Quality use of publicly subsidised tapentadol in Australia: a population‐based analysis

Author:

Camacho Ximena12ORCID,Schaffer Andrea L.123ORCID,Brett Jonathan124,Pratt Nicole25ORCID,Buckley Nicholas A.26ORCID,Henry David27,Pearson Sallie‐Anne12ORCID

Affiliation:

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

2. NHMRC Centre of Research Excellence in Medicines Intelligence Sydney New South Wales Australia

3. The Bennett Institute for Applied Data Science, Nuffield Department of Primary Care Health Sciences University of Oxford Oxford UK

4. Clinical Pharmacology and Toxicology St Vincent's Hospital Sydney New South Wales Australia

5. Quality Use of Medicines and Pharmacy Research Centre, Clinical and Health Sciences University of South Australia Adelaide South Australia Australia

6. Biomedical Informatics and Digital Health, Faculty of Medicine and Health The University of Sydney Sydney New South Wales Australia

7. Institute for Evidence Based Healthcare, Bond University Gold Coast Queensland Australia

Abstract

AbstractBackgroundSustained‐release (SR) tapentadol was listed on Australia's Pharmaceutical Benefits Scheme (PBS) in 2014 for chronic severe pain requiring long‐term opioid treatment. Dispensings have increased since listing despite declining trends in other PBS‐listed opioids. Preferential prescribing of SR opioids may increase the risk of dependence and accidental overdose, particularly when used to treat acute pain.AimsTo explore the quality use of publicly subsidised tapentadol in Australia.MethodsWe examined annual initiation rates and patterns of use of tapentadol (SR) in the dispensing records of a 10% random sample of PBS‐eligible Australians (2014–2021). We used national tapentadol sales data to assess the proportion of sales attributable to the PBS.ResultsTapentadol initiation increased from 2014, peaking at 7.5/1000 adult population in 2019 before declining to 5.3/1000 in 2021. We identified 63 766 new users between 2014 and 2020, of whom 92.8% discontinued in the first year following initiation, 58.0% had only a single dispensing and 34.3% had no other opioids dispensed in the 3 months before or after initiation. 27.8% of new users were dispensed tapentadol on the same day as potentially interacting medicines. There was a sustained drop in the proportion of sales attributable to the PBS from June 2020 onwards, from an average of 69.1%, to 63.9% of pack sales.ConclusionsPatterns of use suggest tapentadol (SR) is generally used for short duration. Although most tapentadol sold in Australia is subsidised, there is evidence of a shift towards private sales.

Funder

National Health and Medical Research Council

Publisher

Wiley

Subject

Internal Medicine

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