Fijnvandraat K, Derkx B, Peters M, Bijlmer R, Sturk A, Prins M H, van Deventer S J, ten Cate J W
Emma Kinder Ziekenhuis/Children's Academic Medical Center, University of Amsterdam, The Netherlands.
Thromb Haemost. 1995 Jan;73(1):15-20.
In 35 consecutively admitted children (mean age: 4.3 years) with a clinical diagnosis of meningococcal septic shock (MSS), activation of the coagulation and fibrinolytic pathways was evaluated directly at admittance to the paediatric intensive care unit (ICU). The association of clinical signs and haemostatic abnormalities was assessed. All patients had signs of extensive activation of the coagulation system. The 28-day mortality was 26%. Protein C activity was strongly reduced, especially in non-survivors in whom it was significantly lower than in survivors (5% versus 23%; p < 0.0001). There was a strong negative correlation between protein C activity and the mean size of the skin lesions (r = -0.71, p < 0.001). These results suggest that an acquired protein C deficiency in MSS is related to the pathogenesis of purpura fulminans. Furthermore, no increase in C4b-binding protein (C4BP) and no decrease in the ratio free protein S/total protein S was observed, suggesting that a deficiency of free protein S as a result of increased C4BP does not play a pathogenetic role in meningococcal septic shock.
在35例临床诊断为脑膜炎球菌性败血症休克(MSS)且连续入院的儿童(平均年龄:4.3岁)中,在其进入儿科重症监护病房(ICU)时直接评估凝血和纤溶途径的激活情况。评估临床体征与止血异常之间的关联。所有患者均有凝血系统广泛激活的体征。28天死亡率为26%。蛋白C活性显著降低,尤其是在非幸存者中,其显著低于幸存者(5%对23%;p<0.0001)。蛋白C活性与皮肤病变的平均大小之间存在强烈的负相关(r=-0.71,p<0.001)。这些结果表明,MSS中获得性蛋白C缺乏与暴发性紫癜的发病机制有关。此外,未观察到C4b结合蛋白(C4BP)增加,游离蛋白S/总蛋白S的比值也未降低,这表明由于C4BP增加导致的游离蛋白S缺乏在脑膜炎球菌性败血症休克中不发挥致病作用。