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在疑似肝素诱导的血小板减少症情况下,绝对未成熟血小板计数可能预测抗PF4-肝素免疫测定检测结果。

Absolute immature platelet counts in the setting of suspected heparin-induced thrombocytopenia may predict anti-PF4-heparin immunoassay testing results.

作者信息

Chen Wei, Ha Jennifer P, Hong Hong, Maitta Robert W

机构信息

University Hospitals Cleveland Medical Center, Case Western Reserve University School of Medicine, Cleveland, OH, United States.

University Hospitals Cleveland Medical Center, Case Western Reserve University School of Medicine, Cleveland, OH, United States.

出版信息

Transfus Apher Sci. 2018 Aug;57(4):507-511. doi: 10.1016/j.transci.2018.04.001. Epub 2018 Apr 11.

DOI:10.1016/j.transci.2018.04.001
PMID:29661682
Abstract

BACKGROUND

Heparin-induced-thrombocytopenia (HIT) is a disease mediated by antibodies to platelet factor 4 (PF4)-heparin complexes. Immature platelet fraction (%-IPF) and absolute immature platelet count (A-IPC) measure newly-released platelets into circulation and can prove useful in differentiating patients with thrombocytopenic presentations due to consumptive or hypoproduction processes. Therefore, we evaluated utility of A-IPC in a cohort of thrombocytopenic patients suspected of HIT.

PATIENTS AND METHODS

Twenty-six thrombocytopenic patients (<150 × 10/L) tested for anti-PF4-heparin and 36 non-thrombocytopenic controls were included. Platelet count, %-IPF, and A-IPC were determined at time of anti-PF4-heparin testing.

RESULTS

Sixteen patients tested anti-PF4-heparin negative and 10 tested positive. Patients with positive anti-PF4-heparin did not differ in A-IPC from normal range (7.2 ± 2.9 × 10/L vs. 7.1 ± 3.2 × 10/L respectively; p = 0.97). However, there was a significant A-IPC decrease in patients negative for anti-PF4-heparin compared to normal range and those testing anti-PF4-heparin positive (4.2 ± 3.1 × 10/L vs. 7.1 ± 3.2 × 10/L vs. 7.2 ± 2.9 × 10/L respectively, p < 0.01). An A-IPC of greater than 5 × 10/L characterized 80% of anti-PF4-heparin positive cases.

CONCLUSION

A-IPC measurements can complement anti-PF4-heparin testing of patients suspected of HIT while potentially predicting anti-PF4-heparin immunoassay results.

摘要

背景

肝素诱导的血小板减少症(HIT)是一种由针对血小板因子4(PF4)-肝素复合物的抗体介导的疾病。未成熟血小板分数(%-IPF)和绝对未成熟血小板计数(A-IPC)可测量新释放到循环中的血小板,有助于鉴别因消耗性或低生成性过程导致血小板减少的患者。因此,我们评估了A-IPC在疑似HIT的血小板减少患者队列中的作用。

患者与方法

纳入26例血小板减少患者(血小板计数<150×10⁹/L)进行抗PF4-肝素检测,并纳入36例非血小板减少对照。在进行抗PF4-肝素检测时测定血小板计数、%-IPF和A-IPC。

结果

16例患者抗PF4-肝素检测为阴性,10例为阳性。抗PF4-肝素阳性患者的A-IPC与正常范围无差异(分别为7.2±2.9×10⁹/L和7.1±3.2×10⁹/L;p=0.97)。然而,抗PF4-肝素阴性患者的A-IPC与正常范围及抗PF4-肝素阳性患者相比显著降低(分别为4.2±3.1×10⁹/L、7.1±3.2×10⁹/L和7.2±2.9×10⁹/L,p<0.01)。A-IPC大于5×10⁹/L可诊断80%的抗PF4-肝素阳性病例。

结论

A-IPC测量可补充疑似HIT患者的抗PF4-肝素检测,同时可能预测抗PF4-肝素免疫测定结果。

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