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Systematic Review with Trial Sequential Analysis of Prophylactic Antibiotics for Acute Pancreatitis
Background/Objectives: Prophylactic antibiotics (PAB) are being still widely used for treatment of acute pancreatitis (AP) despite trials showing no firm evidence of efficacy. We aimed to evaluate effects of PAB for AP in a meta-analysis and the need for further research by trial sequential analysis...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9495153/ https://www.ncbi.nlm.nih.gov/pubmed/36139970 http://dx.doi.org/10.3390/antibiotics11091191 |
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author | Poropat, Goran Goričanec, Karla Lacković, Alojzije Kresović, Andrea Lončarić, Antun Marušić, Martina |
author_facet | Poropat, Goran Goričanec, Karla Lacković, Alojzije Kresović, Andrea Lončarić, Antun Marušić, Martina |
author_sort | Poropat, Goran |
collection | PubMed |
description | Background/Objectives: Prophylactic antibiotics (PAB) are being still widely used for treatment of acute pancreatitis (AP) despite trials showing no firm evidence of efficacy. We aimed to evaluate effects of PAB for AP in a meta-analysis and the need for further research by trial sequential analysis (TSA). Methods: Medline, Scopus and Web of Science were searched for randomized clinical trials. Primary outcomes were all infections and mortality. Secondary outcomes comprised infected pancreatic necrosis (IPN), specific infections, organ failure, surgical interventions, and length of hospital stay. Results: Twenty-one trials with 1383 pts were included. PAB were received by 703 pts, while 680 were controls. Mortality was similar with RR 0.85 (95% CI 0.66–1.10). Infections were significantly reduced (RR 0.60; 95% CI 0.49–0.74), mainly due to decreased risk of sepsis (RR 0.43; 95% CI 0.25–0.73) and urinary tract infections (RR 0.46; 95% CI 0.25–0.86). No significant reduction for IPN was shown (RR 0.81; 95% CI 0.63–1.04). Length of hospital stay was diminished by MD −6.65 (95% CI −8.86 to −4.43) days. TSA for all infections showed that the cumulative Z score crossed both conventional and monitoring boundaries at 526 pts from a heterogeneity-corrected required information size of 1113 pts based on a 40% incidence of infections in the control group, RRR of 30%, alpha 5%, beta 20%, and heterogeneity 56%. Conclusions: PABs decrease the rate of infections in AP, mainly due to RRR of extra-pancreatic infections, requiring no further research. No significant effect is shown on IPN and mortality, although firmer evidence is needed. |
format | Online Article Text |
id | pubmed-9495153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94951532022-09-23 Systematic Review with Trial Sequential Analysis of Prophylactic Antibiotics for Acute Pancreatitis Poropat, Goran Goričanec, Karla Lacković, Alojzije Kresović, Andrea Lončarić, Antun Marušić, Martina Antibiotics (Basel) Systematic Review Background/Objectives: Prophylactic antibiotics (PAB) are being still widely used for treatment of acute pancreatitis (AP) despite trials showing no firm evidence of efficacy. We aimed to evaluate effects of PAB for AP in a meta-analysis and the need for further research by trial sequential analysis (TSA). Methods: Medline, Scopus and Web of Science were searched for randomized clinical trials. Primary outcomes were all infections and mortality. Secondary outcomes comprised infected pancreatic necrosis (IPN), specific infections, organ failure, surgical interventions, and length of hospital stay. Results: Twenty-one trials with 1383 pts were included. PAB were received by 703 pts, while 680 were controls. Mortality was similar with RR 0.85 (95% CI 0.66–1.10). Infections were significantly reduced (RR 0.60; 95% CI 0.49–0.74), mainly due to decreased risk of sepsis (RR 0.43; 95% CI 0.25–0.73) and urinary tract infections (RR 0.46; 95% CI 0.25–0.86). No significant reduction for IPN was shown (RR 0.81; 95% CI 0.63–1.04). Length of hospital stay was diminished by MD −6.65 (95% CI −8.86 to −4.43) days. TSA for all infections showed that the cumulative Z score crossed both conventional and monitoring boundaries at 526 pts from a heterogeneity-corrected required information size of 1113 pts based on a 40% incidence of infections in the control group, RRR of 30%, alpha 5%, beta 20%, and heterogeneity 56%. Conclusions: PABs decrease the rate of infections in AP, mainly due to RRR of extra-pancreatic infections, requiring no further research. No significant effect is shown on IPN and mortality, although firmer evidence is needed. MDPI 2022-09-03 /pmc/articles/PMC9495153/ /pubmed/36139970 http://dx.doi.org/10.3390/antibiotics11091191 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Systematic Review Poropat, Goran Goričanec, Karla Lacković, Alojzije Kresović, Andrea Lončarić, Antun Marušić, Martina Systematic Review with Trial Sequential Analysis of Prophylactic Antibiotics for Acute Pancreatitis |
title | Systematic Review with Trial Sequential Analysis of Prophylactic Antibiotics for Acute Pancreatitis |
title_full | Systematic Review with Trial Sequential Analysis of Prophylactic Antibiotics for Acute Pancreatitis |
title_fullStr | Systematic Review with Trial Sequential Analysis of Prophylactic Antibiotics for Acute Pancreatitis |
title_full_unstemmed | Systematic Review with Trial Sequential Analysis of Prophylactic Antibiotics for Acute Pancreatitis |
title_short | Systematic Review with Trial Sequential Analysis of Prophylactic Antibiotics for Acute Pancreatitis |
title_sort | systematic review with trial sequential analysis of prophylactic antibiotics for acute pancreatitis |
topic | Systematic Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9495153/ https://www.ncbi.nlm.nih.gov/pubmed/36139970 http://dx.doi.org/10.3390/antibiotics11091191 |
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