TY - JOUR
T1 - Efficacy and safety of cryoballoon ablation in patients with heart failure and reduced left ventricular ejection fraction ― A multicenter study
AU - Heeger, Christian Hendrik
AU - Abdin, Amr
AU - Mathew, Shibu
AU - Reissmann, Bruno
AU - Yalin, Kivanc
AU - Liosis, Spyridon
AU - Fink, Thomas
AU - Proietti, Riccardo
AU - Eitel, Charlotte
AU - Vogler, Julia
AU - Lemeš, Christine
AU - Maurer, Tilman
AU - Rillig, Andreas
AU - Meyer-Saraei, Roza
AU - Graf, Tobias
AU - Wohlmuth, Peter
AU - Goldmann, Britta
AU - Ouyang, Feifan
AU - Kuck, Karl Heinz
AU - Metzner, Andreas
AU - Tilz, Roland Richard
N1 - Funding Information:
C.-H.H. received travel grants and research grants by Medtronic, Claret Medical, SentreHeart, Biosense Webster and Cardiofocus. KHK received travel grants and research grants from Biosense Webster, Stereotaxis, Prorhythm, Medtronic, Edwards, Cryocath, and is a consultant to St. Jude Medical, Biosense Webster, Prorhythm, and Stereotaxis. He received speaker’s honoraria from Medtronic. R.R.T. received travel grants from St. Jude Medical, Topera, Biosense Webster, Daiichi Sankyo, SentreHeart and Speaker’s Bureau Honoraria from Biosense Webster, Biotronik, Pfizer, Topera, Bristol-Myers Squibb; Bayer, Sano Aventis and research grants by Cardiofocus. AM received speaker’s honoraria and travel grants from Medtronic, Biosense Webster and Cardiofocus. K.Y. received an educational and research grant by the Turkish Society of Cardiology. C.E. received travel grants and educational grants by Medtronic. All other authors have no relevant disclosures.
Publisher Copyright:
© 2019, Japanese Circulation Society. All rights reserved.
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2019
Y1 - 2019
N2 - Background: Second-generation cryoballoon (CB2)-based pulmonary vein isolation (PVI) has demonstrated encouraging results in the treatment of atrial fibrillation (AF). This study sought to assess data on the safety, efficacy and clinical success of CB2-based PVI in patients with heart failure (HF) and reduced ejection fraction (HFrEF). Methods and Results: CB2-based PVI was performed in 551 consecutive patients in 3 highly experienced EP centers. Patients with HF and LVEF ≤40% were included (HFrEF group, n=50/551, 9.1%). Data were compared with propensity score-matched patients without HF and preserved left ventricular EF (LVEF) (n=50, control group). The median LVEF was HFrEF: 37% (35, 40) and control: 55% (55, 55), P<0.0001. Major periprocedural complications were registered in 4/50 (8%, HFrEF group) and 3/50 (6%, control group), P=0.695. The 12-month freedom from AF recurrence was 73.1% (95% confidence interval (CI): 61–88, HFrEF group) and 72.6% (95% CI: 61–87, control group), P=0.25. NYHA class decreased from 2.4±0.8 (baseline) to 1.7±0.8 at 12-month follow-up (P<0.0001). LVEF improved from a median of 37% (35, 40) prior to ablation to a median of 55% (40, 55), P<0.0001. Conclusions: CB2-based PVI in patients with HFrEF appeared to be safe, was associated with comparable periprocedural complications and showed promising clinical success rates equal to those for patients with preserved LVEF. NYHA class and LVEF significantly improved at 12-month follow-up.
AB - Background: Second-generation cryoballoon (CB2)-based pulmonary vein isolation (PVI) has demonstrated encouraging results in the treatment of atrial fibrillation (AF). This study sought to assess data on the safety, efficacy and clinical success of CB2-based PVI in patients with heart failure (HF) and reduced ejection fraction (HFrEF). Methods and Results: CB2-based PVI was performed in 551 consecutive patients in 3 highly experienced EP centers. Patients with HF and LVEF ≤40% were included (HFrEF group, n=50/551, 9.1%). Data were compared with propensity score-matched patients without HF and preserved left ventricular EF (LVEF) (n=50, control group). The median LVEF was HFrEF: 37% (35, 40) and control: 55% (55, 55), P<0.0001. Major periprocedural complications were registered in 4/50 (8%, HFrEF group) and 3/50 (6%, control group), P=0.695. The 12-month freedom from AF recurrence was 73.1% (95% confidence interval (CI): 61–88, HFrEF group) and 72.6% (95% CI: 61–87, control group), P=0.25. NYHA class decreased from 2.4±0.8 (baseline) to 1.7±0.8 at 12-month follow-up (P<0.0001). LVEF improved from a median of 37% (35, 40) prior to ablation to a median of 55% (40, 55), P<0.0001. Conclusions: CB2-based PVI in patients with HFrEF appeared to be safe, was associated with comparable periprocedural complications and showed promising clinical success rates equal to those for patients with preserved LVEF. NYHA class and LVEF significantly improved at 12-month follow-up.
UR - http://www.scopus.com/inward/record.url?scp=85069970453&partnerID=8YFLogxK
U2 - 10.1253/circj.CJ-19-0151
DO - 10.1253/circj.CJ-19-0151
M3 - Journal articles
C2 - 31257357
AN - SCOPUS:85069970453
SN - 1346-9843
VL - 83
SP - 1653
EP - 1659
JO - Circulation Journal
JF - Circulation Journal
IS - 8
ER -