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

dc.contributor.authorMartinsson Andreas
dc.contributor.authorTörngren Charlotta
dc.contributor.authorNielsen Susanne J
dc.contributor.authorPan Emily
dc.contributor.authorHansson Emma C
dc.contributor.authorTaha Amar
dc.contributor.authorJeppsson Anders
dc.contributor.organizationfi=kirurgia|en=Surgery|
dc.contributor.organization-code2607309
dc.converis.publication-id181013421
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/181013421
dc.date.accessioned2025-08-27T20:49:50Z
dc.date.available2025-08-27T20:49:50Z
dc.description.abstract<p>Objective<br></p><p>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. <br></p><p>Methods<br></p><p>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). <br></p><p>Results<br></p><p>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. <br></p><p>Conclusion<br></p><p>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.</p>
dc.identifier.eissn1468-201X
dc.identifier.jour-issn1355-6037
dc.identifier.olddbid200313
dc.identifier.oldhandle10024/183340
dc.identifier.urihttps://www.utupub.fi/handle/11111/46054
dc.identifier.urlhttps://doi.org/10.1136/heartjnl-2023-322922
dc.identifier.urnURN:NBN:fi-fe2025082784974
dc.language.isoen
dc.okm.affiliatedauthorPan, Emily
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherBMJ PUBLISHING GROUP
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1136/heartjnl-2023-322922
dc.relation.ispartofjournalHeart
dc.source.identifierhttps://www.utupub.fi/handle/10024/183340
dc.titleRenin-angiotensin system inhibition after surgical aortic valve replacement for aortic stenosis
dc.year.issued2023

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