1. Percutaneous Implantation of the CoreValve® Self-expanding Valve Prosthesis in Patients With Severe Aortic Stenosis and Porcelain Aorta: Medium-term Follow-up
- Author
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Raimundo Ocaranza-Sanchez, José M. de la Torre Hernández, César Morís, Ramiro Trillo-Nouche, Diego López-Otero, Isaac Pascual, Manuel F. Jiménez-Navarro, Pablo Avanzas, Belén Cid-Álvarez, Juan H. Alonso-Briales, Fernando Alfonso, Antonio J. Muñoz-García, and Raquel del Valle
- Subjects
Male ,medicine.medical_specialty ,Time Factors ,Percutaneous ,Kaplan-Meier Estimate ,Prosthesis Design ,Aortography ,Risk Assessment ,Severity of Illness Index ,Statistics, Nonparametric ,Transcatheter Aortic Valve Replacement ,Imaging, Three-Dimensional ,Predictive Value of Tests ,Internal medicine ,medicine ,Humans ,Minimally Invasive Surgical Procedures ,Hospital Mortality ,Prospective Studies ,Prospective cohort study ,Geriatric Assessment ,Aged ,Proportional Hazards Models ,Aged, 80 and over ,business.industry ,Vascular disease ,Incidence (epidemiology) ,Hazard ratio ,Calcinosis ,Aortic Valve Stenosis ,General Medicine ,medicine.disease ,Survival Analysis ,Confidence interval ,Surgery ,Stenosis ,Treatment Outcome ,Spain ,Heart Valve Prosthesis ,Multivariate Analysis ,cardiovascular system ,Cardiology ,Female ,Tomography, X-Ray Computed ,business ,Dyslipidemia ,Follow-Up Studies - Abstract
W Aortic stenosis A B S T R A C T Introduction and objectives: There is little information on the use of transcatheter aortic valve implantation in patients with severe aortic stenosis and porcelain aorta. The primary aim of this study was to analyze death from any cause after CoreValve W implantation in patients with severe aortic stenosis, with and without porcelain aorta. Methods: In this multicenter, observational prospective study, carried out in 3 hospitals, percutaneous aortic valves were implanted in 449 patients with severely calcified aortic stenosis. Of these, 36 (8%) met the criteria for porcelain aorta. The primary end-point was death from any cause at 2 years. Results: Patients with porcelain aorta more frequently had extracardiac vascular disease (11 (30.6%) vs 49 (11.9%); P=.002), prior coronary revascularization (15 (41.7%) vs 98 (23.7%); P=.017), and dyslipidemia (26 (72.2%) vs 186 (45%); P=.02). In these patients, there was greater use of general anesthesia (15 (41.7%) vs 111 (16.9%); P=.058) and axillary access (9 (25%) vs 34 (8.2%); P=.004). The success rate of the procedure (94.4 vs 97.3%; P=.28) and the incidence of complications (7 (19.4%) vs 48 (11.6%); P=.20) were similar in both groups. There were no statistically significant differences in the primary end point at 24 months of follow-up (8 (22.2%) vs 66 (16%); P=.33). The only predictive variable for the primary end point was the presence of complications during implantation (hazard ratio=2.6; 95% confidence interval, 1.5- 4.5; P=.001). Conclusions: In patients with aortic stenosis and porcelain aorta unsuitable for surgery, percutaneous implantation of the CoreValve W self-expanding valve prosthesis is safe and feasible.
- Published
- 2013