Heart failure & cardiomyopathies

Clinical Profile, Associated Events and Safety of Vericiguat in a Real-World Cohort: The VERITA Study

ESC Heart FailPublished Prospective observational cohort study

Authors' conclusion

In clinical practice, treatment with vericiguat is associated with substantial improvements in functional class and quality of life and a reduction in hospitalizations for HF, with a low risk of adverse effects.

Study context

Population
Patients with heart failure with reduced ejection fraction (HFrEF) and recent HF worsening episodes requiring intravenous therapy52 with ≥6 months' follow-up
Participants
103 patients
Outcome
Change during follow-up (NYHA class, EQ-5D, VAS, HF hospitalizations)
Follow-up
Median 303 days
Methodological detailssingle-group, HF outpatient clinic
  • Single-group
  • HF outpatient clinic

Main finding

As reported in the abstract

New York Heart Association (NYHA) class III / II from 67.3% / 32.7% to 22.4% / 75.5% at study end
P < 0.001
EQ-5D from 0.83 ± 0.13 to 0.87 ± 0.12
P = 0.032
Visual analogue scale (VAS) from 60 to 79
P = 0.005
HF hospitalizations/decompensations: 2.3 ± 1.4 in previous 12 months, decreased with vericiguat to 0.79 ± 1.14
P < 0.001

Observational data: associations, not effects.

Further findings

OutcomeValues
Target dose of 10 mg achievedVericiguat 78.8%

Safety

OutcomeValues
Symptomatic hypotension; treatment discontinuation; death · study endVericiguat Symptomatic hypotension 13.5% · Discontinued treatment 11.5% · Died 7.7%
  • Symptomatic hypotension; treatment discontinuation; death: 50% of deaths for HF

Original publication

Clinical Profile, Associated Events and Safety of Vericiguat in a Real-World Cohort: The VERITA Study. ESC Heart Fail. Published 18 August 2024. doi:10.1002/ehf2.15032

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