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Medication safety risks to be managed in national implementation of automatic substitution of biological medicines: a qualitative study

OBJECTIVES: To explore relevant Finnish stakeholders’ perceptions on the automatic substitution of biological medicines with particular focus on medication safety and issues that need to be considered to create an appropriate model for automatic biological product substitution. DESIGN: Qualitative i...

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Autores principales: Tolonen, Hanna M, Airaksinen, Marja SA, Ruokoniemi, Päivi, Hämeen-Anttila, Katri, Shermock, Kenneth M, Kurki, Pekka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830661/
https://www.ncbi.nlm.nih.gov/pubmed/31662405
http://dx.doi.org/10.1136/bmjopen-2019-032892
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author Tolonen, Hanna M
Airaksinen, Marja SA
Ruokoniemi, Päivi
Hämeen-Anttila, Katri
Shermock, Kenneth M
Kurki, Pekka
author_facet Tolonen, Hanna M
Airaksinen, Marja SA
Ruokoniemi, Päivi
Hämeen-Anttila, Katri
Shermock, Kenneth M
Kurki, Pekka
author_sort Tolonen, Hanna M
collection PubMed
description OBJECTIVES: To explore relevant Finnish stakeholders’ perceptions on the automatic substitution of biological medicines with particular focus on medication safety and issues that need to be considered to create an appropriate model for automatic biological product substitution. DESIGN: Qualitative interview study. METHODS: Data were collected in semistructured individual (n=17), pair (n=7) and group (n=8) interviews (32 interviews, 62 participants) in 2018. Participants represented a wide range of stakeholders involved in the pharmacotherapy process: community pharmacists (n=8 interviews), authorities (n=7), prescribers (n=7), pharmaceutical industry and wholesalers (n=6), patients/customers (n=2), hospital pharmacists (n=1) and nurses (n=1). Inductive content analysis was performed. RESULTS: Benefits of automatic substitution were identified as cost savings, more patients receiving biological treatments and enhanced continuity of treatment. Six major risk categories were identified: (1) the patient’s medication is interrupted or complicated temporarily or permanently, (2) the patient uses two products with the same active substance, (3) the traceability of the product is compromised, (4) the patient cannot get into healthcare in case of problems, (5) the patient does not receive substitution-related advice from a pharmacy and (6) the patient is distracted by the support material he/she receives. Several risk mitigation measures were commonly mentioned: medication and device counselling by pharmacists (n=23), infrequent substitution interval (n=15) and better knowledge on biosimilars among healthcare providers (n=13). CONCLUSION: Automatic substitution of biologics is associated with risks that should be prospectively managed before implementing the procedure. The substitution also introduces new tasks and communication needs to those involved in actual medication use process, particularly to community pharmacists who will be responsible for substitution and counselling the patients.
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spelling pubmed-68306612019-11-20 Medication safety risks to be managed in national implementation of automatic substitution of biological medicines: a qualitative study Tolonen, Hanna M Airaksinen, Marja SA Ruokoniemi, Päivi Hämeen-Anttila, Katri Shermock, Kenneth M Kurki, Pekka BMJ Open Qualitative Research OBJECTIVES: To explore relevant Finnish stakeholders’ perceptions on the automatic substitution of biological medicines with particular focus on medication safety and issues that need to be considered to create an appropriate model for automatic biological product substitution. DESIGN: Qualitative interview study. METHODS: Data were collected in semistructured individual (n=17), pair (n=7) and group (n=8) interviews (32 interviews, 62 participants) in 2018. Participants represented a wide range of stakeholders involved in the pharmacotherapy process: community pharmacists (n=8 interviews), authorities (n=7), prescribers (n=7), pharmaceutical industry and wholesalers (n=6), patients/customers (n=2), hospital pharmacists (n=1) and nurses (n=1). Inductive content analysis was performed. RESULTS: Benefits of automatic substitution were identified as cost savings, more patients receiving biological treatments and enhanced continuity of treatment. Six major risk categories were identified: (1) the patient’s medication is interrupted or complicated temporarily or permanently, (2) the patient uses two products with the same active substance, (3) the traceability of the product is compromised, (4) the patient cannot get into healthcare in case of problems, (5) the patient does not receive substitution-related advice from a pharmacy and (6) the patient is distracted by the support material he/she receives. Several risk mitigation measures were commonly mentioned: medication and device counselling by pharmacists (n=23), infrequent substitution interval (n=15) and better knowledge on biosimilars among healthcare providers (n=13). CONCLUSION: Automatic substitution of biologics is associated with risks that should be prospectively managed before implementing the procedure. The substitution also introduces new tasks and communication needs to those involved in actual medication use process, particularly to community pharmacists who will be responsible for substitution and counselling the patients. BMJ Publishing Group 2019-10-28 /pmc/articles/PMC6830661/ /pubmed/31662405 http://dx.doi.org/10.1136/bmjopen-2019-032892 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Qualitative Research
Tolonen, Hanna M
Airaksinen, Marja SA
Ruokoniemi, Päivi
Hämeen-Anttila, Katri
Shermock, Kenneth M
Kurki, Pekka
Medication safety risks to be managed in national implementation of automatic substitution of biological medicines: a qualitative study
title Medication safety risks to be managed in national implementation of automatic substitution of biological medicines: a qualitative study
title_full Medication safety risks to be managed in national implementation of automatic substitution of biological medicines: a qualitative study
title_fullStr Medication safety risks to be managed in national implementation of automatic substitution of biological medicines: a qualitative study
title_full_unstemmed Medication safety risks to be managed in national implementation of automatic substitution of biological medicines: a qualitative study
title_short Medication safety risks to be managed in national implementation of automatic substitution of biological medicines: a qualitative study
title_sort medication safety risks to be managed in national implementation of automatic substitution of biological medicines: a qualitative study
topic Qualitative Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830661/
https://www.ncbi.nlm.nih.gov/pubmed/31662405
http://dx.doi.org/10.1136/bmjopen-2019-032892
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