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Pilot Implementation of Falsified Medicines Directive in Hospital Pharmacy to Develop Best Practices for Medicine Decommissioning Process
Background: The introduction of a medicines verification and decommissioning system into the hospital pharmacy may result in an increased workload for pharmacy staff. The pilot implementation allows us to understand all the implications of the process, optimize process workflows, and estimate the ti...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7151703/ https://www.ncbi.nlm.nih.gov/pubmed/32182834 http://dx.doi.org/10.3390/pharmacy8010034 |
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author | Merks, Piotr Świeczkowski, Damian Zerhau, Mikołaj Gawronska, Anna Kowalczuk, Anna Gajewski, Klaudiusz Däinghaus, Ralf Jaguszewski, Miłosz Brindley, David |
author_facet | Merks, Piotr Świeczkowski, Damian Zerhau, Mikołaj Gawronska, Anna Kowalczuk, Anna Gajewski, Klaudiusz Däinghaus, Ralf Jaguszewski, Miłosz Brindley, David |
author_sort | Merks, Piotr |
collection | PubMed |
description | Background: The introduction of a medicines verification and decommissioning system into the hospital pharmacy may result in an increased workload for pharmacy staff. The pilot implementation allows us to understand all the implications of the process, optimize process workflows, and estimate the time and cost of implementation. Methods: All the packages received at the hospital pharmacy had a 2D data matrix codes and were scanned. We analyzed the time needed to unpack a variety of products, scan them, and receive the notification. Results: In total, 144 packages were scanned at an average time of 3.05 s, with most (86.9%) under 4 s. Manual decommissioning using handheld scanners was less efficient than the automated solution tested and resulted in an additional 0.4 full-time equivalent hours per million packages per year. The pattern and total time of manual scanning depended not only on the quantity but also the size of the package and type of packing. Conclusions: This evaluation of scanning performance allows optimizing the process at operational, technical, and resource levels for medicine verification and decommissioning. |
format | Online Article Text |
id | pubmed-7151703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-71517032020-04-20 Pilot Implementation of Falsified Medicines Directive in Hospital Pharmacy to Develop Best Practices for Medicine Decommissioning Process Merks, Piotr Świeczkowski, Damian Zerhau, Mikołaj Gawronska, Anna Kowalczuk, Anna Gajewski, Klaudiusz Däinghaus, Ralf Jaguszewski, Miłosz Brindley, David Pharmacy (Basel) Article Background: The introduction of a medicines verification and decommissioning system into the hospital pharmacy may result in an increased workload for pharmacy staff. The pilot implementation allows us to understand all the implications of the process, optimize process workflows, and estimate the time and cost of implementation. Methods: All the packages received at the hospital pharmacy had a 2D data matrix codes and were scanned. We analyzed the time needed to unpack a variety of products, scan them, and receive the notification. Results: In total, 144 packages were scanned at an average time of 3.05 s, with most (86.9%) under 4 s. Manual decommissioning using handheld scanners was less efficient than the automated solution tested and resulted in an additional 0.4 full-time equivalent hours per million packages per year. The pattern and total time of manual scanning depended not only on the quantity but also the size of the package and type of packing. Conclusions: This evaluation of scanning performance allows optimizing the process at operational, technical, and resource levels for medicine verification and decommissioning. MDPI 2020-03-09 /pmc/articles/PMC7151703/ /pubmed/32182834 http://dx.doi.org/10.3390/pharmacy8010034 Text en © 2020 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 | Article Merks, Piotr Świeczkowski, Damian Zerhau, Mikołaj Gawronska, Anna Kowalczuk, Anna Gajewski, Klaudiusz Däinghaus, Ralf Jaguszewski, Miłosz Brindley, David Pilot Implementation of Falsified Medicines Directive in Hospital Pharmacy to Develop Best Practices for Medicine Decommissioning Process |
title | Pilot Implementation of Falsified Medicines Directive in Hospital Pharmacy to Develop Best Practices for Medicine Decommissioning Process |
title_full | Pilot Implementation of Falsified Medicines Directive in Hospital Pharmacy to Develop Best Practices for Medicine Decommissioning Process |
title_fullStr | Pilot Implementation of Falsified Medicines Directive in Hospital Pharmacy to Develop Best Practices for Medicine Decommissioning Process |
title_full_unstemmed | Pilot Implementation of Falsified Medicines Directive in Hospital Pharmacy to Develop Best Practices for Medicine Decommissioning Process |
title_short | Pilot Implementation of Falsified Medicines Directive in Hospital Pharmacy to Develop Best Practices for Medicine Decommissioning Process |
title_sort | pilot implementation of falsified medicines directive in hospital pharmacy to develop best practices for medicine decommissioning process |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7151703/ https://www.ncbi.nlm.nih.gov/pubmed/32182834 http://dx.doi.org/10.3390/pharmacy8010034 |
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