Reconsidering the Polypill for Management of Cardiovascular Risk Factors in Underserved Patients.
Autor: | Macaulay TE; Department of Pharmacy Practice and Science, University of Kentucky College of Pharmacy, 789 S. Limestone Street, TODD 223, Lexington, KY, 40536, USA. Tracy.macaulay@uky.edu., Sheridan E; Cardiology Clinical Pharmacist, ProMedica Toledo Hospital/Russell J. Ebeid Children's Hospital, Toledo, OH, USA., Ward S; Cardiovascular Clinical Pharmacist - Heart Failure, UofL Health-Jewish Hospital, Louisville, KY, USA. |
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Jazyk: | angličtina |
Zdroj: | Current cardiology reports [Curr Cardiol Rep] 2021 Feb 17; Vol. 23 (3), pp. 19. Date of Electronic Publication: 2021 Feb 17. |
DOI: | 10.1007/s11886-021-01448-9 |
Abstrakt: | Purpose of Review: The recent publication of "Polypill for Cardiovascular Disease Prevention in an Underserved Population" study prompts a thoughtful review of known care disparities in cardiovascular disease management in underserved patients. A polypill approach as a population health solution to this complex problem should also be reviewed. Recent Findings: Muñoz and colleagues open-label, randomized controlled trial of polypill vs. usual care was undertaken in minority patients at a federally qualified health center. The polypill, containing atorvastatin, amlodipine, losartan, and hydrochlorothiazide resulted in statistically significant improvements in systolic blood pressure and low-density lipoprotein levels (p = 0.003 and p < 0.001, respectively). The significant results of this study demonstrate the ability of a polypill approach to safely lower blood pressure, lipids, and thus estimated 10-year risk of CVD and are consistent with findings observed in previous literature. Uniquely, findings in a largely non-Hispanic Black patient population, offer an opportunity to examine this approach to combat important disparities in care in an underserved U.S. community. Further outcomes-based studies are warranted to explore the validity of these results and long-term safety of polypill treatment and are likely necessary prior to FDA approval and availability of a polypill product. |
Databáze: | MEDLINE |
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