Adjustable intragastric balloon for treatment of obesity: a multicentre, open-label, randomised clinical trial

被引:54
|
作者
Abu Dayyeh, Barham K. [1 ]
Maselli, Daniel B. [1 ]
Rapaka, Babusai [1 ]
Lavin, Thomas [2 ]
Noar, Mark [3 ]
Hussan, Hisham [4 ]
Chapman, Christopher G. [5 ]
Popov, Violeta [6 ]
Jirapinyo, Pichamol [8 ]
Acosta, Andres [1 ]
Vargas, Eric J. [1 ]
Storm, Andrew C. [1 ]
Bazerbachi, Fateh [7 ]
Ryou, Marvin [8 ]
French, Matthew [2 ]
Noria, Sabrena [4 ]
Molina, Daniel [9 ]
Thompson, Christopher C. [8 ]
机构
[1] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN 55905 USA
[2] Surg Associates Louisiana, Metairie, LA USA
[3] Endoscop MicroSurg Associates, Towson, MD USA
[4] Ohio State Univ, Div Gastroenterol Hepatol & Nutr, Wexner Med Ctr, Columbus, OH 43210 USA
[5] Univ Chicago Med, Div Gastroenterol Hepatol & Nutr, Chicago, IL USA
[6] NYU Langone Hlth, VA Med Ctr, Div Gastroenterol, New York, NY USA
[7] St Cloud Hosp, CentraCare, Intervent Endoscopy Program, St Cloud, MN USA
[8] Brigham & Womens Hosp, Div Gastroenterol, Boston, MA 02115 USA
[9] Tech Resources Int, Biostat & Clin Data Management, Bethesda, MD USA
来源
LANCET | 2021年 / 398卷 / 10315期
关键词
SEMAGLUTIDE; 2.4; MG; WEIGHT MANAGEMENT; BARIATRIC SURGERY;
D O I
10.1016/S0140-6736(21)02394-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Intragastric balloons are anatomy-preserving, minimally invasive obesity therapies. Enhanced tolerance and durability could help broaden clinical adoption. We investigated the safety and efficacy of an adjustable intragastric balloon (aIGB) in adults with obesity. Methods In this prospective, multicentre, open-label, randomised clinical trial done at seven US sites, adults aged 22-65 years with obesity were randomly assigned (2:1) to aIGB with lifestyle intervention or lifestyle intervention alone (control) for 32 weeks. Balloon volume could be increased to facilitate weight loss or decreased for tolerability. Coprimary endpoints included mean percentage total bodyweight loss and responder rate (>= 5% total bodyweight loss) at 32 weeks. We used a multiple imputed intention-to-treat population analysis. This study was registered with ClinicalTrials.gov , NCT02812160. Findings Between Aug 9,2016, and Dec 7,2018, we randomly assigned 288 patients to aIGB (n=187 [65%]) or control (n=101 [35%]) groups. Mean total bodyweight loss at 32 weeks was 15.0% (95% CI 13.9-16.1) in the aIGB group versus 3.3% (2.0-4.6) in the control group (p<0.0001). Clinical response was observed in 171 (92%) patients in the aIGB group. Adjustments to the aIGB occurred in 145 (80%) patients for weight loss plateau or intolerance. Upward volume adjustment facilitated an additional mean 5.2% (4.5-5.8) total bodyweight loss. Downward volume adjustment allowed 21 (75%) patients in the aIGB group to complete the full duration of therapy. Intolerance caused early removal of the device in 31 (17%) patients. No micronutrient deficiencies were observed in the aIGB cohort. Device-related serious adverse events were observed in seven (4%) patients, without any deaths. Interpretation When aIGB was combined with lifestyle modification, significant weight loss was achieved and maintained for 6 months following removal. Balloon volume adjustability permitted individualised therapy, maximising weight loss and tolerance. Copyright (C) 2021 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1965 / 1973
页数:9
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