News | Heart Failure | October 02, 2015

ENCORE Study Finds Autonomic Regulation Therapy Benefits Extend Beyond 12 Months

Patients in extension of ANTHEM-HF study showed continued improvement in heart pump function, reduction in heart failure symptom burden

October 2, 2015 — Cyberonics Inc. announced results from the extension of the ANTHEM-HF clinical study (ENCORE Study). Results of the study presented by a prominent heart failure (HF) specialist during a major cardiology congress in the United States show that autonomic regulation therapy (ART) in patients with moderate to severe chronic HF and impaired heart function is well-tolerated, safe, improves the heart's ability to pump blood, and reduces the frequency and severity of symptoms associated with chronic HF. More than 10 million people in the United States and Europe have chronic HF, a syndrome characterized by the heart's inability to pump sufficient blood to meet the metabolic demands of the body.

Results from the ENCORE clinical study were presented during a late breaking clinical trials session at the 19th Annual Meeting of the Heart Failure Society of America (HFSA) and showed that patients with chronic, reduced ejection fraction HF on stable pharmacological therapy and treated with ART for 12 months via electrical stimulation of the cervical vagus nerve experienced a statistically and clinically significant:

  • Improvement in heart pump function: Average left ventricular ejection fraction increased from 33.2 percent at baseline to 39.5 percent; average left ventricular end-systolic volume decreased 10 percent from 102 ml to 92 ml;
  • Reduction in HF symptom burden: New York Heart Association (NYHA) class improved in 94 percent of patients;
  • Improvement in quality of life (assessed by Minnesota Living with HF Questionnaire);
  • Increase in functional capacity (assessed by six-minute walk distance); and
  • Improvement in autonomic regulation of resting heart rate.

University of Minnesota Professor of Medicine Inder Anand, M.D., D.Phil. (Oxon), chair of the ANTHEM-HF clinical study steering committee and until recently director of the Heart Failure Program, VA Medical Center, Minneapolis, Minnesota, commented, "Patients with heart failure continue to be at high risk of increased morbidity and mortality. They need new therapies, such as ART, that work synergistically with evolving forms of drug therapy. The results from the extension of the ANTHEM-HF study presented during a late breaking clinical trials session at HFSA provide important insights into the safety and durability of ART. During the 6- to 12-month follow-up period, none of the patients experienced serious adverse events related to ART, and the improvements in cardiac function both in terms of ejection fraction and reverse remodeling suggest that ART is ready to be tested in a randomized, control trial in which a larger cohort of optimally-managed chronic HF patients from the U.S. and the EU would be randomized to a treatment group and a control group to more extensively evaluate safety and efficacy."

Sponsored by Cyberonics, the ENCORE study was a prospective, multi-center, open-label, extension of the ANTHEM-HF study during which the effects of ART were evaluated in chronic HF patients with NYHA Class II and III heart failure, QRS complex interval less than 150 milliseconds, and reduced heart pumping function (left ventricular ejection fraction less than 40 percent). According to investigators, patients enrolled in the study received optimal HF pharmacological therapy prior to and during all phases of study.

Forty-nine patients previously enrolled in the ANTHEM-HF study elected to participate in the ENCORE study and received ART for an additional 6 months (12 months total). All patients received continuously cyclic, natural-frequency ART previously described in the publication of ANTHEM-HF results. Safety was assessed throughout the ENCORE study and outcome measures were assessed after 12 months of ART and compared to baseline values of the ENCORE cohort.

For more information:

Related Content

Abbott Secures FDA Approval for MRI Compatibility on Ellipse ICD
Technology | Implantable Cardioverter Defibrillator (ICD)| September 22, 2017
Abbott announced U.S. Food and Drug Administration (FDA) approval for magnetic resonance (MR)-conditional labeling for...
Edwards Inspiris Resilia Valve Receives FDA Approval
News | Heart Valve Technology| September 21, 2017
Edwards Lifesciences Corp. recently received U.S. Food and Drug Administration (FDA) approval for its Inspiris Resilia...
MyoKardia Presents Additional Positive Data From Phase 2 PIONEER-HCM Study at HFSA 2017
News | Heart Failure| September 21, 2017
MyoKardia Inc. announced that additional positive data from the first patient cohort of its Phase 2 PIONEER-HCM study...
DISRUPT BTK Study Shows Positive Results With Lithoplasty in Calcified Lesions Below the Knee
News | Peripheral Artery Disease (PAD)| September 20, 2017
Shockwave Medical reported positive results from the DISRUPT BTK Study, which were presented at the annual...
Heart Failure Market to Surpass $16 Billion by 2026
News | Heart Failure| September 19, 2017
The heart failure space across the seven key markets of the U.S., France, Germany, Italy, Spain, the U.K. and Japan is...
Corindus Announces First Patient Enrolled in PRECISION GRX Registry
News | Robotic Systems| September 18, 2017
September 18, 2017 — Corindus Vascular Robotics Inc.
Two-Year ILLUMENATE Trial Data Demonstrate Efficacy of Stellarex Drug-Coated Balloon
News | Drug-Eluting Balloons| September 18, 2017
Philips announced the two-year results from the ILLUMENATE European randomized clinical trial (EU RCT) demonstrating...
Sentinel Cerebral Protection System Significantly Reduces Stroke and Mortality in TAVR
News | Embolic Protection Devices| September 18, 2017
September 18, 2017 – Claret Medical announced publication of a new study in the...
Fysicon Receives FDA Approval for QMAPP Hemodynamic Monitoring System
Technology | Hemodynamic Monitoring Systems| September 18, 2017
Fysicon announced that it has been granted 510(k) clearance by the U.S. Food and Drug Administration (FDA) for its...
Overlay Init