Section of Cardiac Electrophysiology, Division of Cardiology, Department of Medicine (Z.H.T., J.E.O., A.B., J.P.), University of California.
Department of Medicine (J.W.S.), University of California.
Circ Arrhythm Electrophysiol. 2019 Jul;12(7):e007171. doi: 10.1161/CIRCEP.119.007171. Epub 2019 Jun 28.
Conventional definitions of sudden cardiac death (SCD) presume cardiac cause. We studied the World Health Organization-defined SCDs autopsied in the POST SCD study (Postmortem Systematic Investigation of SCD) to determine whether premortem characteristics could identify autopsy-defined sudden arrhythmic death (SAD) among presumed SCDs.
Between January 2, 2011, and January 4, 2016, we prospectively identified all 615 World Health Organization-defined SCDs (144 witnessed) 18 to 90 years in San Francisco County for medical record review and autopsy via medical examiner surveillance. Autopsy-defined SADs had no extracardiac or acute heart failure cause of death. We used 2 nested sets of premortem predictors-an emergency medical system set and a comprehensive set adding medical record data-to develop Least Absolute Selection and Shrinkage Operator models of SAD among witnessed and unwitnessed cohorts.
Of 615 presumed SCDs, 348 (57%) were autopsy-defined SAD. For witnessed cases, the emergency medical system model (area under the receiver operator curve 0.75 [0.67-0.82]) included presenting rhythm of ventricular tachycardia/fibrillation and pulseless electrical activity, while the comprehensive (area under the receiver operator curve 0.78 [0.70-0.84]) added depression. If only ventricular tachycardia/fibrillation witnessed cases (n=48) were classified as SAD, sensitivity was 0.46 (0.36-0.57), and specificity was 0.90 (0.79-0.97). For unwitnessed cases, the emergency medical system model (area under the receiver operator curve 0.68 [0.64-0.73]) included black race, male sex, age, and time since last seen normal, while the comprehensive (area under the receiver operator curve 0.75 [0.71-0.79]) added use of β-blockers, antidepressants, QT-prolonging drugs, opiates, illicit drugs, and dyslipidemia. If only unwitnessed cases <1 hour (n=59) were classified as SAD, sensitivity was 0.18 (0.13-0.22) and specificity was 0.95 (0.90-0.97).
Our models identify premortem characteristics that can better specify autopsy-defined SAD among presumed SCDs and suggest the World Health Organization definition can be improved by restricting witnessed SCDs to ventricular tachycardia/fibrillation or nonpulseless electrical activity rhythms and unwitnessed cases to <1 hour since last normal, at the cost of sensitivity.
传统的心脏性猝死 (SCD) 定义假定为心脏原因。我们研究了在 POST SCD 研究(死后系统性 SCD 调查)中进行尸检的世界卫生组织定义的 SCD,以确定在假定的 SCD 中,是否可以通过生前特征来识别尸检定义的心律失常性 SAD(SAD)。
2011 年 1 月 2 日至 2016 年 1 月 4 日,我们前瞻性地确定了旧金山县所有 615 例世界卫生组织定义的 SCD(144 例有目击者),通过法医监测进行医疗记录审查和尸检。尸检定义的 SAD 无心脏外或急性心力衰竭死亡原因。我们使用了 2 组嵌套的生前预测因素-急诊医疗系统组和添加医疗记录数据的综合组-为有目击者和无目击者队列开发 SAD 的最小绝对选择和收缩运算符模型。
在 615 例假定的 SCD 中,348 例(57%)为尸检定义的 SAD。对于有目击者的病例,急诊医疗系统模型(接受者操作特征曲线下面积 0.75 [0.67-0.82])包括室性心动过速/颤动和无脉电活动的表现节律,而综合模型(接受者操作特征曲线下面积 0.78 [0.70-0.84])增加了抑郁。如果只将室性心动过速/颤动有目击者的病例(n=48)分类为 SAD,则敏感性为 0.46(0.36-0.57),特异性为 0.90(0.79-0.97)。对于无目击者的病例,急诊医疗系统模型(接受者操作特征曲线下面积 0.68 [0.64-0.73])包括黑种人、男性、年龄和最后一次正常观察到的时间,而综合模型(接受者操作特征曲线下面积 0.75 [0.71-0.79])增加了β受体阻滞剂、抗抑郁药、QT 延长药物、阿片类药物、非法药物和血脂异常的使用。如果仅将无目击者的<1 小时病例(n=59)分类为 SAD,则敏感性为 0.18(0.13-0.22),特异性为 0.95(0.90-0.97)。
我们的模型确定了可以更好地确定尸检定义的 SAD 的生前特征,并表明可以通过将有目击者的 SCD 限制为室性心动过速/颤动或无脉电活动节律以及将无目击者的 SCD 限制为<1 小时来改善世界卫生组织的定义。最后一次正常,以牺牲敏感性为代价。