Maternal Fetal Medicine Research Program, Department of Obstetrics and Gynecology, Perelman School of Medicine, University of Pennsylvania, Philadelphia.
Maternal Fetal Medicine Research Program, Department of Obstetrics and Gynecology, Perelman School of Medicine, University of Pennsylvania, Philadelphia.
Am J Obstet Gynecol. 2023 Dec;229(6):672.e1-672.e8. doi: 10.1016/j.ajog.2023.06.038. Epub 2023 Jun 21.
Rectovaginal colonization with Group B Streptococcus during pregnancy has historically been shown to be associated with an increased risk of clinical chorioamnionitis and peripartum infectious morbidity.
Newer observational data in the era of intrapartum antibiotic prophylaxis suggest a possible reversal of this association; however, it is unclear if this is related to differences in labor management for those with and without Group B Streptococcus colonization. We therefore sought to assess the association between intrapartum antibiotic prophylaxis for Group B Streptococcus colonization and clinical chorioamnionitis within the context of a randomized induction of labor trial with a standardized labor protocol.
We performed an exploratory secondary analysis of a randomized trial of patients undergoing term induction at a tertiary care center. Patients received third trimester Group B Streptococcus screening and intrapartum antibiotic prophylaxis as routine care. Group B Streptococcus detection was performed using a carrot broth-enhanced subculture to Group B Streptococcus Detect approach (Hardy Diagnostics, Santa Maria, CA). Labor management was protocolized per the trial. Patients with unknown Group B Streptococcus status or who did not receive intrapartum antibiotic prophylaxis, if indicated, were excluded. The primary outcome was diagnosis of clinical chorioamnionitis, compared between patients who received intrapartum antibiotic prophylaxis for known Group B Streptococcus positive status (by culture, history, or Group B Streptococcus bacteriuria) and those who were Group B Streptococcus negative and did not receive intrapartum antibiotic prophylaxis. Secondary outcomes included postpartum endometritis, wound infection, a composite maternal peripartum infectious morbidity, and neonatal outcomes.
A total of 491 patients were enrolled in the trial. Of these, 466 had a known Group B Streptococcus status and received or did not receive intrapartum antibiotic prophylaxis accordingly and were included in this analysis: 292 (62.7%) were Group B Streptococcus negative and did not receive intrapartum antibiotic prophylaxis, and 174 (37.3%) were Group B Streptococcus positive and received intrapartum antibiotic prophylaxis. The majority of patients were Non-Hispanic Black (78.1%) and nulliparous (59.7%). There were no differences in demographic, clinical, induction or labor characteristics between groups. Patients who were Group B Streptococcus positive had a 49% lower rate of clinical chorioamnionitis (8.1% vs 14.7%, odds ratio, 0.51; P=.03) and a lower rate of peripartum infectious morbidity (8.1% vs 15.8%, odds ratio, 0.47; P=.02) compared to those who were Group B Streptococcus negative. Infants born to patients who were Group B Streptococcus positive were significantly less likely to be admitted to the neonatal intensive care unit (3.4% vs 15.1%, P<.001).
Although Group B Streptococcus colonization has historically been considered a risk factor for clinical chorioamnionitis, in the era of universal antibiotic prophylaxis for Group B Streptococcus positive patients, our findings support the point that intrapartum antibiotic prophylaxis for Group B Streptococcus positivity is associated with lower rates of clinical chorioamnionitis and peripartum infectious morbidity among patients undergoing induction with protocolized labor management. These findings demonstrate that intrapartum antibiotic prophylaxis for Group B Streptococcus may protect against perinatal infectious morbidity, a phenomenon that warrants further investigation.
妊娠期间 B 组链球菌直肠阴道定植与临床绒毛膜羊膜炎和围产期感染性发病率增加有关。
在使用产时抗生素预防的时代,新的观察性数据表明这种关联可能发生逆转;然而,尚不清楚这是否与有和没有 B 组链球菌定植的患者在产时管理方面的差异有关。因此,我们试图评估 B 组链球菌定植患者接受产时抗生素预防与随机诱导分娩试验中临床绒毛膜羊膜炎之间的关联,该试验采用标准化产程方案。
我们对在三级保健中心进行足月诱导分娩的患者进行了一项随机试验的探索性二次分析。患者在孕晚期接受 B 组链球菌筛查和产时抗生素预防。B 组链球菌检测使用胡萝卜肉汤增强的亚培养物进行,方法是使用 B 组链球菌检测(Hardy Diagnostics,Santa Maria,CA)。根据试验方案进行产程管理。排除 B 组链球菌状态未知或未接受产时抗生素预防(如果需要)的患者。主要结局是比较已知 B 组链球菌阳性(通过培养、病史或 B 组链球菌菌尿)和 B 组链球菌阴性且未接受产时抗生素预防的患者中临床绒毛膜羊膜炎的诊断。次要结局包括产后子宫内膜炎、伤口感染、产妇围产期感染性发病率的复合结局和新生儿结局。
共有 491 名患者参加了试验。其中,466 名患者具有已知的 B 组链球菌状态,并根据情况接受或未接受产时抗生素预防,这些患者被纳入本分析:292 名(62.7%)为 B 组链球菌阴性且未接受产时抗生素预防,174 名(37.3%)为 B 组链球菌阳性且接受产时抗生素预防。大多数患者为非西班牙裔黑人(78.1%)和初产妇(59.7%)。两组在人口统计学、临床、诱导和产程特征方面无差异。B 组链球菌阳性患者的临床绒毛膜羊膜炎发生率低 49%(8.1%比 14.7%,比值比,0.51;P=.03),围产期感染性发病率低 15%(8.1%比 15.8%,比值比,0.47;P=.02),与 B 组链球菌阴性患者相比。B 组链球菌阳性患者的婴儿更不可能被收治新生儿重症监护病房(3.4%比 15.1%,P<.001)。
尽管 B 组链球菌定植一直被认为是临床绒毛膜羊膜炎的危险因素,但在使用产时抗生素预防 B 组链球菌阳性患者的时代,我们的发现支持这样的观点,即产时抗生素预防 B 组链球菌阳性与接受产时抗生素预防的患者中临床绒毛膜羊膜炎和围产期感染性发病率降低有关。这些发现表明,B 组链球菌产时抗生素预防可能有助于预防围产期感染性发病率,这一现象值得进一步研究。