Dłuski Dominik, Mierzyński Radzisław, Poniedziałek-Czajkowska Elżbieta, Leszczyńska-Gorzelak Bożena
Chair and Department of Obstetrics and Perinatology, Medical University of Lublin, Street: Jaczewskiego 8, 20-954 Lublin, Poland.
Chair and Department of Obstetrics and Perinatology, Medical University of Lublin, Lublin, Poland.
J Perinat Med. 2018 May 24;46(4):411-417. doi: 10.1515/jpm-2017-0059.
(1) To evaluate the prevalence of inherited thrombophilia in pregnant women with adverse pregnancy outcomes: intrauterine growth retardation (IUGR), preeclampsia (PE) and placental abruption. (2) To assess the impact of inherited thrombophilia on the nature of obstetric complications. (3) To assess levels of protein S, protein C, antithrombin III and homocysteine in pregnant women with adverse pregnancy outcomes.
The study comprised 162 pregnant women. The patients were divided into three test groups and one control group. In all 162 patients the following tests were completed: activated protein C resistance (APC-R), the level of free protein S, activity of protein C, antithrombin III and the level of homocysteine. The data were statistically analyzed via χ2 of independence or homogeneity test.
In 32 of 162 patients participating in clinical research thrombophilia was diagnosed (10 patients with APC-R, 21 patients with protein S deficiency, one patient with hyperhomocysteinemia): seven patients belonged to the control group and 25 patients had diagnosed adverse pregnancy outcomes (P=0.04). In 32 patients with diagnosed thrombophilia, level of protein S was decreased (P=0.04). Protein S deficiency was diagnosed, when level of protein S was lower than 30% in the second trimester and lower than 24% in the third trimester. The incidence of activated protein C resistance caused by the mutation of factor V Leiden was in six patients (5.9%) with adverse pregnancy outcomes, and in four patients (6.6%) from the control group. Results were not statistically significant. No protein C deficiency was diagnosed (diagnosis: level<60%), but in 50% of patients with thrombophilia level of protein C was over the norm (P=0.02). The level of antithrombin III was often decreased in patients with preeclampsia - (32.4%), then in the other patients - (17.2%) (P=0.04), but no patient was diagnosed with antithrombin III deficiency (diagnosis: level<60%).
Tests for thrombophilia should be carried out in women with adverse pregnancy outcomes in their history, who are planning pregnancy, to start anticoagulant prophylaxis. Our study supports the thesis that tests for thrombophilia should be carried out in women with a history of adverse pregnancy outcomes and who are planning a pregnancy to start anticoagulant prophylaxis.
(1)评估有不良妊娠结局的孕妇(宫内生长受限、先兆子痫和胎盘早剥)遗传性易栓症的患病率。(2)评估遗传性易栓症对产科并发症性质的影响。(3)评估有不良妊娠结局的孕妇中蛋白S、蛋白C、抗凝血酶III和同型半胱氨酸的水平。
该研究纳入162名孕妇。患者被分为三个试验组和一个对照组。对所有162名患者完成了以下检查:活化蛋白C抵抗(APC-R)、游离蛋白S水平、蛋白C活性、抗凝血酶III和同型半胱氨酸水平。通过独立性或同质性检验的χ2对数据进行统计学分析。
在参与临床研究的162名患者中,有32名被诊断为易栓症(10名APC-R患者,21名蛋白S缺乏患者,1名高同型半胱氨酸血症患者):7名患者属于对照组,25名患者有诊断明确的不良妊娠结局(P = 0.04)。在32名诊断为易栓症的患者中,蛋白S水平降低(P = 0.04)。当蛋白S水平在孕中期低于30%且在孕晚期低于24%时,诊断为蛋白S缺乏。由莱顿V因子突变引起的活化蛋白C抵抗发生率在有不良妊娠结局的6名患者(5.9%)和对照组的4名患者(6.6%)中。结果无统计学意义。未诊断出蛋白C缺乏(诊断标准:水平<60%),但在50%的易栓症患者中,蛋白C水平高于正常(P = 0.02)。先兆子痫患者中抗凝血酶III水平常降低 - (32.4%),其他患者中 - (17.2%)(P = 0.04),但无患者被诊断为抗凝血酶III缺乏(诊断标准:水平<60%)。
对于有不良妊娠史且计划怀孕的女性,应进行易栓症检测,以便开始抗凝预防。我们的研究支持这样的论点,即对于有不良妊娠史且计划怀孕的女性,应进行易栓症检测,以便开始抗凝预防。