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Overall performance of a drug–drug interaction clinical decision support system: quantitative evaluation and end-user survey
BACKGROUND: Clinical decision support systems are implemented in many hospitals to prevent medication errors and associated harm. They are however associated with a high burden of false positive alerts and alert fatigue. The aim of this study was to evaluate a drug–drug interaction (DDI) clinical de...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8864797/ https://www.ncbi.nlm.nih.gov/pubmed/35193547 http://dx.doi.org/10.1186/s12911-022-01783-z |
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author | Van De Sijpe, Greet Quintens, Charlotte Walgraeve, Karolien Van Laer, Eva Penny, Jens De Vlieger, Greet Schrijvers, Rik De Munter, Paul Foulon, Veerle Casteels, Minne Van der Linden, Lorenz Spriet, Isabel |
author_facet | Van De Sijpe, Greet Quintens, Charlotte Walgraeve, Karolien Van Laer, Eva Penny, Jens De Vlieger, Greet Schrijvers, Rik De Munter, Paul Foulon, Veerle Casteels, Minne Van der Linden, Lorenz Spriet, Isabel |
author_sort | Van De Sijpe, Greet |
collection | PubMed |
description | BACKGROUND: Clinical decision support systems are implemented in many hospitals to prevent medication errors and associated harm. They are however associated with a high burden of false positive alerts and alert fatigue. The aim of this study was to evaluate a drug–drug interaction (DDI) clinical decision support system in terms of its performance, uptake and user satisfaction and to identify barriers and opportunities for improvement. METHODS: A quantitative evaluation and end-user survey were performed in a large teaching hospital. First, very severe DDI alerts generated between 2019 and 2021 were evaluated retrospectively. Data collection comprised alert burden, override rates, the number of alert overrides reviewed by pharmacists and the resulting pharmacist recommendations as well as their acceptance rate. Second, an e-survey was carried out among prescribers to assess satisfaction, usefulness and relevance of DDI alerts as well as reasons for overriding. RESULTS: A total of 38,409 very severe DDI alerts were generated, of which 88.2% were overridden by the prescriber. In 3.2% of reviewed overrides, a recommendation by the pharmacist was provided, of which 79.2% was accepted. False positive alerts were caused by a too broad screening interval and lack of incorporation of patient-specific characteristics, such as QTc values. Co-prescribing of a non-vitamin K oral anticoagulant and a low molecular weight heparin accounted for 49.8% of alerts, of which 92.2% were overridden. In 88 (1.1%) of these overridden alerts, concurrent therapy was still present. Despite the high override rate, the e-survey revealed that the DDI clinical decision support system was found useful by prescribers. CONCLUSIONS: Identified barriers were the lack of DDI-specific screening intervals and inclusion of patient-specific characteristics, both leading to a high number of false positive alerts and risk for alert fatigue. Despite these barriers, the added value of the DDI clinical decision support system was recognized by prescribers. Hence, integration of DDI-specific screening intervals and patient-specific characteristics is warranted to improve the performance of the DDI software. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12911-022-01783-z. |
format | Online Article Text |
id | pubmed-8864797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88647972022-02-23 Overall performance of a drug–drug interaction clinical decision support system: quantitative evaluation and end-user survey Van De Sijpe, Greet Quintens, Charlotte Walgraeve, Karolien Van Laer, Eva Penny, Jens De Vlieger, Greet Schrijvers, Rik De Munter, Paul Foulon, Veerle Casteels, Minne Van der Linden, Lorenz Spriet, Isabel BMC Med Inform Decis Mak Research BACKGROUND: Clinical decision support systems are implemented in many hospitals to prevent medication errors and associated harm. They are however associated with a high burden of false positive alerts and alert fatigue. The aim of this study was to evaluate a drug–drug interaction (DDI) clinical decision support system in terms of its performance, uptake and user satisfaction and to identify barriers and opportunities for improvement. METHODS: A quantitative evaluation and end-user survey were performed in a large teaching hospital. First, very severe DDI alerts generated between 2019 and 2021 were evaluated retrospectively. Data collection comprised alert burden, override rates, the number of alert overrides reviewed by pharmacists and the resulting pharmacist recommendations as well as their acceptance rate. Second, an e-survey was carried out among prescribers to assess satisfaction, usefulness and relevance of DDI alerts as well as reasons for overriding. RESULTS: A total of 38,409 very severe DDI alerts were generated, of which 88.2% were overridden by the prescriber. In 3.2% of reviewed overrides, a recommendation by the pharmacist was provided, of which 79.2% was accepted. False positive alerts were caused by a too broad screening interval and lack of incorporation of patient-specific characteristics, such as QTc values. Co-prescribing of a non-vitamin K oral anticoagulant and a low molecular weight heparin accounted for 49.8% of alerts, of which 92.2% were overridden. In 88 (1.1%) of these overridden alerts, concurrent therapy was still present. Despite the high override rate, the e-survey revealed that the DDI clinical decision support system was found useful by prescribers. CONCLUSIONS: Identified barriers were the lack of DDI-specific screening intervals and inclusion of patient-specific characteristics, both leading to a high number of false positive alerts and risk for alert fatigue. Despite these barriers, the added value of the DDI clinical decision support system was recognized by prescribers. Hence, integration of DDI-specific screening intervals and patient-specific characteristics is warranted to improve the performance of the DDI software. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12911-022-01783-z. BioMed Central 2022-02-22 /pmc/articles/PMC8864797/ /pubmed/35193547 http://dx.doi.org/10.1186/s12911-022-01783-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Van De Sijpe, Greet Quintens, Charlotte Walgraeve, Karolien Van Laer, Eva Penny, Jens De Vlieger, Greet Schrijvers, Rik De Munter, Paul Foulon, Veerle Casteels, Minne Van der Linden, Lorenz Spriet, Isabel Overall performance of a drug–drug interaction clinical decision support system: quantitative evaluation and end-user survey |
title | Overall performance of a drug–drug interaction clinical decision support system: quantitative evaluation and end-user survey |
title_full | Overall performance of a drug–drug interaction clinical decision support system: quantitative evaluation and end-user survey |
title_fullStr | Overall performance of a drug–drug interaction clinical decision support system: quantitative evaluation and end-user survey |
title_full_unstemmed | Overall performance of a drug–drug interaction clinical decision support system: quantitative evaluation and end-user survey |
title_short | Overall performance of a drug–drug interaction clinical decision support system: quantitative evaluation and end-user survey |
title_sort | overall performance of a drug–drug interaction clinical decision support system: quantitative evaluation and end-user survey |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8864797/ https://www.ncbi.nlm.nih.gov/pubmed/35193547 http://dx.doi.org/10.1186/s12911-022-01783-z |
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