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Nafamostat mesilate for prevention of post-endoscopic retrograde cholangiopancreatography pancreatitis: A systematic review and meta-analysis based on prospective, randomized, and controlled trials

OBJECTIVES: To evaluate the efficacy of nafamostat mesilate in the prevention of post–endoscopic retrograde cholangiopancreatography pancreatitis (PEP) by conduct a systematic review and meta-analysis. METHOD: We retrieved for all randomized controlled trials (RCTs) about compare nafamostat mesilate...

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Autores principales: Xie, Yu, Cheng, Ziyao, Deng, Cunliang, Deng, Mingming, Zhang, Hailong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578773/
https://www.ncbi.nlm.nih.gov/pubmed/37832051
http://dx.doi.org/10.1097/MD.0000000000035174
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author Xie, Yu
Cheng, Ziyao
Deng, Cunliang
Deng, Mingming
Zhang, Hailong
author_facet Xie, Yu
Cheng, Ziyao
Deng, Cunliang
Deng, Mingming
Zhang, Hailong
author_sort Xie, Yu
collection PubMed
description OBJECTIVES: To evaluate the efficacy of nafamostat mesilate in the prevention of post–endoscopic retrograde cholangiopancreatography pancreatitis (PEP) by conduct a systematic review and meta-analysis. METHOD: We retrieved for all randomized controlled trials (RCTs) about compare nafamostat mesilate with placebo in preventing PEP published before August 23, 2022, in 5 major electronic databases. The primary outcome was PEP rate, and the secondary outcome was post-ERCP hyperamylasemia (PEHA) rate. Subgroup analyses were performed to reveal the factors that may affect the preventive effect of nafamostat. Assessment of the quality of evidence was conducted based on Grading of Recommendations, Assessment, Development and Evaluations (GRADE) system. RESULTS: According to the search strategy and criteria of inclusion and exclusion, 8 articles with a number of 3210 patients were included. The PEP incidence of the nafamostat group was inferior compared with the placebo group (4.6% vs 8.5%, RR = 0.50, 95% CI: 0.38–0.66). Subgroup analyses revealed that nafamostat had a preventive effect on patients with different risk stratification (High-risk: RR = 0.61, 95% CI: 0.43–0.86, Low-risk: RR = 0.28; 95% CI: 0.17–0.47). Different doses (20 mg: RR = 0.50, 95% CI: 0.36–0.69, 50 mg: RR = 0.45, 95% CI: 0.27–0.74) and duration (<12 hour: RR = 0.55, 95% CI: 0.37–0.81, ≥12 h: RR = 0.44, 95% CI: 0.29–0.66) of administration of nafamostat are adequate for the prevention of PEP, but postoperative administration may not help (preoperative: RR = 0.52, 95% CI: 0.39–0.69, postoperative: RR = 0.54, 95% CI: 0.23–1.23). Nafamostat may not efficacious in preventing severe PEP (Mild: RR = 0.49, 95% CI, 0.35–0.68, Moderate: RR = 0.47, 95% CI: 0.25–0.86, Severe: RR = 0.91, 95% CI, 0.25–3.29) or in low-quality studies (Low-quality: RR = 0.69, 95% CI: 0.13–3.60, High-quality: RR = 0.49, 95% CI: 0.37–0.65). CONCLUSION: Preoperative use of nafamostat can effectively prevent PEP in patients with various risk stratification. Nafamostat can prevent mild and moderate PEP, but may not prevent severe PEP and PEHA. There should be more high-quality RCTs in future to strengthen the evidence of nafamostat in preventing PEP.
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spelling pubmed-105787732023-10-17 Nafamostat mesilate for prevention of post-endoscopic retrograde cholangiopancreatography pancreatitis: A systematic review and meta-analysis based on prospective, randomized, and controlled trials Xie, Yu Cheng, Ziyao Deng, Cunliang Deng, Mingming Zhang, Hailong Medicine (Baltimore) Systematic Review and Meta-Analysis OBJECTIVES: To evaluate the efficacy of nafamostat mesilate in the prevention of post–endoscopic retrograde cholangiopancreatography pancreatitis (PEP) by conduct a systematic review and meta-analysis. METHOD: We retrieved for all randomized controlled trials (RCTs) about compare nafamostat mesilate with placebo in preventing PEP published before August 23, 2022, in 5 major electronic databases. The primary outcome was PEP rate, and the secondary outcome was post-ERCP hyperamylasemia (PEHA) rate. Subgroup analyses were performed to reveal the factors that may affect the preventive effect of nafamostat. Assessment of the quality of evidence was conducted based on Grading of Recommendations, Assessment, Development and Evaluations (GRADE) system. RESULTS: According to the search strategy and criteria of inclusion and exclusion, 8 articles with a number of 3210 patients were included. The PEP incidence of the nafamostat group was inferior compared with the placebo group (4.6% vs 8.5%, RR = 0.50, 95% CI: 0.38–0.66). Subgroup analyses revealed that nafamostat had a preventive effect on patients with different risk stratification (High-risk: RR = 0.61, 95% CI: 0.43–0.86, Low-risk: RR = 0.28; 95% CI: 0.17–0.47). Different doses (20 mg: RR = 0.50, 95% CI: 0.36–0.69, 50 mg: RR = 0.45, 95% CI: 0.27–0.74) and duration (<12 hour: RR = 0.55, 95% CI: 0.37–0.81, ≥12 h: RR = 0.44, 95% CI: 0.29–0.66) of administration of nafamostat are adequate for the prevention of PEP, but postoperative administration may not help (preoperative: RR = 0.52, 95% CI: 0.39–0.69, postoperative: RR = 0.54, 95% CI: 0.23–1.23). Nafamostat may not efficacious in preventing severe PEP (Mild: RR = 0.49, 95% CI, 0.35–0.68, Moderate: RR = 0.47, 95% CI: 0.25–0.86, Severe: RR = 0.91, 95% CI, 0.25–3.29) or in low-quality studies (Low-quality: RR = 0.69, 95% CI: 0.13–3.60, High-quality: RR = 0.49, 95% CI: 0.37–0.65). CONCLUSION: Preoperative use of nafamostat can effectively prevent PEP in patients with various risk stratification. Nafamostat can prevent mild and moderate PEP, but may not prevent severe PEP and PEHA. There should be more high-quality RCTs in future to strengthen the evidence of nafamostat in preventing PEP. Lippincott Williams & Wilkins 2023-10-13 /pmc/articles/PMC10578773/ /pubmed/37832051 http://dx.doi.org/10.1097/MD.0000000000035174 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal.
spellingShingle Systematic Review and Meta-Analysis
Xie, Yu
Cheng, Ziyao
Deng, Cunliang
Deng, Mingming
Zhang, Hailong
Nafamostat mesilate for prevention of post-endoscopic retrograde cholangiopancreatography pancreatitis: A systematic review and meta-analysis based on prospective, randomized, and controlled trials
title Nafamostat mesilate for prevention of post-endoscopic retrograde cholangiopancreatography pancreatitis: A systematic review and meta-analysis based on prospective, randomized, and controlled trials
title_full Nafamostat mesilate for prevention of post-endoscopic retrograde cholangiopancreatography pancreatitis: A systematic review and meta-analysis based on prospective, randomized, and controlled trials
title_fullStr Nafamostat mesilate for prevention of post-endoscopic retrograde cholangiopancreatography pancreatitis: A systematic review and meta-analysis based on prospective, randomized, and controlled trials
title_full_unstemmed Nafamostat mesilate for prevention of post-endoscopic retrograde cholangiopancreatography pancreatitis: A systematic review and meta-analysis based on prospective, randomized, and controlled trials
title_short Nafamostat mesilate for prevention of post-endoscopic retrograde cholangiopancreatography pancreatitis: A systematic review and meta-analysis based on prospective, randomized, and controlled trials
title_sort nafamostat mesilate for prevention of post-endoscopic retrograde cholangiopancreatography pancreatitis: a systematic review and meta-analysis based on prospective, randomized, and controlled trials
topic Systematic Review and Meta-Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578773/
https://www.ncbi.nlm.nih.gov/pubmed/37832051
http://dx.doi.org/10.1097/MD.0000000000035174
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