SynthesisBMC cardiovascular disorders2026
Safety and efficacy of single versus dual arterial access in transfemoral transcatheter aortic valve implantation: a systematic review and meta-analysis of propensity-matched cohort.
Synthesis in BMC cardiovascular disorders, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Single-Access Transfemoral TAVI with a Balloon Expandable Valve: Age-Stratified Analysis of Clinical Outcomes.Journal of clinical medicine · 2026Article
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
purpose of reviewTransfemoral transcatheter aortic valve implantation (TAVI) is an established treatment for severe aortic stenosis (AS). Although dual arterial access (DAA) is commonly used for catheter control and haemodynamic monitoring, single arterial access (SAA) has emerged as a minimalist strategy aimed at reducing procedural complexity and access-site complications. However, comparative outcome data remain limited. RECENT
findingsFour propensity score-matched observational studies comprising 540 patients (50.4% SAA) were included. Compared with DAA, SAA was associated with a significantly lower risk of total vascular complications (odds ratio [OR] 0.34, 95% confidence interval [CI] 0.17–0.67; p < 0.001), largely driven by reductions in minor access-site events (OR 0.44, 95% CI 0.20–0.95; p = 0.04), while rates of major vascular complications were similar between groups. There were no significant differences in all-cause mortality, stroke or transient ischaemic attack, paravalvular leak, or major bleeding. SAA was also associated with shorter procedural time (mean difference [MD] -17.1 min, 95% CI -32.8, -1.4; p = 0.03) and lower contrast volume use (MD -28.6 mL, 95% CI -55.3, -1.9; p = 0.04), although substantial heterogeneity was observed. In patients with symptomatic severe AS undergoing transfemoral TAVI, SAA appears to be a safe and feasible alternative to DAA and is associated with fewer vascular complications without compromising major clinical outcomes. Future prospective and randomised studies incorporating procedural complexity and device-specific outcomes are needed to confirm these results and better define optimal patient selection.
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