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全血阻抗聚集检测法可检测肝素诱导的血小板减少症抗体。

Whole blood impedance aggregometry detects heparin-induced thrombocytopenia antibodies.

机构信息

Department of Haematology and Transfusion Medicine, Royal North Shore Hospital, Northern Blood Research Centre, University of Sydney, St Leonards, NSW, Australia.

出版信息

Thromb Res. 2010 May;125(5):e234-9. doi: 10.1016/j.thromres.2009.12.001. Epub 2010 Jan 6.

Abstract

Heparin-induced thrombocytopenia (HIT) is a serious complication of heparin use. IgG antibodies to complexes of platelet factor 4 (PF4) and heparin trigger the clinical manifestations of HIT. Only a subset of these antibodies will activate platelets and these can only be identified with platelet aggregation (functional) assays. Heparin-induced platelet aggregation (HIPA) and (14)C-serotonin release (SRA) assays for HIT are time-consuming and complex to perform. We have developed a whole blood impedance (WBI) test using the new Multiplate analyser. All samples referred to our laboratory over a 10 month period were screened for heparin-PF4 antibodies by an ELISA method (Zymutest HIA IgG). The 4T's score was used to assess HIT pretest probability. Twenty antibody positive samples were further tested by all three functional assays: light transmission aggregometry (LTA), SRA and WBI. Thirteen out of twenty samples were positive by LTA (10 patients) and 15 by WBI (11 patients). SRA, considered to be the gold standard, was used as a confirmatory test and 11 were found to be positive (10 patients); four discrepant samples were weakly positive by WBI. The prevalence of a positive functional test was strongly correlated with the 4T's clinical risk score, but a small number of low-risk patients had positive functional assays. In this study, the WBI assay detected all SRA positive patients and was positive for two others suggesting greater sensitivity. The rapid and easy to perform assay may be a useful tool for haematology laboratories to detect platelet-activating HIT antibodies.

摘要

肝素诱导的血小板减少症(HIT)是肝素使用的严重并发症。IgG 抗体与血小板因子 4(PF4)和肝素复合物触发 HIT 的临床表现。只有这些抗体的一部分会激活血小板,这些只能通过血小板聚集(功能)测定来识别。肝素诱导的血小板聚集(HIPA)和(14)C-血清素释放(SRA)测定用于 HIT 既耗时又复杂。我们使用新的 Multiplate 分析仪开发了一种全血阻抗(WBI)测试。在 10 个月的时间里,我们将所有送往我们实验室的样本通过 ELISA 方法(Zymutest HIA IgG)筛选肝素-PF4 抗体。使用 4T's 评分评估 HIT 测试前的可能性。20 个抗体阳性样本进一步通过所有三种功能测定进行测试:光传输聚集测定(LTA)、SRA 和 WBI。13 个样本在 LTA 中呈阳性(10 个患者),15 个样本在 WBI 中呈阳性(11 个患者)。SRA 被认为是金标准,用作确认测试,发现 11 个样本呈阳性(10 个患者);4 个不一致的样本在 WBI 中呈弱阳性。阳性功能测试的流行率与 4T's 临床风险评分密切相关,但少数低风险患者的功能测试呈阳性。在这项研究中,WBI 测定法检测到所有 SRA 阳性患者,并且对另外两个患者呈阳性,提示敏感性更高。该快速且易于执行的测定法可能是血液学实验室检测血小板激活 HIT 抗体的有用工具。

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