Greenspon A J, Kidwell G A
Department of Medicine, Jefferson Medical College, Philadelphia, PA.
Prog Cardiovasc Dis. 1993 May-Jun;35(6):399-406. doi: 10.1016/0033-0620(93)90024-8.
Late potentials arise from areas of slowly depolarizing myocardium and may represent the substrate for sustained VTs. Because they may be recorded from the body surface using signal-averaging techniques, they represent a noninvasive marker for potential malignant ventricular arrhythmias. The effects of antiarrhythmic drugs on the SAECG and late potentials are reviewed in this article. Unfortunately, there is no SAECG parameter (either total QRS, late potential, or frequency content) that appears to be useful in predicting drug efficacy. However, there are type-specific changes in global ventricular activation that can be quantified by the SAECG. These changes may be useful in categorizing the effects of new type I antiarrhythmic drugs. The effects of antiarrhythmic drugs on tachycardia cycle length are complex and probably represent combined effects of the drug on conduction and refractoriness. Such changes cannot be reliably categorized by the SAECG. Medical therapy of sustained VTs cannot be guided by the SAECG.
晚电位源于心肌缓慢去极化区域,可能是持续性室性心动过速的基质。由于可使用信号平均技术从体表记录到它们,所以晚电位代表了潜在恶性室性心律失常的一种非侵入性标志物。本文综述了抗心律失常药物对信号平均心电图(SAECG)和晚电位的影响。遗憾的是,没有任何SAECG参数(无论是总QRS波、晚电位还是频率成分)似乎可用于预测药物疗效。然而,整体心室激动存在特定类型的变化,可通过SAECG进行量化。这些变化可能有助于对新型I类抗心律失常药物的作用进行分类。抗心律失常药物对心动过速周期长度的影响很复杂,可能代表了药物对传导和不应期的综合作用。此类变化无法通过SAECG可靠地分类。SAECG不能指导持续性室性心动过速的药物治疗。