激素避孕对止血系统的影响

E. Kudinova
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During COCs intake, an increase in the fibrinogen content was noted in patients of both groups, which, however, did not exceed the reference values. During the correlation analysis, it was found that in groups 1 and 2, the parameters of the fibrinogen baseline, D-dimer and the corresponding indicators after 1 month of COCs intake had a strong correlation with each other (r=0.845, r=0.864). However, group 1 had higher levels of fibrinogen and fibrin degradation products (D-dimer) (p<0.0001) versus those in group 2. The study on the trend of prothrombin time (PTT) and activated partial thromboplastin time (APTT) during COCs intake in female patients with HA and UCTD revealed an acceleration of indicators (p<0.01) versus those before COCs intake. At the same time, the change in blood clotting markers was not realized by episodes of thrombosis in any of the patients. Conclusion: patients with UCTD had changes that characterized the activation of thrombogenesis. 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引用次数: 0

摘要

目的:研究合并口服避孕药(COC)的女性高雄激素症(HA)和月经紊乱(MDs)患者在有无未分化结缔组织增生(UCTD)情况下的止血指标。患者与方法:研究结果将28例HA和MDs女性患者分为2组:1 ~ 22例(平均年龄22.1±3.2岁)合并UCTD患者,2 ~ 6例(平均年龄20.5±1.8岁)未合并UCTD患者。测定各组患者月经第2 ~ 3天血液中激素含量、服用COCs 1个月前后的止血参数及同型半胱氨酸水平。结果:分析显示血小板活化标志物、凝血联和纤溶水平升高。在摄入COCs期间,两组患者的纤维蛋白原含量均有所增加,但未超过参考值。相关性分析发现,1、2组患者服用COCs 1个月后纤维蛋白原基线、d -二聚体参数及相应指标之间存在较强相关性(r=0.845, r=0.864)。然而,与2组相比,1组的纤维蛋白原和纤维蛋白降解产物(d -二聚体)水平更高(p<0.0001)。对HA和UCTD女性患者服用COCs时凝血酶原时间(PTT)和活化部分凝血活素时间(APTT)变化趋势的研究显示,与服用COCs前相比,这些指标均有所加速(p<0.01)。与此同时,任何患者的血栓发作都没有实现凝血标志物的变化。结论:UCTD患者具有以血栓形成激活为特征的改变。当计划激素避孕时,有必要挑选出一组HA和UCTD症状的女性患者,因为他们最容易发生血栓形成事件。关键词:高雄激素,联合口服避孕药,血栓形成,结缔组织发育不良,高同型半胱氨酸血症。引用本文:库丁诺娃(库丁诺娃):激素避孕对止血系统的影响。俄罗斯妇女与儿童健康杂志。2023;6(2):130-137。DOI: 10.32364 / 2618-8430-2023-6-2-130-137。
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Hormonal contraception in terms of effect on the hemostasis system
Aim: to study the hemostasis indicators in female patients with hyperandrogenism (HA) and menstrual disorders (MDs) during combined oral contraceptive (COC) intake, depending on the presence of undifferentiated connective tissue displasia (UCTD). Patients and Methods: the study results of 28 female patients with HA and MDs were divided into 2 groups: group 1 — 22 patients (mean age 22.1±3.2 years) with UCTD, group 2 — 6 patients (mean age 20.5±1.8 years) without UCTD. The content of hormones in the blood (on the 2nd–3rd day of the menstrual period), the parameters of hemostasis before and after 1 month of COCs intake, and the level of homocysteine were determined in all patients. Results: the analysis revealed an increase in the levels of platelet activation markers, coagulation link and fibrinolysis. During COCs intake, an increase in the fibrinogen content was noted in patients of both groups, which, however, did not exceed the reference values. During the correlation analysis, it was found that in groups 1 and 2, the parameters of the fibrinogen baseline, D-dimer and the corresponding indicators after 1 month of COCs intake had a strong correlation with each other (r=0.845, r=0.864). However, group 1 had higher levels of fibrinogen and fibrin degradation products (D-dimer) (p<0.0001) versus those in group 2. The study on the trend of prothrombin time (PTT) and activated partial thromboplastin time (APTT) during COCs intake in female patients with HA and UCTD revealed an acceleration of indicators (p<0.01) versus those before COCs intake. At the same time, the change in blood clotting markers was not realized by episodes of thrombosis in any of the patients. Conclusion: patients with UCTD had changes that characterized the activation of thrombogenesis. When planning hormonal contraception, it is necessary to single out a group of female patients with HA and signs of UCTD as the most vulnerable in relation to an increased risk of thrombogenic events. KEYWORDS: hyperandrogenism, combined oral contraceptive, thrombosis, connective tissue dysplasia, hyperhomocysteinemia. FOR CITATION: Kudinova E.G. Hormonal contraception in terms of effect on the hemostasis system. Russian Journal of Woman and Child Health. 2023;6(2):130–137 (in Russ.). DOI: 10.32364/2618-8430-2023-6-2-130-137.
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CiteScore
0.60
自引率
0.00%
发文量
14
审稿时长
12 weeks
期刊最新文献
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