Impact of first-line cryoablation for atrial fibrillation on healthcare utilization, arrhythmia disease burden and efficacy outcomes: real-world evidence from the Cryo Global Registry.


Journal

Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing
ISSN: 1572-8595
Titre abrégé: J Interv Card Electrophysiol
Pays: Netherlands
ID NLM: 9708966

Informations de publication

Date de publication:
Apr 2023
Historique:
received: 27 06 2022
accepted: 29 09 2022
medline: 4 4 2023
pubmed: 5 11 2022
entrez: 4 11 2022
Statut: ppublish

Résumé

Cryoballoon ablation (CBA) is an effective first-line treatment for symptomatic atrial fibrillation (AF), as recently demonstrated by three randomized trials. This sub-analysis of the Cryo Global Registry aims to examine current clinical practices of first-line CBA. AF patients treated with first-line CBA were compared to CBA in antiarrhythmic drug (AAD)-refractory patients at 12 months. Efficacy was examined using time-to-first atrial arrhythmia recurrence following a 90-day blanking period. Healthcare utilization was evaluated by repeat ablations and hospitalizations. Disease burden was examined by assessing quality of life (QOL) and patients' reporting of symptoms. Of 1394 patients, 433 (31.1%) were treated with first-line CBA, which was more frequent in high-volume centers. Serious procedure-related adverse event rates were similar. Efficacy at 12 months was higher in the first-line group (87.8 vs. 81.6%, HR In this global real-world experience, first-line CBA in patients with symptomatic AF is effective, with a larger symptom reduction compared with CBA after AAD failure and without a difference in healthcare utilization at mid-term follow-up. https://clinicaltrials.gov/ct2/show/NCT02752737.

Sections du résumé

BACKGROUND BACKGROUND
Cryoballoon ablation (CBA) is an effective first-line treatment for symptomatic atrial fibrillation (AF), as recently demonstrated by three randomized trials. This sub-analysis of the Cryo Global Registry aims to examine current clinical practices of first-line CBA.
METHODS METHODS
AF patients treated with first-line CBA were compared to CBA in antiarrhythmic drug (AAD)-refractory patients at 12 months. Efficacy was examined using time-to-first atrial arrhythmia recurrence following a 90-day blanking period. Healthcare utilization was evaluated by repeat ablations and hospitalizations. Disease burden was examined by assessing quality of life (QOL) and patients' reporting of symptoms.
RESULTS RESULTS
Of 1394 patients, 433 (31.1%) were treated with first-line CBA, which was more frequent in high-volume centers. Serious procedure-related adverse event rates were similar. Efficacy at 12 months was higher in the first-line group (87.8 vs. 81.6%, HR
CONCLUSIONS CONCLUSIONS
In this global real-world experience, first-line CBA in patients with symptomatic AF is effective, with a larger symptom reduction compared with CBA after AAD failure and without a difference in healthcare utilization at mid-term follow-up.
CLINICAL TRIAL REGISTRATION BACKGROUND
https://clinicaltrials.gov/ct2/show/NCT02752737.

Identifiants

pubmed: 36331681
doi: 10.1007/s10840-022-01388-6
pii: 10.1007/s10840-022-01388-6
doi:

Substances chimiques

Anti-Arrhythmia Agents 0

Banques de données

ClinicalTrials.gov
['NCT02752737']

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

711-722

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Références

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Auteurs

Giulio Zucchelli (G)

Second Division of Cardiology, Azienda Ospedaliero Universitaria Pisana, Via Roma, 67, 56126, Pisa, Italy. g.zucchelli@ao-pisa.toscana.it.

K R Julian Chun (KRJ)

Cardioangiologisches Centrum Bethanien, Frankfurt, Germany.

Surinder Kaur Khelae (SK)

Institut Jantung Negara, National Heart Institute, Kuala Lumpur, Malaysia.

Csaba Földesi (C)

Gottsegen György Országos Kardiovaszkuláris Intézet, Budapest, Hungary.

Fred J Kueffer (FJ)

Medtronic, Inc, Minneapolis, MN, USA.

Kelly A van Bragt (KA)

Medtronic, Inc, Minneapolis, MN, USA.

Fernando Scazzuso (F)

Instituto Cardiovascular de Buenos Aires, Buenos Aires, Argentina.

Young-Keun On (YK)

Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.

Fawzia Al-Kandari (F)

Chest Disease Hospital, Kuwait City, Kuwait.

Ken Okumura (K)

Saiseikai Kumamoto Hospital, Kumamoto, Japan.

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