中枢神经系统感染儿童的多器官功能障碍

K. Ermolenko, K. V. Pshenisnov, Y. Aleksandrovich, I. V. Aleksandrovich, Alexandr I. Konev
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引用次数: 0

摘要

背景:多器官功能障碍综合征是儿童危重病最危险的并发症之一,有助于决定疾病的预后。目的:本研究旨在探讨严重中枢神经系统(CNS)感染患儿多器官功能障碍综合征的特征,并确定决定疾病结局的因素。材料与方法:这项单中心、回顾性、观察性研究共纳入 98 名患者,其中包括 66 名男孩(67%)和 32 名女孩(33%)。平均年龄为 3.6 ± 2.5 岁。格拉斯哥昏迷量表(GCS)评分为(8.8 ± 2.4)分。43(44%)名患者被诊断为休克。在重症监护室(ICU)的平均治疗时间为(9.5±6.2)天,机械通气时间为(6.0±3.9)天,死亡率为 9%。根据结果,患儿被分为 I 组(康复,88 人)和 II 组(死亡,10 人)。所有指标均记录在进入重症监护室后的最初 12 小时内。结果:当pSOFA量表评分为10分时,观察到最明显的心血管功能障碍现象,如Teicholtz射血分数下降(62.3 L/min),与pSOFA量表评分为8分的患儿指标相比,具有统计学意义。在所有患者中,无论年龄大小,pSOFA评分与Teicholtz射血分数之间都存在中等强度的负相关,在7-17岁儿童中更为明显(R = -0.41; p = 0.008)。在 7-17 岁儿童中,心率与 pSOFA 评分之间呈正相关(R = 0.72;p = 0.009)。在评估 pSOFA 评分和 Phoenix 败血症评分对重症监护室第一天治疗结果的判别能力时,后者具有更大的预后意义(曲线下面积,0.866 vs 0.838;灵敏度,76% vs 72%;特异性,82% vs 79%)。结论低心输出量综合征和全身缺氧是导致严重中枢神经系统感染患儿死亡的关键因素。射血分数在预测儿童重症中枢神经系统感染的预后方面具有很高的临床意义,与年龄无关,因此可以利用这一参数进行目标导向治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multiple-organ dysfunction in children with central nervous system infections
BACKGROUND: Multiple-organ dysfunction syndrome is one of the most dangerous complications of critical illness in children, which helps determine the disease outcomes. AIM: This study aimed to examine the features of multiple-organ dysfunction syndrome in children with severe central nervous system (CNS) infection and identify factors that determine disease outcomes. MATERIALS AND METHODS: This single-center, retrospective, observational study enrolled 98 patients, which included 66 (67%) boys and 32 (33%) girls. The average age was 3.6 ± 2.5 years. The Glasgow coma scale (GCS) score was 8.8 ± 2.4 points. Shock was diagnosed in 43 (44%) patients. The average treatment duration in the intensive care unit (ICU) was 9.5 ± 6.2 days, the duration of mechanical ventilation was 6.0 ± 3.9 days, and the mortality rate was 9%. Depending on the outcome, the children were divided into groups I (recovery, n = 88) and II (death, n = 10). All indicators were recorded in the first 12 h from ICU admission. RESULTS: The most pronounced phenomena of cardiovascular dysfunction, such as decreased Teicholtz ejection fraction (62.3 L/min), were observed when the pSOFA scale score was 10 points, which was statistically significant when compared with the indicators in children with a pSOFA scale score of 8 points. In all patients, regardless of age, a negative correlation of moderate strength was found between the pSOFA scale score and the Teicholtz ejection fraction, and it was pronounced in children aged 7–17 years (R = –0.41; p = 0.008). A positive correlation was found between heart rate and pSOFA scale score in children aged 7–17 years (R = 0.72; p = 0.009). In the evaluation of the discriminatory ability of the pSOFA scale and Phoenix sepsis scores regarding the outcome on the first day of treatment in the ICU, the latter has greater prognostic significance (area under the curve, 0.866 vs 0.838; sensitivity, 76% vs 72%; specificity, 82% vs 79%). CONCLUSIONS: Low cardiac output syndrome and systemic hypoxia are key factors associated with fatal outcomes in children with severe CNS infections. The high clinical significance of the ejection fraction in predicting the outcomes of severe CNS infections in children, regardless of age, allows the use of this parameter for goal-oriented therapy.
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