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Risk control drives risk assessment and risk review: A cause and effect model of pharmaceutical drug recall on patient safety

BACKGROUND: Pharmaceutical drug recall is a relentless issue that is composed of multidimensional criteria. The distinct criteria that contributed to drug recalls have been identified in previous literature; however, there is limited information regarding the causal relationships between each criter...

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Autores principales: Lin, Irene D, Hertig, John B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10184228/
https://www.ncbi.nlm.nih.gov/pubmed/37197446
http://dx.doi.org/10.1177/27550834231170075
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author Lin, Irene D
Hertig, John B
author_facet Lin, Irene D
Hertig, John B
author_sort Lin, Irene D
collection PubMed
description BACKGROUND: Pharmaceutical drug recall is a relentless issue that is composed of multidimensional criteria. The distinct criteria that contributed to drug recalls have been identified in previous literature; however, there is limited information regarding the causal relationships between each criterion. Highlighting key influential aspects and criteria of pharmaceutical drug recall is critical in addressing this ongoing issue and promoting patient safety. OBJECTIVE: The objective of this study is as follows: (1) identify critical criteria of pharmaceutical drug recalls for improvements, (2) determine the interrelationships among the criteria, and (3) define the causal relationships of pharmaceutical drug recall and provide theoretical insights and practice recommendations to minimize risks associated with pharmaceutical recalls and maximize patient safety. DESIGN: This study proposes five aspects and 42 criteria to identify the impact of pharmaceutical drug recalls on patient safety by evaluating the interrelationships between the criteria by employing the fuzzy decision-making trial and evaluation laboratory method. METHODS: A group of 11 professionals across the pharmaceutical industry, hospitals, ambulatory care, regulatory authority, and community care settings were selected for interviews. RESULTS: Risk control is the influencing aspect of pharmaceutical drug recalls that has the most substantial impact on risk assessment and risk review; it generates medium effects on risk communication and technology. Risk assessment, risk communication, and risk review demonstrated comparative weak interrelationships, while risk communication exhibits a weak unidirectional effect on risk review. Finally, risk assessment exerts a weak influence on technology application and development. Product contamination, product subpotent or superpotent, injury to patients, product not sterile or impure, and system detectability of hazards have the strongest influence in the causal group of pharmaceutical drug recalls. CONCLUSION: The study shows that risk control drives risk assessment and risk review in the pharmaceutical industry manufacturing process. To achieve patient safety, this study suggests focusing on risk control strategies, as this aspect displays the most substantial effect on influencing other critical risk management aspects such as risk assessment and risk review.
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spelling pubmed-101842282023-05-16 Risk control drives risk assessment and risk review: A cause and effect model of pharmaceutical drug recall on patient safety Lin, Irene D Hertig, John B J Med Access Medicine Quality and Pharmaceutical Manufacturing - What Does Good Look Like? BACKGROUND: Pharmaceutical drug recall is a relentless issue that is composed of multidimensional criteria. The distinct criteria that contributed to drug recalls have been identified in previous literature; however, there is limited information regarding the causal relationships between each criterion. Highlighting key influential aspects and criteria of pharmaceutical drug recall is critical in addressing this ongoing issue and promoting patient safety. OBJECTIVE: The objective of this study is as follows: (1) identify critical criteria of pharmaceutical drug recalls for improvements, (2) determine the interrelationships among the criteria, and (3) define the causal relationships of pharmaceutical drug recall and provide theoretical insights and practice recommendations to minimize risks associated with pharmaceutical recalls and maximize patient safety. DESIGN: This study proposes five aspects and 42 criteria to identify the impact of pharmaceutical drug recalls on patient safety by evaluating the interrelationships between the criteria by employing the fuzzy decision-making trial and evaluation laboratory method. METHODS: A group of 11 professionals across the pharmaceutical industry, hospitals, ambulatory care, regulatory authority, and community care settings were selected for interviews. RESULTS: Risk control is the influencing aspect of pharmaceutical drug recalls that has the most substantial impact on risk assessment and risk review; it generates medium effects on risk communication and technology. Risk assessment, risk communication, and risk review demonstrated comparative weak interrelationships, while risk communication exhibits a weak unidirectional effect on risk review. Finally, risk assessment exerts a weak influence on technology application and development. Product contamination, product subpotent or superpotent, injury to patients, product not sterile or impure, and system detectability of hazards have the strongest influence in the causal group of pharmaceutical drug recalls. CONCLUSION: The study shows that risk control drives risk assessment and risk review in the pharmaceutical industry manufacturing process. To achieve patient safety, this study suggests focusing on risk control strategies, as this aspect displays the most substantial effect on influencing other critical risk management aspects such as risk assessment and risk review. SAGE Publications 2023-05-11 /pmc/articles/PMC10184228/ /pubmed/37197446 http://dx.doi.org/10.1177/27550834231170075 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Medicine Quality and Pharmaceutical Manufacturing - What Does Good Look Like?
Lin, Irene D
Hertig, John B
Risk control drives risk assessment and risk review: A cause and effect model of pharmaceutical drug recall on patient safety
title Risk control drives risk assessment and risk review: A cause and effect model of pharmaceutical drug recall on patient safety
title_full Risk control drives risk assessment and risk review: A cause and effect model of pharmaceutical drug recall on patient safety
title_fullStr Risk control drives risk assessment and risk review: A cause and effect model of pharmaceutical drug recall on patient safety
title_full_unstemmed Risk control drives risk assessment and risk review: A cause and effect model of pharmaceutical drug recall on patient safety
title_short Risk control drives risk assessment and risk review: A cause and effect model of pharmaceutical drug recall on patient safety
title_sort risk control drives risk assessment and risk review: a cause and effect model of pharmaceutical drug recall on patient safety
topic Medicine Quality and Pharmaceutical Manufacturing - What Does Good Look Like?
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10184228/
https://www.ncbi.nlm.nih.gov/pubmed/37197446
http://dx.doi.org/10.1177/27550834231170075
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