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A systematic review and meta-analysis of randomised controlled trials of delayed primary wound closure in contaminated abdominal wounds
A systematic review and meta-analysis was conducted to compare surgical site infection (SSI) between delayed primary (DPC) and primary wound closure (PC) in complicated appendicitis and other contaminated abdominal wounds. Medline and Scopus were searched from their beginning to November 2013 to ide...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162947/ https://www.ncbi.nlm.nih.gov/pubmed/25221617 http://dx.doi.org/10.1186/1749-7922-9-49 |
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author | Siribumrungwong, Boonying Noorit, Pinit Wilasrusmee, Chumpon Thakkinstian, Ammarin |
author_facet | Siribumrungwong, Boonying Noorit, Pinit Wilasrusmee, Chumpon Thakkinstian, Ammarin |
author_sort | Siribumrungwong, Boonying |
collection | PubMed |
description | A systematic review and meta-analysis was conducted to compare surgical site infection (SSI) between delayed primary (DPC) and primary wound closure (PC) in complicated appendicitis and other contaminated abdominal wounds. Medline and Scopus were searched from their beginning to November 2013 to identify randomised controlled trials (RCTs) comparing SSI and length of stay between DPC and PC. Studies’ selection, data extraction, and risk of bias assessment were done by two independent authors. The risk ratio and unstandardised mean difference were pooled for SSI and length of stay, respectively. Among 8 eligible studies, 5 studies were done in complicated appendicitis, 2 with mixed complicated appendicitis and other types of abdominal operation and 1 with ileostomy closure. Most studies (75%) had high risk of bias in sequence generation and allocation concealment. Among 6 RCTs of complicated appendicitis underwent open appendectomy, the SSI between PC and DPC were not significantly different with a risk ratio of 0.89 (95% CI: 0.46, 1.73). DPC had a significantly 1.6 days (95% CI: 1.41, 1.79) longer length of stay than PC. Our evidence suggested there might be no advantage of DPC over PC in reducing SSI in complicated appendicitis. However, this was based on a small number of studies with low quality. A large scale RCT is further required. |
format | Online Article Text |
id | pubmed-4162947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41629472014-09-14 A systematic review and meta-analysis of randomised controlled trials of delayed primary wound closure in contaminated abdominal wounds Siribumrungwong, Boonying Noorit, Pinit Wilasrusmee, Chumpon Thakkinstian, Ammarin World J Emerg Surg Review A systematic review and meta-analysis was conducted to compare surgical site infection (SSI) between delayed primary (DPC) and primary wound closure (PC) in complicated appendicitis and other contaminated abdominal wounds. Medline and Scopus were searched from their beginning to November 2013 to identify randomised controlled trials (RCTs) comparing SSI and length of stay between DPC and PC. Studies’ selection, data extraction, and risk of bias assessment were done by two independent authors. The risk ratio and unstandardised mean difference were pooled for SSI and length of stay, respectively. Among 8 eligible studies, 5 studies were done in complicated appendicitis, 2 with mixed complicated appendicitis and other types of abdominal operation and 1 with ileostomy closure. Most studies (75%) had high risk of bias in sequence generation and allocation concealment. Among 6 RCTs of complicated appendicitis underwent open appendectomy, the SSI between PC and DPC were not significantly different with a risk ratio of 0.89 (95% CI: 0.46, 1.73). DPC had a significantly 1.6 days (95% CI: 1.41, 1.79) longer length of stay than PC. Our evidence suggested there might be no advantage of DPC over PC in reducing SSI in complicated appendicitis. However, this was based on a small number of studies with low quality. A large scale RCT is further required. BioMed Central 2014-09-06 /pmc/articles/PMC4162947/ /pubmed/25221617 http://dx.doi.org/10.1186/1749-7922-9-49 Text en © Siribumrungwong et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Siribumrungwong, Boonying Noorit, Pinit Wilasrusmee, Chumpon Thakkinstian, Ammarin A systematic review and meta-analysis of randomised controlled trials of delayed primary wound closure in contaminated abdominal wounds |
title | A systematic review and meta-analysis of randomised controlled trials of delayed primary wound closure in contaminated abdominal wounds |
title_full | A systematic review and meta-analysis of randomised controlled trials of delayed primary wound closure in contaminated abdominal wounds |
title_fullStr | A systematic review and meta-analysis of randomised controlled trials of delayed primary wound closure in contaminated abdominal wounds |
title_full_unstemmed | A systematic review and meta-analysis of randomised controlled trials of delayed primary wound closure in contaminated abdominal wounds |
title_short | A systematic review and meta-analysis of randomised controlled trials of delayed primary wound closure in contaminated abdominal wounds |
title_sort | systematic review and meta-analysis of randomised controlled trials of delayed primary wound closure in contaminated abdominal wounds |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162947/ https://www.ncbi.nlm.nih.gov/pubmed/25221617 http://dx.doi.org/10.1186/1749-7922-9-49 |
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