Stine Yde Nielsen, Elke Hoffmann-Lücke, Tine Brink Henriksen, Camilla Mirian Hartvigsen, Rikke Bek Helmig, Mohammed Rohi Khalil, Jens Kjølseth Møller, Lars Henning Pedersen, May Murra, Eva Greibe
{"title":"产前预防性青霉素预防早发 B 组链球菌病的时机和剂量:评估母体和脐带血的浓度。","authors":"Stine Yde Nielsen, Elke Hoffmann-Lücke, Tine Brink Henriksen, Camilla Mirian Hartvigsen, Rikke Bek Helmig, Mohammed Rohi Khalil, Jens Kjølseth Møller, Lars Henning Pedersen, May Murra, Eva Greibe","doi":"10.1136/archdischild-2024-326986","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Timing of administration of antibiotics and concentrations in maternal blood and the umbilical cord blood are important prerequisites for optimal intrapartum antibiotic prophylaxis (IAP) of neonatal early-onset group B streptococcus (GBS) disease. This cohort study aimed to explore penicillin concentrations in mothers and infants at birth in relation to time elapsed from administration to delivery and to the minimal inhibitory concentration (MIC) for GBS.</p><p><strong>Main outcome measures: </strong>Penicillin G concentrations in maternal and umbilical cord blood in relation to time and dose from administration to time of delivery.</p><p><strong>Results: </strong>In 44 mother-infant dyads, median maternal penicillin G concentration was 0.2 mg/L (IQR 0-0.8 mg/L; range 0-1.6 mg/L). Median infant penicillin G concentration was 1.2 mg/L (IQR 0.5-5.0 mg/L; range 0-12.7 mg/L). In all infants (N=38) born less than 4 hours after the latest IAP administration, penicillin G concentrations far exceeded MIC (0.125 mg/L), even after short time intervals between IAP administration and birth. 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引用次数: 0
摘要
目的:抗生素的给药时机以及母体血液和脐带血中的浓度是对新生儿早发型乙型链球菌(GBS)疾病进行最佳产前抗生素预防(IAP)的重要前提。这项队列研究旨在探讨出生时母婴体内的青霉素浓度与从用药到分娩的时间以及对 GBS 的最小抑菌浓度 (MIC) 的关系:产妇和脐带血中青霉素 G 的浓度与从用药到分娩的时间和剂量的关系:44对母婴中,母体青霉素G浓度中位数为0.2毫克/升(IQR为0-0.8毫克/升;范围为0-1.6毫克/升)。婴儿青霉素 G 浓度中位数为 1.2 毫克/升(IQR 0.5-5.0 毫克/升;范围 0-12.7 毫克/升)。在最近一次注射 IAP 后不到 4 小时出生的所有婴儿(38 人)中,青霉素 G 的浓度都远远超过了 MIC 值(0.125 mg/L),即使注射 IAP 和出生之间的间隔时间很短也是如此。在 44 对母婴组合中,母婴体内的青霉素 G 浓度与婴儿体内的青霉素 G 浓度相比非常低;特别是在 20 个只服用过一次 IAP 的婴儿体内,青霉素 G 浓度非常高:结论:在注射 IAP 后不到 4 小时出生的婴儿的脐带血中发现了高浓度的青霉素 G,远高于 GBS 的 MIC 值。
Timing and dosage of intrapartum prophylactic penicillin for preventing early-onset group B streptococcal disease: assessing maternal and umbilical cord blood concentration.
Objective: Timing of administration of antibiotics and concentrations in maternal blood and the umbilical cord blood are important prerequisites for optimal intrapartum antibiotic prophylaxis (IAP) of neonatal early-onset group B streptococcus (GBS) disease. This cohort study aimed to explore penicillin concentrations in mothers and infants at birth in relation to time elapsed from administration to delivery and to the minimal inhibitory concentration (MIC) for GBS.
Main outcome measures: Penicillin G concentrations in maternal and umbilical cord blood in relation to time and dose from administration to time of delivery.
Results: In 44 mother-infant dyads, median maternal penicillin G concentration was 0.2 mg/L (IQR 0-0.8 mg/L; range 0-1.6 mg/L). Median infant penicillin G concentration was 1.2 mg/L (IQR 0.5-5.0 mg/L; range 0-12.7 mg/L). In all infants (N=38) born less than 4 hours after the latest IAP administration, penicillin G concentrations far exceeded MIC (0.125 mg/L), even after short time intervals between IAP administration and birth. The highest plasma concentrations were reached in umbilical cord blood within 1 hour from IAP administration to birth.For 44 mother-infant dyads, maternal concentrations were very low compared with their infants'; particularly, very high concentrations were seen in the 20 infants with only one dose of IAP.
Conclusion: High concentrations of penicillin G were found in umbilical cord blood of infants born less than 4 hours after IAP administration, well above the MIC for GBS.
期刊介绍:
Archives of Disease in Childhood is an international peer review journal that aims to keep paediatricians and others up to date with advances in the diagnosis and treatment of childhood diseases as well as advocacy issues such as child protection. It focuses on all aspects of child health and disease from the perinatal period (in the Fetal and Neonatal edition) through to adolescence. ADC includes original research reports, commentaries, reviews of clinical and policy issues, and evidence reports. Areas covered include: community child health, public health, epidemiology, acute paediatrics, advocacy, and ethics.