Biosense Webster, Inc., a global leader in cardiac arrhythmia treatment and part of Johnson & Johnson MedTech,i announced new findings from the Q-FFICIENCY study were published in the Journal of Cardiovascular Electrophysiology demonstrating treatment with the QDOT MICRO™ Catheter significantly improved control of atrial fibrillation (AFib), relief of symptoms and overall quality of life.
Q-FFICIENCY evaluated the safety and 12-month efficacy of the novel QDOT MICRO™ Catheter temperature-controlled, contact force-sensing, radiofrequency (RF) catheter in patients with paroxysmal AFib.2
Based on patient-reported outcomes, the study found a 99% and 93.1% improvement in control of AFib and relief of AFib symptoms, respectively, at 12-month follow-up compared to baseline, and 87.9% of patients experienced a meaningful clinical improvement in quality of life.1
"These findings highlight the advantage of treatment with the QDOT MICRO™ Catheter in patients with paroxysmal AFib, demonstrating that patients have fewer symptoms and a significant improvement in their quality of life along with a low incidence of cardioversion and hospitalizations following temperature-controlled RF ablation treatment," said Ayman A. Hussein, MD, Director of Cardiac Electrophysiological Outcomes Research and Director of the Center for Atrial Fibrillation, Cleveland Clinic and the publication's corresponding author.ii "Paired with previously published Q-FFICIENCY study data showing that the unique design of the QDOT MICRO™ Catheter enhanced efficiency and efficacy without compromising safety, the benefit of treatment with this state-of-the art tool is clear for both patients and physicians."
The QDOT MICRO™ Catheter is a next-generation RF ablation catheter that incorporates advanced, high-energy ablation, improved temperature monitoring, optimized irrigation, and higher signal resolution. In QMODE+™ setting, the catheter allows the delivery of very high-power, short-duration ablation – 90 watts for up to four seconds, significantly improving ablation efficiency.2 The QDOT MICRO™ Catheter is fully integrated with the CARTO® 3 System, enabling efficient and consistent lesion creation with a simplified workflow and lower total procedure time.2 Earlier this year, Biosense Webster announced the publication of the Q-FFICIENCY safety and 12-month efficacy data in JACC: Clinical Electrophysiology, which showed that the QDOT MICRO™ Catheter delivered high clinical success with 86% of patients experiencing freedom from symptomatic recurrence while catheter-related primary adverse events remained low at 1.8%.2
"AFib places a substantial burden on patients' daily lives and healthcare resources, including physician visits, drug costs and side effects, and hospitalizations. At Biosense Webster, we are focused on improving patient outcomes, while offering innovative solutions for physicians treating the growing number of AFib patients today," said Jasmina Brooks, President, Biosense Webster, Inc. "As the Q-FFICIENCY study findings demonstrate, use of the temperature-controlled QDOT MICRO™ Catheter allows physicians to customize treatment for each patient, reduce procedural times and offer significant benefits to patients through improving their quality of life."
AFib is the most common type of cardiac arrhythmia affecting an estimated 37.5 million people globally.3 Responsible for more than 450,000 hospitalizations and nearly 5 million physician visits in the U.S. annually, AFib places a heavy burden on patients, their caregivers and healthcare systems.4 Despite these projections, many people are unfamiliar with AFib symptoms, available treatment options and the importance of early treatment to avoid disease progression.5 Catheter ablation is a safe and effective procedure to restore the heart's incorrect electrical signals, which causes an abnormal heart rhythm.6
About Q-FFICIENCY Study
In this prospective, multicenter, nonrandomized study, patients with drug-refractory, symptomatic paroxysmal AFib underwent PV isolation with the QDOT MICRO™ Catheter with very high-power short-duration as the primary ablation mode, which modulates power to maintain target temperature during 90 watt ablations for up to 4 seconds, with optional use of the conventional-power temperature-controlled mode (25 to 50 watts) for PV touch-up or non-PV ablation. The primary safety endpoint was incidence of primary adverse events within seven days of ablation. The primary effectiveness endpoint was freedom from documented atrial tachyarrhythmia recurrence and acute procedural, repeat ablation, and antiarrhythmic drug (AAD) failure. The primary safety and efficacy endpoints were met.
Patients' quality of life was assessed with the Atrial Fibrillation Effect on Quality-of-Life Tool (AFEQT), a questionnaire that measures symptoms, daily activities, treatment concerns and satisfaction at baseline and throughout 12 months following treatment with the QDOT MICRO™ Catheter.1
An 79.9% reduction in Class I/III AAD use was reported, with >50% of participants discontinuing all AADs postablation.1 Compared with the 12-month preablation period, the cardioversion rate decreased by 93.9% (P<0.0001) during the evaluation period.1 Hospitalizations were also low following ablation, with 80.9% (95% CI, 74.8%–86.9%) and 88.8% (95% CI, 84.0%–93.7%) Kaplan-Meier estimated 12-month freedom from all-cause and cardiovascular hospitalizations, respectively.1
About QDOT MICRO™ Catheteriii
The Biosense Webster QDOT MICRO™ Catheters and related accessory devices are indicated for catheter-based cardiac electrophysiological mapping (stimulating and recording) and, when used in conjunction with a compatible radiofrequency generator, for the treatment of:
For more information please visit, www.biosensewebster.co
