Key result
Self-reported low medication adherence shows no link to therapeutic inertia in patients with hypertension.
Why the study?
Therapeutic inertia remains prevalent in hypertension management, but the degree to which self-reported antihypertensive adherence is associated with therapeutic inertia under intensive blood pressure goals remains unclear.
Is self-reported medication adherence associated with therapeutic inertia in hypertensive patients above intensive BP goals?
Cross-Sectional (n=1,009)
Is self-reported medication adherence associated with therapeutic inertia in hypertensive patients above intensive BP goals?
Self-reported medication adherence was not associated with therapeutic inertia in patients with hypertension above intensive BP goals, suggesting other factors drive the failure to intensify therapy.
Therapeutic inertia in uncontrolled hypertension persists independent of adherence; leaves open prospective identification of clinician- and system-level drivers.
BACKGROUND: Therapeutic inertia (TI), failure to intensify antihypertensive medication when blood pressure (BP) is above goal, remains prevalent in hypertension management. The degree to which self-reported antihypertensive adherence is associated with TI with intensive BP goals remains unclear. METHODS AND RESULTS: Cross-sectional analysis was performed of the 12-month visit of participants in the intensive arm of SPRINT (Systolic Blood Pressure Intervention Trial), which randomized adults to intensive (<120 mm Hg) versus standard (<140 mm Hg) systolic BP goals. TI was defined as no increase in antihypertensive regimen intensity score, which incorporates medication number and dose, when systolic BP is ≥120 mm Hg. Self-reported adherence was assessed using the 8-Item Morisky Medication Adherence Scale (MMAS-8) and categorized as low (MMAS-8 score <6), medium (MMAS-8 score 6 to <8), and high (MMAS-8 score 8). Poisson regressions estimated prevalence ratios (PRs) and 95% CIs for TI associated with MMAS-8. Among 1009 intensive arm participants with systolic BP >120 mm Hg at the 12-month visit (mean age, 69.6 years; 35.2% female, 28.8% non-Hispanic Black), TI occurred in 50.8% of participants. Participants with low adherence (versus high) were younger and more likely to be non-Hispanic Black or smokers. The prevalence of TI among patients with low, medium, and high adherence was 45.0%, 53.5%, and 50.4%, respectively. After adjustment, neither low nor medium adherence (versus high) were associated with TI (PR, 1.11 [95% CI, 0.87-1.42]; PR, 1.08 [95% CI, 0.84-1.38], respectively). CONCLUSIONS: Although clinician uncertainty about adherence is often cited as a reason for why antihypertensive intensification is withheld when above BP goals, we observed no evidence of an association between self-reported adherence and TI.
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Jacobs et al. (2024) conducted a cross-sectional in Hypertension (n=1,009). Low self-reported medication adherence vs. High self-reported medication adherence was evaluated on Therapeutic inertia (no increase in antihypertensive regimen intensity score when systolic BP is ≥120 mm Hg) (PR 1.11, 95% CI 0.87-1.42). Self-reported low medication adherence was not associated with therapeutic inertia compared to high adherence among patients with hypertension (PR 1.11; 95% CI 0.87-1.42).
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