Paroxysmal atrial fibrillation ablation with a novel temperature‐controlled CF‐sensing catheter: Q‐FFICIENCY clinical and healthcare utilization benefits

Author:

Hussein Ayman A.1ORCID,Delaughter M. Craig2,Monir George3ORCID,Natale Andrea4ORCID,Dukkipati Srinivas5,Oza Saumil6,Daoud Emile7ORCID,Di Biase Luigi8ORCID,Mansour Moussa9,Fishel Robert10,Valderrabano Miguel11,Ellenbogen Kenneth12ORCID,Osorio Jose13,

Affiliation:

1. Cleveland Clinic Foundation Cleveland Ohio USA

2. Texas Health Heart & Vascular Arlington Texas USA

3. AdventHealth Orlando Orlando Florida USA

4. Texas Cardiac Arrhythmia Institute Austin Texas USA

5. Mount Sinai School of Medicine New York New York USA

6. St. Vincent's Medical Center Jacksonville Florida USA

7. Ohio State University Medical Center Columbus Ohio USA

8. Montefiore Medical Center at Albert Einstein College of Medicine Bronx New York USA

9. Massachusetts General Hospital Boston Massachusetts USA

10. JFK Medical Center Atlantis Florida USA

11. Houston Methodist DeBakey Heart & Vascular Center Houston Methodist Research Institute Houston Texas USA

12. Virginia Commonwealth University Richmond Virginia USA

13. Grandview Medical Center Alabama Cardiovascular Group Birmingham Alabama USA

Abstract

AbstractIntroductionThe prospective, nonrandomized, multicenter Q‐FFICIENCY study demonstrated the safety and 12‐month efficacy of paroxysmal atrial fibrillation (AF) ablation with the novel QDOT MICRO temperature‐controlled, contact force‐sensing, radiofrequency (RF) catheter. Participants underwent pulmonary vein isolation with very high‐power short‐duration (vHPSD) mode (90 W, ≤4 s) alone or combined with conventional‐power temperature‐controlled (CPTC) mode (25–50 W). This study aimed to assess quality‐of‐life (QOL) and healthcare utilization (HCU) benefits experienced by Q‐FFICIENCY study participants.MethodsBesides evaluating procedural efficiency, QOL and HCU were assessed through 12 months postablation via Atrial Fibrillation Effect on Quality‐of‐Life Tool (AFEQT) score, antiarrhythmic drug (AAD) use, and incidence of cardioversion and cardiovascular hospitalization.ResultsOf 191 participants enrolled, 166 were ablated with the new catheter. Compared to baseline, statistically significant, clinically meaningful improvements in composite and subcategories of AFEQT scores were observed at 3 months and sustained through 12 months (12‐month increase, 29.3–44.2 points). Class I/III AAD use decreased from 97.6% (162/166) at baseline to 19.6% (31/158) during Months 6–12, representing a significant 79.9% reduction. The cardioversion rate significantly declined by 93.9% from 31.3% (12 months preablation) to 1.9% (evaluation period). One‐year Kaplan–Meier estimates of freedom from all‐cause and cardiovascular hospitalization were 80.9% (95% confidence interval [CI], 74.8%–86.9%) and 88.8% (95% CI, 84.0%–93.7%), respectively.ConclusionsParoxysmal AF ablation with the novel temperature‐controlled RF catheter in vHPSD mode, alone or with CPTC mode, led to clinically meaningful improvement in QOL and significant reduction in AAD use, cardioversion, and cardiovascular hospitalization.

Publisher

Wiley

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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