Abstract
Background
Statins are widely prescribed for the primary and secondary prevention of cardiovascular disease (CVD), but their effectiveness is dependent on the level of adherence and persistence.
Objectives
This study aimed to explore the patterns of switching, adherence and persistence among the Australian general population with newly dispensed statins.
Methods
A retrospective cohort study was conducted using a random sample of data from the Australian national prescription claims data. Switching, adherence to and persistence with statins were assessed for people starting statins from 1 January 2015 to 31 December 2019. Switching was defined as either switching to another intensity of statin, to another statin or to a non-statin agent. Non-persistence to treatment was defined as discontinuation (i.e. ≥90 days with no statin) of coverage. Adherence was measured using proportion of days covered (PDC), and patients with PDC < 0.80 were considered non-adherent. Cox proportional hazard models were used to compare discontinuation, switching and reinitiation between different statins.
Results
A cohort of 141,062 people dispensed statins and followed over a median duration of 2.5 years were included. Of the cohort, 29.3% switched statin intensity, 28.4% switched statin type, 3.7% switched to ezetimibe and in 2.7%, ezetimibe was added as combination therapy during the study period. Overall, 58.8% discontinued statins based on the 90-day gap criteria, of whom 55.2% restarted. The proportion of people non-adherent was 24.0% at 6 months to 49.0% at 5 years. People on low and moderate intensity statins were more likely to discontinue compared to those on high-intensity statins (hazard ratio [HR] 1.20, 95% confidence interval [CI] 1.09–1.31), (HR 1.28, 95%CI 1.14–1.42), respectively. Compared to maintaining same statin type and intensity, switching statins, which includes up-titration (HR 0.77, 95%CI 0.70 to 0.86) was associated with less likelihood of discontinuation after reinitiation.
Conclusions
Long-term persistence and adherence to statins remains generally poor among Australians, which limits the effectiveness of these medicines and the consequent health impact they may provide for individuals (and by extension, the population impact when poor persistence and adherence is considered in the statin-taking population). Switching between statins is prevalent in one third of statin users, although any clinical benefit of the observed switching trend is unknown. This, combined with the high volume of statin prescriptions, highlights the need for better strategies to address poor persistence and adherence.
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Abbreviations
- CVD:
-
Cardiovascular disease
- PBS:
-
Pharmaceutical Benefits Scheme
- LDL-C:
-
Low-density lipoprotein cholesterol
- PCSK9:
-
Proprotein convertase subtilisin/kexin type 9
- PDC:
-
Proportion of days covered
- GPs:
-
General practitioners
- PBAC:
-
Pharmaceutical Benefits Advisory Committee
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Data are accessible or available upon request.
Funding
Amgen Australia Pty Ltd. has provided financial support to Monash University for analyses that describe the current burden and treatment of CVD in Australia, of which this manuscript forms a part.
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ST conceptualized the study, performed the analysis, validated and cross-checked analysis outputs with assistance from ROA and wrote the initial draft of the manuscript; CM, AJO, JI, MP, EZ and DL contributed to writing of the manuscript; JI, DT, SL provided constructive feedback and expert advice; ROA provided statistical support and expert feedback. ZA contributed to writing of the manuscript and supervised the project.
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ROA declares no conflict of interest. Authors ZA, EZ, ST, CM, MP, AO and DL have received research funding from Amgen Australia Pty Ltd. underlying this manuscript. JI has received funding from AstraZeneca, Amgen, Dementia Australia, National Breast Cancer Foundation and National Health and Medical Research Council. DT is employed by Amgen Australia Pty Ltd., and SL was employed by Amgen Australia Pty Ltd. at the time of development of the research and is now employed by Amgen Europe GmbH. EZ reports grant support from Amgen, AstraZeneca, Pfizer, and Shire, outside the submitted work. DL declares grants from Abbvie, Amgen, AstraZeneca, Bristol-Myers Squibb, Pfizer and Sanofi, and past participation in advisory boards and/or receipt of honoraria from Abbvie, Amgen, Astellas, AstraZeneca, Bristol-Myers Squibb, Edwards Lifesciences, Novartis, Pfizer, Sanofi and Shire, outside the submitted work.
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Talic, S., Marquina, C., Ofori-Asenso, R. et al. Switching, Persistence and Adherence to Statin Therapy: a Retrospective Cohort Study Using the Australian National Pharmacy Data. Cardiovasc Drugs Ther 36, 867–877 (2022). https://doi.org/10.1007/s10557-021-07199-7
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DOI: https://doi.org/10.1007/s10557-021-07199-7