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Quality of Life Among Implantable Cardioverter-Defibrillator Recipients in the Primary Prevention Therapeutic Era
PETER W. GROENEVELD, M.D., M.S.*†‡, MARY A. MATTA, M.S., JANICE J. SUH, B.S., FEIFEI YANG, M.S. and JUDY A. SHEA, Ph.D.†‡
From the   *Philadelphia Veterans Affairs Medical Center, Philadelphia, Pennsylvania ;   Division of General Internal Medicine, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania ; and   Leonard Davis Institute of Health Economics, University of Pennsylvania, Philadelphia, Pennsylvania
Correspondence to  Address for reprints: Peter W. Groeneveld, M.D., M.S., 1229 Blockley Hall, 423 Guardian Drive, Philadelphia, PA 19104-6021. Fax: 215-573-8778; e-mail: peter.groeneveld@va.gov

This research was supported by an unrestricted grant from the Institute for Health Technology Studies (InHealth), Washington, DC. Dr. Groeneveld was additionally supported by a Research Career Development Award from the Department of Veterans Affairs' Health Services Research and Development Service.

Copyright 2007, The Authors. Journal compilation ©2007, Blackwell Publishing, Inc.
KEYWORDS
defibrillatorsimplantablequality of life

(PACE 2007; 30:463–471)

ABSTRACT

Background: Although patients receiving implantable cardioverter-defibrillators (ICDs) for primary prevention of sudden cardiac death are the fastest growing segment of the ICD recipient population, the quality-of-life (QOL) effects of the ICD among primary prevention patients are not well understood. The purpose of this study was to measure and compare the health-related QOL among primary and secondary prevention ICD recipients, and to determine predictive factors for high or low QOL in each group.

Methods: Forty-five primary prevention and 75 secondary prevention ICD recipients receiving routine care in electrophysiology clinics within the University of Pennsylvania Health System were assessed using several well-validated general and ICD-specific QOL instruments.

Results: Between primary and secondary prevention patients, there were no significant differences in EuroQol 5D (medians: 0.84 vs 0.84, P = 0.71), Health Utilities Index (medians: 0.88 vs 0.85, P = 0.95), Short Form-12 aggregate physical summary (means: 45 vs 46, P = 0.64), and Short Form-12 aggregate mental summary (means: 46 vs 47, P = 0.93) scores. Both primary and secondary prevention patients viewed their devices favorably according to the Florida Patient Acceptance Survey scale, with no significant differences between group means (80 vs 83, P = 0.71). However, substantial fractions of both primary and secondary prevention recipients had particular concerns about lifting (40%), sexual activity (19%), and driving (14%).

Conclusions: QOL does not significantly differ between primary prevention and secondary prevention ICD recipients. Device recipients had comparable QOL to published, nationwide QOL estimates among non-ICD patients of similar age. The ICD was highly acceptable to most primary and secondary prevention patients.


Received November 16, 2006; revised December 9, 2006; accepted December 10, 2006.

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1540-8159.2007.00694.x About DOI

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