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Adverse events caused by potential drug-drug interactions in an intensive care unit of a teaching hospital
OBJECTIVE: To evaluate the incidence of potential drug-drug interactions in an intensive care unit of a hospital, focusing on antimicrobial drugs. METHODS: This cross-sectional study analyzed electronic prescriptions of patients admitted to the intensive care unit of a teaching hospital between Janu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação de Medicina Intensiva Brasileira -
AMIB
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4738821/ https://www.ncbi.nlm.nih.gov/pubmed/26761473 http://dx.doi.org/10.5935/0103-507X.20150060 |
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author | Alvim, Mariana Macedo da Silva, Lidiane Ayres Leite, Isabel Cristina Gonçalves Silvério, Marcelo Silva |
author_facet | Alvim, Mariana Macedo da Silva, Lidiane Ayres Leite, Isabel Cristina Gonçalves Silvério, Marcelo Silva |
author_sort | Alvim, Mariana Macedo |
collection | PubMed |
description | OBJECTIVE: To evaluate the incidence of potential drug-drug interactions in an intensive care unit of a hospital, focusing on antimicrobial drugs. METHODS: This cross-sectional study analyzed electronic prescriptions of patients admitted to the intensive care unit of a teaching hospital between January 1 and March 31, 2014 and assessed potential drug-drug interactions associated with antimicrobial drugs. Antimicrobial drug consumption levels were expressed in daily doses per 100 patient-days. The search and classification of the interactions were based on the Micromedex(®) system. RESULTS: The daily prescriptions of 82 patients were analyzed, totaling 656 prescriptions. Antimicrobial drugs represented 25% of all prescription drugs, with meropenem, vancomycin and ceftriaxone being the most prescribed medications. According to the approach of daily dose per 100 patient-days, the most commonly used antimicrobial drugs were cefepime, meropenem, sulfamethoxazole + trimethoprim and ciprofloxacin. The mean number of interactions per patient was 2.6. Among the interactions, 51% were classified as contraindicated or significantly severe. Highly significant interactions (clinical value 1 and 2) were observed with a prevalence of 98%. CONCLUSION: The current study demonstrated that antimicrobial drugs are frequently prescribed in intensive care units and present a very high number of potential drug-drug interactions, with most of them being considered highly significant. |
format | Online Article Text |
id | pubmed-4738821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Associação de Medicina Intensiva Brasileira -
AMIB |
record_format | MEDLINE/PubMed |
spelling | pubmed-47388212016-02-11 Adverse events caused by potential drug-drug interactions in an intensive care unit of a teaching hospital Alvim, Mariana Macedo da Silva, Lidiane Ayres Leite, Isabel Cristina Gonçalves Silvério, Marcelo Silva Rev Bras Ter Intensiva Original Article OBJECTIVE: To evaluate the incidence of potential drug-drug interactions in an intensive care unit of a hospital, focusing on antimicrobial drugs. METHODS: This cross-sectional study analyzed electronic prescriptions of patients admitted to the intensive care unit of a teaching hospital between January 1 and March 31, 2014 and assessed potential drug-drug interactions associated with antimicrobial drugs. Antimicrobial drug consumption levels were expressed in daily doses per 100 patient-days. The search and classification of the interactions were based on the Micromedex(®) system. RESULTS: The daily prescriptions of 82 patients were analyzed, totaling 656 prescriptions. Antimicrobial drugs represented 25% of all prescription drugs, with meropenem, vancomycin and ceftriaxone being the most prescribed medications. According to the approach of daily dose per 100 patient-days, the most commonly used antimicrobial drugs were cefepime, meropenem, sulfamethoxazole + trimethoprim and ciprofloxacin. The mean number of interactions per patient was 2.6. Among the interactions, 51% were classified as contraindicated or significantly severe. Highly significant interactions (clinical value 1 and 2) were observed with a prevalence of 98%. CONCLUSION: The current study demonstrated that antimicrobial drugs are frequently prescribed in intensive care units and present a very high number of potential drug-drug interactions, with most of them being considered highly significant. Associação de Medicina Intensiva Brasileira - AMIB 2015 /pmc/articles/PMC4738821/ /pubmed/26761473 http://dx.doi.org/10.5935/0103-507X.20150060 Text en http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Alvim, Mariana Macedo da Silva, Lidiane Ayres Leite, Isabel Cristina Gonçalves Silvério, Marcelo Silva Adverse events caused by potential drug-drug interactions in an intensive care unit of a teaching hospital |
title | Adverse events caused by potential drug-drug interactions in an
intensive care unit of a teaching hospital |
title_full | Adverse events caused by potential drug-drug interactions in an
intensive care unit of a teaching hospital |
title_fullStr | Adverse events caused by potential drug-drug interactions in an
intensive care unit of a teaching hospital |
title_full_unstemmed | Adverse events caused by potential drug-drug interactions in an
intensive care unit of a teaching hospital |
title_short | Adverse events caused by potential drug-drug interactions in an
intensive care unit of a teaching hospital |
title_sort | adverse events caused by potential drug-drug interactions in an
intensive care unit of a teaching hospital |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4738821/ https://www.ncbi.nlm.nih.gov/pubmed/26761473 http://dx.doi.org/10.5935/0103-507X.20150060 |
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