Key result
Nontargeted guideline-directed medical treatment was associated with higher all-cause mortality compared to optimally targeted treatment (67.8% vs 37.8%; HR 1.49; 95% CI 1.05-2.13).
Why the study?
Target doses of guideline-directed medical treatment are often underused in real-world conditions, including in patients with comorbid heart failure and atrial fibrillation.
Does optimally targeted GDMT improve survival and reduce cardiovascular death or HF hospitalization in patients with AF and HFrEF or HFmrEF?
Cohort (n=374)
Does optimally targeted GDMT improve survival and reduce cardiovascular death or HF hospitalization in patients with AF and HFrEF or HFmrEF?
Answers are grounded in this paper and cite their sources.
Achievement of target doses of GDMT in patients with concurrent AF and HFrEF/HFmrEF is low (30.7%), and failure to reach these targets is associated with significantly worse clinical outcomes.
Heart failure (HF) and atrial fibrillation (AF) commonly coexist in real-life clinical practice. Among patients with HF with reduced ejection fraction (HFrEF) or HF with mildly reduced ejection fraction (HFmrEF), guidelines call for evidence-based target doses of renin-angiotensin-aldosterone system inhibitors and beta-blockers. However, target doses of guideline-directed medical treatment (GDMT) are often underused in real-world conditions, including HF-AF comorbidity. This retrospective cohort study of a randomized trial (Motivational Interviewing to Support Oral AntiCoagulation adherence in patients with nonvalvular AF) included hospitalized patients with AF and HFrEF or HFmrEF. Optimally targeted GDMT was defined as intake of evidence-based target doses of renin-angiotensin-aldosterone system and beta-blockers at 3 months after discharge. Rates of optimally targeted GDMT achievement across the baseline estimated glomerular filtration rate (eGFR) were assessed. Independent predictors of nontargeted GDMT and its association with all-cause mortality and the composite of cardiovascular death or HF hospitalization were assessed by regression analyses. In total, 374 patients with AF and HFrEF or HFmrEF were studied. At 3 months after discharge, 30.7% received target doses of GDMT medications. The rate of optimally targeted GDMT was reduced by 11% for every 10 mg/min/1.73 m 2 decrease in baseline eGFR [adjusted β = 0.99; 95% confidence interval (CI), 0.98-0.99] levels. After a median 31-month follow-up period, 37.8% patients in the optimally targeted GDMT group died, as compared with 67.8% (adjusted hazard ratio: 1.49; 95% CI, 1.05-2.13) in the nontargeted GDMT group. The risk of cardiovascular death or HF hospitalization was also higher in these patients (adjusted hazard ratio: 1.60; 95% CI, 1.17-2.20). Target doses of all HF drugs were reached in roughly one-third of patients with AF and HFrEF or HFmrEF 3 months after hospital discharge. Nontargeted GDMT was more frequent across lower eGFR levels and was associated with worse outcomes.
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Moysidis et al. (2023) conducted a cohort in Heart failure and atrial fibrillation (n=374). Nontargeted guideline-directed medical treatment vs. Optimally targeted guideline-directed medical treatment was evaluated on All-cause mortality (HR 1.49, 95% CI 1.05-2.13). Nontargeted guideline-directed medical treatment was associated with higher all-cause mortality compared to optimally targeted treatment (67.8% vs 37.8%; HR 1.49; 95% CI 1.05-2.13).
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