Cryothermal ablation treatment of atrial flutter - Experience with a new 9 french 8 mm tip catheter
Cryothermal ablation treatment of atrial flutter - Experience with a new 9 french 8 mm tip catheter
复制标题
DOI:
10.1007/s10840-005-5840-3
复制
发表时间:
2005-01-01
影响因子:
1.8
通讯作者:
Affinito, V
中科院分区:
文献类型:
--
作者:
Montenero, AS;Bruno, N;Affinito, V
Background: Cardiac cryoablation has been used to successfully treat a variety of arrhythmias. Objective: This study documents our experience with a new 9 French (FR) 8 mm. cryocatheter for ablation treatment of symptomatic atrial flutter.Methods: A total of 77 consecutive patients with symptomatic atrial flutter were treated. Electrophysiological studies (EPS) were performed with diagnostic catheters and ablation was performed with a 9FR, 8 mm tip, quadripolar cryocatheter (Freezor(R) MAX catheter, CryoCath Technologies Inc., Kirkland, Canada). Cryoablation at -75degreesC for 8 minutes was performed, beginning at the inferior rim of the coronary sinus (CS) os and creating a posterior line to the Eustachian ridge. Safety, bidirectional isthmus block at intervention, and recurrence at 3 months post procedure were assessed.Results: There were no adverse events reported. All patients remained free of discomfort on cryoenergy delivery. The acute success rate at intervention was 96 % for all patients and 100 % for those with common atrial flutter. Follow-up data from 47 patients showed 33 (70 %) patients without conduction recurrence on repeat EPS at 3 months. Although, 1 (2 %) patient had both symptom and conduction recurrence. Data available from 53 acutely successful patients at 6 month clinical follow-up showed that 48 (91 %) patients were asymptomatic and 5 (9 %) patients had recurrence documented by ECG and/or patient diary records.Conclusions: Our experience with a new 9FR, 8 mm tip, quadripolar cryocatheter yielded a high success rate at intervention and an excellent safety profile. Although repeat EPS at 3 months post ablation identified conduction recurrence in 30 % of patients, at 6 month clinical follow-up only 9 % of patients had recurrence. Further monitoring is necessary to assess whether the relatively low recurrence rate observed at 6 month clinical follow-up is maintained over the long term.