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使用新型肝素中和检测卡的TEG® 6s凝血检测:技术验证及正常参考范围的确定

TEG® 6s coagulation testing with a novel heparin neutralization cartridge: Technical validation and determination of normal reference ranges.

作者信息

Hartmann Jan, Dias Joao, Shilo Alexandra, Bynagari Yamini, Garrett Brandon, Jeske Walter, Manukyan Zorayr, Mkhitaryan Karen, Adelmann Dieter, Subramaniam Kathirvel, Sakai Tetsuro

机构信息

Global Medical Office, Haemonetics Corporation, Boston, MA, US.

Machaon Diagnostics, Inc, Berkeley, CA, US.

出版信息

Am J Clin Pathol. 2025 Jan 28;163(1):12-19. doi: 10.1093/ajcp/aqae088.

Abstract

OBJECTIVES

We sought to establish normal reference ranges (NRRs) for a novel TEG 6s cartridge (TEG 6s Citrated: K, KH, RTH, FFH [Global Hemostasis]) (Haemonetics Corporation, Boston, MA, US).

METHODS

Healthy volunteers (≥18 years of age) included in this single-arm study provided single samples of whole blood. Primary end points included TEG parameters in the citrated kaolin (CK), CK with heparinase (CKH), RapidTEG with heparinase (CRTH), and functional fibrinogen with heparinase (CFFH) assays.

RESULTS

Evaluable data were contributed by 164 volunteers (48.8% female; 62% White/Caucasian). The following NRRs were established: CK maximum amplitude (MA), 51.0 to 67.6 mm; CKH-MA, 51.8 to 67.9 mm; CRTH-MA, 53.0 to 68.9 mm; CFFH-MA, 15.3 to 34.4 mm; CK reaction time, 5.0 to 9.1 minutes; CKH reaction time, 4.9 to 9.4 minutes; CKH lysis 30 minutes after MA, 0% to 3.2%. Duplicate measurements demonstrated high reproducibility. CFFH-MA correlated with Clauss fibrinogen concentration (Pearson correlation coefficient, 0.74). Laboratory-based studies demonstrated maintenance of the relationship between CFFH-MA and fibrinogen up to 1344 mg/dL (hyperfibrinogenemic samples) and acceptability of heparin neutralization up to concentrations of low molecular weight and unfractionated heparin of 1.3 IU/mL and 5 IU/mL, respectively.

CONCLUSIONS

This study established NRRs for the Global Hemostasis cartridge and serves as a proof of concept for the validity of results obtained using this cartridge.

摘要

目的

我们试图为一种新型血栓弹力图6s检测卡(血栓弹力图6s枸橼酸盐法:K、KH、RTH、FFH [整体止血功能])(美国马萨诸塞州波士顿市海莫尼克斯公司)建立正常参考范围(NRRs)。

方法

纳入这项单臂研究的健康志愿者(≥18岁)提供全血单样本。主要终点包括枸橼酸高岭土(CK)、含肝素酶的枸橼酸高岭土(CKH)、含肝素酶的快速血栓弹力图(CRTH)以及含肝素酶的功能性纤维蛋白原(CFFH)检测中的血栓弹力图参数。

结果

164名志愿者(48.8%为女性;62%为白人/高加索人)提供了可评估数据。建立了以下正常参考范围:CK最大振幅(MA),51.0至67.6毫米;CKH-MA,51.8至67.9毫米;CRTH-MA,53.0至68.9毫米;CFFH-MA,15.3至34.4毫米;CK反应时间,5.0至9.1分钟;CKH反应时间,4.9至9.4分钟;MA后30分钟的CKH溶解率,0%至3.2%。重复测量显示出高重现性。CFFH-MA与Clauss纤维蛋白原浓度相关(皮尔逊相关系数,0.74)。基于实验室的研究表明,在纤维蛋白原浓度高达1344毫克/分升(高纤维蛋白原血症样本)时,CFFH-MA与纤维蛋白原之间的关系保持不变,并且分别在低分子量肝素浓度达1.3国际单位/毫升和普通肝素浓度达5国际单位/毫升时,肝素中和效果良好。

结论

本研究为整体止血功能检测卡建立了正常参考范围,并证明了使用该检测卡获得的结果的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1a7/11775113/891c49704967/aqae088_fig1.jpg

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