TY - JOUR
T1 - Impact of Cardiac Resynchronization Therapy on Exercise Performance, Functional Capacity, and Quality of Life in Systolic Heart Failure With QRS Prolongation
T2 - COMPANION Trial Sub-Study
AU - De Marco, Teresa
AU - Wolfel, Eugene
AU - Feldman, Arthur M.
AU - Lowes, Brian
AU - Higginbotham, Michael B.
AU - Ghali, Jalal K.
AU - Wagoner, Lynne
AU - Kirlin, Philip C.
AU - Kennett, Jerry D.
AU - Goel, Satish
AU - Saxon, Leslie A.
AU - Boehmer, John P.
AU - Mann, David
AU - Galle, Elizabeth
AU - Ecklund, Fred
AU - Yong, Patrick
AU - Bristow, Michael R.
N1 - Funding Information:
During the trial duration, the following investigators participated in the COMPANION Functional Capacity Substudy (listed in descending order of the number of randomly assigned patients). S. Krueger, Bryan LGH Medical Center, Lincoln, NE; F. McGrew, Baptist Memorial, Memphis, TN; L. Wagoner, University of Cincinnati, OH; J. K. Ghali, Willis-Knighton Hospital; Shreveport, LA; P. Kirlin, Methodist Hospital of Indianapolis, IN; P. Fenster, University of Arizona Medical Center, Tucson; P. Desai, Amarillo Heart Group, Amarillo, TX; J. Aranda, University of Florida, Gainesville; R. Starling, Cleveland Clinic Foundation, OH; J. Coman, Hillcrest Medical Center, Tulsa, OK; D. Mann, Baylor and Veterans Administration Medical Center, Houston, TX; J. T. Heywood, Loma Linda University Medical Center, Loma Linda, CA; B. Lowes, University of Colorado Health Sciences Center, Denver, CO; J. Kennett, Boone Hospital-Missouri Heart Center, Columbia, MO; P. Steiner, University of California San Francisco, CA; A. Ciuffo, Sentera Norfolk General Hospital, Norfolk, VA; A. Banks, United Hospital-St. Paul Heart Clinic, St. Paul, MN; K. Crossen, North Mississippi Medical Center, Tupelo; J. G. Rogers, Washington University – Barnes, St. Louis, MO; M. Gilbert, University of Utah Medical Center, Salt Lake City; J. Franklin, Baylor-Dallas, Dallas, TX; M. Johnson, Orlando Regional Medical Center, FL; N. Erenrich, JFK Medical Center, West Palm Beach, FL; F. W. Smart, Tulane Hospital and Clinic, New Orleans, LA; S. P. Graham, Buffalo General Hospital, Buffalo, NY; A. Smith, Emory University School of Medicine, Atlanta, GA; M. Jessup, Hospital of the University of Pennsylvania, Philadelphia; G. S. Greer, Baptist Medical Center-Arkansas Cardiology, Little Rock, AR; J. P. Boehmer, The Milton S. Hershey Medical Center, Hershey, PA; A. Seals, Memorial Hospital, Jacksonville, FL; M. Kukin, Mount Sinai Medical Center, New York, NY; G. Bhat, Jewish Hospital–University of Louisville, KY; P. S. Bernstein, St. Luke's Medical Center, Milwaukee, WI; R. L. Berkowitz, Hackensack University, Hackensack, NJ; T. A. Frank, Carolinas Medical Center–The Sanger Clinic, Charlotte, NC; A. Interian Jr., Jackson Memorial Hospital, Miami, FL; A. Heroux, Rush Presbyterian-St. Luke's Medical Center, Chicago, IL; M. A. Silver, Christ Hospital and Medical Center, Oaklawn, IL; D. Renlund, LDS Hospital, Salt Lake City, UT; R. McBride, Cardiovascular Associates of Virginia, Roanoke; M. Flemming, St. John Hospital-Detroit, St. Clair Shores, MI; S. Khan, Cedars-Sinai Medical Center, Los Angeles, CA; R. Corbisiero, Deborah Heart and Lung Center, Brown Mills, NJ; G. Haas, Riverside Methodist Hospital, Columbus, OH; B. S. Clemson, St. Francis Medical Center, Peoria, IL; R. Bourge, University of Alabama, Birmingham, AL; J. Hare, The Johns Hopkins Hospital, Baltimore, MD; C. S. Liang, Strong Memorial Hospital, Rochester, NY; C. O'Connor, Duke University Medical Center, Durham, NC; S. Erhlich, Mission Hospital Regional Medical Center, Mission Viejo, CA; R. Hershberger, Oregon Health Sciences University, Portland; R. Tung, Research Medical Center, Kansas City, MO; A. Labib, St. Elizabeth's Hospital, Youngstown, OH; R. Doshi, Sunrise Medical Center, Las Vegas, NV; R. Oren, University of Iowa Hospitals and Clinics, Iowa City; J. Beard, Providence Hospital, Columbia, SC; S. Gottlieb, University of Maryland, Baltimore; C. Porter, University of Kansas Medical Center, Kansas City; S. Murali, University of Pittsburgh Medical Center, PA; K. Turk, St. Elizabeth Regional Medical Center, Lincoln, NE; B. Knight, University of Michigan Hospital, Ann Arbor; D. Wilber, Loyola University of Chicago, Maywood, IL; F. Abi-Samra, Ochsner Hospital, New Orleans, LA; J. Bergin, University of Virginia, Charlottesville; M. T. Olivari, Abbott Northwestern, Minneapolis, MN; J. Holmberg, St. Joseph Hospital, Omaha, NE; A. Anderson, University of Chicago, IL; C. Sueta, University of North Carolina, Chapel Hill.
PY - 2008/2
Y1 - 2008/2
N2 - Background: A total of 405 participants in the Comparison of Medical Therapy, Pacing, and Defibrillation in Heart Failure trial were prospectively enrolled in an exercise sub-study designed to study the influence of cardiac resynchronization therapy (CRT) on measures of exercise capacity, functional capacity, and quality of life (QOL). Methods and Results: Substudy eligibility included New York Heart Association (NYHA) functional Class III or IV heart failure, left ventricular ejection fraction ≤0.35, QRS interval of ≥120 ms, normal sinus rhythm, a heart failure hospitalization (or equivalent) within 1 year, a peak VO2 ≤22 mL·kg·min, the ability to walk 150 to 425 meters in 6 minutes, forced expiratory volume in 1 second/forced vital capacity ≥50%, and no clinical indication for a pacemaker or implantable cardioverter-defibrillator. Patients were randomized in a 1:4 ratio to optimal medical therapy (OPT) or to OPT plus CRT. Cardiopulmonary exercise testing (peak VO2 and 6-minute walk distance [6MWD]) and assessment of NYHA functional class and QOL were assessed at baseline and at 3 and 6 months of assigned therapy. There was no significant improvement in peak VO2 at 6 months in the CRT group compared with the OPT group (+0.63 mL·kg·min) by unadjusted analysis (P = .05) or by analyses adjusted for missing data. Thus the primary end point of the study was not met. There was significantly greater improvement in the 6MWD in the CRT group compared with the OPT group at both 3 and 6 months by both statistical methods (P ≤ .045). Likewise, a greater proportion of CRT patients improved by 1 or more NYHA functional classes (P < .01) at 3 months and had better QOL scores (P < .01) at 3 and 6 months compared with the OPT patients. Baseline peak VO2 predicted clinical events (time to death, time to death or first hospitalization, or time to death and first heart failure hospitalization: P < .05) in CRT participants. Conclusion: CRT patients with moderate to advanced symptoms of systolic heart failure and prolonged QRS intervals benefit from the addition of CRT to OPT in terms of exercise capacity, functional status, and QOL. CRT should be considered standard therapy in this select group of heart failure patients.
AB - Background: A total of 405 participants in the Comparison of Medical Therapy, Pacing, and Defibrillation in Heart Failure trial were prospectively enrolled in an exercise sub-study designed to study the influence of cardiac resynchronization therapy (CRT) on measures of exercise capacity, functional capacity, and quality of life (QOL). Methods and Results: Substudy eligibility included New York Heart Association (NYHA) functional Class III or IV heart failure, left ventricular ejection fraction ≤0.35, QRS interval of ≥120 ms, normal sinus rhythm, a heart failure hospitalization (or equivalent) within 1 year, a peak VO2 ≤22 mL·kg·min, the ability to walk 150 to 425 meters in 6 minutes, forced expiratory volume in 1 second/forced vital capacity ≥50%, and no clinical indication for a pacemaker or implantable cardioverter-defibrillator. Patients were randomized in a 1:4 ratio to optimal medical therapy (OPT) or to OPT plus CRT. Cardiopulmonary exercise testing (peak VO2 and 6-minute walk distance [6MWD]) and assessment of NYHA functional class and QOL were assessed at baseline and at 3 and 6 months of assigned therapy. There was no significant improvement in peak VO2 at 6 months in the CRT group compared with the OPT group (+0.63 mL·kg·min) by unadjusted analysis (P = .05) or by analyses adjusted for missing data. Thus the primary end point of the study was not met. There was significantly greater improvement in the 6MWD in the CRT group compared with the OPT group at both 3 and 6 months by both statistical methods (P ≤ .045). Likewise, a greater proportion of CRT patients improved by 1 or more NYHA functional classes (P < .01) at 3 months and had better QOL scores (P < .01) at 3 and 6 months compared with the OPT patients. Baseline peak VO2 predicted clinical events (time to death, time to death or first hospitalization, or time to death and first heart failure hospitalization: P < .05) in CRT participants. Conclusion: CRT patients with moderate to advanced symptoms of systolic heart failure and prolonged QRS intervals benefit from the addition of CRT to OPT in terms of exercise capacity, functional status, and QOL. CRT should be considered standard therapy in this select group of heart failure patients.
KW - 6-minute walk distance
KW - New York Heart Association functional class
KW - Peak VO
UR - http://www.scopus.com/inward/record.url?scp=38349098526&partnerID=8YFLogxK
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U2 - 10.1016/j.cardfail.2007.08.003
DO - 10.1016/j.cardfail.2007.08.003
M3 - Article
C2 - 18226768
AN - SCOPUS:38349098526
SN - 1071-9164
VL - 14
SP - 9
EP - 18
JO - Journal of Cardiac Failure
JF - Journal of Cardiac Failure
IS - 1
ER -