Ernstbrunner Lukas, Korn Gundobert, Ernstbrunner Erich, Auffarth Alexander, Tauber Mark, Resch Herbert, Moroder Philipp
a Department of Traumatology and Sports Injuries , Paracelsus Medical University , Salzburg , Austria .
b General Practitioner Office , Vienna , Austria , and .
Brain Inj. 2016;30(1):43-7. doi: 10.3109/02699052.2015.1087593. Epub 2015 Nov 18.
The goal of this study was to investigate if S100B serum protein could predict secondary intracranial haemorrhagic events (SIHEs) after mild head injury (mHI) in patients taking low-dose acetylsalicylic acid (LDA), making routinely repeated head computed tomography (RRHCT) scans unnecessary.
Three hundred and eight-two patients with mHI, older than 60 years and taking LDA prophylaxis were enrolled. Primary head CT and RRHCT scans within 3 and 48 hours to trauma were performed. Additionally, S100B serum protein levels were evaluated at admission and predictive power for SIHEs was analysed.
Fifty-nine per cent were female and the mean age of all included patients was 81.8 ± 8.9 years. In four patients SIHEs were diagnosed. Sensitivity and the negative predictive value of S100B serum protein (cut-off value 0.10 µg l(-1)) were 75.0% and 98.6%, respectively. Specificity was 19.0% and the positive predictive value 1.0% (306 false positive values). In patients without bleeding, the median S100B value was 0.18 (IQR = 0.12-0.34) and in the ones with SIHEs, the median was 0.11 (IQR = 0.10-1.16) (p > 0.05). The discriminatory power of S100B in the ROC analysis was 0.399 (95% CI = 0.079-0.720; p > 0.05).
S100B cannot be considered as an effective diagnostic tool in the prediction or exclusion of SIHE in older patients with mHIs taking LDA prophylaxis.
本研究的目的是调查在服用低剂量乙酰水杨酸(LDA)的患者中,S100B血清蛋白是否能够预测轻度颅脑损伤(mHI)后的继发性颅内出血事件(SIHEs),从而无需进行常规重复头颅计算机断层扫描(RRHCT)。
纳入382例年龄大于60岁且正在接受LDA预防治疗的mHI患者。在创伤后3小时和48小时内进行了初次头颅CT和RRHCT扫描。此外,在入院时评估了S100B血清蛋白水平,并分析了其对SIHEs的预测能力。
59%为女性,所有纳入患者的平均年龄为81.8±8.9岁。4例患者被诊断为SIHEs。S100B血清蛋白(临界值0.10µg l(-1))的敏感性和阴性预测值分别为75.0%和98.6%。特异性为19.0%,阳性预测值为1.0%(306例假阳性值)。在无出血的患者中,S100B的中位数为0.18(IQR=0.12-0.34),在发生SIHEs的患者中,中位数为0.11(IQR=0.10-1.16)(p>0.05)。在ROC分析中,S100B的鉴别能力为0.399(95%CI=0.079-0.720;p>0.05)。
对于正在接受LDA预防治疗的老年mHI患者,S100B不能被视为预测或排除SIHEs的有效诊断工具。