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Thermocool smarttouch ablation catheter

Manufactured by Johnson & Johnson
Sourced in United States

The ThermoCool SmartTouch Ablation Catheter is a medical device used in cardiac procedures. It is designed to deliver controlled radiofrequency energy to targeted areas of the heart to treat certain heart rhythm disorders.

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2 protocols using thermocool smarttouch ablation catheter

1

CF-sensing Catheter Ablation Guidance

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A ThermoCool SmartTouch Ablation Catheter (Biosense Webster Inc., Irvine, CA, USA), which is a novel CF-sensing quadripolar ablation catheter with a 3.5-mm external irrigation tip electrode, was used in our study. The ablation catheter was inserted into the right femoral vein and advanced into the right atrium under the guidance of the CARTO 3 electroanatomic mapping system (Biosense Webster Inc.). When the catheter was suspended in the right atrial cavity without endocardial contact, the CF value was calibrated to 0 g (the non-contact baseline value). Then, real-time CF data and the direction of the force vector were shown to the operators. We reconstructed the three-dimensional geometric model of the right atrium and the RVOT under the guidance of the CARTO 3 mapping system in fast anatomical mapping mode.
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2

Comparison of CPAP and PVI Treatments for Sleep Apnea

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In patients who were randomized to CPAP therapy (AirSense 10 Autoset, ResMed Inc., San Diego, California), we selected the auto set mode for CPAP pressure (between 3 and 15 cm H 2 O) during tolerance testing. Data were downloaded from the CPAP software (RescanÒ, ResMed) to estimate the residual AHI.
Treatment PVI was performed using conscious sedation (midazolam and fentanyl). Five experienced operators performed all the procedures. PVI was achieved with cryoballoon ablation (28-mm Arctic Front Advance cryoballoon catheter and Achieve pulmonary vein catheter; Medtronic Inc.) or radiofrequency (RF) ablation [CARTO 3 (Biosense webster, Diamond Bar, California) system with ThermoCool SmartTouch ablation catheter (Biosense webster) and 12-or 22-polar Lasso pulmonary vein catheter (Johnson & Johnson, New Brunswick, New Jersey)]. Antiarrhythmic drugs were routinely used for 6-8 weeks after PVI. Ablation was considered a failure if antiarrhythmic drugs had to be continued beyond, or reinstituted after, the blanking period.
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