Prescribing and deprescribing trends in schizophrenia: An overview of inpatients in Belgium and in the Canadian province of Québec

Author:

Lagreula Juliette12ORCID,Dagenais‐Beaulé Vincent34,de Timary Philippe56,Elens Laure78,Dalleur Olivia19

Affiliation:

1. Clinical Pharmacy Research Group (CLIP)‐Louvain Drug Research Institute (LDRI) UCLouvain Brussels Belgium

2. Fonds de la Recherche Scientifique – FNRS Brussels Belgium

3. Pharmacy Department & Lady Davis Institute for Medical Research Jewish General Hospital Montreal Québec Canada

4. Faculté de Pharmacie Université de Montréal Montreal Québec Canada

5. Institute of Neuroscience (IoNS) UCLouvain Brussels Belgium

6. Adult Psychiatry Department Cliniques Universitaires Saint‐Luc Brussels Belgium

7. Integrated PharmacoMetrics, PharmacoGenomics and PharmacoKinetics (PMGK)‐Louvain Drug Research Institute (LDRI) UCLouvain Brussels Belgium

8. Louvain Center for Toxicology and Applied Pharmacology (LTAP)‐Institut de Recherche Expérimentale et Clinique (IREC) UCLouvain Brussels Belgium

9. Pharmacy Department Cliniques Universitaires Saint‐Luc Brussels Belgium

Abstract

AbstractAlthough switching to antipsychotic monotherapy improves patient outcomes in schizophrenia, antipsychotic deprescribing is rarely performed, and its use varies between countries, as do psychotropic prescribing patterns. This study aimed to determine factors associated with antipsychotic deprescribing at discharge after a psychiatric hospitalization and to compare psychotropic prescribing patterns between Belgium and Québec, Canada. Data on adult inpatients with schizophrenia were collected retrospectively in seven hospitals. At discharge, the number of antipsychotics had decreased in 22.2% of the 63 Canadian patients and 9.9% of the 516 Belgian patients. A number of factors increased the likelihood of antipsychotic deprescribing: a hospitalization in the Canadian hospital (aOR = 4.13, 95% CI 1.48–11.5), living in a residential facility (aOR = 2.51, 95% CI 1.05–4.39), ≥2 previous antipsychotic trials (aOR = 15.38, 95% CI 3.62–65.36), having an antipsychotic side effect (aOR = 1.86, 95% CI 1.01–3.44) and being in a general hospital (aOR = 2.28, 95% CI 1.09–4.75). Patients on a long‐acting injectable antipsychotic (aOR = 0.51, 95% CI 0.26–0.98), with prior clozapine use (aOR = 0.36, 95% CI 0.13–0.95), greater antipsychotic exposure (aOR = 0.35, 95% CI 0.2–0.61) and more hypno‐sedatives (aOR = 0.65, 95% CI 0.43–0.98), were less likely to be deprescribed. Specific deprescribing interventions could target patients who are less likely to be deprescribed.

Funder

Fonds De La Recherche Scientifique - FNRS

Publisher

Wiley

Subject

Pharmacology,Toxicology,General Medicine

Reference60 articles.

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