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Lumped-Parameter and Finite Element Modeling of Heart Failure with Preserved Ejection Fraction
Published on: February 13, 2021
Mortality and guideline-directed medical therapy in real-world heart failure patients with reduced ejection fraction
Peter A McCullough1, Hirsch S Mehta2, Colin M Barker3
1Texas A & M College of Medicine, Dallas, Texas, USA.
Insights
Guideline-directed medical therapy (GDMT) for heart failure with reduced ejection fraction (HFrEF) is underutilized. Patients not receiving GDMT face a 29% higher mortality risk, underscoring the importance of optimal treatment.
Area of Science:
- Cardiology
- Pharmacology
- Public Health
Background:
- Heart failure with reduced ejection fraction (HFrEF) is a significant cause of morbidity and mortality.
- Guideline-directed medical therapy (GDMT) has been proven to reduce mortality in HFrEF patients.
- Real-world data on GDMT prevalence and its impact on mortality in HFrEF is crucial for clinical practice improvement.
Purpose of the Study:
- To determine the prevalence of guideline-directed medical therapy (GDMT) in US patients with heart failure with reduced ejection fraction (HFrEF).
- To evaluate the association between GDMT and all-cause mortality in HFrEF patients.
- To identify potential gaps in GDMT implementation in a real-world setting.
Main Methods:
- Retrospective cohort study using the Optum Integrated File (2007-2019Q3).
- Identified adult patients with a history of HFrEF.
- Defined GDMT as prescription fills for a beta-blocker plus an ACE inhibitor, ARB, or ARNI within 6 months post-diagnosis. Assessed 2-year all-cause mortality using Cox regression.
Main Results:
- The study included 14,880 HFrEF patients; 70% received GDMT, and 57% had concurrent medication fills.
- Patients not on GDMT exhibited a 29% increased risk of all-cause mortality compared to those on GDMT (HR 1.29; 95% CI [1.19-1.40]; p < .0001).
- A sensitivity analysis showed a 37% increased mortality risk for patients not on GDMT compared to those on concurrent GDMT medication fills.
Conclusions:
- Inadequate guideline-directed medical therapy (GDMT) is associated with a significant excess mortality risk in real-world HFrEF populations.
- A substantial proportion of HFrEF patients are not receiving optimal GDMT, highlighting a critical gap in care.
- Adherence to GDMT is essential for improving survival outcomes in patients with heart failure with reduced ejection fraction.
Objective:
To estimate the prevalence of guideline-directed medical therapy (GDMT) in commercially insured US patients with heart failure with reduced ejection fraction (HFrEF) and examine the effect of GDMT on all-cause mortality. GDMT for HFrEF includes pharmacologic therapies such as β-blockers (BB), angiotensin-converting enzyme inhibitors (ACE-I), angiotensin receptor blockers (ARB), angiotensin receptor-neprilysin (ARNI), mineralocorticoid receptor antagonists (MRA), and sodium-glucose cotransporter inhibitors to reduce morbidity and mortality.
Methods:
Patients in the Optum Integrated File from 2007 to 2019Q3, ≥18 years, with history of HFrEF, were identified. Patients prescribed both a BB and either an ACE-I, ARB, or ARNI during 6-month post-diagnosis were assigned to the GDMT cohort. All others were assigned to the not on GDMT cohort. The GDMT cohort was further classified by those patients with a record of prescription fills for both classes of medications concurrently (GDMT concurrent medication fills). Mortality at 2 years was assessed with a Cox regression model accounting for baseline demographics, comorbidities, and diuretic use.
Results:
This study identified 14 880 HFrEF patients, of which 70% had a record of GDMT, and 57% had a record of concurrent prescriptions. Patients in the not on GDMT cohort had 29% increased risk of mortality versus GDMT (hazard ratio 1.29; 95% CI (1.19-1.40); p < .0001). As a sensitivity analysis, the effect of patients not on GDMT compared to GDMT with concurrent medication fills was more pronounced, with a 37% increased mortality risk.
Conclusion:
In a real-world population of HFrEF patients, inadequate GDMT confers a 29% excess mortality risk over the 2-year follow-up.
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