HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Use of the wearable cardioverter defibrillator in high-risk cardiac patients: data from the Prospective Registry of Patients Using the Wearable Cardioverter Defibrillator (WEARIT-II Registry).

AbstractBACKGROUND:
Prospective data on the safety and efficacy of the wearable cardioverter defibrillator (WCD) in a real-world setting are lacking. The Prospective Registry of Patients Using the Wearable Defibrillator (WEARIT-II) Registry was designed to provide real-world data on the WCD as a strategy during a period of risk stratification.
METHODS AND RESULTS:
The WEARIT-II Registry enrolled 2000 patients with ischemic (n=805, 40%), or nonischemic cardiomyopathy (n=927, 46%), or congenital/inherited heart disease (n=268) prescribed WCD between August 2011 and February 2014. Clinical data, arrhythmia events, implantable cardioverter defibrillator implantation, and improvement in ejection fraction were captured. The median age was 62 years; the median ejection fraction was 25%. The median WCD wear time was 90 days, with median daily use of 22.5 hours. There was a total of 120 sustained ventricular tachyarrhythmias in 41 patients, of whom 54% received appropriate WCD shock. Only 10 patients (0.5%) received inappropriate WCD therapy. The rate of sustained ventricular tachyarrhythmias by 3 months was 3% among patients with ischemic cardiomyopathy and congenital/inherited heart disease, and 1% among nonischemic patients (P=0.02). At the end of WCD use, 840 patients (42%) were implanted with an implantable cardioverter defibrillator. The most frequent reason not to implant an implantable cardioverter defibrillator following WCD use was improvement in ejection fraction.
CONCLUSIONS:
The WEARIT-II Registry demonstrates a high rate of sustained ventricular tachyarrhythmias at 3 months in at-risk patients who are not eligible for an implantable cardioverter defibrillator, and suggests that the WCD can be safely used to protect patients during this period of risk assessment.
AuthorsValentina Kutyifa, Arthur J Moss, Helmut Klein, Yitschak Biton, Scott McNitt, Bonnie MacKecknie, Wojciech Zareba, Ilan Goldenberg
JournalCirculation (Circulation) Vol. 132 Issue 17 Pg. 1613-9 (Oct 27 2015) ISSN: 1524-4539 [Electronic] United States
PMID26316618 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2015 American Heart Association, Inc.
Chemical References
  • Cardiovascular Agents
Topics
  • Aged
  • Arrhythmias, Cardiac (drug therapy, etiology, prevention & control, therapy)
  • Cardiomyopathies (complications)
  • Cardiovascular Agents (therapeutic use)
  • Combined Modality Therapy
  • Death, Sudden, Cardiac (prevention & control)
  • Defibrillators (adverse effects, statistics & numerical data)
  • Defibrillators, Implantable (statistics & numerical data)
  • Electric Countershock (instrumentation)
  • Female
  • Follow-Up Studies
  • Heart Defects, Congenital (complications)
  • Humans
  • Male
  • Middle Aged
  • Myocardial Ischemia (complications)
  • Patient Compliance
  • Prescriptions (statistics & numerical data)
  • Prospective Studies
  • Registries
  • Stroke Volume

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: