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S100B并非小儿创伤性脑损伤可靠的预后指标。

S100B is not a reliable prognostic index in paediatric TBI.

作者信息

Piazza O, Storti M P, Cotena S, Stoppa F, Perrotta D, Esposito G, Pirozzi N, Tufano R

机构信息

Department of Anaesthesia and Intensive Care, University of Naples Federico II, Naples, Italy.

出版信息

Pediatr Neurosurg. 2007;43(4):258-64. doi: 10.1159/000103304.

Abstract

BACKGROUND

As far as paediatric traumatic brain injury is concerned, it is difficult to quantify the extent of the primary insult, to monitor secondary changes and to predict neurological outcomes by means of the currently used diagnostic tools: physical examination, Glasgow Coma Scale (GCS) score and computed tomography. For this reason, several papers focused on the use of biochemical markers (S100B, neuron-specific enolase) to detect and define the severity of brain damage and predict outcome after traumatic head injury or cardiac arrest.

OBJECTIVE

The aim of this paper is measuring the range of S100B serum concentrations in children affected by traumatic brain injury and describing the possible roles of this protein in the reaction to trauma.

METHODS

Fifteen children aged 1-15 years were included in the study. Traumatic brain injury severity was defined by paediatric GCS score as mild (9 patients), moderate (2 patients) or severe (4 patients). Blood samples for S100B serum measurement were taken at emergency department admission and after 48 h.

RESULTS

The serum S100B concentration was higher in the group of severe trauma patients, who scored the lowest on the GCS at admission, and among them, the highest values were reported by the children with concomitant peripheral lesions.

CONCLUSIONS

The role of S100B in paediatric traumatic brain injury has not been clarified yet, and the interpretation of its increase when the head trauma is associated with other injuries needs the understanding of the physiopathological mechanisms that rule its release in the systemic circulation. The levels of S100B in serum after a brain injury could be related to the mechanical discharge from a destroyed blood-brain barrier, or they could be due to the active expression by the brain, as a part of its involvement in the systemic inflammatory reaction. Early increase of this protein is not a reliable prognostic index of neurological outcome after pediatric traumatic brain injury, since even very elevated values are compatible with a complete neurological recovery.

摘要

背景

就小儿创伤性脑损伤而言,目前使用的诊断工具(体格检查、格拉斯哥昏迷量表(GCS)评分和计算机断层扫描)难以量化原发性损伤的程度、监测继发性变化以及预测神经学预后。因此,多篇论文聚焦于使用生化标志物(S100B、神经元特异性烯醇化酶)来检测和界定脑损伤的严重程度,并预测创伤性颅脑损伤或心脏骤停后的预后。

目的

本文旨在测定创伤性脑损伤患儿血清S100B浓度范围,并描述该蛋白在创伤反应中的可能作用。

方法

15名年龄在1至15岁的儿童纳入本研究。创伤性脑损伤严重程度根据小儿GCS评分分为轻度(9例)、中度(2例)或重度(4例)。在急诊科入院时及48小时后采集用于测定血清S100B的血样。

结果

重度创伤患者组血清S100B浓度较高,这些患者入院时GCS评分最低,其中伴有周围损伤的儿童报告的S100B值最高。

结论

S100B在小儿创伤性脑损伤中的作用尚未明确,当头部创伤与其他损伤相关时,对其升高的解读需要了解其在全身循环中释放的生理病理机制。脑损伤后血清中S100B水平可能与受损血脑屏障的机械性释放有关,也可能是由于大脑的主动表达,作为其参与全身炎症反应的一部分。该蛋白的早期升高并非小儿创伤性脑损伤后神经学预后的可靠指标,因为即使值非常高也可能与完全的神经学恢复相符。

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