Key result
Target ACEi/ARB and ≥50% beta-blocker doses linked to ~58% lower 1-year mortality or HF hospitalization.
Why the study?
Titration patterns of ACEis/ARBs and beta-blockers, quality of life changes over 6 months, and associated 1-year outcomes required investigation in a real-world HFrEF population.
Does achieving higher guideline-recommended doses of ACEis/ARBs and beta-blockers improve 1-year outcomes and quality of life in patients with HFrEF?
Cohort (n=1,110)
Yes
Does achieving higher guideline-recommended doses of ACEis/ARBs and beta-blockers improve 1-year outcomes and quality of life in patients with HFrEF?
Effect estimate: HR 0.42 (95% CI 0.24-0.73)
In a real-world HFrEF cohort, achieving higher guideline-recommended doses of ACEis/ARBs and beta-blockers is associated with significantly lower 1-year mortality and HF hospitalization, yet most patients remain under-dosed.
Higher doses associated with lower HFrEF events; leaves open causal benefit and need for RCTs before practice change.
AIMS: We investigated titration patterns of angiotensin-converting enzyme inhibitors (ACEis)/angiotensin receptor blockers (ARBs) and beta-blockers, quality of life (QoL) over 6 months, and associated 1 year outcome [all-cause mortality/heart failure (HF) hospitalization] in a real-world population with HF with reduced ejection fraction (HFrEF). METHODS AND RESULTS: Participants with HFrEF (left ventricular ejection fraction <40%) from a prospective multi-centre study were examined for use and dose [relative to guideline-recommended maintenance dose (GRD)] of ACEis/ARBs and beta-blockers at baseline and 6 months. 'Stay low' was defined as <50% GRD at both time points, 'stay high' as ≥50% GRD, and 'up-titrate' and 'down-titrate' as dose trajectories. Among 1110 patients (mean age 63 ± 13 years, 16% women, 26% New York Heart Association Class III/IV), 714 (64%) were multi-ethnic Asians from Singapore and 396 were from New Zealand (mainly European ethnicity). Baseline use of either ACEis/ARBs or beta-blockers was high (87%). Loop diuretic was prescribed in >80% of patients, mineralocorticoid receptor antagonist in about half of patients, and statins in >90% of patients. At baseline, only 11% and 9% received 100% GRD for each drug class, respectively, with about half (47%) achieving ≥50% GRD for ACEis/ARBs or beta-blockers. At 6 months, a large majority remained in the 'stay low' category, one third remained in 'stay high', whereas 10-16% up-titrated and 4-6% down-titrated. Patients with lower (vs. higher) N-terminal pro-beta-type natriuretic peptide levels were more likely to be up-titrated or be in 'stay high' for ACEis/ARBs and beta-blockers (P = 0.002). Ischaemic aetiology, prior HF hospitalization, and enrolment in Singapore (vs. New Zealand) were independently associated with higher odds of 'staying low' (all P < 0.005) for prescribed doses of ACEis/ARBs and beta-blockers. Adjusted for inverse probability weighting, ≥100% GRD for ACEis/ARBs [hazard ratio (HR) = 0.42; 95% confidence interval (CI) 0.24-0.73] and ≥50% GRD for beta-blockers (HR = 0.58; 95% CI 0.37-0.90) (vs. Nil) were associated with lower hazards for 1 year composite outcome. Country of enrolment did not modify the associations of dose categories with 1 year composite outcome. Higher medication doses were associated with greater improvements in QoL. CONCLUSIONS: Although HF medication use at baseline was high, most patients did not have these medications up-titrated over 6 months. Multiple clinical factors were associated with changes in medication dosages. Further research is urgently needed to investigate the causes of lack of up-titration of HF therapy (and its frequency), which could inform strategies for timely up-titration of HF therapy based on clinical and biochemical parameters.
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Teng et al. (2023) conducted a cohort in Heart failure with reduced ejection fraction (HFrEF) (n=1,110). ACEis/ARBs and beta-blockers vs. Nil was evaluated on 1 year composite outcome (all-cause mortality or heart failure hospitalization) (HR 0.42, 95% CI 0.24-0.73). Achieving ≥100% guideline dose for ACEis/ARBs (HR 0.42; 95% CI 0.24-0.73) and ≥50% for beta-blockers (HR 0.58; 95% CI 0.37-0.90) reduced 1-year mortality or HF hospitalization compared to no use.
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