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In search of a standard when analyzing medication adherence in patients with heart failure using claims data: a
Katrin Krueger1, Nina Griese-Mammen1, Ingrid Schubert2
1Department of Medicine, ABDA - Federal Union of German Associations of Pharmacists, Unter den Linden 19-23, D-10117, Berlin, Germany.
Insights
Medication non-adherence in heart failure patients is a significant issue. This review found varied methods for measuring adherence using claims data, highlighting a need for standardized reporting to improve patient outcomes.
Area of Science:
- Pharmacoeconomics
- Health Services Research
- Cardiology
Background:
- Medication non-adherence is a critical factor impacting patient outcomes in heart failure.
- Claims data offer a valuable resource for assessing adherence in large populations.
- Standardized methods for operationalizing adherence measures are lacking.
Purpose of the Study:
- To systematically review the operationalization of medication adherence measures in heart failure patients using claims data.
- To identify common methodologies and variations in adherence assessment.
- To highlight areas for improvement in reporting adherence measurement.
Main Methods:
- Systematic literature search of MEDLINE, EMBASE, and Cochrane databases.
- Inclusion of 28 studies assessing medication adherence in heart failure.
- Quality assessment using the Quality in Prognosis Studies tool.
Main Results:
- Medication possession ratio (11 studies) and proportion of days covered (15 studies) were common adherence measures.
- Wide variation existed in assumptions for dosage, switching within classes, stockpiling, and censoring events (hospital stays, death).
- Reporting quality of methodologies varied significantly, with no gold standard identified.
Conclusions:
- Current methods for quantifying medication adherence in heart failure using claims data lack standardization.
- Comprehensive reporting of methodological parameters is essential for accurate assessment.
- Standardized approaches are needed to improve the reliability and comparability of adherence research.
Abstract:
To determine and address medication non-adherence is important and may improve patient outcomes. Our aim was to perform a systematic review on the operationalization of adherence measures in patients with heart failure using claims data. We searched the MEDLINE, EMBASE, and Cochrane databases. A quality check of the full-text articles was performed using the Quality in Prognosis Studies tool. We included 28 studies. Eleven studies used the medication possession ratio, 15 the proportion of days covered, and six studies used own methods to calculate medication adherence. Almost all studies used an observation period of 1 year. Twenty-one studies considered angiotensin converting enzyme inhibitors or angiotensin receptor antagonists, 17 beta-blockers, 11 diuretics, eight mineralocorticoid receptor antagonists, six digitalis-glycosides, and six statins. Eight studies looked at single substance classes; 18 studies analyzed more than one drug class. Different assumptions for the dosage were used. In seven studies, switching within therapeutic classes was allowed. Three studies allowed stockpiling, nine studies censored hospital stays, and four studies censored death. Seventeen studies dichotomized the results, applying the cutoff ≥ 0.8 to define a patient as adherent. Eight studies analyzed adherence as a continuous value. The reporting quality of the methodology applied varied widely between studies. A gold standard is currently not available for the quantification of medication adherence in patients with chronic heart failure via claims data. To assess the methodology, the following parameters should be described: method of measurements, observation period, substances, dosing, switches, stockpiling, truncations, statistical analysis, and cutoff for adherence.
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