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A Systematic Review of the Legal Considerations Surrounding Medicines Management
Background and Objectives: There is a paucity of integrated knowledge regarding legal considerations required to ensure patient safety through safe medicines management. This study explores the legal considerations surrounding medicines management, providing a synthesis of existing knowledge. An int...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7828352/ https://www.ncbi.nlm.nih.gov/pubmed/33450903 http://dx.doi.org/10.3390/medicina57010065 |
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author | Vaismoradi, Mojtaba Jordan, Sue Logan, Patricia A. Amaniyan, Sara Glarcher, Manela |
author_facet | Vaismoradi, Mojtaba Jordan, Sue Logan, Patricia A. Amaniyan, Sara Glarcher, Manela |
author_sort | Vaismoradi, Mojtaba |
collection | PubMed |
description | Background and Objectives: There is a paucity of integrated knowledge regarding legal considerations required to ensure patient safety through safe medicines management. This study explores the legal considerations surrounding medicines management, providing a synthesis of existing knowledge. An integrative systematic review of the current international knowledge was performed. Materials and Methods: The search encompassed the online databases of PubMed (including Medline), Scopus, CINAHL, and Web of Science using MeSH terms and relevant keywords relating to the legal considerations of medicines management in healthcare settings. Results: The search process led to the identification of 6051 studies published between 2010 and 2020, of which six articles were found to be appropriate for data analysis and synthesis based on inclusion criteria. Research methods were varied and included qualitative interviews, mixed-methods designs, retrospective case reports and cross-sectional interrupted time-series analysis. Their foci were on the delegation of medicines management, pharmacovigilance and reporting of adverse drug reactions (ADRs) before and after legislation by nurses, physicians and pharmacists, medico-legal litigation, use of forced medication and the prescription monitoring program. Given the heterogenicity of the studies in terms of aims and research methods, a meta-analysis could not be performed and, therefore, our review findings are presented narratively under the categories of ‘healthcare providers’ education and monitoring tasks’, ‘individual and shared responsibility’, and ‘patients’ rights’. Conclusion: This review identifies legal aspects surrounding medicines management, including supervision and monitoring of the effects of medicines; healthcare providers’ knowledge and attitudes; support and standardised tools for monitoring and reporting medicines’ adverse side effects/ADRs; electronic health record systems; individual and shared perceptions of responsibility; recognition of nurses’ roles; detection of sentinel medication errors; covert or non-voluntary administration of medication, and patient participation. |
format | Online Article Text |
id | pubmed-7828352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78283522021-01-25 A Systematic Review of the Legal Considerations Surrounding Medicines Management Vaismoradi, Mojtaba Jordan, Sue Logan, Patricia A. Amaniyan, Sara Glarcher, Manela Medicina (Kaunas) Review Background and Objectives: There is a paucity of integrated knowledge regarding legal considerations required to ensure patient safety through safe medicines management. This study explores the legal considerations surrounding medicines management, providing a synthesis of existing knowledge. An integrative systematic review of the current international knowledge was performed. Materials and Methods: The search encompassed the online databases of PubMed (including Medline), Scopus, CINAHL, and Web of Science using MeSH terms and relevant keywords relating to the legal considerations of medicines management in healthcare settings. Results: The search process led to the identification of 6051 studies published between 2010 and 2020, of which six articles were found to be appropriate for data analysis and synthesis based on inclusion criteria. Research methods were varied and included qualitative interviews, mixed-methods designs, retrospective case reports and cross-sectional interrupted time-series analysis. Their foci were on the delegation of medicines management, pharmacovigilance and reporting of adverse drug reactions (ADRs) before and after legislation by nurses, physicians and pharmacists, medico-legal litigation, use of forced medication and the prescription monitoring program. Given the heterogenicity of the studies in terms of aims and research methods, a meta-analysis could not be performed and, therefore, our review findings are presented narratively under the categories of ‘healthcare providers’ education and monitoring tasks’, ‘individual and shared responsibility’, and ‘patients’ rights’. Conclusion: This review identifies legal aspects surrounding medicines management, including supervision and monitoring of the effects of medicines; healthcare providers’ knowledge and attitudes; support and standardised tools for monitoring and reporting medicines’ adverse side effects/ADRs; electronic health record systems; individual and shared perceptions of responsibility; recognition of nurses’ roles; detection of sentinel medication errors; covert or non-voluntary administration of medication, and patient participation. MDPI 2021-01-13 /pmc/articles/PMC7828352/ /pubmed/33450903 http://dx.doi.org/10.3390/medicina57010065 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Vaismoradi, Mojtaba Jordan, Sue Logan, Patricia A. Amaniyan, Sara Glarcher, Manela A Systematic Review of the Legal Considerations Surrounding Medicines Management |
title | A Systematic Review of the Legal Considerations Surrounding Medicines Management |
title_full | A Systematic Review of the Legal Considerations Surrounding Medicines Management |
title_fullStr | A Systematic Review of the Legal Considerations Surrounding Medicines Management |
title_full_unstemmed | A Systematic Review of the Legal Considerations Surrounding Medicines Management |
title_short | A Systematic Review of the Legal Considerations Surrounding Medicines Management |
title_sort | systematic review of the legal considerations surrounding medicines management |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7828352/ https://www.ncbi.nlm.nih.gov/pubmed/33450903 http://dx.doi.org/10.3390/medicina57010065 |
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