Topic Highlight Open Access
Copyright ©The Author(s) 2016. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Feb 14, 2016; 22(6): 1975-2004
Published online Feb 14, 2016. doi: 10.3748/wjg.v22.i6.1975
Laparoscopic and robot-assisted laparoscopic digestive surgery: Present and future directions
Juan C Rodríguez-Sanjuán, Marcos Gómez-Ruiz, Soledad Trugeda-Carrera, Carlos Manuel-Palazuelos, Antonio López-Useros, Manuel Gómez-Fleitas, Department of General Surgery, University Hospital Marqués de Valdecilla, 39008 Santander, Spain
Juan C Rodríguez-Sanjuán, Marcos Gómez-Ruiz, Soledad Trugeda-Carrera, Carlos Manuel-Palazuelos, Antonio López-Useros, Manuel Gómez-Fleitas, Department of Medical and Surgical Sciences, University of Cantabria, 39010 Santander, Spain
Author contributions: All the authors equally contributed to the writing of the manuscript and approved the final version.
Conflict-of-interest statement: The authors declare they have not any conflict of interests.
Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Correspondence to: Juan C Rodríguez-Sanjuán, MD, PhD, Associate Professor, Department of General Surgery, University Hospital Marqués de Valdecilla, Av/ Marqués de Valdecilla S/N, 39008 Santander, Spain. cgdrsj@humv.es
Telephone: +34-94-2203458
Received: April 29, 2015
Peer-review started: May 7, 2015
First decision: June 3, 2015
Revised: June 20, 2015
Accepted: November 30, 2015
Article in press: December 1, 2015
Published online: February 14, 2016
Processing time: 269 Days and 16.3 Hours

Abstract

Laparoscopic surgery is applied today worldwide to most digestive procedures. In some of them, such as cholecystectomy, Nissen’s fundoplication or obesity surgery, laparoscopy has become the standard in practice. In others, such as colon or gastric resection, the laparoscopic approach is frequently used and its usefulness is unquestionable. More complex procedures, such as esophageal, liver or pancreatic resections are, however, more infrequently performed, due to the high grade of skill necessary. As a result, there is less clinical evidence to support its implementation. In the recent years, robot-assisted laparoscopic surgery has been increasingly applied, again with little evidence for comparison with the conventional laparoscopic approach. This review will focus on the complex digestive procedures as well as those whose use in standard practice could be more controversial. Also novel robot-assisted procedures will be updated.

Key Words: Laparoscopy; Robotic surgery; Colectomy; Esophagectomy; Gastrectomy; Obesity surgery; Liver resection; Pancreatectomy; Laparoscopic training

Core tip: Laparoscopic surgery is increasingly used in the treatment of digestive diseases. New procedures are performed and novel technologies are applied. In addition, robot-assisted laparoscopic surgery has appeared as a useful tool for the digestive surgeon. The aim of this paper is to up-date the recent advances and scientific evidence supporting clinical practice.



INTRODUCTION

Laparoscopic surgery has spread worldwide these days and many digestive procedures have become the standard practice. The rapid development in technology and improvement in surgeon skills have allowed that virtually every complex surgical technique, usually performed through open approaches, has been accomplished laparoscopically. Numerous reports favoring this approach have been published recently.

Caution interpreting literature is, however, necessary. There is a risk for selection and publication bias. Selection bias is possible because most favorable (in terms of location, number and tumor size) cases could have been operated on through a laparoscopic approach. Publication bias could also happen, since it is generally recognized a trend to report studies only with good outcomes and those exhibiting significant differences, which can lead to an overestimation of the laparoscopic approach. This publication bias can also be induced by some journal editors, who could prefer to publish papers with positive and spectacular outcomes more than negative and poor results. In addition, most published studies have been performed at large academic institutions by experienced surgeons, which could not reflect the current general practice.

Although feasibility of most laparoscopic procedures in general surgery has been shown, some have concerns about reproducibility, at least for the most complex techniques.

There are also concerns about costs of minimally invasive techniques in the era of cost containment. The advantage could come from shortening hospital stays and possibly diminishing some complications, but the disadvantage is more expensive surgical material and longer operating room times.

All of these considerations can be applied with robotic-assisted surgery, a novel approach applied today in most surgical procedures, and this approach is becoming used more and more.

The scope of this review tries to update most digestive surgical procedures, which precludes a systematic review. Outstanding papers were reviewed, but we especially focused on most of the recent work.

MINIMALLY INVASIVE COLORECTAL SURGERY

Laparoscopic procedures started in 1902 when George Kelling, a German surgeon, used a laparoscope to assess the peritoneal cavity in a dog[1]. This procedure was followed by different studies until 1987 when Mouret in France performed the first video assisted laparoscopic cholecystectomy. In 1993 this technique was established by consensus as the gold standard for the treatment of cholelithiasis[2]. Since then, laparoscopy has been successfully used to perform fundoplications, appendectomies, splenectomies, nephrectomies and a long etcetera.

Colorectal cancer is the second cause of death in western countries[3]. Despite the progress in the different medical treatments and radiotherapy, surgery remains as the only potentially curative approach for this disease. The implementation of laparoscopic surgery in the field of colorectal surgery faced bigger difficulties because of the need of working in a broader surgical field that involved several quadrants, moving apart the small bowel, dissecting the retroperitoneal planes and removing a big sized specimen[4]. Despite all these difficulties, Jacobs et al[5] in 1991 reported the first laparoscopic sigmoidectomy for colon cancer starting a new era for colorectal surgery.

The enthusiasm for laparoscopic colorectal resections for cancer suffered a setback when in 1993 Alexander et al[6] reported the first case of wound recurrence three months after a right colectomy for colon cancer. Tomita et al[4] published their experience in laparoscopic colorectal resections in 1999 reporting a 1% wound recurrence similar to the one reported in open surgery. We have needed more than 20 years in order to have clinical evidence to demonstrate the benefits of laparoscopic surgery over open surgery in the treatment of rectal tumors.

A prospective comparative study performed at the Barcelona Clinic Hospital comparing laparoscopic and open colonic resections with 219 patients with a 98 mo mean follow-up, demonstrated that the laparoscopic surgery group had a faster recovery after surgery and less morbidity with a longer survival and a lower local recurrence rate[7,8].

Several multicentric prospective randomized studies have shown the advantages of laparoscopic colonic surgery in terms of complications, postoperative recovery and oncological safety (COST, COLOR and CLASSIC)[9-11].

There is not yet enough evidence in the case of rectal surgery. The conclusions of many retrospective studies make us think that this approach will have several advantages but solid data is still lacking.

Some studies such as the prospectively performed by Ströhlein et al[12] comparing laparoscopic and open surgery, conclude that the laparoscopic surgery group has the same oncological results, with faster recovery and a shorter hospital stay, finding statistically significant differences in mid and lower rectal tumors. This study presents a high conversion rate of 22%.

Braga et al[13] published a prospective and randomized study with 168 patients comparing open and laparoscopic surgery for rectal cancer with a 5-year follow-up. This study concludes that postoperative morbidity and postoperative stay were significantly lower in the laparoscopic group. Survival and local recurrence were similar in both groups with better scores in the quality of live tests in the laparoscopic group after the first year. Long term costs were similar in both groups. Conversion rate in the laparoscopic group was 7.5%.

In a review of the literature presented by Indar and Efron[14], the results of several prospective randomized trials were analyzed. From this review we can say that laparoscopic rectal surgery is safe, with good results in terms of morbidity, leaks and hospital stay. The conversion rate ranged from 3% to 29%. A higher conversion rate could be due to a lack of experience of the surgeons even though in some studies this rate was not reduced with a progression in the learning curve[15]. The factors associated with conversion in the CLASSIC trial[16] were a high body mass index (BMI), inaccessibility of the tumor, fixation of the tumor, and loss of definition of the surgical planes. Pugliese et al[17] have shown a significant increase in the anastomotic leak rate in the converted cases. Other alarming data is the increase of local recurrence rate up to 16% in those cases converted during laparoscopic surgery for rectal cancer, as shown by Ströhlein et al[12]. Scheidbach et al[18] presented a prospective study with 1409 patients with a 10-year follow-up about the impact of conversion in colorectal laparoscopic surgery. They observed statistically significant differences in terms of a higher blood loss, more postoperative complications, more anastomotic leaks and a decrease of the survival rate in the cases converted to open surgery.

The COREAN Trial was a randomized and prospective study performed by three Korean centers with a wide experience, recruiting 170 patients in the laparoscopic arm and 170 patients in the open group, with a 3-year follow-up. There was a very low conversion rate of 2% maybe because of the huge laparoscopic experience of these centers. There were no statistical difference in the oncological results in both groups and in the surgical specimen quality. The laparoscopic group showed a faster recovery with less need of postoperative pain-killers, a faster recovery of oral intake and a better quality of life 3 years after surgery[19].

In a meta-analysis published by Anderson et al[20] including 1403 cases of laparoscopic rectal surgery and 1577 cases of open rectal surgery, there was no difference in terms of survival or oncological results.

The Finnish trial published by Kellokumpu et al[21] comparing open surgery vs laparoscopic surgery for rectal cancer concluded that the laparoscopic approach offered a faster recovery after surgery, lower blood loss and a shorter in hospital stay with less complications in the long term. Survival and local recurrence were similar in both groups. Conversion rate in the laparoscopic group was up to 22%.

In the cohort retrospective study from Brazil, Melani et al[22] analyzed 84 rectal cancer patients that had undertaken surgery between 2000 and 2003, 50% with a laparoscopic approach and 50% with an open procedure. Follow-up was longer than 5 years in both groups and they found no difference in terms of complications, survival and oncological results. No conversion rate data was provided and the authors admitted a selection bias since the study was not randomized.

Park et al[23] published a comparative study of two groups with mid-low rectal tumors in which they performed ultralow intersphincteric dissection with an open approach vs a laparoscopic approach. Oncological and survival results were similar in both groups after a 3-year follow-up, but the authors concluded that the laparoscopic surgery group had less postoperative morbidity, a shorter hospital stay and a faster functional recovery.

In 2013, the COLOR II trial results after a 3-year follow-up were published. 1103 patients from 30 centers were recruited and randomized either to laparoscopic or open surgery[24]. The authors conclude that the laparoscopic group patients had less blood loss, a shorter time to start bowel movements and a shorter hospital stay, with statistically significant differences. No difference in specimen quality was observed. Postoperative morbidity and mortality were also similar. Conversion rate was 17% even though the surgical teams were selected among centers with experience in laparoscopic colorectal surgery.

In a recently published study[25], the authors analyze data from 3 randomized and controlled trials that compare laparoscopic vs open surgery for rectal cancer. The mean follow up was of 124.5 mo in the laparoscopic group and 136.6 mo in the open group. Disease free survival after a 10-year follow-up were similar in both groups. There was a tendency towards a lower local recurrence in the stage III tumors treated with laparoscopic surgery.

In summary, we can say that laparoscopic colonic surgery is feasible and completely comparable to open surgery, with advantages in postoperative complications and hospital stay. Rectal laparoscopic resection is also feasible and the studies performed to date suggest that short and long-term outcomes are comparable to open surgery.

Robotic colorectal surgery

Despite the advantages of the laparoscopic approach for colorectal surgery, this approach has some limitations such as loss of the 3D vision, limitations in the freedom degrees of the surgical instruments, the amplification of the physiological tremor and the “fulcrum” effect.

The implementation of robotic technology avoids this disadvantages and improves the ergonomics of the surgeon[26]. Uhrich et al[27] proved that the uncomfortable positions during laparoscopic surgery increase surgeons fatigue and iatrogenic injuries.

The development of robotic surgery started in the mid-80s of the 20th century mainly focused in the development of tele-surgery. The FDA approved the use of Da Vinci system (Intuitive Surgical, Sunnyvale, CA, United States) in 2000, and nowadays is the only robotic system available for minimally invasive surgery.

The first article published about robotic colonic surgery using Da Vinci Surgical System was from Weber et al[28] reporting a right colectomy and a sigmoidectomy for benign diseases. At the same time, other authors published their first robotic colonic surgery case reports[29-31].

In 2004, D'Annibale et al[32] reported 53 patients that had undertaken robotic colonic resections. In this group, 22 were resections for oncological reasons. They concluded that the operative and postoperative results were similar to those obtained with conventional laparoscopic instruments. Braumann et al[33] published the first 5 robotic colonic resections performed in Germany in 2005.

Pigazzi et al[34] and Hellan et al[35] published the first article reporting robotic rectal resections in 2006. These authors reported the first series of 39 consecutive resections for rectal cancer, concluding that this technique is safe and feasible.

In Asia, the first robotic rectal surgery with total mesorectal excision was performed by Baik in June 2006[36]. The same author published the first extended resection with hysterectomy[37]. Ng et al[38] reported the first robotic abdominoperineal resection in Hong Kong.

Few data are available regarding the value of robotic colonic resections but the results seem to be similar to those reported by conventional laparoscopic approaches[39]. No final conclusions can be made at this moment.

Robotic rectal resections for rectal cancer

There are not many articles regarding robotic rectal resections in the scientific literature. Hopefully, the ROLARR (Robotic vs Laparoscopic Resection for Rectal cancer) trial results will be available in a few months and will give some valuable information.

Baek et al[40] analyzed the results of 64 rectal resections for cancer with no operative mortality, a mean blood loss of 200 mL, a conversion rate of 9.4% and a leak rate of 7.7%. The mean of harvested lymph nodes was 14.5, the distal margin was 3.4 cm and the circumferential margin was negative in all cases. They found a local recurrence in 6 patients after an interval of 23 mo. The disease free survival rate was 73.7%.

Luca et al[41], performed a study analyzing sexual and urinary function in 74 patients after robotic rectal resections concluding that robotic instrumentation helped to preserve sexual and urinary function after total mesorectal excision.

Biffi et al[42], studied the blood loss during robotic rectal resections and reported that only one case of their series of 49 patients required blood transfusion, by contrast with patients with open surgery who required blood transfusion in 12 cases of 105.

Shiomi et al[43], in a study with 113 consecutive robotic rectal resections, 12 of them having T4 tumors, observed no conversion and no hospital mortality. The frequency of Clavien III/IV complications was 2.7%. They concluded that robotic instrumentation was helpful in performing advanced dissections with a very low morbidity and conversion rates.

Robotic vs laparoscopic surgery for rectal cancer comparative studies

deSouza et al[44] compared the results obtained with robotic surgery in 36 consecutive cases against those obtained in 46 cases with laparoscopic assisted surgery using a hand port for the splenic flexure. The authors conclude that robotic total mesorectal excision is feasible and safe, and comparable with open surgery in terms of perioperative and anatomopathological results. There was a statistically significant difference in the tumor location, with more mid and low rectal tumor in the robotic group.

Kwak et al[45] in another retrospective study concluded that the results of robotic surgery were comparable to those obtained with a laparoscopic group. This study was performed by a single surgeon with a huge experience in minimally invasive surgery for the treatment of rectal cancer. He recognizes a selection bias in this study and concludes that prospective, multicentric and randomized studies are necessary.

A very interesting study from Kang et al[46], compared three groups of patients with mid and low rectal tumors treated with either open, laparoscopic or robotic approach. They observed that the robotic group had a faster postoperative recovery with a lower hospital stay, less pain and better specimen quality. The disease free survival rate was similar in all groups three years after surgery.

Fernandez et al[47], retrospectively compared a group of patients treated with a robotic approach vs a group treated with a laparoscopic approach. They performed a low anterior resection in all cases with low anastomosis. They observed no difference in blood loss, postoperative morbidity or surgical specimen quality but, nevertheless, they recognized that the robotic group had lower tumors with a more advanced disease and more chemo radiation. The conversion rate was 17% in the laparoscopic group and 8% in the robotic group.

Patriti et al[48] performed a study comparing 29 patients with robotic rectal resections against 37 treated with a laparoscopic approach with a one-year follow-up. They obtained similar results in both groups with a higher conversion rate in the laparoscopic group: 7% vs 0%.

Lin et al[49], performed a meta-analysis concluding that robotic surgery is clearly superior in terms of conversion rate. Another meta-analysis of studies comparing robotic vs laparoscopic surgery for rectal cancer performed by Trastulli et al[50] suggested that the robotic surgery group had a statistically significant difference in conversion rate without significant differences in operation time, hospital stay, postoperative morbimortality or surgical specimen quality. The meta-analysis performed by Ortiz-Oshiro et al[51] had similar conclusions.

In the systematic review of the literature performed by Scarpinata and Aly[52] excluding the studies that referred to colonic resections, they suggested that there is evidence that robotic surgery may offer a better short term results, mainly in obese or male patients. It also may be better in those cases with previous radiotherapy and lower tumors. There was no evidence of any difference in terms of leakages, circumferential margins or preservation of the autonomous function.

A study performed by a Taiwanese group[53], compared the postoperative results of 64 patients with ultralow anterior resection and intersphincteric dissection. Twenty-eight patients had undertaken a conventional laparoscopic approach and 36 a robotic approach. They found statistically significant differences in terms of surgical time - longer in the case of robotic surgery - and in the number of definitive stomas, which was 46.4% in the laparoscopic group vs 19.4% in the robotic surgery group. The authors conclude that this kind of procedure is feasible and safe with robotic instrumentation, with better functional outcomes and that surgical time will diminish as the experience of the surgeons increases.

Casillas et al[54], analyzed the results of robotic colorectal surgery performed in a single institution by a single surgeon. They compared 200 laparoscopic cases vs 144 robotic cases. They observed a shorter hospital stay and a lower complication rate in the case of robotic surgery.

Park et al[55], performed a prospective study with 217 patients that undertook minimally invasive surgery for rectal cancer. 133 patients had robotic surgery while 84 had a conventional laparoscopic approach. There were statistically significant differences in favor of the robotic approach in terms of hospital stay and conversion rates (0% vs 7.1%). Overall survival rate and disease free survival rate were similar in both groups with a 5-year follow-up. Saklani et al[56] have reported similar results in a 3-year follow up study.

In a recently published meta-analysis, Xiong et al[57] made a comparative analysis between laparoscopic and robotic rectal surgery in terms of safety and efficacy. They identified 8 studies with an overall number of 1229 patients, 554 robotic cases vs 675 laparoscopic cases. The authors concluded that the robotic approach is safe and feasible, but they did not find statistically significant differences in circumferential margins or in sexual function after surgery.

In summary, rectal robotic excision is feasible and safe, is comparable to laparoscopic surgery in terms of short and long-term outcomes, with some advantages such as shorter hospital stay, lower conversion rates and better functional results. Some particular conditions such as lower rectal tumors, male and/or obese patients or locally advanced rectal tumors may be indications that could benefit the most from the robotic approach.

Robotic colorectal surgery learning curve

The use of robotic instrumentation in rectal surgery requires not only training in surgical technique but also training in the use of the robotic system. This training has the specific handicap of the loss of the tactile feedback. The procedure is performed from a console far from the patient. This requires an excellent coordination between the surgeon and the surgical assistant.

The advantages that robotic technology provides make, for an expert surgeon in open surgery, less necessary the previous training in conventional laparoscopic surgery. The surgeon expert in conventional laparoscopic procedures has to make a specific training in robotic surgery. No differences have been observed in the learning curve for robotic surgery in surgeons with previous training in laparoscopic surgery vs those without that training.

Giulianotti et al[58] observed that the robotic surgery learning curve was short for easy procedures as suture knotting or instrument use. They also observed that the training for advanced surgical procedures required previous experience in open and laparoscopic surgery.

Very few studies analyze the learning curve in robotic surgery. Bokhari et al[59] estimated following the Cumulative Summation (CUSUM) technique that 50 robotic rectal procedures are necessary for a surgeon to be proficient in this procedure. Sng et al[60] have recently published an article reporting a multiphasic learning curve. In the first phase (around 35 initial cases) the surgeon performs selected easy cases. In the second phase, with a worse CUSUM, the surgeon performs more complex cases (to 100 cases). Finally the surgeon enters in a consolidation phase.

Buchs et al[61] have reported that the learning curve can be reduced using simulation in an animal/cadaver model or through the visualization of video clips or attending to courses.

In a recent study, Byrn et al[62] compared their initial 43 robotic rectal surgery cases with the following 42 cases observing a significant reduction of surgical time and costs.

Other considerations concerning training are made at the end of the paper.

Cost-effectiveness studies

One of the most criticized aspects of robotic colorectal surgery is the increase of cost per procedure. Cost analysis may vary depending on the criteria we use and the items we analyze. Rectal cancer process is very long and the analysis of costs of this process may vary a lot if we analyze just the perioperative period or a 5-year period including stoma cost, quality of life or local recurrence. The cost analysis also varies a lot depending on the health care system characteristics. There are not yet high quality articles that are conclusive about the cost issue.

Delaney et al[63] reported a significant increase of in-hospital costs with robotic colorectal surgery: 2946 dollars per laparoscopic procedure vs 3721.5 dollars per robotic resection. This increase was mainly attributed to the increase in intraoperative costs.

However Rawlings et al[64] did not find any statistically significant difference when they analyzed intraoperative, staff and surgical time costs.

Park et al[55] compared robotic with laparoscopic rectal cases with 150 laparoscopic rectal cases and concluded that the robotic approach increased the perioperative costs. These authors recommended cost effectiveness studies including long-term results, oncological results and functional outcomes. Bodner et al[65] have reported similar results.

MINIMALLY INVASIVE ESOPHAGECTOMY

The esophageal cancer frequency - mainly adenocarcinoma - is increasing worldwide, presently being the 8th in the incidence ranking and 6th in mortality[66].

For patients with advanced loco-regional disease (T2-T4a and N +, stages II and III), controlled randomized trials and a large meta-analysis have shown a clear benefit in disease-free survival in patients treated with chemo-radiotherapy and surgery[67]. However, esophagectomy is one of the most complex procedures of the gastro-intestinal surgery, with a high postoperative morbidity and mortality, mainly of respiratory origin[68]. The potential advantages of minimally invasive procedures, especially regarding a decrease in pulmonary complications, have been studied for the last 4 decades[69]. Minimally invasive esophagectomy (MIE) includes conventional pure laparoscopy/thoracoscopy, hybrid procedures (celiotomy/thoracotomy; celiotomy/thoracoscopy), hand-assisted surgery and, more recently, robot-assisted esophagectomy.

The first thoracoscopic esophagectomy was performed in 1992 by Cuschieri[70]. Later, other experiences have been published: some reporting less than 5 cases of MIE Ivor Lewis each[71], larger series of three-field esophagectomy -McKeown technique such as that of Luketich et al[72] in 2003 with 222 patients, that of Palanivelu et al[73] in 2006 with 130 cases or others including hybrid procedures[74]. Three meta-analysis have compared MIE with open esophagectomy and find a benefit of MIE in a hospital stay, respiratory complications and overall morbidity[75-77]. Current evidences suggest that MIE is a feasible and safe technique with benefits in the short term. As a result, indications have been expanded from the Barrett’s esophagus with high grade dysplasia to locally advanced tumors after neoadjuvant therapy, which are also the indications of open esophagectomy[74]. Some aspects such as oncological outcomes, anastomosis location or patient positioning are, however, controversial. There are to date only a few works reporting long-term oncological outcomes and they have a short follow-up and a small number of patients, but they have failed, up to now, to show benefits by comparison with open esophagectomy[78,79]. Probably, because of this, and despite the MIE procedures increasing, today only 30% of esophagectomies are performed worldwide through minimally invasive approaches, with 20% in 2009 in Japan or 19% in the United Kingdom in the last 8 years[80-82].

Patient positioning influences the MIE technique. In the MIE as well as in the open technique, the left lateral decubitus has been more frequently used, although the prone decubitus is now been increasingly used. In 2012, the first controlled randomized trial analyzing this position was published[83]. Fifty-nine MIE patients who were operated on in prone decubitus were compared with 56 patients treated by esophagectomy through a thoracotomy in semi lateral left decubitus. A significant decrease in respiratory complications in the MIE group was found by comparison with the open group (9% vs 29%). It is not clear whether the benefits are due to the position or the minimally invasive approach or, more probably, a combination of both. However, recent studies comparing both positions[84,85] show that the prone decubitus provides some advantages such as better oxygenation and exposition of the surgical field, which lead to improved postoperative outcomes. As a result, the prone decubitus is being increasingly used.

Regarding the anastomosis location, the McKeown technique with cervical anastomosis, using thoracoscopy only for the esophageal mobilization, has been the most used procedure to date since a lower skill is needed by comparison with the intrathoracic anastomosis. However, the McKeown technique is associated with high complication rates such as recurrent laryngeal nerve injury, and anastomosis leak. As a result, there is a tendency to perform more intrathoracic anastomoses. In 2012 a large series of 1000 MIE patients compared 481 cases treated by the McKeown technique with 530 with the Ivor Lewis procedure[86]. The outcomes in both groups were similar with low mortality rate and a similar number of retrieved lymph nodes, but the authors concluded that Ivor Lewis MIE is preferable because a lower frequency of recurrent laryngeal nerve injury and a mortality rate of 0.9%, not higher than that of McKeown. Similar outcomes were found in another study from 2014 comparing 103 Ivor Lewis MIE with 185 McKeown MIE[87], with significantly better results found in the first group: overall morbidity (16.5% vs 31.4%), respiratory complications (8.7% vs 25.9%), anastomosis leak (1.9% vs 13%), anastomosis stenosis (0% vs 4.9%), and recurrent laryngeal nerve injury (1% vs 7.0%).

Nevertheless, intrathoracic anastomosis in difficult to do through a minimally invasive approach, so there is a limited number of papers reporting more than 50 cases each in the last 2 years[88-92].

Robot-assisted esophagectomy

Some limitations of the MIE can be overcome by the aid of the robotic systems, which provide some advantages such as a tridimensional view of a field selected for the surgeon instead of the assistant-, the 7 degrees of freedom allowing movements similar to open surgery, the tremor suppression resulting in a better precision, and a better ergonomics which leads to less surgeon fatigue. All of these advantages are even greater in small surgical fields, with few instrument exchanges as the thoracic phase of an esophagectomy is.

The first robot-assisted MIE using the Da Vinci system was published by Kernstine et al[93] in 2004. A few short series, between 6 and 47 cases, have been reported since then, always with cervical anastomosis[94-99]. The first robot-assisted Ivor Lewis series were published from 2013 to now, reporting 22[100], 17[101], and 50[102] cases, respectively, all with the patient in lateral decubitus. In 2014 our group published the first series of robot-assisted Ivor Lewis in prone decubitus with intrathoracic manual anastomosis[103]. We feel that the prone position makes the dissection and lymphadenectomy easier, in an optimal field. We had no respiratory complication in 39 cases, although a stapled anastomosis, either transthoracic or transoral, is more difficult. The robotic assistance makes a manual intrathoracic anastomosis easier and allowed us to use the prone position and its potential advantages without flawing short and long-term oncological outcomes, as we recently reported in a series of 21 cases[104].

Despite these potential advantages, the evidence to show any possible superiority of the robot-assisted MIE over either open esophagectomy or conventional thoracoscopic esophagectomy is still very limited. Since 2012 a single center controlled randomized trial has been ongoing in the Netherlands to compare the robot-assisted and open esophagectomy[105], with a recruitment prevision of 112 patients - 56 per arm and a follow-up of 5 years. However, for stronger evidence, multicentric trials with a large number of patients is needed.

MINIMALLY INVASIVE GASTRECTOMY

Gastric cancer incidence is decreasing but is still fourth in the world ranking and accounts for 10% of the overall cancer deaths. There are wide geographic variations, not only in incidence but in their clinical features also. Fifty percent of world cases are diagnosed in Asia and it is the most common cancer in South Korea[106]. In the western world there is a trend for tumors to be advanced at diagnosis, to locate more proximally, to be histologically diffuse, and the patients tend to be older - 10 years more on average, to have an increased body mass index and more comorbidities[107]. Because of these differences, two classification systems have been developed - the Japanese Gastric Cancer Association (JGCA) and the Union for International Cancer Control (UICC/TNM)[108,109]. Also, different concepts concerning the optimal surgery, the reconstruction type and the minimally invasive surgery implementation have arisen between the West and the East. Fortunately, unification of the classification systems and approximation of the lymphadenectomy extent have been achieved in the last decade. As a result, the D2 lymphadenectomy has been implemented in the West[110,111] and in the East now is accepted that no more than a D2 lymphadenectomy is mandatory[112].

The same as in other procedures, minimally invasive gastrectomy (MIG) in case of cancer could show some advantages. These techniques were pioneered by Kitano et al[113] in 1992 with a laparoscopic -assisted gastrectomy. Since then, the development has been determined, not only by the tumor features - location and stage, but also by the above mentioned differences between the West and the East. In general, the high incidence or early tumors in the East led to 7341 distal and 1103 total laparoscopic gastrectomies in 2009 in Japan, and 3783 laparoscopic procedures in South Korea, in contrast with 245 in Spain between 2005 and 2008 and 133 in the United Kingdom between 2011 and 2012[114].

Laparoscopic distal gastrectomy

For tumors in early stage and distal location, literature is profuse in retrospective studies, case series and comparative studies but there are seldom randomized controlled trials (RCTs) comparing Laparoscopic distal gastrectomy (LDG) with open gastrectomy and they have a limited case number[115-122]. Despite the limitations, LDG appears to have advantages over open gastrectomy in terms of postoperative pain, recovery of gastrointestinal and pulmonary function, hospital stay and return to normal activity. The complexity of a proper lymphadenectomy - especially if a D2 is mandatory, and the concerns about oncological safety has slowed down its generalization[123].

Additional evidence has been provided by several meta-analysis[124-127], some of them with more than 3000 patients including advanced stages[128-131] and the most recent with 2144 cases[132]. All coincide in the LDG perioperative advantages - blood losses, overall morbidity, hospital stay - and that oncological results are not inferior to those of open surgery, although more operative time is spent.

Currently two multicentric phase III RCTs are ongoing, one from the Japan Clinical Oncology Group[133] and another from the Korean Laparoendoscopic Gastrointestinal Surgery[134]. The joined recruitment prevision is more than 2300 patients and the results are expected for 2015.

At the moment, and after the international expert group meeting, the LDG is accepted for distal tumors cT1-2 cN0 and the laparoscopic total gastrectomy (LTG) for proximal tumors cT1 cN0, although no consensus was achieved for other stages[135].

Literature data concerning LDG in locally advanced tumors (stage II and III) are even scantier. Only two RCTs have compared MIG and open gastrectomy[136,137]. Two meta-analysis, have been published: the first included 7 studies with 174 laparoscopic and 278 open gastrectomies[138], and the second analyzed 10 studies with 495 laparoscopic and 544 open gastrectomies, both with D2 lymphadenectomy[139]. Both coincide in that the minimally invasive approach in advanced gastric cancer is associated with a longer operative time, but less blood losses, pain, postoperative complications and hospital stay. Similar lymph node number and overall survival were found in the two approaches.

A recently published phase II prospective clinical trial with 157 patients concluded that laparoscopic gastrectomy with D2 lymphadenectomy for advanced gastric cancer is technically feasible and safe, with acceptable morbidity and mortality rates[140].

More high quality RCTs comparing open and laparoscopic gastrectomy are needed, as well as multicentric studies. Even so, some aspects will probably not able to be applied to the West due to the above mentioned clinical and histological differences.

Laparoscopic total gastrectomy

The Laparoscopic total gastrectomy (LTG) spreading has been slower worldwide, even in Korea and Japan, due to the need of an esophagogastric anastomosis, which is technically demanding, and because of the low incidence of the proximal gastric cancer in the East. The first relatively large series appeared in 2009, such as that of Shinohara et al[141] with 57 patients or the multicentric study from South Korea by Jeong et al[142] of 131 laparoscopic-assisted total gastrectomies. Both conclude that LTG is feasible and safe - morbidity of 31% and 19%, respectively with no mortality, it is possible to retrieve sufficient lymph nodes - 46 and 35, respectively - although with long operative times - 4.5 h on average.

In the West, the European pioneer groups in this field, such as Dulucq et al[143] or Huscher et al[144] published a series of only 8 and 11 LTG, respectively. In 2013, a specialized center, the MSKCC published a series of 17 cases[145].

Three recent meta-analysis[146-148] also suggest that, in skilled hands, LTG has better perioperative outcomes than the open procedure in terms of blood losses, pain, resumption of oral intake, hospital stay, with no inferiority concerning lymph node retrieved and survival. However, the operative times are longer.

A phase II multicentric prospective trial (KLASS-03) in patients with stage I gastric cancer is currently ongoing, with the aim of assessing perioperative morbidity and mortality of LTG by comparison with the open procedure[149].

Robot-assisted gastrectomy

The main advantages of the robotic systems have already been discussed. In the case of gastric cancer, these potential advantages lie in a better precision for the lymphadenectomy and an improved skill for intracorporeal anastomosis[150]. Hashizume et al[151] published the first Robot-assisted gastrectomy (RAG) in 2002, but because the procedure is technically complex and the equipment is expensive, the spreading has been slow. Several groups have compared the RAG with the laparoscopic and open techniques. The Yonsei University group published in 2009 the initial experience with 100 patients, extended to 236 cases more (73% subtotal and 27% total) in 2011 of RAG compared with 591 laparoscopic (81% subtotal and 19% total). They concluded that RAG seems to have better short-term results with comparable oncological outcomes[152,153]. Other published series until 2012 support these conclusions, although the largest one reports less than 40 cases[154,155]. The first meta-analysis, also from 2012, compared 268 RAG with 650 laparoscopic gastrectomies[156]. Significant differences were not found in overall morbidity, hospital stay, or number of lymph nodes retrieved.

Interesting, to make the most of the benefits of the robotic assistance, the morbidity due to anastomotic leak must be minimal. A study analyzing postoperative complications in 5839 patients (4542 open, 861 laparoscopic and 436 robotic gastrectomies) concluded that, even in expert hands, minimally invasive techniques are associated with an increased risk of anastomotic leak by comparison with open gastrectomy, although the overall morbidity and mortality rates were similar[157].

Since 2012, seven new meta-analysis have been published, analyzing between 404 and 762 RAG patients[158-164]. All concluded that RAG was associated with lower blood loss and shorter hospital stay, with an adequate lymphadenectomy, by comparison with the laparoscopic and open gastrectomy, although with longer operative times.

More high quality studies are needed to clearly define the role of RAG.

MINIMALLY INVASIVE BARIATRIC SURGERY

Obesity is a world health problem of epidemic dimension in western countries[165,166]. A WHO report estimates that more than 1600 million people are overweight and 400 million people have frank obesity[167]. The increase in obesity prevalence is associated with a rise in the associated disease prevalence such as diabetes mellitus, hypertension, hyperlipidemia, obstructive sleep apnea, cardiovascular and pulmonary disorders, some tumors, osteoarticular disorders, and depression[167,168]. Life expectancy of obese patient is approximately reduced by 12 years[167]. Bariatric surgery has been shown to be the most effective treatment to achieve significant and sustained weight loss[169-173] and also improves every cardiovascular risk factor, with the exception of the hypercholesterolemia[174]. These comorbidities lead to an increased consumption of health resources, and as a result, to increased costs of obesity treatment.

The therapy of this disorder includes both medical and surgical treatment. The former is based on a multidisciplinary approach with the participation of endocrinologists, dieticians and psychologists. The aim is to achieve a change in the life style, promoting physical exercise and healthy nutritional habits with the support of multiple drugs of limited efficacy[175,176]. The current surgical techniques can be divided into restrictive (adjustable gastric banding and sleeve gastrectomy), malabsorptive (biliopancreatic diversion) and mixed (gastric bypass)[177,178]. Since 1993, these techniques are being increasingly performed laparoscopically with preference over the open approach[179]. Laparoscopy in obesity surgery offers several advantages: less pain, lower frequency of wound infection and incisional hernia, less postoperative complications, shorter hospital stay, faster recovery and better cosmetic results[180]. Several early studies on vertical banding gastroplasty[181], adjusted gastric banding[182], and Roux-en-Y gastric bypass[183-186], support some of these advantages, although the mortality rate did not decrease, probably because of the limited number of cases in each series. Later, several reviews[187,188], including the 2009 Cochrane study, compared laparoscopic and open surgery, but no statistically significant difference was found regarding mortality, morbidity, reoperations or weight loss.

Two reviews of observational studies conclude that the frequency of incisional hernia and wound infection are lower in laparoscopic surgery, although lacking a direct comparison with open procedures. The systematic review by Reoch et al[180] analyzed 6 randomized studies including 510 patients with a minimum follow-up of 12 mo. The risks of reoperation, wound infection, incisional hernia, anastomotic leak and cause of death were studied. They found that in the laparoscopically treated patients a 75% and 89% decrease of wound infection and incisional hernia risk, respectively. The risk of reoperation, anastomotic leak, and death cause were, nevertheless, similar in the laparoscopic and open surgery groups. Another review of 361 studies including 85048 patients[189] analyzed the 30 d mortality and found a 0.28% rate for biliopancreatic diversion and duodenal switch and 1% for revisional surgery.

The restrictive procedures are associated with lower mortality rates than the mixed techniques, and the malabsorptive procedures have the highest mortality. In the meta-analysis by Buchwald et al[189] a higher mortality is found in open surgery by comparison with the laparoscopic procedures, with the exception of BPD/DS. Higher complication rate has, however, been reported in laparoscopic cases[190]. Flum et al[191] published a population-based study of Medicare beneficiaries and found a laparoscopic surgery mortality at 30 d, 90 d and 1 year of 2%, 2.8% and 4.6%, respectively as well as higher mortality for individuals older than 65 years.

Morino et al[192] studied the mortality risk factors of several bariatric procedures, such as gastric bypass, banding gastroplasty, adjusted gastric banding, biliopancreatic diversion, biliointestinal diversion and other procedures in a 13871 patient retrospective analysis. They concluded that the laparoscopic approach significantly reduces the mortality risk, and the surgical technique, the open approach, a prolonged operative time, associated comorbidities and the surgeon experience increased the risk.

Mortality associated to laparoscopic bariatric procedures has been shown to be lower in centres with more than 100 cases per year (0.3%) than in those with less than 100 (1.2%)[193].

In summary, the laparoscopic approach significantly reduces the overall mortality risk, since the hazard of thromboembolism as well as other complications decreases by comparison with open surgery. However the evidence level of long term outcomes of most review studies are low since many patients are lost to follow-up in many series.

Robot-assisted bariatric surgery

Robot-assisted bariatric surgery (RABS) has been used since 1998, when a gastric band was put from the distance[194], and shows some advantages over the laparoscopic techniques, which have some limitations related with a poor ergonomics due to a limited instrument mobility due to the abdominal wall width, and hepatomegaly. RABS suppresses the position port limitation as well as the physiological tremor and confers a better ergonomics[195]. The three dimensional view allows a more precise dissection[196] and a decrease in blood loss. A shorter learning curve by comparison with conventional laparoscopy has been claimed[197].

Several studies report that RABS is safe with lower complications than the laparoscopic techniques. Edelson et al[198] compared 287 robotic and 120 laparoscopic gastric banding cases, and they did not find any significant difference in intraoperative or postoperative complications, hospital stay or operative time; the time was, however, significantly lower in patients with a BMI > 50 kg/m2 operated on through a robotic approach (91 min vs 103 min). Fourman et al[199] reported similar findings in a literature review of RABS which included gastric banding.

The gastric bypass has been used since 2000, with satisfactory outcomes[200]. Lower complication rates than those of the laparoscopic approach, without mortality or anastomotic leaks have been published[199,201-205]. Others also report significantly less anastomotic failures with RABS[206]. Skilled teams have achieved similar operative times and even shorter[199,206,207], with comparable long-term results concerning weight loss and comorbidity improvement.

In a review of 1686 patients comparing laparoscopic and robotic bypass, similar results were found regarding anastomotic leaks, postoperative complications, operative time and hospital stay[208]. However, an advantage was found in a decrease of the anastomosis stenosis rate at 6 mo. Most groups coincide in that anastomosis leak is lower with RABS, although without reaching statistical significance.

The vertical gastrectomy or sleeve gastrectomy (SG) has become in one of the most popular bariatric procedures due to its effectiveness in reducing weight. Overweight losses as high as 61% after 24 mo have been reported[209], as well as comorbidity improvement such as diabetes resolution in 47%-66%[210,211]. Other advantage are the lower operative time needed, the shorter hospital stay and the lower frequency of complications, by comparison with the laparoscopic GB. Since the use of robotic surgery has been limited to the most complex procedures - revisional surgery and gastric bypass, there are only a few studies on SG[199,211-217] which do not show any significant difference concerning complication frequency - stenosis, bleeding-, mortality or hospital stay. One study reports a lower fistula frequency and a shorter stay in the robotic cases, but without statistical significance[218]. This technique, when performed with robot assistance, is associated with longer operative times and is more expensive, and thus is controversial its generalized use. However, it is proposed as a way to learn robotic skills before performing the gastric bypass.

The Scopinaro biliopancreatic diversion (BPD) and the biliopancreatic bypass with duodenal switch (DS) are more effective than the gastric bypass in achieving weight loss and improvement of obesity associated comorbidities[219,220] but due to their complexity, higher complication rates and the need of nutritional control, are the least used. The first results of these procedures performed through a laparoscopic approach were published by Ren et al[221] in 2000, with a 2.5% mortality. In a systematic review, a 30-d mortality of 0.1% for restrictive procedures, 0.5% for gastric bypass and 1.1% for BPB/DS were reported 59. Sudan et al[222] reported a series of 59 robotic BPB/DS without mortality, anastomotic leaks, bleeding, sepsis or pulmonary thromboembolism.

The main criticism to RABS is its high cost, as well as the longer operative time, especially because of the preoperative docking time needed. This however, can be minimized with increasing experience of the surgical team.

LIVER SURGERY

Nowadays, laparoscopic resection is increasingly being performed for both benign and malignant liver lesions. This review will focus on the latter.

There are several options to perform a laparoscopic liver resection (LLR): totally laparoscopic, hand-assisted and hybrid resection. In the latter, the liver is mobilized laparoscopically, with the hilar dissection and parenchymal division performed through an abdominal incision, usually epigastric as described by Koffron et al[223]. Hand-assisted laparoscopy and the hybrid technique have been recommended as a bridge to the totally laparoscopic technique as the first steps of surgeons not familiar with complex laparoscopic procedures[224]. There is not sufficient data supporting the superiority of any technique over the other in terms of operative time, blood losses or complication rates[225].

Every type or liver resection has been performed: from non-anatomic resection to segmentectomy or right lobectomy, removing from one tumor node to multiple nodes[226]. Pedicle control can be done, the same as in open surgery, in order to minimize bleeding.

Laparoscopic liver surgery is associated with some potential benefits by comparison with the open technique. There is a better view due to magnification and favorable vision angles. This is the case of the adrenal glands and the area around the inferior vena cava, since these structures are located on the dorsal side of the liver and are best seen by a laparoscope inserted through the umbilicus[227]. There is also less bleeding with less transfusion needs, as most papers show[226], explained in part by the laparoscopic magnification, and decreased venous oozing from the cut surface under pneumoperitoneum[227]. Another explanation is a longer portal clamping time by comparison with open surgery, as reported in some works[228], although this is not seen in others[226]. The lower analgesia requirements are due to less postoperative pain[228]. A lower frequency of postoperative complications has been claimed; several papers have reported a trend to decreased complications rates, although without significant differences[229-232]. Particularly, a lower overall incidence of pulmonary complications has been reported[233]. A recent published metaanalysis reports a significant decrease in the complication rate of laparoscopic cases[226], but other studies find similar complications in laparoscopic and open groups[228]. Other advantages are shorter in - hospital stays - due to less pain and less complications-, better cosmetic results. Lower frequency of incisional hernia. Further resections, if necessary, or even salvage transplantation in the case of hepatocellular carcinoma (HCC) are probably easier and this could increase the re-resection rates. All of this without compromising the oncologic aims as free borders (R0 resection)[228]. Increased liver regeneration has been reported in living donor patients operated by laparoscopy by comparison with open procedures[234]. Although the reason is unclear and these findings have to be confirmed, the diminished acute-phase stress response and improved immune system function reported after laparoscopic surgery could explain this in part.

There are however some concerns regarding the laparoscopic technique. The first is the problem of venous gas embolism[230]. Since the pneumoperitoneum rises intrabdominal pressure, an increased risk of CO2 embolism is possible, although because of its greater solubility than nitrogen, it is much safer. Also, the use of argon beam coagulation could increase the risk of argon gas embolism. As a result, some authors recommend its avoidance or extremely cautious use[224], only over minor bleeding points and opening one port to allow venting excessive gas pressure. Concerns also remain regarding the oncologic adequacy of LLR compared with open liver resection as well as failure to detect occult lesions, which is especially important in the case of metastases. This will be discussed later. There is a potential risk of tumor dissemination (port metastasis, peritoneal carcinomatosis). In case of major bleeding, the restriction on movements make the suture difficult[227], leading to important risks. On the other hand, laparoscopic procedures might result in additional hospital costs due to the need for laparoscopic instrumentation, and possibly longer operative times. However, these costs can be offset by shorter lengths of stay. Estimates of costs in some centers find that the laparoscopic approach is not associated with higher costs[230].

The advent of minimally invasive liver surgery could result in overuse of these procedures. Some authors have stated with caution that laparoscopic procedures could lead to their use in cases where surgery is not indicated and therefore that laparoscopic procedures should only be used when an open procedure is clearly indicated. However, some authors argue that in some cases, especially when faced with diagnostic and therapeutic dilemmas, laparoscopic procedures might be considered instead of conservative nonsurgical management[231].

Most published papers report case series of laparoscopic resections, usually comprising a small number of patients. To date there are no published randomized clinical trials. In addition, few works have reported comparisons with open resection. This is probably due to the difficulty of putting together a team skilled in both advanced laparoscopic and open hepatic surgery.

Conversion rates are variable. The reasons are oncological, bleeding, strong adhesions due to previous surgery and no progression for anatomical reasons.

Transection methods are variable but any energy device or staplers can be used. For deeper transection, an ultrasonic aspirator (CUSA or equivalent) or the clamp-crushing technique can be used[224].

Indications for LLR are the same as those of open surgery: large and symptomatic benign lesions, diagnostic concerns and, especially malignant tumors. The latter comprise any type of malignancy, but most frequently, colo-rectal metastases, HCC and cholangiocarcinoma. Our discussion will be focused on the malignant lesions.

Recently, the Second International Consensus Conference published their recommendations for LLR. They found these were not inferior to open resection in mortality, postoperative complications, margin negativity, overall survival, and costs. Laparoscopy was superior in length of stay. Also, technical recommendations were provided. They state that minor LLR (less than 3 segments) is “confirmed to be a standard practice in surgery but is still in an assessment phase”. They also state that “major LLR is an innovative procedure and is still in an exploration or learning phase and has incompletely defined risks”[224].

LIVER METASTASES

When several years ago laparoscopic LLR began, some concerns regarding liver metastasis resections arose: will free margins can be achieved? Will small metastases be found[235]? No trials comparing open and laparoscopic metastasis resection were available in 2009 when the few available studies reported an 80%-87% 3-year overall survival[235]. Nowadays we have some studies which allow comparing several aspects of open and laparoscopic surgery.

As mentioned above for liver resections in general, most published papers concerning metastasis reports a negligible or nihil mortality with a trend to a lower complication rate in laparoscopic series[226,232], although this is not seen in other works[229,236]. Also, the bleeding and transfusion needs are significantly lower than in open surgery[226,229,237-239].

The mean operation time ranges from 180 to 377 min - depending on the resection extent - which is similar to the time spent in open resections[226,229,237-239].

The length of stay ranges from 3.7 to 7.3 d[226,229,237-239] and 18.3 in a study from Japan[230] but is significantly shorter in laparoscopic resections in all of them.

Concerning oncologic outcomes, the papers report R0 resection rates ranging 82.7%-100%, not different from those obtained in open resections[226,229,232]. The long-term outcomes - overall and disease-free survival - are also similar. The 5-year overall survival rate found in the metaanalysis by Schiffman et al[226] is 51.4%, although rates as high as 76% have been reported[226]. In addition, non-significant differences have been found when compared with survival after open procedures[226,229,232,237]. Importantly, no significant difference between laparoscopic and open resections disease-free survival has been found[226,237], reflecting that no missed metastasis was left behind after laparoscopic procedures.

HCC

Resection is the usual therapy for HCC in non-cirrhotic patients. However, most cases in the western world arise in cirrhotic patients. This implies to deal with a liver with some functional impairment as well as more fibrotic tissues. Current guidelines recommend resection only in solitary tumors when portal hypertension has been excluded and serum bilirubin is normal[240]. Although the best candidates are those patients with tumors up to 5 cm of diameter, resection in bigger tumors is also acceptable[240]. Anatomic resections are recommended because of its better survival rate than wedge resections[230,240].

In 2007 some benefits - reduced blood losses and morbidity in cirrhotic patients as compared with open resections, especially with lower frequency of postoperative ascites - were already recognized for the laparoscopic approach[241]. The possible benefits of laparoscopy in cirrhotic patients can be due to preservation of the abdominal wall and round ligament, which avoids interruption of collateral circulation and, therefore, preventing a rise in portal pressure; less mobilization and manipulation of the liver which reduces liver trauma; avoidance of exposure of the abdominal viscera, which allows to restrict fluid requirements and decreases electrolytic and protein losses; and by reduction of intraoperative blood losses.

A recent metaanalysis of studies dealing with HCC in both cirrhotic and non-cirrhotic patients found lower rates of bleeding and transfusion requirements in laparoscopic resections, by comparison with open procedures[242]. There were no significant differences in operation time. Concerning complications, lower rates of postoperative ascites and liver insufficiency were found. However, the frequency of other complications such as bile leakage, postoperative bleeding, intra-abdominal abscess, and mortality was similar[242,243]. These results ought to be interpreted cautiously since not all the analyzed patients were cirrhotic. The length of hospital stay appeared to be similar after both approaches[242].

Concerning oncologic results, significant differences in free margin rates have not been found[242], although in a non-randomized study it was significantly higher in LLR than in open surgery[244]. Both overall and disease-free survival have been shown to be similar in cirrhotic patients[242-244]. Also, tumor recurrence seemed similar[242-244].

As a result, LLR for hepatocellular carcinoma appears feasible and safe both in cirrhotic and non-cirrhotic patients, provided the functional status of the latter is acceptable. Also, oncologic long-term results are not inferior to those of open surgery.

CHOLANGIOCARCINOMA

Laparoscopy can be used in cholangiocarcinoma both for staging work-up and for therapy.

Cholangiocarcinoma (CC) has considerable rates of unresectability due to the common invasion of vessels, secondary and tertiary biliary duct divisions, presence of distant lymph node metastases and peritoneal metastases. Staging laparoscopy (SL), often combined with ultrasound, detects many of this settings, therefore avoiding unnecessary laparotomies and has been used with staging purposes for many years. The usefulness appears to have decreased considering reports from 2002 and from 2011, showing a drop both in efficacy (41.8% to 14%) and accuracy (72% to 32%)[245]. This decrease can be explained by the continuous improvement in imaging techniques which detect today minimal disease. As a result, today the most extended opinion is that SL only is indicated in case of concerns of unresectable disease on imaging techniques or in patients with high risk of holding it, as T2/T3 cases of the Jarnagin-Blumgart staging system are[246].

On the other hand, experience with laparoscopic treatment of CC is short, with most papers reporting only a few cases of laparoscopic[247,248] or robot-assisted laparoscopic treatment[249]. Two case series report 14 cases each. Yu et al[250] treated 8 Bismuth I tumors by local excision and 6 Bismuth II cases by partial hepatectomy. The R0 resection rate was 100% in the former but only 60% in the latter. Importantly, they do not perform caudate lobe excision. Overall, there was no mortality and there was 35.7% of biliary fistula. They report two tumor recurrences. Gumbs et al[251] report a multicenter experience of 9 intrahepatic and 5 perihilar CC. The former were treated by partial hepatectomy as well as 3 of the perihilar tumors, with a conversion rates of 11% and 20%, respectively. No caudate lobe resection was carried out. The R0 resection rate was 77.7% in the intrahepatic and 80% in the perihilar CC. In the intrahepatic CC the mortality and morbidity rates were 11% and 33%, respectively, whereas in the perihilar CC there was no mortality or complications. The survival rates were 66.6% at 22 mo in the intrahepatic and 100% at 10 mo in the perihilar CC.

Concerning robot-assisted surgery, there is an anecdotal published case of hilar CC treated by extended right hepatectomy and bile duct excision[249]. They had free margins with no complications.

This scanty experience allow us to conclude that laparoscopic treatment of CC is feasible and that the rates of mortality, morbidity and survival are comparable to the open surgical procedures.

In the absence or randomized control trials is difficult to reach any conclusion concerning superiority of laparoscopic over open resection. For the moment, only clinical data mainly coming from case series performed in highly specialized centers show comparable oncological results and some advantages in hospital stay.

LIVING-DONOR LIVER TRANSPLANT

Right lobe living donor liver transplantation is the usual way of adult-to-adult live liver transplantation. Laparoscopic approach for liver procurement has been used in a few reports. The procedure has been performed as totally laparoscopic right or left hepatectomy[252-257] and laparoscopically assisted using a hand port system[256,257]. Also, the hybrid technique has been performed[256] because some authors claim a shortening in the prolonged operative times of the procedure with this technique[256]. The reported donor outcomes were satisfactory with low complication rates -most of them minor- and without mortality[252-257].

Some studies have compared the laparoscopic and open techniques. Baker et al[234] studied donor right hepatectomies and found in the donor similar rates of complications, estimated blood losses, and hospital stays, as well as shorter operative times and higher liver regeneration volumes in the laparoscopic group. Kim et al[258] studied left lateral sectionectomies and found a significantly shorter hospital stay and time to oral diet in the laparoscopic group. Duration of operation, blood loss, warm ischemia time and complications were comparable, with no deaths in any group.

In summary, every liver resection procedure seems safely feasible through a laparoscopic approach provided the surgeon has proper training in both complex laparoscopic and liver procedures. The learning curve for this training has been estimated in 60 cases[259]. Short and long-term results for metastases and hepatocellular carcinoma are as good as in open procedures, with shorter in-hospital stay and a trend for less complications and intraoperative bleeding. The Second International Consensus Conference considers that there are insufficient evidence from few centers to give any recommendation[224].

ROBOTIC HEPATECTOMY

Theoretical advantages of robotic over laparoscopic hepatectomy are increased freedom degrees of the instrument movements, abolition of the physiologic hand tremor and 3-dimensional view. Also easier suture ligation for vessel control rather than stapling has been claimed as well as easier retrohepatic dissection thus facilitating access to the hepatic veins[260,261]. Intracorporeal suturing and tying in difficult locations can also be facilitated by the robotic technology.

Among the disadvantages of robotic hepatectomy are the longer times required to dock the robot, to exchange instruments, and to reposition or redock the instruments if the viewing field has to be changed. Also, the lack of tactile sensation when suturing and knot tying might lead to injury due to uncontrolled tissue overstretching or suture disruption[262].

Although the published experience on robotic hepatectomy is scanty, Ho et al[262] published a systematic review in 2013 comprising data of more than 200 patients. The procedures performed included wedge resection, segmentectomy, right and left hepatectomy and left lateral segmentectomy for both benign and malignant diseases. A right live donor hepatectomy was also done. The conversion rate was 4.6%. Mean operation time was variable, ranging 200 to 507 min. The morbidity rate was 20.3%, with bile collections and abdominal abscess being the most frequent complications. No mortality has been reported. It can be concluded that robotic liver resection is safe and feasible when performed by experienced surgeons.

Because of the relatively short follow-up, results concerning cancer-specific survival are scanty and most papers only report some recurrence cases. As a result it is too early to draw any conclusion concerning oncological results.

Some studies comparing robotic vs laparoscopic hepatectomy in both benign and malignant lesions have been published.

Ji et al[261] showed that robotic hepatectomy is safe and feasible, with slightly lower complication and conversion rates than traditional laparoscopic and open resections. However, longer operative times and hospital stays were found by comparison with laparoscopic procedures, as well as increased costs. On the other hand, Berber et al[263] did not find significant differences in operative time in a comparison between a small series of robotic and laparoscopic resections.

Tsung et al[260] recently reported 51 robotic resections. Importantly, liver mobilization and adhesiolysis were carried out by conventional laparoscopy prior to robotic docking for transection. When compared with matched laparoscopic resections, no significant differences in blood losses, postoperative complication rates, mortality rates, postoperative intensive care unit admission rate, length of stay or margin involvement were found. Robotic resections used up more operation room time, although leading to less conversions than laparoscopic resections did.

In summary, although robotic liver resection is feasible in skilled hands, experience is very short. Indeed, the Second International Consensus Conference considers that there is insufficient data for evaluation[224].

PANCREATIC SURGERY

Different types of laparoscopic pancreatic resection are performed: tumor enucleation, distal pancreatectomy, central pancreatectomy, pancreatico-duodenectomy and total pancreatectomy, although the latter is anecdotal. These techniques have been used for both benign (chronic pancreatitis, cystic tumors) and malignant diseases.

Tumor enucleation

Although in general formal pancreatic resection is recommended for most tumors, enucleation can be performed for neuroendocrine neoplasms if tumor size does not exceed 2 cm and if no findings of malignancy are detected on preoperative staging[264]. Pancreatic tumor enucleation can be easily performed by laparoscopy with excellent morbidity and mortality outcomes[265].

Distal pancreatectomy (pancreatic left resection)

This is the most frequently performed type of laparoscopic pancreatectomy for both benign and malignant diseases[266,267].

Distal pancreatectomy can be accomplished with or without splenic preservation. Splenectomy could adversely influence oncologic long-term outcomes, in addition to predispose to infectious complications. As a result, efforts to preserve the spleen should be done in case of benign or low grade malignancies, provided that splenic vessels are not involved with the tumor. More controversial is splenic preservation in case of adenocarcinoma. Whatever the case, if the spleen is to be preserved, two techniques are used[264,268]: in the first, section of the splenic vessels both at the level of transection of the pancreas and at the splenic hilum is performed, leaving the short gastric vessels as the only blood flow supply. In the second technique, the splenic vessels are preserved by meticulous ligation of all the branches reaching the pancreas. However, patency of splenic vein - although not that of the artery - can be compromised after a laparoscopic DP in as high as 35%[269]. The frequency of splenic infarction and appearance of gastric varices is higher in case of splenic vessel section[268].

Blood losses have been reported to be significantly lower in case of a laparoscopic approach by comparison with open procedures[270-273]. Localizing small tumors by laparoscopy or laparoscopic ultrasonography can be difficult and this leads to conversion in many cases. Other causes of conversion can be bleeding or difficult structure identification which lead to conversion in 17%-30% of cases[270-272]. Obesity is significantly associated to conversion[271].

The complication rate has been reported significantly lower in laparoscopic cases[271,274], although the severity grade was similar than in open procedures[263]. Other papers showed similar rates[272,273]. Tran Cao et al[267] studied a nationwide database and compared the short-term outcomes of 382 minimally invasive distal pancreatectomy (mainly laparoscopic and some robotic) with those of open distal pancreatectomy. They found a significant reduction in overall perioperative morbidity among patients undergoing minimally invasive surgery, including a significant decrease in hemorrhagic complications and postoperative infections in laparoscopically treated patients. Results of five meta-analyses[266] support these findings concerning overall perioperative morbidity, although clinically relevant pancreatic fistula frequency was significantly lower in laparoscopic cases only in one of the analyzed studies.

Patients converted from laparoscopic to open surgery have significantly more severe complications than those with not converted[271] which reflects the need of proper selection for a laparoscopic approach. The reported mortality ranges 0%-1%[267,271,273].

Some have reported operation times significantly longer in laparoscopic than in open procedures[271], but others find similar duration[273].

The hospital stay has also been reported to be significantly lower with a laparoscopic approach[27,270,271,273].

A recently published meta-analyses[275], comprising data of 3701 patients, all of them from non-randomized studies, confirmed most of the above mentioned findings: superiority of laparoscopic over open DP in terms of blood loss, time to first oral intake, and hospital stay. Mean operation time, mortality -0.4% in DP-morbidity and safety showed no difference. However, data concerning oncologic radicality and effectiveness are limited.

Distal pancreatectomy for adenocarcinoma

Most articles report a mixture of benign and malignant diseases as indication of distal pancreatectomy (DP). As a result, to reach conclusions concerning safety and oncological outcomes when dealing with adenocarcinomas is difficult. A few papers compare open and laparoscopic approaches only in case of pancreatic adenocarcinoma. Kooby et al[270] performed a multicenter matched analysis of 23 laparoscopic procedures compared with 189 open procedures and found no significant differences in positive margin rates, number of nodes examined or overall survival. The median follow-up was only 10 mo and, thus, it is premature to conclude that the long-term results are as safe as in open procedures. Magge et al[272] compared 28 patients with 34 operated on by an open approach. They found not significant differences in margin-negative resection (open, 88%; laparoscopic, 86%) and median lymph node clearance. Also, no significant differences were found for overall survival or risk of local recurrence.

Distal pancreatectomy for neuroendocrine tumors:

A recent paper compared laparoscopic an open DP performed for neuroendocrine tumors[274]. The laparoscopic procedure showed no mortality, a significant lower complication rate and shorter hospital stay. No significant difference was found concerning margin involvement, long-term survival, and overall costs.

In summary, DP is feasible, safe and reproducible for most laparoscopy skilled surgeons. Concerning its use in case of adenocarcinoma, it also appears as safe as open DP but more studies analyzing long-term results are needed.

Robotic distal pancreatectomy

Theoretical advantages and disadvantages of robotic surgery have been discussed earlier. The published papers dealing with robotic DP are still scanty.

Zureikat et al[276] report 83 robotic DP with no mortality and a low rate of severe complications, although with 43% cases of pancreatic fistula. The average operative time was 256 min and 2% required conversion.

Waters et al[277] compared 17 robotic against 32 open and 28 laparoscopic DP. Cystic tumors predominated among the indications of robotic resection. In this group, longer operative times, similar blood losses, no mortality, shorter hospital stay and lower hospital costs were found. Higher rates of splenic preservation were achieved in comparison with the open and laparoscopic approaches. Daouadi et al[278] compared 30 robotic DP and 94 laparoscopic DP patients. The robotic DP group included more adenocarcinomas. Significant differences in blood loss, hospital stay, or morbidity were not found. However, there was a statistically significant 36% increase in R0 resection with robotic surgery, as well as more lymph nodes harvested. Also the conversion rate was lower.

The study by Kang et al[279] included 20 robotic and 25 laparoscopic DP for benign and borderline malignant lesions. Although the intent was to preserve the spleen, the overall rate of splenic preservation was very low. A higher splenic preservation rate was achieved with the robotic approach. This took longer operative times and had increased costs compared to laparoscopic cases.

In summary, although feasible and safe, robotic DP has not yet shown clear advantages over laparoscopic DP.

Central pancreatectomy

This technique can be applied for the treatment of benign or borderline lesions of the pancreas situated in the pancreas neck. Although uncommonly performed, this technique is feasible by laparoscopy[265-280].

A review from 2013[281] collected 51 published cases operated on through total laparoscopy or robotic assistance. Pancreatic reconstruction was done with a Roux-en-Y pancreato-jejunostomy, or pancreato-gastrostomy. The procedure was long with a mean time of 356 min. Blood loss was minimal in most cases. Mortality was nil, but morbidity was high, mainly due to pancreatic fistula (46%).

When performed by a robotic approach, the procedure is associated with long operative times (mean: 394 min) and a 23% of severe complications, although without mortality[276].

Pancreaticoduodenectomy

Three techniques are currently employed for LPD: pure laparoscopy (PL), hand-assisted (HA) laparoscopy, and laparoscopic-assisted (LA) surgery. In contrast with DP, where only resection is to be performed, the pancreaticoduodenectomy (PD) requires a complex resection as well as pancreatico-jejunal, hepato-jejunal and gastro-jejunal anastomoses. As a result, although feasible, the difficulty of the procedure makes that experience with laparoscopic pancreaticoduodenectomy is limited to a few case series.

Gumbs et al[282] analyzed most reported cases until 2011 comprising 285 patients, although only 32% had pancreatic adenocarcinoma. The most important findings for the entire cohort were a 9% conversion rate, 2% mortality, 48% morbidity and a length of stay of 12 d. Margin involvement was found in 0.4% with an average of retrieved lymph nodes of 15. The mean disadvantage was a long operation time ranging from 263 to 750 min.

Direct comparison between laparoscopic and open PD has been performed by some groups. The first[273], which included 60% of patients with malignant tumors - pancreatic, biliary, ampullary - found significantly lower blood losses, and hospital stay as well as more lymph node harvested in the laparoscopic group. However, the average operative time was significantly increased. There were no differences in overall complications, pancreatic fistula, delayed gastric emptying, and resection margin involvement. The main finding of the second study[283] was a significant reduction in blood losses and, thus, the transfusion need in the laparoscopic patients although it did not show relevant differences in morbidity.

Asbun and Stauffer[284] compared 53 laparoscopic and 215 open PD. They found significant differences favoring laparoscopic PD blood losses, transfusions, length of hospital stay, length of ICU stay (P < 0.001), and number of lymph nodes retrieved although the operative time was significantly longer. The rates of overall complications, pancreas fistula, delayed gastric emptying, margin involvement were not significantly different.

Kuroki et al[283] compared 20 laparoscopic and 31 open PD. They also report a significant reduction of blood losses and transfusion need but they did not find significant differences in morbidity.

Song et al[285] report a comparison between 137 laparoscopic and 2055 open pylorus-preserving PD for periampullary tumors. A shorter hospital stay and a lower analgesic consumption was seen in the laparoscopic cases. No other difference was found including complications, blood losses margin involvement or lymph nodes retrieved.

In a recent systematic review of several series[286], the operative time averaged 464.3 min (338-710 min) with conversion in 9.1% of patients. The mean estimated blood loss was 575 mL. Average mortality was 1.9% and morbidity ranged between 18.1% and 64.2%, with pancreatic fistula ranging between 4.5% and 52.3% of patients. An average of 14.4 lymph nodes were retrieved and 4.4% of cases had marginal involvement.

In summary, laparoscopic PD is feasible and as safe as the open procedure in highly skilled hands and high-volume centers. Long operative times are needed. Decreased blood losses seem to be the main advantage. Concerning its use in case of adenocarcinoma, more studies are needed.

Robotic PD

Published experiences concerning robotic PD are even less common. Zureikat et al[276] report 132 cases with a 90 d mortality rate of 3.8% and a frequency of severe complications (III-IV) of 21%. The frequency of pancreatic fistula was 17%, although only 3.7% were of grade C. Conversion was needed in 8%. The procedure took long operative times (mean 527 min), and although decreased with improved experience, the last cases of the series lasted over 400 min.

In the systematic review by Boggi et al[286], the robotic PD used up more operative time and had higher pancreatic fistula rate by comparison with pure laparoscopic PD (but not laparoscopically assisted PD). However, significant differences were not found concerning overall morbidity or mortality (2.7%, 1.1%, and 2.4% for pure laparoscopic, laparoscopically assisted, and robotic PD, respectively).

Another systematic review analyzed several non-randomized studies comparing open and robotic pancreatectomies, most of them PD[287]. It included 137 cases of robotic PD and 203 open PD. The median conversion rate was 10%. Overall complications, reoperation rate, and margin involvement were significantly lower in robotic group, with no significant difference in postoperative pancreatic fistula, and mortality. In one study included in this review[288] involving only PD, a significant increase in the R0 resection rate, with 100 % of patients in the robotic group compared with 87% in the open group.

A recently published paper[289] comparing robotic and open PD, report similar findings such as lower blood losses, shorter hospital stay, longer operative times with no significant difference in morbidity, mortality, as well as R0 resection rate and number of lymph nodes retrieved in case of malignancy. Patients with pancreatic adenocarcinoma of both groups had similar overall and disease-free survival.

In summary, the same as laparoscopic PD, robotic PD is feasible in highly skilled hands and high-volume centers. Although the very short published experience makes to reach firm conclusions difficult, it suggests that robotic PD is as safe as laparoscopic PD with some advantages over open PD. However, the former is more time-consuming.

TRAINING IN LAPAROSCOPIC SURGERY

In 1889 Halsted established at the Johns Hopkins Hospital the need of a new training system in surgery. Nowadays, it is rewarding to see how surgeons can be proficient in several techniques when they repeat them in a simulator[290].

Today, traditional methods are not enough to teach and learn surgical skills because of the reductions in training hours during the residency programs and the lack of time of the surgeons to adequately teach these techniques. On the other hand, laparoscopic surgery learning curve and the risk of severe complications when inexperienced surgeons perform these procedures, make it more difficult for residents to learn minimally invasive techniques.

Costs per procedure have increased with minimally invasive procedures and technology is making the surgical environment more complex. A surgeon does not learn alone anymore, and they depend on a complex team that has to be trained and work together. As a result, surgical training models are evolving to serve as a complement to the standard surgical training in the theatre[291].

Current situation of surgical residents training

With the arrival of laparoscopic surgery to the surgical departments in the 90s, the surgical resident training has suffered a huge transformation with a decrease in its autonomy. This has resulted in the need of additional training to obtain the confidence and maturity of judgment. As a result, the number of fellowships has dramatically increased during the last ten years. This change has enlarged the surgical training[290].

Laparoscopic surgery training programs have evolved in several ways in the different countries. Sweden or The Netherlands have national programs limited to basic procedures (cholecystectomy) using training techniques as virtual reality[292]. In the United States and Canada, the surgical training method is structured and the program of the American College of Surgeons (ACS) demands the inclusion of basic training in the Fundamentals of Laparoscopic Surgery (FLS) in the residency programs[293]. Spain has a limited training of two 3-d courses for the residents, one basic and another for advanced training[294]. In Latin America, the project of Laparoscopia Avanzada Práctica (LAP), pretends to bring near a big number of countries to basic programs in laparoscopic training[295].

How does the resident get trained in laparoscopic surgery? The curricular model

One of the most important aspects of the residency program is that training has to be based in a curricular model. Based on the premises that experts indicate[296], these curricula have to be: (1) Endorsed by an accredited training institution (ACS) with a clear message regarding how this surgical training will be; (2) If simulation is used as a training tool, this demands a new and different approach of the instructors; (3) Training has to be integrated with clinical practice; (4) Adequate simulators have to be used in the correct timing and they should be validated for training; (5) The features and different types of surgical simulators are continuously changing. This has to be taken into account in order to plan the update of these simulators; (6) Residents must have reserved time to use simulators in their training; and (7) Financing has to be sustainable using business principles.

How do surgical simulators contribute to laparoscopic training?

Virtual reality (VR) simulators provide surgical training without supervision in a safe environment for both patient and trainees. Skills obtained in the VR simulator can be transferred to the theatre. However, evidence is only limited to basic surgical skills and laparoscopic cholecystectomy. There is no evidence yet of the effect of VR simulators on advanced laparoscopic procedures[297]. The introduction of haptic feedback in these VR simulators has not increased the validation of laparoscopic surgical competences[298]. In summary, all the trails that compare the training using VR simulators and standard laparoscopic training in the theatre observe a higher performance after training with VR, confirming that current training using structured simulation is more efficient than traditional training[291]. Supported by these findings, countries such as Sweden or The Netherlands have established a structured training for laparoscopic cholecystectomy based in the use of VR simulators. This has allowed these countries validate resident competency before being trained in the theatre[299,300].

Animal models for resident training in advanced laparoscopic techniques (Nissen, Colectomy) are the more realistic models, but they are limited in some countries because of religious beliefs or laws. All these reasons are behind the substitution of these animals by synthetic models or even by simulated models with “ex vivo” viscera[301]. Without any doubt, the animal model most frequently used is the porcine model, mainly in colorectal surgery training[302]. Despite this, it is not possible to define nowadays when competency is reached with an animal model, if this model is the best one for laparoscopic training and if what is learned in this model is translated into clinical practice.

There are few studies about the use of cadaveric human models[303]. These models have been used for training in laparoscopic skills, such as cholecystectomy, and have demonstrated the increase of capacitation by comparison with VR simulators. We believe that this model has to be reserved for advanced laparoscopic procedures (colorectal or bariatric surgery) that require a huge degree of realism. Leblanc et al[304] assessed the use of fresh human cadavers for surgical training in laparoscopic sigmoidectomy. They observed that the use of this model improved clinical practice in terms of dissection, traction/counter traction, eye-hand coordination, suture, bleeding control and theatre time comparing with the use of a VR simulator. Palter et al[305] studied the sequencing of VR simulators with human cadaver models for training in colorectal laparoscopic surgery. He added a cognitive module in order to help the participants to understand the procedure and how to plan and execute a right colectomy or a sigmoidectomy. He observed that this training approach improved the technical knowledge and the performance in the theatre in comparison with the traditional training during the residency program.

Hybrid models are those that use a complex robotized mannequin together with the abdomen/thorax of a live animal. These models allow us a high laparoscopic realism simulation while we adjust the cardiologic/respiratory parameters of the robotized mannequin. This way we are able to simulate for example a coronary event during the simulated laparoscopic procedure.

In other opportunities[306], scenarios can be created to train the laparoscopic surgery team in a simulated theatre with a hybrid patient (SimMan 3G; Laerdal) and a laparoscopic VR simulator (Lap Mentor Express, Simbionix). These authors observed that the global assessment of the team showed a high qualification. Powers et al[307] observed that these simulation models let us discriminate between the technical and non-technical abilities in residents and experienced surgeons. The target of this innovative multidisciplinary simulation is to identify the problem and to start with the adequate solution by the surgical team.

Zendejas et al[308] observed in a recent review that whenever simulator is used, it has huge advantages in laparoscopic or open surgery training comparing with no simulator use. These authors also observed that adding the use of simulators to the traditional training is more effective than the use of traditional training alone.

Our model for laparoscopic surgery training for residents

Following the experience of authors such as Haluck et al[296], we think that the University Hospital Marqués de Valdecilla resident training meets a number of requirements[309]: (1) Our curriculum in laparoscopic procedures is developed during the full residency period. We think like Sadideen et al[310] that the first steps in surgical skill training have to be done outside the theatre and that practice is the most important thing to achieve automaticity in surgical skills. In the clinical environment, the needs of the patient prevail over the needs of the trainee; (2) The curriculum is compound by 19 laparoscopic modules; this allows the trainee to progressively gain competence as he learns. At the same time, each year modules are more technically advanced; (3) We support training in a simulated environment and advance in the learning curve during simulation. We have observed that doing gastrointestinal anastomosis and colonic resections this curve is shorter and increases patient safety[311]; (4) Working with the most realistic models in each training phase, we observed that an important part of the initial training can be performed with low cost animal “ex vivo” models. Some examples are gastrointestinal anastomosis, cholecystectomy or gastric bypass; (5) The modular curriculum covers not only technical skills competencies but also teamwork competencies during crisis in laparoscopic surgery procedures. Teamwork competencies are trained in hybrid simulators; (6) The training process of the resident is assessed with Global Rating Scales of Operative Performance. Even though we also apply this assessment to the clinical practice, it is very difficult to move this assessment to the professional competence[312]; and (7) The ACS accredits this training program and the center where it is developed.

We think that progress is very difficult and it may be necessary a trial/error system that let us advance. Learning from other programs that have tried, failed or succeeded may be a key point[313].

Current challenges of resident training in laparoscopic surgery

For most of the groups around the world, the most important challenge is defining how simulation based training can be implemented and improve the training system. There are many questions to be answered, as we cannot say with scientific evidence in which degree simulated training improves results or quality in clinical practice and patient safety.

Simulators have to improve their benefits and design, and objective measures have to be developed so we can say in which degree the trainee acquires the adequate clinical competencies that can be translated in to the theatre[314].

How can we keep and improve the acquired training during residency?

Mattar et al[315] observed that general surgery residency inadequately prepares trainees for fellowship results of a survey of fellowship program directors.

Fellowship programs are well established in countries such as the United States, Canada, United Kingdom or Australia. On the other hand, they have not had a good degree of implementation in the rest of Europe or in Eastern countries. These fellowship programs are advanced laparoscopic surgery training programs that have their own problems. Fellowships coexist with residency programs in the same institution and the continuous advance of new surgical techniques and the complexity of the surgical equipment make that some of the training is short in time or objectives. These reasons are making fellowships more and more specific as the recent fellowships in robotic colorectal surgery or rectal surgery is[316].

The development of national training programs in advanced laparoscopic surgery, such as the one developed in the United Kingdom[317] in laparoscopic colorectal surgery (Lapco) have shown good results in terms of short- and long-term training and have had a positive impact on the trainee learning curves[318,319].

There are an increasing number of short length training courses in advanced laparoscopic surgery. They are usually limited to 3-5 d and they include live procedures performed by expert surgeons in most of the cases. Some theoretical knowledge is also given either during the course or on-line and, in some cases, the trainees have the opportunity to practice the technique on an animal or cadaver model. These courses have been mostly developed in colorectal, bariatric and upper gastro-intestinal surgery.

The impact of these courses on the training of the participant will depend on his previous experience in laparoscopic or open surgery. This way, we see that surgeons that come to a course with previous laparoscopic experience posteriorly implement the acquired knowledge during the course in a 60%-70%. Without this experience the degree of implementation is under 25%[320,321]. Kinoshita et al[322] have demonstrated in Japan that after a training course in gastric laparoscopic surgery the number of laparoscopic gastrectomies increased in a 50% in the participating institutions. Participants answered to the survey saying that they felt improvement in their surgical skills in 100% of the initial procedures. On the other hand, Brunckhorst et al[323] say that there is very poor evidence concerning the training value of live operations and that very few high quality studies have been performed in this field.

Our point of view is that these 3-5 d courses provide knowledge and skills that help the trainee in starting laparoscopic surgery in an already established unit. These courses also help surgeons in sharing experience with experts.

In summary, we can say that current literature consistently proves the positive impact of simulation in theatre time and the scores in predefined performance but, however, this is not enough to ensure the transfer of these lab acquired skills to the theatre.

Which is the future of surgical training?

We are living a huge technological advance in all social scopes and also in surgical training[324]. In this context, the acquisition of knowledge is progressively moving to e-learning platforms that reduce classroom hours. This system includes interactive feedback with the instructor, assessment of the procedure and interaction with other participants. This system may also be combined with VR training[325].

VR simulators for laparoscopic surgery have been importantly improved with haptic technologies. In the near future, it may even be possible to import real 3D images to VR software. This may allow the trainees to perform real operations in virtual surgical fields that look like the real ones. Modelling this imported images, the trainee may even be able to work in fields with anatomical variations[326].

“Virtual cadavers” based on 3D images reconstructed from computerized tomographies will replace human cadaver and animal models. It will be possible to create huge libraries with this “virtual cadavers”. The exposure to multiple scenarios during the same basic procedure will make easier the trainee progress from competency to expertise.

Tele-simulation will be possible thanks to this libraries allowing tele-training. Virtual environments as second life (SL) will be used to completely represent a training centre or meeting room. These environments are already available in the market and can make possible the interaction of scenarios, patients, VR simulators, lectures or videoclips. Surgeons will be able to build their own virtual clinic or whatever they may need to simulate according to the level of competency that is trained[327].

Tele-mentoring[328] using robots as RP-7 (RP-7, Intouch Health, Santa Barbara, California) makes possible active mentoring of the trainees with verbal instructions or changing position of the instruments/camera when needed. It also makes possible a passive mentoring just with verbal instructions. This tele-mentoring seems to be a valuable tool for training minimally invasive procedures.

Now is the moment when all this separate tools, laparoscopic surgery, tele-presence, VR, digital image, networking… join together making tele-surgery possible. A surgeon is able to be miles away from the theatre and assist a surgical procedure.

Robotic surgery has been progressively incorporated to advanced laparoscopic procedures and has made those procedures easier. Robotics will facilitate the training of those surgical procedures. Mixing VR or virtual libraries with the surgical console of the robotic surgical systems will make it possible to train the procedure before doing it in the real world. It will make training a particular procedure in a particular patient possible.

In summary, we should imagine a surgeon being trained in his work environment in complex minimally invasive procedures by anther surgeon that is “on-line”. Robotic surgical systems will be present in daily work and training.

Footnotes

P- Reviewer: Hata T, Muller-Stich BP S- Editor: Yu J L- Editor: A E- Editor: Ma S

References
1.  Gonzalez Contreras QH, Rápalo H. Cirugía laparoscópica de colon y recto. Rev Gastroenterol Mex. 2008;73 Suppl 1:153-156.  [PubMed]  [DOI]  [Cited in This Article: ]
2.  Harrell AG, Heniford BT. Minimally invasive abdominal surgery: lux et veritas past, present, and future. Am J Surg. 2005;190:239-243.  [PubMed]  [DOI]  [Cited in This Article: ]
3.  Haggar FA, Boushey RP. Colorectal cancer epidemiology: incidence, mortality, survival, and risk factors. Clin Colon Rectal Surg. 2009;22:191-197.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1215]  [Cited by in F6Publishing: 1343]  [Article Influence: 103.3]  [Reference Citation Analysis (0)]
4.  Tomita H, Marcello PW, Milsom JW. Laparoscopic surgery of the colon and rectum. World J Surg. 1999;23:397-405.  [PubMed]  [DOI]  [Cited in This Article: ]
5.  Jacobs M, Verdeja JC, Goldstein HS. Minimally invasive colon resection (laparoscopic colectomy). Surg Laparosc Endosc. 1991;1:144-150.  [PubMed]  [DOI]  [Cited in This Article: ]
6.  Alexander RJ, Jaques BC, Mitchell KG. Laparoscopically assisted colectomy and wound recurrence. Lancet. 1993;341:249-250.  [PubMed]  [DOI]  [Cited in This Article: ]
7.  Lacy AM, García-Valdecasas JC, Delgado S, Castells A, Taurá P, Piqué JM, Visa J. Laparoscopy-assisted colectomy versus open colectomy for treatment of non-metastatic colon cancer: a randomised trial. Lancet. 2002;359:2224-2229.  [PubMed]  [DOI]  [Cited in This Article: ]
8.  Lacy AM, Delgado S, Castells A, Prins HA, Arroyo V, Ibarzabal A, Pique JM. The long-term results of a randomized clinical trial of laparoscopy-assisted versus open surgery for colon cancer. Ann Surg. 2008;248:1-7.  [PubMed]  [DOI]  [Cited in This Article: ]
9.  Fleshman J, Sargent DJ, Green E, Anvari M, Stryker SJ, Beart RW, Hellinger M, Flanagan R, Peters W, Nelson H. Laparoscopic colectomy for cancer is not inferior to open surgery based on 5-year data from the COST Study Group trial. Ann Surg. 2007;246:655-62; discussion 662-4.  [PubMed]  [DOI]  [Cited in This Article: ]
10.  Veldkamp R, Kuhry E, Hop WC, Jeekel J, Kazemier G, Bonjer HJ, Haglind E, Påhlman L, Cuesta MA, Msika S. Laparoscopic surgery versus open surgery for colon cancer: short-term outcomes of a randomised trial. Lancet Oncol. 2005;6:477-484.  [PubMed]  [DOI]  [Cited in This Article: ]
11.  Jayne DG, Guillou PJ, Thorpe H, Quirke P, Copeland J, Smith AM, Heath RM, Brown JM. Randomized trial of laparoscopic-assisted resection of colorectal carcinoma: 3-year results of the UK MRC CLASICC Trial Group. J Clin Oncol. 2007;25:3061-3068.  [PubMed]  [DOI]  [Cited in This Article: ]
12.  Ströhlein MA, Grützner KU, Jauch KW, Heiss MM. Comparison of laparoscopic vs. open access surgery in patients with rectal cancer: a prospective analysis. Dis Colon Rectum. 2008;51:385-391.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 106]  [Cited by in F6Publishing: 117]  [Article Influence: 7.3]  [Reference Citation Analysis (0)]
13.  Braga M, Vignali A, Gianotti L, Zuliani W, Radaelli G, Gruarin P, Dellabona P, Di Carlo V. Laparoscopic versus open colorectal surgery: a randomized trial on short-term outcome. Ann Surg. 2002;236:759-766; disscussion 767.  [PubMed]  [DOI]  [Cited in This Article: ]
14.  Indar A, Efron J. Laparoscopic surgery for rectal cancer. Perm J. 2009;13:47-52.  [PubMed]  [DOI]  [Cited in This Article: ]
15.  Park JS, Kang SB, Kim SW, Cheon GN. Economics and the laparoscopic surgery learning curve: comparison with open surgery for rectosigmoid cancer. World J Surg. 2007;31:1827-1834.  [PubMed]  [DOI]  [Cited in This Article: ]
16.  Guillou PJ, Quirke P, Thorpe H, Walker J, Jayne DG, Smith AM, Heath RM, Brown JM; MRC CLASICC trial group. Short-term endpoints of conventional versus laparoscopic-assisted surgery in patients with colorectal cancer (MRC CLASICC trial): multicentre, randomised controlled trial. Lancet. 2005;365:1718-1726.  [PubMed]  [DOI]  [Cited in This Article: ]
17.  Pugliese R, Di Lernia S, Sansonna F, Scandroglio I, Maggioni D, Ferrari GC, Costanzi A, Magistro C, De Carli S. Results of laparoscopic anterior resection for rectal adenocarcinoma: retrospective analysis of 157 cases. Am J Surg. 2008;195:233-238.  [PubMed]  [DOI]  [Cited in This Article: ]
18.  Scheidbach H, Garlipp B, Oberländer H, Adolf D, Köckerling F, Lippert H. Conversion in laparoscopic colorectal cancer surgery: impact on short- and long-term outcome. J Laparoendosc Adv Surg Tech A. 2011;21:923-927.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 27]  [Cited by in F6Publishing: 29]  [Article Influence: 2.2]  [Reference Citation Analysis (0)]
19.  Kang SB, Park JW, Jeong SY, Nam BH, Choi HS, Kim DW, Lim SB, Lee TG, Kim DY, Kim JS. Open versus laparoscopic surgery for mid or low rectal cancer after neoadjuvant chemoradiotherapy (COREAN trial): short-term outcomes of an open-label randomised controlled trial. Lancet Oncol. 2010;11:637-645.  [PubMed]  [DOI]  [Cited in This Article: ]
20.  Anderson C, Uman G, Pigazzi A. Oncologic outcomes of laparoscopic surgery for rectal cancer: a systematic review and meta-analysis of the literature. Eur J Surg Oncol. 2008;34:1135-1142.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 86]  [Cited by in F6Publishing: 94]  [Article Influence: 5.9]  [Reference Citation Analysis (0)]
21.  Kellokumpu IH, Kairaluoma MI, Nuorva KP, Kautiainen HJ, Jantunen IT. Short- and long-term outcome following laparoscopic versus open resection for carcinoma of the rectum in the multimodal setting. Dis Colon Rectum. 2012;55:854-863.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 35]  [Cited by in F6Publishing: 39]  [Article Influence: 3.3]  [Reference Citation Analysis (0)]
22.  Melani AG, Fregnani JH, Matos D. Treatment of rectal adenocarcinoma by laparoscopy and conventional route: a brazilian comparative study on operative time, postoperative complications, oncological radicality and survival. Rev Col Bras Cir. 2011;38:245-252.  [PubMed]  [DOI]  [Cited in This Article: ]
23.  Park JS, Choi GS, Jun SH, Hasegawa S, Sakai Y. Laparoscopic versus open intersphincteric resection and coloanal anastomosis for low rectal cancer: intermediate-term oncologic outcomes. Ann Surg. 2011;254:941-946.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 82]  [Cited by in F6Publishing: 88]  [Article Influence: 7.3]  [Reference Citation Analysis (0)]
24.  van der Pas MH, Haglind E, Cuesta MA, Fürst A, Lacy AM, Hop WC, Bonjer HJ. Laparoscopic versus open surgery for rectal cancer (COLOR II): short-term outcomes of a randomised, phase 3 trial. Lancet Oncol. 2013;14:210-218.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1030]  [Cited by in F6Publishing: 883]  [Article Influence: 80.3]  [Reference Citation Analysis (0)]
25.  Ng SS, Lee JF, Yiu RY, Li JC, Hon SS, Mak TW, Leung WW, Leung KL. Long-term oncologic outcomes of laparoscopic versus open surgery for rectal cancer: a pooled analysis of 3 randomized controlled trials. Ann Surg. 2014;259:139-147.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 50]  [Cited by in F6Publishing: 54]  [Article Influence: 5.4]  [Reference Citation Analysis (0)]
26.  Lanfranco AR, Castellanos AE, Desai JP, Meyers WC. Robotic surgery: a current perspective. Ann Surg. 2004;239:14-21.  [PubMed]  [DOI]  [Cited in This Article: ]
27.  Uhrich ML, Underwood RA, Standeven JW, Soper NJ, Engsberg JR. Assessment of fatigue, monitor placement, and surgical experience during simulated laparoscopic surgery. Surg Endosc. 2002;16:635-639.  [PubMed]  [DOI]  [Cited in This Article: ]
28.  Weber PA, Merola S, Wasielewski A, Ballantyne GH. Telerobotic-assisted laparoscopic right and sigmoid colectomies for benign disease. Dis Colon Rectum. 2002;45:1689-1694; discussion 1695-6.  [PubMed]  [DOI]  [Cited in This Article: ]
29.  DeNoto G, Rubach E, Ravikumar TS. A standardized technique for robotically performed sigmoid colectomy. J Laparoendosc Adv Surg Tech A. 2006;16:551-556.  [PubMed]  [DOI]  [Cited in This Article: ]
30.  Talamini M, Campbell K, Stanfield C. Robotic gastrointestinal surgery: early experience and system description. J Laparoendosc Adv Surg Tech A. 2002;12:225-232.  [PubMed]  [DOI]  [Cited in This Article: ]
31.  Vibert E, Denet C, Gayet B. Major digestive surgery using a remote-controlled robot: the next revolution. Arch Surg. 2003;138:1002-1006.  [PubMed]  [DOI]  [Cited in This Article: ]
32.  D’Annibale A, Morpurgo E, Fiscon V, Trevisan P, Sovernigo G, Orsini C, Guidolin D. Robotic and laparoscopic surgery for treatment of colorectal diseases. Dis Colon Rectum. 2004;47:2162-2168.  [PubMed]  [DOI]  [Cited in This Article: ]
33.  Braumann C, Menenakos C, Rueckert JC, Mueller JM, Jacobi CA. Computer-assisted laparoscopic repair of “upside-down” stomach with the Da Vinci system. Surg Laparosc Endosc Percutan Tech. 2005;15:285-289.  [PubMed]  [DOI]  [Cited in This Article: ]
34.  Pigazzi A, Ellenhorn JD, Ballantyne GH, Paz IB. Robotic-assisted laparoscopic low anterior resection with total mesorectal excision for rectal cancer. Surg Endosc. 2006;20:1521-1525.  [PubMed]  [DOI]  [Cited in This Article: ]
35.  Hellan M, Anderson C, Ellenhorn JD, Paz B, Pigazzi A. Short-term outcomes after robotic-assisted total mesorectal excision for rectal cancer. Ann Surg Oncol. 2007;14:3168-3173.  [PubMed]  [DOI]  [Cited in This Article: ]
36.  Baik SH, Lee WJ, Rha KH, Kim NK, Sohn SK, Chi HS, Cho CH, Lee SK, Cheon JH, Ahn JB. Robotic total mesorectal excision for rectal cancer using four robotic arms. Surg Endosc. 2008;22:792-797.  [PubMed]  [DOI]  [Cited in This Article: ]
37.  Baik SH, Kim YT, Ko YT, Kang CM, Lee WJ, Kim NK, Sohn SK, Chi HS, Cho CH, Lee SK. Simultaneous robotic total mesorectal excision and total abdominal hysterectomy for rectal cancer and uterine myoma. Int J Colorectal Dis. 2008;23:207-208.  [PubMed]  [DOI]  [Cited in This Article: ]
38.  Ng SS, Lee JF, Yiu RY, Li JC, Hon SS. Telerobotic-assisted laparoscopic abdominoperineal resection for low rectal cancer: report of the first case in Hong Kong and China with an updated literature review. World J Gastroenterol. 2007;13:2514-2518.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in CrossRef: 14]  [Cited by in F6Publishing: 11]  [Article Influence: 0.6]  [Reference Citation Analysis (0)]
39.  Shin JY. Comparison of Short-term Surgical Outcomes between a Robotic Colectomy and a Laparoscopic Colectomy during Early Experience. J Korean Soc Coloproctol. 2012;28:19-26.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 46]  [Cited by in F6Publishing: 44]  [Article Influence: 3.7]  [Reference Citation Analysis (0)]
40.  Baek JH, McKenzie S, Garcia-Aguilar J, Pigazzi A. Oncologic outcomes of robotic-assisted total mesorectal excision for the treatment of rectal cancer. Ann Surg. 2010;251:882-886.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 128]  [Cited by in F6Publishing: 123]  [Article Influence: 8.8]  [Reference Citation Analysis (0)]
41.  Luca F, Valvo M, Ghezzi TL, Zuccaro M, Cenciarelli S, Trovato C, Sonzogni A, Biffi R. Impact of robotic surgery on sexual and urinary functions after fully robotic nerve-sparing total mesorectal excision for rectal cancer. Ann Surg. 2013;257:672-678.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 131]  [Cited by in F6Publishing: 143]  [Article Influence: 13.0]  [Reference Citation Analysis (0)]
42.  Biffi R, Luca F, Pozzi S, Cenciarelli S, Valvo M, Sonzogni A, Radice D, Ghezzi TL. Operative blood loss and use of blood products after full robotic and conventional low anterior resection with total mesorectal excision for treatment of rectal cancer. J Robot Surg. 2011;5:101-107.  [PubMed]  [DOI]  [Cited in This Article: ]
43.  Shiomi A, Kinugasa Y, Yamaguchi T, Tomioka H, Kagawa H. Robot-assisted rectal cancer surgery: short-term outcomes for 113 consecutive patients. Int J Colorectal Dis. 2014;29:1105-1111.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 38]  [Cited by in F6Publishing: 37]  [Article Influence: 3.7]  [Reference Citation Analysis (0)]
44.  deSouza AL, Prasad LM, Ricci J, Park JJ, Marecik SJ, Zimmern A, Blumetti J, Abcarian H. A comparison of open and robotic total mesorectal excision for rectal adenocarcinoma. Dis Colon Rectum. 2011;54:275-282.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 58]  [Cited by in F6Publishing: 65]  [Article Influence: 5.0]  [Reference Citation Analysis (0)]
45.  Kwak JM, Kim SH, Kim J, Son DN, Baek SJ, Cho JS. Robotic vs laparoscopic resection of rectal cancer: short-term outcomes of a case-control study. Dis Colon Rectum. 2011;54:151-156.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 142]  [Cited by in F6Publishing: 153]  [Article Influence: 11.8]  [Reference Citation Analysis (0)]
46.  Kang J, Yoon KJ, Min BS, Hur H, Baik SH, Kim NK, Lee KY. The impact of robotic surgery for mid and low rectal cancer: a case-matched analysis of a 3-arm comparison--open, laparoscopic, and robotic surgery. Ann Surg. 2013;257:95-101.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 148]  [Cited by in F6Publishing: 158]  [Article Influence: 14.4]  [Reference Citation Analysis (0)]
47.  Fernandez R, Anaya DA, Li LT, Orcutt ST, Balentine CJ, Awad SA, Berger DH, Albo DA, Artinyan A. Laparoscopic versus robotic rectal resection for rectal cancer in a veteran population. Am J Surg. 2013;206:509-517.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 38]  [Cited by in F6Publishing: 45]  [Article Influence: 4.1]  [Reference Citation Analysis (0)]
48.  Patriti A, Ceccarelli G, Bartoli A, Spaziani A, Biancafarina A, Casciola L. Short- and medium-term outcome of robot-assisted and traditional laparoscopic rectal resection. JSLS. 2009;13:176-183.  [PubMed]  [DOI]  [Cited in This Article: ]
49.  Lin S, Jiang HG, Chen ZH, Zhou SY, Liu XS, Yu JR. Meta-analysis of robotic and laparoscopic surgery for treatment of rectal cancer. World J Gastroenterol. 2011;17:5214-5220.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in CrossRef: 88]  [Cited by in F6Publishing: 87]  [Article Influence: 6.7]  [Reference Citation Analysis (0)]
50.  Trastulli S, Farinella E, Cirocchi R, Cavaliere D, Avenia N, Sciannameo F, Gullà N, Noya G, Boselli C. Robotic resection compared with laparoscopic rectal resection for cancer: systematic review and meta-analysis of short-term outcome. Colorectal Dis. 2012;14:e134-e156.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 204]  [Cited by in F6Publishing: 192]  [Article Influence: 16.0]  [Reference Citation Analysis (0)]
51.  Ortiz-Oshiro E, Sánchez-Egido I, Moreno-Sierra J, Pérez CF, Díaz JS, Fernández-Represa JÁ. Robotic assistance may reduce conversion to open in rectal carcinoma laparoscopic surgery: systematic review and meta-analysis. Int J Med Robot. 2012;8:360-370.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 60]  [Cited by in F6Publishing: 66]  [Article Influence: 5.5]  [Reference Citation Analysis (0)]
52.  Scarpinata R, Aly EH. Does robotic rectal cancer surgery offer improved early postoperative outcomes? Dis Colon Rectum. 2013;56:253-262.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 111]  [Cited by in F6Publishing: 104]  [Article Influence: 9.5]  [Reference Citation Analysis (0)]
53.  Kuo LJ, Lin YK, Chang CC, Tai CJ, Chiou JF, Chang YJ. Clinical outcomes of robot-assisted intersphincteric resection for low rectal cancer: comparison with conventional laparoscopy and multifactorial analysis of the learning curve for robotic surgery. Int J Colorectal Dis. 2014;29:555-562.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 38]  [Cited by in F6Publishing: 38]  [Article Influence: 3.8]  [Reference Citation Analysis (0)]
54.  Casillas MA, Leichtle SW, Wahl WL, Lampman RM, Welch KB, Wellock T, Madden EB, Cleary RK. Improved perioperative and short-term outcomes of robotic versus conventional laparoscopic colorectal operations. Am J Surg. 2014;208:33-40.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 75]  [Cited by in F6Publishing: 60]  [Article Influence: 5.5]  [Reference Citation Analysis (0)]
55.  Park EJ, Cho MS, Baek SJ, Hur H, Min BS, Baik SH, Lee KY, Kim NK. Long-term oncologic outcomes of robotic low anterior resection for rectal cancer: a comparative study with laparoscopic surgery. Ann Surg. 2015;261:129-137.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 158]  [Cited by in F6Publishing: 169]  [Article Influence: 18.8]  [Reference Citation Analysis (0)]
56.  Saklani AP, Lim DR, Hur H, Min BS, Baik SH, Lee KY, Kim NK. Robotic versus laparoscopic surgery for mid-low rectal cancer after neoadjuvant chemoradiation therapy: comparison of oncologic outcomes. Int J Colorectal Dis. 2013;28:1689-1698.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 50]  [Cited by in F6Publishing: 52]  [Article Influence: 4.7]  [Reference Citation Analysis (0)]
57.  Xiong B, Ma L, Zhang C, Cheng Y. Robotic versus laparoscopic total mesorectal excision for rectal cancer: a meta-analysis. J Surg Res. 2014;188:404-414.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 75]  [Cited by in F6Publishing: 65]  [Article Influence: 6.5]  [Reference Citation Analysis (0)]
58.  Giulianotti PC, Coratti A, Angelini M, Sbrana F, Cecconi S, Balestracci T, Caravaglios G. Robotics in general surgery: personal experience in a large community hospital. Arch Surg. 2003;138:777-784.  [PubMed]  [DOI]  [Cited in This Article: ]
59.  Bokhari MB, Patel CB, Ramos-Valadez DI, Ragupathi M, Haas EM. Learning curve for robotic-assisted laparoscopic colorectal surgery. Surg Endosc. 2011;25:855-860.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 294]  [Cited by in F6Publishing: 299]  [Article Influence: 21.4]  [Reference Citation Analysis (0)]
60.  Sng KK, Hara M, Shin JW, Yoo BE, Yang KS, Kim SH. The multiphasic learning curve for robot-assisted rectal surgery. Surg Endosc. 2013;27:3297-3307.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 115]  [Cited by in F6Publishing: 109]  [Article Influence: 9.9]  [Reference Citation Analysis (0)]
61.  Buchs NC, Pugin F, Volonté F, Hagen ME, Morel P. Impact of robotic general surgery course on participants’ surgical practice. Surg Endosc. 2013;27:1968-1972.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 4]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
62.  Byrn JC, Hrabe JE, Charlton ME. An initial experience with 85 consecutive robotic-assisted rectal dissections: improved operating times and lower costs with experience. Surg Endosc. 2014;28:3101-3107.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 45]  [Cited by in F6Publishing: 34]  [Article Influence: 3.4]  [Reference Citation Analysis (0)]
63.  Delaney CP, Lynch AC, Senagore AJ, Fazio VW. Comparison of robotically performed and traditional laparoscopic colorectal surgery. Dis Colon Rectum. 2003;46:1633-1639.  [PubMed]  [DOI]  [Cited in This Article: ]
64.  Rawlings AL, Woodland JH, Vegunta RK, Crawford DL. Robotic versus laparoscopic colectomy. Surg Endosc. 2007;21:1701-1708.  [PubMed]  [DOI]  [Cited in This Article: ]
65.  Bodner J, Augustin F, Wykypiel H, Fish J, Muehlmann G, Wetscher G, Schmid T. The da Vinci robotic system for general surgical applications: a critical interim appraisal. Swiss Med Wkly. 2005;135:674-678.  [PubMed]  [DOI]  [Cited in This Article: ]
66.  Pennathur A, Gibson MK, Jobe BA, Luketich JD. Oesophageal carcinoma. Lancet. 2013;381:400-412.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1629]  [Cited by in F6Publishing: 1865]  [Article Influence: 169.5]  [Reference Citation Analysis (5)]
67.  Grimm JC, Valero V, Molena D. Surgical indications and optimization of patients for resectable esophageal malignancies. J Thorac Dis. 2014;6:249-257.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 6]  [Reference Citation Analysis (0)]
68.  Markar SR, Karthikesalingam A, Thrumurthy S, Low DE. Volume-outcome relationship in surgery for esophageal malignancy: systematic review and meta-analysis 2000-2011. J Gastrointest Surg. 2012;16:1055-1063.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 202]  [Cited by in F6Publishing: 203]  [Article Influence: 16.9]  [Reference Citation Analysis (0)]
69.  Tsujimoto H, Takahata R, Nomura S, Yaguchi Y, Kumano I, Matsumoto Y, Yoshida K, Horiguchi H, Hiraki S, Ono S. Video-assisted thoracoscopic surgery for esophageal cancer attenuates postoperative systemic responses and pulmonary complications. Surgery. 2012;151:667-673.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 60]  [Cited by in F6Publishing: 66]  [Article Influence: 5.5]  [Reference Citation Analysis (0)]
70.  Cuschieri A, Shimi S, Banting S. Endoscopic oesophagectomy through a right thoracoscopic approach. J R Coll Surg Edinb. 1992;37:7-11.  [PubMed]  [DOI]  [Cited in This Article: ]
71.  Huang L, Onaitis M. Minimally invasive and robotic Ivor Lewis esophagectomy. J Thorac Dis. 2014;6 Suppl 3:S314-S321.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 9]  [Reference Citation Analysis (0)]
72.  Luketich JD, Alvelo-Rivera M, Buenaventura PO, Christie NA, McCaughan JS, Litle VR, Schauer PR, Close JM, Fernando HC. Minimally invasive esophagectomy: outcomes in 222 patients. Ann Surg. 2003;238:486-494; discussion 494-495.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 658]  [Cited by in F6Publishing: 724]  [Article Influence: 34.5]  [Reference Citation Analysis (0)]
73.  Palanivelu C, Prakash A, Senthilkumar R, Senthilnathan P, Parthasarathi R, Rajan PS, Venkatachlam S. Minimally invasive esophagectomy: thoracoscopic mobilization of the esophagus and mediastinal lymphadenectomy in prone position--experience of 130 patients. J Am Coll Surg. 2006;203:7-16.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 314]  [Cited by in F6Publishing: 306]  [Article Influence: 17.0]  [Reference Citation Analysis (0)]
74.  Yamamoto M, Weber JM, Karl RC, Meredith KL. Minimally invasive surgery for esophageal cancer: review of the literature and institutional experience. Cancer Control. 2013;20:130-137.  [PubMed]  [DOI]  [Cited in This Article: ]
75.  Biere SS, Cuesta MA, van der Peet DL. Minimally invasive versus open esophagectomy for cancer: a systematic review and meta-analysis. Minerva Chir. 2009;64:121-133.  [PubMed]  [DOI]  [Cited in This Article: ]
76.  Nagpal K, Ahmed K, Vats A, Yakoub D, James D, Ashrafian H, Darzi A, Moorthy K, Athanasiou T. Is minimally invasive surgery beneficial in the management of esophageal cancer? A meta-analysis. Surg Endosc. 2010;24:1621-1629.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 245]  [Cited by in F6Publishing: 220]  [Article Influence: 15.7]  [Reference Citation Analysis (0)]
77.  Sgourakis G, Gockel I, Radtke A, Musholt TJ, Timm S, Rink A, Tsiamis A, Karaliotas C, Lang H. Minimally invasive versus open esophagectomy: meta-analysis of outcomes. Dig Dis Sci. 2010;55:3031-3040.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 119]  [Cited by in F6Publishing: 127]  [Article Influence: 9.1]  [Reference Citation Analysis (0)]
78.  Osugi H, Takemura M, Higashino M, Takada N, Lee S, Kinoshita H. A comparison of video-assisted thoracoscopic oesophagectomy and radical lymph node dissection for squamous cell cancer of the oesophagus with open operation. Br J Surg. 2003;90:108-113.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 178]  [Cited by in F6Publishing: 160]  [Article Influence: 7.6]  [Reference Citation Analysis (0)]
79.  Smithers BM, Gotley DC, Martin I, Thomas JM. Comparison of the outcomes between open and minimally invasive esophagectomy. Ann Surg. 2007;245:232-240.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 298]  [Cited by in F6Publishing: 286]  [Article Influence: 16.8]  [Reference Citation Analysis (0)]
80.  D’Journo XB, Thomas PA. Current management of esophageal cancer. J Thorac Dis. 2014;6 Suppl 2:S253-S264.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 65]  [Reference Citation Analysis (0)]
81.  Kawakubo H, Takeuchi H, Kitagawa Y. Current status and future perspectives on minimally invasive esophagectomy. Korean J Thorac Cardiovasc Surg. 2013;46:241-248.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 15]  [Cited by in F6Publishing: 19]  [Article Influence: 1.7]  [Reference Citation Analysis (0)]
82.  Burdall OC, Boddy AP, Fullick J, Blazeby J, Krysztopik R, Streets C, Hollowood A, Barham CP, Titcomb D. A comparative study of survival after minimally invasive and open oesophagectomy. Surg Endosc. 2015;29:431-437.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 49]  [Cited by in F6Publishing: 46]  [Article Influence: 4.6]  [Reference Citation Analysis (0)]
83.  Biere SS, van Berge Henegouwen MI, Maas KW, Bonavina L, Rosman C, Garcia JR, Gisbertz SS, Klinkenbijl JH, Hollmann MW, de Lange ES. Minimally invasive versus open oesophagectomy for patients with oesophageal cancer: a multicentre, open-label, randomised controlled trial. Lancet. 2012;379:1887-1892.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1067]  [Cited by in F6Publishing: 1154]  [Article Influence: 96.2]  [Reference Citation Analysis (0)]
84.  Jarral OA, Purkayastha S, Athanasiou T, Darzi A, Hanna GB, Zacharakis E. Thoracoscopic esophagectomy in the prone position. Surg Endosc. 2012;26:2095-2103.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 21]  [Cited by in F6Publishing: 17]  [Article Influence: 1.4]  [Reference Citation Analysis (0)]
85.  Tanaka E, Okabe H, Kinjo Y, Tsunoda S, Obama K, Hisamori S, Sakai Y. Advantages of the prone position for minimally invasive esophagectomy in comparison to the left decubitus position: better oxygenation after minimally invasive esophagectomy. Surg Today. 2015;45:819-825.  [PubMed]  [DOI]  [Cited in This Article: ]
86.  Luketich JD, Pennathur A, Awais O, Levy RM, Keeley S, Shende M, Christie NA, Weksler B, Landreneau RJ, Abbas G. Outcomes after minimally invasive esophagectomy: review of over 1000 patients. Ann Surg. 2012;256:95-103.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 533]  [Cited by in F6Publishing: 590]  [Article Influence: 49.2]  [Reference Citation Analysis (0)]
87.  Lin J, Kang M, Lin J, Chen S, Deng F, Han W, Lin R. [Short-term efficacy comparison between Ivor-Lewis approach and McKeown approach in minimally invasive esophagectomy]. Zhonghua Wei Chang Wai Ke Za Zhi. 2014;17:888-891.  [PubMed]  [DOI]  [Cited in This Article: ]
88.  Ai B, Zhang Z, Liao Y. Laparoscopic and thoracoscopic esophagectomy with intrathoracic anastomosis for middle or lower esophageal carcinoma. J Thorac Dis. 2014;6:1354-1357.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 12]  [Reference Citation Analysis (0)]
89.  Zhang J, Xu M, Guo M, Mei X, Liu C. [Analysis of postoperative quality of life in patients with middle thoracic esophageal carcinoma undergoing minimally invasive Ivor-Lewis esophagectomy]. Zhonghua Weichang Waike Zazhi. 2014;17:915-919.  [PubMed]  [DOI]  [Cited in This Article: ]
90.  Xie MR, Liu CQ, Guo MF, Mei XY, Sun XH, Xu MQ. Short-term outcomes of minimally invasive Ivor-Lewis esophagectomy for esophageal cancer. Ann Thorac Surg. 2014;97:1721-1727.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 35]  [Cited by in F6Publishing: 39]  [Article Influence: 3.9]  [Reference Citation Analysis (0)]
91.  Zhang R, Kang N, Xia W, Che Y, Wan J, Yu Z. Thoracoscopic purse string technique for minimally invasive Ivor Lewis esophagectomy. J Thorac Dis. 2014;6:148-151.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 5]  [Reference Citation Analysis (0)]
92.  Noble F, Kelly JJ, Bailey IS, Byrne JP, Underwood TJ. A prospective comparison of totally minimally invasive versus open Ivor Lewis esophagectomy. Dis Esophagus. 2013;26:263-271.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 53]  [Cited by in F6Publishing: 57]  [Article Influence: 5.2]  [Reference Citation Analysis (0)]
93.  Kernstine KH, DeArmond DT, Karimi M, Van Natta TL, Campos JH, Yoder MR, Everett JE. The robotic, 2-stage, 3-field esophagolymphadenectomy. J Thorac Cardiovasc Surg. 2004;127:1847-1849.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 90]  [Cited by in F6Publishing: 92]  [Article Influence: 4.6]  [Reference Citation Analysis (0)]
94.  Bodner JC, Zitt M, Ott H, Wetscher GJ, Wykypiel H, Lucciarini P, Schmid T. Robotic-assisted thoracoscopic surgery (RATS) for benign and malignant esophageal tumors. Ann Thorac Surg. 2005;80:1202-1206.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 1]  [Reference Citation Analysis (0)]
95.  Boone J, Schipper ME, Moojen WA, Borel Rinkes IH, Cromheecke GJ, van Hillegersberg R. Robot-assisted thoracoscopic oesophagectomy for cancer. Br J Surg. 2009;96:878-886.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 103]  [Cited by in F6Publishing: 108]  [Article Influence: 7.2]  [Reference Citation Analysis (0)]
96.  Puntambekar SP, Rayate N, Joshi S, Agarwal G. Robotic transthoracic esophagectomy in the prone position: experience with 32 patients with esophageal cancer. J Thorac Cardiovasc Surg. 2011;142:1283-1284.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 46]  [Cited by in F6Publishing: 40]  [Article Influence: 3.1]  [Reference Citation Analysis (0)]
97.  van Hillegersberg R, Boone J, Draaisma WA, Broeders IA, Giezeman MJ, Borel Rinkes IH. First experience with robot-assisted thoracoscopic esophagolymphadenectomy for esophageal cancer. Surg Endosc. 2006;20:1435-1439.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 156]  [Cited by in F6Publishing: 157]  [Article Influence: 8.7]  [Reference Citation Analysis (0)]
98.  Kim DJ, Hyung WJ, Lee CY, Lee JG, Haam SJ, Park IK, Chung KY. Thoracoscopic esophagectomy for esophageal cancer: feasibility and safety of robotic assistance in the prone position. J Thorac Cardiovasc Surg. 2010;139:53-59.e1.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 86]  [Cited by in F6Publishing: 81]  [Article Influence: 5.4]  [Reference Citation Analysis (0)]
99.  Suda K, Ishida Y, Kawamura Y, Inaba K, Kanaya S, Teramukai S, Satoh S, Uyama I. Robot-assisted thoracoscopic lymphadenectomy along the left recurrent laryngeal nerve for esophageal squamous cell carcinoma in the prone position: technical report and short-term outcomes. World J Surg. 2012;36:1608-1616.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 96]  [Cited by in F6Publishing: 104]  [Article Influence: 8.7]  [Reference Citation Analysis (0)]
100.  Cerfolio RJ, Bryant AS, Hawn MT. Technical aspects and early results of robotic esophagectomy with chest anastomosis. J Thorac Cardiovasc Surg. 2013;145:90-96.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 66]  [Cited by in F6Publishing: 76]  [Article Influence: 6.3]  [Reference Citation Analysis (0)]
101.  Sarkaria IS, Rizk NP, Finley DJ, Bains MS, Adusumilli PS, Huang J, Rusch VW. Combined thoracoscopic and laparoscopic robotic-assisted minimally invasive esophagectomy using a four-arm platform: experience, technique and cautions during early procedure development. Eur J Cardiothorac Surg. 2013;43:e107-e115.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 64]  [Cited by in F6Publishing: 71]  [Article Influence: 6.5]  [Reference Citation Analysis (0)]
102.  de la Fuente SG, Weber J, Hoffe SE, Shridhar R, Karl R, Meredith KL. Initial experience from a large referral center with robotic-assisted Ivor Lewis esophagogastrectomy for oncologic purposes. Surg Endosc. 2013;27:3339-3347.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 57]  [Cited by in F6Publishing: 54]  [Article Influence: 4.9]  [Reference Citation Analysis (0)]
103.  Trugeda S, Fernández-Díaz MJ, Rodríguez-Sanjuán JC, Palazuelos CM, Fernández-Escalante C, Gómez-Fleitas M. Initial results of robot-assisted Ivor-Lewis oesophagectomy with intrathoracic hand-sewn anastomosis in the prone position. Int J Med Robot. 2014;10:397-403.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 25]  [Cited by in F6Publishing: 30]  [Article Influence: 3.0]  [Reference Citation Analysis (0)]
104.  Trugeda Carrera MS, Fernández-Díaz MJ, Rodríguez-Sanjuán JC, Manuel-Palazuelos JC, de Diego García EM, Gómez-Fleitas M. [Initial results of robotic esophagectomy for esophageal cancer]. Cir Esp. 2015;93:396-402.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 6]  [Article Influence: 0.7]  [Reference Citation Analysis (0)]
105.  van der Sluis PC, Ruurda JP, van der Horst S, Verhage RJ, Besselink MG, Prins MJ, Haverkamp L, Schippers C, Rinkes IH, Joore HC. Robot-assisted minimally invasive thoraco-laparoscopic esophagectomy versus open transthoracic esophagectomy for resectable esophageal cancer, a randomized controlled trial (ROBOT trial). Trials. 2012;13:230.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 125]  [Cited by in F6Publishing: 117]  [Article Influence: 9.8]  [Reference Citation Analysis (0)]
106.  Jemal A, Bray F, Center MM, Ferlay J, Ward E, Forman D. Global cancer statistics. CA Cancer J Clin. 2011;61:69-90.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 23762]  [Cited by in F6Publishing: 25335]  [Article Influence: 1948.8]  [Reference Citation Analysis (7)]
107.  Strong VE, Song KY, Park CH, Jacks LM, Gonen M, Shah M, Coit DG, Brennan MF. Comparison of gastric cancer survival following R0 resection in the United States and Korea using an internationally validated nomogram. Ann Surg. 2010;251:640-646.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 250]  [Cited by in F6Publishing: 282]  [Article Influence: 20.1]  [Reference Citation Analysis (0)]
108.  Japanese Gastric Cancer Association. Japanese classification of gastric carcinoma: 3rd English edition. Gastric Cancer. 2011;14:101-112.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2390]  [Cited by in F6Publishing: 2751]  [Article Influence: 211.6]  [Reference Citation Analysis (0)]
109.  American Joint Committee on Cancer (AJCC) cancer staging manual 7th ed. Chicago: Springer, Inc 2010; .  [PubMed]  [DOI]  [Cited in This Article: ]
110.  Ajani JA, Bentrem DJ, Besh S, D’Amico TA, Das P, Denlinger C, Fakih MG, Fuchs CS, Gerdes H, Glasgow RE. Gastric cancer, version 2.2013: featured updates to the NCCN Guidelines. J Natl Compr Canc Netw. 2013;11:531-546.  [PubMed]  [DOI]  [Cited in This Article: ]
111.  Okines A, Verheij M, Allum W, Cunningham D, Cervantes A. Gastric cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2010;21 Suppl 5:v50-v54.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 208]  [Cited by in F6Publishing: 247]  [Article Influence: 17.6]  [Reference Citation Analysis (0)]
112.  Japanese Gastric Cancer Association. Japanese gastric cancer treatment guidelines 2010 (ver. 3). Gastric Cancer. 2011;14:113-123.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1723]  [Cited by in F6Publishing: 1863]  [Article Influence: 143.3]  [Reference Citation Analysis (0)]
113.  Kitano S, Iso Y, Moriyama M, Sugimachi K. Laparoscopy-assisted Billroth I gastrectomy. Surg Laparosc Endosc. 1994;4:146-148.  [PubMed]  [DOI]  [Cited in This Article: ]
114.  Antonakis PT, Ashrafian H, Isla AM. Laparoscopic gastric surgery for cancer: where do we stand? World J Gastroenterol. 2014;20:14280-14291.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in CrossRef: 19]  [Cited by in F6Publishing: 19]  [Article Influence: 1.9]  [Reference Citation Analysis (0)]
115.  Kitano S, Shiraishi N, Fujii K, Yasuda K, Inomata M, Adachi Y. A randomized controlled trial comparing open vs laparoscopy-assisted distal gastrectomy for the treatment of early gastric cancer: an interim report. Surgery. 2002;131:S306-S311.  [PubMed]  [DOI]  [Cited in This Article: ]
116.  Hayashi H, Ochiai T, Shimada H, Gunji Y. Prospective randomized study of open versus laparoscopy-assisted distal gastrectomy with extraperigastric lymph node dissection for early gastric cancer. Surg Endosc. 2005;19:1172-1176.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 1]  [Reference Citation Analysis (0)]
117.  Strong VE, Devaud N, Allen PJ, Gonen M, Brennan MF, Coit D. Laparoscopic versus open subtotal gastrectomy for adenocarcinoma: a case-control study. Ann Surg Oncol. 2009;16:1507-1513.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 144]  [Cited by in F6Publishing: 153]  [Article Influence: 10.2]  [Reference Citation Analysis (0)]
118.  Lee JH, Han HS, Lee JH. A prospective randomized study comparing open vs laparoscopy-assisted distal gastrectomy in early gastric cancer: early results. Surg Endosc. 2005;19:168-173.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 308]  [Cited by in F6Publishing: 321]  [Article Influence: 16.1]  [Reference Citation Analysis (0)]
119.  Kim YW, Yoon HM, Yun YH, Nam BH, Eom BW, Baik YH, Lee SE, Lee Y, Kim YA, Park JY. Long-term outcomes of laparoscopy-assisted distal gastrectomy for early gastric cancer: result of a randomized controlled trial (COACT 0301). Surg Endosc. 2013;27:4267-4276.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 87]  [Cited by in F6Publishing: 103]  [Article Influence: 9.4]  [Reference Citation Analysis (0)]
120.  Kim HH, Hyung WJ, Cho GS, Kim MC, Han SU, Kim W, Ryu SW, Lee HJ, Song KY. Morbidity and mortality of laparoscopic gastrectomy versus open gastrectomy for gastric cancer: an interim report--a phase III multicenter, prospective, randomized Trial (KLASS Trial). Ann Surg. 2010;251:417-420.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 562]  [Cited by in F6Publishing: 609]  [Article Influence: 43.5]  [Reference Citation Analysis (0)]
121.  Takiguchi S, Fujiwara Y, Yamasaki M, Miyata H, Nakajima K, Sekimoto M, Mori M, Doki Y. Laparoscopy-assisted distal gastrectomy versus open distal gastrectomy. A prospective randomized single-blind study. World J Surg. 2013;37:2379-2386.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 75]  [Cited by in F6Publishing: 88]  [Article Influence: 8.8]  [Reference Citation Analysis (0)]
122.  Kim YW, Baik YH, Yun YH, Nam BH, Kim DH, Choi IJ, Bae JM. Improved quality of life outcomes after laparoscopy-assisted distal gastrectomy for early gastric cancer: results of a prospective randomized clinical trial. Ann Surg. 2008;248:721-727.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 475]  [Cited by in F6Publishing: 496]  [Article Influence: 31.0]  [Reference Citation Analysis (0)]
123.  Lee J, Kim YM, Woo Y, Obama K, Noh SH, Hyung WJ. Robotic distal subtotal gastrectomy with D2 lymphadenectomy for gastric cancer patients with high body mass index: comparison with conventional laparoscopic distal subtotal gastrectomy with D2 lymphadenectomy. Surg Endosc. 2015;29:3251-3260.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 73]  [Cited by in F6Publishing: 88]  [Article Influence: 9.8]  [Reference Citation Analysis (0)]
124.  Chen XZ, Hu JK, Yang K, Wang L, Lu QC. Short-term evaluation of laparoscopy-assisted distal gastrectomy for predictive early gastric cancer: a meta-analysis of randomized controlled trials. Surg Laparosc Endosc Percutan Tech. 2009;19:277-284.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 52]  [Cited by in F6Publishing: 54]  [Article Influence: 3.6]  [Reference Citation Analysis (0)]
125.  Kodera Y, Fujiwara M, Ohashi N, Nakayama G, Koike M, Morita S, Nakao A. Laparoscopic surgery for gastric cancer: a collective review with meta-analysis of randomized trials. J Am Coll Surg. 2010;211:677-686.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 98]  [Cited by in F6Publishing: 109]  [Article Influence: 7.8]  [Reference Citation Analysis (0)]
126.  Ohtani H, Tamamori Y, Noguchi K, Azuma T, Fujimoto S, Oba H, Aoki T, Minami M, Hirakawa K. Meta-analysis of laparoscopy-assisted and open distal gastrectomy for gastric cancer. J Surg Res. 2011;171:479-485.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 40]  [Cited by in F6Publishing: 46]  [Article Influence: 3.3]  [Reference Citation Analysis (0)]
127.  Zorcolo L, Rosman AS, Pisano M, Marcon F, Restivo A, Nigri GR, Fancellu A, Melis M. A meta-analysis of prospective randomized trials comparing minimally invasive and open distal gastrectomy for cancer. J Surg Oncol. 2011;104:544-551.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 13]  [Cited by in F6Publishing: 12]  [Article Influence: 0.9]  [Reference Citation Analysis (0)]
128.  Viñuela EF, Gonen M, Brennan MF, Coit DG, Strong VE. Laparoscopic versus open distal gastrectomy for gastric cancer: a meta-analysis of randomized controlled trials and high-quality nonrandomized studies. Ann Surg. 2012;255:446-456.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 277]  [Cited by in F6Publishing: 288]  [Article Influence: 24.0]  [Reference Citation Analysis (0)]
129.  Zeng YK, Yang ZL, Peng JS, Lin HS, Cai L. Laparoscopy-assisted versus open distal gastrectomy for early gastric cancer: evidence from randomized and nonrandomized clinical trials. Ann Surg. 2012;256:39-52.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 155]  [Cited by in F6Publishing: 158]  [Article Influence: 13.2]  [Reference Citation Analysis (0)]
130.  Jiang L, Yang KH, Guan QL, Cao N, Chen Y, Zhao P, Chen YL, Yao L. Laparoscopy-assisted gastrectomy versus open gastrectomy for resectable gastric cancer: an update meta-analysis based on randomized controlled trials. Surg Endosc. 2013;27:2466-2480.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 63]  [Cited by in F6Publishing: 57]  [Article Influence: 5.2]  [Reference Citation Analysis (0)]
131.  Wang Y, Wang S, Huang ZQ, Chou WP. Meta-analysis of laparoscopy assisted distal gastrectomy and conventional open distal gastrectomy for EGC. Surgeon. 2014;12:53-58.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 8]  [Cited by in F6Publishing: 10]  [Article Influence: 0.9]  [Reference Citation Analysis (0)]
132.  Inokuchi M, Sugita H, Otsuki S, Sato Y, Nakagawa M, Kojima K. Laparoscopic distal gastrectomy reduced surgical site infection as compared with open distal gastrectomy for gastric cancer in a meta-analysis of both randomized controlled and case-controlled studies. Int J Surg. 2015;15:61-67.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 15]  [Cited by in F6Publishing: 17]  [Article Influence: 1.9]  [Reference Citation Analysis (0)]
133.  Nakamura K, Katai H, Mizusawa J, Yoshikawa T, Ando M, Terashima M, Ito S, Takagi M, Takagane A, Ninomiya M. A phase III study of laparoscopy-assisted versus open distal gastrectomy with nodal dissection for clinical stage IA/IB gastric Cancer (JCOG0912). Jpn J Clin Oncol. 2013;43:324-327.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 99]  [Cited by in F6Publishing: 98]  [Article Influence: 8.2]  [Reference Citation Analysis (0)]
134.  Kim HH, Han SU, Kim MC, Hyung WJ, Kim W, Lee HJ, Ryu SW, Cho GS, Kim CY, Yang HK. Prospective randomized controlled trial (phase III) to comparing laparoscopic distal gastrectomy with open distal gastrectomy for gastric adenocarcinoma (KLASS 01). J Korean Surg Soc. 2013;84:123-130.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 79]  [Cited by in F6Publishing: 90]  [Article Influence: 8.2]  [Reference Citation Analysis (0)]
135.  Brar S, Law C, McLeod R, Helyer L, Swallow C, Paszat L, Seevaratnam R, Cardoso R, Dixon M, Mahar A. Defining surgical quality in gastric cancer: a RAND/UCLA appropriateness study. J Am Coll Surg. 2013;217:347-57.e1.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 33]  [Cited by in F6Publishing: 39]  [Article Influence: 3.5]  [Reference Citation Analysis (0)]
136.  Huscher CG, Mingoli A, Sgarzini G, Sansonetti A, Di Paola M, Recher A, Ponzano C. Laparoscopic versus open subtotal gastrectomy for distal gastric cancer: five-year results of a randomized prospective trial. Ann Surg. 2005;241:232-237.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 650]  [Cited by in F6Publishing: 648]  [Article Influence: 34.1]  [Reference Citation Analysis (0)]
137.  Cai J, Wei D, Gao CF, Zhang CS, Zhang H, Zhao T. A prospective randomized study comparing open versus laparoscopy-assisted D2 radical gastrectomy in advanced gastric cancer. Dig Surg. 2011;28:331-337.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 119]  [Cited by in F6Publishing: 130]  [Article Influence: 10.0]  [Reference Citation Analysis (0)]
138.  Martínez-Ramos D, Miralles-Tena JM, Cuesta MA, Escrig-Sos J, Van der Peet D, Hoashi JS, Salvador-Sanchís JL. Laparoscopy versus open surgery for advanced and resectable gastric cancer: a meta-analysis. Rev Esp Enferm Dig. 2011;103:133-141.  [PubMed]  [DOI]  [Cited in This Article: ]
139.  Wei HB, Wei B, Qi CL, Chen TF, Huang Y, Zheng ZH, Huang JL, Fang JF. Laparoscopic versus open gastrectomy with D2 lymph node dissection for gastric cancer: a meta-analysis. Surg Laparosc Endosc Percutan Tech. 2011;21:383-390.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 1]  [Reference Citation Analysis (0)]
140.  Lee JH, Son SY, Lee CM, Ahn SH, Park do J, Kim HH. Morbidity and mortality after laparoscopic gastrectomy for advanced gastric cancer: results of a phase II clinical trial. Surg Endosc. 2013;27:2877-2885.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 33]  [Cited by in F6Publishing: 35]  [Article Influence: 3.2]  [Reference Citation Analysis (0)]
141.  Shinohara T, Kanaya S, Taniguchi K, Fujita T, Yanaga K, Uyama I. Laparoscopic total gastrectomy with D2 lymph node dissection for gastric cancer. Arch Surg. 2009;144:1138-1142.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 87]  [Cited by in F6Publishing: 97]  [Article Influence: 6.9]  [Reference Citation Analysis (0)]
142.  Jeong GA, Cho GS, Kim HH, Lee HJ, Ryu SW, Song KY. Laparoscopy-assisted total gastrectomy for gastric cancer: a multicenter retrospective analysis. Surgery. 2009;146:469-474.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 83]  [Cited by in F6Publishing: 92]  [Article Influence: 6.1]  [Reference Citation Analysis (0)]
143.  Dulucq JL, Wintringer P, Perissat J, Mahajna A. Completely laparoscopic total and partial gastrectomy for benign and malignant diseases: a single institute’s prospective analysis. J Am Coll Surg. 2005;200:191-197.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 64]  [Cited by in F6Publishing: 53]  [Article Influence: 2.8]  [Reference Citation Analysis (0)]
144.  Huscher CG, Mingoli A, Sgarzini G, Brachini G, Binda B, Di Paola M, Ponzano C. Totally laparoscopic total and subtotal gastrectomy with extended lymph node dissection for early and advanced gastric cancer: early and long-term results of a 100-patient series. Am J Surg. 2007;194:839-844; discussion 844.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 84]  [Cited by in F6Publishing: 90]  [Article Influence: 5.3]  [Reference Citation Analysis (0)]
145.  LaFemina J, Viñuela EF, Schattner MA, Gerdes H, Strong VE. Esophagojejunal reconstruction after total gastrectomy for gastric cancer using a transorally inserted anvil delivery system. Ann Surg Oncol. 2013;20:2975-2983.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 42]  [Cited by in F6Publishing: 47]  [Article Influence: 4.3]  [Reference Citation Analysis (0)]
146.  Wang W, Li Z, Tang J, Wang M, Wang B, Xu Z. Laparoscopic versus open total gastrectomy with D2 dissection for gastric cancer: a meta-analysis. J Cancer Res Clin Oncol. 2013;139:1721-1734.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 25]  [Cited by in F6Publishing: 25]  [Article Influence: 2.3]  [Reference Citation Analysis (0)]
147.  Haverkamp L, Weijs TJ, van der Sluis PC, van der Tweel I, Ruurda JP, van Hillegersberg R. Laparoscopic total gastrectomy versus open total gastrectomy for cancer: a systematic review and meta-analysis. Surg Endosc. 2013;27:1509-1520.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 131]  [Cited by in F6Publishing: 138]  [Article Influence: 11.5]  [Reference Citation Analysis (0)]
148.  Chen K, Xu XW, Zhang RC, Pan Y, Wu D, Mou YP. Systematic review and meta-analysis of laparoscopy-assisted and open total gastrectomy for gastric cancer. World J Gastroenterol. 2013;19:5365-5376.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in CrossRef: 59]  [Cited by in F6Publishing: 67]  [Article Influence: 6.1]  [Reference Citation Analysis (0)]
149.  Laparoscopy-assisted Total Gastrectomy for Clinical Stage I Gastric Cancer (KLASS-03).  Available from: https://clinicaltrials.gov/ct2/show/NCT01584336.  [PubMed]  [DOI]  [Cited in This Article: ]
150.  Hur H, Kim JY, Cho YK, Han SU. Technical feasibility of robot-sewn anastomosis in robotic surgery for gastric cancer. J Laparoendosc Adv Surg Tech A. 2010;20:693-697.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 55]  [Cited by in F6Publishing: 59]  [Article Influence: 4.5]  [Reference Citation Analysis (0)]
151.  Hashizume M, Shimada M, Tomikawa M, Ikeda Y, Takahashi I, Abe R, Koga F, Gotoh N, Konishi K, Maehara S. Early experiences of endoscopic procedures in general surgery assisted by a computer-enhanced surgical system. Surg Endosc. 2002;16:1187-1191.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 187]  [Cited by in F6Publishing: 161]  [Article Influence: 7.3]  [Reference Citation Analysis (0)]
152.  Song J, Oh SJ, Kang WH, Hyung WJ, Choi SH, Noh SH. Robot-assisted gastrectomy with lymph node dissection for gastric cancer: lessons learned from an initial 100 consecutive procedures. Ann Surg. 2009;249:927-932.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 213]  [Cited by in F6Publishing: 214]  [Article Influence: 14.3]  [Reference Citation Analysis (0)]
153.  Woo Y, Hyung WJ, Pak KH, Inaba K, Obama K, Choi SH, Noh SH. Robotic gastrectomy as an oncologically sound alternative to laparoscopic resections for the treatment of early-stage gastric cancers. Arch Surg. 2011;146:1086-1092.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 147]  [Cited by in F6Publishing: 162]  [Article Influence: 12.5]  [Reference Citation Analysis (0)]
154.  Yoon HM, Kim YW, Lee JH, Ryu KW, Eom BW, Park JY, Choi IJ, Kim CG, Lee JY, Cho SJ. Robot-assisted total gastrectomy is comparable with laparoscopically assisted total gastrectomy for early gastric cancer. Surg Endosc. 2012;26:1377-1381.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 93]  [Cited by in F6Publishing: 98]  [Article Influence: 7.5]  [Reference Citation Analysis (0)]
155.  Huang KH, Lan YT, Fang WL, Chen JH, Lo SS, Hsieh MC, Li AF, Chiou SH, Wu CW. Initial experience of robotic gastrectomy and comparison with open and laparoscopic gastrectomy for gastric cancer. J Gastrointest Surg. 2012;16:1303-1310.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 94]  [Cited by in F6Publishing: 105]  [Article Influence: 8.8]  [Reference Citation Analysis (0)]
156.  Xiong B, Ma L, Zhang C. Robotic versus laparoscopic gastrectomy for gastric cancer: a meta-analysis of short outcomes. Surg Oncol. 2012;21:274-280.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 61]  [Cited by in F6Publishing: 66]  [Article Influence: 5.5]  [Reference Citation Analysis (0)]
157.  Kim KM, An JY, Kim HI, Cheong JH, Hyung WJ, Noh SH. Major early complications following open, laparoscopic and robotic gastrectomy. Br J Surg. 2012;99:1681-1687.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 108]  [Cited by in F6Publishing: 116]  [Article Influence: 9.7]  [Reference Citation Analysis (0)]
158.  Liao GX, Xie GZ, Li R, Zhao ZH, Sun QQ, Du SS, Ren C, Li GX, Deng HJ, Yuan YW. Meta-analysis of outcomes compared between robotic and laparoscopic gastrectomy for gastric cancer. Asian Pac J Cancer Prev. 2013;14:4871-4875.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 28]  [Cited by in F6Publishing: 27]  [Article Influence: 2.7]  [Reference Citation Analysis (0)]
159.  Xiong J, Nunes QM, Tan C, Ke N, Chen Y, Hu W, Liu X, Mai G. Comparison of short-term clinical outcomes between robotic and laparoscopic gastrectomy for gastric cancer: a meta-analysis of 2495 patients. J Laparoendosc Adv Surg Tech A. 2013;23:965-976.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 27]  [Cited by in F6Publishing: 31]  [Article Influence: 2.8]  [Reference Citation Analysis (0)]
160.  Marano A, Choi YY, Hyung WJ, Kim YM, Kim J, Noh SH. Robotic versus Laparoscopic versus Open Gastrectomy: A Meta-Analysis. J Gastric Cancer. 2013;13:136-148.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 86]  [Cited by in F6Publishing: 93]  [Article Influence: 8.5]  [Reference Citation Analysis (0)]
161.  Hyun MH, Lee CH, Kim HJ, Tong Y, Park SS. Systematic review and meta-analysis of robotic surgery compared with conventional laparoscopic and open resections for gastric carcinoma. Br J Surg. 2013;100:1566-1578.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 73]  [Cited by in F6Publishing: 74]  [Article Influence: 7.4]  [Reference Citation Analysis (0)]
162.  Liao G, Chen J, Ren C, Li R, Du S, Xie G, Deng H, Yang K, Yuan Y. Robotic versus open gastrectomy for gastric cancer: a meta-analysis. PLoS One. 2013;8:e81946.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 34]  [Cited by in F6Publishing: 37]  [Article Influence: 3.4]  [Reference Citation Analysis (0)]
163.  Zong L, Seto Y, Aikou S, Takahashi T. Efficacy evaluation of subtotal and total gastrectomies in robotic surgery for gastric cancer compared with that in open and laparoscopic resections: a meta-analysis. PLoS One. 2014;9:e103312.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 43]  [Cited by in F6Publishing: 46]  [Article Influence: 4.6]  [Reference Citation Analysis (0)]
164.  Shen WS, Xi HQ, Chen L, Wei B. A meta-analysis of robotic versus laparoscopic gastrectomy for gastric cancer. Surg Endosc. 2014;28:2795-2802.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 63]  [Cited by in F6Publishing: 72]  [Article Influence: 7.2]  [Reference Citation Analysis (0)]
165.  Bhatt DL, Steg PG, Ohman EM, Hirsch AT, Ikeda Y, Mas JL, Goto S, Liau CS, Richard AJ, Röther J. International prevalence, recognition, and treatment of cardiovascular risk factors in outpatients with atherothrombosis. JAMA. 2006;295:180-189.  [PubMed]  [DOI]  [Cited in This Article: ]
166.  Lobstein T, Leach RJ. Tackling obesities: future choices. International comparisons of obesity trends, determinants and responses-evidence review.  Available from: http://www.bis.gov.uk/assets/ foresight/docs/obesity/06 page.pdf.URN 07/926A1.  [PubMed]  [DOI]  [Cited in This Article: ]
167.  World Health Organization. World Health Report 2002. Accessed January 13, 2004.  Available from: http://www.who.int/whr/2002/en/whr02_en.pdf.  [PubMed]  [DOI]  [Cited in This Article: ]
168.  Must A, Spadano J, Coakley EH, Field AE, Colditz G, Dietz WH. The disease burden associated with overweight and obesity. JAMA. 1999;282:1523-1529.  [PubMed]  [DOI]  [Cited in This Article: ]
169.  O’Brien P, Brown W, Dixon J. Revisional surgery for morbid obesity--conversion to the Lap-Band system. Obes Surg. 2000;10:557-563.  [PubMed]  [DOI]  [Cited in This Article: ]
170.  Christou NV, MacLean LD. Effect of bariatric surgery on long-term mortality. Adv Surg. 2005;39:165-179.  [PubMed]  [DOI]  [Cited in This Article: ]
171.  Linner JH. Comparative effectiveness of gastric bypass and gastroplasty: a clinical study. Arch Surg. 1982;117:695-700.  [PubMed]  [DOI]  [Cited in This Article: ]
172.  Christou NV, Sampalis JS, Liberman M, Look D, Auger S, McLean AP, MacLean LD. Surgery decreases long-term mortality, morbidity, and health care use in morbidly obese patients. Ann Surg. 2004;240:416-423; discussion 423-424.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 912]  [Cited by in F6Publishing: 843]  [Article Influence: 42.2]  [Reference Citation Analysis (0)]
173.  MacLean LD, Rhode BM, Sampalis J, Forse RA. Results of the surgical treatment of obesity. Am J Surg. 1993;165:155-60; discussion 160-2.  [PubMed]  [DOI]  [Cited in This Article: ]
174.  Sjöström L, Lindroos AK, Peltonen M, Torgerson J, Bouchard C, Carlsson B, Dahlgren S, Larsson B, Narbro K, Sjöström CD. Lifestyle, diabetes, and cardiovascular risk factors 10 years after bariatric surgery. N Engl J Med. 2004;351:2683-2693.  [PubMed]  [DOI]  [Cited in This Article: ]
175.  North American Association for the Study of Obesity and the National Heart, Lung, and Blood Institute The Practical Guide: Identification, Evaluation, and Treatment of Overweight and Obesity in Adults. Bethesda, MD: National Institutes of Health 2000; .  [PubMed]  [DOI]  [Cited in This Article: ]
176.  North American Association for the Study of Obesity (NAASO) and the National Heart Clinical Guidelines on the Identification, Evaluation, and Treatment of Overweight and Obesity in Adults: The Evidence Report. Bethesda, MD: National Institutes of Health 1998; .  [PubMed]  [DOI]  [Cited in This Article: ]
177.  Papamargaritis DK, Pournaras DJ, Le Roux CW. Techniques, assessment, and effectiveness of bariatric surgery in combating obesity. Surgery. 2010;3:123-136.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1]  [Cited by in F6Publishing: 1]  [Article Influence: 0.1]  [Reference Citation Analysis (0)]
178.  Dixon JB, le Roux CW, Rubino F, Zimmet P. Bariatric surgery for type 2 diabetes. Lancet. 2012;379:2300-2311.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 218]  [Cited by in F6Publishing: 194]  [Article Influence: 16.2]  [Reference Citation Analysis (0)]
179.  Nguyen NT, Hinojosa M, Fayad C, Varela E, Wilson SE. Use and outcomes of laparoscopic versus open gastric bypass at academic medical centers. J Am Coll Surg. 2007;205:248-255.  [PubMed]  [DOI]  [Cited in This Article: ]
180.  Reoch J, Mottillo S, Shimony A, Filion KB, Christou NV, Joseph L, Poirier P, Eisenberg MJ. Safety of laparoscopic vs open bariatric surgery: a systematic review and meta-analysis. Arch Surg. 2011;146:1314-1322.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 92]  [Cited by in F6Publishing: 88]  [Article Influence: 7.3]  [Reference Citation Analysis (0)]
181.  Azagra JS, Goergen M, Ansay J, De Simone P, Vanhaverbeek M, Devuyst L, Squelaert J. Laparoscopic gastric reduction surgery. Preliminary results of a randomized, prospective trial of laparoscopic vs open vertical banded gastroplasty. Surg Endosc. 1999;13:555-558.  [PubMed]  [DOI]  [Cited in This Article: ]
182.  de Wit LT, Mathus-Vliegen L, Hey C, Rademaker B, Gouma DJ, Obertop H. Open versus laparoscopic adjustable silicone gastric banding: a prospective randomized trial for treatment of morbid obesity. Ann Surg. 1999;230:800-805; discussion 805-807.  [PubMed]  [DOI]  [Cited in This Article: ]
183.  Nguyen NT, Goldman C, Rosenquist CJ, Arango A, Cole CJ, Lee SJ, Wolfe BM. Laparoscopic versus open gastric bypass: a randomized study of outcomes, quality of life, and costs. Ann Surg. 2001;234:279-289; discussion 289-291.  [PubMed]  [DOI]  [Cited in This Article: ]
184.  Sundbom M, Gustavsson S. Randomized clinical trial of hand-assisted laparoscopic versus open Roux-en-Y gastric bypass for the treatment of morbid obesity. Br J Surg. 2004;91:418-423.  [PubMed]  [DOI]  [Cited in This Article: ]
185.  Westling A, Gustavsson S. Laparoscopic vs open Roux-en-Y gastric bypass: a prospective, randomized trial. Obes Surg. 2001;11:284-292.  [PubMed]  [DOI]  [Cited in This Article: ]
186.  Luján JA, Frutos MD, Hernández Q, Liron R, Cuenca JR, Valero G, Parrilla P. Laparoscopic versus open gastric bypass in the treatment of morbid obesity: a randomized prospective study. Ann Surg. 2004;239:433-437.  [PubMed]  [DOI]  [Cited in This Article: ]
187.  Colquitt JL, Picot J, Loveman E, Clegg AJ. Surgery for obesity. Cochrane Database Syst Rev. 2009;CD003641.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3437]  [Cited by in F6Publishing: 2598]  [Article Influence: 2598.0]  [Reference Citation Analysis (0)]
188.  Gentileschi P, Kini S, Catarci M, Gagner M. Evidence-based medicine: open and laparoscopic bariatric surgery. Surg Endosc. 2002;16:736-744.  [PubMed]  [DOI]  [Cited in This Article: ]
189.  Buchwald H, Estok R, Fahrbach K, Banel D, Sledge I. Trends in mortality in bariatric surgery: a systematic review and meta-analysis. Surgery. 2007;142:621-632; discussion 632-635.  [PubMed]  [DOI]  [Cited in This Article: ]
190.  Jones KB, Afram JD, Benotti PN, Capella RF, Cooper CG, Flanagan L, Hendrick S, Howell LM, Jaroch MT, Kole K. Open versus laparoscopic Roux-en-Y gastric bypass: a comparative study of over 25,000 open cases and the major laparoscopic bariatric reported series. Obes Surg. 2006;16:721-727.  [PubMed]  [DOI]  [Cited in This Article: ]
191.  Flum DR, Belle SH, King WC, Wahed AS, Berk P, Chapman W, Pories W, Courcoulas A, McCloskey C, Mitchell J. Perioperative safety in the longitudinal assessment of bariatric surgery. N Engl J Med. 2009;361:445-454.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1041]  [Cited by in F6Publishing: 933]  [Article Influence: 62.2]  [Reference Citation Analysis (0)]
192.  Morino M, Toppino M, Forestieri P, Angrisani L, Allaix ME, Scopinaro N. Mortality after bariatric surgery: analysis of 13,871 morbidly obese patients from a national registry. Ann Surg. 2007;246:1002-1007; discussion 1007-1009.  [PubMed]  [DOI]  [Cited in This Article: ]
193.  Nguyen NT, Paya M, Stevens CM, Mavandadi S, Zainabadi K, Wilson SE. The relationship between hospital volume and outcome in bariatric surgery at academic medical centers. Ann Surg. 2004;240:586-593; discussion 593-594.  [PubMed]  [DOI]  [Cited in This Article: ]
194.  Cadiere GB, Himpens J, Vertruyen M, Favretti F. The world’s first obesity surgery performed by a surgeon at a distance. Obes Surg. 1999;9:206-209.  [PubMed]  [DOI]  [Cited in This Article: ]
195.  Cadière GB, Himpens J, Vertruyen M, Bruyns J, Germay O, Leman G, Izizaw R. Evaluation of telesurgical (robotic) NISSEN fundoplication. Surg Endosc. 2001;15:918-923.  [PubMed]  [DOI]  [Cited in This Article: ]
196.  Talamini MA, Chapman S, Horgan S, Melvin WS. A prospective analysis of 211 robotic-assisted surgical procedures. Surg Endosc. 2003;17:1521-1524.  [PubMed]  [DOI]  [Cited in This Article: ]
197.  Yu SC, Clapp BL, Lee MJ, Albrecht WC, Scarborough TK, Wilson EB. Robotic assistance provides excellent outcomes during the learning curve for laparoscopic Roux-en-Y gastric bypass: results from 100 robotic-assisted gastric bypasses. Am J Surg. 2006;192:746-749.  [PubMed]  [DOI]  [Cited in This Article: ]
198.  Edelson PK, Dumon KR, Sonnad SS, Shafi BM, Williams NN. Robotic vs. conventional laparoscopic gastric banding: a comparison of 407 cases. Surg Endosc. 2011;25:1402-1408.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 38]  [Cited by in F6Publishing: 26]  [Article Influence: 1.9]  [Reference Citation Analysis (0)]
199.  Fourman MM, Saber AA. Robotic bariatric surgery: a systematic review. Surg Obes Relat Dis. 2012;8:483-488.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 73]  [Cited by in F6Publishing: 66]  [Article Influence: 5.5]  [Reference Citation Analysis (0)]
200.  Horgan S, Vanuno D. Robots in laparoscopic surgery. J Laparoendosc Adv Surg Tech A. 2001;11:415-419.  [PubMed]  [DOI]  [Cited in This Article: ]
201.  Jacobsen G, Berger R, Horgan S. The role of robotic surgery in morbid obesity. J Laparoendosc Adv Surg Tech A. 2003;13:279-283.  [PubMed]  [DOI]  [Cited in This Article: ]
202.  Snyder BE, Wilson T, Scarborough T, Yu S, Wilson EB. Lowering gastrointestinal leak rates: a comparative analysis of robotic and laparoscopic gastric bypass. J Robot Surg. 2008;2:159-163.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 35]  [Cited by in F6Publishing: 29]  [Article Influence: 1.8]  [Reference Citation Analysis (0)]
203.  Moser F, Horgan S. Robotically assisted bariatric surgery. Am J Surg. 2004;188:38S-44S.  [PubMed]  [DOI]  [Cited in This Article: ]
204.  Parini U, Fabozzi M, Brachet Contul R, Millo P, Loffredo A, Allieta R, Nardi M, Lale-Murix E. Laparoscopic gastric bypass performed with the Da Vinci Intuitive Robotic System: preliminary experience. Surg Endosc. 2006;20:1851-1857.  [PubMed]  [DOI]  [Cited in This Article: ]
205.  Sanchez BR, Mohr CJ, Morton JM, Safadi BY, Alami RS, Curet MJ. Comparison of totally robotic laparoscopic Roux-en-Y gastric bypass and traditional laparoscopic Roux-en-Y gastric bypass. Surg Obes Relat Dis. 2005;1:549-554.  [PubMed]  [DOI]  [Cited in This Article: ]
206.  Snyder BE, Wilson T, Leong BY, Klein C, Wilson EB. Robotic-assisted Roux-en-Y Gastric bypass: minimizing morbidity and mortality. Obes Surg. 2010;20:265-270.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 74]  [Cited by in F6Publishing: 75]  [Article Influence: 5.0]  [Reference Citation Analysis (0)]
207.  Mohr CJ, Nadzam GS, Curet MJ. Totally robotic Roux-en-Y gastric bypass. Arch Surg. 2005;140:779-786.  [PubMed]  [DOI]  [Cited in This Article: ]
208.  Markar SR, Karthikesalingam AP, Venkat-Ramen V, Kinross J, Ziprin P. Robotic vs. laparoscopic Roux-en-Y gastric bypass in morbidly obese patients: systematic review and pooled analysis. Int J Med Robot. 2011;7:393-400.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 68]  [Cited by in F6Publishing: 60]  [Article Influence: 4.6]  [Reference Citation Analysis (0)]
209.  Fischer L, Hildebrandt C, Bruckner T, Kenngott H, Linke GR, Gehrig T, Büchler MW, Müller-Stich BP. Excessive weight loss after sleeve gastrectomy: a systematic review. Obes Surg. 2012;22:721-731.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 132]  [Cited by in F6Publishing: 143]  [Article Influence: 11.9]  [Reference Citation Analysis (0)]
210.  Lee WJ, Chong K, Ser KH, Lee YC, Chen SC, Chen JC, Tsai MH, Chuang LM. Gastric bypass vs sleeve gastrectomy for type 2 diabetes mellitus: a randomized controlled trial. Arch Surg. 2011;146:143-148.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 327]  [Cited by in F6Publishing: 320]  [Article Influence: 24.6]  [Reference Citation Analysis (1)]
211.  Gill RS, Birch DW, Shi X, Sharma AM, Karmali S. Sleeve gastrectomy and type 2 diabetes mellitus: a systematic review. Surg Obes Relat Dis. 2010;6:707-713.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 185]  [Cited by in F6Publishing: 175]  [Article Influence: 12.5]  [Reference Citation Analysis (0)]
212.  Diamantis T, Alexandrou A, Nikiteas N, Giannopoulos A, Papalambros E. Initial experience with robotic sleeve gastrectomy for morbid obesity. Obes Surg. 2011;21:1172-1179.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 50]  [Cited by in F6Publishing: 52]  [Article Influence: 4.3]  [Reference Citation Analysis (0)]
213.  Ayloo S, Buchs NC, Addeo P, Bianco FM, Giulianotti PC. Robot-assisted sleeve gastrectomy for super-morbidly obese patients. J Laparoendosc Adv Surg Tech A. 2011;21:295-299.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 62]  [Cited by in F6Publishing: 65]  [Article Influence: 5.0]  [Reference Citation Analysis (0)]
214.  Abdalla RZ, Garcia RB, Luca CR, Costa RI, Cozer Cde O. Brazilian experience in obesity surgery robot-assisted. Arq Bras Cir Dig. 2012;25:33-35.  [PubMed]  [DOI]  [Cited in This Article: ]
215.  Vilallonga R, Fort JM, Gonzalez O, Caubet E, Boleko A, Neff KJ, Armengol M. The Initial Learning Curve for Robot-Assisted Sleeve Gastrectomy: A Surgeon’s Experience While Introducing the Robotic Technology in a Bariatric Surgery Department. Minim Invasive Surg. 2012;2012:347131.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 21]  [Cited by in F6Publishing: 34]  [Article Influence: 2.8]  [Reference Citation Analysis (0)]
216.  Elli E, Gonzalez-Heredia R, Sarvepalli S, Masrur M. Laparoscopic and robotic sleeve gastrectomy: short- and long-term results. Obes Surg. 2015;25:967-974.  [PubMed]  [DOI]  [Cited in This Article: ]
217.  Kannan U, Ecker BL, Choudhury R, Dempsey DT, Williams NN, Dumon KR. Laparoscopic hand-assisted versus robotic-assisted laparoscopic sleeve gastrectomy: experience of 103 consecutive cases. Surg Obes Relat Dis. 2015;Epub ahead of print.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 1]  [Reference Citation Analysis (0)]
218.  Romero RJ, Kosanovic R, Rabaza JR, Seetharamaiah R, Donkor C, Gallas M, Gonzalez AM. Robotic sleeve gastrectomy: experience of 134 cases and comparison with a systematic review of the laparoscopic approach. Obes Surg. 2013;23:1743-1752.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 60]  [Cited by in F6Publishing: 59]  [Article Influence: 5.4]  [Reference Citation Analysis (0)]
219.  Buchwald H, Avidor Y, Braunwald E, Jensen MD, Pories W, Fahrbach K, Schoelles K. Bariatric surgery: a systematic review and meta-analysis. JAMA. 2004;292:1724-1737.  [PubMed]  [DOI]  [Cited in This Article: ]
220.  Prachand VN, Davee RT, Alverdy JC. Duodenal switch provides superior weight loss in the super-obese (BMI > or =50 kg/m2) compared with gastric bypass. Ann Surg. 2006;244:611-619.  [PubMed]  [DOI]  [Cited in This Article: ]
221.  Ren CJ, Patterson E, Gagner M. Early results of laparoscopic biliopancreatic diversion with duodenal switch: a case series of 40 consecutive patients. Obes Surg. 2000;10:514-523; discussion 524.  [PubMed]  [DOI]  [Cited in This Article: ]
222.  Sudan R, Podolsky E. Totally robot-assisted biliary pancreatic diversion with duodenal switch: single dock technique and technical outcomes. Surg Endosc. 2015;29:55-60.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 18]  [Cited by in F6Publishing: 10]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
223.  Koffron AJ, Kung RD, Auffenberg GB, Abecassis MM. Laparoscopic liver surgery for everyone: the hybrid method. Surgery. 2007;142:463-468; discussion 468.e1-2.  [PubMed]  [DOI]  [Cited in This Article: ]
224.  Wakabayashi G, Cherqui D, Geller DA, Buell JF, Kaneko H, Han HS, Asbun H, O’Rourke N, Tanabe M, Koffron AJ. Recommendations for laparoscopic liver resection: a report from the second international consensus conference held in Morioka. Ann Surg. 2015;261:619-629.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 69]  [Cited by in F6Publishing: 77]  [Article Influence: 8.6]  [Reference Citation Analysis (0)]
225.  Hasegawa Y, Koffron AJ, Buell JF, Wakabayashi G. Approaches to laparoscopic liver resection: a meta-analysis of the role of hand-assisted laparoscopic surgery and the hybrid technique. J Hepatobiliary Pancreat Sci. 2015;22:335-341.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 35]  [Cited by in F6Publishing: 37]  [Article Influence: 4.1]  [Reference Citation Analysis (0)]
226.  Schiffman SC, Kim KH, Tsung A, Marsh JW, Geller DA. Laparoscopic versus open liver resection for metastatic colorectal cancer: a metaanalysis of 610 patients. Surgery. 2015;157:211-222.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 101]  [Cited by in F6Publishing: 97]  [Article Influence: 9.7]  [Reference Citation Analysis (0)]
227.  Wakabayashi G, Cherqui D, Geller DA, Han HS, Kaneko H, Buell JF. Laparoscopic hepatectomy is theoretically better than open hepatectomy: preparing for the 2nd International Consensus Conference on Laparoscopic Liver Resection. J Hepatobiliary Pancreat Sci. 2014;21:723-731.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 97]  [Cited by in F6Publishing: 103]  [Article Influence: 10.3]  [Reference Citation Analysis (0)]
228.  Simillis C, Constantinides VA, Tekkis PP, Darzi A, Lovegrove R, Jiao L, Antoniou A. Laparoscopic versus open hepatic resections for benign and malignant neoplasms--a meta-analysis. Surgery. 2007;141:203-211.  [PubMed]  [DOI]  [Cited in This Article: ]
229.  de’Angelis N, Eshkenazy R, Brunetti F, Valente R, Costa M, Disabato M, Salloum C, Compagnon P, Laurent A, Azoulay D. Laparoscopic versus open resection for colorectal liver metastases: a single-center study with propensity score analysis. J Laparoendosc Adv Surg Tech A. 2015;25:12-20.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 37]  [Cited by in F6Publishing: 40]  [Article Influence: 4.4]  [Reference Citation Analysis (0)]
230.  Koffron AJ, Auffenberg G, Kung R, Abecassis M. Evaluation of 300 minimally invasive liver resections at a single institution: less is more. Ann Surg. 2007;246:385-392; discussion 392-394.  [PubMed]  [DOI]  [Cited in This Article: ]
231.  Koffron A, Geller D, Gamblin TC, Abecassis M. Laparoscopic liver surgery: Shifting the management of liver tumors. Hepatology. 2006;44:1694-1700.  [PubMed]  [DOI]  [Cited in This Article: ]
232.  Montalti R, Berardi G, Laurent S, Sebastiani S, Ferdinande L, Libbrecht LJ, Smeets P, Brescia A, Rogiers X, de Hemptinne B. Laparoscopic liver resection compared to open approach in patients with colorectal liver metastases improves further resectability: Oncological outcomes of a case-control matched-pairs analysis. Eur J Surg Oncol. 2014;40:536-544.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 1]  [Reference Citation Analysis (0)]
233.  Fuks D, Cauchy F, Ftériche S, Nomi T, Schwarz L, Dokmak S, Scatton O, Fusco G, Belghiti J, Gayet B. Laparoscopy Decreases Pulmonary Complications in Patients Undergoing Major Liver Resection: A Propensity Score Analysis. Ann Surg. 2015;Epub ahead of print.  [PubMed]  [DOI]  [Cited in This Article: ]
234.  Baker TB, Jay CL, Ladner DP, Preczewski LB, Clark L, Holl J, Abecassis MM. Laparoscopy-assisted and open living donor right hepatectomy: a comparative study of outcomes. Surgery. 2009;146:817-823; discussion 823-825.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 103]  [Cited by in F6Publishing: 96]  [Article Influence: 6.4]  [Reference Citation Analysis (0)]
235.  Buell JF, Cherqui D, Geller DA, O’Rourke N, Iannitti D, Dagher I, Koffron AJ, Thomas M, Gayet B, Han HS, Wakabayashi G, Belli G, Kaneko H, Ker CG, Scatton O, Laurent A, Abdalla EK, Chaudhury P, Dutson E, Gamblin C, D’Angelica M, Nagorney D, Testa G, Labow D, Manas D, Poon RT, Nelson H, Martin R, Clary B, Pinson WC, Martinie J, Vauthey JN, Goldstein R, Roayaie S, Barlet D, Espat J, Abecassis M, Rees M, Fong Y, McMasters KM, Broelsch C, Busuttil R, Belghiti J, Strasberg S, Chari RS; World Consensus Conference on Laparoscopic Surgery. The international position on laparoscopic liver surgery: The Louisville Statement, 2008. Ann Surg. 2009;250:825-830.  [PubMed]  [DOI]  [Cited in This Article: ]
236.  Guerron AD, Aliyev S, Agcaoglu O, Aksoy E, Taskin HE, Aucejo F, Miller C, Fung J, Berber E. Laparoscopic versus open resection of colorectal liver metastasis. Surg Endosc. 2013;27:1138-1143.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 57]  [Cited by in F6Publishing: 54]  [Article Influence: 4.5]  [Reference Citation Analysis (0)]
237.  Iwahashi S, Shimada M, Utsunomiya T, Imura S, Morine Y, Ikemoto T, Arakawa Y, Mori H, Kanamoto M, Yamada S. Laparoscopic hepatic resection for metastatic liver tumor of colorectal cancer: comparative analysis of short- and long-term results. Surg Endosc. 2014;28:80-84.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 41]  [Cited by in F6Publishing: 38]  [Article Influence: 3.5]  [Reference Citation Analysis (0)]
238.  Cheung TT, Poon RT, Yuen WK, Chok KS, Tsang SH, Yau T, Chan SC, Lo CM. Outcome of laparoscopic versus open hepatectomy for colorectal liver metastases. ANZ J Surg. 2013;83:847-852.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 42]  [Cited by in F6Publishing: 51]  [Article Influence: 4.6]  [Reference Citation Analysis (0)]
239.  Nguyen KT, Gamblin TC, Geller DA. World review of laparoscopic liver resection-2,804 patients. Ann Surg. 2009;250:831-841.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 836]  [Cited by in F6Publishing: 859]  [Article Influence: 57.3]  [Reference Citation Analysis (0)]
240.  European Association For The Study Of The Liver; European Organisation For Research And Treatment Of Cancer. EASL-EORTC clinical practice guidelines: management of hepatocellular carcinoma. J Hepatol. 2012;56:908-943.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 4059]  [Cited by in F6Publishing: 4423]  [Article Influence: 368.6]  [Reference Citation Analysis (2)]
241.  Belli G, Fantini C, D’Agostino A, Cioffi L, Langella S, Russolillo N, Belli A. Laparoscopic versus open liver resection for hepatocellular carcinoma in patients with histologically proven cirrhosis: short- and middle-term results. Surg Endosc. 2007;21:2004-2011.  [PubMed]  [DOI]  [Cited in This Article: ]
242.  Xiong JJ, Altaf K, Javed MA, Huang W, Mukherjee R, Mai G, Sutton R, Liu XB, Hu WM. Meta-analysis of laparoscopic vs open liver resection for hepatocellular carcinoma. World J Gastroenterol. 2012;18:6657-6668.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in CrossRef: 112]  [Cited by in F6Publishing: 119]  [Article Influence: 9.9]  [Reference Citation Analysis (0)]
243.  Ahn KS, Kang KJ, Kim YH, Kim TS, Lim TJ. A propensity score-matched case-control comparative study of laparoscopic and open liver resection for hepatocellular carcinoma. J Laparoendosc Adv Surg Tech A. 2014;24:872-877.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 30]  [Cited by in F6Publishing: 33]  [Article Influence: 3.7]  [Reference Citation Analysis (0)]
244.  Memeo R, de’Angelis N, Compagnon P, Salloum C, Cherqui D, Laurent A, Azoulay D. Laparoscopic vs. open liver resection for hepatocellular carcinoma of cirrhotic liver: a case-control study. World J Surg. 2014;38:2919-2926.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 111]  [Cited by in F6Publishing: 120]  [Article Influence: 13.3]  [Reference Citation Analysis (0)]
245.  Rotellar F, Pardo F. Laparoscopic staging in hilar cholangiocarcinoma: Is it still justified? World J Gastrointest Oncol. 2013;5:127-131.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in CrossRef: 9]  [Cited by in F6Publishing: 9]  [Article Influence: 0.8]  [Reference Citation Analysis (0)]
246.  Jarnagin WR, Fong Y, DeMatteo RP, Gonen M, Burke EC, Bodniewicz BS J, Youssef BA M, Klimstra D, Blumgart LH. Staging, resectability, and outcome in 225 patients with hilar cholangiocarcinoma. Ann Surg. 2001;234:507-517; discussion 517-519.  [PubMed]  [DOI]  [Cited in This Article: ]
247.  Machado MA, Makdissi FF, Surjan RC, Mochizuki M. Laparoscopic resection of hilar cholangiocarcinoma. J Laparoendosc Adv Surg Tech A. 2012;22:954-956.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 27]  [Cited by in F6Publishing: 30]  [Article Influence: 2.5]  [Reference Citation Analysis (0)]
248.  Cho A, Yamamoto H, Kainuma O, Muto Y, Yanagibashi H, Tonooka T, Masuda T. Laparoscopy in the management of hilar cholangiocarcinoma. World J Gastroenterol. 2014;20:15153-15157.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in CrossRef: 22]  [Cited by in F6Publishing: 18]  [Article Influence: 1.8]  [Reference Citation Analysis (0)]
249.  Giulianotti PC, Sbrana F, Bianco FM, Addeo P. Robot-assisted laparoscopic extended right hepatectomy with biliary reconstruction. J Laparoendosc Adv Surg Tech A. 2010;20:159-163.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 79]  [Cited by in F6Publishing: 79]  [Article Influence: 5.6]  [Reference Citation Analysis (0)]
250.  Yu H, Wu SD, Chen DX, Zhu G. Laparoscopic resection of Bismuth type I and II hilar cholangiocarcinoma: an audit of 14 cases from two institutions. Dig Surg. 2011;28:44-49.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 37]  [Cited by in F6Publishing: 41]  [Article Influence: 3.2]  [Reference Citation Analysis (0)]
251.  Gumbs AA, Jarufe N, Gayet B. Minimally invasive approaches to extrapancreatic cholangiocarcinoma. Surg Endosc. 2013;27:406-414.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 58]  [Cited by in F6Publishing: 65]  [Article Influence: 5.4]  [Reference Citation Analysis (0)]
252.  Han HS, Cho JY, Yoon YS, Hwang DW, Kim YK, Shin HK, Lee W. Total laparoscopic living donor right hepatectomy. Surg Endosc. 2015;29:184.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 71]  [Cited by in F6Publishing: 84]  [Article Influence: 8.4]  [Reference Citation Analysis (0)]
253.  Rotellar F, Pardo F, Benito A, Martí-Cruchaga P, Zozaya G, Lopez L, Hidalgo F, Sangro B, Herrero I. Totally laparoscopic right-lobe hepatectomy for adult living donor liver transplantation: useful strategies to enhance safety. Am J Transplant. 2013;13:3269-3273.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 66]  [Cited by in F6Publishing: 71]  [Article Influence: 6.5]  [Reference Citation Analysis (0)]
254.  Samstein B, Cherqui D, Rotellar F, Griesemer A, Halazun KJ, Kato T, Guarrera J, Emond JC. Totally laparoscopic full left hepatectomy for living donor liver transplantation in adolescents and adults. Am J Transplant. 2013;13:2462-2466.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 76]  [Cited by in F6Publishing: 86]  [Article Influence: 7.8]  [Reference Citation Analysis (0)]
255.  Soubrane O, Perdigao Cotta F, Scatton O. Pure laparoscopic right hepatectomy in a living donor. Am J Transplant. 2013;13:2467-2471.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 107]  [Cited by in F6Publishing: 119]  [Article Influence: 10.8]  [Reference Citation Analysis (0)]
256.  Suh KS, Yi NJ, Kim T, Kim J, Shin WY, Lee HW, Han HS, Lee KU. Laparoscopy-assisted donor right hepatectomy using a hand port system preserving the middle hepatic vein branches. World J Surg. 2009;33:526-533.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 56]  [Cited by in F6Publishing: 41]  [Article Influence: 2.9]  [Reference Citation Analysis (0)]
257.  Koffron AJ, Kung R, Baker T, Fryer J, Clark L, Abecassis M. Laparoscopic-assisted right lobe donor hepatectomy. Am J Transplant. 2006;6:2522-2525.  [PubMed]  [DOI]  [Cited in This Article: ]
258.  Kim KH, Jung DH, Park KM, Lee YJ, Kim DY, Kim KM, Lee SG. Comparison of open and laparoscopic live donor left lateral sectionectomy. Br J Surg. 2011;98:1302-1308.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 110]  [Cited by in F6Publishing: 109]  [Article Influence: 8.4]  [Reference Citation Analysis (0)]
259.  Vigano L, Laurent A, Tayar C, Tomatis M, Ponti A, Cherqui D. The learning curve in laparoscopic liver resection: improved feasibility and reproducibility. Ann Surg. 2009;250:772-782.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 280]  [Cited by in F6Publishing: 292]  [Article Influence: 19.5]  [Reference Citation Analysis (0)]
260.  Tsung A, Geller DA, Sukato DC, Sabbaghian S, Tohme S, Steel J, Marsh W, Reddy SK, Bartlett DL. Robotic versus laparoscopic hepatectomy: a matched comparison. Ann Surg. 2014;259:549-555.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 220]  [Cited by in F6Publishing: 238]  [Article Influence: 23.8]  [Reference Citation Analysis (0)]
261.  Ji WB, Wang HG, Zhao ZM, Duan WD, Lu F, Dong JH. Robotic-assisted laparoscopic anatomic hepatectomy in China: initial experience. Ann Surg. 2011;253:342-348.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 128]  [Cited by in F6Publishing: 133]  [Article Influence: 10.2]  [Reference Citation Analysis (0)]
262.  Ho CM, Wakabayashi G, Nitta H, Ito N, Hasegawa Y, Takahara T. Systematic review of robotic liver resection. Surg Endosc. 2013;27:732-739.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 79]  [Cited by in F6Publishing: 67]  [Article Influence: 5.6]  [Reference Citation Analysis (0)]
263.  Berber E, Akyildiz HY, Aucejo F, Gunasekaran G, Chalikonda S, Fung J. Robotic versus laparoscopic resection of liver tumours. HPB (Oxford). 2010;12:583-586.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 131]  [Cited by in F6Publishing: 139]  [Article Influence: 9.9]  [Reference Citation Analysis (0)]
264.  Fritz S, Büchler M, Werner J. Surgery of the pancreas: minimally invasive approaches. Philadelphia: Elsevier Saunders 2012; 967-971.  [PubMed]  [DOI]  [Cited in This Article: ]
265.  Stauffer JA, Asbun HJ. Minimally invasive pancreatic surgery. Semin Oncol. 2015;42:123-133.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 30]  [Cited by in F6Publishing: 32]  [Article Influence: 3.2]  [Reference Citation Analysis (0)]
266.  Place TL, Nau P, Mezhir JJ. Minimally invasive pancreatectomy for cancer: a critical review of the current literature. J Gastrointest Surg. 2015;19:375-386.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 9]  [Cited by in F6Publishing: 10]  [Article Influence: 1.1]  [Reference Citation Analysis (0)]
267.  Tran Cao HS, Lopez N, Chang DC, Lowy AM, Bouvet M, Baumgartner JM, Talamini MA, Sicklick JK. Improved perioperative outcomes with minimally invasive distal pancreatectomy: results from a population-based analysis. JAMA Surg. 2014;149:237-243.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 60]  [Cited by in F6Publishing: 55]  [Article Influence: 5.5]  [Reference Citation Analysis (0)]
268.  Zhou ZQ, Kim SC, Song KB, Park KM, Lee JH, Lee YJ. Laparoscopic spleen-preserving distal pancreatectomy: comparative study of spleen preservation with splenic vessel resection and splenic vessel preservation. World J Surg. 2014;38:2973-2979.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 36]  [Cited by in F6Publishing: 36]  [Article Influence: 4.0]  [Reference Citation Analysis (0)]
269.  Yoon YS, Lee KH, Han HS, Cho JY, Jang JY, Kim SW, Lee WJ, Kang CM, Park SJ, Han SS. Effects of laparoscopic versus open surgery on splenic vessel patency after spleen and splenic vessel-preserving distal pancreatectomy: a retrospective multicenter study. Surg Endosc. 2015;29:583-588.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 25]  [Cited by in F6Publishing: 29]  [Article Influence: 2.9]  [Reference Citation Analysis (0)]
270.  Kooby DA, Hawkins WG, Schmidt CM, Weber SM, Bentrem DJ, Gillespie TW, Sellers JB, Merchant NB, Scoggins CR, Martin RC. A multicenter analysis of distal pancreatectomy for adenocarcinoma: is laparoscopic resection appropriate? J Am Coll Surg. 2010;210:779-785, 786-787.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 229]  [Cited by in F6Publishing: 236]  [Article Influence: 16.9]  [Reference Citation Analysis (0)]
271.  Jayaraman S, Gonen M, Brennan MF, D’Angelica MI, DeMatteo RP, Fong Y, Jarnagin WR, Allen PJ. Laparoscopic distal pancreatectomy: evolution of a technique at a single institution. J Am Coll Surg. 2010;211:503-509.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 126]  [Cited by in F6Publishing: 122]  [Article Influence: 8.7]  [Reference Citation Analysis (0)]
272.  Magge D, Gooding W, Choudry H, Steve J, Steel J, Zureikat A, Krasinskas A, Daouadi M, Lee KK, Hughes SJ. Comparative effectiveness of minimally invasive and open distal pancreatectomy for ductal adenocarcinoma. JAMA Surg. 2013;148:525-531.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 95]  [Cited by in F6Publishing: 108]  [Article Influence: 9.8]  [Reference Citation Analysis (0)]
273.  Stauffer JA, Rosales-Velderrain A, Goldberg RF, Bowers SP, Asbun HJ. Comparison of open with laparoscopic distal pancreatectomy: a single institution’s transition over a 7-year period. HPB (Oxford). 2013;15:149-155.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 48]  [Cited by in F6Publishing: 50]  [Article Influence: 4.5]  [Reference Citation Analysis (0)]
274.  Xourafas D, Tavakkoli A, Clancy TE, Ashley SW. Distal pancreatic resection for neuroendocrine tumors: is laparoscopic really better than open? J Gastrointest Surg. 2015;19:831-840.  [PubMed]  [DOI]  [Cited in This Article: ]
275.  Mehrabi A, Hafezi M, Arvin J, Esmaeilzadeh M, Garoussi C, Emami G, Kössler-Ebs J, Müller-Stich BP, Büchler MW, Hackert T. A systematic review and meta-analysis of laparoscopic versus open distal pancreatectomy for benign and malignant lesions of the pancreas: it’s time to randomize. Surgery. 2015;157:45-55.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 190]  [Cited by in F6Publishing: 196]  [Article Influence: 21.8]  [Reference Citation Analysis (0)]
276.  Zureikat AH, Moser AJ, Boone BA, Bartlett DL, Zenati M, Zeh HJ. 250 robotic pancreatic resections: safety and feasibility. Ann Surg. 2013;258:554-559; discussion 559-562.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 256]  [Cited by in F6Publishing: 262]  [Article Influence: 23.8]  [Reference Citation Analysis (0)]
277.  Waters JA, Canal DF, Wiebke EA, Dumas RP, Beane JD, Aguilar-Saavedra JR, Ball CG, House MG, Zyromski NJ, Nakeeb A. Robotic distal pancreatectomy: cost effective? Surgery. 2010;148:814-823.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 175]  [Cited by in F6Publishing: 178]  [Article Influence: 12.7]  [Reference Citation Analysis (0)]
278.  Daouadi M, Zureikat AH, Zenati MS, Choudry H, Tsung A, Bartlett DL, Hughes SJ, Lee KK, Moser AJ, Zeh HJ. Robot-assisted minimally invasive distal pancreatectomy is superior to the laparoscopic technique. Ann Surg. 2013;257:128-132.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 233]  [Cited by in F6Publishing: 222]  [Article Influence: 20.2]  [Reference Citation Analysis (0)]
279.  Kang CM, Kim DH, Lee WJ, Chi HS. Conventional laparoscopic and robot-assisted spleen-preserving pancreatectomy: does da Vinci have clinical advantages? Surg Endosc. 2011;25:2004-2009.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 147]  [Cited by in F6Publishing: 156]  [Article Influence: 11.1]  [Reference Citation Analysis (0)]
280.  Kang CM, Kim DH, Lee WJ, Chi HS. Initial experiences using robot-assisted central pancreatectomy with pancreaticogastrostomy: a potential way to advanced laparoscopic pancreatectomy. Surg Endosc. 2011;25:1101-1106.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 58]  [Cited by in F6Publishing: 57]  [Article Influence: 4.1]  [Reference Citation Analysis (0)]
281.  Machado MA, Surjan RC, Epstein MG, Makdissi FF. Laparoscopic central pancreatectomy: a review of 51 cases. Surg Laparosc Endosc Percutan Tech. 2013;23:486-490.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 30]  [Cited by in F6Publishing: 34]  [Article Influence: 3.4]  [Reference Citation Analysis (0)]
282.  Gumbs AA, Rodriguez Rivera AM, Milone L, Hoffman JP. Laparoscopic pancreatoduodenectomy: a review of 285 published cases. Ann Surg Oncol. 2011;18:1335-1341.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 82]  [Cited by in F6Publishing: 99]  [Article Influence: 7.6]  [Reference Citation Analysis (0)]
283.  Kuroki T, Adachi T, Okamoto T, Kanematsu T. A non-randomized comparative study of laparoscopy-assisted pancreaticoduodenectomy and open pancreaticoduodenectomy. Hepatogastroenterology. 2012;59:570-573.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 52]  [Cited by in F6Publishing: 63]  [Article Influence: 5.7]  [Reference Citation Analysis (0)]
284.  Asbun HJ, Stauffer JA. Laparoscopic vs open pancreaticoduodenectomy: overall outcomes and severity of complications using the Accordion Severity Grading System. J Am Coll Surg. 2012;215:810-819.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 287]  [Cited by in F6Publishing: 313]  [Article Influence: 26.1]  [Reference Citation Analysis (0)]
285.  Song KB, Kim SC, Hwang DW, Lee JH, Lee DJ, Lee JW, Park KM, Lee YJ. Matched Case-Control Analysis Comparing Laparoscopic and Open Pylorus-preserving Pancreaticoduodenectomy in Patients With Periampullary Tumors. Ann Surg. 2015;262:146-155.  [PubMed]  [DOI]  [Cited in This Article: ]
286.  Boggi U, Amorese G, Vistoli F, Caniglia F, De Lio N, Perrone V, Barbarello L, Belluomini M, Signori S, Mosca F. Laparoscopic pancreaticoduodenectomy: a systematic literature review. Surg Endosc. 2015;29:9-23.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 127]  [Cited by in F6Publishing: 128]  [Article Influence: 12.8]  [Reference Citation Analysis (0)]
287.  Zhang J, Wu WM, You L, Zhao YP. Robotic versus open pancreatectomy: a systematic review and meta-analysis. Ann Surg Oncol. 2013;20:1774-1780.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 66]  [Cited by in F6Publishing: 70]  [Article Influence: 6.4]  [Reference Citation Analysis (0)]
288.  Chalikonda S, Aguilar-Saavedra JR, Walsh RM. Laparoscopic robotic-assisted pancreaticoduodenectomy: a case-matched comparison with open resection. Surg Endosc. 2012;26:2397-2402.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 186]  [Cited by in F6Publishing: 187]  [Article Influence: 15.6]  [Reference Citation Analysis (0)]
289.  Chen S, Chen JZ, Zhan Q, Deng XX, Shen BY, Peng CH, Li HW. Robot-assisted laparoscopic versus open pancreaticoduodenectomy: a prospective, matched, mid-term follow-up study. Surg Endosc. 2015;29:3698-3711.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 128]  [Cited by in F6Publishing: 137]  [Article Influence: 15.2]  [Reference Citation Analysis (0)]
290.  Eberlein TJ. A new paradigm in surgical training. J Am Coll Surg. 2014;218:511-518.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 14]  [Cited by in F6Publishing: 13]  [Article Influence: 1.3]  [Reference Citation Analysis (0)]
291.  Willaert W, Van De Putte D, Van Renterghem K, Van Nieuwenhove Y, Ceelen W, Pattyn P. Training models in laparoscopy: a systematic review comparing their effectiveness in learning surgical skills. Acta Chir Belg. 2013;113:77-95.  [PubMed]  [DOI]  [Cited in This Article: ]
292.  Schijven M, Jakimowicz J. Virtual reality surgical laparoscopic simulators. Surg Endosc. 2003;17:1943-1950.  [PubMed]  [DOI]  [Cited in This Article: ]
293.  Mittal MK, Dumon KR, Edelson PK, Acero NM, Hashimoto D, Danzer E, Selvan B, Resnick AS, Morris JB, Williams NN. Successful implementation of the american college of surgeons/association of program directors in surgery surgical skills curriculum via a 4-week consecutive simulation rotation. Simul Healthc. 2012;7:147-154.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 20]  [Cited by in F6Publishing: 23]  [Article Influence: 1.9]  [Reference Citation Analysis (0)]
294.  Targarona EM, Salvador Sanchís JL, Morales-Conde S. [Advanced training in laparoscopic surgery: what is the best model?]. Cir Esp. 2010;87:1-3.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 16]  [Cited by in F6Publishing: 11]  [Article Influence: 0.7]  [Reference Citation Analysis (0)]
295.  Shuchleib S. La enseñanza de la cirugía laparoscópica. Proyecto LAP (Laparoscopia Avanzada Práctica). Seclaendosurgery.com (on line) 2007, No. 18.  Available from: http://www.seclaendosurgery.com.  [PubMed]  [DOI]  [Cited in This Article: ]
296.  Haluck RS, Satava RM, Fried G, Lake C, Ritter EM, Sachdeva AK, Seymour NE, Terry ML, Wilks D. Establishing a simulation center for surgical skills: what to do and how to do it. Surg Endosc. 2007;21:1223-1232.  [PubMed]  [DOI]  [Cited in This Article: ]
297.  Yiannakopoulou E, Nikiteas N, Perrea D, Tsigris C. Virtual reality simulators and training in laparoscopic surgery. Int J Surg. 2015;13:60-64.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 107]  [Cited by in F6Publishing: 110]  [Article Influence: 11.0]  [Reference Citation Analysis (0)]
298.  Beyer-Berjot L, Aggarwal R. Toward technology-supported surgical training: the potential of virtual simulators in laparoscopic surgery. Scand J Surg. 2013;102:221-226.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 16]  [Cited by in F6Publishing: 19]  [Article Influence: 1.7]  [Reference Citation Analysis (0)]
299.  van Dongen KW, Ahlberg G, Bonavina L, Carter FJ, Grantcharov TP, Hyltander A, Schijven MP, Stefani A, van der Zee DC, Broeders IA. European consensus on a competency-based virtual reality training program for basic endoscopic surgical psychomotor skills. Surg Endosc. 2011;25:166-171.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 60]  [Cited by in F6Publishing: 53]  [Article Influence: 3.8]  [Reference Citation Analysis (0)]
300.  Harrysson I, Hull L, Sevdalis N, Darzi A, Aggarwal R. Development of a knowledge, skills, and attitudes framework for training in laparoscopic cholecystectomy. Am J Surg. 2014;207:790-796.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 17]  [Cited by in F6Publishing: 15]  [Article Influence: 1.5]  [Reference Citation Analysis (0)]
301.  Botden SM, Christie L, Goossens R, Jakimowicz JJ. Training for laparoscopic Nissen fundoplication with a newly designed model: a replacement for animal tissue models? Surg Endosc. 2010;24:3134-3140.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 16]  [Cited by in F6Publishing: 15]  [Article Influence: 1.1]  [Reference Citation Analysis (0)]
302.  Bosker R, Groen H, Hoff C, Totte E, Ploeg R, Pierie JP. Early learning effect of residents for laparoscopic sigmoid resection. J Surg Educ. 2013;70:200-205.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 10]  [Cited by in F6Publishing: 10]  [Article Influence: 0.9]  [Reference Citation Analysis (0)]
303.  Sharma M, Macafee D, Horgan AF. Basic laparoscopic skills training using fresh frozen cadaver: a randomized controlled trial. Am J Surg. 2013;206:23-31.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 32]  [Cited by in F6Publishing: 24]  [Article Influence: 2.2]  [Reference Citation Analysis (0)]
304.  Leblanc F, Senagore AJ, Ellis CN, Champagne BJ, Augestad KM, Neary PC, Delaney CP; Colorectal Surgery Training Group. Hand-assisted laparoscopic sigmoid colectomy skills acquisition: augmented reality simulator versus human cadaver training models. J Surg Educ. 2010;67:200-204.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 36]  [Cited by in F6Publishing: 30]  [Article Influence: 2.1]  [Reference Citation Analysis (0)]
305.  Palter VN, Grantcharov TP. Development and validation of a comprehensive curriculum to teach an advanced minimally invasive procedure: a randomized controlled trial. Ann Surg. 2012;256:25-32.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 99]  [Cited by in F6Publishing: 101]  [Article Influence: 8.4]  [Reference Citation Analysis (0)]
306.  Kjellin A, Hedman L, Escher C, Felländer-Tsai L. Hybrid simulation: bringing motivation to the art of teamwork training in the operating room. Scand J Surg. 2014;103:232-236.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 11]  [Cited by in F6Publishing: 16]  [Article Influence: 1.6]  [Reference Citation Analysis (0)]
307.  Powers KA, Rehrig ST, Irias N, Albano HA, Malinow A, Jones SB, Moorman DW, Pawlowski JB, Jones DB. Simulated laparoscopic operating room crisis: An approach to enhance the surgical team performance. Surg Endosc. 2008;22:885-900.  [PubMed]  [DOI]  [Cited in This Article: ]
308.  Zendejas B, Brydges R, Hamstra SJ, Cook DA. State of the evidence on simulation-based training for laparoscopic surgery: a systematic review. Ann Surg. 2013;257:586-593.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 213]  [Cited by in F6Publishing: 223]  [Article Influence: 20.3]  [Reference Citation Analysis (0)]
309.  Martín Parra JI, Manuel Palazuelos JC, Gómez Fleitas M. [Pursuing quality in simulation-based surgical education]. Cir Esp. 2013;91:623-624.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3]  [Cited by in F6Publishing: 3]  [Article Influence: 0.3]  [Reference Citation Analysis (0)]
310.  Sadideen H, Kneebone R. Practical skills teaching in contemporary surgical education: how can educational theory be applied to promote effective learning? Am J Surg. 2012;204:396-401.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 73]  [Cited by in F6Publishing: 69]  [Article Influence: 5.8]  [Reference Citation Analysis (0)]
311.  Rodríguez-Sanjuán JC, Manuel-Palazuelos C, Fernández-Díez MJ, Gutiérrez-Cabezas JM, Alonso-Martín J, Redondo-Figuero C, Herrera-Noreña LA, Gómez-Fleitas M. [Assessment of resident training in laparoscopic surgery based on a digestive system anastomosis model in the laboratory]. Cir Esp. 2010;87:20-25.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 13]  [Cited by in F6Publishing: 11]  [Article Influence: 0.7]  [Reference Citation Analysis (0)]
312.  Manuel-Palazuelos JC, Alonso-Martín J, Rodríguez-Sanjuan JC, Fernández Díaz MJ, Gutiérrez Cabezas JM, Revuelta-Alvarez S, Morales-García DJ, Herrera Noreña L, Gómez-Fleitas M. [Surgical resident training program in minimally invasive surgery experimental laboratory (CENDOS)]. Cir Esp. 2009;85:84-91.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 7]  [Cited by in F6Publishing: 7]  [Article Influence: 0.5]  [Reference Citation Analysis (0)]
313.  Singh P, Aggarwal R, Zevin B, Grantcharov T, Darzi A. A global Delphi consensus study on defining and measuring quality in surgical training. J Am Coll Surg. 2014;219:346-53.e7.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 26]  [Cited by in F6Publishing: 30]  [Article Influence: 3.0]  [Reference Citation Analysis (0)]
314.  Stefanidis D, Arora S, Parrack DM, Hamad GG, Capella J, Grantcharov T, Urbach DR, Scott DJ, Jones DB. Research priorities in surgical simulation for the 21st century. Am J Surg. 2012;203:49-53.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 65]  [Cited by in F6Publishing: 69]  [Article Influence: 5.8]  [Reference Citation Analysis (0)]
315.  Mattar SG, Alseidi AA, Jones DB, Jeyarajah DR, Swanstrom LL, Aye RW, Wexner SD, Martinez JM, Ross SB, Awad MM. General surgery residency inadequately prepares trainees for fellowship: results of a survey of fellowship program directors. Ann Surg. 2013;258:440-449.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 517]  [Cited by in F6Publishing: 590]  [Article Influence: 53.6]  [Reference Citation Analysis (0)]
316.  Plerhoples TA, Greco RS, Krummel TM, Melcher ML. Symbiotic or parasitic? A review of the literature on the impact of fellowships on surgical residents. Ann Surg. 2012;256:904-908.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 16]  [Cited by in F6Publishing: 15]  [Article Influence: 1.4]  [Reference Citation Analysis (0)]
317.  Plerhoples TA; LAPCO. National Training Programme in Laparoscopic Colorectal Surgery.  Available from: http://www.lapco.nhs.uk.  [PubMed]  [DOI]  [Cited in This Article: ]
318.  Miskovic D, Ni M, Wyles SM, Kennedy RH, Francis NK, Parvaiz A, Cunningham C, Rockall TA, Gudgeon AM, Coleman MG. Is competency assessment at the specialist level achievable? A study for the national training programme in laparoscopic colorectal surgery in England. Ann Surg. 2013;257:476-482.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 76]  [Cited by in F6Publishing: 83]  [Article Influence: 7.5]  [Reference Citation Analysis (0)]
319.  Kelly M, Bhangu A, Singh P, Fitzgerald JE, Tekkis PP. Systematic review and meta-analysis of trainee- versus expert surgeon-performed colorectal resection. Br J Surg. 2014;101:750-759.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 46]  [Cited by in F6Publishing: 48]  [Article Influence: 4.8]  [Reference Citation Analysis (0)]
320.  Targarona EM, Balagué C, Martínez C, Hernández MP, Segade M, Franco L, Garriga J, Trías M. [Medium term results on introducing colorrectal laparoscopic surgery into clinical practice after having an intensive training course]. Cir Esp. 2011;89:282-289.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 14]  [Cited by in F6Publishing: 14]  [Article Influence: 1.1]  [Reference Citation Analysis (0)]
321.  Manuel Palazuelos C, Alonso Martín J, Martín Parra JI, Gómez Ruiz M, Maestre JM, Redondo Figuero C, Castillo Diego J, Gómez Fleitas M. [Effects of surgical simulation on the implementation of laparoscopic colorectal procedures]. Cir Esp. 2014;92:100-106.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 4]  [Cited by in F6Publishing: 5]  [Article Influence: 0.5]  [Reference Citation Analysis (0)]
322.  Kinoshita T, Kanehira E, Matsuda M, Okazumi S, Katoh R. Effectiveness of a team participation training course for laparoscopy-assisted gastrectomy. Surg Endosc. 2010;24:561-566.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 18]  [Cited by in F6Publishing: 14]  [Article Influence: 0.9]  [Reference Citation Analysis (0)]
323.  Brunckhorst O, Challacombe B, Abboudi H, Khan MS, Dasgupta P, Ahmed K. Systematic review of live surgical demonstrations and their effectiveness on training. Br J Surg. 2014;101:1637-1643.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 27]  [Cited by in F6Publishing: 26]  [Article Influence: 2.6]  [Reference Citation Analysis (0)]
324.  Kim S, Dunkin BJ, Paige JT, Eggerstedt JM, Nicholas C, Vassilliou MC, Spight DH, Pliego JF, Rush RM, Lau JN. What is the future of training in surgery? Needs assessment of national stakeholders. Surgery. 2014;156:707-717.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 30]  [Cited by in F6Publishing: 26]  [Article Influence: 2.6]  [Reference Citation Analysis (0)]
325.  Evgeniou E, Loizou P. The theoretical base of e-learning and its role in surgical education. J Surg Educ. 2012;69:665-669.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 45]  [Cited by in F6Publishing: 27]  [Article Influence: 2.3]  [Reference Citation Analysis (0)]
326.  Nagendran M, Gurusamy KS, Aggarwal R, Loizidou M, Davidson BR. Virtual reality training for surgical trainees in laparoscopic surgery. Cochrane Database Syst Rev. 2013;8:CD006575.  [PubMed]  [DOI]  [Cited in This Article: ]
327.  Satava RM. Emerging trends that herald the future of surgical simulation. Surg Clin North Am. 2010;90:623-633.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 48]  [Cited by in F6Publishing: 48]  [Article Influence: 3.4]  [Reference Citation Analysis (0)]
328.  Bogen EM, Augestad KM, Patel HR, Lindsetmo RO. Telementoring in education of laparoscopic surgeons: An emerging technology. World J Gastrointest Endosc. 2014;6:148-155.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in CrossRef: 46]  [Cited by in F6Publishing: 35]  [Article Influence: 3.5]  [Reference Citation Analysis (0)]