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更新后的指导意见:围产期 B 族链球菌感染的预防和管理。

Updated Guidance: Prevention and Management of Perinatal Group B Infection.

机构信息

Division of Neonatology and.

Center for Pediatric Clinical Effectiveness, Children's Hospital of Philadelphia, Philadelphia, PA.

出版信息

Neoreviews. 2021 Mar;22(3):e177-e188. doi: 10.1542/neo.22-3-e177.

Abstract

Group B (GBS) remains the most common cause of neonatal early-onset sepsis among term infants and a major cause of late-onset sepsis among both term and preterm infants. The American Academy of Pediatrics and the American College of Obstetricians and Gynecologists published separate but aligned guidelines in 2019 and 2020 for the prevention and management of perinatal GBS disease. Together, these replace prior consensus guidelines provided by the Centers for Disease Control and Prevention. Maternal intrapartum antibiotic prophylaxis based on antenatal screening for GBS colonization remains the primary recommended approach to prevent perinatal GBS disease, though the optimal window for screening is changed to 36 0/7 to 37 6/7 weeks of gestation rather than beginning at 35 0/7 weeks' gestation. Penicillin, ampicillin, or cefazolin are recommended for prophylaxis, with clindamycin and vancomycin reserved for cases of significant maternal penicillin allergy. Pregnant women with a history of penicillin allergy are now recommended to undergo skin testing, because confirmation of or delabeling from a penicillin allergy can provide both short- and long-term health benefits. Aligned with the American Academy of Pediatrics recommendations for evaluating newborns for all causes of early-onset sepsis, separate consideration should be given to infants born at less than 35 weeks' and more than or equal to 35 weeks' gestation when performing GBS risk assessment. Empiric antibiotics are recommended for infants at high risk for GBS early-onset disease. Although intrapartum antibiotic prophylaxis is effective in preventing GBS early-onset disease, currently there is no approach for the prevention of GBS late-onset disease.

摘要

B 组链球菌(GBS)仍然是足月婴儿早发性新生儿败血症的最常见原因,也是足月和早产儿晚发性败血症的主要原因。美国儿科学会和美国妇产科医师学会在 2019 年和 2020 年分别发布了针对围产期 GBS 疾病预防和管理的单独但一致的指南。这些指南共同取代了疾病控制与预防中心提供的先前共识指南。基于 GBS 定植的产前筛查进行产时抗生素预防仍然是预防围产期 GBS 疾病的主要推荐方法,尽管筛查的最佳窗口已从 35 孕周提前至 36 周零 7 天至 37 周零 6 天。青霉素、氨苄西林或头孢唑啉被推荐用于预防,克林霉素和万古霉素保留用于有严重青霉素过敏的病例。现在建议对有青霉素过敏史的孕妇进行皮肤试验,因为青霉素过敏的确认或去标签可以提供短期和长期的健康益处。与美国儿科学会对所有早发性败血症病因评估新生儿的建议一致,在进行 GBS 风险评估时,应分别考虑出生胎龄小于 35 周和大于或等于 35 周的婴儿。对于 GBS 早发性疾病风险高的婴儿,建议使用经验性抗生素。虽然产时抗生素预防可有效预防 GBS 早发性疾病,但目前尚无预防 GBS 晚发性疾病的方法。

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