{"title":"Myocardial Injury and Incidence of Early Recurrence of Atrial Fibrillation after Catheter Ablation between Two Types of Cryoballoon Systems.","authors":"Satoko Shiomi, Michifumi Tokuda, Ui Takato, Ryutaro Sakurai, Yoshito Yamazaki, Takuya Matsumoto, Hidenori Sato, Hirotsuna Oseto, Masaaki Yokoyama, Kenichi Tokutake, Seigo Yamashita, Teiichi Yamane","doi":"10.1536/ihj.25-374","DOIUrl":null,"url":null,"abstract":"<p><p>Two types of cryoballoon (CB) systems are currently available for catheter ablation of atrial fibrillation (AF). It is not clear how the difference between POLARx (Boston Scientific) and AFA-Pro (Medtronic) relates to myocardial injury and the incidence of early recurrence of fibrillation (ERAF).Patients (n = 137) who underwent catheter ablation for paroxysmal AF by 2 CB devices were included (AFA-Pro in 87; POLARx in 50). We assessed creatine kinase (CK)-MB pre and post-procedure, ERAF, and the number of atrial premature contractions (APCs) at Holter monitoring 1 month and 3 months after the procedure. The change ratio was defined by the following formula: (post-procedure/pre-procedure). ERAF is defined as the recurrence of AF within 90 days after the procedure.The 2 groups did not differ significantly in the number of CB applications or the percentage of touch-up applications by radiofrequency catheter. The CK-MB change ratio was considerably higher in the POLARx group than the AFA-Pro group (19.3 ± 21.6 versus 27.4 ± 21.3; P = 0.036). The incidence of ERAF was similar between the 2 groups (15% versus 24%; P = 0.23). Additionally, there were no significant differences in the number of APCs (120 [39-784] versus 147 [43-1039]; P = 0.70) or AF recurrence (3% versus 12%; P = 0.10).POLARx causes stronger myocardial injury than AFA-Pro but does not increase ERAF and APC numbers.</p>","PeriodicalId":13711,"journal":{"name":"International heart journal","volume":" ","pages":"20-26"},"PeriodicalIF":1.3000,"publicationDate":"2026-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International heart journal","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1536/ihj.25-374","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/17 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0
Abstract
Two types of cryoballoon (CB) systems are currently available for catheter ablation of atrial fibrillation (AF). It is not clear how the difference between POLARx (Boston Scientific) and AFA-Pro (Medtronic) relates to myocardial injury and the incidence of early recurrence of fibrillation (ERAF).Patients (n = 137) who underwent catheter ablation for paroxysmal AF by 2 CB devices were included (AFA-Pro in 87; POLARx in 50). We assessed creatine kinase (CK)-MB pre and post-procedure, ERAF, and the number of atrial premature contractions (APCs) at Holter monitoring 1 month and 3 months after the procedure. The change ratio was defined by the following formula: (post-procedure/pre-procedure). ERAF is defined as the recurrence of AF within 90 days after the procedure.The 2 groups did not differ significantly in the number of CB applications or the percentage of touch-up applications by radiofrequency catheter. The CK-MB change ratio was considerably higher in the POLARx group than the AFA-Pro group (19.3 ± 21.6 versus 27.4 ± 21.3; P = 0.036). The incidence of ERAF was similar between the 2 groups (15% versus 24%; P = 0.23). Additionally, there were no significant differences in the number of APCs (120 [39-784] versus 147 [43-1039]; P = 0.70) or AF recurrence (3% versus 12%; P = 0.10).POLARx causes stronger myocardial injury than AFA-Pro but does not increase ERAF and APC numbers.
期刊介绍:
Authors of research articles should disclose at the time of submission any financial arrangement they may have with a company whose product figures prominently in the submitted manuscript or with a company making a competing product. Such information will be held in confidence while the paper is under review and will not influence the editorial decision, but if the article is accepted for publication, the editors will usually discuss with the authors the manner in which such information is to be communicated to the reader.