Respiratory Diseases Branch, Centers for Disease Control and Prevention, Atlanta, Georgia.
Connecticut Department of Public Health, Hartford.
JAMA Pediatr. 2019 Mar 1;173(3):224-233. doi: 10.1001/jamapediatrics.2018.4826.
Invasive disease owing to group B Streptococcus (GBS) remains an important cause of illness and death among infants younger than 90 days in the United States, despite declines in early-onset disease (EOD; with onset at 0-6 days of life) that are attributed to intrapartum antibiotic prophylaxis (IAP). Maternal vaccines to prevent infant GBS disease are currently under development.
To describe incidence rates, case characteristics, antimicrobial resistance, and serotype distribution of EOD and late-onset disease (LOD; with onset at 7-89 days of life) in the United States from 2006 to 2015 to inform IAP guidelines and vaccine development.
DESIGN, SETTING, AND PARTICIPANTS: This study used active population-based and laboratory-based surveillance for invasive GBS disease conducted through Active Bacterial Core surveillance in selected counties of 10 states across the United States. Residents of Active Bacterial Core surveillance areas who were younger than 90 days and had invasive GBS disease in 2006 to 2015 were included. Data were analyzed from December 2017 to April 2018.
Group B Streptococcus isolated from a normally sterile site.
Early-onset disease and LOD incidence rates and associated GBS serotypes and antimicrobial resistance.
The Active Bacterial Core surveillance program identified 1277 cases of EOD and 1387 cases of LOD. From 2006 to 2015, EOD incidence declined significantly from 0.37 to 0.23 per 1000 live births (P < .001), and LOD rates remained stable (mean, 0.31 per 1000 live births). Among the mothers of 1277 infants with EOD, 617 (48.3%) had no indications for IAP and did not receive it, and 278 (21.8%) failed to receive IAP despite having indications. Serotype data were available for 1743 of 1897 patients (91.3%) from 7 sites that collect GBS isolates. Among patients with EOD, serotypes Ia (242 [27.3%]) and III (242 [27.3%]) were most common. Among patients with LOD, serotype III was most common (481 [56.2%]), and this increased from 2006 to 2015 from 0.12 to 0.20 cases per 1000 live births (P < .001). Serotype IV caused 53 cases (6.2%) of EOD and LOD combined. The 6 most common serotypes (Ia, Ib, II, III, IV, and V) caused 881 EOD cases (99.3%) and 853 LOD cases (99.7%). No β-lactam resistance was identified; 359 isolates (20.8%) tested showed constitutive clindamycin resistance. In 2015, an estimated 840 EOD cases and 1265 LOD cases occurred nationally.
The rates of LOD among US infants are now higher than EOD rates. Combined with addressing IAP implementation gaps, an effective vaccine covering the most common serotypes might further reduce EOD rates and help prevent LOD, for which there is no current public health intervention.
在美国,尽管由于分娩期间使用抗生素预防(IAP)而导致早发性疾病(EOD;发病时间为 0-6 天)有所下降,但由于 B 组链球菌(GBS)引起的侵袭性疾病仍然是导致 90 天以下婴儿发病和死亡的一个重要原因。目前正在开发用于预防婴儿 GBS 疾病的母体疫苗。
描述美国 2006 年至 2015 年期间 EOD 和晚发性疾病(发病时间为 7-89 天)的发病率、病例特征、抗微生物药物耐药性和血清型分布,为 IAP 指南和疫苗开发提供信息。
设计、地点和参与者:本研究使用了美国 10 个州的选定县进行的基于人群的主动和基于实验室的侵袭性 GBS 疾病监测,该监测通过主动细菌核心监测进行。2006 年至 2015 年期间,年龄在 90 天以下且患有侵袭性 GBS 疾病的居住在主动细菌核心监测地区的居民被纳入研究。数据分析于 2017 年 12 月至 2018 年 4 月进行。
从正常无菌部位分离出 B 组链球菌。
EOD 和 LOD 的发病率和相关 GBS 血清型和抗微生物药物耐药性。
主动细菌核心监测计划确定了 1277 例 EOD 和 1387 例 LOD。从 2006 年至 2015 年,EOD 发病率从 0.37 降至 0.23/1000 活产儿(P < .001),而 LOD 率保持稳定(平均为 0.31/1000 活产儿)。在 1277 例 EOD 婴儿的母亲中,617 例(48.3%)无 IAP 适应证且未接受 IAP,278 例(21.8%)尽管有适应证但未接受 IAP。来自 7 个收集 GBS 分离株的地点的 1743 名患者(91.3%)提供了血清型数据。在 EOD 患者中,血清型 Ia(242 [27.3%])和 III(242 [27.3%])最为常见。在 LOD 患者中,血清型 III 最为常见(481 [56.2%]),从 2006 年到 2015 年,这一比例从 0.12 升至 0.20/1000 活产儿(P < .001)。血清型 IV 导致 53 例(6.2%)EOD 和 LOD 合并感染。最常见的 6 种血清型(Ia、Ib、II、III、IV 和 V)导致 881 例 EOD 病例(99.3%)和 853 例 LOD 病例(99.7%)。未发现β-内酰胺类耐药性;359 株(20.8%)测试显示出固有克林霉素耐药性。2015 年,全国估计发生了 840 例 EOD 病例和 1265 例 LOD 病例。
美国婴儿 LOD 率现在高于 EOD 率。在解决 IAP 实施差距的同时,一种覆盖最常见血清型的有效疫苗可能会进一步降低 EOD 率,并有助于预防目前尚无公共卫生干预措施的 LOD。