Renin-angiotensin system inhibition after surgical aortic valve replacement for aortic stenosis.

aortic valve stenosis epidemiology pharmacology, clinical

Journal

Heart (British Cardiac Society)
ISSN: 1468-201X
Titre abrégé: Heart
Pays: England
ID NLM: 9602087

Informations de publication

Date de publication:
17 Jul 2023
Historique:
received: 04 05 2023
accepted: 28 06 2023
medline: 18 7 2023
pubmed: 18 7 2023
entrez: 17 7 2023
Statut: aheadofprint

Résumé

The optimal medical therapy after surgical aortic valve replacement (SAVR) for aortic stenosis remains unknown. Renin-angiotensin system (RAS) inhibitors could potentially improve cardiac remodelling and clinical outcomes after SAVR. All patients undergoing SAVR due to aortic stenosis in Sweden 2006-2020 and surviving 6 months after surgery were included. The primary outcome was major adverse cardiovascular events (MACEs; all-cause mortality, stroke or myocardial infarction). Secondary endpoints included the individual components of MACE and cardiovascular mortality. Time-updated adjusted Cox regression models were used to compare patients with and without RAS inhibitors. Subgroup analyses were performed, as well as a comparison between angiotensin-converting enzyme (ACE) inhibitors and angiotensin II receptor blockers (ARBs). A total of 11 894 patients (mean age, 69.5 years, 40.4% women) were included. Median follow-up time was 5.4 (2.7-8.5) years. At baseline, 53.6% of patients were dispensed RAS inhibitors, this proportion remained stable during follow-up. RAS inhibition was associated with a lower risk of MACE (adjusted hazard ratio (aHR) 0.87 (95% CI 0.81 to 0.93), p<0.001), mainly driven by a lower risk of all-cause death (aHR 0.79 (0.73 to 0.86), p<0.001). The lower MACE risk was consistent in all subgroups except for those with mechanical prostheses (aHR 1.07 (0.84 to 1.37), p for interaction=0.040). Both treatment with ACE inhibitors (aHR 0.89 (95% CI 0.82 to 0.97)) and ARBs (0.87 (0.81 to 0.93)) were associated with lower risk of MACE. The results of this study suggest that medical therapy with an RAS inhibitor after SAVR is associated with a 13% lower risk of MACE and a 21% lower risk of all-cause death.

Identifiants

pubmed: 37460192
pii: heartjnl-2023-322922
doi: 10.1136/heartjnl-2023-322922
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: AJ has received fees for consultancy from AstraZeneca, Werfen and LFB Biotechnologies, all unrelated to the present work.

Auteurs

Andreas Martinsson (A)

Department of Cardiology, Sahlgrenska University Hospital, Goteborg, Sweden andreas.s.martinsson@vgregion.se.
Department of Molecular and Clinical Medicine, University of Gothenburg Sahlgrenska Academy, Goteborg, Sweden.

Charlotta Törngren (C)

Department of Molecular and Clinical Medicine, University of Gothenburg Sahlgrenska Academy, Goteborg, Sweden.
Department of Cardiothoracic Surgery, Sahlgrenska University Hospital, Goteborg, Sweden.

Susanne J Nielsen (SJ)

Department of Molecular and Clinical Medicine, University of Gothenburg Sahlgrenska Academy, Goteborg, Sweden.
Department of Cardiothoracic Surgery, Sahlgrenska University Hospital, Goteborg, Sweden.

Emily Pan (E)

Department of Cardiovascular Medicine, Harvard Medical School, Boston, Massachusetts, USA.
University of Turku, Turku, Finland.

Emma C Hansson (EC)

Cardiothoracic Surgery, Sahlgrenska University Hospital, Gothenburg, Sweden.
Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Amar Taha (A)

Department of Cardiology, Sahlgrenska University Hospital, Goteborg, Sweden.
Department of Molecular and Clinical Medicine, University of Gothenburg Sahlgrenska Academy, Goteborg, Sweden.

Anders Jeppsson (A)

Department of Molecular and Clinical Medicine, University of Gothenburg Sahlgrenska Academy, Goteborg, Sweden.
Cardiothoracic Surgery, Sahlgrenska University Hospital, Gothenburg, Sweden.

Classifications MeSH