Does TAVR with a self-expanding valve provide similar 5-year clinical outcomes compared to surgical aortic valve replacement in intermediate-risk patients with severe aortic stenosis?
1,660 patients with symptomatic severe aortic valve stenosis deemed to be at intermediate risk of 30-day surgical mortality, mean age 79.8 years, 43.6% female, mean STS PROM score 4.5%, from 87 centers in Europe and North America.
Transcatheter aortic valve replacement (TAVR) with a self-expanding, supra-annular transcatheter bioprosthesis
Surgical aortic valve replacement with a surgical bioprosthesis
Composite of death or disabling stroke at 5 yearscomposite
In intermediate-risk patients with severe aortic stenosis, TAVR and surgery provide similar rates of death or disabling stroke at 5 years, though TAVR is associated with superior hemodynamics at the cost of higher rates of paravalvular leak, pacemakers, and reinterventions.
Importance In patients with severe aortic valve stenosis at intermediate surgical risk, transcatheter aortic valve replacement (TAVR) with a self-expanding supra-annular valve was noninferior to surgery for all-cause mortality or disabling stroke at 2 years. Comparisons of longer-term clinical and hemodynamic outcomes in these patients are limited. Objective To report prespecified secondary 5-year outcomes from the Symptomatic Aortic Stenosis in Intermediate Risk Subjects Who Need Aortic Valve Replacement (SURTAVI) randomized clinical trial. Design, Setting, and Participants SURTAVI is a prospective randomized, unblinded clinical trial. Randomization was stratified by investigational site and need for revascularization determined by the local heart teams. Patients with severe aortic valve stenosis deemed to be at intermediate risk of 30-day surgical mortality were enrolled at 87 centers from June 19, 2012, to June 30, 2016, in Europe and North America. Analysis took place between August and October 2021. Intervention Patients were randomized to TAVR with a self-expanding, supra-annular transcatheter or a surgical bioprosthesis. Main Outcomes and Measures The prespecified secondary end points of death or disabling stroke and other adverse events and hemodynamic findings at 5 years. An independent clinical event committee adjudicated all serious adverse events and an independent echocardiographic core laboratory evaluated all echocardiograms at 5 years. Results A total of 1660 individuals underwent an attempted TAVR (n = 864) or surgical (n = 796) procedure. The mean (SD) age was 79.8 (6.2) years, 724 (43.6%) were female, and the mean (SD) Society of Thoracic Surgery Predicted Risk of Mortality score was 4.5% (1.6%). At 5 years, the rates of death or disabling stroke were similar (TAVR, 31.3% vs surgery, 30.8%; hazard ratio, 1.02 95% CI, 0.85-1.22; P = .85). Transprosthetic gradients remained lower (mean SD, 8.6 5.5 mm Hg vs 11.2 6.0 mm Hg; P lt; .001) and aortic valve areas were higher (mean SD, 2.2 0.7 cm 2 vs 1.8 0.6 cm 2 ; P lt; .001) with TAVR vs surgery. More patients had moderate/severe paravalvular leak with TAVR than surgery (11 3.0% vs 2 0.7%; risk difference, 2.37% 95% CI, 0.17%- 4.85%; P = .05). New pacemaker implantation rates were higher for TAVR than surgery at 5 years (289 39.1% vs 94 15.1%; hazard ratio, 3.30 95% CI, 2.61-4.17; log-rank P lt; .001), as were valve reintervention rates (27 3.5% vs 11 1.9%; hazard ratio, 2.21 95% CI, 1.10-4.45; log-rank P = .02), although between 2 and 5 years only 6 patients who underwent TAVR and 7 who underwent surgery required a reintervention. Conclusions and Relevance Among intermediate-risk patients with symptomatic severe aortic stenosis, major clinical outcomes at 5 years were similar for TAVR and surgery. TAVR was associated with superior hemodynamic valve performance but also with more paravalvular leak and valve reinterventions.
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Nicolas M. Van Mieghem
G. Michael Deeb
Lars Søndergaard
JAMA Cardiology
University of Michigan
Columbia University
University of Pittsburgh
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Mieghem et al. (Wed,) studied this question.
www.synapsesocial.com/papers/6995afa083d686757580cce9 — DOI: https://doi.org/10.1001/jamacardio.2022.2695