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The Association Between Cephalosporin and Hypoprothrombinemia: A Systematic Review and Meta-Analysis
Cephalosporins that contain the N-methylthiotetrazole side chain (NMTT-cephalosporin) have been reported to be associated with coagulation-related adverse events; however, a comprehensive evaluation regarding the association is lacking. A systematic review and meta-analysis were conducted to assess...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6843226/ https://www.ncbi.nlm.nih.gov/pubmed/31623191 http://dx.doi.org/10.3390/ijerph16203937 |
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author | Park, Gi Hyue Kim, Seungyeon Kim, Min Soo Yu, Yun Mi Kim, Gun Hee Lee, Jeong Sang Lee, Euni |
author_facet | Park, Gi Hyue Kim, Seungyeon Kim, Min Soo Yu, Yun Mi Kim, Gun Hee Lee, Jeong Sang Lee, Euni |
author_sort | Park, Gi Hyue |
collection | PubMed |
description | Cephalosporins that contain the N-methylthiotetrazole side chain (NMTT-cephalosporin) have been reported to be associated with coagulation-related adverse events; however, a comprehensive evaluation regarding the association is lacking. A systematic review and meta-analysis were conducted to assess the safety profile of NMTT-cephalosporins with respect to hypoprothrombinemia and bleeding. The MEDLINE, Embase, Cochrane, and RISS databases were systematically searched for clinical studies up to October 2018. The association between NMTT-cephalosporins and hypoprothrombinemia was estimated using an odds ratio (OR) with a 95% confidence interval (CI). A total of 15 studies on cefamandole, cefoperazone, cefotetan, cefmetazole, and moxalactam were identified and included in the meta-analysis. Hypoprothrombinemia (OR 1.676, 95% CI 1.275–2.203) and prothrombin time (PT) prolongation (OR 2.050, 95% CI 1.398–3.005) were significantly associated with NMTT-cephalosporins, whereas bleeding was not (OR 1.359, 95% CI 0.920–2.009). Subgroup analyses revealed that cefoperazone (OR 2.506, 95% CI 1.293–4.860), cefamandole (OR 3.247, 95% CI 1.083–9.733), and moxalactam (OR 3.367, 95% CI 1.725–6.572) were significantly associated with hypoprothrombinemia. An Antimicrobial Stewardship Program led by a multidisciplinary team could play a critical role in monitoring cephalosporin-related hypoprothrombinemia or PT prolongation in patients with underlying clinical conditions at risk for bleeding. The multidisciplinary team could also assist in communicating the potential safety concerns regarding NMTT-cephalosporin use with healthcare professionals to decrease the risk of adverse events. |
format | Online Article Text |
id | pubmed-6843226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68432262019-11-25 The Association Between Cephalosporin and Hypoprothrombinemia: A Systematic Review and Meta-Analysis Park, Gi Hyue Kim, Seungyeon Kim, Min Soo Yu, Yun Mi Kim, Gun Hee Lee, Jeong Sang Lee, Euni Int J Environ Res Public Health Article Cephalosporins that contain the N-methylthiotetrazole side chain (NMTT-cephalosporin) have been reported to be associated with coagulation-related adverse events; however, a comprehensive evaluation regarding the association is lacking. A systematic review and meta-analysis were conducted to assess the safety profile of NMTT-cephalosporins with respect to hypoprothrombinemia and bleeding. The MEDLINE, Embase, Cochrane, and RISS databases were systematically searched for clinical studies up to October 2018. The association between NMTT-cephalosporins and hypoprothrombinemia was estimated using an odds ratio (OR) with a 95% confidence interval (CI). A total of 15 studies on cefamandole, cefoperazone, cefotetan, cefmetazole, and moxalactam were identified and included in the meta-analysis. Hypoprothrombinemia (OR 1.676, 95% CI 1.275–2.203) and prothrombin time (PT) prolongation (OR 2.050, 95% CI 1.398–3.005) were significantly associated with NMTT-cephalosporins, whereas bleeding was not (OR 1.359, 95% CI 0.920–2.009). Subgroup analyses revealed that cefoperazone (OR 2.506, 95% CI 1.293–4.860), cefamandole (OR 3.247, 95% CI 1.083–9.733), and moxalactam (OR 3.367, 95% CI 1.725–6.572) were significantly associated with hypoprothrombinemia. An Antimicrobial Stewardship Program led by a multidisciplinary team could play a critical role in monitoring cephalosporin-related hypoprothrombinemia or PT prolongation in patients with underlying clinical conditions at risk for bleeding. The multidisciplinary team could also assist in communicating the potential safety concerns regarding NMTT-cephalosporin use with healthcare professionals to decrease the risk of adverse events. MDPI 2019-10-16 2019-10 /pmc/articles/PMC6843226/ /pubmed/31623191 http://dx.doi.org/10.3390/ijerph16203937 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Park, Gi Hyue Kim, Seungyeon Kim, Min Soo Yu, Yun Mi Kim, Gun Hee Lee, Jeong Sang Lee, Euni The Association Between Cephalosporin and Hypoprothrombinemia: A Systematic Review and Meta-Analysis |
title | The Association Between Cephalosporin and Hypoprothrombinemia: A Systematic Review and Meta-Analysis |
title_full | The Association Between Cephalosporin and Hypoprothrombinemia: A Systematic Review and Meta-Analysis |
title_fullStr | The Association Between Cephalosporin and Hypoprothrombinemia: A Systematic Review and Meta-Analysis |
title_full_unstemmed | The Association Between Cephalosporin and Hypoprothrombinemia: A Systematic Review and Meta-Analysis |
title_short | The Association Between Cephalosporin and Hypoprothrombinemia: A Systematic Review and Meta-Analysis |
title_sort | association between cephalosporin and hypoprothrombinemia: a systematic review and meta-analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6843226/ https://www.ncbi.nlm.nih.gov/pubmed/31623191 http://dx.doi.org/10.3390/ijerph16203937 |
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