2016
DOI: 10.1016/j.soard.2016.02.006
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Endoscopic treatments of obesity: a comprehensive review

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Cited by 25 publications
(14 citation statements)
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“…The Full Sense Bariatric Device (Baker, Michigan) is an endoscopically placed stent that traverses the gastroesophageal junction (GEJ) and places pressure on the distal esophagus and gastric cardia to induce satiety. This temporary metal device has not yet been studied in randomized controlled clinical trials and is not FDA approved …”
Section: Non‐space‐occupying Therapiesmentioning
confidence: 99%
“…The Full Sense Bariatric Device (Baker, Michigan) is an endoscopically placed stent that traverses the gastroesophageal junction (GEJ) and places pressure on the distal esophagus and gastric cardia to induce satiety. This temporary metal device has not yet been studied in randomized controlled clinical trials and is not FDA approved …”
Section: Non‐space‐occupying Therapiesmentioning
confidence: 99%
“…335 Bariatric surgery in liver transplantation may be performed more frequently in the future in patients with earlystage liver disease, to reduce weight-related CVE; however, the efficacy of this approach requires verification by welldesigned clinical studies. 354 Noninvasive endoscopic techniques, such as use of the endobarrier, 355,356 may be effective and safer alternative approaches but their role in transplant recipients has to be assessed.…”
Section: Lifestyle Changesmentioning
confidence: 99%
“…Currently, the balloons are required, per FDA guidance, to be removed after 6 months because of concern that they slowly deflate and migrate, causing complications such as obstruction. At the time of removal, there has been up to 30%–50% mean EWL [31]. One such balloon, the BioEnterics Intragastric Balloon (Inamed Corp., Santa Barbara, CA, USA), now known as the Orbera balloon (Obalon Therapeutics, Carlsbad, CA, USA), showed a 58% ± 19% EWL at the time of removal (6 months), 39% ± 14% at 1 year, 25% ± 8% at 2 years, and 17% ± 8% at 5 years after removal [32] in a study of 122 patients.…”
Section: Endoscopic Bariatric Techniquesmentioning
confidence: 99%
“…It is left in place for 6 months. Although patients treated with the device showed a mean 32% EWL, a significant decrease in HbA 1c , and a significant decrease in antidiabetic drug requirement, the trial for this procedure was prematurely terminated because of the incidence of hepatic abscesses [31, 39]. The EndoBarrier has CE mark approval in Europe and is indicated for patients with type-2 diabetes and obesity, but is not approved for sale in the U.S. [40].…”
Section: Endoscopic Bariatric Techniquesmentioning
confidence: 99%
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