Ketura Verheye, Ine Vangrieken, Kato De Pril, Els Mehuys, Koen Boussery, Thierry Christiaens, Ellen Van Leeuwen
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引用次数: 0
Abstract
Background
Long-term antidepressant use is widespread in high-income countries. While general practitioners (GPs) are central in reviewing and discontinuing antidepressants, community pharmacists (CP) may support this process. However, barriers and facilitators to CP involvement remain underexplored.
Aim
This study aims to explore CPs' perceptions of long-term antidepressant discontinuation and their roles in the antidepressants discontinuation process and to identify key barriers and facilitators for engaging in this process.
Methods
A cross-sectional online survey was conducted among Belgian CPs. Items assessing perceived roles and barriers/facilitators were rated on Likert scales and categorized by mean scores.
Results
A total of 190 CPs completed the survey. Pharmacists identified their main responsibilities as informing patients, compounding tapering formulations and contacting physicians during tapering when problems arise. The only barrier classified as major was resistance from GPs to antidepressant discontinuation. Eleven major facilitators were identified, including patient-initiated requests, good GP collaboration, strong trust relationships with patients and access to guidelines, information and education on discontinuation of antidepressants.
Conclusion
CPs currently tend to adopt a largely reactive approach towards discontinuing long-term antidepressants. Interventions aiming to promote more proactive engagement may focus on clarifying roles and responsibilities, strengthening collaboration with GPs and supporting pharmacists through education, practical resources and communication training.
期刊介绍:
Basic & Clinical Pharmacology and Toxicology is an independent journal, publishing original scientific research in all fields of toxicology, basic and clinical pharmacology. This includes experimental animal pharmacology and toxicology and molecular (-genetic), biochemical and cellular pharmacology and toxicology. It also includes all aspects of clinical pharmacology: pharmacokinetics, pharmacodynamics, therapeutic drug monitoring, drug/drug interactions, pharmacogenetics/-genomics, pharmacoepidemiology, pharmacovigilance, pharmacoeconomics, randomized controlled clinical trials and rational pharmacotherapy. For all compounds used in the studies, the chemical constitution and composition should be known, also for natural compounds.