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肝素诱导的血小板减少症/血栓形成:临床病理综述

Heparin-induced thrombocytopaenia/thrombosis: a clinicopathologic review.

作者信息

Dave P A

机构信息

Clinical Pathologist and Haematologist, MP Shah Hospital, Nairobi, Kenya.

出版信息

East Afr Med J. 2009 Dec;86(12 Suppl):S62-70.

Abstract

BACKGROUND

Heparin is widely used for the prophylaxis of venous thrombo-embolism and pulmonary embolism. Thrombocytopaenia and the sequale of thrombosis are uncommon adverse effects of therapy which are associated with high morbidity and mortality.

OBJECTIVE

To review the clinical-pathologic features of heparin induced thrombocytopaenia/thrombosis.

DATA SOURCES

Reputable haematology journals and the internet in English. Searches included thrombosis, heparin, and heparin induced thrombocytopaenia.

DATA SELECTION

Only relevant journals and internet sources were selected for this review. In particular leading journals in thrombosis and anticoagulants.

DATA EXTRACTION

High quality abstracts, papers and internet articles were the main source of information.

DATA SYNTHESIS

Information from the selected abstracts and papers was used'for the paper.

CONCLUSION

The clinical effects of heparin induced thrombocytopaenia/thrombosis (HIT/T) include venous and arterial events the latter of which include limb ischaemia, myocardial infarction and stroke. The pathogenesis of this complication is related the formation of heparin-platelet factor 4 antibodies which can be demonstrated in the laboratory by functional and immunoassays. Management requires alternative anticoagulation with agents that have no cross reactivity with heparin platelet factor 4 antibodies. These agents include danapranoid, direct thrombin inhibitors and newer agents like fondaparinux and rivaroxaban with anti Xa activity.

摘要

背景

肝素广泛用于预防静脉血栓栓塞和肺栓塞。血小板减少症以及血栓形成的后遗症是治疗中不常见的不良反应,与高发病率和死亡率相关。

目的

综述肝素诱导的血小板减少症/血栓形成的临床病理特征。

资料来源

英文的著名血液学杂志和互联网。检索词包括血栓形成、肝素和肝素诱导的血小板减少症。

资料选择

本综述仅选择相关的杂志和互联网来源。特别是血栓形成和抗凝领域的领先杂志。

资料提取

高质量的摘要、论文和互联网文章是主要信息来源。

资料综合

所选摘要和论文中的信息用于撰写本文。

结论

肝素诱导的血小板减少症/血栓形成(HIT/T)的临床影响包括静脉和动脉事件,后者包括肢体缺血、心肌梗死和中风。这种并发症的发病机制与肝素-血小板因子4抗体的形成有关,可通过功能和免疫测定在实验室中证实。治疗需要用与肝素血小板因子4抗体无交叉反应的药物进行替代抗凝。这些药物包括达那肝素、直接凝血酶抑制剂以及具有抗Xa活性的新型药物如磺达肝癸钠和利伐沙班。

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