학술논문

One-year results of gastric peroral endoscopic myotomy for refractory gastroparesis: a French multicenter study.
Document Type
Journal Article
Source
Endoscopy. 2021, Vol. 53 Issue 5, p480-490. 11p.
Subject
*GASTROPARESIS
*ODDS ratio
*MYOTOMY
*GASTROINTESTINAL motility
*ESOPHAGUS
*RESEARCH
*RESEARCH methodology
*RETROSPECTIVE studies
*MEDICAL cooperation
*EVALUATION research
*TREATMENT effectiveness
*COMPARATIVE studies
*ESOPHAGEAL achalasia
*LONGITUDINAL method
Language
ISSN
0013-726X
Abstract
Background: Data on the long-term outcomes of gastric peroral endoscopic myotomy (G-POEM) for refractory gastroparesis are lacking. We report the results of a large multicenter long-term follow-up study of G-POEM for refractory gastroparesis.Methods: This was a retrospective multicenter study of all G-POEM operations performed in seven expert French centers for refractory gastroparesis with at least 1 year of follow-up. The primary endpoint was the 1-year clinical success rate, defined as at least a 1-point improvement in the Gastroparesis Cardinal Symptom Index (GCSI).Results: 76 patients were included (60.5 % women; age 56 years). The median symptom duration was 48 months. The median gastric retention at 4 hours (H4) before G-POEM was 45 % (interquartile range [IQR] 29 % - 67 %). The median GCSI before G-POEM was 3.6 (IQR 2.8 - 4.0). Clinical success was achieved in 65.8 % of the patients at 1 year, with a median rate of reduction in the GCSI score of 41 %. In logistic regression analysis, only a high preoperative GCSI satiety subscale score was predictive of clinical success (odds ratio [OR] 3.41, 95 % confidence interval [CI] 1.01 - 11.54; P = 0.048), while a high rate of gastric retention at H4 was significantly associated with clinical failure (OR 0.97, 95 %CI 0.95 - 1.00; P = 0.03).Conclusions: The results confirm the efficacy of G-POEM for the treatment of refractory gastroparesis, as evidenced by a 65.8 % clinical success rate at 1 year. Although G-POEM is promising, prospective sham-controlled trials are urgently needed to confirm its efficacy and identify the patient populations who will benefit most from this procedure. [ABSTRACT FROM AUTHOR]