Purpose: To provide a descriptive analysis of adherence to secondary prevention therapies and mortality among post myocardial infarction (MI) Medicare beneficiaries.
Methods: The 2006-2007 5% national sample of Medicare claims data were used. Beneficiaries ≥65 years old, hospitalized for acute MI between January 1 and December 31, 2006, were identified using a validated algorithm. Only those who survived for ≥90 days were included in analysis. Patients with ESRD and disabilities were excluded. Three classes of secondary prevention medications were examined: statins, beta-blockers, and ACEI/ARBs. Patients were classified as adherent if proportion of days covered during follow-up for a class of medication was ≥ 0.8.
Results: Of the 11,472 patients identified, 58.3% female, 87.7% white, 37.9% lived in the South, and 42.1% were 75-85 year olds. Among 5,036 statin users, 34.7% were adherent; a greater proportion of the non-adherent patients were from the South (38.4% vs. 36.5%; p=0.0069) compared to adherent patients. Among beta-blocker users (6,016), 38.9% were adherent; a higher proportion of the non-adherent patients were black (10.3% vs. 8.1%; p=0.0109) and from the Northeast (24.0% vs. 21.0%; p=0.0015) compared to adherent patients. Among 5,327 ACEI/ARBs users, 32.4% were adherent; non-adherent patients were more likely to be black (11.1% vs. 9.3%; p=0.0363) compared to adherent patients. Overall, 16.1% of patients died within a year. Across all three classes of medications, non-adherent patients were more likely to die within a year compared to adherent patients: statins (15.8 % vs. 1.8%; p<.0001), beta-blockers (20.9% vs. 2.4%; p<.0001), and ACEI/ARBs (18.9 % vs. 2.6%; p<.0001).
Conclusion: There are racial and geographic disparities in adherence to secondary prevention therapies among elderly post-MI patients and nonadherence is associated with a higher risk of mortality. Further research needs to identify predictors of such disparities and appropriate measures need to be designed to improve medication adherence.