Heart failure & cardiomyopathies

Angiotensin Receptor-Neprilysin Inhibitors in Concurrent Heart Failure with Reduced Ejection Fraction and Kidney Failure

ESC Heart FailPublished Retrospective cohort study

Main findingResult — go to the resultHazard ratio 0.86 95% CI 0.75–0.97

Authors' conclusion

Among HFrEF patients with kidney failure receiving replacement therapy, ARNI use was associated with lower risks of all-cause mortality, any hospitalization and cardiovascular mortality compared with RAS blockers, particularly in those with good adherence to therapy.

Study context

Population
Patients with heart failure with reduced ejection fraction (HFrEF) and kidney failure receiving replacement therapy, Korean National Health Insurance Service database, 2017–2021after IPTW weighting
Participants
2,104 vs 2,191
Exposure
Angiotensin receptor-neprilysin inhibitor (ARNI) vs renin-angiotensin system (RAS) blockers
  • ARNIn = 2,104
  • RAS blockersn = 2,191reference
Outcome
Composite of:
  • All-cause mortality
  • Any hospitalization
Follow-up
Median 19.1 months
Methodological detailsinverse probability of treatment weighting, nationwide claims database
  • Inverse probability of treatment weighting
  • Nationwide claims database

Main finding

As reported in the abstract

Hazard ratio

0.86

95% CI 0.75–0.97

ARNIvs RAS blockers
HR 0.86 (95% CI 0.75–0.97)

Observational data: associations, not effects.

Secondary outcomes

OutcomeHR (95% CI)
All-cause mortality0.68 (0.54–0.86)
Any hospitalization0.86 (0.75–0.98)
CV mortality0.68 (0.52–0.89)

Primary endpoint by subgroup (age, sex, comorbidities, medications)

Consistent associations across subgroups

Primary endpoint by ARNI adherence

Good adherence linked to lower risk; non-adherence showed no benefit

Original publication

Angiotensin Receptor-Neprilysin Inhibitors in Concurrent Heart Failure with Reduced Ejection Fraction and Kidney Failure. ESC Heart Fail. Published 3 July 2025. doi:10.1002/ehf2.15359

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.