Applied Evidence

Ejection fraction is back to normal—now what?

Author and Disclosure Information

Heart failure treatment guidelines don’t address whether to change a patient’s medications should the EF improve. This evidence review provides guidance.


 

References

PRACTICE RECOMMENDATIONS

Assess the ejection fraction (EF) of all heart failure patients, and treat those with reduced EF according to established guidelines. A

Reassess EF only when the clinical situation demands it; there is no need for routine EF surveillance. B

Continue to treat patients with heart failure medications even after their EF has normalized. C

Strength of recommendation (SOR)

A Good-quality patient-oriented evidence
B Inconsistent or limited-quality patient-oriented evidence
C Consensus, usual practice, opinion, disease-oriented evidence, case series

CASE Joe H is a 64-year-old African American man with a history of heart failure, hypertension, coronary artery disease (CAD), type 2 diabetes, chronic kidney disease, atrial fibrillation, and gout. His ejection fraction (EF), measured several years ago by echocardiography, was 20%, and he has New York Heart Association class II–III symptoms. Joe is taking an angiotensin-converting enzyme (ACE) inhibitor, a beta-blocker, an aldosterone antagonist, a loop diuretic, a nitrate, and digoxin, and he has an implantable cardioverter defibrillator (ICD). He recently spent 2 days in the hospital after being admitted for chest pain.

As an inpatient, Joe underwent stress echocardiography, which showed no inducible ischemia and an EF of 50%. Should the normalization of Joe’s EF prompt a change in his therapy?

Heart failure (HF), which affects an estimated 5 million Americans, is the leading cause of hospitalization in people older than 65 years.1 The condition—characterized by signs and symptoms of congestion and objective evidence of structural or functional heart disease—has historically been divided into 2 categories: Patients with HF and a reduced ejection fraction (EF) were said to have systolic dysfunction, while the term “diastolic dysfunction” was applied to those with HF and a preserved EF.

The distinction between systolic and diastolic dysfunction is not so simple, though, and the definition of diastolic dysfunction, in particular, is not so clearcut.

Diastolic dysfunction is sometimes described on the basis of echocardiographic criteria, such as the ratio of early-to-late diastolic filling, short deceleration times, and isovolumic relaxation times.2,3 But demographic and physiologic variables make interpretation of these parameters difficult, and the parameters themselves are not uniformly applied. What’s more, echocardiographic evidence of diastolic dysfunction is not specific to HF with a preserved EF.4 Some patients may be shown to have diastolic dysfunction and reduced EF.

As understanding of these variations grows, momentum about the need to change the clinical terminology has begun to develop. The suggested revision is simply to distinguish between HF with reduced EF and HF with preserved EF.5

To provide the best possible care for HF patients—including those who, like Joe, have gone from a reduced to a normal EF after receiving aggressive treatment—you need to be familiar with these changing parameters, recent research findings, and implications for treatment.

Managing both types of HF: What the evidence shows

Evidence-based management of HF with reduced EF is distinctly different from that of HF with preserved EF (TABLE).6-8 In fact, the vast majority of the evidence involves patients with reduced EF, as most randomized clinical trials (RCTs)—and the only trials demonstrating a reduction in mortality—have excluded patients with preserved EF. Thus, in diagnosing and treating HF patients, it is crucial to assess for, and to distinguish between, the 2 EF states. Documentation of this assessment is a core quality measure for HF management, according to the Joint Commission.9

Treating HF with reduced EF. Barring any contraindications, ACE inhibitors and beta-blockers are core treatments for patients with reduced EF.8 Aldosterone antagonists are also indicated for patients with reduced EF who have, or recently had, rest dyspnea. They are also indicated for patients with reduced EF who are 3 to 14 days post-MI and have diabetes or symptomatic HF.8 Nitrates are indicated for African American patients who have persistent symptoms despite treatment with ACE inhibitors, beta-blockers, and diuretics, as needed.8 Consider an ICD as well, as these devices have been found to significantly reduce the risk of death for patients who have an EF <35% with either ischemic cardiomyopathy or symptomatic HF.

Treating HF with preserved EF. Because of the dearth of trials involving patients with HF and a preserved EF, there is limited evidence-based treatment. Nonetheless, it is reasonable to control signs and symptoms of congestion with diuretics.6 In addition, the CHARM-Preserved trial demonstrated the efficacy of candesartan—an angiotensin receptor blocker—in decreasing rates of hospital admissions among symptomatic patients with a preserved EF.10

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