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Review

A Systematic Review of the Legal Considerations Surrounding Medicines Management

1
Faculty of Nursing and Health Sciences, Nord University, 8049 Bodø, Norway
2
Department of Nursing, Swansea University, Swansea SA2 8PP, UK
3
Faculty of Science, Charles Sturt University, Bathurst 2795, Australia
4
Student Research Center, Semnan University of Medical Sciences, Semnan 3514799442, Iran
5
Institute of Nursing Science and Practice, Paracelsus Medical University, 5020 Salzburg, Austria
*
Author to whom correspondence should be addressed.
Medicina 2021, 57(1), 65; https://doi.org/10.3390/medicina57010065
Received: 4 December 2020 / Revised: 6 January 2021 / Accepted: 10 January 2021 / Published: 13 January 2021
(This article belongs to the Special Issue Meta-Research in the Medico-Scientific Field)
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. View Full-Text
Keywords: clinical practice; law; legal; adverse drug reactions; pharmacovigilance; medicines management; patient safety clinical practice; law; legal; adverse drug reactions; pharmacovigilance; medicines management; patient safety
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MDPI and ACS Style

Vaismoradi, M.; Jordan, S.; Logan, P.A.; Amaniyan, S.; Glarcher, M. A Systematic Review of the Legal Considerations Surrounding Medicines Management. Medicina 2021, 57, 65. https://doi.org/10.3390/medicina57010065

AMA Style

Vaismoradi M, Jordan S, Logan PA, Amaniyan S, Glarcher M. A Systematic Review of the Legal Considerations Surrounding Medicines Management. Medicina. 2021; 57(1):65. https://doi.org/10.3390/medicina57010065

Chicago/Turabian Style

Vaismoradi, Mojtaba, Sue Jordan, Patricia A. Logan, Sara Amaniyan, and Manela Glarcher. 2021. "A Systematic Review of the Legal Considerations Surrounding Medicines Management" Medicina 57, no. 1: 65. https://doi.org/10.3390/medicina57010065

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