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小儿肝素诱导的血小板减少症——文献综述及1例用达那肝素钠治疗的新病例

Heparin-induced thrombocytopenia in paediatric patients--a review of the literature and a new case treated with danaparoid sodium.

作者信息

Ranze O, Ranze P, Magnani H N, Greinacher A

机构信息

Institut für Immunologie und Transfusionsmedizin, Ernst-Moritz-Arndt Universität, Greifswald, Germany.

出版信息

Eur J Pediatr. 1999 Dec;158 Suppl 3:S130-3. doi: 10.1007/pl00014338.

DOI:10.1007/pl00014338
PMID:10650852
Abstract

UNLABELLED

The immunological form of heparin-induced thrombocytopenia (HIT) is a potentially life-threatening adverse reaction of heparin medication. It is mediated by multimolecular complexes consisting of platelet factor 4 (PF4)-heparin-IgG which bind to platelets via platelet Fc gamma receptors. Cross-linking of multiple Fc gamma receptors results in platelet activation, platelet aggregation and enhanced thrombin generation with a increasing risk of developing new thrombosis. In children, data on HIT are sparse. This review of the literature reports on 8 children aged 3 months to 15 years and 14 newborns suffering from HIT. Additionally, we report one new case treated with danaparoid sodium. Thrombotic complications were venous (n = 12) and arterial (n = 15). The children received heparin either for a spontaneous thrombotic event, for severe cardiac diseases or to maintain patency of intravascular catheters which are used for nutrition, blood sampling, and for application of medication. After diagnosis of HIT they were further anticoagulated with aspirin, warfarin, danaparoid sodium, lepirudin or low molecular weight heparin.

CONCLUSION

Although HIT is less frequently reported in newborns and children, paediatricians should be aware of HIT in childhood as a potential complication of heparin application. The widespread practice of flushing catheters with heparin should also be debated in view of the risk of triggering the primary immune-response of HIT. In 1999, treatment options for further parenteral anticoagulation of HIT patients are danaparoid sodium (a low-molecular weight heparinoid) and lepirudin (a direct thrombin inhibitor).

摘要

未标记

肝素诱导的血小板减少症(HIT)的免疫形式是肝素治疗中一种潜在的危及生命的不良反应。它由血小板因子4(PF4)-肝素-IgG组成的多分子复合物介导,该复合物通过血小板Fcγ受体与血小板结合。多个Fcγ受体的交联导致血小板活化、血小板聚集和凝血酶生成增加,从而增加发生新血栓形成的风险。在儿童中,关于HIT的数据很少。这篇文献综述报告了8名年龄在3个月至15岁的儿童和14名患有HIT的新生儿。此外,我们报告了1例用达那肝素钠治疗的新病例。血栓并发症为静脉血栓(n = 12)和动脉血栓(n = 15)。这些儿童接受肝素治疗的原因包括自发性血栓事件、严重心脏病或维持用于营养、采血和用药的血管内导管通畅。诊断为HIT后,他们进一步用阿司匹林、华法林、达那肝素钠、比伐卢定或低分子量肝素进行抗凝治疗。

结论

尽管新生儿和儿童中HIT的报道较少,但儿科医生应意识到儿童期HIT是肝素应用的潜在并发症。鉴于存在引发HIT原发性免疫反应的风险,肝素冲洗导管的广泛做法也应进行讨论。1999年,HIT患者进一步胃肠外抗凝的治疗选择是达那肝素钠(一种低分子量类肝素)和比伐卢定(一种直接凝血酶抑制剂)。

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