Safety and efficacy of lumen-apposing metal stents and double-pigtail plastic stents for endoscopic ultrasound-guided drainage of walled-off necrosis; a systematic review and meta-analysis

What is the best endoscopic treatment option for the walled-off necrosis (WON)? A brief comparison of lumen-apposing metal stents (LAMS), bi-flanged metallic stents (BFMS) and double-pigtail plastic stents (DPS) for the treatment of WON patients. How can we limit the adverse events and provide bette...

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Veröffentlicht in:Annals of medicine (Helsinki) 2023-12, Vol.55 (1), p.578-591
Hauptverfasser: Khizar, Hayat, Yufei, Hu, Yanhua, Wu, Wangyang, Chen, Ying, Bian, Chenyu, Le, Zhicheng, Huang, Ali, Kamran, Jianfeng, Yang
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Sprache:eng
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Zusammenfassung:What is the best endoscopic treatment option for the walled-off necrosis (WON)? A brief comparison of lumen-apposing metal stents (LAMS), bi-flanged metallic stents (BFMS) and double-pigtail plastic stents (DPS) for the treatment of WON patients. How can we limit the adverse events and provide better treatment. Patients with walled-off necrosis (WON) are still challenging to treat safely and effectively. Recently, double-pigtail plastic stents (DPS), bi-flanged metallic stents (BFMS), and lumen-apposing metal stents (LAMS) have been employed with endoscopic ultrasound-guided (EUS-guided) drainage. However, there is little solid evidence to support the effectiveness and safety of using stents. This study aims to compare the outcomes of the LAMS and the PS. Till July 2022, a thorough database search was done, and studies that met the criteria were chosen. By using the RevMan software, the technical and clinical success and other secondary outcomes were calculated. Subgroup analysis was performed between the LAMS and the BFMS. Fifteen studies (two randomized controlled trials and thirteen observational) with 687 patients receiving metal stents and 771 patients receiving plastic stents were selected for final analysis. There was no significant risk of bias or publication bias. The odds ratios (OR) for technical and clinical success were 0.36 (95% confidence interval (95% CI) 0.08, 1.52) and 2.26 (95%CI 1.62, 3.15), respectively. The OR for overall adverse events was 0.74 (95% CI 0.41, 1.34). In subgroup analysis, the LAMS and the BFMS showed the same outcomes. Compared to DPS, LAMS had better clinical outcomes and fewer side effects when treating patients with WON.
ISSN:0785-3890
1365-2060
DOI:10.1080/07853890.2022.2164048