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A pilot study of implementation of endoscopic sleeve gastroplasty (ESG) in Norway.
Tønnesen, Christer Julseth; Hjelmesæth, Jøran; Aabakken, Lars; Lund, Randi Størdal; Johnson, Line Kristin; Hertel, Jens Kristoffer; Kalager, Mette; Løberg, Magnus; Bretthauer, Michael.
Afiliación
  • Tønnesen CJ; Clinical Effectiveness Research Group, University of Oslo, Oslo, Norway.
  • Hjelmesæth J; Clinical Effectiveness Research Group, Oslo University Hospital, Oslo, Norway.
  • Aabakken L; Section of Gastroenterology, Department of Transplantation Medicine, Oslo University Hospital, Oslo, Norway.
  • Lund RS; Department of Endocrinology, Obesity and Nutrition, Vestfold Hospital Trust, Tønsberg, Norway.
  • Johnson LK; Department of Endocrinology, Morbid Obesity and Preventive Medicine Institute of Clinical Medicine, University of Oslo, Norway.
  • Hertel JK; Clinical Effectiveness Research Group, University of Oslo, Oslo, Norway.
  • Kalager M; Clinical Effectiveness Research Group, Oslo University Hospital, Oslo, Norway.
  • Løberg M; Section of Gastroenterology, Department of Transplantation Medicine, Oslo University Hospital, Oslo, Norway.
  • Bretthauer M; Institute of Clinical Medicine, University of Oslo, Norway.
Scand J Gastroenterol ; 58(10): 1180-1184, 2023.
Article en En | MEDLINE | ID: mdl-37128713
BACKGROUND AND AIM: Bariatric surgery is the most effective treatment for obesity but is invasive and associated with serious complications. Endoscopic sleeve gastroplasty (ESG) is a less invasive weight loss procedure to reduce the stomach volume by full-thickness sutures. ESG has been adopted in many countries, but implementation at Scandinavian centres has not yet been documented. We performed a clinical pilot trial at a Norwegian centre with the primary objective to assess the feasibility of the ESG procedure. PATIENTS AND METHODS: We included the first 10 patients treated with ESG at a Norwegian centre in a single-arm pilot study. The eligibility criteria were either a body mass index (BMI) of 40-49.9 kg/m2, BMI 35-39.9 kg/m2 and at least one obesity-related comorbidity, or BMI 30-34.9 kg/m2 and type 2 diabetes. Patient follow-up resembled the scheme used for bariatric surgery at the center, including dietary plans and outpatient visits. RESULTS: All procedures were technically successful except for one patient who had adhesions between the stomach and anterior abdominal wall, related to a prior hernia repair, resulting in less-than-intended stomach volume reduction. Mean total body weight loss (TBWL) after 26 and 52 weeks was 12.2% (95% CI 8.1-16.2) and 9.1% (95% CI 3.3 - 15.0). One patient experienced a minor suture-induced diaphragmatic injury, which was successfully managed conservatively. CONCLUSIONS: This first Scandinavian clinical trial of ESG, documenting the implementation of the procedure at a Norwegian center, demonstrated acceptable feasibility and safety, with large variations in individual weight loss during the 52-week follow-up period.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Obesidad Mórbida / Gastroplastia / Diabetes Mellitus Tipo 2 Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Scand J Gastroenterol Año: 2023 Tipo del documento: Article País de afiliación: Noruega

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Obesidad Mórbida / Gastroplastia / Diabetes Mellitus Tipo 2 Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Scand J Gastroenterol Año: 2023 Tipo del documento: Article País de afiliación: Noruega