Key result
LVEF improvement after sacubitril/valsartan in non-ischaemic cardiomyopathy is linked to ~58% fewer major events.
Why the study?
The PARADIGM-HF study did not analyse the effect of ventricular remodelling on heart failure patients with different aetiologies receiving sacubitril/valsartan, which may affect clinical outcomes.
Does sacubitril/valsartan treatment improve left ventricular remodelling and clinical outcomes differently in non-ischaemic versus ischaemic heart failure patients?
Cohort (n=1,576)
Does sacubitril/valsartan treatment improve left ventricular remodelling and clinical outcomes differently in non-ischaemic versus ischaemic heart failure patients?
Hazard Ratio: 0.42 (95% CI 0.31–0.58)
p-value: p=<0.001
Sacubitril/valsartan induces greater left ventricular reverse remodelling in non-ischaemic heart failure compared to ischaemic heart failure, which correlates with improved clinical outcomes.
NICM patients with LVEF gains after SAC/VAL showed outcome associations absent in ICM; leaves open aetiology-specific remodelling effects.
AIMS: Although the beneficial effect of sacubitril/valsartan (SAC/VAL) compared to enalapril was consistent across ischaemic cardiomyopathy (ICM) and non-ischaemic cardiomyopathy (NICM) groups, the PARADIGM-HF study did not analyse the effect of ventricular remodelling on patients with different aetiologies, which may affect clinical treatment outcomes. This study aimed to compare left ventricular ejection fraction (LVEF) following SAC/VAL treatment and its association with clinical outcomes. METHODS AND RESULTS: A total of 1576 patients were analysed. Patients were grouped by LVEF changes following SAC/VAL treatment for 8-month period. LVEF improvement ≥15% was defined as 'significant improvement', and <5% or worse was classified as 'lack of improvement'. The primary outcome was a composite of cardiovascular death and unplanned hospitalization for heart failure. Patients with NICM had lower baseline LVEF but improvement was significantly greater comparing to those with ICM (baseline 28.0 ± 7.7% vs. 30.1 ± 7.1%, P < 0.001, LVEF increase of 11.1 ± 12.6% vs. 6.7 ± 10.2%, P < 0.001). The effect of functional improvement of SAC/VAL on NICM patients showed bimodal distribution. Primary endpoints were inversely associated with LVEF changes in NICM patients: adjusted hazard ratio was 0.42 [95% confidence interval (CI) 0.31-0.58, P < 0.001] for NICM patients with significant improvement, and was 1.73 (95% CI 1.38-2.16, P < 0.001) for NICM patients but lack of improvement. Primary endpoints of ICM patients did not demonstrate an association with LVEF changes. CONCLUSION: Patients with NICM had higher degree of LVEF improvement than those with ICM following SAC/VAL treatment, and significant improvement of LVEF in NICM patients indicates favourable outcome.
No takes yet. Share an insight, caveat, or question.
Lee et al. (2020) conducted a cohort in Heart failure (ischaemic and non-ischaemic cardiomyopathy) (n=1,576). Significant LVEF improvement (≥15%) following sacubitril/valsartan treatment vs. Lack of LVEF improvement (<5% or worse) was evaluated on Composite of cardiovascular death and unplanned hospitalization for heart failure (HR 0.42, 95% CI 0.31-0.58, p=<0.001). Significant LVEF improvement after sacubitril/valsartan in non-ischaemic cardiomyopathy was associated with reduced cardiovascular death or HF hospitalization (HR 0.42; 95% CI 0.31-0.58; P<0.001).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: