Heart failure & cardiomyopathiesSecondary analysis

Implantable Cardioverter-Defibrillators in Ischaemic Versus Non-Ischaemic Heart Failure: Insights from the VICTORIA Trial

Eur J Heart FailPublished

  • Secondary analysis of the VICTORIA randomised trial
  • propensity-score adjusted

Authors' conclusion

Among patients with HFrEF with recent decompensation, presence of an ICD was associated with a reduction in SCD, but did not translate to a reduction in the risk of cardiovascular or all-cause death.

Study context

Population
Patients with HFrEF and recent heart failure (HF) decompensation, by HF aetiology (ischaemic vs non-ischaemic)53.6% ischaemic
Participants
5,040 patients
Comparison
Pre-existing ICD vs no ICD
  • ICDn = 1,399
Primary endpoint
SCD, CV death (including SCD) and all-cause death
Follow-up
Median 10.8 months

Primary result

As reported in the abstract

SCD, CV death, all-cause death
ICD vs No ICDAdjusted hazard ratio (95% CI)
SCD
0.64(0.43–0.96)
CV death
0.99(0.83–1.18)
all-cause death
1.02(0.87–1.19)

Further findings

OutcomeaHR (95% CI)
SCD by HF aetiology (subgroup) — ICD vs No ICD · ischaemic HF0.61 (0.38–0.98)
SCD by HF aetiology (subgroup) — ICD vs No ICD · non-ischaemic HF0.72 (0.36–1.43)
SCD in women with ischaemic HF (subgroup)0.2 (0.05–0.82)
  • Sudden cardiac death (SCD) by HF aetiology (subgroup): interaction P = 0.69
  • SCD in women with ischaemic HF (subgroup): interaction P = 0.029

ICD use, women vs men

ICD use in women vs men
16.4% vs. 26.8%

SCD by AF (subgroup)

AF modulated ICD effect on SCD; no benefit with AF
  • interaction P = 0.015

Original publication

Implantable Cardioverter-Defibrillators in Ischaemic Versus Non-Ischaemic Heart Failure: Insights from the VICTORIA Trial. Eur J Heart Fail. Published 20 June 2025. doi:10.1002/ejhf.3731

Summarised from the published abstract; every number is checked against it