De Marco Teresa, Wolfel Eugene, Feldman Arthur M, Lowes Brian, Higginbotham Michael B, Ghali Jalal K, Wagoner Lynne, Kirlin Philip C, Kennett Jerry D, Goel Satish, Saxon Leslie A, Boehmer John P, Mann David, Galle Elizabeth, Ecklund Fred, Yong Patrick, Bristow Michael R
University of California, San Francisco Medical Center, San Francisco, CA, USA.
J Card Fail. 2008 Feb;14(1):9-18. doi: 10.1016/j.cardfail.2007.08.003.
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).
Substudy eligibility included New York Heart Association (NYHA) functional Class III or IV heart failure, left ventricular ejection fraction < or =0.35, QRS interval of > or =120 ms, normal sinus rhythm, a heart failure hospitalization (or equivalent) within 1 year, a peak VO2 < or =22 mL x kg x min, the ability to walk 150 to 425 meters in 6 minutes, forced expiratory volume in 1 second/forced vital capacity > or =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 x kg x 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 < or = .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.
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.
心力衰竭的药物治疗、起搏和除颤比较试验(Comparison of Medical Therapy, Pacing, and Defibrillation in Heart Failure trial)中的405名参与者被前瞻性纳入一项运动子研究,该子研究旨在探讨心脏再同步治疗(CRT)对运动能力、功能能力和生活质量(QOL)指标的影响。
子研究的入选标准包括纽约心脏协会(NYHA)心功能Ⅲ级或Ⅳ级心力衰竭、左心室射血分数≤0.35、QRS间期≥120毫秒、正常窦性心律、1年内有心力衰竭住院史(或同等情况)、峰值摄氧量≤22毫升·千克·分钟、6分钟内能够行走150至425米、1秒用力呼气量/用力肺活量≥50%,且无起搏器或植入式心脏复律除颤器的临床指征。患者按1:4的比例随机分为接受最佳药物治疗(OPT)或OPT加CRT。在基线以及指定治疗的3个月和6个月时,进行心肺运动测试(峰值摄氧量和6分钟步行距离[6MWD])以及NYHA心功能分级和QOL评估。未经调整的分析显示,与OPT组相比,CRT组在6个月时的峰值摄氧量无显著改善(+0.63毫升·千克·分钟)(P = 0.05),对缺失数据进行调整后的分析结果亦是如此。因此,该研究的主要终点未达到。两种统计方法均显示,与OPT组相比,CRT组在3个月和6个月时的6MWD改善更为显著(P≤0.045)。同样,与OPT组患者相比,更多比例的CRT患者在3个月时NYHA心功能分级改善1级或更多(P < 0.01),且在3个月和6个月时生活质量评分更高(P < 0.01)。基线峰值摄氧量可预测CRT参与者的临床事件(死亡时间、死亡或首次住院时间、死亡和首次心力衰竭住院时间:P < 0.05)。
对于有中重度收缩性心力衰竭症状且QRS间期延长的CRT患者,在运动能力、功能状态和生活质量方面,OPT联合CRT治疗有益。对于这部分特定的心力衰竭患者,应考虑将CRT作为标准治疗。