Patterns of suboptimal antipsychotic use and misuse in Australia: What can routinely collected data tell us?

Author:

Brett Jonathan123ORCID,Gillies Malcolm B.1ORCID,Buckley Nicholas A.34ORCID,Pearson Sallie‐Anne1ORCID,Zoega Helga15ORCID

Affiliation:

1. Medicines Intelligence in Health, School of Population Health, Faculty of Medicine and Health UNSW Sydney Sydney New South Wales Australia

2. Clinical Therapeutics Department St Vincent's Hospital Sydney NSW Australia

3. New South Wales Poisons Information Centre Westmead Children's Hospital Sydney NSW Australia

4. Clinical Pharmacology and Toxicology Research Group, Biomedical Informatics and Digital Health University of Sydney Sydney Australia

5. Centre of Public Health Sciences, Faculty of Medicine University of Iceland Reykjavík Iceland

Abstract

AimsThere are increasing concerns about harms related to suboptimal antipsychotic use. Here we describe recent population‐based trends in antipsychotic use and harms in Australia and identify population groups exhibiting patterns of use likely to contribute to these harms.MethodsUsing population‐based data from the Australian Pharmaceutical Benefits Scheme (2015‐2020), poisoning calls to the New South Wales (NSW) Poisons Information Centre (2015‐2020) and poisoning deaths in all coronial records (2005‐2018) in Australia, we measured trends in the prevalence of antipsychotic use and related deaths and poisonings. We applied latent class analyses to identify patterns of antipsychotic use that may contribute to harms.ResultsQuetiapine and olanzapine had the highest prevalence of use between 2015 and 2020. Noteworthy trends included increases of 9.1% and 30.8% in quetiapine use and poisonings, while olanzapine use decreased by 4.5% but poisonings increased by 32.7%. Quetiapine and olanzapine poisonings and related deaths had the highest rates of co‐ingestion of opioids, benzodiazepines and pregabalin compared to other antipsychotics. We identified six distinct population groups using antipsychotics: (i) ongoing high‐dose use with sedatives (8%), (ii) ongoing use (42%), (iii) ongoing use with analgesics and sedatives (11%), (iv) long‐term low‐dose use (9%), (v) sporadic use (20%) and (vi) sporadic use with analgesics (10%).ConclusionOngoing potentially suboptimal antipsychotic use and associated harms highlight the need to monitor such patterns of use, for example through prescription monitoring systems.

Funder

National Health and Medical Research Council

University of New South Wales

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

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