27 November 2025: Articles
Gastric Bipartition with Functional Duodenum Exclusion (GBp-FDE) as a Possible Surgical Conversion of Sleeve Gastrectomy in Patients with De Novo GERD and Obesity Recidivism: Preliminary Results of a Case Series
Unusual clinical course, Challenging differential diagnosis, Unusual or unexpected effect of treatment, Diagnostic / therapeutic accidents, Unexpected drug reaction, Educational Purpose (only if useful for a systematic review or synthesis)
Victor Ramos Mussa DibDOI: 10.12659/AJCR.950798
Am J Case Rep 2025; 26:e950798
Abstract
BACKGROUND: Sleeve gastrectomy (SG) is widely used in obesity treatment, although it is associated with new onset of gastroesophageal reflux disease (de novo GERD) and weight regain. Roux-en-Y gastric bypass (RYGB) is the standard revisional procedure for GERD, though it offers limited additional weight loss. Ileal-based procedures have demonstrated superior outcomes regarding weight loss but have uncertain results in GERD. This study presents preliminary findings on gastric bipartition with functional duodenal exclusion (GBp-FDE) as a revisional approach following SG in this scenario.
CASE REPORT: A retrospective data analysis was conducted on 10 patients who underwent GBp-FDE due to de novo GERD and obesity recurrence after SG (mean BMI: 37.2±3.2 kg/m²). Nine patients presented with hiatal hernia and 8 with sleeve dilation. GERD was assessed pre- and postoperatively using a validated questionnaire, endoscopy, and contrast radiology. The surgical technique involved a pre-pyloric antroileostomy in Roux-en-Y configuration using a 40% proportion biliopancreatic limb. One-year postoperative findings included pyloric spasm (endoscopy), very preferential contrast flow to the ileum (radiology), and endoscopic access preservation to the duodenum. GERD symptoms resolved in 90% (P=0.0059) and esophagitis healed in 80% (P=0.008), likely due to gastric decompression. Mean percent total weight loss and percent excess weight loss were 35.2±6.6 and 108.0±11.14, respectively.
CONCLUSIONS: GBp-FDE seems to be a promising surgery for managing de novo GERD and obesity recurrence after SG, through SG pouch decompression and ileal stimuli, promoted by the antroileostomy. Further controlled studies with extended follow-up are necessary to validate these findings.
Keywords: Bariatric Surgery, Gastrectomy, Gastric Bypass, Anastomosis, Roux-en-Y, Humans, Duodenum, Gastroesophageal Reflux, obesity, Obesity, Morbid, Recurrence, Reoperation, Retrospective Studies
Introduction
Obesity has reached alarming global prevalence, and metabolic bariatric surgery (MBS) is recognized as the most effective and durable treatment [1]. Several techniques are available, each with distinct mechanisms of action [2,3]. Sleeve gastrectomy is the most widely performed procedure worldwide [4,5], but it is frequently associated with new-onset or worsening gastroesophageal reflux disease. This occurs mainly due to the longitudinal gastrectomy, which reduces gastric compliance, increases intragastric pressure, and alters the esophagogastric junction anatomy [6–8]. A strong correlation has been established between sleeve pouch dilation, obesity recurrence, hiatal hernia (HH), and GERD after SG [9,10]. Conversely, SG preserves gastrointestinal continuity, allowing complete endoscopic evaluation and reducing nutritional deficiencies [11]. Long-term metabolic outcomes and weight loss are satisfactory [12], particularly in patients with body mass index (BMI) <50 kg/m2, although results are slightly inferior to those of RYGB [13].
RYGB was the most performed bariatric procedure worldwide until 2013, when sleeve gastrectomy (SG) started surpassing it in the United States [14]. Despite this shift, RYGB remains widely recommended, demonstrating effective weight loss and metabolic improvements in patients with morbid obesity [15]. It is considered the most effective surgical option for obese individuals with GERD [16,17]. The procedure excludes most of the stomach, duodenum, and proximal jejunum, limiting transoral endoscopic access to these segments [18–23]. For this reason, in regions with high gastric cancer prevalence, resection of the remnant stomach has been proposed as a preventive strategy [24].
Managing patients with GERD and recurrence of weight gain after SG remains challenging, as neither re-sleeve gastrectomy (Re-SG) nor RYGB adequately addresses both conditions. Re-SG may promote further weight loss (WL) in cases of gastric pouch dilation but is suboptimal for GERD control [25]. Conversely, while RYGB effectively treats GERD, it often fails to achieve sustained additional weight loss [26]. Ileal surgeries such as duodenal switch (DS), single anastomosis duodenum-ileostomy with sleeve (SADI-S) and one anastomosis gastric bypass (OAGB) promote further WL, but have questionable results in gastroesophageal reflux control [27]. Transit bipartition (TB) has emerged as a feasible surgical option to deal with obesity recidivism and GERD after SG [28], although studies addressing this operation in severe gastroesophageal reflux disease are lacking.
This case series examines patients presenting with moderate to severe de novo GERD and recurrent weight gain following SG, with associated HH and sleeve pouch dilation in most cases, for whom revision surgery was indicated. Inclusion criteria comprised obesity recurrence and confirmed endoscopic GERD diagnosis per the Lyon consensus [29], using the Los Angeles Endoscopic Esophagitis Classification (LA Classification) [30]. All patients declined operations that included gastrointestinal exclusions for varied reasons: 4 had a family history of digestive tract cancer, 2 had relatives with biliary tree gallstones, 3 knew individuals with malnutrition after other techniques associated with anatomical exclusions, and 1 was concerned about blind gastrointestinal segments. Considering these factors and after thorough discussion about surgical options, GBp-FDE was proposed as a revisional approach to address both GERD and obesity recidivism without anatomical exclusions [31,32]. In cases associated with gastric pouch dilation and/or HH, concomitant re-sleeve and HH repair were performed. The surgery consisted of adding a wide Roux-en-Y antroileostomy on the juxta pre-pyloric anterior gastric wall of the sleeved stomach, aiming to reduce intragastric pressure and alleviate reflux. This anastomosis was also intended to promote preferential gastric flow to the ileum, functionally excluding the duodenum. Duodenal diversion and ileal stimulation – enhanced by a 40% proportion biliopancreatic limb – are expected to support further weight loss via metabolic pathways [33,34].
Preoperative and 1-year postoperative assessments included clinical evaluation of gastroesophageal reflux symptoms using a validated GERD questionnaire [35], which was an adaptation to Portuguese language by Velanovich et al. The GERD questionnaire (Table 1) [36], translated and validated by the authors, aimed at easier comprehension by Brazilians, with the inclusion of regurgitation assessment. Upper endoscopy was performed at both time points to assess hiatal hernia – defined by the distance between the proximal gastric folds and crura constriction, during endoscopic withdrawal – erosive esophagitis per Los Angeles classification [30], and sleeve pouch morphology, including tortuosity, stenosis, or dilation (the latter inferred when endoscopic retroflexion was feasible). Radiological contrast studies were conducted pre- and postoperatively to evaluate HH, pouch tortuosity, stenosis, and pouch dilation (defined as total gastric volume >250 mL) [37]. Postoperative radiological series (300 mL of barium solution) also assessed the preferential contrast flow between the antroileostomy and the pylorus. Three patterns were considered: (1) unidirectional flow to the ileum; (2) preferential flow to the ileum, with minimal contrast passage to the duodenum; (3) split flow between the ileum and the duodenum. The first 2 patterns were interpreted as functional duodenum exclusion. Anthropometric parameters and comorbidity status were monitored throughout the study.
Case Reports
STATISTICAL ANALYSIS:
Continuous variables are summarized as mean±SD, median (P25–P75), minimum–maximum, and the 95% confidence interval of the mean. Categorical variables are presented as counts and percentages, with exact Clopper-Pearson 95% confidence intervals when informative. The number of missing observations is reported per variable.
Longitudinal comparisons (4 time points). Weight and BMI measured at initial, nadir, pre-revision, and 1-year follow-up were analyzed using one-factor repeated-measures ANOVA (within-subjects). Sphericity was evaluated with Mauchly’s test; when violated, degrees of freedom and
Before-after outcomes such as gastroesophageal reflux disease (GERD) and hiatal hernia (HH) were tested with McNemar’s test; in addition to the continuity-corrected chi-square, the exact binomial
The distribution of contrast destination at postoperative seriography (ileum vs duodenum) was compared using an exact binomial test of the ileum proportion against a null of 0.50, with the corresponding exact 95% confidence interval. Results are illustrated with monochrome bar charts in percentages and reported in figure captions.
Descriptive summaries used available data (pairwise). Repeated-measures ANOVA and paired tests were performed on complete cases for the respective variables. No imputation was performed given the sample size and design. Significance and reporting. All tests were two-sided with α=0.05. Exact
Results
Out of a total of 22 individuals, 12 were excluded from this study: 6 for presenting grade A or no esophagitis according to LA classification, 5 due to absence of obesity recidivism, and 1 for not complying with the FU protocol. In the remaining 10 individuals enrolled in this series, during 1-year FU there was a universal reflux symptoms improvement and decrease in validated GERD questionnaire scores (
Radiological oral contrast studies revealed functional duodenal exclusion in all individuals, and unidirectional flow to the ileum was observed in 9 of them (
During 1-year follow-up weight and BMI dropped from 99.7±9.9kg (97.5 [94.5–108.8]) and 37.2±3.2 kg/m2 (37.0 [34.7–38.0]) to 64.5±8.4 kg (62.9 [58.2–70.2]) and 24.0±1.7 kg/m2 (23.8 [23.2–24.9]), respectively (Figures 14 and 15 shows mean weight and BMI evolution since primary operation until 1-year FU of revision). Mean%EWL was 108.0±11.4 (109.9 [102.1–115.0]) and%TWL was 35.2±6.6 (37.8 [33.7–38.4]), 1 year after revision (Figure 16).
All individuals improved their comorbidities, and reduced drugs need, 1 year after revision, summarized in Table 3. Surgical details are available in Video 1 (link).
Discussion
Although sleeve gastrectomy (SG) is the most commonly performed bariatric procedure worldwide [4,5], obesity recurrence and gastroesophageal reflux disease (GERD) remain major concerns postoperatively [38,39]. These complications may limit its indication and often require surgical revision. In this series, all patients met the updated Lyon consensus criteria for GERD [29] and exhibited recidivism of weight gain after primary SG.
Multiple factors contribute to GERD onset or its exacerbation following SG [40]. The marked reduction in gastric volume from longitudinal gastrectomy decreases gastric compliance and elevates intraluminal pressure [41,42]. Additionally, inadvertent injury to the crura and sling fibers of the lower esophageal sphincter may impair the region’s anti-reflux barrier [43,44]. The increased incidence of HH post-SG is well documented and may further drive GERD pathophysiology [10]. In this cohort, HH was present in 90% of patients, potentially contributing to de novo GERD.
These findings underscore the importance of actively assessing for sleeve pouch proximal migration and repairing HH when identified. Furthermore, abdominal fixation of the gastric pouch may help prevent HH formation, gastric rotation, or tortuosity – mechanisms implicated in GERD development [40,45–47].
Gastric dilation typically occurs 2–3 years after SG and, depending on its volume, may contribute to GERD development and recurrent weight gain [25]. A sleeve pouch volume >250 mL within the first 3 years after SG has been strongly linked to GERD and obesity recurrence [48]. This threshold was adopted in the present study, where 80% of patients demonstrated varying degrees of gastric chamber dilation on preoperative radiological assessment. These cases required re-sleeve gastrectomy as part of revisional surgery.
A large percentage of patients with prior SG and pathological GERD are asymptomatic [25]. In this cohort, 90% of individuals reported symptoms during the preoperative phase of revisional surgery, as assessed by a validated GERD questionnaire [35] – a finding that contrasts with the existing literature.
The interval between primary and revisional surgery in this series was longer than typically reported in the literature [49,50], yet did not appear to impact outcomes during the 1-year follow-up.
Although some authors report a 15–25% incidence of de novo GERD following primary RYGB [51,52], conversion to RYGB remains a common recommendation when GERD arises after SG, given its well-established efficacy [53]. However, in cases where GERD after SG is accompanied by obesity recurrence, RYGB may not be the optimal revisional approach due to its limited effectiveness regarding further weight loss [54]. In the clinical context of this study, it is essential to identify the main concern, as other bariatric procedures (eg, OAGB and SADI-S) may offer better obesity and comorbidities control, compared to Roux-en-Y gastric bypass (RYGB), despite their inferiority in GERD mitigation [49,55].
Transit bipartition has emerged as a viable surgical alternative for recurrent weight gain and mild GERD after SG [28]. Nonetheless, its efficacy in patients with severe GERD remains unsupported by consistent evidence. In this case series, the coexistence of obesity and moderate/severe GERD presented a complex challenge for surgical revision. Additionally, patients declined anatomical gastrointestinal exclusions for previously mentioned reasons.
Given this scenario, revision to GBp-FDE was selected, an operation described in the literature [31,32,56]. Anatomically, this technique resembles transit bipartition with some modifications, preserving the safety of antroenterostomies, already well-documented [57–60]. Considering the preliminary report of this conversion, there are no comparative studies with other revisional strategies.
This procedure was recently renamed by the authors as “gastric bipartition with functional duodenum exclusion” (GBp-FDE) to better describe its anatomical similarity with TB (ie, Roux-en-Y antroileostomy over a sleeve pouch) and its functional implications. The preferential flow through the anastomosis, functionally bypassing the duodenum [56], mimics the alimentary route of a long-pouch distal RYGB, which anatomically diverts the duodenum [61–63].
Long-pouch RYGB proved effective in managing gastroesophageal reflux and yielded superior mid-term weight loss compared to short-pouch RYGB [64,65]. The extended gastric pouch in GBp-FDE not only can support sustained weight reduction but also enhance nutritional safety by preserving gastric cellularity. This factor may optimize the gastric phase of digestion and reduce the risk of malabsorption and malnutrition, even when paired with an elongated biliopancreatic limb (BPL) [33,61,66]. Accordingly, in the proposed technique, the biliopancreatic limb was extended to 40% of the total small intestine [56], reaching the ileum and its metabolic and weight loss benefits [67,68], notably enhanced incretin release [33,69]. The additional weight loss also contributes to reduced intra-abdominal pressure, offering further mechanisms for GERD mitigation [70].
The prevailing functional duodenal exclusion observed in GBp-FDE is a novel concept in metabolic surgery, likely resulting from the proximity of a wide antroileostomy to a spastic pylorus [56]. The observed partial or complete pyloric spasm may stem from injury to the anterior vagus nerve branches – intramural within the antrum – during wedge resection of the anterior wall in this region, as part of anastomosis [71]. This hypothesis is an assumption that needs further investigation to be confirmed.
Moreover, disruption of the interstitial cells of Cajal (ICC) network during antral wedge resection can further contribute to pyloric dysmotility. A reduction in ICC density within the antrum has been associated with impaired pyloric function and spasm [72–77]. Further investigation is necessary to confirm this hypothesis. Although pyloric spasm has been observed in GBp-FDE, either complete or partial, it is not possible to infer its role in functional duodenum exclusion, considering the wide antrum-ileal anastomosis near the pylorus could solely promote it. Further investigation is demanded to clarify this.
Functionally, GBp-FDE differs from TB due to the anatomical configuration of the latter, which allows near-equal food flow through both the pylorus and gastroileostomy [78]. This enables the use of a shorter, fixed common channel while maintaining nutritional safety. However, preservation of the pylorus in food pathway in TB, combined with the ileal brake mechanism typical of ileal procedures [79], can impede effective gastric decompression in severe GERD cases, which is the scenario in this series.
In contrast, SADI-S and DS preserve the pyloric sphincter as the only path for ingested food. Consequently, intragastric pressure within the sleeve pouch remains elevated and possibly aggravated by the ileal break effect [80], potentially limiting GERD resolution in more advanced cases, which completely differs from the revision proposed in this case series, which prompts reduced intragastric pressure due to the wide gastrointestinal anastomosis.
Notably, 80% of patients in this series required a re-sleeve procedure due to gastric pouch dilation [25]. A 32-Fr bougie was used and the stapling was performed 2–3 mm lateral to it, followed by staple line invagination. This technique aimed to create a narrow sleeve pouch, that potentially accelerates gastric emptying via the gastroenterostomy, leading to gastric decompression – mechanisms that may contribute to improved GERD control and enhanced metabolic outcomes [81,82]. In this study, complete resolution of erosive esophagitis was achieved in 80% of patients, while all patients had symptoms improvement, reinforcing this hypothesis.
Duodenal exclusion may be a pivotal metabolic mechanism in bariatric surgery [83]. Elevated serum levels of fibroblast growth factor 19 (FGF19) and bile acids, along with partial restoration of postprandial GLP-1 peaks and reductions in GIP and glucagon responses, have been observed following duodenal isolation. This hormonal profile collectively enhances lipid and glycemic regulation [34,84–87]. However, anatomical duodenal exclusion via gastroduodenal partitioning – as seen in RYGB, OAGB, SADI-S, and DS – presents a limitation by obstructing routine endoscopic access to the biliopancreatic papillae [68,88,89]. The potential to achieve functional duodenal isolation, as proposed in this study, could be clinically significant. It preserves standard endoscopic access to the duodenum, as the spastic pylorus seems to yield to the forward pressure of the endoscope, successfully achieved in all patients in this series. Moreover, the absence of a bypassed stomach in GBp-FDE may be particularly advantageous in populations or ethnic groups at increased risk for gastric cancer [90].
In this study, during 1-year FU, the WL achieved resembled the one from other ileal surgeries when used as a rescue procedure after sleeve gastrectomy in individuals with obesity recidivism [27,28,49,55,91–94]. No distinct WL pattern was observed when minimal contrast flow to the duodenum occurs, suggesting the importance of a very preferential flow to the ileum as the goal to be reached in this operation. Again, the role of pyloric spasm in this physiology is not established, and the wide gastrointestinal anastomosis itself could “steal” all the alimentary flow.
Complete comorbidities control was achieved in 80% and partial in 20%, in this series. These results are consistent with the expected outcomes of other ileal metabolic surgeries [33,61,69] and mirrored the revisions of SG when converted to potent ileal operations [27,28,49,91,92].
Marginal ulceration was a concern in GBp-FDE due to its elevated incidence in gastrointestinal anastomoses involving large gastric reservoirs [95]. However, procedures utilizing a long, narrow gastric pouch (eg, OAGB [96], long-pouch-RYGB [61], and TB [60,97) have negligible rates of marginal ulcers. The usual extensive longitudinal gastrectomy in these operations, which removes or isolates most of gastrin- and acid-producing cells [98], may account for the low incidence of marginal ulceration and justify its absence in this series.
This case series is constrained by its retrospective design, limited sample size, and absence of a control group, reducing both clinical and statistical robustness. Furthermore, the lack of esophageal manometry hindered assessment of esophageal function, limiting insight into GERD pathophysiology following primary sleeve gastrectomy (SG) and its effect on motility. The absence of manometric data also precluded evaluation of the revisional procedure’s impact on esophageal motility and lower esophageal sphincter competence. Although postoperative grade A esophagitis has been considered as pathological reflux in this series (sensitivity analyses considered suspected cases as positive), lack of esophageal pHmetry compromised the accurate detection of pathological reflux, particularly in patients with this grade of erosive esophagitis or no esophagitis, after revisional surgery.
The observation of duodenal functional exclusion was inferred from indirect findings obtained via endoscopic and contrast radiological evaluations. Direct pyloric pressure measurements were not performed, representing a limitation in the assessment of pyloric function, warranting further investigations to confirm its occurrence and to clearly elucidate its underlying mechanisms and influence on duodenal diversion. Also, the role of pylorus spasm in functional duodenum exclusion cannot be inferred, as the exclusion may be provided solely by a huge gastric flow diversion towards the ileum, promoted by the wide gastroileal anastomosis.
The 1-year follow-up period is limited, hindering strong conclusions and compromising the nutritional safety of the proposed surgical revision; thus, the results of this case series should be regarded as preliminary. Validation through larger, long-term controlled studies, incorporating comprehensive gastroesophageal physiological assessment, is recommended.
Conclusions
The proposed GBp-FDE, as a revisional approach to SG in patients with de novo GERD and recurrent obesity, aims to decompress the SG pouch via wide gastroileostomy, leading to GERD control; to redirect most of the gastric flow to the ileum, enhancing weight loss and metabolic outcome; and to promote duodenal exclusion without anatomical partitioning, preserving thorough gastrointestinal endoscopic access and increasing metabolic benefits. Controlled studies are necessary to validate these findings.
Figures
Figure 1. (Case 3) Preoperative seriography showing dilated sleeve pouch.
Figure 2. (Case 5) Re-sleeve starting 2 cm proximal to the pylorus.
Figure 4. (Case 5) Spastic pylorus with a forceps passing through, reaching the duodenum.
Figure 3. (Case 5) Delineation of wedge resection area. (A) The red line depicts the pylorus; (B) Wedge resection procedure; (C) Wedge resection completed.
Figure 5. (Case 5) Manual Roux-en-Y antroileostomy. (A) Gastroileostomy – posterior layer; (B) Gastroileostomy – anterior layer; (C) Gastroileostomy completed.
Figure 6. (Case 5) Handsewn end-side entero-enterostomy. (A) End-side Ileo-ileostomy posterior layer; (B) End-side Ileo-ileostomy completed.
Figure 7. Schematic overview of surgery. (A) Schematic diagram of Re-sleeve steps; (B) Schematic diagram of final aspect of GBp-FDE.
Figure 8. Graphical demonstration of symptoms evolution according to validated GERD questionnaire.
Figure 9. Graphical demonstration of erosive esophagitis evolution according to Los Angeles Classification (Grade A was considered as pathological in postoperative period).
Figure 10. Graphical demonstration of hiatal hernia evolution from revision until 1 year follow-up.
Figure 11. (Case 9) One-year postoperative endoscopic findings. (A) Normal gastroesophageal junction; (B) Straight and narrow sleeve pouch; (C) Wide gastro-ileostomy; (D) Spastic pylorus (arrow); (E) Efferent ileum; (F) Duodenum – major papillae (arrow)
Figure 12. (Case 4) Seriography study images. (A) Absence of hiatal hernia and straight sleeve pouch; (B) Contrast flowing through the anastomosis/ileum and no contrast in duodenum. (C) Contrast filling efferent ileal limb from the gastroileostomy
Figure 13. Graphic showing prevalent unidirectional flow to the ileum and no split contrast between ileum and duodenum.
Figure 14. Graphic showing mean weight evolution since the primary surgery until 1 year after revision.
Figure 15. Graphic showing mean BMI evolution since the primary surgery until 1 year after revision.
Figure 16. Graphic showing 1-year postoperative percentage or EWL and TWL. References
1. Blüher M, Obesity: Global epidemiology and pathogenesis: Nat Rev Endocrinol, 2019; 15(5); 288-98
2. Guerreiro V, Neves JS, Salazar D, Long-term weight loss and metabolic syndrome remission after bariatric surgery: The effect of sex, age, metabolic parameters and surgical technique – a 4-year follow-up study: Obes Facts, 2019; 12(6); 639-52
3. Aarts EO, Mahawar K, From the knife to the endoscope – a history of bariatric surgery: Curr Obes Rep, 2020; 9(3); 348-63
4. Welbourn R, Hollyman M, Kinsman R, Bariatric surgery worldwide: Baseline demographic description and one-year outcomes from the Fourth IFSO Global Registry Report 2018: Obes Surg, 2019; 29(3); 782-95
5. English WJ, DeMaria EJ, Hutter MM, American Society for Metabolic and Bariatric Surgery 2018 estimate of metabolic and bariatric procedures performed in the United States: Surg Obes Relat Dis, 2020; 16(4); 457-63
6. Quero G, Fiorillo C, Dallemagne B, The causes of gastroesophageal reflux after laparoscopic sleeve gastrectomy: Quantitative assessment of the structure and function of the esophagogastric junction by magnetic resonance imaging and high-resolution manometry: Obes Surg, 2020; 30(6); 2108-17
7. Rebecchi F, Allaix M, Giaccone C, Gastroesophageal reflux disease and laparoscopic sleeve gastrectomy: A physiopathologic evaluation: Ann Surg, 2014; 260; 909-15
8. Braghetto I, Korn O, Late esophagogastric anatomic and functional changes after sleeve gastrectomy and its clinical consequences with regards to gastroesophageal reflux disease: Dis Esophagus, 2019; 32(6); doz020
9. Ferrer JV, Acosta A, García-Alementa EM, High rate of de novo esophagitis 5 years after sleeve gastrectomy: A prospective multicenter study in Spain: Surg Obes Relat Dis, 2022; 18(4); 546-54
10. Saba J, Bravo M, Rivas E, Incidence of de novo hiatal hernia after laparoscopic sleeve gastrectomy: Obes Surg, 2020; 30(10); 3730-34
11. Kheirvari M, Dadkhah Nikroo N, Jaafarinejad H, The advantages and disadvantages of sleeve gastrectomy; clinical laboratory to bedside review: Heliyon, 2020; 6(2); e03496
12. Himpens J, Dobbeleir J, Peeters G, Long-term results of laparoscopic sleeve gastrectomy for obesity: Ann Surg, 2010; 252(2); 319-24
13. Salminen P, Grönroos S, Helmiö M, Effect of laparoscopic sleeve gastrectomy vs Roux-en-Y gastric bypass on weight loss, comorbidities, and reflux at 10 years in adult patients with obesity: JAMA Surg, 2022; 157(8); 656
14. Campos GM, Khoraki J, Browning MG, Changes in utilization of bariatric surgery in the United States from 1993 to 2016: Ann Surg, 2020; 271(2); 201-9
15. Currie AC, Askari A, Fangueiro A, Mahawar K, Network meta-analysis of metabolic surgery procedures for the treatment of obesity and diabetes: Obes Surg, 2021; 31(10); 4528-41
16. Adil MT, Al-taan O, Rashid F, A systematic review and meta-analysis of the effect of Roux-en-Y gastric bypass on Barrett’s esophagus: Obes Surg, 2019; 29(11); 3712-21
17. Braghetto I, Korn O, Burgos A, Figueroa M, When should be converted laparoscopic sleeve gastrectomy to laparoscopic Roux-en-y gastric bypass due to gastroesophageal reflux?: Arq Bras Cir Dig, 2020; 33(4); e1553
18. Gu L, Fu R, Chen P, In Terms of nutrition, the most suitable method for bariatric surgery: Laparoscopic sleeve gastrectomy or Roux-en-Y gastric bypass? A systematic review and meta-analysis: Obes Surg, 2020; 30(5); 2003-14
19. Hassan Zadeh M, Mohammadi Farsani G, Zamaninour N, Selenium status after Roux-en-Y gastric bypass: Interventions and recommendations: Obes Surg, 2019; 29(11); 3743-48
20. Cheng Q, Hort A, Yoon P, Loi K, Review of the endoscopic, surgical and radiological techniques of treating choledocholithiasis in bariatric Roux-en-Y gastric bypass patients and proposed management algorithm: Obes Surg, 2021; 31(11); 4993-5004
21. Kumar P, Yau H-CV, Trivedi A, Global variations in practices concerning Roux-en-Y gastric bypass – an online survey of 651 bariatric and metabolic surgeons with cumulative experience of 158,335 procedures: Obes Surg, 2020; 30(11); 4339-51
22. Chemaly R, Diab S, Khazen G, Al-Hajj G, Gastroesophageal cancer after gastric bypass surgeries: a systematic review and meta-analysis: Obes Surg, 2022; 32(4); 1300-11
23. Ravacci GR, Ishida R, Torrinhas RS, Potential premalignant status of gastric portion excluded after Roux en-Y gastric bypass in obese women: A pilot study: Sci Rep, 2019; 9(1); 5582
24. Csendes A, Burdiles P, Papapietro K, Results of gastric bypass plus resection of the distal excluded gastric segment in patients with morbid obesity: J Gastrointest Surg, 2005; 9(1); 121-31
25. Sancho Moya C, Bruna Esteban M, Sempere García-Argüelles J, The impact of sleeve gastrectomy on gastroesophageal reflux disease in patients with morbid obesity: Obes Surg, 2022; 32(3); 615-24
26. Thaher O, Daza JFM, Croner RS, Stroh C, Outcome of revisional bariatric surgery after failed sleeve gastrectomy: A German multicenter study: Obes Surg, 2023; 33(11); 3362-72
27. Gallucci P, Marincola G, Pennestrì F, One-Anastomosis Gastric Bypass (OABG) vs. Single Anastomosis Duodeno-Ileal Bypass (SADI) as revisional procedure following sleeve gastrectomy: Results of a multicenter study: Langenbecks Arch Surg, 2024; 409(1); 128
28. Reiser M, Christogianni V, Nehls F, Short-term results of transit bipartition to promote weight loss after laparoscopic sleeve gastrectomy: Annals of Surgery Open, 2021; 2(4); e102
29. Gyawali CP, Yadlapati R, Fass R, Updates to the modern diagnosis of GERD: Lyon consensus 2.0: Gut, 2024; 73(2); 361-71
30. Lundell LR, Dent J, Bennett JR, Endoscopic assessment of oesophagitis: Clinical and functional correlates and further validation of the Los Angeles classification: Gut, 1999; 45(2); 172-80
31. Dib VRM, Madalosso CAS, Domene CE, Sleeve gastrectomy associated with antral lesion resection and Roux-en-Y antrojejunal reconstruction: Surg Sci, 2023; 14(05); 360-76
32. Dib VRM, Madalosso CAS, de Melo PRE, Functional Roux-en-Y gastric bypass (F-RYGB), with preservation of duodenal access: Report of two revisional cases of sleeve gastrectomy: Surg Sci, 2024; 15(03); 135-58
33. Slagter N, van der Laan L, de Heide LJM, Effect of tailoring biliopancreatic limb length based on total small bowel length versus standard limb length in one anastomosis gastric bypass: 1-year outcomes of the TAILOR randomized clinical superiority trial: Br J Surg, 2024; 111(9); znae219
34. de Oliveira GHP, de Moura DTH, Funari MP, Metabolic effects of endoscopic duodenal mucosal resurfacing: A systematic review and meta-analysis: Obes Surg, 2021; 31(3); 1304-12
35. Fornari F, Gruber AC, Lopes A, de B, Cecchetti D, deBarros SGSSymptom questionnaire for gastroesophageal reflux disease: Arq Gastroenterol, 2004; 41(4); 263-67 [in Portuguese]
36. Velanovich V, Vallance SR, Gusz JR, Quality of life scale for gastroesophageal reflux disease: J Am Coll Surg, 1996; 183(3); 217-24
37. Pomerri F, Foletto M, Allegro G, Bernante P, Laparoscopic sleeve gastrectomy – radiological assessment of fundus size and sleeve voiding: Obes Surg, 2011; 21(7); 858-63
38. Guan B, Chong TH, Peng J, Mid-long-term revisional surgery after sleeve gastrectomy: A systematic review and meta-analysis: Obes Surg, 2019; 29(6); 1965-75
39. Elkassem S, Gastroesophageal reflux disease, esophagitis, and Barrett’s Esophagus 3 to 4 years post sleeve gastrectomy: Obes Surg, 2021; 31(12); 5148-55
40. Felinska E, Billeter A, Nickel F, Do we understand the pathophysiology of GERD after sleeve gastrectomy?: Ann N Y Acad Sci, 2020; 1482(1); 26-35
41. Yehoshua RT, Eidelman LA, Stein M, Laparoscopic sleeve gastrectomy – volume and pressure assessment: Obes Surg, 2008; 18(9); 1083
42. Mion F, Tolone S, Garros A, High-resolution impedance manometry after sleeve gastrectomy: Increased intragastric pressure and reflux are frequent events: Obes Surg, 2016; 26(10); 2449-56
43. Zifan A, Kumar D, Cheng LK, Mittal RK, Three-dimensional myoarchitecture of the lower esophageal sphincter and esophageal hiatus using optical sectioning microscopy: Sci Rep, 2017; 7(1); 13188
44. Braghetto I, Csendes A, Korn O, Gastroesophageal reflux disease after sleeve gastrectomy: Surg Laparosc Endosc Percutan Tech, 2010; 20(3); 148-53
45. Filho AMM, Silva LB, Godoy ES, Omentopexy in sleeve gastrectomy reduces early gastroesophageal reflux symptoms: Surg Laparosc Endosc Percutan Tech, 2019; 29(3); 155-61
46. Dalkılıç MS, Gençtürk M, Yılmaz M, The critical role of fixation techniques in preventing sleeve migration: Obes Surg, 2024; 34(8); 3129-30
47. deGodoy EP, Coelho D, Gastric sleeve fixation strategy in laparoscopic vertical gastrectomy: Arq Bras Cir Dig, 2013; 26(Suppl 1); 79-82
48. Deguines J-B, Verhaeghe P, Yzet T, Is the residual gastric volume after laparoscopic sleeve gastrectomy an objective criterion for adapting the treatment strategy after failure?: Surg Obes Relat Dis, 2013; 9(5); 660-66
49. Zaveri H, Surve A, Cottam D, A Multi-institutional study on the mid-term outcomes of single anastomosis duodeno-ileal bypass as a surgical revision option after sleeve gastrectomy: Obes Surg, 2019; 29(10); 3165-73
50. de la Cruz M, Büsing M, Dukovska R, Short- to medium-term results of single-anastomosis duodeno-ileal bypass compared with one-anastomosis gastric bypass for weight recidivism after laparoscopic sleeve gastrectomy: Surg Obes Relat Dis, 2020; 16(8); 1060-66
51. Rebecchi F, Allaix ME, Ugliono E, Increased esophageal exposure to weakly acidic reflux 5 years after laparoscopic Roux-en-Y gastric bypass: Ann Surg, 2016; 264(5); 871-77
52. Suter M, Gastroesophageal reflux disease, obesity, and Roux-en-Y gastric bypass: Complex relationship – A narrative review: Obes Surg, 2020; 30(8); 3178-87
53. Serra FE, Cohen RV, Gastroesophageal reflux disease after sleeve gastrectomy: Dig Med Res, 2024; 7; 5
54. Parmar CD, Mahawar KK, Boyle M, Conversion of sleeve gastrectomy to Roux-en-Y gastric bypass is effective for gastro-oesophageal reflux disease but not for further weight loss: Obes Surg, 2017; 27(7); 1651-58
55. Kermansaravi M, Karami R, Valizadeh R, Five-year outcomes of one anastomosis gastric bypass as conversional surgery following sleeve gastrectomy for weight loss failure: Sci Rep, 2022; 12(1); 10304
56. Dib VRM, de Melo PRRE, Madalosso CAS, Functional Roux-En-Y gastric bypass with diverted sleeve gastrectomy (FRYGB-DSG) as a proposal for obesity and GERD after fundoplication: New concept: Gastroenterology, Hepatology & Digestive Disorders, 2025; 8(2); 1093
57. Pazouki A, Kermansaravi M, Single anastomosis sleeve-jejunal bypass: A new method of bariatric/metabolic surgery: Obes Surg, 2019; 29(11); 3769-70
58. Sewefy AM, Saleh A, The outcomes of single anastomosis sleeve jejunal bypass as a treatment for morbid obesity (two-year follow-up): Surg Endosc, 2021; 35(10); 5698-704
59. Santoro S, Castro LC, Velhote MCP, Sleeve gastrectomy with transit bipartition: A potent intervention for metabolic syndrome and obesity: Ann Surg, 2012; 256(1); 104-10
60. Muzaffer A, Taskin HE, Sleeve gastrectomy with transit bipartition in a series of 883 patients with mild obesity: Early effectiveness and safety outcomes: Surg Endosc, 2022; 36(4); 2631-42
61. Ribeiro R, Pouwels S, Parmar C, Outcomes of long pouch gastric bypass (LPGB): 4-year experience in primary and revision cases: Obes Surg, 2019; 29(11); 3665-71
62. Schauer PR, Ikramuddin S, Hamad G, Laparoscopic gastric bypass surgery: Current technique: Journal of Laparoendoscopic & Advanced Surgical Techniques, 2003; 13(4); 229-39
63. Khwaja HA, Bonanomi G, Bariatric surgery: Techniques, outcomes and complications: Curr Anaesth Crit Care, 2010; 21(1); 31-38
64. Hu S, Wang C, Dong Z, Yang W, Long narrow pouch Roux-en-Y gastric bypass (LN-RYGB) for recurrent weight gain after sleeve gastrectomy: Obes Surg, 2024; 34(9); 3509-12
65. Boerboom A, Cooiman M, Aarts E, An extended pouch in a Roux-En-Y gastric bypass reduces weight regain: 3-year results of a randomized controlled trial: Obes Surg, 2020; 30(1); 3-10
66. Komaei I, Sarra F, Lazzara C, One anastomosis gastric bypass–mini gastric bypass with tailored biliopancreatic limb length formula relative to small bowel length: Preliminary results: Obes Surg, 2019; 29(9); 3062-70
67. Zerrweck C, Herrera A, Sepúlveda EM, Long versus short biliopancreatic limb in Roux-en-Y gastric bypass: Short-term results of a randomized clinical trial: Surg Obes Relat Dis, 2021; 17(8); 1425-30
68. Connell M, Sun WYL, Mocanu V, Management of choledocholithiasis after Roux-en-Y gastric bypass: A systematic review and pooled proportion meta-analysis: Surg Endosc, 2022; 36(9); 6868-77
69. Zorrilla-Nunez LF, Campbell A, Giambartolomei G, The importance of the biliopancreatic limb length in gastric bypass: A systematic review: Surg Obes Relat Dis, 2019; 15(1); 43-49
70. Seeras K, Campbell J, Pryor AD, Considerations in the management of gastroesophageal reflux disease in the morbidly obese: Annals of Esophagus, 2022; 5; 41
71. Zhu TL, Tan JS, Zhang ZX, Vagus nerve anatomy at the lower esophagus and stomach. A study of 100 cadavers: Chin Med J (Engl), 1980; 93(9); 629-36
72. Na HK, Li AA, Gottfried-Blackmore A, Pyloric dysfunction: A review of the mechanisms, diagnosis, and treatment: Gut Liver, 2025; 19(3); 327-45
73. Mostafa RM, Moustafa YM, Hamdy H, Interstitial cells of Cajal, the Maestro in health and disease: World J Gastroenterol, 2010; 16(26); 3239
74. López-Pingarrón L, Almeida H, Soria-Aznar M, Interstitial cells of Cajal and enteric nervous system in gastrointestinal and neurological pathology, relation to oxidative stress: Curr Issues Mol Biol, 2023; 45(4); 3552-72
75. Ward SM, Sanders KM, Involvement of intramuscular interstitial cells of Cajal in neuroeffector transmission in the gastrointestinal tract: J Physiol, 2006; 576(3); 675-82
76. Al-Shboul O, The importance of interstitial cells of Cajal in the gastrointestinal tract: Saudi J Gastroenterol, 2013; 19(1); 3-15
77. Vanderwinden J, Liu H, De Laet M, Vanderhaeghen J, Study of the interstitial cells of Cajal in infantile hypertrophic pyloric stenosis: Gastroenterology, 1996; 111(2); 279-87
78. Bhandari M, Kosta S, Khurana M, Emerging procedures in bariatric metabolic surgery: Surg Clin North Am, 2021; 101(2); 335-53
79. Van Citters GW, Lin HC, The ileal brake: A fifteen-year progress report: Curr Gastroenterol Rep, 1999; 1(5); 404-9
80. Brand B, Jatana S, Morris-Janzen D, Gastroesophageal reflux disease after biliopancreatic diversion-duodenal switch: a systematic review and meta-analysis: Surg Endosc, 2025; 39(7); 4533-44
81. Kelly KA, Gastric emptying of liquids and solids: Roles of proximal and distal stomach: Am J Physiol Gastrointest Liver Physiol, 1980; 239(2); G71-76
82. Chambers AP, Smith EP, Begg DP, Regulation of gastric emptying rate and its role in nutrient-induced GLP-1 secretion in rats after vertical sleeve gastrectomy: Am J Physiol Endocrinol Metab, 2014; 306(4); E424-32
83. De Paula AL, Stival AR, Macedo A: Surg Obes Relat Dis, 2010; 6(3); 296-304
84. de Jonge C, Rensen SS, Verdam FJ, Impact of duodenal-jejunal exclusion on satiety hormones: Obes Surg, 2016; 26(3); 672-78
85. Lee W-J, Almulaifi AM, Tsou J-J, Duodenal–jejunal bypass with sleeve gastrectomy versus the sleeve gastrectomy procedure alone: the role of duodenal exclusion: Surg Obes Relat Dis, 2015; 11(4); 765-70
86. Hoyt JA, Cozzi E, D’Alessio DA, A look at duodenal mucosal resurfacing: Rationale for targeting the duodenum in type 2 diabetes: Diabetes Obes Metab, 2024; 26(6); 2017-28
87. Kaválková P, Mráz M, Trachta P, Endocrine effects of duodenal–jejunal exclusion in obese patients with type 2 diabetes mellitus: J Endocrinol, 2016; 231(1); 11-22
88. Gutierrez JM, Lederer H, Krook JC, Surgical gastrostomy for pancreatobiliary and duodenal access following Roux en Y gastric bypass: J Gastrointest Surg, 2009; 13(12); 2170-75
89. Marchesini JCD, Noda RW, Haida VM, Transenteric ERCP for treatment of choledocholithiasis after duodenal switch: Surg Laparosc Endosc Percutan Tech, 2017; 27(3); e28-30
90. Braghetto I, Martinez G, Korn O, Laparoscopic subtotal gastrectomy in morbid obese patients: A valid option to laparoscopic gastric bypass in particular circumstances (prospective study): Surg Today, 2018; 48(5); 558-65
91. Pizza F, D’Antonio D, Carbonell Asíns JA, One anastomosis gastric bypass after sleeve gastrectomy failure: Des a single procedure fit for all?: Obes Surg, 2021; 31(4); 1722-32
92. Sánchez-Pernaute A, Rubio MÁ, Conde M, Single-anastomosis duodenoileal bypass as a second step after sleeve gastrectomy: Surg Obes Relat Dis, 2015; 11(2); 351-55
93. Zaveri H, Surve A, Cottam D, A multi-institutional study on the mid-term outcomes of single anastomosis duodeno-ileal bypass as a surgical revision option after sleeve gastrectomy: Obes Surg, 2019; 29(10); 3165-73
94. Reiser M, Christogianni V, Nehls F, Short-term results of transit bipartition to promote weight loss after laparoscopic sleeve gastrectomy: Ann Surg Open, 2021; 2(4); e102
95. Chung WC, Jeon EJ, Lee K-M, Incidence and clinical features of endoscopic ulcers developing after gastrectomy: World J Gastroenterol, 2012; 18(25); 3260-66
96. Lee S, Supparamaniam S, Varghese C, Mahawar K, Marginal ulcers following one-anastomosis gastric bypass: A systematic review and meta-analysis: Obes Surg, 2023; 33(9); 2884-97
97. Zhao S, Li R, Zhou J, sun q, wang w, wang d, Sleeve gastrectomy with transit bipartition: a review of the literature: Expert Rev Gastroenterol Hepatol, 2023; 17(5); 451-59
98. Mahawar KK, Jennings N, Balupuri S, Small PK, Sleeve gastrectomy and gastro-oesophageal reflux disease: A complex relationship: Obes Surg, 2013; 23(7); 987-91
Figures
Figure 1. (Case 3) Preoperative seriography showing dilated sleeve pouch.
Figure 2. (Case 5) Re-sleeve starting 2 cm proximal to the pylorus.
Figure 4. (Case 5) Spastic pylorus with a forceps passing through, reaching the duodenum.
Figure 3. (Case 5) Delineation of wedge resection area. (A) The red line depicts the pylorus; (B) Wedge resection procedure; (C) Wedge resection completed.
Figure 5. (Case 5) Manual Roux-en-Y antroileostomy. (A) Gastroileostomy – posterior layer; (B) Gastroileostomy – anterior layer; (C) Gastroileostomy completed.
Figure 6. (Case 5) Handsewn end-side entero-enterostomy. (A) End-side Ileo-ileostomy posterior layer; (B) End-side Ileo-ileostomy completed.
Figure 7. Schematic overview of surgery. (A) Schematic diagram of Re-sleeve steps; (B) Schematic diagram of final aspect of GBp-FDE.
Figure 8. Graphical demonstration of symptoms evolution according to validated GERD questionnaire.
Figure 9. Graphical demonstration of erosive esophagitis evolution according to Los Angeles Classification (Grade A was considered as pathological in postoperative period).
Figure 10. Graphical demonstration of hiatal hernia evolution from revision until 1 year follow-up.
Figure 11. (Case 9) One-year postoperative endoscopic findings. (A) Normal gastroesophageal junction; (B) Straight and narrow sleeve pouch; (C) Wide gastro-ileostomy; (D) Spastic pylorus (arrow); (E) Efferent ileum; (F) Duodenum – major papillae (arrow)
Figure 12. (Case 4) Seriography study images. (A) Absence of hiatal hernia and straight sleeve pouch; (B) Contrast flowing through the anastomosis/ileum and no contrast in duodenum. (C) Contrast filling efferent ileal limb from the gastroileostomy
Figure 13. Graphic showing prevalent unidirectional flow to the ileum and no split contrast between ileum and duodenum.
Figure 14. Graphic showing mean weight evolution since the primary surgery until 1 year after revision.
Figure 15. Graphic showing mean BMI evolution since the primary surgery until 1 year after revision.
Figure 16. Graphic showing 1-year postoperative percentage or EWL and TWL.Tables
Table 1. Gastroesophageal reflux data sheet.
Table 2. Individual endoscopic aspects of patients before revision and 1 year after.
Table 3. Preoperative and postoperative comorbidities and medications.
Table 1. Gastroesophageal reflux data sheet.
Table 2. Individual endoscopic aspects of patients before revision and 1 year after.
Table 3. Preoperative and postoperative comorbidities and medications. In Press
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.949976
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.950290
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.950607
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.950985
Most Viewed Current Articles
07 Dec 2021 : Case report
17,691,734
DOI :10.12659/AJCR.934347
Am J Case Rep 2021; 22:e934347
06 Dec 2021 : Case report
164,491
DOI :10.12659/AJCR.934406
Am J Case Rep 2021; 22:e934406
21 Jun 2024 : Case report
113,090
DOI :10.12659/AJCR.944371
Am J Case Rep 2024; 25:e944371
07 Mar 2024 : Case report
59,175
DOI :10.12659/AJCR.943133
Am J Case Rep 2024; 25:e943133






