Gold Michael R, Higgins Steven, Klein Richard, Gilliam F Roosevelt, Kopelman Harry, Hessen Scott, Payne John, Strickberger S Adam, Breiter David, Hahn Stephen
Medical University of South Carolina, Division of Cardiology, Charleston 29425, USA.
Circulation. 2002 Apr 30;105(17):2043-8. doi: 10.1161/01.cir.0000015508.59749.f5.
Traditionally, a safety margin of at least 10 J between the maximum output of the pulse generator and the energy needed for ventricular defibrillation has been used because lower safety margins were associated with unacceptably high rates of failed defibrillation and sudden cardiac death. The Low Energy Safety Study (LESS) was a prospective, randomized assessment of the safety margin requirements for modern implantable cardioverter-defibrillator (ICD) systems.
A total of 636 patients undergoing initial ICD implantation with a dual-coil lead and active pulse generator were evaluated. The defibrillation threshold (DFT) and enhanced DFT (DFT+ and DFT++) were measured using a modified step-down protocol. Conversion testing of induced ventricular fibrillation before discharge, at 3 months, and at 12 months was performed, as was randomization to chronic programming at either 2 steps above DFT++ or maximal output. The induced ventricular fibrillation data had conversion success rates of 91.4%, 97.9%, 99.1%, 99.6%, and 99.8% for safety margins of 0, 1, 2, 3, and 4 steps above the DFT++, respectively. A margin of 4 to 6 J was adequate to maintain high conversion success over time (98.9% before discharge versus 99.2% at 12 months; P=NS). Over a mean follow-up of 24+/-13 months, conversion of spontaneously occurring ventricular tachyarrhythmias >200 bpm was identical (97.3%), despite a safety margin difference of 5.2+/-1.1 J for the 2-step group versus 20.8+/-4.2 J for maximal output.
With a rigorous implantation algorithm, a safety margin of about 5 J is adequate for safe implantation of modern ICD systems.
传统上,脉冲发生器的最大输出与心室除颤所需能量之间至少保持10 J的安全裕度,因为较低的安全裕度与不可接受的高除颤失败率和心源性猝死率相关。低能量安全研究(LESS)是一项对现代植入式心律转复除颤器(ICD)系统安全裕度要求的前瞻性、随机评估。
共评估了636例接受双线圈导线和有源脉冲发生器初次植入ICD的患者。使用改良的逐步降低方案测量除颤阈值(DFT)和增强除颤阈值(DFT+和DFT++)。在出院时、3个月和12个月进行诱发性室颤的转换测试,并将患者随机分为高于DFT++ 2步或最大输出的慢性程控组。对于高于DFT++ 0、1、2、3和4步的安全裕度,诱发性室颤数据的转换成功率分别为91.4%、97.9%、99.1%、99.6%和99.8%。4至6 J的裕度足以长期维持高转换成功率(出院前为98.9%,12个月时为99.2%;P=无显著性差异)。在平均随访24±13个月期间,尽管2步组的安全裕度为5.2±1.1 J,最大输出组为20.8±4.2 J,但>200次/分的自发性室性快速心律失常的转换率相同(97.3%)。
采用严格的植入算法,约5 J的安全裕度足以安全植入现代ICD系统。