Background Medical Therapy and Clinical Outcomes From the VICTORIA Trial.


Journal

Circulation. Heart failure
ISSN: 1941-3297
Titre abrégé: Circ Heart Fail
Pays: United States
ID NLM: 101479941

Informations de publication

Date de publication:
09 2023
Historique:
medline: 21 9 2023
pubmed: 7 7 2023
entrez: 7 7 2023
Statut: ppublish

Résumé

We examined whether the primary composite outcome (cardiovascular death or heart failure hospitalization) was related to differences in background use and dosing of guideline-directed medical therapy in patients with heart failure with reduced ejection fraction enrolled in VICTORIA (Vericiguat Global Study in Subjects with Heart Failure with Reduced Ejection Fraction), a randomized trial of vericiguat versus placebo. We evaluated the adherence to guideline use of angiotensin-converting enzyme inhibitors, angiotensin-receptor blockers, angiotensin receptor-neprilysin inhibitors, beta-blockers, and mineralocorticoid receptor antagonists. We assessed basic adherence; indication-corrected adherence accounting for guideline indications and contraindications; and dose-corrected adherence (indication-corrected adherence+≥50% of drug dose target). Associations between study treatment and the primary composite outcome according to the adherence to guidelines were assessed using multivariable adjustment; adjusted hazard ratios with 95% CIs and Of 5050 patients, 5040 (99.8%) had medication data at baseline. For angiotensin-converting enzyme inhibitor, angiotensin-receptor blockers, and angiotensin receptor-neprilysin inhibitors, basic adherence to guidelines was 87.4%, indication-corrected was 95.7%, and dose-corrected was 50.9%. For beta-blockers, basic adherence was 93.1%, indication-corrected was 96.2%, and dose-corrected was 45.4%. For mineralocorticoid receptor antagonists, basic adherence was 70.3%, indication-corrected was 87.1%, and dose-corrected was 82.2%. For triple therapy (angiotensin-converting enzyme inhibitors, angiotensin-receptor blockers, or angiotensin receptor-neprilysin inhibitors+beta-blocker+mineralocorticoid receptor antagonist), basic adherence was 59.7%, indication-corrected was 83.3%, and dose-corrected was 25.5%. Using basic or dose-corrected adherence, the treatment effect of vericiguat was consistent across adherence to guidelines groups, with or without multivariable adjustment with no treatment heterogeneity. Patients in VICTORIA were well treated with heart failure with reduced ejection fraction medications. The efficacy of vericiguat was consistent across background therapy with very high adherence to guidelines accounting for patient-level indications, contraindications, and tolerance. URL: https://www. gov; Unique identifier: NCT02861534.

Sections du résumé

BACKGROUND
We examined whether the primary composite outcome (cardiovascular death or heart failure hospitalization) was related to differences in background use and dosing of guideline-directed medical therapy in patients with heart failure with reduced ejection fraction enrolled in VICTORIA (Vericiguat Global Study in Subjects with Heart Failure with Reduced Ejection Fraction), a randomized trial of vericiguat versus placebo.
METHODS
We evaluated the adherence to guideline use of angiotensin-converting enzyme inhibitors, angiotensin-receptor blockers, angiotensin receptor-neprilysin inhibitors, beta-blockers, and mineralocorticoid receptor antagonists. We assessed basic adherence; indication-corrected adherence accounting for guideline indications and contraindications; and dose-corrected adherence (indication-corrected adherence+≥50% of drug dose target). Associations between study treatment and the primary composite outcome according to the adherence to guidelines were assessed using multivariable adjustment; adjusted hazard ratios with 95% CIs and
RESULTS
Of 5050 patients, 5040 (99.8%) had medication data at baseline. For angiotensin-converting enzyme inhibitor, angiotensin-receptor blockers, and angiotensin receptor-neprilysin inhibitors, basic adherence to guidelines was 87.4%, indication-corrected was 95.7%, and dose-corrected was 50.9%. For beta-blockers, basic adherence was 93.1%, indication-corrected was 96.2%, and dose-corrected was 45.4%. For mineralocorticoid receptor antagonists, basic adherence was 70.3%, indication-corrected was 87.1%, and dose-corrected was 82.2%. For triple therapy (angiotensin-converting enzyme inhibitors, angiotensin-receptor blockers, or angiotensin receptor-neprilysin inhibitors+beta-blocker+mineralocorticoid receptor antagonist), basic adherence was 59.7%, indication-corrected was 83.3%, and dose-corrected was 25.5%. Using basic or dose-corrected adherence, the treatment effect of vericiguat was consistent across adherence to guidelines groups, with or without multivariable adjustment with no treatment heterogeneity.
CONCLUSIONS
Patients in VICTORIA were well treated with heart failure with reduced ejection fraction medications. The efficacy of vericiguat was consistent across background therapy with very high adherence to guidelines accounting for patient-level indications, contraindications, and tolerance.
REGISTRATION
URL: https://www.
CLINICALTRIALS
gov; Unique identifier: NCT02861534.

Identifiants

pubmed: 37417824
doi: 10.1161/CIRCHEARTFAILURE.123.010599
doi:

Substances chimiques

Mineralocorticoid Receptor Antagonists 0
Neprilysin EC 3.4.24.11
Angiotensin-Converting Enzyme Inhibitors 0
Angiotensin Receptor Antagonists 0
Adrenergic beta-Antagonists 0
Angiotensins 0

Banques de données

ClinicalTrials.gov
['NCT02861534']

Types de publication

Randomized Controlled Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e010599

Auteurs

Justin A Ezekowitz (JA)

Canadian VIGOUR Centre, University of Alberta, Edmonton, AB, Canada (J.A.E., C.M.W., P.W.A.).

Ciaran J McMullan (CJ)

Merck & Co Inc, Kenilworth, NJ (C.J.M., J.K.).

Cynthia M Westerhout (CM)

Canadian VIGOUR Centre, University of Alberta, Edmonton, AB, Canada (J.A.E., C.M.W., P.W.A.).

Ileana L Piña (IL)

Central Michigan University, Mount Pleasant (I.L.P.).

Jose Lopez-Sendon (J)

IdiPaz Research Institute, Hospital Universitario La Paz, Universidad Autonoma de Madrid, Spain (J.L.-S.).

Kevin J Anstrom (KJ)

Duke Clinical Research Institute, Duke University, Durham, NC (K.J.A., A.F.H.).

Adrian F Hernandez (AF)

Duke Clinical Research Institute, Duke University, Durham, NC (K.J.A., A.F.H.).

Carolyn S P Lam (CSP)

National Heart Centre Singapore and Duke-National University of Singapore (C.S.P.L.).

Christopher M O'Connor (CM)

Inova Heart and Vascular Institute, Falls Church, VA (C.M.O.).

Burkert Pieske (B)

Charité University Medicine German Heart Center, Berlin, Germany (B.P.).

Piotr Ponikowski (P)

Department of Heart Disease, Wroclaw Medical University, Poland (P.P.).

Lothar Roessig (L)

Bayer AG, Wuppertal, Germany (L.R.).

Adriaan A Voors (AA)

University Medical Center Groningen, University of Groningen, the Netherlands (A.A.V.).

Joerg Koglin (J)

Merck & Co Inc, Kenilworth, NJ (C.J.M., J.K.).

Paul W Armstrong (PW)

Canadian VIGOUR Centre, University of Alberta, Edmonton, AB, Canada (J.A.E., C.M.W., P.W.A.).

Javed Butler (J)

Baylor University Medical Center, Dallas, TX (J.B.).

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Classifications MeSH