دورية أكاديمية

Ursodeoxycholic acid for the prevention of symptomatic gallstone disease after bariatric surgery: study protocol for a randomized controlled trial (UPGRADE trial)

التفاصيل البيبلوغرافية
العنوان: Ursodeoxycholic acid for the prevention of symptomatic gallstone disease after bariatric surgery: study protocol for a randomized controlled trial (UPGRADE trial)
المؤلفون: Thomas C. C. Boerlage, Sylke Haal, L. Maurits de Brauw, Yair I. Z. Acherman, Sjoerd Bruin, Arnold W. J. M. van de Laar, Daan E. Moes, Bart A. van Wagensveld, Claire E. E. de Vries, Ruben van Veen, Ruben Schouten, Marcel G. Dijkgraaf, Paul Fockens, Victor E. A. Gerdes, Rogier P. Voermans
المصدر: BMC Gastroenterology, Vol 17, Iss 1, Pp 1-8 (2017)
بيانات النشر: BMC, 2017.
سنة النشر: 2017
المجموعة: LCC:Diseases of the digestive system. Gastroenterology
مصطلحات موضوعية: Gallstones, Bariatric surgery, Roux-en-Y gastric bypass, Sleeve gastrectomy, Ursodeoxycholic acid, Cost-benefit analysis, Diseases of the digestive system. Gastroenterology, RC799-869
الوصف: Abstract Background The number of bariatric interventions for morbid obesity is increasing worldwide. Rapid weight loss is a major risk factor for gallstone development. Approximately 11 % of patients who underwent Roux-en-Y gastric bypass develop symptomatic gallstone disease. Gallstone disease can lead to severe complications and often requires hospitalization and surgery. Ursodeoxycholic acid (UDCA) prevents the formation of gallstones after bariatric surgery. However, randomized controlled trials with symptomatic gallstone disease as primary endpoint have not been conducted. Currently, major guidelines make no definite statement about postoperative UDCA prophylaxis and most bariatric centers do not prescribe UDCA. Methods A randomized, placebo-controlled, double-blind multicenter trial will be performed for which 980 patients will be included. The study population consists of consecutive patients scheduled to undergo Roux-en-Y gastric bypass or sleeve gastrectomy in three bariatric centers in the Netherlands. Patients will undergo a preoperative ultrasound and randomization will be stratified for pre-existing gallstones and for type of surgery. The intervention group will receive UDCA 900 mg once daily for six months. The placebo group will receive similar-looking placebo tablets. The primary endpoint is symptomatic gallstone disease after 24 months, defined as admission or hospital visit for symptomatic gallstone disease. Secondary endpoints consist of the development of gallstones on ultrasound at 24 months, number of cholecystectomies, side-effects of UDCA and quality of life. Furthermore, cost-effectiveness, cost-utility and budget impact analyses will be performed. Discussion The UPGRADE trial will answer the question whether UDCA reduces the incidence of symptomatic gallstone disease after Roux-en-Y gastric bypass or sleeve gastrectomy. Furthermore it will determine if treatment with UDCA is cost-effective. Trial registration Netherlands Trial Register (trialregister.nl) 6135 . Date registered: 21-Nov-2016.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1471-230X
Relation: http://link.springer.com/article/10.1186/s12876-017-0674-x; https://doaj.org/toc/1471-230X
DOI: 10.1186/s12876-017-0674-x
URL الوصول: https://doaj.org/article/ca137538bd74449b9dfe04f730a6b87c
رقم الأكسشن: edsdoj.137538bd74449b9dfe04f730a6b87c
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:1471230X
DOI:10.1186/s12876-017-0674-x