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先天性缺乏患者中的获得性因子XI抑制剂。

Acquired factor XI inhibitors in congenitally deficient patients.

作者信息

Schnall S F, Duffy T P, Clyne L P

机构信息

Department of Medicine, Yale University School of Medicine, New Haven, Connecticut.

出版信息

Am J Hematol. 1987 Dec;26(4):323-8. doi: 10.1002/ajh.2830260405.

Abstract

Four factor XI (F XI)-deficient patients are described, all of whom formed circulating anticoagulants against F X1. In the three most severely affected patients (F XI 0%-6% activity), the anticoagulant appeared to have been stimulated by plasma infusion. However, in the milder case (25% F XI activity), no infusion had been documented. The findings in these cases emphasize the diversity of F XI inhibitors in congenitally deficient patients. Awareness of the potential development of these inhibitors will be helpful in both daily management and perioperative care of such patients.

摘要

本文描述了4例因子XI(F XI)缺乏症患者,他们均形成了针对F X1的循环抗凝剂。在3例受影响最严重的患者(F XI活性为0%-6%)中,抗凝剂似乎是由血浆输注刺激产生的。然而,在症状较轻的病例(F XI活性为25%)中,没有记录到输注情况。这些病例的研究结果强调了先天性缺乏患者中F XI抑制剂的多样性。认识到这些抑制剂的潜在发展,将有助于对此类患者的日常管理和围手术期护理。

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