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Use of a trigger tool to detect adverse drug reactions in an emergency department

BACKGROUND: Although there are systems for reporting adverse drug reactions (ADR), these safety events remain under reported. The low-cost, low-tech trigger tool method is based on the detection of events through clues, and it seems to increase the detection of adverse events compared to traditional...

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Autores principales: de Almeida, Silvana Maria, Romualdo, Aruana, de Abreu Ferraresi, Andressa, Zelezoglo, Giovana Roberta, Marra, Alexandre R., Edmond, Michael B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688728/
https://www.ncbi.nlm.nih.gov/pubmed/29141696
http://dx.doi.org/10.1186/s40360-017-0177-y
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author de Almeida, Silvana Maria
Romualdo, Aruana
de Abreu Ferraresi, Andressa
Zelezoglo, Giovana Roberta
Marra, Alexandre R.
Edmond, Michael B.
author_facet de Almeida, Silvana Maria
Romualdo, Aruana
de Abreu Ferraresi, Andressa
Zelezoglo, Giovana Roberta
Marra, Alexandre R.
Edmond, Michael B.
author_sort de Almeida, Silvana Maria
collection PubMed
description BACKGROUND: Although there are systems for reporting adverse drug reactions (ADR), these safety events remain under reported. The low-cost, low-tech trigger tool method is based on the detection of events through clues, and it seems to increase the detection of adverse events compared to traditional methodologies. This study seeks to estimate the prevalence of adverse reactions to drugs in patients seeking care in the emergency department. METHODS: Retrospective study from January to December, 2014, applying the Institute for Healthcare Improvement (IHI) trigger tool methodology for patients treated at the emergency room of a tertiary care hospital. RESULTS: The estimated prevalence of adverse reactions in patients presenting to the emergency department was 2.3% [CI(95) 1.3% to 3.3%]; 28.6% of cases required hospitalization at an average cost of US$ 5698.44. The most common triggers were hydrocortisone (57% of the cases), diphenhydramine (14%) and fexofenadine (14%). Anti-infectives (19%), cardiovascular agents (14%), and musculoskeletal drugs (14%) were the most common causes of adverse reactions. According to the Naranjo Scale, 71% were classified as possible and 29% as probable. There was no association between adverse reactions and age and sex in the present study. CONCLUSIONS: The use of the trigger tool to identify adverse reactions in the emergency department was possible to identify a prevalence of 2.3%. It showed to be a viable method that can provide a better understanding of adverse drug reactions in this patient population.
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spelling pubmed-56887282017-11-24 Use of a trigger tool to detect adverse drug reactions in an emergency department de Almeida, Silvana Maria Romualdo, Aruana de Abreu Ferraresi, Andressa Zelezoglo, Giovana Roberta Marra, Alexandre R. Edmond, Michael B. BMC Pharmacol Toxicol Research Article BACKGROUND: Although there are systems for reporting adverse drug reactions (ADR), these safety events remain under reported. The low-cost, low-tech trigger tool method is based on the detection of events through clues, and it seems to increase the detection of adverse events compared to traditional methodologies. This study seeks to estimate the prevalence of adverse reactions to drugs in patients seeking care in the emergency department. METHODS: Retrospective study from January to December, 2014, applying the Institute for Healthcare Improvement (IHI) trigger tool methodology for patients treated at the emergency room of a tertiary care hospital. RESULTS: The estimated prevalence of adverse reactions in patients presenting to the emergency department was 2.3% [CI(95) 1.3% to 3.3%]; 28.6% of cases required hospitalization at an average cost of US$ 5698.44. The most common triggers were hydrocortisone (57% of the cases), diphenhydramine (14%) and fexofenadine (14%). Anti-infectives (19%), cardiovascular agents (14%), and musculoskeletal drugs (14%) were the most common causes of adverse reactions. According to the Naranjo Scale, 71% were classified as possible and 29% as probable. There was no association between adverse reactions and age and sex in the present study. CONCLUSIONS: The use of the trigger tool to identify adverse reactions in the emergency department was possible to identify a prevalence of 2.3%. It showed to be a viable method that can provide a better understanding of adverse drug reactions in this patient population. BioMed Central 2017-11-15 /pmc/articles/PMC5688728/ /pubmed/29141696 http://dx.doi.org/10.1186/s40360-017-0177-y Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Research Article
de Almeida, Silvana Maria
Romualdo, Aruana
de Abreu Ferraresi, Andressa
Zelezoglo, Giovana Roberta
Marra, Alexandre R.
Edmond, Michael B.
Use of a trigger tool to detect adverse drug reactions in an emergency department
title Use of a trigger tool to detect adverse drug reactions in an emergency department
title_full Use of a trigger tool to detect adverse drug reactions in an emergency department
title_fullStr Use of a trigger tool to detect adverse drug reactions in an emergency department
title_full_unstemmed Use of a trigger tool to detect adverse drug reactions in an emergency department
title_short Use of a trigger tool to detect adverse drug reactions in an emergency department
title_sort use of a trigger tool to detect adverse drug reactions in an emergency department
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688728/
https://www.ncbi.nlm.nih.gov/pubmed/29141696
http://dx.doi.org/10.1186/s40360-017-0177-y
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