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

IF 1.9 4区 医学 Q2 PATHOLOGY American journal of clinical pathology Pub Date : 2025-01-28 DOI:10.1093/ajcp/aqae088
Jan Hartmann, Joao Dias, Alexandra Shilo, Yamini Bynagari, Brandon Garrett, Walter Jeske, Zorayr Manukyan, Karen Mkhitaryan, Dieter Adelmann, Kathirvel Subramaniam, Tetsuro Sakai
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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.

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使用新型肝素中和试剂盒进行 TEG® 6s 凝血检测:技术验证和正常参考范围的确定。
目的:我们试图为新型 TEG 6s 血盒(TEG 6s Citrated: K, KH, RTH, FFH [Global Hemostasis])(Haemonetics Corporation,波士顿,马萨诸塞州,美国)确定正常参考范围 (NRR)。主要终点包括枸橼酸高岭土(CK)、肝素酶 CK(CKH)、肝素酶 RapidTEG(CRTH)和肝素酶功能性纤维蛋白原(CFFH)测定中的 TEG 参数:164 名志愿者(48.8% 为女性;62% 为白人/高加索人)提供了可评估的数据。确定了以下 NRR: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 CKH 溶解率,0% 至 3.2%。重复测量结果表明重复性很高。CFFH-MA 与克劳斯纤维蛋白原浓度相关(皮尔逊相关系数为 0.74)。基于实验室的研究表明,CFFH-MA 与纤维蛋白原之间的关系可维持到 1344 mg/dL(高纤维蛋白原血症样本),肝素中和的可接受性可达到低分子量肝素和非分数肝素浓度分别为 1.3 IU/mL 和 5 IU/mL:这项研究确定了全球止血血盒的 NRR,证明了使用该血盒所获得结果的有效性。
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来源期刊
CiteScore
7.70
自引率
2.90%
发文量
367
审稿时长
3-6 weeks
期刊介绍: The American Journal of Clinical Pathology (AJCP) is the official journal of the American Society for Clinical Pathology and the Academy of Clinical Laboratory Physicians and Scientists. It is a leading international journal for publication of articles concerning novel anatomic pathology and laboratory medicine observations on human disease. AJCP emphasizes articles that focus on the application of evolving technologies for the diagnosis and characterization of diseases and conditions, as well as those that have a direct link toward improving patient care.
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