Key result
HF hospitalization is linked to ~17% greater odds of low sacubitril/valsartan adherence.
Why the study?
Medication adherence in chronic conditions is a long-term process, and modeling longitudinal trajectories using routinely collected prescription data is a promising method to describe adherence patterns and identify at-risk groups.
What are the long-term adherence trajectories to sacubitril/valsartan and their associated factors in patients with heart failure?
Cohort (n=4,455)
What are the long-term adherence trajectories to sacubitril/valsartan and their associated factors in patients with heart failure?
Odds Ratio: 1.165 (95% CI 1.151–1.179)
Less than half of heart failure patients maintain high adherence to sacubitril/valsartan over 12 months, with polypharmacy and hospitalizations predicting poorer adherence.
Polypharmacy may hinder sacubitril/valsartan adherence; leaves open whether targeted interventions improve persistence in multimorbid HF.
Medication adherence in chronic conditions is a long-term process. Modeling longitudinal trajectories using routinely collected prescription data is a promising method for describing adherence patterns and identifying at-risk groups. The study aimed to characterize distinct long-term sacubitril/valsartan adherence trajectories and factors associated with them in patients with heart failure (HF). Subjects with incident HF starting sac/val in 2017-2018 were identified from the Campania Regional Database for Medication Consumption. We estimated patients' continuous medication availability (CMA9; R package AdhereR) during a 12-month period. We selected groups with similar CMA9 trajectories (Calinski-Harabasz criterion; R package kml). We performed multinomial regression analysis, assessing the relationship between demographic and clinical factors and adherence trajectory groups. The cohort included 4455 subjects, 70% male. Group-based trajectory modeling identified four distinct adherence trajectories: high adherence (42.6% of subjects; CMA mean 0.91 ± 0.08), partial drop-off (19.6%; CMA 0.63 ± 0.13), moderate adherence (19.3%; CMA 0.54 ± 0.11), and low adherence (18.4%; CMA 0.17 ± 0.12). Polypharmacy was associated with partial drop-off adherence (OR 1.194, 95%CI 1.175-1.214), while the occurrence of ≥1 HF hospitalization (OR 1.165, 95%CI 1.151-1.179) or other hospitalizations (OR 1.481, 95%CI 1.459-1.503) were associated with low adherence. This study found that tailoring patient education, providing support, and ongoing monitoring can boost adherence within different groups, potentially improving health outcomes.
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Mucherino et al. (2023) conducted a cohort in Heart failure (n=4,455). Clinical factors (polypharmacy, hospitalizations) was evaluated on Low adherence trajectory (OR 1.165, 95% CI 1.151-1.179). Among patients with heart failure, the occurrence of ≥1 HF hospitalization was associated with low adherence to sacubitril/valsartan (OR 1.165; 95% CI 1.151-1.179).
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