Suppr超能文献

接受普通肝素或低分子量肝素抗凝的患者在体外循环后针对血小板第4因子-肝素的抗体:肝素诱导的血小板减少症的临床意义

Antibodies to platelet factor 4-heparin after cardiopulmonary bypass in patients anticoagulated with unfractionated heparin or a low-molecular-weight heparin : clinical implications for heparin-induced thrombocytopenia.

作者信息

Pouplard C, May M A, Iochmann S, Amiral J, Vissac A M, Marchand M, Gruel Y

机构信息

Departments of Hematology, Anesthesiology and Cardiac Surgery, Gennevilliers, France.

出版信息

Circulation. 1999 May 18;99(19):2530-6. doi: 10.1161/01.cir.99.19.2530.

Abstract

BACKGROUND

Cardiopulmonary bypass (CPB) induces platelet activation with release of platelet factor 4 (PF4), and patients are exposed to high doses of heparin (H). We investigated whether this contributes to the development of antibodies to H-PF4 and heparin-induced thrombocytopenia (HIT).

METHODS AND RESULTS

CPB was performed with unfractionated heparin (UFH) in 328 patients. After surgery, patients received UFH (calcium heparin, 200 IU. kg-1. d-1) (group 1, n=157) or low-molecular-weight heparin (LMWH, Dalteparin, 5000 IU once daily) (group 2, n=171). Eight days after surgery, antibodies to H-PF4 were present in 83 patients (25.3%), 46 in group 1 and 37 in group 2 (P=0.12). Most patients (61%) had IgG1 to H-PF4, but only 8 samples with antibodies induced platelet activation with positive results on serotonin release assay. HIT occurred in 6 patients in group 1, but no thrombocytopenia was observed in subjects receiving LMWH, although 2 had high levels of antibodies with positive serotonin release assay results. When antibodies to H-PF4 were present, mean platelet counts were lower only in patients with FcgammaRIIA R/R131 platelets.

CONCLUSIONS

These results provide evidence that the development of antibodies to H-PF4 after CPB performed with UFH is not influenced by the postoperative heparin treatment. The antibodies associated with high risk of HIT are mainly IgG1, which is present at high titers in the plasma of patients continuously treated with UFH.

摘要

背景

体外循环(CPB)可诱导血小板活化并释放血小板因子4(PF4),且患者会接触高剂量肝素(H)。我们研究了这是否会导致H-PF4抗体及肝素诱导的血小板减少症(HIT)的发生。

方法与结果

328例患者接受了普通肝素(UFH)体外循环。术后,患者接受UFH(肝素钙,200 IU·kg-1·d-1)(第1组,n = 157)或低分子肝素(LMWH,达肝素,每日5000 IU)(第2组,n = 171)。术后8天,83例患者(25.3%)出现H-PF4抗体,第1组46例,第2组37例(P = 0.12)。大多数患者(61%)有针对H-PF4的IgG1,但只有8份抗体样本在5-羟色胺释放试验中诱导血小板活化呈阳性结果。第1组有6例发生HIT,但接受LMWH的患者未观察到血小板减少,尽管有2例5-羟色胺释放试验结果呈阳性且抗体水平较高。当存在H-PF4抗体时,仅FcγRIIA R/R131血小板的患者平均血小板计数较低。

结论

这些结果表明,UFH体外循环后H-PF4抗体的产生不受术后肝素治疗的影响。与HIT高风险相关的抗体主要是IgG1,在持续接受UFH治疗的患者血浆中高滴度存在。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验