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妊娠期止血参考区间。

Haemostatic reference intervals in pregnancy.

机构信息

Department of Clinical Biochemistry, Gentofte Hospital, University of Copenhagen, Denmark.

出版信息

Thromb Haemost. 2010 Apr;103(4):718-27. doi: 10.1160/TH09-10-0704. Epub 2010 Feb 19.

DOI:10.1160/TH09-10-0704
PMID:20174768
Abstract

Haemostatic reference intervals are generally based on samples from non-pregnant women. Thus, they may not be relevant to pregnant women, a problem that may hinder accurate diagnosis and treatment of haemostatic disorders during pregnancy. In this study, we establish gestational age-specific reference intervals for coagulation tests during normal pregnancy. Eight hundred one women with expected normal pregnancies were included in the study. Of these women, 391 had no complications during pregnancy, vaginal delivery, or postpartum period. Plasma samples were obtained at gestational weeks 13-20, 21-28, 29-34, 35-42, at active labor, and on postpartum days 1 and 2. Reference intervals for each gestational period using only the uncomplicated pregnancies were calculated in all 391 women for activated partial thromboplastin time (aPTT), fibrinogen, fibrin D-dimer, antithrombin, free protein S, and protein C and in a subgroup of 186 women in addition for prothrombin time (PT), Owren and Quick PT, protein S activity, and total protein S and coagulation factors II, V, VII, VIII, IX, X, XI, and XII. The level of coagulation factors II, V, X, XI, XII and antithrombin, protein C, aPTT, PT remained largely unchanged during pregnancy, delivery, and postpartum and were within non-pregnant reference intervals. However, levels of fibrinogen, D-dimer, and coagulation factors VII, VIII, and IX increased markedly. Protein S activity decreased substantially, while free protein S decreased slightly and total protein S was stable. Gestational age-specific reference values are essential for the accurate interpretation of a subset of haemostatic tests during pregnancy, delivery, and puerperium.

摘要

止血参考区间通常基于非孕妇的样本。因此,它们可能与孕妇无关,这可能会妨碍怀孕期间止血障碍的准确诊断和治疗。在这项研究中,我们建立了正常妊娠期间凝血试验的特定于妊娠龄的参考区间。801 名预期正常妊娠的女性被纳入研究。其中 391 名女性在妊娠、阴道分娩或产后期间没有并发症。在妊娠 13-20 周、21-28 周、29-34 周、35-42 周、活跃分娩时以及产后第 1 和第 2 天采集血浆样本。在所有 391 名无并发症妊娠的女性中,计算了每个妊娠期间仅使用无并发症妊娠的活化部分凝血活酶时间(aPTT)、纤维蛋白原、纤维蛋白 D-二聚体、抗凝血酶、游离蛋白 S 和蛋白 C 的参考区间,在另外 186 名女性亚组中还计算了凝血酶原时间(PT)、Owren 和 Quick PT、蛋白 S 活性以及总蛋白 S 和凝血因子 II、V、VII、VIII、IX、X、XI 和 XII 的参考区间。凝血因子 II、V、X、XI、XII 和抗凝血酶、蛋白 C、aPTT、PT 在妊娠、分娩和产褥期基本保持不变,且在非妊娠参考区间内。然而,纤维蛋白原、D-二聚体和凝血因子 VII、VIII 和 IX 的水平显著增加。蛋白 S 活性显著下降,而游离蛋白 S 略有下降,总蛋白 S 稳定。妊娠、分娩和产褥期特定于妊娠龄的参考值对于准确解释这组凝血试验至关重要。

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