Monitoring the puerperium microbiota is a necessary condition for diagnosing newborn infections in the early neonatal period

L. Boronina, E. V. Samatova, A. G. Asnovskaya, S. Panova, S. S. Ustyugova, K.V. Zakharchuk
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Abstract

Background: maternal and child healthcare is considered a priority area of the public health services in all countries. Aim: to assess the birth canal microbiota in pregnant women and puerperia for diagnosing potential infections of newborn infants in the early neonatal period. Patients and Methods: this retrospective study analyses the results of microbiological examination of the samples taken from various loci of 1915 pregnant women and/or puerperia and newborn infants in the period of February 1, 2020, to February 28, 2022. The biological material samples for microbiological examination were obtained from the following locations: 1) in the pregnant women and/or puerperia: the posterior vaginal vault, cervical canal, afterbirth, and the uterine cavity; 2) in the newborn infants: the blood, cerebrospinal fluid, tracheal secretions, and the catheter Results: in 38.1% of puerperia, the caesarean section was performed to deliver a baby. In 513 (26.8%) women in labor and their newborns, microbiological tests were not carried out, as they did not have clinical manifestations of infectious diseases. Based on the monitoring of the results of microbiological examination of the biomaterial samples taken from various loci, the following three groups were formed: group 1 — the samples were taken only from the newborns (n=458); group 2 — the samples were taken only from the mothers (n=294); group 3 — the samples were taken both from the mothers and newborns (n=650). Then, group 3 was divided into the following subgroups: the growth of microorganisms was not detected or the normal flora was found (n=459); the potential causative agents of infectious and inflammatory diseases were found in the mother, but not in the newborn (n=161); the same potential causative agents of infectious and inflammatory diseases were detected in the newborn and the mother (n=19); different potential causative agents of infectious and inflammatory diseases were found in the newborn and the mother (n=6); potential causative agents of infectious and inflammatory diseases were detected in the newborns, but not in the mothers (n=5). Escherichia coli (31.6%) and Streptococcus agalactiae (15.7%) were the most prevalent microorganisms in the birth canal of the pregnant women and puerperia. In the newborns, the same agents were most frequently found in the blood or the tracheal secretions. Conclusion: the microbiological monitoring of the birth canal of pregnant women and puerperia, as well as of newborn infants is necessary for a timely prevention or treatment of infectious diseases. KEYWORDS: monitoring, microbiota, puerperia, newborns, infection, bacterial carriage. FOR CITATION: Boronina L.G., Samatova E.V., Asnovskaya A.G. et al. Monitoring the puerperium microbiota is a necessary condition for diagnosing newborn infections in the early neonatal period. Russian Journal of Woman and Child Health. 2023;6(1):13–19 (in Russ.). DOI: 10.32364/2618-8430-2023-6-1-13-19.
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监测产褥期微生物群是诊断新生儿早期感染的必要条件
背景:妇幼保健被认为是所有国家公共卫生服务的一个优先领域。目的:评估孕妇和产褥期产道微生物群对新生儿早期潜在感染的诊断价值。患者和方法:本回顾性研究分析了2020年2月1日至2022年2月28日期间从1915名孕妇和/或产褥期和新生儿的不同位点采集的样本的微生物学检查结果。微生物学检查的生物材料样本取自以下部位:1)孕妇和/或产褥期:阴道后穹窿、子宫颈管、产后和子宫腔;2)新生儿:血液、脑脊液、气管分泌物、导管结果:38.1%的产褥者行剖宫产。513名(26.8%)分娩妇女及其新生儿没有进行微生物检测,因为她们没有传染病的临床表现。根据对各基因座采集的生物材料样本的微生物学检测结果的监测,将其分为以下三组:1组-仅采集新生儿样本(n=458);第2组-仅从母亲身上采集样本(n=294);第三组-样本取自母亲和新生儿(n=650)。然后将第3组分为以下亚组:未检测到微生物生长或发现正常菌群(n=459);在母亲中发现了感染性和炎症性疾病的潜在病原体,但在新生儿中没有发现(n=161);在新生儿和母亲身上检测到相同的感染性和炎症性疾病的潜在病原体(n=19);在新生儿和母亲身上发现了不同的感染性和炎症性疾病的潜在病原体(n=6);在新生儿中检测到传染性和炎症性疾病的潜在病原体,但在母亲中未检测到(n=5)。孕妇和产褥期产道中最常见的微生物为大肠杆菌(31.6%)和无乳链球菌(15.7%)。在新生儿中,同样的物质最常出现在血液或气管分泌物中。结论:对孕妇、产褥期及新生儿产道进行微生物监测是及时预防或治疗传染病的必要措施。关键词:监测,微生物群,产褥期,新生儿,感染,细菌携带。引文:Boronina l.g., Samatova e.v., Asnovskaya A.G.等。监测产褥期微生物群是诊断新生儿早期感染的必要条件。俄罗斯妇女与儿童健康杂志。2023;6(1):13-19。DOI: 10.32364 / 2618-8430-2023-6-1-13-19。
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CiteScore
0.60
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0.00%
发文量
14
审稿时长
12 weeks
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