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Published on: July 24, 2013
Discontinuation of Heart Failure Pharmacotherapy in Older Adults With Frailty
Ryo Nakamaru1,2, Shiori Nishimura2,3, Hiraku Kumamaru2,3
1Department of Cardiovascular Medicine Kyorin University School of Medicine Tokyo Japan.
Insights
Older adults with heart failure often discontinue guideline-directed medical therapy (GDMT). Discontinuation rates increase with frailty, impacting treatment adherence for heart failure patients.
Area of Science:
- Cardiology
- Geriatrics
- Pharmacology
Background:
- Guideline-directed medical therapy (GDMT) is crucial for improving heart failure outcomes.
- The impact of frailty on GDMT discontinuation in heart failure patients requires further investigation.
Purpose of the Study:
- To quantify 12-month discontinuation rates of GDMT in older heart failure patients across different frailty strata.
- To analyze the association between frailty severity and GDMT discontinuation.
Main Methods:
- Retrospective cohort study utilizing a nationwide insurer-based database.
- Inclusion of patients aged ≥65 years hospitalized for heart failure (2014-2022) initiated on GDMT at discharge.
- Assessment of GDMT discontinuation (≥60-day gap) and cumulative incidence within 12 months, stratified by Hospital Frailty Risk Score.
Main Results:
- Analysis of 33,155 patients (mean age 83.2 years).
- Discontinuation rates for angiotensin-converting enzyme inhibitors/angiotensin II receptor blockers/angiotensin receptor-neprilysin inhibitors, β-blockers, and SGLT2is increased significantly with higher frailty scores (P<0.001).
- Mineralocorticoid receptor antagonists showed no significant difference in discontinuation rates across frailty strata (P=0.22).
Conclusions:
- Approximately one-third of older heart failure patients discontinued GDMT within 12 months.
- Frailty is associated with a disproportionately higher rate of GDMT discontinuation.
- Strategies to improve GDMT adherence in frail heart failure patients are warranted.
Background:
Guideline-directed medical therapy (GDMT) improves outcomes in heart failure irrespective of frailty status. Nevertheless, the magnitude of frailty-associated discontinuation of GDMT remains insufficiently studied. We aimed to quantify 12-month discontinuation rates of GDMT across frailty strata.
Methods:
This retrospective cohort study used a nationwide insurer-based database. We identified patients aged ≥65 years who were hospitalized for heart failure between 2014 and 2022 and newly initiated on at least 1 GDMT at discharge, including angiotensin-converting enzyme inhibitors/angiotensin II receptor blockers/angiotensin receptor-neprilysin inhibitors, β-blockers, mineralocorticoid receptor antagonists, or SGLT2is (sodium-glucose cotransporter-2 inhibitors). Discontinuation was defined as a gap of 60 days without a prescription following the expected completion of the dispensed supply. The cumulative incidence of GDMT discontinuation within 12 months was estimated according to Hospital Frailty Risk Score, with death treated as a competing risk.
Results:
We analyzed 33 155 patients (mean age: 83.2 years, women: 53.0%). The initiating rates were as follows: angiotensin-converting enzyme inhibitors/angiotensin II receptor blockers/angiotensin receptor-neprilysin inhibitors 48.3% (N=16 025), β-blockers 54.9% (N=18 197), mineralocorticoid receptor antagonists 44.1% (N=14 608), and SGLT2is 5.9% (N=1948). The Hospital Frailty Risk Score categories were as follows: low (33.2%), intermediate (47.1%), and severe (19.7%). Discontinuation rates increased with frailty severity: angiotensin-converting enzyme inhibitors/angiotensin II receptor blockers/angiotensin receptor-neprilysin inhibitors 27.5%, 39.0%, 45.5% (for low, moderate, and high Hospital Frailty Risk Score, respectively, P<0.001); β-blockers 22.0%, 28.4%, 33.6%, respectively (P<0.001); and SGLT2is, 32.3%, 34.7%, 40.2%, respectively, (P=0.008), but not for mineralocorticoid receptor antagonists 42.2%, 42.5%, and 42.3%, respectively, (P=0.22).
Conclusions:
In older adults with heart failure, approximately one-third discontinued GDMT within 12 months, and discontinuation appeared disproportionately common among those with frailty.
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