Clinical outcomes and complications of single anastomosis duodenal-ileal bypass with sleeve gastrectomy: A 2-year follow-up study in Bogotá, Colombia

Abstract

BACKGROUND

The global prevalence of obesity has increased over the past 40 years, and bariatric surgery has proven to be the most effective therapy for long-term weight loss. Its principles are based on modifying the brain-gut axis by altering the gastrointestinal anatomy and affecting the function of gastrointestinal hormones, thereby modifying satiety signals. Single anastomosis duodeno-ileal bypass with sleeve gastrectomy (SADI-S) combines both techniques and has become an alternative to gastric bypass and biliopancreatic diversion procedures for treating severe obesity and associated metabolic diseases in selected patients.

AIM

To describe the outcomes and complications of SADI-S.

METHODS

We retrospectively analyzed the data of patients who underwent SADI-S laparoscopically at the Clínica Reina Sofía in Bogotá, Colombia. This study assessed the therapeutic effectiveness of SADI-S in terms of short-term preoperative clinical characteristics, postoperative complications, comorbidities, nutritional defi-ciencies, and intraoperative complications during a 2-year follow-up.

RESULTS

Sixty-one patients with a mean body mass index (BMI) of 50 ± 7.1 kg/m² underwent laparoscopic SADI-S. The mean operative time and hospital stays were 143.8 ± 42 min and 2.3 ± 0.8 d, respectively. The mean follow-up period was 18 mo, and the mean BMI decreased to 28.5 ± 12.2 kg/m². The excess BMI loss was 41.8% ± 13.5%, and the weight loss percentage was 81.1% ± 17.0%. Resolution of obesity-related comorbidities, including type 2 diabetes mellitus, hypertension, dyslipidemia, and obstructive sleep apnea, was achieved and defined as complete or partial remission. No intraoperative complications were observed. Short-term complications were observed in four (6.8%) patients. However, larger studies with longer follow-up periods are required to draw definitive conclusions.

CONCLUSION

SADI-S has a low intraoperative and postoperative complication rate and is effective for weight loss and improving obesity-related comorbidities, including hypertension, type 2 diabetes mellitus, dyslipidemia, and sleep apnea syndrome.

Key Words: Extreme obesity; Bariatric surgery; Body mass index; Metabolic syndrome; Cardiovascular diseases; Complications

Core Tip: In this publication, we showcase our institution's experience with single anastomosis duodeno-ileal bypass with sleeve gastrectomy (SADI-S) in Colombia. We provide a comprehensive description of the patient journey, from preoperative to postoperative phases, demonstrating weight loss outcomes and resolution of obesity-related comorbidities. We present procedural complications, immediate postoperative care, and the evolution of patients with early initiation of oral intake, ambulation, and nutritional strategies. Our study emphasizes SADI-S as a viable surgical alternative for extreme obesity and metabolic diseases, highlighting its progressive weight reduction and promising lifestyle modifications for this patient population. Our findings support the effectiveness of SADI-S in the Colombian context.

INTRODUCTION

Obesity is a chronic disease whose global prevalence has significantly increased over the past 40 years[1,2]. Over 1.5 billion adults are estimated to have a body mass index (BMI) greater than 25 kg/m² globally[3-6]. The prevalence of obesity in adults in the United States is approximately 42.4%[2,5,6]. The latest health survey in Colombia (ENSIN 2015) found that 37.8% of the adults in the country were overweight, whereas 18.7% were obese. With over half the population (56.5%) being overweight or obese, obesity is considered a public health problem in Colombia[7].

Treatment of obesity requires a multidisciplinary approach to reduce long-term morbidity and mortality[3,4]. Bariatric and metabolic surgeries are indicated for obese patients who do not respond to medical treatment[8-10].

Among the surgical procedures, laparoscopic sleeve gastrectomy or gastric bypass surgeries[11-15] have shown effectiveness in terms of long-term weight loss and maintenance. The single anastomosis duodeno-ileal bypass with sleeve gastrectomy (SADI-S) combines the restrictive component of sleeve gastrectomy with the malabsorptive component of duodeno-ileal bypass. It simplifies the techniques of biliopancreatic diversion procedures, such as the duodenal switch (DS), where sleeve gastrectomy is followed by a terminolateral duodeno-ileal bypass[16]. SADI-S has demonstrated a low complication rate, requires a single ileo-duodenal anastomosis, and reduces the likelihood of internal hernias by avoiding mesenteric openings. This simplifies the surgical technique and has been associated with good short- and medium-term sustained weight loss[17-19].

The literature has demonstrated that the procedure is safe and effective, with optimal effects on weight loss and reduced metabolic diseases. In 2018, the International Federation for the Surgery of Obesity stated that available short-term data demonstrated the safety and efficacy of this procedure. However, the long-term outcomes of this procedure remain unclear.

Therefore, this retrospective study aimed to analyze our experience with patients undergoing SADI-S, the first of its kind in Colombia. We aimed to describe our institution's experience, identify the rates of intraoperative and postoperative complications, and evaluate weight loss and resolution of obesity-related comorbidities during 2 years of follow-up.

MATERIALS AND METHODS

Retrospective data were collected from patients with extreme obesity who underwent laparoscopic SADI-S as a primary or revision procedure after sleeve gastrectomy at Clínica Reina Sofía, Bogotá, from August 3, 2016 to June 15, 2020, with a follow-up limited to 2 years. Data were retrospectively obtained from medical records of patients attending the bariatric surgery clinic.

The primary objective of this study was to assess the safety of this procedure in terms of intraoperative complications within 30 postoperative days. The secondary objective was to evaluate the weight loss and complications during the follow-up period.

Patients were evaluated in the clinic according to the guidelines of the Colombian Association of Obesity and Bariatric Surgery (ACOCIB - Asociación Colombiana de Obesidad y Cirugía Bariátrica)[20,21].

Inclusion criteria

All patients aged 18-65 years with extreme obesity and obesity-related comorbidities such as type 2 diabetes mellitus, hypertension, dyslipidemia, and obstructive sleep apnea syndrome (OSAS) were included in the study. Extreme obesity was defined as a BMI ≥ 40 kg/m². Patients who had failed sleeve gastrectomies were included, with failure defined as insufficient weight loss after 18 mo (excess weight loss percentage < 50) or a BMI > 35%[20].

Exclusion criteria

Patients with a history of bariatric surgery other than sleeve gastrectomy, severe gastroesophageal reflux disease (GERD - esophagitis equal to or greater than Los Angeles classification grade C)[22], Barrett's esophagus, or giant hiatal hernias (candidates for gastric bypass according to the study protocol) were excluded. Patients with serious pathologies that would not benefit from the intervention or posed a high anesthetic-surgical risk were also excluded. Similarly, patients with active major psychiatric disorders (alcoholism, drug addiction, schizophrenia, etc.) were excluded. Individuals identified by the multidisciplinary team (nutritionist, internist, psychiatrist, and surgeon) to be at risk of lack of support and poor compliance with postoperative medical or nutritional treatment plans and recommendations were excluded.

The reference institution provides a multidisciplinary program for obese patients, including pre- and postoperative counseling, focused on education about lifestyle changes and outpatient follow-up evaluations 8 d after surgery, at 1 mo, once every 3 mo for 1 year, and every 6 mo thereafter.

At this institution, the choice of surgical approach (1- or 2-stage SADI-S) depends on the patient's BMI, medical condition, and the surgeon's judgment.

Surgical technique

An expert bariatric surgery team performed all the procedures. The 58 patients underwent sleeve gastrectomy, which involved dissection of the gastrocolic ligament, followed by preparation of the greater curvature, extending cranially to expose the left diaphragmatic pillar and caudally to the pylorus. The first portion of the duodenum was prepared to expose the gastroduodenal arteries. The next step was vertical gastric resection using a 48 Fr bougie with a section 6 cm from the pylorus. A 60 mm linear cutting stapler was used for all procedures. The staple line was reinforced using a continuously invaginating suture using 3-0 polypropylene. The efferent limb was 300 cm from the ileocecal valve, and a terminolateral antecolic duodenoileal anastomosis was performed in two planes. Continuous polydioxanone (PDS) 3-0 barbed sutures were used for the first plane on the posterior side and PDS 3-0 for the remaining planes. The integrity of the anastomosis was verified using methylene blue and pneumatic tests following the basic principles of the technique described by Sanchez-Pernaute (Figures 1 and 2)[16].

Figure 1 Positioning of trocars for laparoscopic single-anastomosis duodeno-ileal bypass with sleeve gastrectomy.

Figure 2 Sequence of single-anastomosis duodenum ileal bypass with sleeve gastrectomy. A: Dissection of duodenum posterior to gastroduodenal artery; B and C: Forty-five mm stapled line of the duodenum, leaving 5 cm of the duodenum proximal to the pylorus; D: End-to-side duodenal ileostomy in two planes and methylene blue test without leaks; C: Common bile duct; D: Duodenum; AA: Afferent loop; AE: Efferent loop; P: Pylorus; T: Portal triad; DP: Proximal duodenum; DD: Distal duodenum; S: stomach.

Post-procedural weight loss was the primary outcome. For secondary outcomes, the resolution of comorbidities was assessed and classified as complete or partial remission. Complete remission of hypertension was considered achieved when blood pressure was below 130/85 mmHg without medication[23]. In this study, complete remission of type 2 diabetes mellitus was defined as a glycosylated hemoglobin (HbA1c) level of < 6% and normalizing fasting glucose (< 100 mg/dL) without medication for over 1 year. Partial remission was defined as an HbA1c level between 6%-6.5% and fasting glucose levels between 100 and 125 mg/dL without medication[20]. Resolution of hypercholesterolemia and hypertriglyceridemia was evaluated when medication was no longer required, and the values were within normal parameters. The resolution of sleep apnea was defined as the discontinuation of all sleep apnea treatments[24].

This study implemented a standardized, personalized postoperative protocol for bariatric patients. The severity of postoperative complications was evaluated using the Clavien-Dindo classification[25]. The follow-up period was defined as short-term (12-24 mo after surgery) and medium-term (2-5 years after the procedure).

Statistical analysis

Descriptive analyses of the convenience sample of patients included means, standard deviations, percentages, and frequencies. Descriptive analyses were performed on demographic variables, medical history, surgical characteristics, and surgical complications. Qualitative variables are presented using absolute and relative frequencies, whereas quantitative variables are presented using central tendency and dispersion measures based on their distribution. Laboratory parameters and BMI are presented according to the time of measurement, and their comparison was conducted using repeated-measures analysis of variance, with assumptions of independence, normality, and sphericity verified. Post-hoc analysis was conducted using paired t-tests adjusted for Bonferroni correction. The percentage of BMI reduction was compared using the non-parametric Kruskal-Wallis test, and post-hoc analysis was performed using the paired Wilcoxon test with Bonferroni correction.

Ethical considerations

After obtaining approval from the research and ethics committees of the institution, the study was conducted in accordance with the Declaration of Helsinki of 1964 and its subsequent revisions. The informed consent that the patients signed for surgery included the use of personal and surgical data, images, and videos for scientific purposes. All the study participants or their legal guardians provided written informed consent.

Body weight and composition

Weight and body composition were evaluated before surgery and at 3, 6, 9, 12, 18, and 24 mo after surgery. The percentage of excess weight loss (%TWL) was estimated as the percentage of total weight loss (%TWL) as follows:

WL% = 100 × (initial weight - weight at the 2-year follow-up)/initial weight. Reduction of BMI = (initial weight - final weight)/height². %TWL = 100% × reduction in baseline BMI/initial BMI.

RESULTS

Sixty-one patients were included in this study, of whom 40 (65.57%) were female and 21 (34.4%) were male. The mean age of the patients was 39.8 ± 9.54 years. At the time of the procedure, the average weight of the patients was 139.5 ± 28.3 kg, and the average BMI was 50.27 ± 7.6 kg/m². Table 1 shows the patients' preoperative, surgical, and demographic characteristics. All the patients underwent laparoscopic surgery. The SADI-S one-step procedure was performed in 50 (81.9%) patients, while the two-step procedure was performed in 11 (22.4%) patients. In the two-step procedure, the interval between the two surgical sessions ranged from 6-12 mo. Regarding surgical procedures, SADI-S was the primary procedure in 56 (98.36%) patients. In two (4%) patients, SADI-S was performed as a rescue procedure for failed sleeve gastrectomy. For these two patients, duodenal-ileal anastomosis was performed 3 and 6 years after the original sleeve gastrectomy. The average operative time was 144.95 ± 42.24 min (range 69-300 min), and the average postoperative hospital stay was 2.3 ± 0.8 d (range 1-6 d). Simultaneous procedures were performed in three (5.2%) patients, including incisional herniorrhaphy for a giant hernia with mesh in one patient and hiatal hernia repair in two patients. The average time to initiate oral feeding after the procedure was 1.0 ± 0.25 days. The patients were followed in the hospital before and after the operation. The median follow-up time was 18 mo [interquartile range (IQR) 12-24 mo] over 2 years. Weight loss and blood analysis results were obtained by telephone or email for patients living in different countries.

Table 1 Patient demographic and surgical characteristics and preoperative comorbidities, n (%).

Variables
Demographic characteristics
Male sex	21	34.43
Years of age (mean, SD)	39.8	9.54
BMI kg/m2 (mean, SD)	50.27	7.21
Surgical characteristics	n or median	%
Procedure characteristics
Type of surgery, SADI	11	0.224
SADI-S	50	0.819
Synchronous procedure	3	0.052
Operative time minutes (mean, SD)	144.95	42.24
Hospitalization characteristics
Length of stay (days) 1	2	0.034
2	40	0.69
3	12	0.207
4	2	0.034
5	1	0.017
6	1	0.017
1	54	0.931
Start of oral route (d)
2	4	0.069
CPAP discontinuation	14	0.25
Medical history
OSAH	43	70.49
Dyslipidemia	31	50.82
Arterial hypertension	21	34.43
Use of CPAP	14	22.95
Hiatal hernia	14	22.95
Prediabetes	13	21.31
Gastritis	12	19.67
Type 2 diabetes	12	19.67
Hypothyroidism	10	16.39
Smoking	8	13.11
Gastroesophageal reflux	8	13.11
Type 1 diabetes	1	1.64
Complications
Pain	9	14.75
Readmission	4	6.56
Hematoma	2	3.28
Intestinal obstruction	1	1.64
Postoperative ileus	1	1.64
Follow-up time (mean, SD)	19.43	6.91

CPAP: Continuous positive airway pressure; OSAHS: Obstructive sleep apnea/hypopnea syndrome; BMI: Body mass index; SADI: Single anastomosis Duodeno-ileal bypass; SADI-S: Single anastomosis duodeno-ileal bypass with sleeve gastrectomy.

During the study, the patients followed a specific dietary protocol, which involved a liquid diet for the first 15 d postoperatively, followed by sequential progression to a normal diet supplemented with bariatric multivitamins (calcium, vitamin D3, iron, etc.). A nutrition team closely monitored the nutritional status of patients. Additionally, the patients were instructed to initiate early ambulation starting on day 1 after surgery and begin cardiovascular exercise after the first month. These measures were implemented to support patients’ postoperative recovery and overall health.

The most common comorbidity was OSAS (70.49%), followed by dyslipidemia (50.82%) and hypertension (34.43%). Other comorbidities included hypothyroidism in ten (17.2%) patients, GERD in eight (13.8%), and type 2 diabetes mellitus in 19.7%. One (2%) patient received insulin, and 13 (24.1%) were on oral hypoglycemic agents for diabetes management. Thirteen (22.41%) patients were diagnosed with a hiatal hernia based on preoperative endoscopic studies. Among them, seven (12%) patients had hiatal hernias measuring > 2 cm and/or were symptomatic for gastroesophageal reflux. Hiatal hernia repair was performed in these seven patients. Additionally, seven (12.1%) patients had a smoking history, but none were smokers at the time of surgery.

Resolution of comorbidities

Twelve (19.7%) patients had type 2 diabetes mellitus preoperatively. Preoperative tests found that 37 patients had HbA1C levels above 6.5% (average: 6.03 ± 0.99). At 12 mo post-procedure, the average HbA1C of the patients was 5.13% ± 0.34%, and the average fasting blood glucose was 83.49 ± 6.82 mg/dL. None of the patients had HbA1C levels > 5.6% at 24 mo.

Sleep apnea affected 70.49% of the patients at the beginning of the study. Of these, 23% used continuous positive airway pressure (CPAP); at 1 year postoperatively, only 25% reported no longer using CPAP. The resolution of sleep apnea was defined as the cessation of all sleep apnea treatments.

Hypertension was present in 34.43% of patients before the surgical procedure. However, 1 year after the procedure, 70% of the patients had normal blood pressure during their office evaluations, and medications were discontinued, or the doses were reduced.

Follow-up blood tests were performed every 6 mo after surgery. In the first year postoperatively, Figure 3 shows that patients exhibited a reduction in hemoglobin, hematocrit, HbA1C, glucose, total cholesterol, low-density lipoprotein (LDL) cholesterol, and triglyceride levels before surgery (T1) and at the 6-mo postoperative follow-up (T2). At the 1-year follow-up, the levels remained stable compared to those measured at T2. High-density lipoprotein (HDL) cholesterol levels tended to remain consistent with the measurements at T1 and T2, but an increase was observed at T3. Differences were considered statistically significant.

Figure 3 Frequency distribution of laboratory results taken before surgery (T1), at 6 mo (T2), and at one year (T3) of follow-up. A: The median hemoglobin was 14.35 mg/dL [interquartile range (IQR) 1.82] at T1, 13.47 mg/dL (IQR 2.6) at T2, and 13.50 mg/dL (1.37) at T3; B: The median hematocrit was 44.36% (IQR 5.17) at T1, 30.27% (IQR 6.5) at T2, and 40.22% (3.33) at T3; C: Median glycated hemoglobin was 5.81% (IQR 0.75) at T1, 5.1% (IQR 0.48) at T2, and 13.50% (IQR 0.51) at T3; D: Median glucose levels were 97.54 mg/dL (IQR 21.07) at T1, 81.7 mg/dl (IQR 10.99) at T2, and 79 mg/dL (IQR 10.9) at T3; E: Median TSH levels were 2.8 mU/L at T1, 2.10 mU/L at T2, and 2.46mU/L at T3 ; F: Cholesterol at T1 of 179.80 mg/dL (IQR 48.9) dropped at T2 to 143.38 mg/dL (IQR 46) and was maintained at T3 at 143.13 mg/dL (IQR 26); G: High-density lipoprotein levels (HDL) went from 44.1 mg/dL (IQR 10.9) at T1 to 41.35 mg/dL (IQR 12.45) at T2 and 46.5 mg/dL (IQR 13) at T3; H: LDL levels went from 108 mg/dL (IQR 39.6) at T1 to 89.4 mg/dL (IQR 36.31) at T2 and 84.37 mg/dL (IQR 37.67) at T3; I: Triglyceride levels went from 110.8 mg/dL (IQR 64.75) at T1 to 90 mg/dL (IQR 46.09) at T2 and 75.5 mg/dL (IQR 25.8) at T3. T1: Preoperative, T2: 6 mo, T3: 1 year. ^aP < 0.05, ^bP < 0.01, ^cP < 0.01, ^dP < 0.00001. NS: Not significant.

Preoperatively, 22.4% of the patients had elevated triglyceride and cholesterol levels (triglyceride > 150 mg/dL and cholesterol > 200 mg/dL); these levels decreased by 19% and 21%, respectively, after 6 mo. At 24 mo, cholesterol and triglyceride levels in all patients were within the normal range. During the preoperative period, 57 (98.27%) patients had low HDL levels, with an average of 43.23 ± 8.89 mg/dL. This had increased to 50 ± 8.3 mg/dL by the end of the first year. The changes in the mean triglyceride, HDL, and LDL levels are shown in Figure 4.

Figure 4 Frequency distribution of body mass index of patients during follow-up. T1: Pre-surgical, median body mass index (BMI) 49.15 kg/m² [interquartile range (IQR) 5.98]. Postoperative: T2: 2 wk, median BMI 43.73 kg/m² (IQR 7.49); T3: 1 mo, median BMI 41.22 kg/m² (IQR 6.39); T4: 3 mo, median BMI 37.52 kg/m² (IQR 7.56); T5: 6 mo, median BMI 33.91 kg/m² (IQR 7.71); T6: 1 year, median BMI 30.99 kg/m² (IQR 8.02); T7: 2 years, median BMI 29.61 kg/m² (IQR 6.04). ^dP < 0.00001. NS: Not significant.

Regarding vitamin deficiencies at 12 mo, 10.3% of the patients had vitamin B12 Levels below the normal range (reference value: 197-771 pg/mL), and 17.24% had low 25-hydroxyvitamin D levels. Low ferritin levels were reported in three (5.1%) patients. Average calcium levels were 3.86 ± 3.76 mg/dL at 6 mo. Vitamin B12 and 25-hydroxyvitamin D levels were not routinely measured preoperatively. Measurements were taken at 6 mo and every year postoperatively.

At discharge, all patients were prescribed oral bariatric multivitamins three times a day (folic acid 200 mcg, thiamine 3 mg, and vitamin A 1875 IU), calcium (300 mg), vitamin D3 (750 IU), iron (11.25 mg), and a bimonthly intramuscular injection of the vitamin B complex (vitamin B1, 100 mg; vitamin B6, 100 mg; vitamin B12, 5,000 mg). Patients had the option to individually purchase sublingual vitamin B12 (1000 μg twice a week) as a substitute for intramuscular administration.

Weight loss

Figure 4 demonstrates the progressive decrease in BMI from the preoperative point (T1) to the last follow-up 2 years after surgery (T7). The differences were statistically significant in all comparisons except for the T6-T7 period.

Figure 5 shows the weight loss percentage from 2 wk postoperatively (T1) to the last follow-up 2 years (T7) postoperatively. Differences were considered statistically significant for all comparisons.

Figure 5 Frequency distribution of percentage reduction in body mass index of patients during follow-up. Postoperative: T1: 2 wk, median body mass index (BMI) reduction 19.53% [interquartile range (IQR) 9.57]; T2: 3 mo, median BMI reduction 27.58% (IQR 14.46); T3: 6 mo, median BMI reduction 61.71% (IQR 23.78); T4: 1 year, median BMI reduction 79.84% (IQR 35.76); T5: 2 years, median BMI reduction 91.27% (IQR 102.23). ^cP < 0.01, ^dP < 0.00001.

Complications

The most frequent complications were abdominal pain (14.75%), readmission (6.56%), and hematoma (3.28%). One patient experienced intraluminal bleeding, which resolved spontaneously without the need for a blood transfusion. Another patient was diagnosed with ileus on postoperative day 6; however, laparoscopic inspection did not reveal any significant findings. Anastomotic leaks or strictures were not observed. None of the patients experienced volvulus of the duodenal-ileal anastomosis or internal hernia. No intraoperative complications or mortality were reported during the immediate postoperative or follow-up periods. No long-term complications were reported until the end of the follow-up period. The mean follow-up time was 19.43 ± 6.91 mo, with 65% of patients being followed for 2 years.

DISCUSSION

This study presents the initial experience in Colombia with the SADI-S procedure as a surgical approach for extremely obese patients with obesity-related metabolic diseases, confirming the intended effectiveness in weight loss and safety. In an updated statement (2020), the American Society for Metabolic & Bariatric Surgery endorsed SADI-S as an appropriate metabolic procedure; however, there is a lack of evidence regarding intestinal adaptation, nutritional issues, optimal lengths of efferent limbs, and long-term weight loss and recovery after this procedure[17,18].

Different studies have sought to identify an ideal technique that can be individualized and tailored to each patient's requirements to identify the most effective and safe procedure that reduces associated complications. One advantage of SADI-S is the preservation of the pylorus, which reduces the occurrence of dumping syndrome and reactive hypoglycemia reported after other procedures, such as Roux-en-Y gastric bypass (RYGB)[19]. Additionally, preserving a common limb length of 300 cm may be associated with a lower incidence of diarrhea and malabsorption, reducing the occurrence of short bowel syndrome, a risk factor for patients with an intestinal length of < 2 m[19]. Similar to DS, SADI-S has beneficial effects on endocrine and metabolic diseases such as type 2 diabetes mellitus, hypertension, and OSAS, similar to DS[20].

The SADI-S is a modified version of the DS, and its efficacy should be compared based on the mechanism that they share. One advantage of SADI-S over DS is the shorter operative time, with SADI-S averaging 132.70 ± 7.19 min compared to 164.30 ± 7.78 min for DS (P = 0.006)[17-20]. Several studies have documented a low rate of anastomotic leaks and a reduction in the occurrence of internal hernias, as there is no mesenteric opening[17,18]. The procedure can be performed in one or two stages, with the first stage involving sleeve gastrectomy and the second being a single duodenal-ileal anastomosis, typically performed 6-12 mo after the initial procedure[19]. In the series published by Surve et al[21], the average operative time (skin-to-skin) for SADI-S was 121.8 ± 25 min (range 75-182 min). Complication rates after SADI-S have been reported in the literature ranging from 1.6% to 13%, with an overall reoperation rate of 8.2% and an estimated mortality rate of 0.4%[20,22].

In this study, the mean operative time was 143 ± 25 min. There were no intraoperative complications in this series; only 6.8% (n = 4) of the patients experienced early complications within the first 30 d after surgery. No mortality occurred during the immediate postoperative period or follow-up. The mean hospital stay after surgery was 2.3 d, and the mean time from surgery to the initiation of oral feeding was only 1.0 ± 0.25 d.

No cases of internal hernias or volvulus at the duodenal-ileal anastomosis were documented during follow-up. The rate of anastomotic-related complications after SADI-S was lower than those reported for RYGB and DS[25-27]. The reported incidence of anastomotic leaks after DS ranges from 0.5% to 6%, whereas the incidence of internal hernias after RYGB ranges between 0.5% and 16%. The incidence of intestinal obstruction ranges from 0.6% to 3.6%, and the incidence of gastrojejunal stenosis varies from 3% to 11%[27-29].

Studies have documented excess weight loss of 61.7%-87% 1 year after the SADI-S. Two-year weight loss ranges from 83.7% to 93.7%[18,27,28]. In this series, the initial mean BMI was 50 kg/m², and 33% of the participants had a BMI < 30 kg/m² at 1 year. Weight loss during the first year remained consistent throughout the follow-up period, with a median reduction in BMI of 79.84% (IQR, 35.76) at 1 year and a median reduction of 91.27% (IQR, 102) at 2 years. However, no statistically significant differences were observed between groups.

Regarding the resolution of comorbidities, the rates of complete remission of diabetes in non-insulin-dependent patients after a 3-year follow-up were 77.1%, 89.7%, and 96.4% for RYGB, DS, and SADI-S, respectively, and 30.4%, 50%, and 56%, respectively, for insulin-dependent patients[23]. SADI-S, along with associated lifestyle and nutritional changes during follow-up, improved fasting blood glucose levels to an average of 83 mg/dL at 12 mo and reduced the average HbA1C to 5.1%. All patients had HbA1C levels < 5.6% 24 mo after the procedure.

The control of obesity-related metabolic diseases and the outcomes observed in this study are consistent with other evidence described by Sánchez-Pernaute, who reported an average excess weight loss of 72% 2 years after the two-stage SADI-S. The complete remission rates of diabetes mellitus, hypertension, and dyslipidemia were 88%, 60%, and 40%, respectively[18]. Dyslipidemia was resolved in 31.2% of patients and improved by 25%. The rates of remission and improvement in hypertension were 27.7% and 22.2%, respectively[27-31]. This study illustrates the initial experiences in Colombia regarding the performance of SADI-S as a surgical technique for extremely obese patients with obesity-related metabolic diseases, reaffirming the data obtained regarding the effectiveness of weight loss and the procedure's safety.

In a single-center cohort study that included patients who underwent the SADI-S, the overall rates of resolution of diabetes mellitus, hypertension, dyslipidemia, and OSAS were 88.5%, 73.0%, 77.0%, and 85.7%, respectively, with no differences observed between one- and two-stage SADI-S[21]. In this study, OSAS was diagnosed in 76% (n = 44) of the patients using polysomnography at the beginning of the study, of whom 69% were treated with CPAP. At 1 year, 24% (n = 14) of the patients reported resolution of sleep apnea and discontinuation of CPAP. The remaining 45% (n = 22) reported symptom improvement during the follow-up[21].

The results of this study support the efficacy and safety of SADI-S as a treatment for extreme obesity. Long-term follow-up is necessary to evaluate the outcomes of this technique and compare them with those of other procedures in terms of sustained long-term weight loss and occurrence of late complications[32-34].

This is the first national retrospective study on SADI-S; however, several limitations of our analysis should be considered, including its retrospective design, observational nature, small sample size, short follow-up duration, and lack of postoperative polysomnography. Although this study had a limited sample size and short-term follow-up, the results correlate with findings from other studies showing favorable outcomes and the safety of SADI-S as a surgical technique. The significance of this study lies in being the first case series published in Spanish-speaking countries in South America, which helps promote the use of this surgery as a viable alternative for patients with extreme obesity, with very low perioperative mortality and good weight-loss results up to the observation period.

CONCLUSION

SADI-S is an effective procedure for patients with extreme obesity. It has a low rate of intraoperative and postoperative complications, with good outcomes in terms of weight loss and improvement or resolution of associated comorbidities. Our experience confirms the reproducibility of this technique when performed in referral centers. Long-term follow-up studies are required to evaluate sustained weight loss and determine long-term metabolic complications.

ARTICLE HIGHLIGHTS

Research background

The latest health survey in Colombia (ENSIN 2015) found that 37.8% of adults in our country were overweight, while 18.7% were obese. With over half of the population (56.5%) being overweight or obese, this is considered a public health problem in Colombia.

Research motivation

Single anastomosis duodeno-ileal bypass with sleeve gastrectomy (SADI-S) is a safe and effective procedure for weight loss 2 years post-surgery. SADI-S improves and resolves obesity-related comorbidities. SADI-S has shorter operative time compared to duodenal switch.

Research objectives

The primary objective was to assess the safety of the procedure in terms of intraoperative complications and complications within 30 d postoperatively. The secondary objective was to evaluate weight loss and complications during the follow-up period.

Research methods

Retrospective data were collected from patients with extreme obesity who underwent laparoscopic SADI-S as a primary or revision procedure after sleeve gastrectomy at Clínica Reina Sofía in Bogotá.

Research results

The results of this study support the efficacy and safety of SADI-S as a treatment for extreme obesity.

Research conclusions

SADI-S is an effective procedure for patients with extreme obesity. It has a low rate of intraoperative and postoperative complications, with good outcomes in terms of weight loss and improvement/resolution of associated comorbidities. Our experience confirms the reproducibility of the technique when performed in referral centers.

Research perspectives

The significance of the study lies in being the first case series published in Spanish-speaking countries in South America, which helps promote the use of this surgery as a viable alternative for patients with extreme obesity, with very low perioperative mortality and good weight loss results up to the observation period.