Prior Beta-Blocker Therapy for Hypertension and Sex-Based Differences in Heart Failure Among Patients With Incident Coronary Heart Disease.


Journal

Hypertension (Dallas, Tex. : 1979)
ISSN: 1524-4563
Titre abrégé: Hypertension
Pays: United States
ID NLM: 7906255

Informations de publication

Date de publication:
09 2020
Historique:
pubmed: 14 7 2020
medline: 15 4 2021
entrez: 14 7 2020
Statut: ppublish

Résumé

The usefulness of β-blockers has been questioned for patients who have hypertension without a prior manifestation of coronary heart disease or heart failure. In addition, sex-based differences in the efficacy of β-blockers for prevention of heart failure during acute myocardial ischemia have never been evaluated. We explored whether the effect of β-blocker therapy varied according to the sex among patients with hypertension who have no prior history of cardiovascular disease. Data were drawn from the ISACS (International Survey of Acute Coronary Syndromes)-Archives. The study population consisted of 13 764 patients presenting with acute coronary syndromes. There were 2590 patients in whom hypertension was treated previously with β-blocker (954 women and 1636 men). Primary outcome measure was the incidence of heart failure according to Killip class classification. Subsidiary analyses were conducted to estimate the association between heart failure and all-cause mortality at 30 days. Outcome rates were assessed using the inverse probability of treatment weighting and logistic regression models. Estimates were compared by test of interaction on the log scale. Among patients taking β-blockers before admission, there was an absolute difference of 4.6% between women and men in the rate of heart failure (Killip ≥2) at hospital presentation (21.3% versus 16.7%; relative risk ratio, 1.35 [95% CI, 1.10-1.65]). On the opposite, the rate of heart failure was approximately similar among women and men who did not receive β-blockers (17.2% versus 16.1%; relative risk ratio, 1.09 [95% CI, 0.97-1.21]). The test of interaction identified a significant (

Identifiants

pubmed: 32654558
doi: 10.1161/HYPERTENSIONAHA.120.15323
doi:

Substances chimiques

Adrenergic beta-Antagonists 0

Banques de données

ClinicalTrials.gov
['NCT04008173']

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

819-826

Auteurs

Raffaele Bugiardini (R)

From the Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Italy (R.B., O.M., E.C.).

Jinsung Yoon (J)

Electrical Engineering Department, University of California, UCLA, Los Angeles (J.Y.).

Sasko Kedev (S)

University Clinic of Cardiology, Medical Faculty, University "Ss. Cyril and Methodius," Skopje, Macedonia (S.K.).

Goran Stankovic (G)

Department of Cardiology, Clinical Center of Serbia, and Faculty of Medicine, University of Belgrade (G.S.), University of Belgrade, Serbia.

Zorana Vasiljevic (Z)

Faculty of Medicine (Z.V.), University of Belgrade, Serbia.

Davor Miličić (D)

Department for Cardiovascular Diseases, University Hospital Center Zagreb, University of Zagreb, Croatia (D.M.).

Olivia Manfrini (O)

From the Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Italy (R.B., O.M., E.C.).

Mihaela van der Schaar (M)

University of Cambridge, United Kingdom (M.v.d.S.).

Chris P Gale (CP)

Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, United Kingdom (C.P.G.).

Lina Badimon (L)

Cardiovascular Research Institute (ICCC), CiberCV-Institute Carlos III, IIB-Sant Pau, Hospital de la Santa Creu i Sant Pau, Autonomous University of Barcelona, Spain (L.B.).

Edina Cenko (E)

From the Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Italy (R.B., O.M., E.C.).

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