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Conversion of AspireAssist System® to Sleeve Gastrectomy: Technical Video Description.
Vilallonga, Ramon; Bademci, Refik; Roriz-Silva, Renato; Sanchez-Cordero, Sergi; Curbelo, Yuhamy; Almanza, Ariel.
Afiliación
  • Vilallonga R; QUIROBES, Integral Obesity Care, Centro Médico Teknon, C. Marquesa de Vilallonga, 12, 08017, Barcelona, Spain. vilallongapuy@hotmail.com.
  • Bademci R; Endocrine, Metabolic and Bariatric Unit, General Surgery Department, Vall d'Hebron University Hospital, Universitat Autònoma de Barcelona, Center of Excellence for the EAC-BC, Barcelona, Spain. vilallongapuy@hotmail.com.
  • Roriz-Silva R; Camlica Hospital, Istanbul Medipol University, 34767, Istanbul, Turkey.
  • Sanchez-Cordero S; Department of Medicine, Division of General Surgery, Hospital de Base of Porto Velho, Federal University of Rondônia - Unir, Porto Velho, RO, Brazil.
  • Curbelo Y; General Surgery Department, Consorci Sanitari de l'Anoia, Barcelona, Spain.
  • Almanza A; General Surgery Department, Hospital Universitari de Vic (Consorci Hospitalari de Vic), Vic, Spain.
Obes Surg ; 29(8): 2715-2717, 2019 08.
Article en En | MEDLINE | ID: mdl-31183784
ABSTRACT

PURPOSE:

The AspireAssist System® (Aspire Bariatrics, Inc. King of Prussia, PA) is a new endoscopic procedure used to treat obese patients. The aim of this dedicated video is to present a case that required revision surgery due to failure of the AspireAssist System®, and to show how the cannula was removed from the abdomen, and why sleeve gastrectomy (SG) was a good option for revisional surgery in that patient. We aim to discuss technical aspects. PATIENT AND

METHODS:

A 43-year-old female patient who underwent a placement in 2016. Her initial BMI (body mass index) was 38 kg/m2, with a follow-up period of 26 months. A revisional surgery was performed including dissection of the previous gastric fistula and adhesiolysis from the previous AspireAssist System® placement. A complete dissection of the gastrostomy, including removal of all the system, was done. A decision was made, once the incisura angularis and the placement of a 40 Fch bougie showed that the transection could be performed. SG was done. Patients showed an uneventful postoperative course and 4 months follow-up with 45% EWL.

CONCLUSION:

In case of having the device in place, the surgeon must be aware to remove intraoperatively or endoscopically, the device. Surgeons should consider endoscopic removal of the AspireAssist System® before conversion to another procedure (SG or GBP) at least 6 months of the removal. Removal of the AspireAssist System® should be performed endoscopically but direct conversion to another bariatric procedure can be considered, either to SG or GBP depending on the technical intraoperative aspects.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Reoperación / Fístula Gástrica / Remoción de Dispositivos / Gastrectomía / Intubación Gastrointestinal / Obesidad Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Adult / Female / Humans Idioma: En Revista: Obes Surg Asunto de la revista: METABOLISMO Año: 2019 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Reoperación / Fístula Gástrica / Remoción de Dispositivos / Gastrectomía / Intubación Gastrointestinal / Obesidad Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Adult / Female / Humans Idioma: En Revista: Obes Surg Asunto de la revista: METABOLISMO Año: 2019 Tipo del documento: Article País de afiliación: España