One‐year clinical and echocardiographic outcomes of direct implantation of a self‐expanding valve
Autor: | Vicki Zeniou, Haim D. Danenberg, Maria Karmpalioti, Ioannis Iakovou, M Xanthopoulou, Maria Drakopoulou, Georgios Katsimagklis, Konstantinos Stathogiannis, George Latsios, Dimitris Tousoulis, Vassilis Voudris, Sotiris Moraitis, Evangelia Bei, Andreas Synetos, Panagiotis Halvatsiotis, Georgios Benetos, Manolis Vavuranakis, Konstantinos Toutouzas |
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Rok vydání: | 2020 |
Předmět: |
medicine.medical_specialty
Regurgitation (circulation) 030204 cardiovascular system & hematology Transcatheter Aortic Valve Replacement 03 medical and health sciences 0302 clinical medicine Internal medicine medicine Clinical endpoint Humans Radiology Nuclear Medicine and imaging 030212 general & internal medicine Stroke business.industry Incidence (epidemiology) Significant difference Aortic Valve Stenosis General Medicine medicine.disease Stenosis Treatment Outcome Echocardiography Aortic Valve Heart Valve Prosthesis Heart failure Cardiology Permanent pacemaker Cardiology and Cardiovascular Medicine business |
Zdroj: | Catheterization and Cardiovascular Interventions. 98 |
ISSN: | 1522-726X 1522-1946 |
DOI: | 10.1002/ccd.29389 |
Popis: | Objective To present 1 year clinical and echocardiographic outcomes of the randomized DIRECT (Pre-dilatation in Transcatheter Aortic Valve Implantation Trial) trial. Background Intermediate-term data from randomized studies investigating the safety and efficacy of direct implantation are lacking. Methods DIRECT trial randomized 171 consecutive patients with severe aortic stenosis at four tertiary centers to undergo TAVI with the use of self-expanding prostheses with (pre-BAV) or without pre-dilatation (no-BAV). The primary endpoint was device success according to the VARC-2 criteria. All patients underwent a clinical and echocardiographic follow-up at 1 year. All-cause and cardiac mortality, stroke, heart failure hospitalization, and new pacemaker implantation were recorded. Results At 1 year, four deaths were recorded in pre-BAV group (4.7%) and three deaths in no-BAV group (3.5%). There was no difference in Kaplan-Meier plots between the two groups in all-cause mortality at 1 year (log-rank p = .72). Similarly, there was no difference in the incidence of permanent pacemaker implantation between the two groups at 1 year (27/67-40.3% in no-BAV group versus 20/69-29% in pre-BAV group, log-rank p = .24). There was no significant difference between pre-BAV and no BAV group in aortic valve area (1.84 ± 0.39 cm2 vs. 1.85 ± 0.44 cm2 , p = .90), mean aortic valve gradient (8.36 ± 5.04 vs. 8.00 ± 4.04 mmHg, p = .65) and moderate or severe paravalvular regurgitation (5-6.6 vs. 4-5.7%, respectively) at 1 year. The same applied independently from the performance of post-dilatation at baseline. Conclusions Direct, without pre-dilatation, implantation of a self-expanding valve has no impact on one-year clinical and echocardiographic outcomes, independently also from the baseline performance of post-dilatation. |
Databáze: | OpenAIRE |
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