“… 35 Investigations into this concept continued for the next decade, 36 , 37 , 38 , 39 , 40 , 41 , 42 , 43 , 44 but a practical device did not become available until 2014. Initial use of this device—the ensoETM (Attune Medical, Chicago, IL)—was in critical care, emergency medicine, and surgery for patient systemic temperature management 45 , 46 , 47 , 48 , 49 , 50 , 51 , 52 , 53 but adoption for use during PVI has grown rapidly, with a recent analysis of >25,000 patients finding a significant reduction in AEF rate associated with its use. 54 In September 2023, the US Food and Drug Administration (FDA) granted de novo marketing authorization for the device to reduce the likelihood of ablation-related esophageal injury resulting from RF cardiac ablation procedures.…”