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Evidence - Gastric bypass, laparoscopic

  1. Summary of the Literature

    Definitions

    Bariatric surgery refers to surgical procedures that aim to achieve an improvement in comorbidities or their prevention and an improvement in quality of life through sustainable weight reduction. If the surgical procedures have the primary goal of improving the glycemic metabolic situation in pre-existing type 2 diabetes mellitus, this is referred to as metabolic surgery.

    The WHO classification of obesity is based on the Body Mass Index (BMI): body weight divided by height squared (kg/m²). For Europeans, obesity is classified into

    • Grade I (BMI 30–34.9 kg/m²
    • Grade II (BMI 35–39.9 kg/m²
    • Grade III (BMI ≥40 kg/m²

    Obesity is multifactorially caused; ultimately, a positive energy balance leads to the storage of excessively supplied energy mainly in adipose tissue and the liver. Weight reduction is associated, among other things, with an improvement in insulin resistance, blood sugar, blood pressure, blood lipids, gastroesophageal reflux, urinary incontinence, gonarthrosis, spinal complaints, intertrigo, infertility, obstructive sleep apnea syndrome, asthma, and a reduction in the risk of certain cancers.

    Indications for bariatric or metabolic surgery

    Sustainable weight reduction to improve comorbidities and quality of life is possible in higher-grade obesity through dietary, exercise, behavioral, and pharmacotherapy alone or in combination, but is often not achieved [1 - 4]. Compared to conservative measures for weight reduction alone or in combination, surgical therapy is significantly more effective and usually achieves the desired therapeutic goal [5 - 12].

    The indication for a bariatric surgical procedure is given under the following conditions [13 - 16]:

    1. BMI ≥ 40 kg/m² without comorbidities and without contraindications after exhaustion of conservative therapy.

    2. BMI ≥ 35 kg/m² with one or more obesity-associated comorbidities such as type 2 diabetes mellitus, coronary heart disease, heart failure, hyperlipidemia, arterial hypertension, nephropathy, obstructive sleep apnea syndrome, obesity hypoventilation syndrome, Pickwick syndrome, non-alcoholic fatty liver or non-alcoholic steatohepatitis, gastroesophageal reflux disease, asthma, chronic venous insufficiency, urinary incontinence, immobilizing joint disease, fertility restrictions or polycystic ovary syndrome.

    3. Primary indication for a bariatric surgical procedure without prior conservative therapy attempt if one of the following conditions is present:   

    • BMI ≥ 50 kg/m²
    • Conservative therapy attempt is assessed by the multidisciplinary team as not promising or hopeless.
    • In patients with particular severity of concomitant and secondary diseases that do not allow postponement of a surgical procedure.

    A primary indication in the sense of metabolic surgery can be made for BMI ≥ 40 kg/m² and coexisting type 2 diabetes mellitus if the treatment goal is to improve the glycemic metabolic situation more than weight reduction. To establish the indication for surgery, proof of exhausted conservative therapy in the sense of bariatric surgery is not required for these patients [17, American Diabetes Association 2017].

    Contraindications for bariatric or metabolic surgery

    In the following diseases and conditions, bariatric or metabolic surgery - despite currently lacking evidence - is considered contraindicated:

    1. Unstable psychopathological conditions, untreated bulimia nervosa, active substance dependence.

    2. Consumptive underlying diseases, malignant neoplasms, untreated endocrine causes, chronic diseases that worsen due to postoperative catabolic metabolism.

    3. Existing or immediately planned pregnancy.

    If the mentioned diseases and conditions can be successfully treated, a re-evaluation should be performed.

    The following do not constitute contraindications:

    • higher age (≥ 65 years) [18]
    • chronic inflammatory bowel diseases such as Crohn's disease and ulcerative colitis [19]
    • existing desire to have children [20]
    • Type 1 diabetes [21]

     

    Surgical Procedures

    The effective surgical procedures for the treatment of obesity and its comorbidities include:

    • Sleeve gastrectomy (“Sleeve Gastrectomy”, SG)
    • proximal Roux-en-Y gastric bypass (pRYGB)
    • Omega-Loop gastric bypass (MGB)
    • biliopancreatic diversion with/without duodenal switch (BPD or BPD-DS)

    There is no surgical procedure that can be recommended across the board for all patients; rather, the choice of procedure should be individually oriented to the patient's medical, psychosocial, and general life circumstances [22].  The current evidence does not allow the definition of a surgical “gold standard” as a primary procedure in bariatric and metabolic surgery.

    In patients with extreme forms of obesity (BMI > 50 kg/m²) and/or significant comorbidity, staged concepts can be considered, e.g., initially sleeve gastrectomy, then gastric bypass, to reduce perioperative risk [23]. All procedures should ideally be performed laparoscopically.

    1. Sleeve Gastrectomy (“Sleeve Gastrectomy”, SG)

    The SG was initially established in biliopancreatic diversion with duodenal switch (BPD-DS) for additional food restriction and ulcer prophylaxis. Meanwhile, it has established itself as an independent surgical procedure. The SG was first described in 1993 by Marceau [24]. The SG is also very suitable as the first operation of a staged concept in extreme obesity, as the sleeve stomach can be easily converted into a Roux-en-Y gastric bypass, an Omega-Loop gastric bypass, or a postpyloric bypass if necessary [25].

    The excess weight loss 2 years after SG does not differ significantly from the weight loss after pRYGB. After 5 years, the weight loss after SG is around 50%, the remission rate of type 2 diabetes mellitus is 58% [26 – 30].  Compared to gastric bypass, the SG has partially significantly fewer perioperative complications. The morbidity after SG is reported as 7 - 8% [15, 29, 31, 32, 33]. In large centers, the lethality is well below 1% [15]. The most common complications are staple line fistulas, abscesses, or rebleeding.

    Clear contraindications for the SG do not currently exist. Only in cases of preoperatively proven symptomatic and/or therapy-refractory gastroesophageal reflux should the indication be viewed critically [29].

    2. Proximal Roux-en-Y Gastric Bypass (pRYGB)

    The pRYGB was previously referred to as the gold standard of bariatric or metabolic surgery and was first described in 1967 and 1969 by Mason and Ito initially with a relatively large pouch volume. Nowadays, it is performed in the laparoscopic modification by Wittgrove from the 1990s with a very small pouch (< 15 cm ³) [34, 35].

    The pRYGB offers very good long-term results regarding weight reduction and remission of pre-existing type 2 diabetes mellitus. In the meta-analysis by Chang et al., the average weight reduction after pRYGB compared to conservatively treated controls was 14 BMI points, Yu et al. determined 12.6 BMI points [36, 37]. After 5 years, an excess weight loss of 60 - 65% can be expected. The procedure leads on average to remission of pre-existing type 2 diabetes in 75% [16, 37].  In the meta-analysis by Chang et al. [36], a mortality of under 1% is reported for the pRYGB, the morbidity is 21%, and the reoperation rate is 3%.  Thus, the pRYGB has a higher postoperative morbidity and reoperation rate compared to the SG, the incidence of severe complications is comparable. Regarding effectiveness in T2DM, the pRYGB is superior to the SG.

    3.  Omega-Loop Gastric Bypass (MGB)

    The Mini Gastric Bypass, abbreviated MGB, was first performed in 1997 by Rutledge and is considered a safe and effective procedure in bariatric or metabolic surgery. The principle of the MGB is the formation of a long lesser curvature gastric pouch combined with a biliary small intestine loop, whose length can vary. Usually, it has a length from the ligament of Treitz to the gastrojejunostomy of 200 cm. Depending on the severity of obesity, longer biliary limbs (250-300 cm) are also chosen. For severe obesity, a length of 250 cm is recommended, for older patients and vegetarians a length of 180-200 cm, and for type 2 diabetics without massive obesity a length of 150 cm.

    The conversion rate from laparoscopic to open procedure is between 0 and 1.23% [22]. The weight loss of the MGB is a reduction in BMI of 11.3 kg/m² or an excess weight loss between 61 and 69% after 12 months and 72.9 and 77% after 5 years [22, 38, 39]. For type 2 diabetes, remission rates between 51 and 100% are reported [39]. Weight loss and type 2 diabetes remission rate are greater after MGB than after a pRYGB [39].

    The number of postoperative complications after MGB is between 0 - 28.6%. The most common are bleedings that require endoscopic or surgical intervention (0.2 - 28.6%), and anastomotic ulcers (1 - 14.3%). The mortality rate is 0 - 0.5% [38].

    4.1  Biliopancreatic Diversion (BPD)

    The BPD was developed in the 1970s by Scopinaro [40, 41] and separates food passage and digestive secretions similar to the pRYGB, bypassing the duodenum. Internationally, the BPD is considered a standard procedure, but has hardly caught on numerically in Germany.

    In the meta-analysis by Panunzi et al., it was shown that this malabsorptive surgical procedure has the highest remission rates for pre-existing type 2 diabetes mellitus among all bariatric surgical procedures [16]. Diabetes remission could be achieved in 89% of patients after BPD, in 77% of patients after pRYGB, and in 60% of patients after SG. Similar results were also described by Müller-Stich et al. and Mingrone et al. [12, 42]. The same applies to excess weight reduction, although there are no high-quality data on this. 

    The perioperative mortality rate is reported in the meta-analysis by Panunzi et al. as 0.8% for the BPD. The BPD is primarily based on the principle of malabsorption with severe fatty stools, which inevitably leads to reduced nutrient absorption such as fat-soluble vitamins. In various studies, a significant drop in vitamin A and E was observed in up to 40% of patients. Vitamin D deficiency states occur in up to 61% of cases after BPD, iron and ferritin deficits in up to 16%, and zinc deficit in 40 - 68% [43]. In a systematic review by Rodriguez-Carmona et al., it was demonstrated that bone density can decrease significantly after BPD, which poses a significant risk for the development of spontaneous fractures [44].

    Malabsorptive surgical procedures also lead to restricted absorption and reduced effectiveness of therapeutically relevant medications [45].

    The overall complication rate after laparoscopic biliopancreatic diversion is up to 25% (insufficiencies of the gastric staple line, duodenal stump insufficiencies, incisional hernias, strictures of the duodenojejunostomy) [46]. In a retrospective observational study, a significantly higher percentage of necessary postoperative intensive care stays and orotracheal intubation treatments (30.5%) was found after BPD than after gastric bypass and sleeve gastrectomy (12%).  The mortality rate was 6% for BPD, whereas no deaths were reported for SG and pRYGB [47].

    4.2 Biliopancreatic Diversion with Duodenal Switch (BPD-DS)

    The BPD-DS is a complex operation that combines restriction (sleeve gastrectomy) with malabsorption (postpyloric Roux-en-Y reconstruction).

    It was first performed as an open operation in 1988 by Douglas Hess [48]. Due to the good results (sustainable weight reduction, high remission rate of pre-existing type 2 diabetes), the procedure could establish itself and was first performed laparoscopically by Michael Gagner [49]. 

    Meanwhile, the BPD-DS is a procedure that is rather rarely performed worldwide and accounts for at most 2% of all bariatric or metabolic procedures [50]. The reasons are likely the significantly increased perioperative morbidity and mortality compared to other procedures, as well as postoperative deficiencies that can occur in a high percentage despite substitution due to the pronounced malabsorption [15, 51, 52, 53].

  2. Currently ongoing studies on this topic

  3. Literature on this topic

    1. Avenell, A.; Broom, J.; Brown, T.; Poobalan, A.; Aucott, L.; Stearns, S. et al. (2004): Systematic review of the long-term effects and economic consequences of treatments for obesity and implications for health improvement. In: Health Technol Assess 8 (21).

    2. Burguera, B.; Jesús Tur, J.; Escudero, A.J.; Alos, M.; Pagán, A.; Cortés, B. et al. (2015): An intensive lifestyle intervention is an effective treatment of morbid obesity. The TRAMOMTANA study - A two-year randomized controlled clinical trial. In: International journal of endocrinology 2015, p. 194696

    3. Thorogood, A.; Mottillo, S.; Shimony, A.; Filion, K.B.; Joseph, L.; Genest, J. et al. (2011): Isolated aerobic exercise and weight loss. A systematic review and meta-analysis of randomized controlled trials. In: The American journal of medicine 124 (8), pp. 747–755.

    4. Johns, D.J.; Hartmann-Boyce, J.; Jebb, S.A.; Aveyard, P. (2014): Diet or exercise interventions vs combined behavioral weight management programs. A systematic review and meta-analysis of direct comparisons. In: Journal of the Academy of Nutrition and Dietetics 114 (10), pp. 1557–1568.

    5. Dixon, J. B.; Schachter, L. M.; O'Brien, P. E.; Jones, K.; Grima, M.; Lambert, G. et al. (2012): Surgical vs conventional therapy for weight loss treatment of obstructive sleep apnea:a randomized controlled trial. In: Jama 308, pp. 1142–1149.

    6. Sjöström, L.; Peltonen, M.; Jacobson, P.; Sjöström, C. D.; Karason, K.; Wedel, H. et al. (2012): Bariatric surgery and long-term cardiovascular events. In: Jama 307, pp. 56–65.

    7. Cheng, J.; Gao, J.; Shuai, X.; Wang, G.; Tao, K. (2016): The comprehensive summary of surgical versus non-surgical treatment for obesity. A systematic review and meta-analysis of randomized controlled trials. In: Oncotarget 7 (26), pp. 39216–39230.

    8. Schauer, P. R.; Kashyap, S. R.; Wolski, K.; Brethauer, S. A.; Kirwan, J. P.; Pothier, C. E. et al. (2012): Bariatric surgery versus intensive medical therapy in obese patients with diabetes. In: The New England journal of medicine 366, pp. 1567–1576.

    9. Mingrone, G.; Panunzi, S.; Gaetano, A.; Guidone, C.; Iaconelli, A.; Nanni, G. et al. (2015): Bariatric-metabolic surgery versus conventional medical treatment in obese patients with type 2 diabetes: 5 year follow-up of an open-label, single-centre, randomised controlled trial. In: Lancet (London, England) 386 (9997), pp. 964–973.

    10. Courcoulas, A. P.; Belle, S. H.; Neiberg, R. H.; Pierson, S. K.; Eagleton, J. K.; Kalarchian, M. A. et al. (2015): Three-year outcomes of bariatric surgery vs lifestyle intervention for type 2 diabetes mellitus treatment: A randomized clinical trial. In: JAMA surgery 150, pp. 931–940.

    11. Wu, G.-Z.; Cai, B.; Yu, F.; Fang, Z.; Fu, X.-L.; Zhou, H.-S. et al. (2016): Meta-analysis of bariatric surgery versus non-surgical treatment for type 2 diabetes mellitus. In: Oncotarget 7 (52), pp. 87511–87522.

    12. Müller-Stich, B. P.; Senft, J. D.; Warschkow, R.; Kenngott, H. G.; Billeter, A. T.; Vit, G. et al. (2015): Surgical versus medical treatment of type 2 diabetes mellitus in nonseverely obese patients: A systematic review and meta-analysis. In: Annals of surgery 261 (3), pp. 421–429.

    13. Mechanick, J.I.; Youdim, A.; Jones, D.B.; Timothy G.W.; Hurley, D.L.; Molly McMahon, M. et al. (2013): Clinical practice guidelines for the perioperative nutritional, metabolic, and nonsurgical support of the bariatric surgery patient--2013 update: cosponsored by American Association of Clinical Endocrinologists, the Obesity Society, and American Society for Metabolic & Bariatric Surgery. In: Surgery for obesity and related diseases: official journal of the American Society for Bariatric Surgery 9 (2), pp. 159–191.

    14. Boido, A.; Ceriani, V.; Cetta, F.; Lombardi, F.; Pontiroli, A. E. (2015): Bariatric surgery and prevention of cardiovascular events and mortality in morbid obesity: Mechanisms of action and choice of surgery 25, pp. 437–443.

    15. Colquitt, J. L.; Pickett, K.; Loveman, E.; Frampton, G. K. (2014): Surgery for weight loss in adults. In: The Cochrane database of systematic reviews 8, Cd003641.

    16. Panunzi, S.; Gaetano, A. de; Carnicelli, A.; Mingrone, G. (2014): Predictors of remission of diabetes mellitus in severely obese individuals undergoing bariatric surgery: do BMI or procedure choice matter? A meta-analysis. In: Annals of surgery 261, pp. 459–467.

    17. Rubino, F.; Nathan, D.M.; Eckel, R.H.; Schauer, P.R.; Alberti, K.G.; Zimmet, P.Z. et al. (2016): Metabolic surgery in the treatment algorithm for type 2 diabetes. A Joint Statement by International Diabetes Organizations. In: Surgery for obesity and related diseases: official journal of the American Society for Bariatric Surgery 12 (6), pp. 1144–1162.

    18. Giordano, S.; Victorzon, M. (2015): Bariatric surgery in elderly patients: A systematic review 10, pp. 1627–1635.

    19. Aminian, A.; Andalib, A.; Ver, M.R.; Corcelles, R.; Schauer, P.R.; Brethauer, S.A. (2016): Outcomes of Bariatric Surgery in Patients with Inflammatory Bowel Disease. In: Obesity surgery 26 (6), pp. 1186–1190.

    20. Johansson, K.; Cnattingius, S.; Naslund, I.; Roos, N.; Trolle Lagerros, Y.; Granath, F. et al. (2015): Outcomes of pregnancy after bariatric surgery. In: The New England journal of medicine 372 (9), pp. 814–824.

    21. Chow, A.; Switzer, N. J.; Dang, J.; Shi, X.; Gara, C.; Birch, D.W. et al. (2016): A systematic review and meta-analysis of outcomes for type 1 diabetes after bariatric surgery. In: Journal of obesity 2016, p. 6170719.

    22. Padwal, R.; Klarenbach, S.; Wiebe, N.; Birch, D.; Karmali, S.; Manns, B. et al. (2011): Bariatric surgery: A systematic review and network meta-analysis of randomized trials. In: Obesity reviews: an official journal of the International Association for the Study of Obesity 12, pp. 602–621.

    23. Alexandrou, A.; Felekouras, E.; Giannopoulos, A.; Tsigris, C.; Diamantis, T. (2012): What is the actual fate of super-morbid-obese patients who undergo laparoscopic sleeve gastrectomy as the first step of a two-stage weight-reduction operative strategy? In: Obesity surgery 22 (10), pp. 1623–1628.

    24. Marceau, P.; Biron, S.; Bourque, R.A.; Potvin, M.; Hould, F.S.; Simard, S. (1993): Biliopancreatic diversion with a new type of gastrectomy. In: Obesity surgery 3 (1), pp. 29–35.

    25. Regan, J. P.; Inabnet, W. B.; Gagner, M.; Pomp, A. (2003): Early experience with two-stage laparoscopic Roux-en-Y gastric bypass as an alternative in the super-super obese patient. In: Obesity surgery 13 (6), pp. 861–864.

    26. Schauer, P. R.; Bhatt, D. L.; Kirwan, J. P.; Wolski, K.; Brethauer, S. A.; Navaneethan, S. D. et al. (2014): Bariatric surgery versus intensive medical therapy for diabetes--3-year outcomes. In: The New England journal of medicine 370, pp. 2002–2013.

    27. Helmio, M.; Victorzon, M.; Ovaska, J.; Leivonen, M.; Juuti, A.; Peromaa-Haavisto, P. et al. (2014a): Comparison of laparoscopic sleeve gastrectomy and gastric bypass in the treatment of morbid obesity: A prospective randomized controlled multicentre sleevepass study with 4year follow-up. In: Obesity surgery 24 (8), p. 1214.

    28. Lee, W.-J. Chong, K.; Ser, K.-H. Lee, Y.-C.; Chen, S.-C.; Chen, J.-C. et al. (2011b): Gastric bypass vs sleeve gastrectomy for type 2 diabetes mellitus. A randomized controlled trial. In: Archives of surgery (Chicago, Ill.: 1960) 146 (2), pp. 143–148.

    29. Peterli, R.; Borbely, Y.; Kern, B.; Gass, M.; Peters, T.; Thurnheer, M. et al. (2013): Early results of the Swiss Multicentre Bypass or Sleeve Study (SM-BOSS): a prospective randomized trial comparing laparoscopic sleeve gastrectomy and Roux-en-Y gastric bypass. In: Annals of surgery 258, 690-4.

    30. Fischer, L.; Hildebrandt, C.; Bruckner, T.; Kenngott, H.; Linke, G. R.; Gehrig, T. et al. (2012): Excessive weight loss after sleeve gastrectomy: a systematic review. In: Obesity surgery 22, pp. 721–731.

    31. Helmio, M.; Victorzon, M.; Ovaska, J.; Leivonen, M.; Juuti, A.; Peromaa-Haavisto, P. et al. (2014b): Comparison of short-term outcome of laparoscopic sleeve gastrectomy and gastric bypass in the treatment of morbid obesity. A prospective randomized controlled multicenter SLEEVEPASS study with 6-month follow-up. In: Scandinavian journal of surgery: SJS : official organ for the Finnish Surgical Societyand the Scandinavian Surgical Society 103 (3), pp. 175–181.

    32. Osland, E.; Yunus, R. M.; Khan, S.; Alodat, T.; Memon, B.; Memon, M.A. (2016): Postoperative early major and minor complications in laparoscopic vertical sleeve gastrectomy (LVSG) versus laparoscopic Roux-en-Y gastric bypass (LRYGB) procedures. A meta-analysis and systematic review. In: Obesity surgery 26 (10), pp. 2273–2284.

    33. Li, P.; Fu, P.; Chen, J.; Wang, L. H.; Wang, D. R. (2013): Laparoscopic Roux-en-Y gastric bypass vs. laparoscopic sleeve gastrectomy for morbid obesity and diabetes mellitus: A meta-analysis of sixteen recent studies 60, pp. 132–135.

    34. Wittgrove, A. C.; Clark, G. W.; Tremblay, L. J. (1994): Laparascopic gastric bypass, Roux-enY: Preliminary report of five cases. In: Obesity surgery 4, pp. 353–357.

    35. Wittgrove, A. C.; Clark, G. W. (2000): Laparoscopic Gastric Bypass, Roux en – Y 500 Patients: Technique and Results, with 3-60 month follow-up. In: Obesity surgery 10, pp. 233– 239.

    36. Chang, S. H.; Stoll, C. R.; Song, J.; Varela, J. E.; Eagon, C. J.; Colditz, G. A. (2013): The effectiveness and risks of bariatric surgery: an updated systematic review and meta-analysis, 2003-2012. In: JAMA surgery 149, pp. 275–287.

    37. Yu, J.; Zhou, X.; Li, L.; Li, S.; Tan, J.; Li, Y.; Sun, X. (2014): The long-term effects of bariatric surgery for type 2 diabetes: systematic reviewand meta-analysis of randomized and nonrandomized evidence. In: Obesity surgery 25, pp. 143–158.

    38. Georgiadou, D.; Sergentanis, T. N.; Nixon, A.; Diamantis, T.; Tsigris, C.; Psaltopoulou, T. (2014): Efficacy and safety of laparoscopic mini gastric bypass. A systematic review. In: Surgery for obesity and related diseases: official journal of the American Societyfor Bariatric Surgery 10, pp. 984–991.

    39. Quan, Y.; Huang, A.; Ye, M.; Xu, M.; Zhuang, B.; Zhang, P. et al. (2015): Efficacy of laparoscopic mini gastric bypass for obesity and type 2 diabetes mellitus: A systematic review and meta-analysis. In: Gastroenterology Research and Practice 2015, p. 152852.

    40. Scopinaro, N.; Gianetta, E.; Civalleri, D.; Bonalumi, U.; Bacchi, V. (1979): Bilio-pancreatic bypass for obesity: II. Initial experience in man. In: British Journal of Surgery 66 (9), pp. 618– 620.

    41. Scopinaro, N.; Gianetta, E.; Adami, G. F.; Friedman, D.; Traverso, E.; Marinari, G. M. et al. (1996): Biliopancreatic diversion for obesity at eighteen years. In: Surgery 119 (3), pp. 261– 268. 

    42. Mingrone, G.; Panunzi, S.; Gaetano, A.; Guidone, C.; Iaconelli, A.; Nanni, G. et al. (2015): Bariatric-metabolic surgery versus conventional medical treatment in obese patients with type 2 diabetes: 5 year follow-up of an open-label, single-centre, randomised controlled trial. In: Lancet (London, England) 386 (9997), pp. 964–973.

    43. Ballesteros-Pomar, M.D.; González de Francisco, T.; Urioste-Fondo, A.; González-Herraez, L.; Calleja-Fernández, A.; Vidal-Casariego, A. et al. (2016): Biliopancreatic Diversion for Severe Obesity. Long-term effectiveness and nutritional complications. In: Obesity surgery 26 (1), pp. 38–44.

    44. Rodriguez-Carmona, Y.; Lopez-Alavez, F. J.; Gonzalez-Garay, A. G.; Solis-Galicia, C.; Melendez, G.; Serralde-Zuniga, A. E. (2014): Bone mineral density after bariatric surgery. A systematic review. In: International journal of surgery (London, England) 12, pp. 976–982.

    45. Padwal, R.; Brocks, D.; Sharma, A. M. (2009): A systematic review of drug absorption following bariatric surgery and its theoretical implications. In: Obesity reviews: an official journal of the International Association for the Study of Obesity 11, pp. 41–50.

    46. Parikh, M.S.; Laker, S.; Weiner, M.; Hajiseyedjavadi, O.; Ren, C.J. (2006): Objective comparison of complications resulting from laparoscopic bariatric procedures. In: Journal of the American College of Surgeons 202 (2), pp. 252–261.

    47. De La Matta-Martin, M.; Acosta-Martinez, J.; Morales-Conde, S.; Herrera-Gonzalez, A. (2012): Perioperative morbi-mortality associated with bariatric surgery. From systematic biliopancreatic diversion to a tailored laparoscopic gastric bypass or sleeve gastrectomy approach. In: Obesity surgery 22 (7), pp. 1001–1007.

    48. Hess, D. S.; Hess, D. W. (1998): Biliopancreatic diversion with a duodenal switch. In: Obesity surgery 8 (267-282).

    49. Ren, C. J.; Patterson, E.; Gagner, M. (2000): Early results of laparoscopic biliopancreatic diversion with duodenal switch: A case series of 40 consecutive patients. In: Obesity surgery 10, pp. 514–523.

    50. Buchwald, H.; Oien, D.M. (2013): Metabolic/bariatric surgery worldwide 2011. In: Obesity surgery 23 (4), pp. 427–436.

    51. Hedberg, J.; Sundstrom, J.; Sundbom, M. (2014): Duodenal switch versus Roux-en-Y gastric bypass for morbid obesity: systematic reviewand meta-analysis of weight results, diabetes resolution and early complicationsin single-centre comparisons. In: Obesity reviews: an official journal of the International Association for the Studyof Obesity 15, pp. 555–563.

    52. Aasheim, E. T.; Bjorkman, S.; Sovik, T. T.; Engstrom, M.; Hanvold, S. E.; Mala, T. et al. (2009): Vitamin status after bariatric surgery: a randomized study of gastric bypass and duodenal switch. In: The American journal of clinical nutrition 90, pp. 15–22.

    53. Risstad, H.; Søvik, T. T.; Engström, M.; Aasheim, E. T.; Fagerland, M. W.; Olsén, M. F. et al. (2015): Five-year outcomes after laparoscopic gastric bypass and laparoscopic duodenal switch in patients with body mass index of 50 to 60: a randomized clinical trial. In: JAMA surgery 150 (4), pp. 352–361.

  4. Reviews

    Andraos Y. Safety and Efficacy of Trocar Port-Site Closure Using a Biological Plug Closure in Laparoscopic Bariatric Surgery: a Prospective Study. Obes Surg. 2022 Nov;32(11):3796-3806.

    Caiazzo R, Marciniak C, Rémond A, Baud G, Pattou F. Future of bariatric surgery beyond simple weight loss: Metabolic surgery. J Visc Surg. 2023 Apr;160(2S):S55-S62.

    Chierici A, Amoretti P, Drai C, De Fatico S, Barriere J, Schiavo L, Iannelli A.  Does Bariatric Surgery Reduce the Risk of Colorectal Cancer in Individuals with Morbid Obesity? A Systematic Review and Meta-Analysis. Nutrients. 2023 Jan 16;15(2).

    D'Amato S, Sofia M, Agosta M, Litrico G, Sarvà I, La Greca G, Latteri S. The impact of bariatric surgery on colorectal cancer risk. Surg Obes Relat Dis. 2023  Feb;19(2):144-157.

    Intriago JMV, de Moura DTH, do Monte Junior ES, Proença IM, Ribeiro IB, Sánchez-Luna SA, Bernardo WM, de Moura EGH. Endoscopic Vacuum Therapy (EVT) for the Treatment of Post-Bariatric Surgery Leaks and Fistulas: a Systematic Review and Meta-analysis. Obes Surg. 2022 Oct;32(10):3435-3451.

    Lange UG, Mehdorn M, Dietrich A. [Anastomotic techniques in minimally invasive bariatric surgery]. Chirurgie (Heidelb). 2023 Sep;94(9):768-774.

    Monfared S, Weis JJ, Shah SK, Scott DJ, Felinski MM, Wilson EB. The rising tide of revisional surgery: tracking changes in index cases among bariatric-accredited fellowships. Surg Endosc. 2023 Jun;37(6):4824-4828.

    Parmar C, Pouwels S. Oesophageal and Gastric Cancer After Bariatric Surgery: an Up-to-Date Systematic Scoping Review of Literature of 324 Cases. Obes Surg. 2022  Dec;32(12):3854-3862.

    Qureshi H, Saeed N, Jovani M. Updates in Endoscopic Bariatric and Metabolic Therapies. J Clin Med. 2023 Jan 31;12(3).

    Thaher O, Driouch J, Hukauf M, Glatz T, Croner RS, Stroh C. Is development in bariatric surgery in Germany compatible with international standards? A review of 16 years of data. Updates Surg. 2022 Oct;74(5):1571-1579.

  5. Guidelines

  6. literature search

    Literature search on the pages of pubmed.