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纯合子β地中海贫血的凝血筛查试验及凝血因子

Screening coagulation tests and clotting factors in homozygous beta-thalassemia.

作者信息

Caocci L, Alberti M, Burrai P, Corda R

出版信息

Acta Haematol. 1978;60(6):358-64. doi: 10.1159/000207735.

Abstract

In 30 children with homozygous beta-thalassemia the hemostasis screening tests (bleeding time, PT, PTT), platelet count and specific assays of clotting factors were carried out 25 days after their last transfusion. PT, PTT, and bleeding time showed minor variations; considerable thrombocytosis was found in splenectomized patients. Factors IX and XII were decreased in a high proportion of patients, the vitamin K-dependent factors (II, VII, IX, X) were slightly reduced and factors I, V and VIII remained within the normal range in a majority of patients. Hepatic failure resulting in defective protein synthesis does not explain the more marked impairment of factors XI and XII, which might be secondary to activation of the intrinsic coagulation and/or kallikrein systems following intravascular haemolysis and multiple blood transfusions.

摘要

对30名纯合子β地中海贫血患儿在末次输血25天后进行了止血筛查试验(出血时间、PT、PTT)、血小板计数及凝血因子特异性检测。PT、PTT和出血时间变化较小;脾切除患者出现明显的血小板增多。大部分患者的因子IX和XII降低,维生素K依赖因子(II、VII、IX、X)略有降低,多数患者的因子I、V和VIII仍在正常范围内。导致蛋白质合成缺陷的肝功能衰竭并不能解释因子XI和XII更明显的损害,这可能继发于血管内溶血和多次输血后内源性凝血和/或激肽释放酶系统的激活。

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