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Impact of paravalvular regurgitation on the mid-term outcome after transcatheter and surgical aortic valve replacement
Author(s) -
Teemu Laakso,
Mika Laine,
Noriaki Moriyama,
Sebastian Dahlbacka,
Juhani Airaksinen,
Marko Virtanen,
Annastiina Husso,
Tuomas Tauriainen,
Matti Niemelä,
Timo H. Mäkikallio,
Antti Valtola,
Markku Eskola,
Tatu Juvonen,
Fausto Biancari,
Peter Raivio
Publication year - 2020
Publication title -
european journal of cardio-thoracic surgery
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.303
H-Index - 133
eISSN - 1873-734X
pISSN - 1010-7940
DOI - 10.1093/ejcts/ezaa254
Subject(s) - medicine , aortic valve replacement , hazard ratio , cardiology , valve replacement , stenosis , confidence interval , regurgitation (circulation) , incidence (geometry) , aortic valve stenosis , aortic valve , survival rate , surgery , physics , optics
OBJECTIVES The aim of this study was to evaluate the incidence and prognostic impact of paravalvular regurgitation (PVR) on the outcome after transcatheter (TAVR) and surgical aortic valve replacement (SAVR) for aortic stenosis. METHODS The nationwide FinnValve registry included data on 6463 consecutive patients who underwent TAVR (n = 2130) or SAVR (n = 4333) with a bioprosthesis for the treatment of aortic stenosis during 2008–2017. The impact of PVR at discharge after TAVR and SAVR on 4-year mortality was herein investigated. RESULTS The rate of mild PVR was 21.7% after TAVR and 5.2% after SAVR. The rate of moderate-to-severe PVR was 3.7% after TAVR and 0.7% after SAVR. After TAVR, 4-year survival was 69.0% in patients with none-to-trace PVR, 54.2% with mild PVR [adjusted hazard ratio (HR) 1.64, 95% confidence interval (CI) 1.35–1.99] and 48.9% with moderate-to-severe PVR (adjusted HR 1.61, 95% CI 1.10–2.35). Freedom from PVR-related reinterventions was 100% for none-to-mild PVR and 95.2% for moderate-to-severe PVR. After SAVR, mild PVR (4-year survival 78.9%; adjusted HR 1.29, 95% CI 0.93–1.78) and moderate-to-severe PVR (4-year survival 67.8%; adjusted HR 1.36, 95% CI 0.72–2.58) were associated with worse 4-year survival compared to none-to-trace PVR (4-year survival 83.7%), but the difference did not reach statistical significance in multivariable analysis. Freedom from PVR-related reinterventions was 99.5% for none-to-trace PVR patients, 97.9% for mild PVR patients and 77.0% for moderate-to-severe PVR patients. CONCLUSIONS This multicentre study showed that both mild and moderate-to-severe PVR were independent predictors of worse survival after TAVR. Mild and moderate-to-severe PVR are not frequent after SAVR, but tend to decrease survival also in these patients. Clinical trial registration number ClinicalTrials.gov Identifier: NCT03385915.

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