Non-superiority of lumen-apposing metal stents over plastic stents for drainage of walled-off necrosis in a randomised trial
- PMID: 29858393
- PMCID: PMC6582745
- DOI: 10.1136/gutjnl-2017-315335
Non-superiority of lumen-apposing metal stents over plastic stents for drainage of walled-off necrosis in a randomised trial
Abstract
Objective: Although lumen-apposing metal stents (LAMS) are increasingly used for drainage of walled-off necrosis (WON), their advantage over plastic stents is unclear. We compared efficacy of LAMS and plastic stents for WON drainage.
Design: Patients with WON were randomised to endoscopic ultrasound-guided drainage using LAMS or plastic stents. Primary outcome was comparing total number of procedures to achieve treatment success defined as symptom relief in conjunction with WON resolution on CT at 6 months. Secondary outcomes were treatment success, procedure duration, clinical/stent-related adverse events, readmissions, length of hospital stay (LOS) and costs.
Results: 60 patients underwent LAMS (n=31) or plastic stent (n=29) placement. There was no significant difference in total number of procedures performed (median 2 (range 2-7) LAMS vs 3 (range 2-7) plastic, p=0.192), treatment success, clinical adverse events, readmissions, LOS and overall treatment costs between cohorts. Although procedure duration was shorter (15 vs 40 min, p<0.001), stent-related adverse events (32.3% vs 6.9%, p=0.01) and procedure costs (US$12 155 vs US$6609, p<0.001) were higher with LAMS. Significant stent-related adverse events were observed ≥3 weeks postintervention in LAMS cohort. Interim audit resulted in protocol amendment where CT scan was obtained at 3 weeks postintervention followed by LAMS removal if WON had resolved. After protocol amendment, there was no significant difference in adverse events between cohorts.
Conclusion: Except for procedure duration, there was no significant difference in treatment outcomes between LAMS and plastic stents. To minimise adverse events with LAMS, patients should undergo follow-up imaging and stent removal at 3 weeks if WON has resolved.
Trial registration number: NCT02685865.
Keywords: endoscopic ultrasonography; pancreatic disease.
© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2019. All rights reserved. No commercial use is permitted unless otherwise expressly granted.
Conflict of interest statement
Competing interests: SV: Consultant for Olympus Medical Systems Corporation and Boston Scientific Corporation. RH: Consultant for Olympus Medical Systems Corporation and Boston Scientific Corporation.
Figures
Comment in
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EUS-guided treatment of WON using lumen-apposing metal stents: protocol standardisation based on the occurrence of natural healing processes.Gut. 2019 Jul;68(7):1334-1335. doi: 10.1136/gutjnl-2018-316994. Epub 2018 Jul 20. Gut. 2019. PMID: 30030302 No abstract available.
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Single LAMS versus multigate plastic stent drainage of WON; fair comparison or apples versus oranges?Gut. 2019 Oct;68(10):1904-1905. doi: 10.1136/gutjnl-2018-317387. Epub 2018 Oct 9. Gut. 2019. PMID: 30301769 No abstract available.
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Lumen-apposing metal stent acted as an interim role in walled-off necrosis drainage.Gut. 2019 Dec;68(12):2255-2256. doi: 10.1136/gutjnl-2018-317494. Epub 2018 Oct 27. Gut. 2019. PMID: 30368455 No abstract available.
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Non-superiority of lumen-apposing metal stents: Is the evidence conclusive?Gut. 2019 Dec;68(12):2257. doi: 10.1136/gutjnl-2018-317777. Epub 2018 Nov 2. Gut. 2019. PMID: 30389713 No abstract available.
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Authors reply: treatment strategy for necrotising pancreatitis.Gut. 2020 Jan;69(1):189-190. doi: 10.1136/gutjnl-2018-317848. Epub 2018 Nov 17. Gut. 2020. PMID: 30448773 No abstract available.
References
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