Acute and mid-term outcomes of ablation for atrial fibrillation with VISITAG SURPOINT: the Japan MIYABI registry

Author:

Okumura Ken1ORCID,Inoue Koichi23,Goya Masahiko4ORCID,Origasa Hideki5ORCID,Yamazaki Makiho6ORCID,Nogami Akihiko7ORCID

Affiliation:

1. Division of Cardiology, Saiseikai Kumamoto Hospital , 5-3-1 Chikami, Minami-ku, Kumamoto 861-4193 , Japan

2. Division of Cardiology, National Hospital Organization Osaka National Hospital , 2-1-14 Houenzaka, Chuo-ku, Osaka 540-0006 , Japan

3. Cardiovascular Center, Sakurabashi Watanabe Hospital , 2-4-32 Umeda, Kita-ku, Osaka 530-0001 , Japan

4. Department of Cardiovascular Medicine, Tokyo Medical and Dental University , 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8510 , Japan

5. The Institute of Statistical Mathematics , 10-3 Midori-cho, Tachikawa, Tokyo 190-8562 , Japan

6. Department of Clinical Research, Johnson & Johnson K.K. Medical Company, Chiyoda First Building West Tower, 3-5-2 Nishi-Kanda, Chiyoda-ku, Tokyo 101-0065 , Japan

7. Department of Cardiology, Institute of Medicine, University of Tsukuba , 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8575 , Japan

Abstract

Abstract Aims The effectiveness of pulmonary vein isolation (PVI) guided by VISITAG SURPOINT (VS) has been demonstrated in Western populations. However, data for Asian populations are limited. VS settings may differ for Asians, given their smaller body size. This study aimed to describe outcomes of radiofrequency atrial fibrillation (AF) ablation guided by VS in a large Asian population. Methods and results The prospective, observational, multicentre MIYABI registry collected real-world data from patients undergoing VS-guided AF ablation using ThermoCool SmartTouch and ThermoCool SmartTouch SF catheters from 50 Japanese centres. All patients had paroxysmal AF or persistent AF for <6 months. Primary adverse events (PAEs) were evaluated for safety. The primary efficacy endpoint was the proportion of patients with PVI at the end of the procedure. Mid-term effectiveness (up to 12 months) was evaluated by freedom from documented atrial arrhythmias. Of the 1011 patients enrolled, 1002 completed AF ablation. The mean number of VS values per procedure was 428.8 on the anterior wall and 400.4 on the posterior wall. Nine patients (0.9%) experienced PAEs. Upon procedure completion, 99.7% of patients had PVI. Twelve-month freedom from atrial arrhythmia recurrence was 88.5%; 5.7% of patients were re-ablated. At repeat ablation, 54% of RSPV, 73% of RIPV, 70% of LSPV, and 86% of LIPV evaluated remained durably isolated. Conclusion Despite lower anterior wall VS values compared with the CLOSE protocol (≥550), the present study demonstrated comparable efficacy outcomes, indicating that a VS of ≥550 for the anterior wall may not be necessary for Asian patients.

Funder

Johnson & Johnson K.K. Medical Company

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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