Abstract
This study aimed to make a meta-analysis regarding mid-long-term outcomes (≥ 3-year follow-up) after sleeve gastrectomy (SG), focusing on incidence, reasons, and results of revisional surgery. PubMed, EMBASE, and CENTRAL were searched and 32 studies were included. The overall revision rate was 10.4%, but for patients with ≥ 10-year follow-up, the rate was 22.6%. European studies had a higher revision rate (14.4%) than other studies. The most common reason for revision was failure in weight loss, and the most frequent revisional procedure was gastric bypass. Revisional surgery was favorable for weight reduction and comorbidity resolution. In conclusion, revision rate is not rare after SG, especially when looking at long-term follow-up. Bariatric surgeons and patients need to fully understand and deal with the need for revision after SG.
Similar content being viewed by others
Avoid common mistakes on your manuscript.
Introduction
In light of the ever-increasing prevalence of obesity in the world, an increase of bariatric surgery in clinical practice has been seen [1]. Bariatric surgery brings about durable weight reduction as well as significant improvement of obesity-related comorbidities [2]. Sleeve gastrectomy (SG) was originally regarded as a first-step bariatric procedure for severely obese patients. However, with the advantage of relative safety and effective results in the short term, SG became a stand-alone bariatric procedure subsequently [3]. According to the recent data, SG has become the most common bariatric surgery around the world, reaching 45.9%, followed by Roux-en-Y gastric bypass (RYGB) (39.6%) [1].
In spite of postoperative short-term satisfying outcomes, revisional surgery is still unavoidable for some SG patients due to weight loss failure and/or complication during the mid-long-term follow-up period after this procedure [4]. Current literature data regarding the incidence of revisional surgery vary greatly between studies. Some data showed that the rate of revision after SG could be up to 30% [5], while others reported a relatively low percentage of the need for revisional surgery [6, 7]. Therefore, the incidence of revision after SG remains to be answered.
Up to now, there have been some systematic review evaluating the treatment effect of SG, but little attention was paid on its revision [8, 9]. Although a previous meta-analysis had pooled the overall revision rate after SG based on studies with > 7-year follow-up, it had only included few studies, and not conducted subgroup analysis based on follow-up period and region, which may affect the revision rate [10]. In addition, the revisional reasons, revisional procedures, and surgical outcomes have not been previously analyzed using a systematic review and meta-analysis yet. The aim of the current study was to apply a systematic review and meta-analysis of mid-long-term outcomes (≥ 3-year follow-up) after SG, focusing on the incidence, reasons, and treatment results of revisional surgery.
Methods
We conducted a meta-analysis according to the preferred reporting items for systematic reviews and meta-analyses (PRISMA), combined with the recommendations from the Cochrane Collaboration and Meta-analysis of Observational Studies in Epidemiology (MOOSE) [11, 12]. Given that this is an analysis of published articles, with no real concern to individual patients, ethical approval and informed consent were not required.
Literature Search
PubMed, EMBASE, and the Cochrane Central Register of Controlled Trails (CENTRAL) were searched from inception to January 2019. Medical subject headings along with free terms were adopted together for literature search, including (sleeve gastrectomy OR SG OR LSG) AND (long-term OR long term OR mid-term OR midterm OR 3 years OR 4 years OR 5 years OR 6 years OR 7 years OR 8 years OR 9 years OR 10 years) AND (revision OR revisional OR converted OR conversion OR reoperation OR failed). Additionally, we also screened the references of identified articles and reviews for other potential articles.
Inclusion and Exclusion Criteria
Randomized controlled trials (RCT) and observational clinical studies were included if they met the following criteria: (1) providing mid-long-term follow-up (≥ 3 years) outcomes after SG, (2) reporting the incidence of revisional surgery after SG or other information sufficient to calculate the incidence. Non-English studies, reviews, conference abstract, case reports, comments, letters, animal studies, and studies with the number of SG patients less than 20 or reporting zero value of incidence were excluded. In addition, the patients undergoing SG as part of planned two-stage bariatric surgeries were also excluded. For studies enrolled overlapping populations, we only included the study with the most comprehensive information and excluded the other.
Two investigators independently performed the stages of study selection, data extraction, and quality assessment. Regarding disagreements, it would be discussed with a third investigator in order to get the consensus.
Data Extraction and Quality Assessment
After deleting the duplicated articles, titles and abstracts of the remaining articles were screened to examine whether they matched the inclusion criteria or not. Full-text was further reviewed when needed.
Two reviewers independently extracted the following data from each of the included studies using a pre-specified data extraction form: the first author’ name, location, publication year, patients’ characteristics, follow-up duration, and outcomes of interest. The primary outcome of interest was the incidence of revisional surgery after SG. The secondary outcomes included the reasons for revision and the follow-up results after revision. With regard to missing data, the study authors would be contacted for complete information by emails if possible.
Quality assessment of the included trials was conducted based on a quality rating system containing the following 5-point scales: (1) the clarity of definition of revisional surgery; (2) the representativeness of the patients’ sample; (3) the credibility of diagnostic criteria of revisional surgery; (4) the credibility of diagnostic evaluation; (5) the completeness of outcomes. The score rated from 1 to 5 with one meaning the best quality and five meaning the worst quality [13, 14].
Statistical Analysis
Stata (version 11.0) was used for calculating the pooled incidence of revisional surgery. The Cochran Q-statistic and I2 statistic were used to measure between-study heterogeneity. Significant heterogeneity was expected when p value < 0.1 and I2 > 50%, indicating that a random effects model would be used to pool estimates. A fixed effects model would be chosen when between-study heterogeneity was not significant. We also carried out subgroup and sensitivity analyses to explore possible sources of heterogeneity in enrolled studies if feasible and necessary. Pre-specified subgroup analyses included region (Europea, Eastern Asia, Middle East, America), publication year (the Year 2015 or earlier, the Year 2016 or later), and follow-up duration (3–5 years, 5–10 years, ≥ 10 years). Regarding sensitivity analyses, the methods of changing the pooling model (random effects model or fixed effects model) and omitting one study each time were performed. The funnel plot, along with the Begg and Egger tests, was conducted for assessing possible publication bias.
Results
Search Process, Study Characteristics, and Quality Assessment
Our initial literature search yielded 1690 potentially relevant articles. After removal of duplicate articles, there were 1355 titles and abstracts left for screening. Afterwards, 123 studies were reviewed in full-text. And finally, 32 publications (3 RCTs, 29 observational studies) were included in qualitative synthesis and meta-analysis, with a total of 6665 patients [7, 15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45]. The process of study selection is displayed in Fig. 1.
Table 1 showed the study characteristics. These studies adopted data from different regions (e.g., Europea, Eastern Asia, Middle East, America). Patients had different reasons for revisional surgery (e.g., failure in weight loss, gastro-esophageal reflux disease (GERD)). The duration of follow-up ranged from 3 years to more than 10 years.
Meta-analysis of Incidence of Revisional Surgery
All of the included trials involving 6665 patients reported the incidence of revisional surgery after SG. Our data revealed that the incidence rate of revision ranged from 2.5 to 33.0%. Because of significant heterogeneity among these studies (p < 0.001, I2 = 86.8%), a random effects model was used to pool results. The results showed that the pooled incidence of revisional surgery was 10.4% (95% confidence interval (95%CI), 8.5–12.4%) (Fig. 2).
In the sensitivity analysis, the stability of pooled incidence of revisional surgery got confirmation by changing the random effects model to a fixed effects model (p = 6.4%, 95%CI 5.8–7.0%). Additionally, through excluding research one by one, it was found that no individual study would remarkably affect the pooled incidence, with a range from 9.7% (95%CI 7.9–11.6%) to 10.8% (95%CI 8.8–12.8%). The Begg (p = 0.001) or Egger (p < 0.001) test showed that there was significant publication bias in the literature. For this reason, we performed a trim and fill analysis and found that after adding ten studies, the pooled data is still statistically significant. Therefore, the pooled estimate for incidence rate of revision is robust.
Subgroup Analyses of the Incidence of Revision
For the purpose of exploring the potential source of heterogeneity, we performed subgroup analyses by different regions, reasons for revisional surgery, and follow-up duration (Table 2). Grouping the studies by regions led to homogeneous result for four studies conducted in Middle East (p = 0.262, I2 = 25.0%), but not for studies conducted in the other three regions. However, the pooled results showed that European studies (p = 14.4%, 95%CI 10.9–17.8%) have a higher rate of revision than Eastern Asian studies (p = 10.5%, 95%CI 2.1–18.9%), American studies (p = 5.9%, 95%CI 1.1–10.7%), and Middle Eastern studies (p = 4.5%, 95%CI 3.6–5.4%). In addition, grouping the studies by publication years and follow-up duration did not resolve the issue of heterogeneity, but a phenomenon was found that the revisional rate would increase along with longer follow-up times, with 7.4% (95%CI 5.5–9.4%) for the studies with 3–5-year follow-up, 13.3% (95%CI 8.7–18.0%) for the studies with 5–10-year follow-up, and up to 22.6% (95%CI 7.2–38.0%) for the studies with ≥ 10-year follow-up.
Reasons and Surgical Procedures for Revisional Surgery
All but four of the included studies provided information about the reasons for revisional surgery after SG; detailed data is shown in Table 3. From the table, one could see that there were various causes for revision, such as failure in weight loss (including insufficient weight loss (IWL) and weight regain (WR)), GERD, intractable diabetes, gastric stricture, and dysphagia. However, these included studies had some difference regarding the definitions of IWL, WR, and GERD. Generally speaking, IWL was defined as the percentage of excess weight loss (%EWL) < 50% and/or the percentage of excess body mass index loss (%EBMIL) < 50%; WR was considered with > 25% EBMIL and/or EWL regain after an initial sufficient weight loss following SG [20, 23, 35]. GERD was defined by symptom complaints, upper endoscopy, and/or validated scores [20, 21, 24]. Overall, the most common reason for revision was failure in weight loss. For the studies with > 5-year follow-up, the revisional rate due to failure in weight loss was up to 11.8% (95%CI 8.0–15.6%, p < 0.001) (Fig. 3). The pooled rate of revision due to GERD was 3.1% (95%CI 1.5–4.7%). With respect to the surgical procedures for revision, different researchers had different choices, such as RYGB, repeated sleeve gastrectomy (R-SG), biliopancreatic diversion (BPD), duodenal switch (DS), and biliopancreatic diversion and duodenal switch (BPD-DS). The most commonly used procedure was RYGB; less common operations included duodenal-jejunal bypass (DJB) and one-anastomosis gastric bypass (OAGB).
Follow-up Outcomes of Revisional Surgery
Some studies described the follow-up outcomes after revisional surgery [21, 24, 29]. A favorable effect of revisional surgery on weight reduction and comorbidity resolution had been shown in these studies, which was supported by the remission or improvement of diabetes, hypertension, dyslipidemia, and GERD postoperatively. Through comparing data between primary and revisional surgery patients (Table 4), we found that there was higher weight reduction in revisional patients in comparison to primary procedure patients. Therefore, for those patients encountering weight loss failure after SG, it is reasonable to conclude that revisional surgery might be beneficial for them.
Discussion
In the literature, an amount of interest has been devoted to the impact of SG on weight reduction, hypertension, type 2 diabetes mellitus, and dyslipidemia [9]. However, revision after SG did not get enough attention yet. It is well known that patients undergoing AGB procedure would have a high rate of revision after surgery. The question arises whether or not will we convert SG at a similar rate as AGB procedure? This is an important question that needs to be determined. The current study aimed to look at the incidence, reasons, and follow-up outcomes of revisional surgery after SG by systematically outlining the current literature, and found that the revisional rate was up to 10.4% (95%CI, 8.5–12.4%) after SG, based on the studies with ≥ 3-year follow-up.
Although the history of SG procedure is shorter than other bariatric procedures, like RYGB, AGB, and BPD-DS, SG is the most popular bariatric procedure worldwide, being used in a great number of countries [3]. We found that the incidence of revision is higher in European studies than Eastern Asian and American studies. Exact reasons for these differences are still unknown; some possible explanations may be racial difference, different health policy, patients’ different attitudes to revisional surgery, and technical differences in index procedure (such as a larger sleeve or failure in gastric fundus resection). Another noteworthy phenomenon is that with the follow-up time extends, the incidence of revision increases too, from 7.4% with 3–5 year follow-up to 22.6% with ≥ 10-year follow-up. If we include the patients who also encounter weight loss failure or GERD, but not receive revisional surgery, the revisional rate would be higher. So a high rate of revision makes some people wonder whether or not SG should be restricted for use in the future, just like AGB [46]. We also need to know that revisional surgery is always more technically challenging.
Now that we know the high rate of revision after SG, we should then analysis its reasons. Only with a well understanding of these reasons can we make a better choice of surgical patients and decrease the revision rate. Based on our pooled data, the main cause for revision is failure in weight loss, followed by GERD. Failure in weight loss after SG is not due to a single cause but due to a combination of factors, including the dilatation of the gastric fundus and/or antrum, too big gastric bougie, and patients’ non-compliance with postoperative dietary changes and behavior modification [47, 48]. Hence, strict technical demand and postoperative multidisciplinary guidance are very necessary for SG patients. As for the relation between GERD and SG procedure, there has not been consistent conclusion in the literature yet [49]. Some authors reported reduced rate of GERD after SG, while others indicated opposite results [50, 51]. In any case, GERD is an intractable complication for SG patients; if the GERD symptom is already very serious before surgery, SG may not be a good surgery for them.
By reason that quite a few patients need revision in the long-term follow-up, it is essential to explore which revisional surgery is the best choice for these patients. Among our included studies, some provided information about surgical outcomes after conversion. RYGB, R-SG, BPD-DS, and DS all had been chosen for revision. For IWL due to gastric dilatation without comorbidities recurrence, R-SG was suggested with good results; while for patients without significant gastric dilatation, converting to BPD-DS can be an option [23]. Regarding WR, RYGB could be chosen but it was reported that the weight reduction was lower in SG patients converted to RYGB than primary RYGB patients [52]. SADI has also been proposed for treating weight regain with or without comorbidities recurrence, but it is still a relatively new procedure and needs further research [23]. And for failed SG owing to GERD, common revisional surgery is RYGB, which would not increase stomach pressure. Felsenreich et al. found that all the patients with reflux symptoms after SG went into remission after revisional RYGB [21]. What is noteworthy is that comparative studies between two revisional bariatric surgeries are quite few; these points are future research directions because the need to convert a certain percentage of SG patients in the mid-long-term follow-up is an important clinical issue.
This study provides a quantifiable measure of revision issue after SG. However, it has some limitations. One is that patient characteristics and follow-up duration vary differently from one to another study and may cause reporting biases. For this issue, we used random effects model to pool results, in order to get the most conservative estimates. Moreover, we performed subgroup analysis, sensitivity analysis, and trim and fill analysis; the results indicated that the pooled incidence were robust. Another limitation is that data about revisional outcomes is limited, making us unable to run meta-analysis of surgical outcomes after revision. All in all, more research taking patient characteristics into account are warranted, so as to determine which revision surgery is the best for failed SG.
Conclusion
This systematic review and meta-analysis demonstrated that revision rate is not rare after SG, especially when looking at long-term follow-up. The most common reason for revision is failure in weight loss, and the most frequent revisional procedure is RYGB. There is a need for bariatric surgeons and patients to fully understand and deal with the need for revision after SG.
References
Angrisani L, Santonicola A, Iovino P, et al. Bariatric surgery and endoluminal procedures: IFSO worldwide survey 2014. Obes Surg. 2017;27(9):2279–89.
Ricci C, Gaeta M, Rausa E, et al. Long-term effects of bariatric surgery on type II diabetes, hypertension and hyperlipidemia: a meta-analysis and meta-regression study with 5-year follow-up. Obes Surg. 2015;25(3):397–405.
Rosenthal RJ. International sleeve gastrectomy expert panel consensus statement: best practice guidelines based on experience of > 12,000 cases. Surg Obes Relat Dis. 2012;8(1):8–19.
English WJ, DeMaria EJ, Brethauer SA, et al. American Society for Metabolic and Bariatric Surgery estimation of metabolic and bariatric procedures performed in the United States in 2016. Surg Obes Relat Dis. 2018;14(3):259–63.
De Angelis F, Avallone M, Albanese A, et al. Re-sleeve gastrectomy 4 years later: is it still an effective revisional option? Obes Surg. 2018;28(11):3714–6.
Boru CE, Greco F, Giustacchini P, et al. Short-term outcomes of sleeve gastrectomy conversion to R-Y gastric bypass: multi-center retrospective study. Langenbeck Arch Surg. 2018;403(4):473–9.
Boza C, Daroch D, Barros D, et al. Long-term outcomes of laparoscopic sleeve gastrectomy as a primary bariatric procedure. Surg Obes Relat Dis. 2014;10(6):1129–33.
Diamantis T, Apostolou KG, Alexandrou A, et al. Review of long-term weight loss results after laparoscopic sleeve gastrectomy. Surg Obes Relat Dis. 2014;10(1):177–83.
Juodeikis Z, Brimas G. Long-term results after sleeve gastrectomy: a systematic review. Surg Obes Relat Dis. 2017;13(4):693–9.
Clapp B, Wynn M, Martyn C, et al. Long term (7 or more years) outcomes of the sleeve gastrectomy: a meta-analysis. Surg Obes Relat Dis. 2018;14(6):741–7.
Stroup DF, Berlin JA, Morton SC, et al. Meta-analysis of observational studies in epidemiology: a proposal for reporting. Meta-analysis Of Observational Studies in Epidemiology (MOOSE) group. JAMA. 2008;283(15):2000.
Moher D, Liberati A, Tetzlaff J, et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Int J Surg. 2010;8(5):336–41.
Chen J, Wang X, Bai W, et al. Prevalence of heterotopic ossification after cervical total disc arthroplasty: a meta-analysis. Eur Spine J. 2012;21(4):674–80.
Richardson WS, Polashenski WA, Robbins BW. Could our pretest probabilities become evidence based? A prospective survey of hospital practice. J Gen Intern Med. 2003;18(3):203–8.
Ruiz-Tovar J, Carbajo MA, Jimenez JM, et al. Long-term follow-up after sleeve gastrectomy versus Roux-en-Y gastric bypass versus one-anastomosis gastric bypass: a prospective randomized comparative study of weight loss and remission of comorbidities. Surg Endosc. 2019;33(2):401–10.
Altieri MS, Yang J, Nie L, et al. Rate of revisions or conversion after bariatric surgery over 10 years in the state of New York. Surg Obes Relat Dis. 2018;14(4):500–7.
Peterli R, Wolnerhanssen BK, Peters T, et al. Effect of laparoscopic sleeve gastrectomy vs laparoscopic Roux-en-Y gastric bypass on weight loss in patients with morbid obesity: the SM-BOSS randomized clinical trial. JAMA. 2018;319(3):255–65.
Chang D, Lee W, Chen J, et al. Thirteen-year experience of laparoscopic sleeve gastrectomy: surgical risk, weight loss, and revision procedures. Obes Surg. 2018;28(10):2991–7.
Castagneto Gissey L, Casella Mariolo JR, Genco A, et al. 10-year follow-up after laparoscopic sleeve gastrectomy: outcomes in a monocentric series. Surg Obes Relat Dis. 2018;14(10):1480–7.
Kowalewski PK, Olszewski R, Walędziak MS, et al. Long-term outcomes of laparoscopic sleeve gastrectomy—a single-center, retrospective study. Obes Surg. 2018;28(1):130–4.
Felsenreich DM, Ladinig LM, Beckerhinn P, et al. Update: 10 years of sleeve gastrectomy—the first 103 patients. Obes Surg. 2018;28(11):3586–94.
Flølo TN, Andersen JR, Kolotkin RL, et al. Five-year outcomes after vertical sleeve gastrectomy for severe obesity: a prospective cohort study. Obes Surg. 2017;27(8):1944–51.
Noel P, Nedelcu M, Eddbali I, et al. What are the long-term results 8 years after sleeve gastrectomy? Surg Obes Relat Dis. 2017;13(7):1110–5.
Mandeville Y, Van Looveren R, Vancoillie P, et al. Moderating the enthusiasm of sleeve gastrectomy: up to fifty percent of reflux symptoms after ten years in a consecutive series of one hundred laparoscopic sleeve gastrectomies. Obes Surg. 2017;27(7):1797–803.
Schauer PR, Bhatt DL, Kirwan JP, et al. Bariatric surgery versus intensive medical therapy for diabetes—5-year outcomes. New Engl J Med. 2017;376(7):641–51.
Gadiot RP Biter LU, van Mil S, Zengerink HF, et al. Long-term results of laparoscopic sleeve gastrectomy for morbid obesity: 5 to 8-year results. Obes Surg. 2017;27(1):59–63.
Garofalo F, Denis R, Pescarus R, et al. Long-term outcome after laparoscopic sleeve gastrectomy in patients over 65 years old: a retrospective analysis. Surg Obes Relat Dis. 2016;13(1):1–6.
Lessing Y, Pencovich N, Lahat G, et al. Laparoscopic sleeve gastrectomy for diabetics—5-year outcomes. Surg Obes Relat Dis. 2017;13(10):1658–63.
Yilmaz H, Ece I, Sahin M. Revisional surgery after failed laparoscopic sleeve gastrectomy: retrospective analysis of causes, results, and technical considerations. Obes Surg. 2017;27(11):2855–60.
Arman GA, Himpens J, Dhaenens J, et al. Long-term (11+years) outcomes in weight, patient satisfaction, comorbidities, and gastroesophageal reflux treatment after laparoscopic sleeve gastrectomy. Surg Obes Relat Dis. 2016;12(10):1778–86.
Seki Y, Kasama K, Hashimoto K. Long-term outcome of laparoscopic sleeve gastrectomy in morbidly obese Japanese patients. Obes Surg. 2016;26(1):138–45.
Angrisani L, Santonicola A, Hasani A, et al. Five-year results of laparoscopic sleeve gastrectomy: effects on gastroesophageal reflux disease symptoms and co-morbidities. Surg Obes Relat Dis. 2016;12(5):960–8.
Dakour Aridi H, Alami R, Tamim H, et al. Long-term outcomes of laparoscopic sleeve gastrectomy: a Lebanese center experience. Surg Obes Relat Dis. 2016;12(9):1689–96.
Casella G, Soricelli E, Giannotti D, et al. Long-term results after laparoscopic sleeve gastrectomy in a large monocentric series. Surg Obes Relat Dis. 2016;12(4):757–62.
Dogan K, Gadiot RP, Aarts EO, et al. Effectiveness and safety of sleeve gastrectomy, gastric bypass, and adjustable gastric banding in morbidly obese patients: a multicenter, retrospective, matched cohort study. Obes Surg. 2015;25(7):1110–8.
Lee W, Pok E, Almulaifi A, et al. Medium-term results of laparoscopic sleeve gastrectomy: a matched comparison with gastric bypass. Obes Surg. 2015;25(8):1431–8.
Abd Ellatif ME, Abdallah E, Askar W, et al. Long term predictors of success after laparoscopic sleeve gastrectomy. Int J Surg. 2014;12(5):504–8.
Prevot F, Verhaeghe P, Pequignot A, et al. Two lessons from a 5-year follow-up study of laparoscopic sleeve gastrectomy: persistent, relevant weight loss and a short surgical learning curve. Surgery. 2014;155(2):292–9.
Sieber P, Gass M, Kern B, et al. Five-year results of laparoscopic sleeve gastrectomy. Surg Obes Relat Dis. 2014;10(2):243–9.
Rawlins L, Rawlins MP, Brown CC, et al. Sleeve gastrectomy: 5-year outcomes of a single institution. Surg Obes Relat Dis. 2012;9(1):21–5.
Catheline JM, Fysekidis M, Bachner I, et al. Five-year results of sleeve gastrectomy. J Visc Surg. 2013;150(5):307–12.
Abbatini F, Capoccia D, Casella G, et al. Long-term remission of type 2 diabetes in morbidly obese patients after sleeve gastrectomy. Surg Obes Relat Dis. 2013;9(4):498–502.
Sarela AI, Dexter SPL, O'Kane M, et al. Long-term follow-up after laparoscopic sleeve gastrectomy: 8–9-year results. Surg Obes Relat Dis. 2012;8(6):679–84.
Bohdjalian A, Langer FB, Shakeri-Leidenmühler S, et al. Sleeve gastrectomy as sole and definitive bariatric procedure: 5-year results for weight loss and ghrelin. Obes Surg. 2010;20(5):535–40.
Himpens J, Dobbeleir J, Peeters G. Long-term results of laparoscopic sleeve gastrectomy for obesity. Ann Surg. 2010;252(2):319–24.
Shen XJ, Zhang X, Bi JW, et al. Long-term complications requiring reoperations after laparoscopic adjustable gastric banding: a systematic review. Surg Obes Relat Dis. 2015;11(4):956–64.
Shimon O, Keidar A, Orgad R, et al. Long-term effectiveness of laparoscopic conversion of sleeve gastrectomy to a biliopancreatic diversion with a duodenal switch or a Roux-en-Y gastric bypass due to weight loss failure. Obes Surg. 2018;28(6):1724–30.
Quezada N, Hernández J, Pérez G, et al. Laparoscopic sleeve gastrectomy conversion to Roux-en-Y gastric bypass: experience in 50 patients after 1 to 3 years of follow-up. Surg Obes Relat Dis. 2016;12(8):1611–5.
Oor JE, Roks DJ, Unlu C, et al. Laparoscopic sleeve gastrectomy and gastroesophageal reflux disease: a systematic review and meta-analysis. Am J Surg. 2016;211(1):250–67.
Braghetto I, Csendes A, Korn O, et al. Gastroesophageal reflux disease after sleeve gastrectomy. Surg Laparosc Endosc Percutan Tech. 2010;20(3):148–53.
Daes J, Jimenez ME, Said N, et al. Improvement of gastroesophageal reflux symptoms after standardized laparoscopic sleeve gastrectomy. Obes Surg. 2014;24(4):536–40.
Malinka T, Zerkowski J, Katharina I, et al. Three-year outcomes of revisional laparoscopic gastric bypass after failed laparoscopic sleeve gastrectomy: a case-matched analysis. Obes Surg. 2017;27(9):2324–30.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of Interest
The authors declare that they have no conflict of interest.
A Statement of Formal Consent
For this type of study, formal consent is not required.
A Statement of Human and Animal Rights
Given that there are no interventions implemented on patients, ethical approval is not required.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Guan, B., Chong, T.H., Peng, J. et al. Mid-long-term Revisional Surgery After Sleeve Gastrectomy: a Systematic Review and Meta-analysis. OBES SURG 29, 1965–1975 (2019). https://doi.org/10.1007/s11695-019-03842-3
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11695-019-03842-3