Perinatal consequences of innovative tactics for the treatment of recurrent miscarriage in isthmic-cervical insufficiency

R. Ismailov, A. Kaminskyi, K. Chaika, T. Kolomiichenko
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Abstract

Purpose - to improve the effectiveness of the treatment of miscarriage due to isthmic-cervical insufficiency (ICI) by using improved management tactics for women at high risk of ICI. Materials and methods. A two-stage innovating tactic for the treatment of miscarriage caused by ICI was proposed, including the prediction of the ineffectiveness of vaginal cerclage and the implementation of transabdominal cerclage in certain groups of patients. Starting from the pregravid stage, 30 women at risk of ICI were examined, which were conducted according to the developed scheme. 2 patients with a history of failed vaginal cerclage had abdominal cerclage prior to pregnancy and had not yet become pregnant at the time of writing. In 28 remaining women, the course and results of pregnancy were monitored. 3 patients after trachelectomy for cervical cancer were given abdominal cerclage in early pregnancy. 23 pregnant women were subjected to vaginal cerclage prophylactically or for sonographic or physical indications, these women constituted the main group for evaluating the effectiveness of the proposed treatment regimen for miscarriage in ICI. The comparison group consisted of 80 women with intravaginal cerclage, who were managed according to the protocols of the Ministry of Health of Ukraine. Results. The effectiveness of the proposed tactics for the treatment of miscarriage caused by ICI reflects the frequency of miscarriage and its structure. No cases of late miscarriages were observed. The rate of preterm birth significantly decreased from 37.5% to 21.7% (p<0.05), while no cases of early preterm birth (before 28 weeks) were observed. In the structure of miscarriage, 80.0% is the proportion of preterm births at 34-36 weeks of gestation (against 35.5%; p<0.05). The frequency of premature rupture of membranes decreased by 4 times (8.7% vs. 36.3%; p<0.05). The frequency of birth of children in a state of asphyxia decreased by more than 2 times (17.4% vs. 43.4%; p<0.05), and there was not a single case of birth in a state of severe asphyxia. The incidence of complications in the early neonatal period decreased by 20% (43.5% vs. 63.2%; p<0.05), mainly due to a decrease in the frequency of such dangerous complications as respiratory distress syndrome (13.0% vs. 31.6%; p<0.05) and disorders of central nervous system (17.4% vs. 44.7%; p<0.05). Conclusions. The use of the proposed tactics for the treatment of miscarriage caused by CI made it possible to significantly reduce the frequency of miscarriage and improve its structure, avoid cases of spontaneous miscarriages and neonatal deaths, improve the condition of newborns, which makes it possible to recommend the introduction of this tactic in the practical work of obstetric and gynecological institutions. The research was carried out in accordance with the principles of the Helsinki Declaration. The study protocol was approved by the Local Ethics Committee of the participating institution. The informed consent of the patient was obtained for conducting the studies. No conflict of interests was declared by the authors.
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缺血性-宫颈功能不全复发性流产治疗的创新策略对围产期的影响
目的:通过改进对高危妇女缺血性宫颈功能不全(ICI)的管理策略,提高治疗ICI流产的有效性。材料和方法。提出了一种治疗ICI所致流产的两阶段创新策略,包括预测阴道环扎术无效,以及在特定患者群体中实施经腹环扎术。从孕前阶段开始,根据制定的方案对30名有ICI风险的妇女进行了检查。2例有阴道环扎失败史的患者妊娠前有腹部环扎,撰写本文时尚未怀孕。对其余28名妇女的妊娠过程和结果进行了监测。3例宫颈癌气管切除术后妊娠早期行腹部环扎术。23名孕妇预防性或出于超声或生理适应症行阴道环扎术,这些妇女构成了评估ICI流产治疗方案有效性的主要群体。对照组由80名阴道内结扎的妇女组成,根据乌克兰卫生部的规程对她们进行管理。结果。所提出的治疗ICI引起的流产的策略的有效性反映了流产的频率及其结构。未观察到晚期流产病例。早产率由37.5%降至21.7% (p<0.05),未见早期早产(28周前)发生。在流产的结构中,34-36周早产的比例为80.0%(对35.5%;p < 0.05)。胎膜早破的发生率降低了4倍(8.7% vs. 36.3%;p < 0.05)。在窒息状态下出生的孩子的频率下降了2倍以上(17.4%比43.4%;P <0.05),无一例新生儿处于严重窒息状态。新生儿早期并发症发生率下降20% (43.5% vs. 63.2%;P <0.05),主要是由于呼吸窘迫综合征等危险并发症的发生率降低(13.0%比31.6%;P <0.05)和中枢神经系统疾病(17.4% vs. 44.7%;p < 0.05)。结论。采用拟议的策略来治疗产后流产,可以大大减少流产的频率并改善其结构,避免自然流产和新生儿死亡的情况,改善新生儿的状况,因此有可能建议在产科和妇科机构的实际工作中采用这一策略。这项研究是按照《赫尔辛基宣言》的原则进行的。研究方案经参与机构当地伦理委员会批准。获得患者的知情同意进行研究。作者未声明存在利益冲突。
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