First experience with a transseptal puncture using a novel transseptal crossing device with integrated dilator and needle

Background This study aimed to evaluate the feasibility and safety of an innovative “all in one” integrated transseptal crossing device to achieve transseptal puncture (TSP). Methods Twenty patients (10 males, mean age 65.65 ± 9.25 years), indicated to supraventricular left side tachyarrhythmia ablation, underwent TSP using a new-generation integrated crossing device, and a control cohort of twenty patients (10 males, mean age 65.5 ± 10.12 years) underwent TSP using the traditional TSP system. Results In all the study patients, the novel TSP device led to a successful and safe access to the left atrium (LA). The mean transseptal time, defined as the time occurring between the groin puncture and the advancing of the guidewire into the left superior pulmonary vein (PV), was 3 min 33 s ± 44 s, 7 min 5 s ± 36 s in the control cohort. Additionally, we compared the cost of the two systems. No acute complications related to the TSP were noted in both cohorts. Conclusions TSP performed with the new integrated transseptal system is feasible and safe.