Weight loss, cardiovascular risk factors, and quality of life after gastric bypass and duodenal switch: a randomized trial
- PMID: 21893621
- DOI: 10.7326/0003-4819-155-5-201109060-00005
Weight loss, cardiovascular risk factors, and quality of life after gastric bypass and duodenal switch: a randomized trial
Abstract
Background: Gastric bypass and duodenal switch are currently performed bariatric surgical procedures. Uncontrolled studies suggest that duodenal switch induces greater weight loss than gastric bypass.
Objective: To determine whether duodenal switch leads to greater weight loss and more favorable improvements in cardiovascular risk factors and quality of life than gastric bypass.
Design: Randomized, parallel-group trial. (ClinicalTrials.gov registration number: NCT00327912)
Setting: 2 academic medical centers (1 in Norway and 1 in Sweden).
Patients: 60 participants with a body mass index (BMI) between 50 and 60 kg/m(2).
Intervention: Gastric bypass (n = 31) or duodenal switch (n = 29).
Measurements: The primary outcome was the change in BMI after 2 years. Secondary outcomes included anthropometric measures; concentrations of blood lipids, glucose, insulin, C-reactive protein, and vitamins; and health-related quality of life and adverse events.
Results: Fifty-eight of 60 participants (97%) completed the study. The mean reductions in BMI were 17.3 kg/m(2) (95% CI, 15.7 to 19.0 kg/m(2)) after gastric bypass and 24.8 kg/m(2) (CI, 23.0 to 26.5 kg/m(2)) after duodenal switch (mean between-group difference, 7.44 kg/m(2) [CI, 5.24 to 9.64 kg/m(2)]; P < 0.001). Total cholesterol concentration decreased by 0.24 mmol/L (CI, -0.03 to 0.50 mmol/L) (9.27 mg/dL [CI, -1.16 to 19.3 mg/dL]) after gastric bypass and 1.07 mmol/L (CI, 0.79 to 1.35 mmol/L) (41.3 mg/dL [CI, 30.5 to 52.1 mg/dL]) after duodenal switch (mean between-group difference, 0.83 mmol/L [CI, 0.48 to 1.18 mmol/L]; 32.0 mg/dL [CI, 18.5 to 45.6 mg/dL]; P ≤ 0.001). Reductions in low-density lipoprotein cholesterol concentration, anthropometric measures, fat mass, and fat-free mass were also greater after duodenal switch (P ≤ 0.010 for each between-group comparison). Both groups had reductions in blood pressure and mean concentrations of glucose, insulin, and C-reactive protein, with no between-group differences. The duodenal switch group, but not the gastric bypass group, had reductions in concentrations of vitamin A and 25-hydroxyvitamin D. Most Short Form-36 Health Survey dimensional scores improved in both groups, with greater improvement in 1 of 8 domains (bodily pain) after gastric bypass. From surgery until 2 years, 10 participants (32%) had adverse events after gastric bypass and 18 (62%) after duodenal switch (P = 0.021). Adverse events related to malnutrition occurred only after duodenal switch.
Limitation: Clinical experience was greater with gastric bypass than with duodenal switch at the study centers.
Conclusion: Duodenal switch surgery was associated with greater weight loss, greater reductions of total and low-density lipoprotein cholesterol concentrations, and more adverse events. Improvements in other cardiovascular risk factors and quality of life were similar after both procedures.
Primary funding source: South-Eastern Norway Regional Health Authority.
Comment in
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Primum non nocere.Ann Intern Med. 2011 Sep 6;155(5):329-30. doi: 10.7326/0003-4819-155-5-201109060-00012. Ann Intern Med. 2011. PMID: 21893627 No abstract available.
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Bariatric surgery: Weight loss after gastric bypass and duodenal switch.Nat Rev Gastroenterol Hepatol. 2011 Oct 11;8(11):598. doi: 10.1038/nrgastro.2011.180. Nat Rev Gastroenterol Hepatol. 2011. PMID: 21989156 No abstract available.
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Comments regarding a recent article comparing gastric bypass and duodenal switch and its questionable method and results.Surg Obes Relat Dis. 2012 Mar-Apr;8(2):239-40. doi: 10.1016/j.soard.2011.11.010. Epub 2011 Dec 2. Surg Obes Relat Dis. 2012. PMID: 22222300 No abstract available.
Summary for patients in
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Summaries for patients. Outcomes after gastric bypass and duodenal switch surgery.Ann Intern Med. 2011 Sep 6;155(5):I21. doi: 10.7326/0003-4819-155-5-201109060-00001. Ann Intern Med. 2011. PMID: 21893617 No abstract available.
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