Yuan Qiang, Sun Yi-Rui, Wu Xing, Yu Jian, Li Zhi-Qi, Du Zhuo-Ying, Wu Xue-Hai, Zhou Liang-Fu, Hu Jin
Department of Neurosurgery, Huashan Hospital, Fudan University , Shanghai, PR China .
J Neurotrauma. 2016 Jul 15;33(14):1279-91. doi: 10.1089/neu.2015.4205. Epub 2016 Mar 22.
The association between coagulopathy and either isolated traumatic brain injury (TBI) or progressive hemorrhagic injury (PHI) remains controversial. The aims of this study were to evaluate whether isolated TBI induces pronounced coagulopathy, in comparison with non-TBI or TBI in conjunction with other injuries (TBI + other injuries), and to examine whether there is any evidence of a relationship between coagulopathy and PHI in patients who have experienced TBI. The MEDLINE(®) and Embase databases, and the Cochrane Central Register of Controlled Trials (Central), were trawled for relevant studies. Searches covered the period from the inception of each of the databases to June 2015, and were conducted using appropriate combinations of terms and key words based on medical subject headings (MeSH). Studies were included if they compared isolated TBI with a similar severity of injury to other body regions, or compared PHI with non-PHI, with regard to coagulation tests and the prevalence of coagulopathy. We extracted the means and standard deviations (SD) of coagulation test levels, as well as their ranges or the percentage of abnormal coagulation tests, in both cases and controls. A total of 19 studies were included in our systematic review and meta-analysis. Only the mean fibrinogen (FIB) in isolated TBI was found to be significantly higher than in TBI + other injuries (pooled mean difference [MD] 32.09; 95% confidence interval [CI] 4.92-59.25; p = 0.02); in contrast, it was also significantly higher than in non-TBI (pooled MD 15.44; 95% CI 0.28-30.59; p = 0.05). We identified 15 studies that compared coagulopathy between a PHI group and a non-PHI group. The PHI group had a lower platelet count (PLT) value (pooled MD -19.21; 95% CI: -26.99 to -11.44, p < 0.001) and a higher international normalized ratio (INR) value (pooled MD 0.07; 95% CI: 0.02-0.13, p = 0.006) than the non-PHI group, but no differences were observed in the mean activated partial thromboplastin time (APTT) and prothrombin time (PT) between the PHI and non-PHI patients. In addition, PHI was significantly associated with a higher percentage of INR >1.2 (pooled OR 3.49 [95% CI 1.97-6.20], p < 0.001), PLT <100 × 109/L (pooled OR 4.74 [95% CI 2.44-9.20], p < 0.001), and coagulopathy (pooled OR 2.52; 95% CI 1.88- 3.38; p < 0.001), compared with non-PHI. The current clinical evidence does not indicate that the prevalence of coagulopathy in TBI is significantly higher than in injuries of similar severity to other areas of the body, or in multiple injuries with TBI. With respect to the association between coagulopathy and PHI, the occurrence of coagulopathy, INR, and PLT was significantly associated with PHI, but APTT and PT were not found to be associated with PHI. In the future, high quality research will be required to further characterize the effects of coagulopathy on TBI and subsequent PHI.
凝血功能障碍与单纯性创伤性脑损伤(TBI)或进行性出血性损伤(PHI)之间的关联仍存在争议。本研究的目的是评估与非TBI或合并其他损伤的TBI(TBI + 其他损伤)相比,单纯性TBI是否会引发明显的凝血功能障碍,并探讨在经历TBI的患者中,凝血功能障碍与PHI之间是否存在关联证据。我们检索了MEDLINE®、Embase数据库以及Cochrane对照试验中心注册库(Central)中的相关研究。检索涵盖了从各数据库创建之初至2015年6月的时间段,并根据医学主题词(MeSH)使用适当的术语和关键词组合进行检索。如果研究比较了单纯性TBI与身体其他部位相似损伤严重程度,或者就凝血试验和凝血功能障碍患病率比较了PHI与非PHI,则纳入该研究。我们提取了病例组和对照组中凝血试验水平的均值和标准差(SD),以及它们的范围或异常凝血试验的百分比。共有19项研究纳入了我们的系统评价和荟萃分析。仅发现单纯性TBI中的纤维蛋白原(FIB)均值显著高于TBI + 其他损伤(合并均值差[MD] 32.09;95%置信区间[CI] 4.92 - 59.25;p = 0.02);相比之下,它也显著高于非TBI(合并MD 15.44;95% CI 0.28 - 30.59;p = 0.05)。我们确定了15项比较PHI组和非PHI组凝血功能障碍的研究。与非PHI组相比,PHI组的血小板计数(PLT)值较低(合并MD -19.21;95% CI:-26.99至-11.44,p < 0.001),国际标准化比值(INR)值较高(合并MD 0.07;95% CI:0.02 - 0.13,p = 0.006),但在PHI患者和非PHI患者之间,活化部分凝血活酶时间(APTT)和凝血酶原时间(PT)的均值未观察到差异。此外,与非PHI相比,PHI与INR > 1.2的较高百分比(合并OR 3.49 [95% CI 1.97 - 6.20],p < 0.001)、PLT < 100×10⁹/L(合并OR 4.74 [95% CI 2.44 - 9.20],p < 0.001)以及凝血功能障碍(合并OR 2.52;95% CI 1.88 - 3.38;p < 0.001)显著相关。目前的临床证据并未表明TBI中凝血功能障碍的患病率显著高于身体其他部位相似严重程度的损伤或合并TBI的多发伤。关于凝血功能障碍与PHI之间的关联,凝血功能障碍、INR和PLT的发生与PHI显著相关,但未发现APTT和PT与PHI相关。未来,需要高质量的研究来进一步明确凝血功能障碍对TBI及后续PHI的影响。