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Complex and Potentially Harmful Medication Patterns in Heart Failure with Preserved Ejection Fraction - 23/02/21

Doi : 10.1016/j.amjmed.2020.07.023 
Lina M. Brinker, MD a, Matthew C. Konerman, MD, MS b, Pedram Navid, MD c, Michael P. Dorsch, PharmD, MS d, Jennifer McNamara, MS e, Cristen J. Willer, PhD b, f, g, Mary E. Tinetti, MD h, Scott L. Hummel, MD, MS b, i, Parag Goyal, MD, MSc c,
a Department of Internal Medicine, University of Michigan, Ann Arbor 
b Division of Cardiovascular Medicine, Department of Internal Medicine, University of Michigan, Ann Arbor 
c Department of Medicine, Weill Cornell Medicine, New York, NY 
d Department of Clinical Pharmacy, College of Pharmacy, University of Michigan, Ann Arbor 
e University of Michigan Frankel Cardiovascular Center Administration, University of Michigan, Ann Arbor 
f Department of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor 
g Department of Human Genetics, University of Michigan, Ann Arbor 
h Department of Medicine, Yale University School of Medicine, New Haven, CT 
i Section of Cardiology, Ann Arbor Veterans Affairs Health System, Ann Arbor, Mich 

Requests for reprints should be addressed to Parag Goyal MD, MSc, FACC, Department of Medicine; Weill Cornell Medicine, 420 East 70th Street, LH-365, New York, NY, 10063.Department of MedicineWeill Cornell Medicine420 East 70th Street, LH-365New YorkNY10063

Abstract

Background

Complex medication regimens, often present in heart failure with preserved ejection fraction, may increase the risk of adverse drug effects and harm. We sought to characterize this complexity by determining the prevalence of polypharmacy, potentially inappropriate medications, and therapeutic competition (where a medication for 1 condition may worsen another condition) in 1 of the few dedicated heart failure with preserved ejection fraction programs in the United States.

Methods

We conducted chart review on 231 patients with heart failure with preserved ejection fraction seen in the University of Michigan's Heart Failure with Preserved Ejection Fraction Clinic between July 2016 and September 2019. We recorded: 1) standing medications to determine the presence of polypharmacy, defined as ≥10 medications; 2) potentially inappropriate medications based on the 2016 American Heart Association Scientific Statement on drugs that pose a major risk of causing or exacerbating heart failure, the 2019 Beers Criteria update, or a previously described list of medications associated with geriatric syndromes; and 3) competing conditions and subsequent medications that could create therapeutic competition.

Results

The prevalence of polypharmacy was 74%, and the prevalence of potentially inappropriate medications was 100%. Competing conditions were present in 81% of patients, of whom 49% took a medication that created therapeutic competition.

Conclusion

In addition to confirming that polypharmacy was highly prevalent, we found that potentially inappropriate medications and therapeutic competition were also frequently present. This supports the urgent need to develop patient-centered approaches to mitigate the negative effects of complex medication regimens endemic to adults with heart failure with preserved ejection fraction.

El texto completo de este artículo está disponible en PDF.

Graphical abstract

Overview of medication complexity in heart failure with preserved ejection fraction. Several factors contribute to medication complexity, including polypharmacy, use of potentially inappropriate medications, and the presence of therapeutic competition. With increased medication complexity, patients with heart failure with preserved ejection fraction are at higher risk for adverse outcomes. Patient-centered approaches are needed to mitigate the negative effects of medication complexity in heart failure with preserved ejection fraction.



Image, graphical abstract

El texto completo de este artículo está disponible en PDF.

Keywords : Geriatrics, Heart failure, Medications, Polypharmacy


Esquema


 Funding: Data collection was supported by the Cardiovascular Health Improvement Program (CHIP), a biorepository funded by the University of Michigan.
 Conflicts of Interest: PG is supported by the National Institute on Aging grant R03AG056446 and American Heart Association grant 18IPA34170185 and is a recipient of a National Institute on Aging Loan Repayment Plan. SLH is supported by the National Heart, Lung, and Blood Institute grant R01-HL139813 and Veterans Administration grant CARA-009-16F9050. MPD has received honoraria from Jansen and research funding from BMS/Pfizer, Amgen, Agency for Healthcare Research and Quality, NIH/National Institute of Aging, and the American Heart Association. CJW's spouse works at Regeneron.
 Authorship: All authors had access to the data and a role in writing this manuscript.


© 2020  Elsevier Inc. Reservados todos los derechos.
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Vol 134 - N° 3

P. 374-382 - mars 2021 Regresar al número
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