Journal of cardiovascular medicine (Hagerstown, Md.) · 2026
Safety and efficacy of transcatheter aortic valve replacement for native pure aortic valve regurgitation.
СтатьяНазвание и аннотация: Перевод в очереди
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Cavalli Giulio Giovanni, Vallabini Albino, Braccio Maurizio, Spatuzza Paola, Alemanni Rossella, Russo Eleonora, Siena Paola, Palladino Michele, Gallo Nunzio, Arcudi Giuseppe, Di Marco Luca, Leone Alessandro, Greco Francesco, Pacini Davide, Cassese Mauro
Аннотация
AIMS: Transcatheter aortic valve replacement has become the standard of care for high-risk patients with aortic stenosis. Considering the unique procedural challenges posed by native pure aortic regurgitation (NPAR), our aim was to evaluate the early and mid-term results of off-label transcatheter aortic valve replacement (TAVR), investigating the possibility of brief Veno-Arterial extracorporeal membrane oxygenation (VA ECMO) support for most complex procedures.
METHODS: We retrospectively enrolled 65 consecutive patients, who underwent TAVR for NPAR because they were deemed ineligible for surgery. Patients with aortic valve calcification or stenosis were excluded. Primary endpoints were technical and device success according to the VARC-3 criteria. Secondary endpoints were clinical efficacy at 1 year and absence of at least moderate paravalvular leak.
RESULTS: Patients' mean age was 76.15 ± 8.91. We adopted light sedation and local anesthesia in 60 patients (92.3%). High-risk patients (53.8%) were briefly supported with percutaneous femoro-femoral VA ECMO, allowing safer and more precise valve deployment. One intraprocedural death was recorded (1.5%). Although the overall 30-day mortality was 7.7%, primary composite outcomes were significantly better in the second half of the population ( P = 0.023 and P = 0.026). Only one moderate paravalvular leak (1.5%) was detected at 1-month follow-up. Clinical efficacy at 1 year was 76.3%, being available for 38 patients.
CONCLUSION: TAVR is still considered an off-label approach for NPAR because of the increased stroke volume and absence of annular and leaflet calcification, which might increase the complication rate. Nonetheless, a standardized approach, with the aid of brief VA ECMO support for complex cases, should be considered a safe and valid option in high-volume centers for inoperable patients.
METHODS: We retrospectively enrolled 65 consecutive patients, who underwent TAVR for NPAR because they were deemed ineligible for surgery. Patients with aortic valve calcification or stenosis were excluded. Primary endpoints were technical and device success according to the VARC-3 criteria. Secondary endpoints were clinical efficacy at 1 year and absence of at least moderate paravalvular leak.
RESULTS: Patients' mean age was 76.15 ± 8.91. We adopted light sedation and local anesthesia in 60 patients (92.3%). High-risk patients (53.8%) were briefly supported with percutaneous femoro-femoral VA ECMO, allowing safer and more precise valve deployment. One intraprocedural death was recorded (1.5%). Although the overall 30-day mortality was 7.7%, primary composite outcomes were significantly better in the second half of the population ( P = 0.023 and P = 0.026). Only one moderate paravalvular leak (1.5%) was detected at 1-month follow-up. Clinical efficacy at 1 year was 76.3%, being available for 38 patients.
CONCLUSION: TAVR is still considered an off-label approach for NPAR because of the increased stroke volume and absence of annular and leaflet calcification, which might increase the complication rate. Nonetheless, a standardized approach, with the aid of brief VA ECMO support for complex cases, should be considered a safe and valid option in high-volume centers for inoperable patients.