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产时β-内酰胺类抗生素预防 B 族链球菌早发型疾病:我们能否摒弃“产时抗生素预防不足”的概念?

Intrapartum beta-lactam antibiotics for preventing group B streptococcal early-onset disease: can we abandon the concept of 'inadequate' intrapartum antibiotic prophylaxis?

机构信息

Neonatal Intensive Care Unit, Women's and Children's Health Department, Azienda Ospedaliera, University of Modena and Reggio Emilia, Modena, Italy.

Pediatric Post-graduate School, University of Modena and Reggio Emilia, Modena, Italy.

出版信息

Expert Rev Anti Infect Ther. 2020 Jan;18(1):37-46. doi: 10.1080/14787210.2020.1697233. Epub 2019 Dec 6.

Abstract

: Neonatal sepsis remains a serious and potentially fatal illness. Intrapartum antibiotic prophylaxis (IAP) prevents group B streptococcal (GBS) early-onset sepsis. The optimal duration of IAP (adequate IAP) to reduce vertical transmission of GBS has been debated. Understanding the mechanism of action of IAP may help in minimizing neonatal evaluation and unnecessary antibiotic use.: In recent years, several studies on pharmacokinetics and clinical use of IAP have been published. Although penicillin and ampicillin are the most preferred antibiotics, the clinical efficacy of non-beta-lactam antibiotics, including clindamycin and vancomycin, used in cases of penicillin anaphylaxis-associated allergy, remains debatable. This is a narrative review of the literature regarding the impact of 'inadequate' IAP on the clinical management of women and newborns.: Recent evidence suggests that 'inadequate' IAP with beta-lactams is more effective in preventing vertical transmission of GBS than previously thought. Newborns exposed to intrapartum beta-lactams and who are asymptomatic at birth are likely uninfected, irrespective of IAP duration before delivery. Hence, we may abandon the concept of 'inadequate' IAP with beta-lactams in early-onset GBS sepsis, relying primarily on clinical signs observed at birth for managing IAP-exposed neonates.

摘要

新生儿败血症仍然是一种严重且潜在致命的疾病。产时抗生素预防(IAP)可预防 B 组链球菌(GBS)早发性败血症。为减少 GBS 的垂直传播而争论的是 IAP 的最佳持续时间(足够的 IAP)。了解 IAP 的作用机制可能有助于最大限度地减少新生儿评估和不必要的抗生素使用。

近年来,已经发表了几项关于 IAP 的药代动力学和临床应用的研究。虽然青霉素和氨苄西林是最优选的抗生素,但在青霉素过敏相关过敏的情况下使用的非β-内酰胺类抗生素(包括克林霉素和万古霉素)的临床疗效仍然存在争议。这是对文献的叙述性综述,涉及“不充分”的 IAP 对妇女和新生儿临床管理的影响。

最近的证据表明,与以前认为的相比,β-内酰胺类药物的“不充分”IAP 更有效地预防 GBS 的垂直传播。在出生时无症状的暴露于产时β-内酰胺类药物的新生儿,无论分娩前 IAP 持续时间如何,都可能未被感染。因此,我们可能会放弃β-内酰胺类药物治疗早发性 GBS 败血症中“不充分”IAP 的概念,主要依靠出生时观察到的临床体征来管理 IAP 暴露的新生儿。

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