Why the study?
The risk-to-benefit ratio of cardioprotective medications in frail older adults following myocardial infarction is uncertain.
Does frailty reduce the likelihood of being prescribed guideline-recommended cardioprotective medications following myocardial infarction compared to non-frail patients?
Does frailty reduce the likelihood of being prescribed guideline-recommended cardioprotective medications following myocardial infarction compared to non-frail patients?
Frail patients are consistently prescribed fewer guideline-recommended cardioprotective medications following myocardial infarction compared to non-frail patients.
Frail post-MI patients may face undertreatment; confirms prescribing gaps across studies and leaves open optimal frailty-adjusted strategies.
AIMS: The risk-to-benefit ratio of cardioprotective medications in frail older adults is uncertain. The objective was to systematically review prescribing of guideline-recommended cardioprotective medications following myocardial infarction (MI) in people who are frail. DATA SOURCES: Ovid Medline, PubMed and Cochrane were searched from inception to October 2022 for studies that reported prescribing of one or more cardioprotective medication classes post-MI or acute coronary syndromes in people with frailty. STUDY SELECTION: We included observational studies that reported prescribing of cardioprotective medications post-MI stratified by frailty status. RESULTS: Overall, 16 cohort studies published from 2013 to 2022 that used seven different frailty scales were included. Prescribing of all cardioprotective medication classes following MI was lower in frail compared to non-frail people, with absolute rates of prescribing varying substantially across studies. Median prescribing in frail and non-frail people, respectively, was 88.9% (IQR 81.5-96.2) and 93.1% (IQR 92.0-98.9) for aspirin; 68.1% (IQR 61.9-91.2) and 86.7% (IQR 79.5-92.8) for P2Y12-inhibitors; 83.1% (IQR 76.9-91.3) and 94.0% (IQR 87.1-95.9) for lipid-lowering therapy; 67.9% (IQR 60.6-74.0) and 74.7% (IQR 71.3-84.5) for angiotensin-converting enzyme inhibitor/angiotensin II receptor blockers; and 74.1% (IQR 69.2-79) and 77.6% (IQR 71.8-85.9) for beta-blockers. CONCLUSION: People who were frail were less likely to be prescribed guideline recommended medication classes post-MI than those who were non-frail. Further research is needed into treatment benefits and risks in frail people to avoid unnecessarily withholding treatment in this high-risk population, while also minimising potential for medication related harm.
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Doody et al. (2023) studied this question.
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