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Adherence to newer second‐line oral antidiabetic drugs among people with type 2 diabetes—A systematic review.

Authors :
Holdt‐Caspersen, Nynne Sophie
Dethlefsen, Claus
Vestergaard, Peter
Hejlesen, Ole
Hangaard, Stine
Jensen, Morten Hasselstrøm
Source :
Pharmacology Research & Perspectives; Apr2024, Vol. 12 Issue 2, p1-10, 10p
Publication Year :
2024

Abstract

The adherence to oral antidiabetic drugs (OADs) among people with type 2 diabetes (T2D) is suboptimal. However, new OADs have been marketed within the last 10 years. As these new drugs differ in mechanism of action, treatment complexity, and side effects, they may influence adherence. Thus, the aim of this study was to assess the adherence to newer second‐line OADs, defined as drugs marketed in 2012–2022, among people with T2D. A systematic review was performed in CINAHL, Cochrane Trials, Embase, PubMed, PsycINFO, and Scopus. Articles were included if they were original research of adherence to newer second‐line OADs and reported objective adherence quantification. The quality of the articles was assessed using JBI's critical appraisal tools. The overall findings were reported according to the preferred reporting items for systematic reviews and meta‐analyses (PRISMA) guidelines and summarized in a narrative synthesis. All seven included articles were European retrospective cohort studies investigating alogliptin, canagliflozin, dapagliflozin, empagliflozin, and unspecified types of SGLT2i. Treatment discontinuation and medication possession ratio (MPR) were the most frequently reported adherence quantification measures. Within the first 12 months of treatment, 29%–44% of subjects on SGLT2i discontinued the treatment. In terms of MPR, 61.7%–94.9% of subjects on either alogliptin, canagliflozin, dapagliflozin, empagliflozin or an unspecified SGLT2i were adherent. The two investigated adherence quantification measures, treatment discontinuation and MPR, suggest that adherence to the newer second‐line OADs may be better than that of older OADs. However, a study directly comparing older and newer OADs should be done to verify this. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20521707
Volume :
12
Issue :
2
Database :
Complementary Index
Journal :
Pharmacology Research & Perspectives
Publication Type :
Academic Journal
Accession number :
176585799
Full Text :
https://doi.org/10.1002/prp2.1185