EUS- versus ERCP-guided biliary drainage for malignant biliary obstruction: a systematic review and meta-analysis of randomized controlled trials.
Autor: | Barbosa EC; Department of Medicine, Evangelical University of Goiás, Anápolis, Brazil. Electronic address: eduardo.cerchi27@gmail.com., Santo PADE; Diagnostic Imaging and Specialized Diagnosis Unit, University Hospital of Federal University of São Carlos, São Carlos, Brazil., Baraldo S; Department of Endoscopy, Barretos Cancer Hospital, Barretos, Brazil., Nau AL; Department of Pediatric Gastroenterology, Jaraguá Hospital, Jaraguá do Sul, Brazil., Meine GC; Division of Gastroenterology, Department of Internal Medicine, Feevale University, Novo Hamburgo, Brazil. |
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Jazyk: | angličtina |
Zdroj: | Gastrointestinal endoscopy [Gastrointest Endosc] 2024 Sep; Vol. 100 (3), pp. 395-405.e8. Date of Electronic Publication: 2024 Apr 20. |
DOI: | 10.1016/j.gie.2024.04.019 |
Abstrakt: | Background and Aims: Increasing evidence supports EUS-guided biliary drainage (EUS-BD) as a potential alternative to ERCP-guided biliary drainage (ERCP-BD) in the primary treatment of malignant biliary obstruction (MBO). This systematic review and meta-analysis aimed to compare the efficacy and safety of both techniques as the initial approach for MBO. Methods: We systematically searched in MEDLINE, Embase, and Cochrane databases for randomized controlled trials comparing both techniques and reporting at least one of the outcomes of interest. The pooled estimates were calculated using the random-effects model, and I 2 statistics were used to evaluate heterogeneity. Results: We included 6 randomized controlled trials (577 patients). There were no significant differences between both groups in terms of stent patency (mean difference [MD], 8.18 days; 95% confidence interval [CI], -22.55 to 38.91), procedure time (MD, -6.31 minutes; 95% CI, -12.68 to 0.06), and survival (MD, 4.59 days; 95% CI, -34.23 to 43.40). Technical success (risk ratio [RR], 1.04; 95% CI, 0.96-1.13), clinical success (RR, 1.02; 95% CI, 0.96-1.08), overall adverse events (RR, 0.58; 95% CI, 0.24-1.43), and cholangitis (RR, 1.19; 95% CI, 0.39-3.61) were also similar between groups. However, the hospital stay was significantly shorter (MD, -1.03 days; 95% CI, -1.53 to -0.53), and the risk of reintervention (RR, 0.57; 95% CI, 0.37-0.88), postprocedure pancreatitis (RR, 0.15; 95% CI, 0.03-0.66), and tumor ingrowth/overgrowth (RR, 0.28; 95% CI, 0.11-0.70) were significantly lower with EUS-BD. Conclusions: EUS-BD and ERCP-BD had similar efficacy and safety as the initial approach for MBO. However, EUS-BD had a significantly lower risk of reintervention, postprocedure pancreatitis, tumor ingrowth/overgrowth, and reduced hospital stay. Competing Interests: Disclosure All authors disclosed no financial relationships. (Copyright © 2024 American Society for Gastrointestinal Endoscopy. Published by Elsevier Inc. All rights reserved.) |
Databáze: | MEDLINE |
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