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Systematic review and Meta-analysis: One-year outcomes of gastric peroral endoscopic myotomy for refractory gastroparesis

Journal

ALIMENTARY PHARMACOLOGY & THERAPEUTICS
Volume 55, Issue 2, Pages 168-177

Publisher

WILEY
DOI: 10.1111/apt.16725

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A meta-analysis evaluating the mid-term efficacy of gastric peroral endoscopic myotomy (G-POEM) found that it is associated with modest clinical success at 1 year, with a 61% clinical success rate and 8% adverse event rate. Additional studies with longer follow-up are needed to further assess its longer-term efficacy.
Background Several studies have examined the efficacy of gastric peroral endoscopic myotomy (G-POEM) for gastroparesis. Aim To evaluate the mid-term efficacy of G-POEM by meta-analysis of studies with a minimum 1 year of follow-up. Methods We reviewed several databases from inception to 10 June 2021 to identify studies that evaluated the efficacy of G-POEM in refractory gastroparesis, and had at least 1 year of follow-up. Our outcomes of interest were clinical success at 1 year, adverse events, difference in mean pre- and 1 year post-procedure Gastroparesis Cardinal Symptom Index (GCSI) score, and difference in mean pre- and post-procedure EndoFLIP measurements. We analysed data using a random-effects model and assessed heterogeneity by I-2 statistic. Results We included 10 studies comprising 482 patients. Pooled rates (95% CI) of clinical success at 1 year and adverse events were 61% (49%, 71%) and 8% (6%, 11%), respectively. Mean GCSI at 1 year post-procedure was significantly lower than pre-procedure; mean difference (MD) (95% CI) -1.4 (-1.9, -0.9). Mean post-procedure distensibility index was significantly higher than pre-procedure in the clinical success group at 40 and 50 mL volume distension; standardised mean difference (95% CI) 0.82 (0.07, 1.64) and 0.91 (0.32, 1.49), respectively. In the clinical failure group, there was no significant difference between mean pre- and post-procedure EndoFLIP measurements. Conclusions G-POEM is associated with modest clinical success at 1 year. Additional studies with longer follow-up are required to evaluate its longer-term efficacy.

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