Methods of pharmacological correction of intrauterine growth restriction syndrome

O. I. Klycheva, A. B. Khuraseva
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Abstract

Aim . Comparative analysis of the effectiveness of pharmacological correction of intrauterine growth restriction syndrome (IGRS) by monotherapy with diosmin and dipiridamol. Materials and Methods. Retrospective and prospective examination of 80 pregnant women with singleton pregnancy with gestational age from 28 to 36 weeks with confirmed diagnosis of IGRS of 1 or 2 degree asymmetric form was conducted. 75.0% Of pregnant women that participated in the study, were of the average reproductive age (23-29 years of age). The share of young first-time-mother in I group was 10.0%, in II group – 15.0%, the share of age first-time-mothers was 17.5 and 10.0%, respectively. Extended history taking and history analysis, general clinical and obstetric-gynecological examination were conducted, laboratory and ultrasound methods were used. Newborns were evaluated on Apgar scale at birth and in 5 minutes. In the early neonatal period, inborn and transient pathological syndromes were evaluated. Results . In patients receiving diosmin (n=40), reduction  of the resistance index of the right and left uterine arteries  to 0.440±0.004 and 0.460±0.004, respectively,  and of the umbilical artery to 0.56±0.02 was achieved, that is lower than in the group of patients taking dipiridamol (n=40). A positive influence of diosmin on the intrauterine condition of the fetus was found that was manifested by its increased compensatory capacities for adaptation  to chronic hypoxia in reliably higher percent of cases as compared to dipiridamol. After pharmacological correction, a tendency to normalization of the main parameters of the system of hemostasis was found in higher percent in women taking diosmin. This, in turn, produced a favorable influence on the volume of blood loss in physiological deliveries. Thus, in I group the average amount of blood loss was 180±15 ml, while in II group it was 265±15 ml (р<0.05). However, in operative delivery no such differences were obtained. In I group immediately after deliveries 10.0% of newborns were transferred to the resuscitation and intensive care unit, in II group transfer to resuscitation department was required in 37.5% of infants (<0.05). All the rest of children immediately after birth in the satisfactory condition were placed to one ward with mother, and they did not require resuscitation measures.  Conclusion . Increase in the compensatory capacities of the fetus was shown in the conditions of chronic intrauterine hypoxia in a reliably higher percent of cases after pharmacological correction with diosmin. This, in turn, produced a favorable influence on perinatal outcomes, birth of children with a higher parameters of mass and height and health index.
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宫内生长受限综合征的药物矫正方法
的目标。地奥明与双吡达莫单药治疗宫内生长受限综合征(IGRS)疗效比较分析。材料与方法。对80例胎龄28 ~ 36周的单胎妊娠确诊为1度或2度不对称型IGRS的孕妇进行回顾性和前瞻性检查。参与研究的孕妇中有75.0%处于平均生育年龄(23-29岁)。1组中年轻初妈比例为10.0%,2组为15.0%,年龄初妈比例分别为17.5%和10.0%。采用化验室及超声检查方法,进行全面的临床及妇产科检查。新生儿在出生时和5分钟内用阿普加量表进行评估。在新生儿早期,评估先天性和短暂性病理综合征。结果。服用地奥司明的患者(n=40)右、左子宫动脉阻力指数分别降至0.440±0.004和0.460±0.004,脐动脉阻力指数降至0.56±0.02,均低于服用地奥司明组(n=40)。研究发现,地奥司明对胎儿的宫内状况有积极影响,表现为与地吡达莫相比,地奥司明对慢性缺氧适应的代偿能力增加,这一比例明显高于地吡达莫。药理学校正后,止血系统主要参数趋于正常化的趋势在服用地奥司明的妇女中有较高的百分比。这反过来又对生理分娩时的失血量产生了有利的影响。I组平均失血量为180±15 ml, II组平均失血量为265±15 ml (p <0.05)。然而,在手术分娩中没有这种差异。I组新生儿分娩后立即转复苏加护病房的比例为10.0%,II组新生儿需转复苏加护病房的比例为37.5%(<0.05)。其余出生后病情满意的患儿均与母亲同住一室,不需采取复苏措施。结论。增加代偿能力的胎儿显示在慢性宫内缺氧的条件下,在一个可靠的较高百分比的情况下,用地奥司明药理学纠正。这反过来又对围产期结果产生了有利的影响,出生的儿童具有较高的质量和身高参数以及健康指数。
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