Nürnberger W, Platonov A, Stannigel H, Beloborodov V B, Michelmann I, von Kries R, Burdach S, Göbel U
Department of Paediatric Haematology and Oncology, Heinrich-Heine-University, Düsseldorf, Germany.
Eur J Pediatr. 1995 Nov;154(11):896-900. doi: 10.1007/BF01957501.
Neisseria meningitidis infection may present as meningitis or as severe, fulminant sepsis. In order to classify individual patients early according to the expected course of the disease, we developed a score named Neisseria sepsis index [NESI]. The NESI was defined using the parameters heart rate, mean arterial blood pressure, base excess and presence of acute subcutaneous bleeding and/or skin necroses (minimal value [= no evidence for sepsis] NESI 0; maximum value [= most severe sepsis] NESI 8). Seventeen patients with documented, systemic N. meningitidis infection were prospectively assessed for the terminal complement complex (TCC), serum tumour necrosis factor alpha (TNF alpha) levels (as laboratory parameters for severity of sepsis) and NESI score. The evaluation was immediately performed when the patients were admitted to the hospital. The 17 patients showed the following distribution of data: NESI 0 (n = 4), NESI 1 (n = 6), NESI 2 (n = 0), NESI 3 (n = 1), NESI 4 (n = 2), NESI 5 (n = 2), NESI 6 (n = 0), NESI 7 (n = 1), NESI 8 (n = 1). Mortality was 4/17 patients, all had NESI > or = 5. TCC values ranged from 647-6461 ng/ml (normal range: 130-360 ng/ml); and was not correlated to NESI. TNF alpha values ranged from 10-910 pg/ml and were correlated to NESI (r2 = 0.71, n = 17, P < 0.001). In patients with fatal outcome, TNF alpha was 600 +/- 160 pg/ml (mean +/- SEM) and in surviving patients 130 +/- 50 pg/ml (mean +/- SEM). TNF alpha was increased in 15/17 patients when compared to normal controls (< 27 pg/ml). CONCLUSION. The NESI is based on few clinical, objective data, that are available in every hospital. NESI appears to offer an instrument: (1) for making decisions in regard to appropriate monitoring and treatment of vital organ function; and (2) for assessing the quality of care for this life-threatening infection.
脑膜炎奈瑟菌感染可能表现为脑膜炎或严重的暴发性败血症。为了根据疾病的预期病程对个体患者进行早期分类,我们开发了一种名为奈瑟菌败血症指数(NESI)的评分系统。NESI是根据心率、平均动脉压、碱剩余以及是否存在急性皮下出血和/或皮肤坏死等参数来定义的(最小值[=无败血症证据]NESI为0;最大值[=最严重败血症]NESI为8)。对17例有记录的全身性脑膜炎奈瑟菌感染患者进行前瞻性评估,检测其终末补体复合物(TCC)、血清肿瘤坏死因子α(TNFα)水平(作为败血症严重程度的实验室参数)以及NESI评分。患者入院时立即进行评估。17例患者的数据分布如下:NESI 0(n = 4),NESI 1(n = 6),NESI 2(n = 0),NESI 3(n = 1),NESI 4(n = 2),NESI 5(n = 2),NESI 6(n = 0),NESI 7(n = 1),NESI 8(n = 1)。死亡率为4/17例患者,所有死亡患者的NESI均≥5。TCC值范围为647 - 6461 ng/ml(正常范围:130 - 360 ng/ml);且与NESI无关。TNFα值范围为10 - 910 pg/ml,与NESI相关(r2 = 0.71,n = 17,P < 0.001)。死亡患者的TNFα为600±160 pg/ml(平均值±标准误),存活患者为130±50 pg/ml(平均值±标准误)。与正常对照组(<27 pg/ml)相比,17例患者中有15例的TNFα升高。结论。NESI基于很少的临床客观数据,这些数据在每家医院都可获取。NESI似乎提供了一种工具:(1)用于对重要器官功能的适当监测和治疗做出决策;(2)用于评估这种危及生命感染的护理质量。