Adherence, Persistence, and Switching Among People Prescribed Sodium Glucose Co-transporter 2 Inhibitors: A Nationwide Retrospective Cohort Study.


Journal

Advances in therapy
ISSN: 1865-8652
Titre abrégé: Adv Ther
Pays: United States
ID NLM: 8611864

Informations de publication

Date de publication:
11 2019
Historique:
received: 08 08 2019
pubmed: 5 9 2019
medline: 26 6 2020
entrez: 5 9 2019
Statut: ppublish

Résumé

Non-adherence and non-persistence to diabetes medications are associated with worse clinical outcomes. In this study, we aimed to characterise the 1-year switching, adherence, and persistence patterns among people with diabetes aged 18 years and older prescribed sodium-glucose co-transporter 2 inhibitors (SGLT2is) in Australia. Using data from Australia's national Pharmaceutical Benefits Scheme (PBS), we identified 11,981 adults (mean age 60.9 years; 40.5% female) newly initiated on SGLT2is (5993 dapagliflozin; 5988 empagliflozin) from September 2015 to August 2017. Adherence was assessed via the proportion of days covered (PDC), persistence was defined as the continuous use of SGLT2i without a gap of ≥ 90 days, and switching was defined as the first change from dapagliflozin to empagliflozin or vice versa. Generalised linear models (GLMs) were used to compare the adherence (PDC = continuous), logistic regression models were used to compare the likelihoods of being adherent (PDC ≥ 0.80), and Cox proportional hazard models were used to compare the likelihoods of persistence and switching between people prescribed empagliflozin and dapagliflozin. Overall, 65.8% (7879/11,981) of people dispensed SGLT2is were adherent (PDC ≥ 0.80) and 72.1% (8644/11,981) were persistent at 12 months. The mean PDC was 0.79 ± 0.27. The use of empagliflozin was associated with higher adherence (PDC = continuous) [odds ratio (OR) 1.04, 95% confidence interval (CI) 1.03-1.05], being adherent (OR 1.39, 95% CI 1.29-1.51), and persisting for 12 months [hazard ratio (HR) 1.14, 95% CI 1.06-1.22] compared with dapagliflozin. Only 4.3% (509/11,981) of people switched between the SGLT2i. Compared with dapagliflozin, people initiated on empagliflozin were less likely to switch [HR 0.46, 95% CI 0.38-0.55]. A considerable proportion of Australians prescribed SGLT2is were non-adherent or non-persistent. However, empagliflozin was associated with better adherence and persistence rates and a lower likelihood of switching compared with dapagliflozin.

Identifiants

pubmed: 31482509
doi: 10.1007/s12325-019-01077-3
pii: 10.1007/s12325-019-01077-3
doi:

Substances chimiques

Hypoglycemic Agents 0
Sodium-Glucose Transporter 2 Inhibitors 0

Banques de données

figshare
['10.6084/m9.figshare.9712703']

Types de publication

Journal Article

Langues

eng

Pagination

3265-3278

Auteurs

Richard Ofori-Asenso (R)

Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, VIC, Australia. richard.ofori-asenso@monash.edu.

Danny Liew (D)

Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, VIC, Australia.

Samanta Lalic (S)

Centre for Medicine Use and Safety, Faculty of Pharmacy and Pharmaceutical Sciences, Monash University, Melbourne, VIC, Australia.

Mohsen Mazidi (M)

Division of Food and Nutrition Science, Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.

Dianna J Magliano (DJ)

Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, VIC, Australia.
Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.

Zanfina Ademi (Z)

Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, VIC, Australia.

J Simon Bell (JS)

Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, VIC, Australia.
Centre for Medicine Use and Safety, Faculty of Pharmacy and Pharmaceutical Sciences, Monash University, Melbourne, VIC, Australia.
School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, Australia.

Jenni Ilomaki (J)

Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, VIC, Australia.
Centre for Medicine Use and Safety, Faculty of Pharmacy and Pharmaceutical Sciences, Monash University, Melbourne, VIC, Australia.

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Classifications MeSH