Real-world comparative effectiveness of sacubitril/valsartan versus RAS inhibition alone in patients with de novo heart failure

ESC Heart Fail. 2025 Jun;12(3):1682-1692. doi: 10.1002/ehf2.15183. Epub 2025 Jan 30.

Abstract

Aims: Large-scale, real-world data on early initiation of sacubitril/valsartan in patients newly diagnosed (de novo) with HF with reduced ejection fraction (HFrEF) are limited. We examined the effectiveness of sacubitril/valsartan versus angiotensin-converting enzyme inhibitor (ACEi)/angiotensin receptor blocker (ARB) on all-cause and cause-specific hospitalizations among patients with de novo HFrEF from the Optum® dataset in the United States.

Methods: This retrospective cohort study included adult patients with de novo HFrEF (diagnosed ≤30 days) with left ventricular ejection fraction (LVEF) ≤40% who were first prescribed with sacubitril/valsartan or ACEi/ARB from 1 January 2016 to 31 March 2020. The primary endpoint (all-cause hospitalization) and secondary endpoints were analysed in propensity score-matched cohorts.

Results: A cohort of 3290 patients with de novo HFrEF who were prescribed with sacubitril/valsartan and a propensity-matched cohort of 6580 patients who were prescribed with ACEi/ARB were analysed. Overall, the mean (SD) age of patients was 63 (14) years, 34% were women, and baseline characteristics were balanced across treatment groups. Hypertension (67%), diabetes (33%) and chronic kidney disease (28%) were highly prevalent comorbidities. Patients in the sacubitril/valsartan cohort when compared with the ACEi/ARB cohort had lower annual rates of all-cause hospitalizations [incidence rate ratio (IRR): 0.81, 95% confidence interval (CI): 0.75-0.89, P < 0.001], cardiovascular (CV) hospitalizations (IRR: 0.80, 95% CI: 0.73-0.87, P < 0.001) and HF hospitalizations (IRR: 0.86, 95% CI: 0.78-0.95, P = 0.002).

Conclusions: Among patients with de novo HFrEF, sacubitril/valsartan (compared with that of ACEi/ARB) was associated with fewer all-cause, CV and HF hospitalizations. These findings are consistent with clinical trial evidence suggesting potential benefits of early initiation of sacubitril/valsartan in patients with HFrEF, including those soon after diagnosis.

Keywords: angiotensin receptor blocker; angiotensin‐converting enzyme inhibitor; de novo; heart failure; sacubitril/valsartan.

Publication types

  • Comparative Study
  • Multicenter Study

MeSH terms

  • Aged
  • Aminobutyrates* / administration & dosage
  • Aminobutyrates* / therapeutic use
  • Angiotensin Receptor Antagonists / therapeutic use
  • Angiotensin-Converting Enzyme Inhibitors* / therapeutic use
  • Biphenyl Compounds*
  • Drug Combinations
  • Female
  • Follow-Up Studies
  • Heart Failure* / drug therapy
  • Heart Failure* / physiopathology
  • Hospitalization
  • Humans
  • Male
  • Middle Aged
  • Renin-Angiotensin System / drug effects
  • Retrospective Studies
  • Stroke Volume / physiology
  • Tetrazoles* / therapeutic use
  • Treatment Outcome
  • Valsartan* / administration & dosage
  • Valsartan* / therapeutic use
  • Ventricular Function, Left* / physiology

Substances

  • Aminobutyrates
  • Angiotensin Receptor Antagonists
  • Angiotensin-Converting Enzyme Inhibitors
  • Biphenyl Compounds
  • Drug Combinations
  • sacubitril and valsartan sodium hydrate drug combination
  • Tetrazoles
  • Valsartan

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