Why the study?
Although TAVI complications requiring emergent cardiac surgery have become rare, guidelines mandate on-site cardiac surgery, contributing to access disparities and prolonged waiting times.
Does performing TAVI in centers without on-site cardiac surgery compared to centers with on-site cardiac surgery affect outcomes in high-risk patients with symptomatic severe aortic stenosis?
Does performing TAVI in centers without on-site cardiac surgery compared to centers with on-site cardiac surgery affect outcomes in high-risk patients with symptomatic severe aortic stenosis?
The TRACS trial is designed to determine if TAVI can be safely and effectively performed in centers without on-site cardiac surgery, potentially expanding access to care.
Answers are grounded in this paper and cite their sources.
Rare ECS after TAVI may ease on-site surgery mandates; leaves open whether guidelines should relax center requirements.
BACKGROUND: Transcatheter aortic valve implantation (TAVI) has emerged as an effective and safe treatment for patients with symptomatic aortic stenosis. The indication to TAVI should be agreed upon by a Heart Team, and the procedure should be performed in centers with on-site cardiac surgery. However, TAVI complications requiring emergent cardiac surgery (ECS) have become very rare. Concurrently, access disparities and prolonged waiting times are pressing issues due to increasing clinical demand of TAVI. Many solutions have been proposed and one of them is the possibility of performing TAVI in centers without on-site cardiac surgery. METHODS AND DESIGN: The Transcatheter Aortic-Valve Implantation with or without on-site Cardiac Surgery (TRACS) trial is a prospective, randomized, multicenter, open-label study with blinded adjudicated evaluation of outcomes. Patients with symptomatic severe aortic stenosis and deemed inoperable, at high surgical risk, or presenting with at least 1 clinical factor compromising the benefit/risk ratio for ECS, will be randomized to undergo TAVI either in centers with or without on-site cardiac surgery. The primary endpoint will be the composite occurrence of all-cause death, stroke, and hospital readmission for cardiovascular causes at one year. The safety endpoint will include death attributable to periprocedural complications actionable by ECS. The study aims to enroll 566 patients. IMPLICATIONS: The TRACS trial aims to address critical gaps in knowledge regarding the safety and efficacy of TAVI procedures performed in centers without on-site cardiac surgery, potentially improving access and outcomes for high-risk patients. TRIAL REGISTRATION: ClinicalTrials.gov NCT05751577.
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Iannopollo et al. (2024) studied this question.
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