左旋硬化对经剖腹产出生的转基因婴儿脑电波活动形成的影响:公开随机试验的结果

Т. С. Тумаева, Лариса Александровна Балыкова, А. С. Моторкина
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引用次数: 1

摘要

新生儿的大脑活动影响出生后的适应,这种适应的紊乱会导致未成熟有机体的器官和系统的功能障碍,并在更遥远的成熟时期引起疾病的发展。目的:研究左卡尼汀对剖宫产足月儿脑电活动形成动态的影响。方法。该研究包括剖宫产分娩的足月婴儿(妊娠期38-40周),围生期伴有中枢神经系统缺氧损伤(脑缺血)。儿童被随机分为标准(推荐)治疗组和标准治疗组,左卡尼汀(加左卡尼汀)- 30%口服溶液,剂量为100mg /kg /天,从出生第7天开始,持续3周。采用脑电图(EEG)测定大鼠自然睡眠第3 ~ 6天、第3、6、12个月时的脑电活动。结果:45例患儿随机分为标准治疗组和标准治疗加左卡尼汀组,分别有44例和40例患儿完成了研究。最初,在接受左卡尼汀治疗的16/40(40%)儿童和实验组19/44(43%)儿童中检测到年龄相关脑活动的延迟形成(p = 0.767),在17(43%)和16 (36%)(p = 0.565)中检测到脑电图睡眠模式紊乱并产生背景异常(p = 0.565),在1(3%)和2(5%)儿童中检测到病理图元素(p = 0.536)。根据动态脑电图控制结果,1年后左卡尼汀组患儿脑功能障碍发生率较低,标准治疗组为32例(80%),对照组为42例(96%)(p = 0.028)。结论。在新生儿期给予左卡尼汀可降低在生命第一年结束时发生脑功能障碍的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Влияние левокарнитина на динамику формирования электробиологической активности головного мозга у доношенных детей, рожденных путем кесарева сечения: результаты открытого рандомизированного исследования
The brain activity of a newborn affects postnatal adaptation, the disorder of which can cause dysfunction of organs and systems of the immature organism and the development of diseases in more distant periods of maturation. Objective: Our aim was to study the effect of levocarnitine on dynamics of the brain bioelectrical activity formation in term infants delivered by cesarean section. Methods. The study included term infants (gestation period 38–40 weeks) delivered by cesarean section, with perinatal hypoxic lesion of the central nervous system (cerebral ischemia). Children were randomized into groups of standard (recommended) treatment and standard treatment enhanced with levocarnitine (plus levocarnitine) — 30% oral solution at a dose of 100 mg/kg per day for 3 weeks starting from the 7th day of life. The brain bioelectrical activity was assessed with electroencephalography (EEG) of the natural sleep period on the 3rd–6th day and then at 3, 6, and 12 months. Results. 45 children were randomized into groups of standard treatment and standard treatment plus levocarnitine, of which 44 and 40 children completed the study, respectively. Initially, the delayed formation of age-related brain activity was detected in 16/40 (40%) children receiving levocarnitine and in 19/44 (43%) in the experimental group (p = 0.767), disturbances in the EEG sleep pattern with generation of background anomalies — in 17 (43%) and 16 (36%) (p = 0.565), pathological graph elements — in 1 (3%) and 2 (5%) children (p = 0.536), respectively. According to the dynamic EEG control results, it was found that after 1 year the cerebral dysfunction was registered less frequently in children receiving levocarnitine — in 32 (80%) vs. 42 (96%) children in the group of standard treatment (p = 0.028). Conclusion. Adminisration of levocarnitine in the neonatal period reduces the risk of developing cerebral dysfunction by the end of the first year of life.
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