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Drug incompatibilities in the adult intensive care unit of a university hospital
OBJECTIVES: This study sought to identify the physical and chemical incompatibilities among the drugs administered intravenously to patients admitted to an adult intensive care unit. We also aimed to establish pharmaceutical guidelines for administering incompatible drugs. METHODS: This cross-sectio...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação de Medicina Intensiva Brasileira -
AMIB
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4943052/ https://www.ncbi.nlm.nih.gov/pubmed/27410410 http://dx.doi.org/10.5935/0103-507X.20160029 |
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author | Marsilio, Naiane Roveda da Silva, Daiandy Bueno, Denise |
author_facet | Marsilio, Naiane Roveda da Silva, Daiandy Bueno, Denise |
author_sort | Marsilio, Naiane Roveda |
collection | PubMed |
description | OBJECTIVES: This study sought to identify the physical and chemical incompatibilities among the drugs administered intravenously to patients admitted to an adult intensive care unit. We also aimed to establish pharmaceutical guidelines for administering incompatible drugs. METHODS: This cross-sectional, prospective, and quantitative study was conducted from July to September 2015. Drug incompatibilities were identified based on an analysis of the patient prescriptions available in the hospital online management system. A pharmaceutical intervention was performed using the guidelines on the preparation and administration of incompatible drugs. Adherence to those guidelines was subsequently assessed among the nursing staff. RESULTS: A total of 100 prescriptions were analyzed; 68 were incompatible with the intravenous drugs prescribed. A total of 271 drug incompatibilities were found, averaging 4.0 ± 3.3 incompatibilities per prescription. The most commonly found drug incompatibilities were between midazolam and hydrocortisone (8.9%), between cefepime and midazolam (5.2%), and between hydrocortisone and vancomycin (5.2%). The drugs most commonly involved in incompatibilities were midazolam, hydrocortisone, and vancomycin. The most common incompatibilities occurred when a drug was administered via continuous infusion and another was administered intermittently (50%). Of the 68 prescriptions that led to pharmaceutical guidelines, 45 (66.2%) were fully adhered to by the nursing staff. CONCLUSION: Patients under intensive care were subjected to a high rate of incompatibilities. Drug incompatibilities can be identified and eliminated by the pharmacist on the multidisciplinary team, thereby reducing undesirable effects among patients. |
format | Online Article Text |
id | pubmed-4943052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Associação de Medicina Intensiva Brasileira -
AMIB |
record_format | MEDLINE/PubMed |
spelling | pubmed-49430522016-07-14 Drug incompatibilities in the adult intensive care unit of a university hospital Marsilio, Naiane Roveda da Silva, Daiandy Bueno, Denise Rev Bras Ter Intensiva Original Article OBJECTIVES: This study sought to identify the physical and chemical incompatibilities among the drugs administered intravenously to patients admitted to an adult intensive care unit. We also aimed to establish pharmaceutical guidelines for administering incompatible drugs. METHODS: This cross-sectional, prospective, and quantitative study was conducted from July to September 2015. Drug incompatibilities were identified based on an analysis of the patient prescriptions available in the hospital online management system. A pharmaceutical intervention was performed using the guidelines on the preparation and administration of incompatible drugs. Adherence to those guidelines was subsequently assessed among the nursing staff. RESULTS: A total of 100 prescriptions were analyzed; 68 were incompatible with the intravenous drugs prescribed. A total of 271 drug incompatibilities were found, averaging 4.0 ± 3.3 incompatibilities per prescription. The most commonly found drug incompatibilities were between midazolam and hydrocortisone (8.9%), between cefepime and midazolam (5.2%), and between hydrocortisone and vancomycin (5.2%). The drugs most commonly involved in incompatibilities were midazolam, hydrocortisone, and vancomycin. The most common incompatibilities occurred when a drug was administered via continuous infusion and another was administered intermittently (50%). Of the 68 prescriptions that led to pharmaceutical guidelines, 45 (66.2%) were fully adhered to by the nursing staff. CONCLUSION: Patients under intensive care were subjected to a high rate of incompatibilities. Drug incompatibilities can be identified and eliminated by the pharmacist on the multidisciplinary team, thereby reducing undesirable effects among patients. Associação de Medicina Intensiva Brasileira - AMIB 2016 /pmc/articles/PMC4943052/ /pubmed/27410410 http://dx.doi.org/10.5935/0103-507X.20160029 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 Marsilio, Naiane Roveda da Silva, Daiandy Bueno, Denise Drug incompatibilities in the adult intensive care unit of a university hospital |
title | Drug incompatibilities in the adult intensive care unit of a
university hospital |
title_full | Drug incompatibilities in the adult intensive care unit of a
university hospital |
title_fullStr | Drug incompatibilities in the adult intensive care unit of a
university hospital |
title_full_unstemmed | Drug incompatibilities in the adult intensive care unit of a
university hospital |
title_short | Drug incompatibilities in the adult intensive care unit of a
university hospital |
title_sort | drug incompatibilities in the adult intensive care unit of a
university hospital |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4943052/ https://www.ncbi.nlm.nih.gov/pubmed/27410410 http://dx.doi.org/10.5935/0103-507X.20160029 |
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