Women with persistent atrial fibrillation need more than pulmonary vein isolation: personalised extra-pulmonary vein ablation strategy vs. pulmonary vein isolation alone in the TAILORED-AF trial.
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Deisenhofer Isabel, Seitz Julien, Nguyen-Tu Marie-Sophie, Lotteau Sabine, Bars Clément, Albenque Jean-Paul, Busch Sonia, Gitenay Edouard, Mountantonakis Stavros, Roux Antoine, Horvilleur Jérôme, Bakouboula Babe, Oza Saumil, Abbey Selim, Theodore Guillaume, Lepillier Antoine, Guyomar Yves, Bessière Francis, Smit Jaap Jan, Rajendra Anil, Cooper Daniel H, Rashid Haroon, De Potter Tom, De Chillou Christian, Goldbarg Seth, Verma Atul, Morales Gustavo, Milpied Paola, Hummel John D, Kalifa Jérôme
Аннотация
METHODS AND RESULTS: In TAILORED-AF, 370 patients were randomised to either a personalised, artificial intelligence (AI)-guided tailored ablation or to PVI-only. AF substrate mapping data and 12-month ablation outcomes were compared between women and men. Overall, 21% patients were female (70.4 ± 6.9 vs. 64.5 ± 8.5 years for men, P < 0.001). While spatio-temporal dispersion extent was similar between groups, left atrial low-voltage surface area (<0.2 mV) was significantly larger in women (P < 0.01). In women, the single-procedure freedom from AF (76% vs. 50%, log-rank P < 0.001) and any atrial arrhythmia (56% vs. 38%, log-rank P < 0.05) were significantly superior to PVI alone with a tailored procedure. In the PVI-only group, the single-procedure freedom from AF (50% vs. 70%, log-rank P < 0.001) and any atrial arrhythmia (38% vs. 61%, log-rank P < 0.001) were significantly lower in women. After a tailored ablation, no significant differences were observed between women and men regarding freedom from AF (76% vs. 91%, log-rank P = 0.07) or any atrial arrhythmia (56% vs. 62%, log-rank P = 0.69) free survival.
CONCLUSION: Compared to men, PVI-only in women with persistent AF leads to a significantly lower freedom from atrial arrhythmia. A personalised spatio-temporal dispersion-targeted ablation strategy led to a higher rate of freedom from any atrial arrhythmia than standard PVI after a single procedure in women and comparable outcomes between women and men.
REGISTRATION IDENTIFICATION: clinicaltrials.gov NCT04702451.