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Prediction of clinically relevant adverse drug events in surgical patients

BACKGROUND: Risk stratification of hospital patients for adverse drug events would enable targeting patients who may benefit from interventions aimed at reducing drug-related morbidity. It would support clinicians and hospital pharmacists in selecting patients to deliver a more efficient health care...

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Autores principales: Bos, Jacqueline M., Kalkman, Gerard A., Groenewoud, Hans, van den Bemt, Patricia M. L. A., De Smet, Peter A. G. M., Nagtegaal, J. Elsbeth, Wieringa, Andre, van der Wilt, Gert Jan, Kramers, Cornelis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107128/
https://www.ncbi.nlm.nih.gov/pubmed/30138343
http://dx.doi.org/10.1371/journal.pone.0201645
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author Bos, Jacqueline M.
Kalkman, Gerard A.
Groenewoud, Hans
van den Bemt, Patricia M. L. A.
De Smet, Peter A. G. M.
Nagtegaal, J. Elsbeth
Wieringa, Andre
van der Wilt, Gert Jan
Kramers, Cornelis
author_facet Bos, Jacqueline M.
Kalkman, Gerard A.
Groenewoud, Hans
van den Bemt, Patricia M. L. A.
De Smet, Peter A. G. M.
Nagtegaal, J. Elsbeth
Wieringa, Andre
van der Wilt, Gert Jan
Kramers, Cornelis
author_sort Bos, Jacqueline M.
collection PubMed
description BACKGROUND: Risk stratification of hospital patients for adverse drug events would enable targeting patients who may benefit from interventions aimed at reducing drug-related morbidity. It would support clinicians and hospital pharmacists in selecting patients to deliver a more efficient health care service. This study aimed to develop a prediction model that helps to identify patients on the day of hospital admission who are at increased risk of developing a clinically relevant, preventable adverse drug event during their stay on a surgical ward. METHODS: Data of the pre-intervention measurement period of the P-REVIEW study were used. This study was designed to assess the impact of a multifaceted educational intervention on clinically relevant, preventable adverse drug events in surgical patients. Thirty-nine variables were evaluated in a univariate and multivariate logistic regression analysis, respectively. Model performance was expressed in the Area Under the Receiver Operating Characteristics. Bootstrapping was used for model validation. RESULTS: 6780 admissions of patients at surgical wards were included during the pre-intervention period of the PREVIEW trial. 102 patients experienced a clinically relevant, adverse drug event during their hospital stay. The prediction model comprised five variables: age, number of biochemical tests ordered, heparin/LMWH in therapeutic dose, use of opioids, and use of cardiovascular drugs. The AUROC was 0.86 (95% CI 0.83–0.88). The model had a sensitivity of 80.4% and a specificity of 73.4%. The positive and negative predictive values were 4.5% and 99.6%, respectively. Bootstrapping generated parameters in the same boundaries. CONCLUSIONS: The combined use of a limited set of easily ascertainable patient characteristics can help physicians and pharmacists to identify, at the time of admission, surgical patients who are at increased risk of developing ADEs during their hospital stay. This may serve as a basis for taking extra precautions to ensure medication safety in those patients.
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spelling pubmed-61071282018-08-30 Prediction of clinically relevant adverse drug events in surgical patients Bos, Jacqueline M. Kalkman, Gerard A. Groenewoud, Hans van den Bemt, Patricia M. L. A. De Smet, Peter A. G. M. Nagtegaal, J. Elsbeth Wieringa, Andre van der Wilt, Gert Jan Kramers, Cornelis PLoS One Research Article BACKGROUND: Risk stratification of hospital patients for adverse drug events would enable targeting patients who may benefit from interventions aimed at reducing drug-related morbidity. It would support clinicians and hospital pharmacists in selecting patients to deliver a more efficient health care service. This study aimed to develop a prediction model that helps to identify patients on the day of hospital admission who are at increased risk of developing a clinically relevant, preventable adverse drug event during their stay on a surgical ward. METHODS: Data of the pre-intervention measurement period of the P-REVIEW study were used. This study was designed to assess the impact of a multifaceted educational intervention on clinically relevant, preventable adverse drug events in surgical patients. Thirty-nine variables were evaluated in a univariate and multivariate logistic regression analysis, respectively. Model performance was expressed in the Area Under the Receiver Operating Characteristics. Bootstrapping was used for model validation. RESULTS: 6780 admissions of patients at surgical wards were included during the pre-intervention period of the PREVIEW trial. 102 patients experienced a clinically relevant, adverse drug event during their hospital stay. The prediction model comprised five variables: age, number of biochemical tests ordered, heparin/LMWH in therapeutic dose, use of opioids, and use of cardiovascular drugs. The AUROC was 0.86 (95% CI 0.83–0.88). The model had a sensitivity of 80.4% and a specificity of 73.4%. The positive and negative predictive values were 4.5% and 99.6%, respectively. Bootstrapping generated parameters in the same boundaries. CONCLUSIONS: The combined use of a limited set of easily ascertainable patient characteristics can help physicians and pharmacists to identify, at the time of admission, surgical patients who are at increased risk of developing ADEs during their hospital stay. This may serve as a basis for taking extra precautions to ensure medication safety in those patients. Public Library of Science 2018-08-23 /pmc/articles/PMC6107128/ /pubmed/30138343 http://dx.doi.org/10.1371/journal.pone.0201645 Text en © 2018 Bos et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Bos, Jacqueline M.
Kalkman, Gerard A.
Groenewoud, Hans
van den Bemt, Patricia M. L. A.
De Smet, Peter A. G. M.
Nagtegaal, J. Elsbeth
Wieringa, Andre
van der Wilt, Gert Jan
Kramers, Cornelis
Prediction of clinically relevant adverse drug events in surgical patients
title Prediction of clinically relevant adverse drug events in surgical patients
title_full Prediction of clinically relevant adverse drug events in surgical patients
title_fullStr Prediction of clinically relevant adverse drug events in surgical patients
title_full_unstemmed Prediction of clinically relevant adverse drug events in surgical patients
title_short Prediction of clinically relevant adverse drug events in surgical patients
title_sort prediction of clinically relevant adverse drug events in surgical patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107128/
https://www.ncbi.nlm.nih.gov/pubmed/30138343
http://dx.doi.org/10.1371/journal.pone.0201645
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