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输注浓缩物所诱导的超正常抗凝血酶III水平在急性早幼粒细胞白血病中对抑制凝血酶生成无效。

Supranormal antithrombin III levels induced by concentrate administration are ineffective in quenching thrombin generation in acute promyelocytic leukemia.

作者信息

Rodeghiero F, Castaman G, Gugliotta L, Mattioli Belmonte M, Falanga A, Bottasso B, Barbui T, Mannucci P M

机构信息

Department of Hematology, San Bortolo Hospital, Vicenza, Italy.

出版信息

Thromb Res. 1993 Feb 15;69(4):377-85. doi: 10.1016/0049-3848(93)90037-o.

Abstract

Coagulation abnormalities occurring in patients with acute promyelocytic leukemia (APL) are partially corrected by heparin administration. This study was undertaken to verify if "supra-normal" levels of antithrombin III (AT-III) are similarly able to quench intravascular thrombin generation triggered by APL cells. Eight patients with APL were randomly assigned to receive either 50 U/kg (Group A) or 100 U/kg (Group B) of an AT-III concentrate, starting on the first day of chemotherapy and continuing for 7 days thereafter. Fibrinopeptide A (FPA), prothrombin fragment F1+2 and thrombin-AT III complexes, measured before and 15 minutes after each AT-III infusion, decreased significantly after each infusion, but the effect was minimal and short-lived, despite the achievement of post-infusion levels of AT-III activity well above 150% (Group A) or 200% (Group B). Small amounts of heparin were consistently detected in AT-III concentrates and post-infusion plasma samples. The short-lived quenching of thrombin generation after AT-III concentrate could be partially explained by the infusion of heparin, rather than by supranormal AT-III levels.

摘要

急性早幼粒细胞白血病(APL)患者出现的凝血异常可通过给予肝素得到部分纠正。本研究旨在验证“超正常”水平的抗凝血酶III(AT-III)是否同样能够抑制由APL细胞引发的血管内凝血酶生成。8例APL患者被随机分配,从化疗第一天开始接受50 U/kg(A组)或100 U/kg(B组)的AT-III浓缩物,并持续7天。在每次输注AT-III之前和之后15分钟测量的纤维蛋白肽A(FPA)、凝血酶原片段F1+2和凝血酶-AT III复合物,在每次输注后均显著降低,但尽管输注后AT-III活性水平远高于150%(A组)或200%(B组),其效果仍微乎其微且持续时间短。在AT-III浓缩物和输注后血浆样本中始终检测到少量肝素。AT-III浓缩物后凝血酶生成的短暂抑制可能部分是由于肝素的输注,而非超正常的AT-III水平。

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