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Medication safety risks to be managed in national implementation of automatic substitution of biological medicines: a qualitative study.
- Source :
-
BMJ open [BMJ Open] 2019 Oct 28; Vol. 9 (10), pp. e032892. Date of Electronic Publication: 2019 Oct 28. - Publication Year :
- 2019
-
Abstract
- 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.<br />Design: Qualitative interview study.<br />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.<br />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).<br />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.<br />Competing Interests: Competing interests: HMT has participated in a congress for which participation fee was sponsored by Roche Oy.<br /> (© 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.)
- Subjects :
- Adult
Attitude to Health
Continuity of Patient Care
Cost Savings
Drug Costs
Finland
Health Policy
Humans
Qualitative Research
Biosimilar Pharmaceuticals adverse effects
Biosimilar Pharmaceuticals economics
Biosimilar Pharmaceuticals standards
Patient Safety
Risk Management
Stakeholder Participation
Subjects
Details
- Language :
- English
- ISSN :
- 2044-6055
- Volume :
- 9
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- BMJ open
- Publication Type :
- Academic Journal
- Accession number :
- 31662405
- Full Text :
- https://doi.org/10.1136/bmjopen-2019-032892