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Adverse drug events in hospital: pilot study with trigger tool
OBJECTIVE: To estimate the frequency of and to characterize the adverse drug events at a terciary care hospital. METHODS: A retrospective review was carried out of 128 medical records from a hospital in Rio de Janeiro in 2007, representing 2,092 patients. The instrument used was a list of triggers,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Faculdade de Saúde Pública da Universidade de São
Paulo
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206103/ https://www.ncbi.nlm.nih.gov/pubmed/24626548 http://dx.doi.org/10.1590/S0034-8910.2013047004735 |
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author | Rozenfeld, Suely Giordani, Fabiola Coelho, Sonia |
author_facet | Rozenfeld, Suely Giordani, Fabiola Coelho, Sonia |
author_sort | Rozenfeld, Suely |
collection | PubMed |
description | OBJECTIVE: To estimate the frequency of and to characterize the adverse drug events at a terciary care hospital. METHODS: A retrospective review was carried out of 128 medical records from a hospital in Rio de Janeiro in 2007, representing 2,092 patients. The instrument used was a list of triggers, such as antidotes, abnormal laboratory analysis results and sudden suspension of treatment, among others. A simple random sample of patients aged 15 and over was extracted. Oncologic and obstetric patients were excluded as were those hospitalized for less than 48 hours or in the emergency room. Social and demographic characteristics and those of the disease of patients who underwent adverse events were compared with those of patients who did not in order to test for differences between the groups. RESULTS: Around 70.0% of the medical records assessed showed at least one trigger. Adverse drug events triggers had an overall positive predictive value of 14.4%. The incidence of adverse drug events was 26.6 per 100 patients and 15.6% patients suffered one or more event. The median length of stay for patients suffering an adverse drug event was 35.2 days as against 10.7 days for those who did not (p < 0.01). The pharmacological classes most commonly associated with an adverse drug event were related to the cardiovascular system, nervous system and alimentary tract and metabolism. The most common active substances associated with an adverse drug event were tramadol, dypirone, glibenclamide and furosemide. Over 80.0% of events provoked or contributed to temporary harm to the patient and required intervention and 6.0% may have contributed to the death of the patient. It was estimated that in the hospital, 131 events involving drowsiness or fainting 33 involving falls, and 33 episodes of hemorrhage related to adverse drug effects occur annually. CONCLUSIONS: Almost one-sixth of in-patients (16,0%) suffered an adverse drug event. The instrument used may prove useful as a technique for monitoring and evaluating patient care results. Psycothropic therapy should be critically appraised given the frequency of associated events, such as excessive sedation, lethargy, and hypotension. |
format | Online Article Text |
id | pubmed-4206103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Faculdade de Saúde Pública da Universidade de São
Paulo |
record_format | MEDLINE/PubMed |
spelling | pubmed-42061032015-01-07 Adverse drug events in hospital: pilot study with trigger tool Rozenfeld, Suely Giordani, Fabiola Coelho, Sonia Rev Saude Publica Original Articles OBJECTIVE: To estimate the frequency of and to characterize the adverse drug events at a terciary care hospital. METHODS: A retrospective review was carried out of 128 medical records from a hospital in Rio de Janeiro in 2007, representing 2,092 patients. The instrument used was a list of triggers, such as antidotes, abnormal laboratory analysis results and sudden suspension of treatment, among others. A simple random sample of patients aged 15 and over was extracted. Oncologic and obstetric patients were excluded as were those hospitalized for less than 48 hours or in the emergency room. Social and demographic characteristics and those of the disease of patients who underwent adverse events were compared with those of patients who did not in order to test for differences between the groups. RESULTS: Around 70.0% of the medical records assessed showed at least one trigger. Adverse drug events triggers had an overall positive predictive value of 14.4%. The incidence of adverse drug events was 26.6 per 100 patients and 15.6% patients suffered one or more event. The median length of stay for patients suffering an adverse drug event was 35.2 days as against 10.7 days for those who did not (p < 0.01). The pharmacological classes most commonly associated with an adverse drug event were related to the cardiovascular system, nervous system and alimentary tract and metabolism. The most common active substances associated with an adverse drug event were tramadol, dypirone, glibenclamide and furosemide. Over 80.0% of events provoked or contributed to temporary harm to the patient and required intervention and 6.0% may have contributed to the death of the patient. It was estimated that in the hospital, 131 events involving drowsiness or fainting 33 involving falls, and 33 episodes of hemorrhage related to adverse drug effects occur annually. CONCLUSIONS: Almost one-sixth of in-patients (16,0%) suffered an adverse drug event. The instrument used may prove useful as a technique for monitoring and evaluating patient care results. Psycothropic therapy should be critically appraised given the frequency of associated events, such as excessive sedation, lethargy, and hypotension. Faculdade de Saúde Pública da Universidade de São Paulo 2013-12 /pmc/articles/PMC4206103/ /pubmed/24626548 http://dx.doi.org/10.1590/S0034-8910.2013047004735 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Rozenfeld, Suely Giordani, Fabiola Coelho, Sonia Adverse drug events in hospital: pilot study with trigger tool |
title | Adverse drug events in hospital: pilot study with trigger
tool |
title_full | Adverse drug events in hospital: pilot study with trigger
tool |
title_fullStr | Adverse drug events in hospital: pilot study with trigger
tool |
title_full_unstemmed | Adverse drug events in hospital: pilot study with trigger
tool |
title_short | Adverse drug events in hospital: pilot study with trigger
tool |
title_sort | adverse drug events in hospital: pilot study with trigger
tool |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206103/ https://www.ncbi.nlm.nih.gov/pubmed/24626548 http://dx.doi.org/10.1590/S0034-8910.2013047004735 |
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