TBICheck:在轻度创伤性脑损伤患者中排除CT扫描的快速测试

Jean-Charles Sanchez
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摘要

TBICheck TM快速检测是一种免疫层析快速检测,能够帮助诊断疑似脑病变的轻度创伤性脑损伤(mTBI)患者。它定量测定全血、血清或血浆中心脏型脂肪酸结合蛋白(H-FABP)水平。本研究的目的是评估其技术性能,并在两个不同的mTBI患者队列中测试其作为检测mTBI患者脑病变的潜在诊断工具。实验材料和方法描述:采用标准样品的连续稀释法确定TBICheck TM横向流动法的线性和定量下限(LLOQ)。使用TBICheck TM Reader读取结果,TBICheck TM Reader是一种基于反射率测量的移动光度免疫分析仪,以捕获光密度。将所得结果与经典的ELISA检测方法、Meso Scale Diagnostics (MSD)进行比较。患者队列:纳入了两个不同的成年mTBI患者队列:回顾性队列包括82例患者,前瞻性队列包括65例患者。计算H-FABP曲线下面积(AUC)、特异性(SP)、敏感性(SE)和阴性预测值(NPV)。结果H-FABP在0.5 ~ 25 ng/mL范围内的剂量响应符合线性回归。血中下限为0.5 ng/mL。比较MSD ELISA和TBICheck TM浓度时,发现Spearman相关性高(ρ=0.933, p<0.001)。在回顾性队列中,当临床敏感性设置为100%时,特异性值为32.9%。在前瞻性队列中,SP值上升至66.1%,SE为100%,即根据入院时血清H-FABP浓度,10例患者中有6例可能出院。结论采用TBICheck TM快速检测方法定量测定成人mTBI患者的H-FABP,可减少ct扫描,减少辐射暴露,避免急诊候诊时间过长。它可以节省医院资源,并帮助医生为患者提供最合适的治疗。
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TBICheck: a rapid test to rule-out CT scans in mild Traumatic Brain Injury patients
Introduction The TBICheck TM Rapid test is an immunochromatographic rapid test capable of assisting in the triage of patients with mild Traumatic Brain Injury (mTBI) suspected of brain lesions. It quantitatively determines heart-type Fatty Acid Binding Protein (H-FABP) levels in whole blood, serum, or plasma. The aim of the present study was to evaluate its technical performance and test it in two different cohorts of mTBI patients as a potential diagnostic tool for detecting brain lesions in patients with mTBI. Material and methods Description of the assay: Linearity and low limit of quantification (LLOQ) of TBICheck TM lateral flow assay were determined using serial dilution of standardized samples. Results were read using the TBICheck TM Reader, a mobile photometric immunoassay analyzer based on reflectance measurements to capture the optical density. Obtained results were compared to classical ELISA assays, Meso Scale Diagnostics (MSD). Patient cohorts: Two different cohorts of adult mTBI patients were included: a retrospective one including 82 patients and a prospective one including 65 patients. Values of H-FABP area under the curve (AUC), specificity (SP), sensitivity (SE) and negative predictive value (NPV) were calculated. Results The H-FABP dose response fitted a linear regression within the range of 0.5-25 ng/mL. LLOQ in blood was 0.5 ng/mL. High Spearman correlation was found (ρ=0.933, p<0.001) when MSD ELISA and TBICheck TM concentrations were compared. In the retrospective cohort, when the clinical sensitivity was set at 100%, a specificity value of 32.9% was obtained. In the prospective cohort, the SP value raised to 66.1% with 100% SE, meaning that 6 out of 10 patients might be discharged on the basis of their serum H-FABP concentration at hospital admission. Conclusions The quantification of H-FABP by using the TBICheck TM Rapid test on adult mTBI patients may allow to rule out the need of a CT-scan reducing the radiation exposure and avoiding the long waiting times in emergency units. It may lead to savings in hospital resources and assists medical doctors to provide the most appropriate treatment to the patients.
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