Why the study?
The necessity and safety of continued guideline-directed medical therapy after recovery in heart failure with improved ejection fraction remains uncertain.
Does the withdrawal of guideline-directed medical therapy increase adverse cardiac remodeling or all-cause mortality in patients with heart failure with improved ejection fraction?
Meta-Analysis (n=4,773)
Does the withdrawal of guideline-directed medical therapy increase adverse cardiac remodeling or all-cause mortality in patients with heart failure with improved ejection fraction?
In patients with heart failure with improved ejection fraction, withdrawal of guideline-directed medical therapy—particularly RAAS inhibitors—significantly increases the risk of mortality and structural relapse, mandating lifelong continuation of therapy for the vast majority of patients.
Continue GDMT lifelong in HFimpEF; reinforces consensus and extends HFrEF evidence to improved EF.
Heart failure with reduced ejection fraction (HFrEF) and heart failure with improved ejection fraction (HFimpEF) represent dynamic states modifiable by pharmacologic therapy. Guideline Directed Medical Therapy (GDMT) reduces morbidity and mortality in HFrEF, but the necessity and safety of continued GDMT after recovery in HFimpEF remains uncertain and the safety of stopping therapy in these patients is unclear. We conducted a systematic review and meta-analysis of randomized controlled trials and observational studies comparing GDMT withdrawal with continuation in HFimpEF. Five studies involving 4,773 patients were included. Withdrawal of comprehensive GDMT, defined as discontinuing two or more than two drug classes of GDMT, significantly increased the risk of relapse of adverse cardiac remodelling (RR = 9.35, p = 0.02). Critically, stopping renin-angiotensin-aldosterone system inhibitors (RAASi) was associated with a higher risk of all-cause mortality (RR=1.50, 95%CI=1.09_2.07; p=0.01). In contrast, withdrawal of beta-blockers alone showed no significant effect on mortality. These findings highlight that the recovery of HFimpEF is often contingent on continued GDMT. Withdrawal, particularly of multiple agents or RAASi carries substantial risk of relapse and death. Our findings mandate a paradigm of continued, lifelong GDMT for vast majority of HFimpEF patients as they remain vulnerable despite apparent recovery, and continuation of GDMT is essential to prevent relapse and improve survival. Selective withdrawal may only be considered in highly selected patients under strict monitoring until reliable predictors of durable recovery are established.
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Rehman et al. (2026) conducted a meta-analysis in Heart failure with improved ejection fraction (HFimpEF) (n=4,773). Withdrawal of Guideline-Directed Medical Therapy (GDMT) vs. Continuation of GDMT was evaluated on all-cause mortality (RR 1.50, 95% CI 1.09-2.07, p=0.01).
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