Prognostic Impact of Prefrailty and Frailty in Women Undergoing TAVR: Insights From the WIN-TAVI Registry.
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Petrovic Marija, Spirito Alessandro, Sartori Samantha, Vogel Birgit, Tchetche Didier, Petronio Anna Sonia, Mehilli Julinda, Lefevre Thierry, Presbitero Patrizia, Capranzano Piera, Pileggi Brunna, Iadanza Alessandro, Sardella Gennaro, van Mieghem Nicolas M, Meliga Emanuele, Feng Yihan, Dumonteil Nicolas, Cohen Rebecca, Fraccaro Chiara, Trabattoni Daniela, Mikhail Ghada, Ferrer-Gracia Maria-Cruz, Naber Christoph, Sharma Samin K, Watanabe Yusuke, Morice Marie-Claude, Dangas George D, Chieffo Alaide, Mehran Roxana
Аннотация
METHODS: Women at intermediate or high surgical risk with severe aortic stenosis undergoing TAVR from the prospective multicentre WIN-TAVI (Women's International Transcatheter Aortic Valve Implantation) registry were stratified based on the number of Fried frailty criteria (weight loss, exhaustion, low physical activity, slow gait, weakness) met: nonfrail (no criteria), prefrail (1 or 2 criteria), or frail (3 or more criteria). The primary outcome at 1 year was the Valve Academic Research Consortium 2 (VARC-2) efficacy end point, a composite of mortality, stroke, myocardial infarction, hospitalisation for valve-related symptoms or heart failure, and valve-related dysfunction; secondary outcomes included the composite of VARC-2 life-threatening or major bleeding.
RESULTS: Out of 1019 women, 297 (29.1%) met at least 1 frailty criterion: 264 (25.9%) had prefrailty and 33 (3.2%) frailty. The 1-year risk of the primary outcome was significantly higher in prefrail and frail (20.2%) than in nonfrail (14.9%) women (adjusted hazard ratio [aHR] 1.51, 95% confidence interval [CI] 1.07-2.12). The risk of VARC-2 life-threatening or major bleeding was higher in prefrail or frail (19.9%) than in nonfrail (10.0%) women (aHR 2.06, 95% CI 1.42-2.97). These risks were consistently increased in the prefrail and frail groups assessed separately.
CONCLUSIONS: In women undergoing TAVR, the presence of prefrailty or frailty conferred an increased risk of the VARC-2 efficacy end point and of VARC-2 life-threatening or major bleeding.