Hunt Harriet, Stanworth Simon, Curry Nicola, Woolley Tom, Cooper Chris, Ukoumunne Obioha, Zhelev Zhivko, Hyde Chris
Institute of Health Research, University of Exeter Medical School, University of Exeter, Exeter, UK.
Cochrane Database Syst Rev. 2015 Feb 16;2015(2):CD010438. doi: 10.1002/14651858.CD010438.pub2.
Trauma-induced coagulopathy (TIC) is a disorder of the blood clotting process that occurs soon after trauma injury. A diagnosis of TIC on admission is associated with increased mortality rates, increased burdens of transfusion, greater risks of complications and longer stays in critical care. Current diagnostic testing follows local hospital processes and normally involves conventional coagulation tests including prothrombin time ratio/international normalized ratio (PTr/INR), activated partial prothrombin time and full blood count. In some centres, thromboelastography (TEG) and rotational thromboelastometry (ROTEM) are standard tests, but in the UK they are more commonly used in research settings.
The objective was to determine the diagnostic accuracy of thromboelastography (TEG) and rotational thromboelastometry (ROTEM) for TIC in adult trauma patients with bleeding, using a reference standard of prothrombin time ratio and/or the international normalized ratio.
We ran the search on 4 March 2013. Searches ran from 1970 to current. We searched The Cochrane Library, MEDLINE (OvidSP), EMBASE Classic and EMBASE, eleven other databases, the web, and clinical trials registers. The Cochrane Injuries Group's specialised register was not searched for this review as it does not contain diagnostic test accuracy studies. We also screened reference lists, conducted forward citation searches and contacted authors.
We included all cross-sectional studies investigating the diagnostic test accuracy of TEG and ROTEM in patients with clinically suspected TIC, as well as case-control studies. Participants were adult trauma patients in both military and civilian settings. TIC was defined as a PTr/INR reading of 1.2 or greater, or 1.5 or greater.
We piloted and performed all review stages in duplicate, including quality assessment using the QUADAS-2 tool, adhering to guidance in the Cochrane Handbook for Diagnostic Test Accuracy Reviews. We analysed sensitivity and specificity of included studies narratively as there were insufficient studies to perform a meta-analysis.
Three studies were included in the final analysis. All three studies used ROTEM as the test of global haemostatic function, and none of the studies used TEG. Tissue factor-activated assay EXTEM clot amplitude (CA) was the focus of the accuracy measurements in blood samples taken near to the point of admission. These CAs were not taken at a uniform time after the start of the coagulopathic trace; the time varied from five minutes, to ten minutes and fifteen minutes. The three included studies were conducted in the UK, France and Afghanistan in both civilian and military trauma settings. In two studies, median Injury Severity Scores were 12, inter-quartile range (IQR) 4 to 24; and 22, IQR 12 to 34; and in one study the median New Injury Severity Score was 34, IQR 17 to 43.There were insufficient included studies examining each of the three ROTEM CAs at 5, 10 and 15 minutes to make meta-analysis and investigation of heterogeneity valid. The results of the included studies are thus reported narratively and illustrated by a forest plot and results plotted on the receiver operating characteristic (ROC) plane.For CA5 the accuracy results were sensitivity 70% (95% CI 47% to 87%) and specificity 86% (95% CI 82% to 90%) for one study, and sensitivity 96% (95% CI 88% to 100%) and specificity 58% (95% CI 44% to 72%) for the other.For CA10 the accuracy results were sensitivity 100% (95% CI 94% to 100%) and specificity 70% (95% CI 56% to 82%).For CA15 the accuracy results were sensitivity 88% (95% CI 69% to 97%) and specificity 100% (95% CI 94% to 100%).No uninterpretable ROTEM study results were mentioned in any of the included studies.Risk of bias and concerns around applicability of findings was low across all studies for the patient and flow and timing domains. However, risk of bias and concerns around applicability of findings for the index test domain was either high or unclear, and the risk of bias for the reference standard domain was high. This raised concerns around the interpretation of the sensitivity and specificity results of the included studies, which may be misleading.
AUTHORS' CONCLUSIONS: We found no evidence on the accuracy of TEG and very little evidence on the accuracy of ROTEM. The value of accuracy estimates are considerably undermined by the small number of included studies, and concerns about risk of bias relating to the index test and the reference standard. We are unable to offer advice on the use of global measures of haemostatic function for trauma based on the evidence on test accuracy identified in this systematic review. This evidence strongly suggests that at present these tests should only be used for research. We consider more thoroughly what this research could be in the Discussion section.
创伤性凝血病(TIC)是创伤损伤后不久发生的一种凝血过程紊乱。入院时诊断为TIC与死亡率增加、输血负担加重、并发症风险增加以及重症监护时间延长相关。目前的诊断检测遵循当地医院流程,通常包括传统凝血试验,如凝血酶原时间比值/国际标准化比值(PTr/INR)、活化部分凝血活酶时间和全血细胞计数。在一些中心,血栓弹力图(TEG)和旋转血栓弹力测定法(ROTEM)是标准检测方法,但在英国,它们更常用于研究环境。
以凝血酶原时间比值和/或国际标准化比值为参考标准,确定血栓弹力图(TEG)和旋转血栓弹力测定法(ROTEM)对有出血的成年创伤患者TIC的诊断准确性。
我们于2013年3月4日进行检索。检索时间范围从1970年至当前。我们检索了考克兰图书馆、MEDLINE(OvidSP)、EMBASE经典版和EMBASE、其他11个数据库、网络以及临床试验注册库。本次综述未检索考克兰损伤组的专门注册库,因为其中不包含诊断试验准确性研究。我们还筛选了参考文献列表,进行了向前引用检索并联系了作者。
我们纳入了所有调查TEG和ROTEM对临床疑似TIC患者诊断试验准确性的横断面研究以及病例对照研究。参与者为军事和民用环境中的成年创伤患者。TIC定义为PTr/INR读数为1.2或更高,或1.5或更高。
我们对所有综述阶段进行了双人试点和操作,包括使用QUADAS - 2工具进行质量评估,遵循考克兰诊断试验准确性综述手册中的指南。由于纳入研究数量不足,无法进行Meta分析,我们对纳入研究的敏感性和特异性进行了叙述性分析。
主要结果:最终分析纳入了三项研究。所有三项研究均使用ROTEM作为整体止血功能测试,且无一研究使用TEG。组织因子激活试验EXTEM凝血振幅(CA)是入院时采集血样准确性测量的重点。这些CA并非在凝血异常轨迹开始后的统一时间采集;时间从5分钟到10分钟和15分钟不等。纳入的三项研究在英国、法国和阿富汗的民用和军事创伤环境中进行。在两项研究中,损伤严重程度评分中位数分别为12,四分位间距(IQR)4至24;以及22,IQR 12至34;在一项研究中,新损伤严重程度评分中位数为34,IQR 17至43。纳入研究中在5分钟、10分钟和15分钟对三项ROTEM CA进行检查的数量不足,无法进行Meta分析和异质性研究。因此,纳入研究的结果以叙述方式报告,并通过森林图说明,结果绘制在受试者工作特征(ROC)平面上。对于CA5,一项研究的准确性结果为敏感性70%(95%CI 47%至87%),特异性86%(95%CI 82%至90%);另一项研究的敏感性为96%(95%CI 88%至100%),特异性为58%(95%CI 44%至72%)。对于CA10,准确性结果为敏感性100%(95%CI 94%至100%),特异性70%(95%CI 56%至82%)。对于CA15,准确性结果为敏感性88%(95%CI 69%至97%),特异性100%(95%CI 9
4%至100%)。纳入研究中均未提及无法解释的ROTEM研究结果。在所有研究中,患者、流程和时间领域的偏倚风险及对结果适用性的担忧较低。然而,指标试验领域的偏倚风险及对结果适用性的担忧较高或不明确,参考标准领域的偏倚风险较高。这引发了对纳入研究敏感性和特异性结果解释的担忧,这些结果可能具有误导性。
我们未发现关于TEG准确性的证据,关于ROTEM准确性的证据也极少。纳入研究数量少以及对指标试验和参考标准偏倚风险的担忧,极大地削弱了准确性估计值的价值。基于本系统综述中确定的试验准确性证据,我们无法就创伤止血功能的整体测量方法的使用提供建议。该证据强烈表明,目前这些检测仅应用于研究。我们在讨论部分更全面地考虑了这项研究可能的方向。