Undén Johan, Astrand Ramona, Waterloo Knut, Ingebrigtsen Tor, Bellner Johan, Reinstrup Peter, Andsberg Gunnar, Romner Bertil
Department of Anaesthesiology and Intensive Care, Halmstad Regional Hospital, Halmstad, and Neurointensive Care Unit, Department of Neurosurgery, Lund University Hospital, Sweden.
Neurocrit Care. 2007;6(2):94-9. doi: 10.1007/s12028-007-0005-0.
S100B is viewed as the most promising biomarker for brain damage. It has been proposed that this marker is useful in a Neurointensive Care Unit (NICU) as a monitoring parameter. This study aims to examine the clinical usefulness of daily serum S100B measurements in this setting.
Prospective consecutive inclusion of patients.
A total of 79 patients with confirmed or suspected head injury or cerebrovascular insults (CVIs) (based upon patient history, computed tomography (CT) and/or magnetic resonance imaging (MRI) and neurological examination including coma scoring) who required neurointensive care were included in the study.
Sampling for S100B was performed at admission and daily until patients were discharged from the NICU. S100B measurements were statistically compared to occurrence of secondary complications and outcome according to Glasgow Outcome Scale (GOS), with focus on clinical prediction.
17 of 79 patients (22%) had secondary neurological complications. Mean S100B levels were found to be an independent parameter associated with these complications (P=0.03). Mean S100B levels were higher in patients with complications compared to those without on both the complication day (P=0.033) and the day after (P=0.015), but not the day prior to the complication (P=0.62). S100B did not predict secondary neurological complication. Neither mean (P=0.182) nor peak (P=0.370) S100B levels were associated with or predicted outcome according to dichotomised GOS.
Daily S100B measurements are associated with secondary complications but not to outcome. However, daily S100B levels do not predict secondary complications, which limit the usefulness of this brain biomarker in this setting.
S100B被视为脑损伤最具前景的生物标志物。有人提出,该标志物在神经重症监护病房(NICU)作为监测参数很有用。本研究旨在探讨在此环境下每日测定血清S100B的临床实用性。
对患者进行前瞻性连续纳入。
本研究共纳入79例确诊或疑似头部损伤或脑血管损伤(CVI)(基于患者病史、计算机断层扫描(CT)和/或磁共振成像(MRI)以及包括昏迷评分在内的神经学检查)且需要神经重症监护的患者。
入院时及每日进行S100B采样,直至患者从NICU出院。根据格拉斯哥预后量表(GOS),将S100B测量值与继发性并发症的发生情况及预后进行统计学比较,重点关注临床预测。
79例患者中有17例(22%)发生继发性神经并发症。发现平均S100B水平是与这些并发症相关的独立参数(P = 0.03)。与未发生并发症的患者相比,发生并发症的患者在并发症当天(P = 0.033)和次日(P = 0.015)的平均S100B水平更高,但在并发症前一天无差异(P = 0.62)。S100B不能预测继发性神经并发症。根据二分法GOS,平均(P = 0.182)和峰值(P = 0.370)S100B水平均与预后无关或不能预测预后。
每日测定S100B与继发性并发症相关,但与预后无关。然而,每日S100B水平不能预测继发性并发症,这限制了这种脑生物标志物在此环境下的实用性。