Abi-Samra Freddy, Gutterman David
, 1516 Jefferson Hwy, New Orleans, LA, 70121, USA.
MD Medical College of Wisconsin, Milwaukee, WI, 53226, USA.
Heart Fail Rev. 2016 Nov;21(6):645-660. doi: 10.1007/s10741-016-9571-6.
Heart failure is a major health problem worldwide and, despite effective therapies, is expected to grow by almost 50 % over the next 15 years. Five-year mortality remains high at 50 % over 5 years. Because of the economic burden and large impact on quality of life, substantial effort has focused on treatments with multiple medical (beta-blockers, angiotensin-converting enzyme inhibitors and angiotensin receptor blockers (ARB), aldosterone antagonists, and combination of ARB/neprilysin blockers, ivabradine) and device therapies (ICD, CRT) which have been implemented to reduce disease burden and mortality. However, in the past decade only two new medical therapies and no devices have been approved by the US FDA for the treatment of heart failure. This review highlights the preclinical and clinical literature, and the implantation procedure, related to a relatively new therapeutic device for heart failure; cardiac contractility modulation (CCM). CCM delivers a biphasic high-voltage bipolar signal to the RV septum during the absolute refractory period, eliciting an acute increase in global contractility, and chronically producing a sustained improvement in quality of life, exercise tolerance, and heart failure symptoms. The technology is used commercially in Europe with nearly 3000 patients implanted worldwide. Indications include patients with reduced EF and normal or slightly prolonged QRS duration, thus filling an important therapeutic gap among the 2/3 of patients with heart failure who do not meet criteria for CRT. The mechanism by which CCM provides benefit can be seen at the cellular level where improved calcium handling (phosphorylation of phospholamban, upregulation of SERCA-2A), reversal of the fetal myocyte gene program associated with heart failure, and reverse remodeling are observed. Recent retrospective studies indicate a long-term mortality benefit. A pivotal randomized controlled study is currently being completed in the USA. CCM appears to be an effective, safe technology for the treatment of heart failure with reduced ejection fraction.
心力衰竭是一个全球性的重大健康问题,尽管有有效的治疗方法,但预计在未来15年内将增长近50%。五年死亡率在5年内仍高达50%。由于经济负担和对生活质量的巨大影响,大量努力集中在多种药物治疗(β受体阻滞剂、血管紧张素转换酶抑制剂和血管紧张素受体阻滞剂(ARB)、醛固酮拮抗剂以及ARB/中性肽链内切酶抑制剂、伊伐布雷定联合治疗)和器械治疗(植入式心脏复律除颤器(ICD)、心脏再同步治疗(CRT))上,这些治疗已被用于减轻疾病负担和降低死亡率。然而,在过去十年中,美国食品药品监督管理局(US FDA)仅批准了两种新的药物治疗方法,且没有批准新的器械用于治疗心力衰竭。本综述重点介绍了与一种相对较新的心力衰竭治疗器械——心脏收缩力调制(CCM)相关的临床前和临床文献以及植入过程。CCM在绝对不应期向右心室间隔输送双相高压双极信号,引发整体收缩力急性增加,并长期持续改善生活质量、运动耐量和心力衰竭症状。该技术在欧洲已商业化应用,全球有近3000名患者植入。适应症包括射血分数降低且QRS时限正常或略延长的患者,从而填补了2/3不符合CRT标准的心力衰竭患者中的一个重要治疗空白。CCM产生益处的机制可在细胞水平上观察到,即改善钙处理(受磷蛋白磷酸化、肌浆网钙ATP酶2A(SERCA-2A)上调)、逆转与心力衰竭相关的胎儿心肌细胞基因程序以及逆向重构。最近的回顾性研究表明其具有长期死亡率获益。一项关键的随机对照研究目前正在美国完成。CCM似乎是一种治疗射血分数降低的心力衰竭的有效、安全技术。