Benchimol D, Dartigues J F, Benchimol H, Drouillet F, Lauribe P, Marazanof M, Couffinhal T, Bonnet J
Service de Cardiologie et Maladies Vasculaires, Hôpital Cardiologique, Pessac, France.
Am J Cardiol. 1995 Aug 1;76(4):241-4. doi: 10.1016/s0002-9149(99)80073-3.
To assess hemostatic risk factors for sudden death in patients with stable angina, 323 consecutive patients were recruited prospectively. Patients with clinical heart failure or recent myocardial infarction were excluded. The following clinical variables were recorded: age, gender, smoking habits, hypertension, previous myocardial infarction, left ventricular hypertrophy, and severe ventricular arrhythmia. Angiographic variables included coronary extent, assessed from Jenkins' and mean atherosclerotic scores, and left ventricular ejection fraction. Lipid variables included total cholesterol, triglycerides, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, and apolipoproteins A-I and B. Hemostatic factors included fibrinogen, fibrinopeptide A, antithrombin III, factor VIII antigen, factor VIII coagulant, protein C, plasminogen, alpha 2 antiplasmin, euglobulin clot lysis time, tissue plasminogen activator before and after venous occlusion, and plasminogen activator inhibitor. There were 34 deaths, 19 of which were sudden during the follow-up period (60 +/- 17 months). The association between each variable and the risk of sudden death was assessed by calculating the relative risk with the Cox univariate model. All significant predictors from the univariate analysis were then incorporated in a Cox multivariate model to select the independent predictors of sudden death. The independent predictors of sudden death were left ventricular hypertrophy (p < 0.04), lower left ventricular ejection fraction (p < 0.04), and shorter euglobulin clot lysis time after venous occlusion (p < 0.02), whereas fibrinogen (p < 0.07) and Jenkins' score (p < 0.08) were borderline. Determination of hemostatic variables, especially those pertaining to dynamic fibrinolysis, may thus be of value in assessing risk of sudden death.
为评估稳定型心绞痛患者猝死的止血危险因素,前瞻性招募了323例连续患者。排除临床心力衰竭或近期心肌梗死患者。记录以下临床变量:年龄、性别、吸烟习惯、高血压、既往心肌梗死、左心室肥厚和严重室性心律失常。血管造影变量包括根据詹金斯评分和平均动脉粥样硬化评分评估的冠状动脉病变范围以及左心室射血分数。血脂变量包括总胆固醇、甘油三酯、高密度脂蛋白胆固醇、低密度脂蛋白胆固醇以及载脂蛋白A-I和B。止血因素包括纤维蛋白原、纤维蛋白肽A、抗凝血酶III、因子VIII抗原、因子VIII凝血活性、蛋白C、纤溶酶原、α2抗纤溶酶、优球蛋白凝块溶解时间、静脉闭塞前后的组织纤溶酶原激活物以及纤溶酶原激活物抑制剂。随访期间有34例死亡,其中19例为猝死(60±17个月)。通过Cox单变量模型计算相对风险来评估每个变量与猝死风险之间的关联。然后将单变量分析中所有显著预测因素纳入Cox多变量模型,以选择猝死的独立预测因素。猝死的独立预测因素为左心室肥厚(p<0.04)、较低的左心室射血分数(p<0.04)以及静脉闭塞后较短的优球蛋白凝块溶解时间(p<0.02),而纤维蛋白原(p<0.07)和詹金斯评分(p<0.08)处于临界值。因此,测定止血变量,尤其是与动态纤维蛋白溶解有关的变量,可能对评估猝死风险有价值。