Division of Neonatology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
Clin Infect Dis. 2022 Oct 12;75(8):1405-1415. doi: 10.1093/cid/ciac222.
This study was performed to determine the incidence of group B Streptococcus (GBS) disease among extremely preterm infants and assess to risk of death or neurodevelopmental impairment (NDI) at a corrected age of 18-26 months.
In this observational cohort study of infants enrolled in a multicenter registry, the incidence of GBS disease was assessed in infants born in 1998-2016 at 22-28 weeks' gestation and surviving for >12 hours. The composite outcome, death or NDI, was assessed in infants born in 1998-2014 at 22-26 weeks' gestation. Infection was defined as GBS isolation in blood or cerebrospinal fluid culture at ≤72 hours (early-onset disease [EOD]) or >72 hours (late-onset disease [LOD]) after birth. Using Poisson regression models, the outcome was compared in infants with GBS disease, infants infected with other pathogens, and uninfected infants.
The incidence of GBS EOD (2.70/1000 births [95% confidence interval (CI), 2.15-3.36]) and LOD (8.47/1000 infants [7.45-9.59]) did not change significantly over time. The adjusted relative risk of death/NDI was higher among infants with GBS EOD than in those with other infections (adjusted relative risk, 1.22 [95% CI, 1.02-1.45]) and uninfected infants (1.44 [1.23-1.69]). Risk of death/NDI did not differ between infants with GBS LOD and comparator groups. GBS LOD occurred at a significantly later age than non-GBS late-onset infection. Among infants surviving >30 days, the risk of death was higher with GBS LOD (adjusted relative risk, 1.90 [95% CI, 1.36-2.67]), compared with uninfected infants.
In a cohort of extremely preterm infants, the incidence of GBS disease did not change during the study period. The increased risk of death or NDI with GBS EOD, and of death among some infants with GBS LOD, supports the need for novel preventive strategies for disease reduction.
NCT00063063.
本研究旨在确定极早产儿中 B 群链球菌(GBS)病的发生率,并评估校正年龄为 18-26 个月时的死亡或神经发育障碍(NDI)风险。
在这项对纳入多中心登记处的婴儿进行的观察性队列研究中,评估了 1998 年至 2016 年出生于 22-28 周且存活时间超过 12 小时的婴儿中 GBS 病的发生率。在 1998 年至 2014 年出生于 22-26 周的婴儿中,评估了复合结局(死亡或 NDI)。感染的定义为出生后≤72 小时(早发型疾病[EOD])或>72 小时(晚发型疾病[LOD])时血或脑脊液培养中分离出 GBS。使用泊松回归模型,将患有 GBS 病、感染其他病原体的婴儿和未感染的婴儿的结局进行比较。
GBS EOD(2.70/1000 例活产[95%置信区间(CI),2.15-3.36])和 LOD(8.47/1000 例婴儿[7.45-9.59])的发生率在研究期间无显著变化。与其他感染(调整后的相对风险,1.22[95%CI,1.02-1.45])和未感染婴儿(1.44[1.23-1.69])相比,GBS EOD 婴儿的死亡/NDI 风险更高。GBS LOD 婴儿与对照组的死亡/NDI 风险无差异。GBS LOD 发生在明显较晚的年龄,而非非 GBS 晚发型感染。在存活时间超过 30 天的婴儿中,GBS LOD 的死亡风险更高(调整后的相对风险,1.90[95%CI,1.36-2.67]),与未感染的婴儿相比。
在一组极早产儿中,GBS 病的发生率在研究期间没有变化。GBS EOD 增加的死亡或 NDI 风险,以及一些 GBS LOD 婴儿的死亡风险,支持需要新的预防策略来减少疾病。
NCT00063063。