Device Therapies Among Patients Receiving Primary Prevention Implantable Cardioverter‐Defibrillators in the Cardiovascular Research Network

Author:

Greenlee Robert T.1,Go Alan S.2,Peterson Pamela N.34,Cassidy‐Bushrow Andrea E.5,Gaber Charles6,Garcia‐Montilla Romel1,Glenn Karen A.7,Gupta Nigel8,Gurwitz Jerry H.9,Hammill Stephen C.10,Hayes John J.1,Kadish Alan11,Magid David J.7,McManus David D.9,Multerer Deborah1,Powers J. David7,Reifler Liza M.7,Reynolds Kristi12,Schuger Claudio6,Sharma Param P.1,Smith David H.13,Suits Mary1,Sung Sue Hee2,Varosy Paul D.14,Vidaillet Humberto J.1,Masoudi Frederick A.4

Affiliation:

1. Marshfield Clinic, Marshfield, WI

2. Kaiser Permanente Northern California, Oakland, CA

3. Denver Health Medical Center, Denver, CO

4. University of Colorado Anschutz Medical Campus, Aurora, CO

5. Henry Ford Health System, Detroit, MI

6. University of Michigan, Ann Arbor, MI

7. Kaiser Permanente Colorado, Denver, CO

8. Kaiser Los Angeles Medical Center, Los Angeles, CA

9. University of Massachusetts Medical School, Worcester, MA

10. Mayo Clinic, Rochester, MN

11. Touro College, New York, NY

12. Kaiser Permanente Southern California, Pasadena, CA

13. Kaiser Permanente Northwest, Portland, OR

14. Department of Veterans Affairs Eastern Colorado Health System, Denver, CO

Abstract

Background Primary prevention implantable cardioverter‐defibrillators (ICDs) reduce mortality in selected patients with left ventricular systolic dysfunction by delivering therapies (antitachycardia pacing or shocks) to terminate potentially lethal arrhythmias; inappropriate therapies also occur. We assessed device therapies among adults receiving primary prevention ICDs in 7 healthcare systems. Methods and Results We linked medical record data, adjudicated device therapies, and the National Cardiovascular Data Registry ICD Registry. Survival analysis evaluated therapy probability and predictors after ICD implant from 2006 to 2009, with attention to Centers for Medicare and Medicaid Services Coverage With Evidence Development subgroups: left ventricular ejection fraction, 31% to 35%; nonischemic cardiomyopathy <9 months’ duration; and New York Heart Association class IV heart failure with cardiac resynchronization therapy defibrillator. Among 2540 patients, 35% were <65 years old, 26% were women, and 59% were white. During 27 (median) months, 738 (29%) received ≥1 therapy. Three‐year therapy risk was 36% (appropriate, 24%; inappropriate, 12%). Appropriate therapy was more common in men (adjusted hazard ratio [HR], 1.84; 95% confidence interval [CI], 1.43–2.35). Inappropriate therapy was more common in patients with atrial fibrillation (adjusted HR, 2.20; 95% CI, 1.68–2.87), but less common among patients ≥65 years old versus younger (adjusted HR, 0.72; 95% CI, 0.54–0.95) and in recent implants (eg, in 2009 versus 2006; adjusted HR, 0.66; 95% CI, 0.46–0.95). In Centers for Medicare and Medicaid Services Coverage With Evidence Development analysis, inappropriate therapy was less common with cardiac resynchronization therapy defibrillator versus single chamber (adjusted HR, 0.55; 95% CI, 0.36–0.84); therapy risk did not otherwise differ for Centers for Medicare and Medicaid Services Coverage With Evidence Development subgroups. Conclusions In this community cohort of primary prevention patients receiving ICD, therapy delivery varied across demographic and clinical characteristics, but did not differ meaningfully for Centers for Medicare and Medicaid Services Coverage With Evidence Development subgroups.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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