Miller Connie H
Division of Hereditary Blood Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia 30345, USA.
Clin Obstet Gynecol. 2006 Dec;49(4):844-9. doi: 10.1097/01.grf.0000211953.59336.94.
Diagnosis of thrombotic disorders depends on the performance of a panel of laboratory tests for individual components of the coagulation mechanism. Although genetic tests are simple and accurate, most disorders still require functional or immunologic tests for diagnosis. Tests for the most important thrombotic defects are described. These tests may be significantly altered by pregnancy, hormones, thrombotic events, systemic illness, and anticoagulant therapy. These changes make some thrombotic disorders difficult to diagnose during pregnancy. Testing before pregnancy for women with a personal or family history of thrombosis will simplify the interpretation.
血栓形成性疾病的诊断依赖于针对凝血机制各个组成部分进行一系列实验室检查。尽管基因检测简单且准确,但大多数疾病的诊断仍需要功能或免疫检测。文中描述了针对最重要的血栓形成缺陷的检测。这些检测可能会因妊娠、激素、血栓形成事件、全身性疾病及抗凝治疗而发生显著改变。这些变化使得某些血栓形成性疾病在孕期难以诊断。对于有个人或家族血栓形成病史的女性,在孕前进行检测将简化结果的解读。