Systematic Reviews Open Access
Copyright ©The Author(s) 2025. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastrointest Surg. May 27, 2025; 17(5): 103758
Published online May 27, 2025. doi: 10.4240/wjgs.v17.i5.103758
Efficacy of reinforcing sutures in preventing anastomotic leakage after surgery for rectal cancer: A systematic review and metaanalysis
Zi-Xuan Zhuang, Yang Zhang, Xu-Yang Yang, Zi-Qiang Wang, Xiang-Bing Deng, Ming-Ming Zhang, Colorectal Cancer Center, Department of General Surgery, West China Hospital of Sichuan University, Chengdu 610041, Sichuan Province, China
ORCID number: Zi-Xuan Zhuang (0000-0003-0057-9107); Yang Zhang (0000-0003-0138-0028); Xu-Yang Yang (0000-0002-4522-5962); Zi-Qiang Wang (0000-0002-2874-1535); Xiang-Bing Deng (0000-0002-9208-7398); Ming-Ming Zhang (0009-0001-6198-2330).
Co-corresponding authors: Xiang-Bing Deng and Ming-Ming Zhang.
Author contributions: Zhuang ZX contributed to the design and implementation of the study and the writing of the manuscript; Zhang Y and Yang XY contributed to the statistical analyses and the writing of the manuscript; Deng XB contributed to the design of the study and the revision of the manuscript; Wang ZQ contributed to the performance of the research; Deng XB and Zhang MM contributed to the quality and professional revision, and contributed equally as co-corresponding authors; Zhang MM contributed to the quality and professional revision and the writing of the manuscript.
Conflict-of-interest statement: All the authors report no relevant conflicts of interest for this article.
PRISMA 2009 Checklist statement: The authors have read the PRISMA 2009 Checklist, and the manuscript was prepared and revised according to the PRISMA 2009 Checklist.
Open Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (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: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Ming-Ming Zhang, Professor, Colorectal Cancer Center, Department of General Surgery, West China Hospital of Sichuan University, No. 37 Guoxue Lane, Chengdu 610041, Sichuan Province, China. zhangmm@scu.edu.cn
Received: November 29, 2024
Revised: February 25, 2025
Accepted: March 24, 2025
Published online: May 27, 2025
Processing time: 174 Days and 22.3 Hours

Abstract
BACKGROUND

Anastomotic leakage (AL) is a challenging complication following rectal cancer surgery, often leading to increased morbidity and healthcare costs. The use of reinforcement sutures is expected to reduce the rate of AL, their preventive effects are controversial.

AIM

To determine the efficacy of reinforcing sutures in preventing AL in rectal cancer.

METHODS

A systematic search of major medical databases was conducted to identify studies up to June 2024. Intraoperative and postoperative outcomes were assessed; the primary outcome assessed was the incidence of AL. Pooled odds ratios (ORs) and mean differences (MDs) with a 95% confidence interval (CI) were calculated using fixed-effect or random-effect models under heterogeneity.

RESULTS

This meta-analysis incorporated 20 studies involving 3726 patients. Pooled results demonstrated a statistically significant reduction AL incidence in the reinforced suture group (OR: 0.26, 95%CI: 0.19-0.35, P < 0.001) than the unreinforced suture group. The reinforced suture group also exhibited a shorter hospital stay (MD: -1.17, 95%CI: -1.78 to -0.57, P < 0.001), earlier anal exhaust (MD: -0.13, 95%CI: -0.22 to -0.05, P = 0.002), longer operative time (MD: 15.25, 95%CI: 10.71-19.80, P < 0.001), lower infection rate (OR: 0.54, 95%CI: 0.29-1.00, P = 0.05) and lower reoperation rate (OR: 0.19, 95%CI: 0.08-0.45, P < 0.001).

CONCLUSION

The results substantiate the clinical value of anastomotic reinforcement sutures in reducing AL incidence post-rectal cancer surgery. Nevertheless, these conclusions warrant verification through additional high-quality randomized controlled trials.

Key Words: Rectal cancer; Anastomotic leakage; Reinforcing suture; Meta-analysis; Systematic review

Core Tip: This extensive systematic review rigorously evaluates the effectiveness and safety of trans-anal versus intracorporeal reinforcement sutures in low anterior resection for rectal cancer, offering the most robust methodological appraisal to date. Through heterogeneity assessment, sensitivity and subgroup analyses, and publication bias evaluation, it strengthens evidence quality, addresses outcome variability, and underscores clinical implications. Results inform surgical decision-making by comparing anastomotic leakage risks, postoperative morbidity, and technical feasibility, advocating for standardized practices to optimize colorectal surgical outcomes.



INTRODUCTION

Rectal carcinoma represents a predominant gastrointestinal malignancy globally, with radical resection constituting the cornerstone of contemporary therapeutic strategies[1]. Despite advancements in minimally invasive techniques, widespread adoption of neoadjuvant therapies, and innovations in stapled anastomosis technology, anastomotic leakage (AL) persists as a major concern in rectal cancer surgery. AL predisposes patients to acute complications [longer hospital length of stay, elevated surgical site infections (SSIs), and bowel dysfunction] while correlating with reduced quality of life, elevated local recurrence risks, and compromised disease-specific survival[2,3]. Current evidence indicates AL incidence rates of 3%-28% with associated mortality ranging from 6%-30%[4-6], underscoring the critical need for effective preventive measures in mid-low rectal resections. Diverting stoma, while commonly employed to protect anastomotic integrity and mitigate AL severity, remains controversial due to necessitating secondary surgical procedures and frequent stoma-related complications that significantly increase patient/caregiver burden and impair quality of life[7,8]. Trans-anal drainage tube placement represents another preventive approach aimed at reducing intraluminal pressure. Although some evidence suggests trans-anal drainage tube placement may decrease Grade C leakage rates, its clinical utility remains debated[9].

Current research identifies three primary AL determinants: Surgical technique selection, anastomotic blood supply adequacy, and anastomotic tension presence[10-12]. Among these factors, the anastomotic technique and instruments were assumed to play a pivotal role. The double-stapled anastomosis is a widely applied technique; however, at least two staple lines cross each other in the double-stapled technique, forming a potential ischemic area known as a “dog ear”. Furthermore, stapler removal may cause traumatic tearing at the anastomotic site, particularly in these vulnerable areas, potentially compromising structural integrity[13,14]. Therefore, reinforcing the anastomotic site, especially the “dog ears” area, is considered helpful in reducing postoperative AL. Gadiot et al[14] pioneered the application of tri-quadrangular tension-reducing sutures in circular stapled anastomoses, demonstrating a 62% reduction in leakage incidence compared to conventional single-layer closure. Subsequent single-center randomized controlled trials (RCTs) and retrospective studies have further explored reinforcement suture outcomes, though multicenter prospective RCTs remain absent. Thus, we conducted this systematic review and meta-analysis to draw a preliminary conclusion about the effectiveness and safety of anastomotic reinforcement sutures as an alternative technique in preventing AL after rectal cancer surgery.

MATERIALS AND METHODS
Protocol registration

This systematic review follows the recommendations of the Assessing the methodological quality of systematic reviews guidelines[15] and adheres to the PRISMA reporting standards[16]. We followed a priori protocol registered at the International Prospective Register of Systematic Reviews (PROSPERO registration number: CRD42024500080, https://www.crd.york.ac.uk/prospero/). All authors had access to the study data and reviewed and approved the final manuscript.

Literature search

The systematic search employed medical subject headings (MeSH) terms combined with text word strategies across eight databases (PubMed, Embase, Web of Science, Cochrane Library, Sinomed, Wangfang, VIP, China National Knowledge Infrastructure) through the Cochrane Collaborative Network. Search parameters incorporated controlled vocabulary (“anastomotic leak[MeSH]”) and free-text terms: (“anastomotic leakage” OR leak*) AND (“reinforcing suture” OR suture) AND (“rectal cancer” OR “rectal neoplasms” OR “rectal tumor”). Prospective trial registries (ClinicalTrials.gov, International Clinical Trials Registry Platform) and supplementary grey literature were interrogated, with search currency extended through June 2024.

Inclusion and exclusion criteria

Studies were included based on the following criteria: (1) Population comprising histologically confirmed rectal adenocarcinoma patients; (2) Original articles compared anastomotic suture reinforcement and not strengthened in laparoscopic rectal cancer resection; and (3) Availability of primary outcome data, including but not limited to AL incidence. Exclusion criteria comprised: (1) Non-primary research formats (systematic reviews, correspondence articles, case series); (2) Duplicate datasets (retaining most recent/Largest cohort); and (3) Unobtainable full-text documentation after interlibrary loan requests.

Study selection

Dual investigators independently screened retrieved records using predefined eligibility thresholds. Publications satisfying inclusion parameters underwent blinded full-text appraisal, with discrepancies resolved through iterative consensus-building or consultation with a third independent reviewer. Final inclusion validation strictly followed Population, Intervention, Comparison, Outcomes and Study design framework criteria.

Outcomes and definition

Two independent investigators conducted blinded data extraction from all eligible studies that applied the International Study Group of Rectal Cancer criteria for AL diagnosis. The studies employed diverse anastomotic reinforcement techniques (interrupted sutures, continuous sutures). These technical variations were systematically evaluated in subgroup analyses to assess their impact on outcomes, ensuring comparability across studies. The extracted data encompassed: First author, year of publication, country, study design, number of participants, number of cases, age, sex, body mass index, tumor-node-metastasis stage, American Society of Anesthesiologists status, distance of tumor from the anus, tumor size, reinforced anastomosis method, anastomotic reinforcing sutures and the implementation of prophylactic ileostomy. The outcome indicators include surgical safety (surgical time, intraoperative blood loss) and postoperative recovery (total hospital stay, first anal exhaust time, AL rate, anastomotic bleeding rate, anastomotic stricture rate, infection rate, intestinal obstruction rate, reoperation rate). For studies reporting medians with interquartile ranges, we applied established transformation methods to estimate means and standard deviations[17,18]. Technical variations in reinforcement methodologies, including interrupted sutures, continuous sutures, and barbed sutures. Suture materials primarily consisted of absorbable sutures, with some studies utilizing antimicrobial-coated variants. These variations were accounted for in subgroup analyses to assess their impact on outcomes.

Study quality

Dual investigators conducted blinded quality assessments using domain-specific instruments: Cochrane RoB 2.0 for RCTs and Newcastle-Ottawa Scale[19] for observational studies. Evidence synthesis stratified studies into three validity tiers: High (Newcastle-Ottawa Scale 7-9), moderate (4-6), and low methodological rigor (0-3). Inter-rater discrepancies underwent independent adjudication by a tertiary methodological expert.

Statistical analysis

Meta-analytic procedures were executed in RevMan 5.3 (Cochrane Collaboration, United Kingdom) employing a DerSimonian-Laird random-effects model[20]. Continuous measures were expressed as standardized mean differences (MD) with 95% confidence intervals (CI), while dichotomous outcomes were quantified through Mantel-Haenszel odds ratios (OR) and 95%CI. Heterogeneity assessment incorporated Cochran’s Q-test (χ2, P < 0.05) supplemented by I2 quantification, with I2 ≥ 50% defining substantial heterogeneity thresholds. Results visualization utilized forest plots with predictive intervals.

RESULTS
Literature search

The systematic search identified 1033 articles, with 208 duplicates removed. Title/abstract screening qualified 43 publications for full-text evaluation, of which 23 were excluded due to: Inaccessible raw datasets, data redundancy with included studies, and unobtainable full-texts. The final evidence synthesis incorporated 20 methodologically sound studies, with complete selection protocol detailed in Figure 1.

Figure 1
Figure 1 Flow diagram of the literature search.
Study characteristics

The twenty included articles comprised sixteen observational studies and four RCTs, encompassing 3726 participants[21-40]. Geographically, seventeen studies originated from China, two from Japan, and one from South Korea. The publication timeline spanned from August 2007 to March 2023, with study durations ranging from 14 to 76 months. Individual study sample sizes varied between 58 and 403 cases, cumulatively totaling 3726 patients undergoing laparoscopic anterior resection with double-stapled anastomosis for rectal malignancies located within 15 cm of the anal verge. Among the 20 studies, five used trans-anal reinforcing suture[21,32,37-39], fifteen studies employed intracorporeal laparoscopic reinforcing sutures[22-31,33-36,40]. Regarding the suture method, five studies used interrupted suture reinforcement[21-23,27,31], twelve studies used continuous suture reinforcement[24-26,28,30,32,34-37,39,40], and one study employed both suture reinforcement methods simultaneously[38]. Additionally, three studies implemented prophylactic ileostomy for individuals with preoperative or intraoperative risk factors[21,28,36]. Furthermore, six studies mentioned routine intraoperative air leakage tests to observe the adequacy of the anastomosis[21-25,27], and two studies also mentioned postoperative contrast enema radiography to help detect asymptomatic AL[23,25]. Seven studies reported the observation period for defining anastomotic leaks[21-23,27,28,31,32]. Supplementary Table 1 delineates key methodological attributes of included studies, with meta-analytic covariates systematically indexed in Table 1. The quality evaluations of the RCT and non-RCT articles are shown in Figure 2 and Table 2, respectively.

Figure 2
Figure 2 Quality assessment of the included articles according to the Cochrane risk of bias assessment tool. A: Risk of bias graph; B: Risk of bias summary.
Table 1 The outcomes in the included studies, n (%).
Ref.
Outcome of interest
Length of the operation, minutes
Intraoperative blood loss, mL
Length of hospital stay, days
Anal exhaust time, days
Anastomotic bleeding
Anastomotic leakage
Grading of anastomotic leakage, A/B/C
Deaths related to AL
Anastomotic stricture
Intestinal obstruction
Infection
Reoperation
Baek et al[21]Experimental (n = 47)198.3 ± 75.7174.5 ± 348.011.0 ± 5.61.5 ± 0.9N/A3 (6.4)N/ANANANANA2 (4.3)
Control (n = 63)212.1 ± 65.0188.4 ± 301.59.8 ± 6.71.5 ± 1.2NA5 (7.9)NANANANANA2 (3.2)
Maeda et al[22]Experimental (n = 91)NANANANANA3 (3.3)NA0 (0)NANANANA
Control (n = 110)NANANANANA15 (13.6)NA0 (0)NANANANA
He et al[23]Experimental (n = 145)NANANANANA5 (3.4)NANANANANANA
Control (n = 146)NANANANANA17 (11.6)NANANANANANA
Lin et al[24]Experimental (n = 142)147.5 ± 35.05100 ± 73.967.5 ± 3.182.5 ± 0.8NA4 (2.82)0/2/2NA0 (0)NANANA
Control (n = 150)130 ± 32.07100 ± 75.018 ± 4.123 ± 0.8NA15 (10.0)0/13/2NA0 (0)NANANA
Ban et al[25]Experimental (n = 168)150.4 ± 25.160.5 ± 43.9NANANA8 (4.8)3/3/2NA12 (7.1)25 (14.9)NA2 (1.2)
Control (n = 151)146.6 ± 20.258.2 ± 46.3NANANA17 (11.3)2/2/13NA17 (13.1)17 (11.3)NA13 (8.6)
Zhang et al[26]Experimental (n = 198)109.04 ± 24.0956.46 ± 8.326.61 ± 0.78NA0 (0)4 (2.0)NA0 (0)NA2 (1.0)1 (0.5)NA
Control (n = 205)100.33 ± 28.9156.46 ± 8.327.34 ± 1.95NA1 (0.5)19 (9.3)NA0 (0)NA1 (0.5)1 (0.5)NA
Hashida et al[27]Experimental (n = 72)NANANANANA1 (1.4)NANANANANANA
Control (n = 81)NANANANANA10 (12.3)NANANANANANA
Yi et al[28]Experimental (n = 99)196.41 ± 76.7172.72 ± 27.8711.52 ± 3.732.75 ± 1.11NA2 (2.0)NANANA3 (3.0)1 (1.0)NA
Control (n = 146)182.39 ± 49.1077.21 ± 49.5213.79 ± 5.912.86 ± 1.28NA12 (8.2)NANANA3 (2.0)0 (0)NA
Jin et al[29]Experimental (n = 123)124.66 ± 25.2748.77 ± 18.878.11 ± 2.102.63 ± 0.77NA4 (3.25)NANANA2 (1.62)2 (1.62)NA
Control (n = 135)116.73 ± 38.0752.15 ± 22.2610.87 ± 4.662.84 ± 0.58NA19 (14.07)NANANA6 (4.44)10 (7.41)NA
Yang et al[30]Experimental (n = 38)160.23 ± 3.85114.90 ± 9.858.12 ± 0.563.15 ± 0.09NA1 (2.63)NANANA1 (2.63)0 (0)NA
Control (n = 38)128.95 ± 2.46119.54 ± 6.278.06 ± 0.513.17 ± 0.07NA6 (15.79)NANANA0 (0)1 (2.63)NA
Zhang et al[31]Experimental (n = 60)158.62 ± 30.1754.74 ± 10.486.84 ± 1.561.89 ± 0.55NA2 (3.33)2/0/0NANANANANA
Control (n = 60)150.02 ± 28.9556.81 ± 9.967.69 ± 2.032.32 ± 0.64NA9 (15)1/7/1NANANANANA
Zhang et al[32]Experimental (n = 26)143.4 ± 2.591.4 ± 7.9NA3.3 ± 0.12 (7.7)0 (0)NANA7 (26.9)NA0 (0)NA
Control (n = 32)118.4 ± 2.077.5 ± 6.3NA3.2 ± 0.14 (12.5)6 (18.8)NANA9 (28.1)NA4 (12.5)NA
Chen et al[33]Experimental (n = 56)211 ± 91119 ± 3810.1 ± 3.22.9 ± 0.71 (1.8)1 (1.8)NA0 (0)NANANA0 (0)
Control (n = 64)174 ± 57121 ± 4610.7 ± 3.13.1 ± 0.73 (4.7)8 (12.5)NA0 (0)NANANA6 (9.4)
Luo et al[34]Experimental (n = 86)160.2 ± 3.8127 ± 98.1 ± 0.53.02 ± 0.09NA2 (2.3)NANANA4 (4.7)6 (7)NA
Control (n = 129)128.9 ± 2.4114 ± 68 ± 0.53.18 ± 0.07NA13 (10.1)NANANA8 (6.2)8 (6.2)NA
Wu et al[35]Experimental (n = 84)227.73 ± 91.258.44 ± 46.18NA3.61 ± 0.76NA5 (6)NANANANANANA
Control (n = 170)203.91 ± 61.6152.91 ± 64.5NA3.72 ± 0.91NA11 (6.5)NANANANANANA
Liu et al[36]Experimental (n = 63)NANANANANA2 (3.2)0/2/00 (0)0 (0)NANA0 (0)
Control (n = 68)NANANANANA9 (13.2)0/4/51 (1.5)2 (2.9)NANA5 (7.4)
Liu et al[37]Experimental (n = 53)180.1 ± 12.985.9 ± 24.34.8 ± 1.11.19 ± 0.280 (0)0 (0)NANANANA0 (0)0 (0)
Control (n = 44)179.8 ± 11.278.2 ± 29.15.2 ± 1.41.19 ± 0.301 (2.3)3 (6.8)NANANANA1 (2.3)2 (4.5)
Liu et al[38]Continuous suture (n = 43)103.9 ± 30.386.0 ± 59.98.17 ± 1.522.29 ± 0.640 (0)2 (4.7)0/1/1NANANA0 (0)1 (2.3)
Interrupted suture (n = 42)115.1 ± 41.280.2 ± 59.98.15 ± 1.692.22 ± 0.690 (0)2 (4.8)0/2/0NANANA1 (2.4)0 (0)
Control (n = 42)103.8 ± 26.297.0 ± 47.912.13 ± 1.572.50 ± 0.941 (2.4)7 (16.7)1/3/3NANANA0 (0)3 (7.1)
Xing et al[39]Experimental (n = 30)140.05 ± 2.5191.43 ± 7.9NA3.33 ± 0.50NA1 (3.3)NANANANANANA
Control (n = 30)119.4 ± 2.4988.93 ± 6.41NA3.27 ± 0.45NA5 (16.7)NANANANANANA
Zheng et al[40]Experimental (n = 113)NANA8.11 ± 2.102.63 ± 0.77NA5 (4.42)NANANA2(1.77)3(2.65)NA
Control (n = 125)NANA10.87 ± 4.662.84 ± 0.58NA16 (12.8)NANANA10(8)6(4.8)NA
Table 2 The Newcastle-Ottawa scale for assessing the quality of included studies.
Ref.
Is the case definition adequate
Representativeness of the cases
Selection of Controls
Definition of Controls
Comparability of cases and controls on the basis of the design or analysis
Ascertainment of exposure
Same method of ascertainment for cases and controls
Non-response rate
Quality assessment score
Baek SJ et al[21]11111117
Maeda K et al[22]111111118
Lin et al[24]111111118
Ban et al[25]111111118
Zhang et al[26]111111118
Hashida et al[27]11111117
Yi et al[28]111121119
Jin et al[29]11111117
Zhang et al[32]111121119
Chen et al[33]11111117
Luo et al[34]111121119
Wu et al[35]11111117
Liu et al[36]11111117
Liu et al[37]111111118
Liu D et al[38]11111117
Zheng et al[40]111111118
Primary outcomes

AL: All twenty studies (3726 patients)[21-40] reported AL rates, with five studies specifying AL severity[24,25,31,36,38]. Pooled analysis demonstrated significantly lower AL incidence in the reinforced suture group vs controls (OR: 0.26, 95%CI: 0.19-0.35, P < 0.001, Figure 3A and Table 3).

Figure 3
Figure 3 Primary outcome and secondary outcomes. A: Anastomotic leakage (primary outcome); B: Length of the operation; C: Intraoperative blood loss; D: Length of hospital stay; E: Anal exhaust time; F: Anastomotic bleeding; G: Anastomotic stricture; H: Intestinal obstruction; I: Infection; J: Reoperation. CI: Confidence interval.
Table 3 The pooled outcomes.
Outcomes of interest
Number of studies
Number of patients
MD or OR (95%CI)
P value
I2, %
Primary outcome
    Anastomotic leakage 2037260.26 (0.19, 0.35)< 0.0010
Secondary outcome
    Length of the operation15271215.25 (10.71, 19.80)< 0.00197
    Intraoperative blood loss1527122.04 (-2.35, 6.42)0.3691
    Length of hospital stay122259-1.17 (-1.78, -0.57)< 0.00195
    Anal exhaust time142228-0.13 (-0.22, -0.05)0.00291
    Anastomotic bleeding57630.41 (0.13, 1.25)0.120
    Anastomotic stricture35080.65 (0.35, 1.21)0.170
    Intestinal obstruction717540.91 (0.58, 1.42)0.6823
    Infection815900.54 (0.29, 1.00)0.050
    Reoperation68620.19 (0.08, 0.45)< 0.0010

Length of the operation: Operative time data from fifteen studies (2712 patients)[21,24-26,28-35,37-39] showed significant heterogeneity (I2 = 97%). The reinforced suture group required prolonged operative durations than non-reinforcing sutures group with significantly difference (MD: 15.25, 95%CI: 10.71-19.80, P < 0.001, Figure 3B).

Intraoperative blood loss: Fifteen studies (2712 patients)[21,24-26,28-35,37-39] reported blood loss measurements with substantial heterogeneity (I2 = 91%). No intergroup difference was observed (MD: 2.04, 95%CI: -2.35 to 6.42, P = 0.36, Figure 3C).

Length of hospital stay: Analysis of twelve studies (2259 patients)[21,24,26,28-31,33,34,37,38,40] revealed high heterogeneity (I2 = 95%). The reinforced group showed significantly shorter hospitalization (MD: -1.17, 95%CI: -1.78 to -0.57, P < 0.001, Figure 3D).

Anal exhaust time: Fourteen studies (2228 patients)[21,24,28-35,37-40] documented bowel function recovery, with marked heterogeneity (I2 = 91%). Earlier anal exhaust occurred in the reinforced group (MD: -0.13, 95%CI: -0.22 to -0.05, P = 0.002, Figure 3E).

Anastomotic bleeding: Five studies (763 patients)[26,32,33,37,38] reported bleeding rates without significant intergroup difference (OR: 0.41, 95%CI: 0.13-1.25, P = 0.12, Figure 3F).

Anastomotic stricture: The rate of anastomotic stricture was reported in three studies (508 patients)[25,32,36]. There was no significant difference between groups (OR: 0.65, 95%CI: 0.35-1.21, P = 0.17, Figure 3G).

Intestinal obstruction: Seven studies (1754 patients)[25,26,28-30,34,40] reported obstruction rates with low heterogeneity (I2 = 23%), showing no significant difference (OR: 0.91, 95%CI: 0.58-1.42, P = 0.68, Figure 3H).

Infection: Eight studies (1590 patients)[26,28-30,32,34,37,40] demonstrated lower infection rates in the reinforced group (OR: 0.54, 95%CI: 0.29-1.00, P = 0.05, Figure 3I).

Reoperation: The incidence of reoperation was reported in six studies (862 patients)[21,25,33,36-38]. The incidence of reoperation with the reinforced suture was significantly lower (OR: 0.19, 95%CI: 0.08-0.45, P = 0.0001, Figure 3J).

Subgroup analysis and sensitivity analysis

Subgroup analyses were conducted to investigate potential heterogeneity sources across studies (Tables 4, 5, 6, and 7). Stratification by study design, reinforcement methodology, reinforcing suture, and prophylactic ileostomy implementation revealed differential outcome patterns. For the primary endpoint, reinforced sutures significantly reduced AL incidence across all subgroups, including RCTs vs observational studies, interrupted vs continuous sutures, transanal vs transabdominal approaches, and low rectal cancer resections. The reduction in Grade C leakage severity reached particular significance (P = 0.001, Figure 4, Supplementary Figure 1). Regarding operative duration, heterogeneity appeared associated with reinforcing suture and ileostomy implementation. Interrupted suturing the “dog ears” area (P = 0.006) and the implementation of prophylactic ileostomy prolong the surgical duration (P = 0.008). Bowel function recovery analysis demonstrated earlier anal exhaust times with transanal reinforcement vs laparoscopic approaches (P < 0.001) and in ileostomy cases vs non-ileostomy controls (P = 0.05). Sensitivity analyses were performed by sequentially excluding individual studies from each outcome assessment. These sequential exclusions demonstrated no significant alterations in the pooled results, confirming the relative stability of the findings.

Figure 4
Figure 4 Comparison of grade C leakage rate. CI: Confidence interval.
Table 4 Results of subgroup analysis of studies - length of the operation.
Study characteristics
Number of studies
Number of patients
OR (95%CI)
I2, %
P value
Total20372615.25 (10.71, 19.80)97< 0.00001
Study design
    RCT454721.59 (12.37, 30.80)970.13
    CCS16317913.02 (6.76, 19.28)98
Reinforced anastomosis method
    Trans-anal reinforcing541012.01 (5.20, 18.82)970.25
    Laparoscopic reinforcing15331617.30 (11.25, 23.35)96
Reinforcing suture
    Interrupted suture69592.58 (-7.02, 12.17)280.006
    Continuous suture13247317.87 (12.88, 22.86)98
Prophylactic ileostomy
    Yes34521.95 (-8.84, 12.74)420.008
    No17327417.69 (13.23, 22.14)97
Table 5 Results of subgroup analysis of studies - intraoperative blood loss.
Study characteristics
Number of studies
Number of patients
OR (95%CI)
I2, %
P value
Total2037262.04 (-2.35, 6.42)910.36
Study design
    RCT4547-1.39 (-5.48, 2.70)730.19
    CCS1631793.19 (-2.39, 8.77)91
Reinforced anastomosis method
    Trans-anal reinforcing54106.13 (-2.21, 14.48)810.26
    Laparoscopic reinforcing1533160.50 (-4.77, 5.78)93
Reinforcing suture
    Interrupted suture6959-2.30 (-5.91, 1.31)00.06
    Continuous suture1324733.88 (-1.41, 9.17)94
Prophylactic ileostomy
    Yes34521.15 (-8.41, 10.72)270.86
    No1732742.14 (-2.62, 6.90)93
Table 6 Results of subgroup analysis of studies - length of hospital stay.
Study characteristics
Number of studies
Number of patients
OR (95%CI)
I2, %
P value
Total203726-1.17 (-1.78, -0.57)950.00002
Study design
    RCT4547-0.34 (-1.23, 0.54)850.10
    CCS163179-1.35 (-2.17, -0.53)96
Reinforced anastomosis method
    Trans-anal reinforcing5410-1.19 (-4.09, 1.72)970.91
    Laparoscopic reinforcing153316-1.02 (-1.55, -0.49)93
Reinforcing suture
    Interrupted suture6959-1.37 (-4.03, 1.28)960.64
    Continuous suture132473-0.73 (-1.22, -0.24)92
Prophylactic ileostomy
    Yes3452-0.69 (-2.27, 0.88)810.50
    No173274-1.29 (-1.99, -0.59)97
Table 7 Results of subgroup analysis of studies - anal exhaust time.
Study characteristics
Number of studies
Number of patients
OR (95%CI)
I2, %
P value
Total203726-0.13 (-0.22, -0.05)910.002
Study design
    RCT4547-0.12 (-0.38, 0.13)860.90
    CCS163179-0.14 (-0.25, -0.03)90
Reinforced anastomosis method
    Trans-anal reinforcing54100.05 (-0.02, 0.13)25< 0.0001
    Laparoscopic reinforcing153316-0.20 (-0.29, -0.11)88
Reinforcing suture
    Interrupted suture6959-0.26 (-0.51, -0.01)490.24
    Continuous suture132473-0.10 (-0.19, 0.00)94
Prophylactic ileostomy
    Yes3452-0.01 (-0.12, 0.09)00.05
    No173274-0.15 (-0.25, -0.06)93
Publication bias

Funnel plots based on AL was shown in Figure 5. There was no evidence of publication bias.

Figure 5
Figure 5 Funnel plot for publication bias basing on anastomotic leakage in included studies. OR: Odds ratio.
DISCUSSION

The International Study Group of Rectal Cancer consensus guidelines established a clinically validated three-grade classification system (A, B, and C) in 2010 to standardize the diagnosis of AL following rectal anterior resection. This system defines AL as transmural defects at colorectal/coloanal anastomotic sites that establish pathological continuity between the intestinal lumen and extraintestinal spaces. Within this framework, grade A leakage (radiologically confirmed) requires no therapeutic intervention, grade B (clinically significant) necessitates non-surgical management, while grade C (life-threatening) mandates urgent reoperation. AL pathogenesis involves multifactorial interactions, with key determinants spanning anatomical, physiological, and clinical domains. Critical risk factors include the distance of the anastomotic site from the anal margin, intestinal cavity pressure, anastomotic tension, local blood supply, operation time, tumor staging, body mass index, age, gender, preoperative adjuvant radiotherapy and chemotherapy, nutrition status, hypoalbuminemia, intraoperative blood loss, etc[10-12].

Reinforcement of the anastomotic suture line remains an essential technical consideration in colorectal surgery. This procedure typically involves applying additional sutures transanally or intracorporeally along the staple line, either completely or partially encircling it with interrupted/continuous stitches. This technique specifically targets the “dog ears” area - the anatomical junction where the linear rectal transection meets the circular sigmoid-rectal end-to-end anastomosis. Strategically placed reinforcing sutures have been demonstrated to effectively decrease anastomotic tension, improve regional perfusion, strengthen vulnerable tissue areas, and close any incipient gaps at the anastomotic site, as evidenced by studies[41,42].

The principal finding of our meta-analysis demonstrates a statistically significant reduction in AL incidence with reinforcement sutures compared to conventional techniques (3.16% vs 11.16%, P < 0.001). Given methodological heterogeneity across studies - including variations in design (RCTs vs observational), reinforcement approaches (interrupted/continuous), surgical access (transanal/intracorporeal), and tumor localization - we performed comprehensive subgroup analyses. These analyses consistently revealed AL risk reduction across all subgroups (Supplementary Figure 1), with particular significance in Grade C leakage mitigation (P = 0.001), corroborated by reduced reoperation rates (1.16% vs 7.17%, P < 0.001). Notably, two transanal reinforcement studies showed nonsignificant AL rate differences. Nonetheless, Baek et al[21] suggests that trans-anal suture reinforcement may reduce the necessity for a diverting ileostomy. Moreover, Liu et al’s research[38], despite not showing a statistically significant variance, demonstrated a tendency towards a lower incidence of AL (4.65% in the trans-anal suture group vs 16.67% in the control group) and a reduced occurrence of grade C AL (one case in the transanal suture group compared to three in the control group), indicating a potential clinical benefit of this approach.

Postoperative hemorrhage predominantly manifests within 24-48 hours following rectal cancer resection, with anastomotic sites representing the most frequent bleeding origin. The use of double stapler anastomosis may encounter several pitfalls: (1) Inadequate closure of blood vessels due to thick tissue or improper selection of stapler height; (2) Accidental displacement during the manual stapling process, resulting in stapling defects; (3) Insufficient staple numbers or the presence of quality defects in some staplers, leading to improper closure of small arteries; and (4) AL or SSI corrodes the arteries. Existing evidence suggests that relying solely on instrument suturing may lead to incomplete suturing during anastomosis, resulting in ineffective nailing of the mucosal layer and an increased risk of anastomotic bleeding. However, in the case of fully reinforced anastomoses, the probability of bleeding may be reduced[43]. Although the current meta-analysis did not demonstrate a significant advantage in reducing anastomotic bleeding with reinforced sutures, the likelihood of bleeding was indeed lower (reinforced group 3/198, control group 10/205).

The primary concerns following reinforced suturing encompass potential impacts on gastrointestinal functional recovery, anastomotic stenosis, and intestinal obstruction. Regarding anastomotic stenosis, cases in the reinforced group may result from luminal narrowing following full-thickness reinforcement, whereas in the non-reinforced group, stenosis may develop secondary to AL, potentially due to localized tissue edema and proliferative changes post-leakage. Our research indicates that reinforced suturing has no discernible effect on this. Contemporary practice predominantly utilizes absorbable sutures with low tissue reactivity, including antimicrobial properties, which minimize inflammatory responses and excessive scar formation. With proficiency in surgical techniques, even in continuous suturing, appropriate suture tension prevents anastomotic stenosis. At the same time, some studies have only sutured the high-risk “dog ear” region, further mitigating iatrogenic stenosis[23,24,33,34]. Current evidence suggests most strictures arise secondarily from leakage-induced inflammatory cascades and granulation tissue hyperplasia[44-46]. Thus, reinforcement sutures may theoretically prevent stricture formation through leakage reduction. Liu et al[37] observed well-healed anastomotic sites without granulation tissue on six-month postoperative colonoscopy. Significantly, Zhang et al[32] reported seven anastomotic strictures caused by trans-anal running full-layer stitches around the entire circular anastomosis with absorbable sutures. Therefore, appropriate suture methods and tension control during full-thickness closure may mitigate stenosis risk. However, at present, there is no consensus on the method of anastomotic reinforcement.

Subgroup analyses identified interrupted suture patterns and prophylactic ileostomy implementation as primary sources of heterogeneity. Given the comparable AL prevention efficacy between techniques, patients undergoing continuous closure may derive greater clinical utility from reduced operative duration. Bowel function recovery analysis revealed significantly earlier time to first flatus with transanal reinforcement vs laparoscopic approaches (MD: -0.73, 95%CI: -1.12 to -0.34). This discrepancy could potentially stem from multifactorial determinants including tumor localization, variations in bowel pre-operative preparation, and time to get out of bed after surgery. Additional heterogeneity contributors encompassed baseline characteristics and intraoperative variables. Current evidence remains insufficiently robust to establish definitive recommendations, necessitating prospective trials controlling for these confounding factors.

Our findings demonstrate that anastomotic reinforcement confers significant protective effects irrespective of surgical approach (trans-anal vs. intracorporeal) or suture technique (interrupted vs. continuous). Current reinforcement methodologies encompass: (1) Trans-anal or intracorporeal access; (2) Interrupted or continuous suturing patterns; and (3) Segmental reinforcement of high-risk “dog-ears” regions vs circumferential reinforcement. Suture material selection primarily involves conventional absorbable sutures (applicable to both techniques) and barbed suture devices (exclusively for continuous closure). Transanal reinforcement proves particularly advantageous in low/ultralow rectal cancer patients with challenging pelvic anatomy (obesity or narrow pelvis). This approach facilitates direct visualization and closure of residual dog-ear defects while enabling concurrent ostomy creation without prolonging operative duration[47]. Additionally, the laparoscopic pneumoperitoneum pressure can detect potential AL during suturing. Modern surgery retractors have enhanced the safety and precision of trans-anal techniques, though inherent risks persist: The distal rectal wall’s anatomical vulnerability, characterized by thin muscular layers and absence of serosal support, creates inherent technical challenges. If the rectum and anus are overstretched during trans-anal sutures, the rectal wall may be injured with stitches, firstly piercing mucosa, and anastomotic stoma can rupture. This complication occurs most frequently during anterior wall reinforcement with continuous suturing techniques, as their uninterrupted suture lines cannot circumvent high-risk regions, whereas interrupted sutures enable precise avoidance[48]. The intracorporeal suture is feasible for an anastomotic site with a high position. In combination with our-self experience, accompanied by the advancements of laparoscopic instruments and operative techniques, the distance from the anastomotic site to the anal verge is no longer the sole determinant. In patients with low body mass index or spacious pelvic anatomy, intracorporeal suturing can be safely implemented even for anastomotic sites located 1-5 cm from the anal verge[49-51].

Existing evidence predominantly supports targeted reinforcement of “dog ear” regions through selective suturing[23,24,33,34]. Our operative findings suggest enhanced safety and efficacy when resecting one of the two corners made by crossing the circular and linear staple lines and strengthening another corner in the meantime. Another critical consideration is that selecting the most appropriate reinforcement methods and surgical approaches is imperative, absolutely avoiding injuries caused by sutures. In most cases, targeted reinforcement of “dog ear” regions or anatomically vulnerable zones proves sufficient. Diverting ileostomy should be implemented without hesitation when encountering insufficient quality of anastomosis, positive leak test, excessive anastomotic tension, or inadequate vascular perfusion.

Regarding postoperative outcomes, the results of the current meta-analysis indicated that the operating time for reinforced anastomosis was significantly prolonged compared to conventional techniques, primarily attributable to the additional suturing steps. Although this temporal increase reached statistical significance, its clinical relevance appeared negligible, as no associations were observed with elevated anesthesia-related complications or other perioperative adverse events. Subgroup analyses further demonstrated that prolonged operative duration was predominantly driven by interrupted suture reinforcement (P = 0.006), whereas continuous barbed suture techniques showed comparable operative times to conventional methods, aligning with existing clinical evidence. Early anal exhaust time and reduced length of hospital stay are considered as advantages of suture reinforcement.

Existing evidence demonstrates that intervention with anastomotic reinforcement sutures can effectively reduce postoperative complications[21]. The reinforced suture group exhibited earlier independent mobility, faster intestinal function recovery, and shorter hospital stays. Yi et al[28] demonstrated a 16.5% reduction in AL incidence correlating with accelerated perioperative recovery in reinforced anastomosis patients, translating to significantly decreased mean hospitalization duration (11.52 days vs 13.79 days, P = 0.035). It is logical to recognize that patients experiencing earlier return of bowel function and lower AL rates would require shorter hospitalization, findings that align with our pooled meta-analytic results. No statistically significant difference emerged in intraoperative blood loss between the techniques. Since all patients included in the studies received treatment at a high-capacity tertiary surgical center, where surgeons with skilled surgical operation and deep anatomical knowledge reserve can be effective in bleeding control during suturing.

SSIs rates in colorectal surgery remain high, ranging from 15% to 30% in some studies[52-55]. These infections impose substantial healthcare costs and prolong hospitalization duration[56]. Reoperation rates could be reduced through effective mitigation of SSI risk. AL facilitates peritoneal contamination through luminal content extravasation, precipitating organ/space infections and systemic inflammatory responses. Emergency reoperation following AL paradoxically heighten infectious morbidity risks. Reinforcement sutures effectively safeguard anastomotic integrity, thereby reducing both SSI occurrence and reoperation necessitated by leakage events. Our findings demonstrate that reinforced anastomotic sutures can effectively diminish leakage-associated secondary infections (OR: 0.54, 95%CI: 0.29-1.00, P = 0.05). Concurrently, due to the reduced incidence of AL, the reinforced suture achieved a lower reoperation rate, which is logically sound, as one of the most common reasons for reoperation after rectal surgery is the management of AL and its associated complications. The reoperation rate naturally reducibility through mitigation of AL occurrence, particularly symptomatic leaks (Grade C leaks). Ban et al’s research[25] confirms this hypothesis, wherein reinforced suturing predominantly attenuated Grade C leak incidence, results corroborated by our subgroup analysis (P = 0.001). With reduced reoperations and postoperative infections, patient recovery becomes more accessible with concurrent shortening of hospitalization duration. In summary, reinforced sutures could effectively reduce postoperative complications.

Our meta-analysis presents distinct advantages compared to existing published analyses. Firstly, our study incorporates an expanded dataset. Specifically, we included one RCT and eight retrospective cohort studies, which were not encompassed in prior systematic reviews. Second, our meta- analysis further performed subgroup analyzes based on study type (RCT or retrospective study), reinforced suture method (transabdominal or transanal), low rectal cancer (within 5-6 cm from the anal verge), etc., which also makes our conclusions more objective. Finally, our study compares reoperation rates between groups and shows that reinforced sutures can help reduce reoperation rates, a finding not covered in previous meta-analyses. While acknowledging these strengths, the synthesized findings require cautious interpretation due to methodological constraints. The systematic search identified 20 qualifying investigations, comprising 4 RCTs and 16 retrospective observational studies. The predominance of observational study designs may introduce selection bias, resulting in a relatively low level of clinical evidence. Second, variations in reinforcement suturing types, suturing methodologies, and tumor location across studies may contribute to heterogeneity and influence outcomes. Third, the absence of longitudinal functional outcome data and cost-effectiveness analyses constrains the generalizability of our conclusions. Future investigations should integrate cost-benefit evaluations to assess reinforced sutures’ economic implications. Finally, as all studies originated from East Asia populations, so it might not completely reveal the effect of reinforcing sutures outside Asia.

CONCLUSION

Our study demonstrates that properly implemented reinforced suturing represents a potentially cost-effective preventive strategy against AL in rectal cancer procedures. Nevertheless, current evidence limitations and interstudy heterogeneity necessitate cautious interpretation of these results. More well-designed large-sample RCTs are needed to assess the efficiency and clarify the indications of reinforced sutures in future research.

Footnotes

Provenance and peer review: Unsolicited article; Externally peer reviewed.

Peer-review model: Single blind

Specialty type: Gastroenterology and hepatology

Country of origin: China

Peer-review report’s classification

Scientific Quality: Grade A, Grade A, Grade A, Grade B

Novelty: Grade A, Grade A, Grade B, Grade D

Creativity or Innovation: Grade A, Grade A, Grade A, Grade B

Scientific Significance: Grade A, Grade A, Grade A, Grade B

P-Reviewer: Dimofte GM; Zhang A S-Editor: Wei YF L-Editor: A P-Editor: Xu ZH

References
1.  Siegel RL, Miller KD, Fuchs HE, Jemal A. Cancer statistics, 2022. CA Cancer J Clin. 2022;72:7-33.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 4235]  [Cited by in RCA: 11075]  [Article Influence: 3691.7]  [Reference Citation Analysis (4)]
2.  Hida K, Okamura R, Sakai Y, Konishi T, Akagi T, Yamaguchi T, Akiyoshi T, Fukuda M, Yamamoto S, Yamamoto M, Nishigori T, Kawada K, Hasegawa S, Morita S, Watanabe M; Japan Society of Laparoscopic Colorectal Surgery. Open versus Laparoscopic Surgery for Advanced Low Rectal Cancer: A Large, Multicenter, Propensity Score Matched Cohort Study in Japan. Ann Surg. 2018;268:318-324.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Full Text (PDF)]  [Cited by in Crossref: 56]  [Cited by in RCA: 80]  [Article Influence: 13.3]  [Reference Citation Analysis (0)]
3.  Taflampas P, Christodoulakis M, Tsiftsis DD. Anastomotic leakage after low anterior resection for rectal cancer: facts, obscurity, and fiction. Surg Today. 2009;39:183-188.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 68]  [Cited by in RCA: 70]  [Article Influence: 4.4]  [Reference Citation Analysis (0)]
4.  Caulfield H, Hyman NH. Anastomotic leak after low anterior resection: a spectrum of clinical entities. JAMA Surg. 2013;148:177-182.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 80]  [Cited by in RCA: 97]  [Article Influence: 8.1]  [Reference Citation Analysis (0)]
5.  Chiarello MM, Fransvea P, Cariati M, Adams NJ, Bianchi V, Brisinda G. Anastomotic leakage in colorectal cancer surgery. Surg Oncol. 2022;40:101708.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 100]  [Cited by in RCA: 71]  [Article Influence: 23.7]  [Reference Citation Analysis (0)]
6.  Sciuto A, Merola G, De Palma GD, Sodo M, Pirozzi F, Bracale UM, Bracale U. Predictive factors for anastomotic leakage after laparoscopic colorectal surgery. World J Gastroenterol. 2018;24:2247-2260.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Full Text (PDF)]  [Cited by in CrossRef: 263]  [Cited by in RCA: 219]  [Article Influence: 31.3]  [Reference Citation Analysis (2)]
7.  Ahmad NZ, Abbas MH, Khan SU, Parvaiz A. A meta-analysis of the role of diverting ileostomy after rectal cancer surgery. Int J Colorectal Dis. 2021;36:445-455.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 22]  [Cited by in RCA: 47]  [Article Influence: 11.8]  [Reference Citation Analysis (0)]
8.  Ihnát P, Guňková P, Peteja M, Vávra P, Pelikán A, Zonča P. Diverting ileostomy in laparoscopic rectal cancer surgery: high price of protection. Surg Endosc. 2016;30:4809-4816.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 60]  [Cited by in RCA: 74]  [Article Influence: 8.2]  [Reference Citation Analysis (0)]
9.  Wang W, Zhang J, Cai J, Zhao X, Wang F. Transanal drainage tube for the prevention of anastomotic leakage in anterior resection for rectal cancer: a systematic review and meta-analysis. Expert Rev Anticancer Ther. 2023;23:431-442.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Reference Citation Analysis (0)]
10.  Kostov GG, Dimov RS, Almeida DD. Risk Factors for Anastomotic Leakage after Low Anterior Resection. Folia Med (Plovdiv). 2020;62:290-294.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Reference Citation Analysis (0)]
11.  González-Valverde FM, Vicente-Ruiz M, Gómez-Ramos MJ. Risk factors of anastomotic leakage in colon cancer. Cir Cir. 2019;87:347-352.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in RCA: 1]  [Reference Citation Analysis (0)]
12.  Kryzauskas M, Bausys A, Degutyte AE, Abeciunas V, Poskus E, Bausys R, Dulskas A, Strupas K, Poskus T. Risk factors for anastomotic leakage and its impact on long-term survival in left-sided colorectal cancer surgery. World J Surg Oncol. 2020;18:205.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Full Text (PDF)]  [Cited by in Crossref: 57]  [Cited by in RCA: 46]  [Article Influence: 9.2]  [Reference Citation Analysis (0)]
13.  Marecik SJ, Chaudhry V, Pearl R, Park JJ, Prasad LM. Single-stapled double-pursestring anastomosis after anterior resection of the rectum. Am J Surg. 2007;193:395-399.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 28]  [Cited by in RCA: 30]  [Article Influence: 1.7]  [Reference Citation Analysis (0)]
14.  Gadiot RP, Dunker MS, Mearadji A, Mannaerts GH. Reduction of anastomotic failure in laparoscopic colorectal surgery using antitraction sutures. Surg Endosc. 2011;25:68-71.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 14]  [Cited by in RCA: 18]  [Article Influence: 1.2]  [Reference Citation Analysis (0)]
15.  Shea BJ, Reeves BC, Wells G, Thuku M, Hamel C, Moran J, Moher D, Tugwell P, Welch V, Kristjansson E, Henry DA. AMSTAR 2: a critical appraisal tool for systematic reviews that include randomised or non-randomised studies of healthcare interventions, or both. BMJ. 2017;358:j4008.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Full Text (PDF)]  [Cited by in Crossref: 3100]  [Cited by in RCA: 5455]  [Article Influence: 681.9]  [Reference Citation Analysis (0)]
16.  Moher D, Liberati A, Tetzlaff J, Altman DG; PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med. 2009;6:e1000097.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Full Text (PDF)]  [Cited by in Crossref: 47017]  [Cited by in RCA: 46623]  [Article Influence: 2913.9]  [Reference Citation Analysis (0)]
17.  Shi J, Luo D, Wan X, Liu Y, Liu J, Bian Z, Tong T. Detecting the skewness of data from the five-number summary and its application in meta-analysis. Stat Methods Med Res. 2023;32:1338-1360.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 2]  [Cited by in RCA: 97]  [Article Influence: 48.5]  [Reference Citation Analysis (0)]
18.  Wan X, Wang W, Liu J, Tong T. Estimating the sample mean and standard deviation from the sample size, median, range and/or interquartile range. BMC Med Res Methodol. 2014;14:135.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Full Text (PDF)]  [Cited by in Crossref: 3433]  [Cited by in RCA: 6756]  [Article Influence: 614.2]  [Reference Citation Analysis (0)]
19.  Wells GA, Shea B, O'Connell D, Peterson J, Welch V, Losos M, Tugwell P.   The Newcastle-Ottawa Scale (NOS) for assessing the quality of nonrandomised studies in meta-analyses. [cited 15 October 2024]. Available from: https://www.ohri.ca/programs/clinical_epidemiology/oxford.asp.  [PubMed]  [DOI]
20.  Cumpston M, Li T, Page MJ, Chandler J, Welch VA, Higgins JP, Thomas J. Updated guidance for trusted systematic reviews: a new edition of the Cochrane Handbook for Systematic Reviews of Interventions. Cochrane Database Syst Rev. 2019;10:ED000142.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 1361]  [Cited by in RCA: 2731]  [Article Influence: 455.2]  [Reference Citation Analysis (0)]
21.  Baek SJ, Kim J, Kwak J, Kim SH. Can trans-anal reinforcing sutures after double stapling in lower anterior resection reduce the need for a temporary diverting ostomy? World J Gastroenterol. 2013;19:5309-5313.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Full Text (PDF)]  [Cited by in CrossRef: 28]  [Cited by in RCA: 28]  [Article Influence: 2.3]  [Reference Citation Analysis (0)]
22.  Maeda K, Nagahara H, Shibutani M, Ohtani H, Sakurai K, Toyokawa T, Muguruma K, Tanaka H, Amano R, Kimura K, Sugano K, Ikeya T, Iseki Y, Hirakawa K. Efficacy of intracorporeal reinforcing sutures for anastomotic leakage after laparoscopic surgery for rectal cancer. Surg Endosc. 2015;29:3535-3542.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 23]  [Cited by in RCA: 29]  [Article Influence: 2.9]  [Reference Citation Analysis (0)]
23.  He Y, Zhu Z, Liu S, Liu L, Hu B, Wan X, Huang Q. [Effect of anastomotic reinforcing sutures on the incidence of anastomotic leakage after laparoscopic radical resection of rectal cancer: a prospective randomized controlled trial]. Zhonghua Wei Chang Wai Ke Za Zhi. 2018;21:431-436.  [PubMed]  [DOI]
24.  Lin H, Yu M, Ye G, Qin S, Fang H, Jing R, Gong T, Luo Y, Zhong M. Intracorporeal reinforcement with barbed suture is associated with low anastomotic leakage rates after laparoscopic low anterior resection for rectal cancer: a retrospective study. BMC Surg. 2022;22:335.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Full Text (PDF)]  [Reference Citation Analysis (0)]
25.  Ban B, Shang A, Shi J. Efficacy of staple line reinforcement by barbed suture for preventing anastomotic leakage in laparoscopic rectal cancer surgery. World J Gastrointest Surg. 2022;14:821-832.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Full Text (PDF)]  [Cited by in CrossRef: 1]  [Cited by in RCA: 8]  [Article Influence: 2.7]  [Reference Citation Analysis (1)]
26.  Zhang HQ, Xu L, Wang ZL, Shao Y, Chen Y, Lu YF, Fu Z. The effect of reinforcing sutures and trans-anal drainage tube on the outcome of laparoscopic resection for rectal cancer: propensity scorematched analysis. Langenbecks Arch Surg. 2023;408:289.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Reference Citation Analysis (0)]
27.  Hashida H, Mizuno R, Iwaki K, Hanabata Y, Kita R, Oshima N, Kitamura K, Kondo M, Kobayashi H, Uryuhara K, Kaihara S. Intracorporeal reinforcing sutures reduce anastomotic leakage in double-stapling anastomosis for laparoscopic rectal surgery. Wideochir Inne Tech Maloinwazyjne. 2022;17:491-497.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Full Text (PDF)]  [Reference Citation Analysis (0)]
28.  Yi X, Liao W, Feng X, Li H, Chen Z, Wang J, Lu X, Wan J, Lin J, Hong X, Diao D. An innovative and convenient technique to reduce anastomotic leakage after double stapling anastomosis: laparoscopic demucositized suture the overlapping point of the "dog ear" area. Updates Surg. 2022;74:1645-1656.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 1]  [Cited by in RCA: 1]  [Article Influence: 0.3]  [Reference Citation Analysis (0)]
29.  Jin CW, Wang Y, Fu Z. [Effect of anastomotic reinforcement suture on the incidence of anastomotic fistula after laparoscopic surgery for low and middle rectal cancer]. Xuzhou Yike Daxue Xuebao. 2022;42:110-114.  [PubMed]  [DOI]  [Full Text]
30.  Yang XD. [The application value of barbed suture in laparoscopic radical resection of rectal cancer to strengthen the anastomosis]. Xitong Yixue. 2022;7:131-134.  [PubMed]  [DOI]  [Full Text]
31.  Zhang Y, Wang X. [Effect of reinforcing ‘dog ear area’ to reduce the risk of anastomotic leakage after laparoscopic TME for rectal cancer]. Jiezhichang Gangmen Waike. 2018;24:545-548.  [PubMed]  [DOI]  [Full Text]
32.  Zhang H, Chen S, Zhang J, Zhou Q, Xu SR. [Effectiveness of transanal reinforced anastomosis in laparoscopic sphincter preserving operation for ultra-low rectal cancer]. Jiezhichang Gangmen Waike. 2021;27:560-563.  [PubMed]  [DOI]  [Full Text]
33.  Chen S, Wu Y, Han S, Mo Q, Ma Y, Song S, Zhao H. [Modification and efficacy observation of laparoscopic dual anastomosis for mid-low rectal cancer]. Zhonghua Wei Chang Wai Ke Za Zhi. 2014;17:1216-1219.  [PubMed]  [DOI]
34.  Luo Y, Yu MH, Chen JJ, Qin J, Qin SL, Huang ZZ, Zhong M. [Application value of barbed suture in reinforcing anastomosis during laparoscopic radical resection of rectal cancer]. Zhonghua Xiaohua Waike Zazhi. 2020;19:1205-1210.  [PubMed]  [DOI]  [Full Text]
35.  Wu YH, Chen H, Liu D, Long YB, Yang N, Yu L, Liu B. [Effect of anastomotic reinforcement and suture on prevention of postoperative anastomotic leakage in laparoscopic radical resection of middle and low rectal cancer and its influence on postoperative recovery]. Xiandai Zhongliu Yixue. 2022;30:4274-4276.  [PubMed]  [DOI]  [Full Text]
36.  Liu TP, Wang HM, Wang HL, Deng C, Tian M. [Clinical study of anastomotic reinforcement suture during laparoscopic rectal cancer TME in reducing postoperative anastomotic leakage]. Zhongwen Keji Qikan Shuju Ku (Quanwen Ban) Yiyao Weisheng. 2023;2:56-59.  [PubMed]  [DOI]
37.  Liu XX, Li YP, Jiang ZW, Gong GW, Pan HF, Wang HF, Shao WJ. [Double stapling combined with transanal suture to strengthen anastomosis for laparoscopic radical resection for rectal cancer]. Jiezhichang Gangmen Waike. 2021;27:107-111+121.  [PubMed]  [DOI]  [Full Text]
38.  Liu D, Liu B, Yang HY, Duan XL, Liu SD, Wu YH, Mao ZJ, Long YB. [Transanal anastomotic reinforcement on anastomotic leakage after laparoscopic radical resection for middle and low rectal cancer]. Xiandai Zhongliu Yixue. 2023;31:2048-2053.  [PubMed]  [DOI]  [Full Text]
39.  Xing HB, Zhang GB, Li GF. [The safety and feasibility of via anus reinforcing to suture stoma amidst laparoscopic ano-preserved procedure for ultra-low rectal cancer]. Zhongguo Gangchangbing Zazhi. 2023;43:16-18.  [PubMed]  [DOI]
40.  Zheng JB  [Clinical study on the application of anastomotic reinforcement suture combined with pelvic floor peritoneal reconstruction in laparoscopic anterior resection of rectal cancer]. M.Sc. Thesis, Jilin University. 2023.  [PubMed]  [DOI]  [Full Text]
41.  Griffen FD, Knight CD Sr, Whitaker JM, Knight CD Jr. The double stapling technique for low anterior resection. Results, modifications, and observations. Ann Surg. 1990;211:745-51; discussion 751.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 133]  [Cited by in RCA: 125]  [Article Influence: 3.6]  [Reference Citation Analysis (0)]
42.  Moore JW, Chapuis PH, Bokey EL. Morbidity and mortality after single- and double-stapled colorectal anastomoses in patients with carcinoma of the rectum. Aust N Z J Surg. 1996;66:820-823.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 31]  [Cited by in RCA: 29]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
43.  Hanna DN, Hawkins AT. Colorectal: Management of Postoperative Complications in Colorectal Surgery. Surg Clin North Am. 2021;101:717-729.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 1]  [Cited by in RCA: 1]  [Article Influence: 0.3]  [Reference Citation Analysis (0)]
44.  Polese L, Vecchiato M, Frigo AC, Sarzo G, Cadrobbi R, Rizzato R, Bressan A, Merigliano S. Risk factors for colorectal anastomotic stenoses and their impact on quality of life: what are the lessons to learn? Colorectal Dis. 2012;14:e124-e128.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 53]  [Cited by in RCA: 61]  [Article Influence: 4.7]  [Reference Citation Analysis (0)]
45.  Lee SY, Kim CH, Kim YJ, Kim HR. Anastomotic stricture after ultralow anterior resection or intersphincteric resection for very low-lying rectal cancer. Surg Endosc. 2018;32:660-666.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 36]  [Cited by in RCA: 43]  [Article Influence: 5.4]  [Reference Citation Analysis (0)]
46.  Kraenzler A, Maggiori L, Pittet O, Alyami MS, Prost À la Denise J, Panis Y. Anastomotic stenosis after coloanal, colorectal and ileoanal anastomosis: what is the best management? Colorectal Dis. 2017;19:O90-O96.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 37]  [Cited by in RCA: 42]  [Article Influence: 5.3]  [Reference Citation Analysis (0)]
47.  Zhuo C, Liang L, Ying M, Li Q, Li D, Li Y, Peng J, Huang L, Cai S, Li X. Laparoscopic Low Anterior Resection and Eversion Technique Combined With a Nondog Ear Anastomosis for Mid- and Distal Rectal Neoplasms: A Preliminary and Feasibility Study. Medicine (Baltimore). 2015;94:e2285.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Full Text (PDF)]  [Cited by in Crossref: 14]  [Cited by in RCA: 16]  [Article Influence: 1.6]  [Reference Citation Analysis (0)]
48.  Velotti N, Manigrasso M, Di Lauro K, Vertaldi S, Anoldo P, Vitiello A, Milone F, Musella M, De Palma GD, Milone M. Barbed suture in gastro-intestinal surgery: A review with a meta-analysis. Surgeon. 2022;20:115-122.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 23]  [Cited by in RCA: 12]  [Article Influence: 4.0]  [Reference Citation Analysis (0)]
49.  Rahbari NN, Weitz J, Hohenberger W, Heald RJ, Moran B, Ulrich A, Holm T, Wong WD, Tiret E, Moriya Y, Laurberg S, den Dulk M, van de Velde C, Büchler MW. Definition and grading of anastomotic leakage following anterior resection of the rectum: a proposal by the International Study Group of Rectal Cancer. Surgery. 2010;147:339-351.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 732]  [Cited by in RCA: 787]  [Article Influence: 52.5]  [Reference Citation Analysis (4)]
50.  Kim CW, Baek SJ, Hur H, Min BS, Baik SH, Kim NK. Anastomotic Leakage After Low Anterior Resection for Rectal Cancer Is Different Between Minimally Invasive Surgery and Open Surgery. Ann Surg. 2016;263:130-137.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 49]  [Cited by in RCA: 56]  [Article Influence: 6.2]  [Reference Citation Analysis (0)]
51.  Fukada M, Matsuhashi N, Takahashi T, Imai H, Tanaka Y, Yamaguchi K, Yoshida K. Risk and early predictive factors of anastomotic leakage in laparoscopic low anterior resection for rectal cancer. World J Surg Oncol. 2019;17:178.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Full Text (PDF)]  [Cited by in Crossref: 22]  [Cited by in RCA: 39]  [Article Influence: 6.5]  [Reference Citation Analysis (0)]
52.  Merkow RP, Ju MH, Chung JW, Hall BL, Cohen ME, Williams MV, Tsai TC, Ko CY, Bilimoria KY. Underlying reasons associated with hospital readmission following surgery in the United States. JAMA. 2015;313:483-495.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 506]  [Cited by in RCA: 580]  [Article Influence: 58.0]  [Reference Citation Analysis (0)]
53.  Zimlichman E, Henderson D, Tamir O, Franz C, Song P, Yamin CK, Keohane C, Denham CR, Bates DW. Health care-associated infections: a meta-analysis of costs and financial impact on the US health care system. JAMA Intern Med. 2013;173:2039-2046.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 1128]  [Cited by in RCA: 1269]  [Article Influence: 105.8]  [Reference Citation Analysis (0)]
54.  Tanner J, Khan D, Aplin C, Ball J, Thomas M, Bankart J. Post-discharge surveillance to identify colorectal surgical site infection rates and related costs. J Hosp Infect. 2009;72:243-250.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 118]  [Cited by in RCA: 118]  [Article Influence: 7.4]  [Reference Citation Analysis (0)]
55.  Hübner M, Diana M, Zanetti G, Eisenring MC, Demartines N, Troillet N. Surgical site infections in colon surgery: the patient, the procedure, the hospital, and the surgeon. Arch Surg. 2011;146:1240-1245.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 87]  [Cited by in RCA: 90]  [Article Influence: 6.4]  [Reference Citation Analysis (0)]
56.  Berríos-Torres SI, Umscheid CA, Bratzler DW, Leas B, Stone EC, Kelz RR, Reinke CE, Morgan S, Solomkin JS, Mazuski JE, Dellinger EP, Itani KMF, Berbari EF, Segreti J, Parvizi J, Blanchard J, Allen G, Kluytmans JAJW, Donlan R, Schecter WP; Healthcare Infection Control Practices Advisory Committee. Centers for Disease Control and Prevention Guideline for the Prevention of Surgical Site Infection, 2017. JAMA Surg. 2017;152:784-791.  [RCA]  [PubMed]  [DOI]  [Full Text]  [Cited by in Crossref: 1394]  [Cited by in RCA: 1985]  [Article Influence: 248.1]  [Reference Citation Analysis (0)]