Centre for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven, the Netherlands.
Department of Neurology, Amsterdam Neuroscience, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
PLoS One. 2019 May 9;14(5):e0216749. doi: 10.1371/journal.pone.0216749. eCollection 2019.
Group B Streptococcus (GBS) is the leading cause of neonatal sepsis and meningitis worldwide. We aimed to estimate the current burden of neonatal invasive GBS disease in the Netherlands, as a first step in providing an evidence base for policy makers on the potential benefits of a future maternal GBS vaccine.
Surveillance of neonatal invasive GBS occurs at the National Reference Laboratory for Bacterial Meningitis, where culture isolates from cerebrospinal fluid and blood are sent by diagnostic laboratories. From the number of cultures we estimated the incidence of neonatal (age 0-90 days) GBS meningitis and sepsis. We constructed a disease progression model informed by literature and expert consultation to estimate the disease burden of neonatal invasive GBS infection. As many neonates with a probable GBS sepsis are never confirmed by blood culture, we further estimated the disease burden of unconfirmed cases of probable GBS sepsis in sensitivity analyses.
An estimated 97 cases and 6.5 deaths occurred in the Netherlands in 2017 due to culture positive neonatal invasive GBS infection. This incidence comprised 15 cases of meningitis and 42 cases of sepsis per 100.000 births, with an estimated mortality of 3.8 per 100.000 live births. A disease burden of 780 disability-adjusted life years (DALY) (95% CI 650-910) or 460 DALY per 100.000 live births was attributed to neonatal invasive GBS infection. In the sensitivity analysis including probable neonatal GBS sepsis the disease burden increased to 71 cases and 550 DALY (95% CI 460-650) per 100.000 live births.
In conclusion, neonatal invasive GBS infection currently causes a substantial disease burden in the Netherlands. However, important evidence gaps are yet to be filled. Furthermore, cases of GBS sepsis lacking a positive blood culture may contribute considerably to this burden potentially preventable by a future GBS vaccine.
B 群链球菌(GBS)是全球导致新生儿败血症和脑膜炎的主要原因。我们旨在估计荷兰目前新生儿侵袭性 GBS 疾病的负担,为决策者提供未来 GBS 疫苗潜在效益的证据基础。
通过国家细菌脑膜炎参考实验室进行新生儿侵袭性 GBS 的监测,诊断实验室将脑脊液和血液的培养分离物送到该实验室。我们根据培养物的数量估计了新生儿(0-90 天龄)GBS 脑膜炎和败血症的发病率。我们构建了一个疾病进展模型,该模型是根据文献和专家咨询意见构建的,用于估计新生儿侵袭性 GBS 感染的疾病负担。由于许多疑似 GBS 败血症的新生儿从未通过血液培养得到证实,因此我们在敏感性分析中进一步估计了疑似 GBS 败血症的未确诊病例的疾病负担。
2017 年,荷兰估计有 97 例和 6.5 例死亡是由培养阳性的新生儿侵袭性 GBS 感染引起的。这一发病率包括每 100,000 例活产中有 15 例脑膜炎和 42 例败血症,估计每 100,000 例活产中有 3.8 例死亡。新生儿侵袭性 GBS 感染导致 780 个残疾调整生命年(DALY)(95%CI 650-910)或每 100,000 例活产中有 460 DALY。在包括疑似新生儿 GBS 败血症的敏感性分析中,疾病负担增加到每 100,000 例活产中有 71 例和 550 DALY(95%CI 460-650)。
总之,新生儿侵袭性 GBS 感染目前在荷兰造成了相当大的疾病负担。然而,仍有重要的证据空白有待填补。此外,缺乏阳性血培养的 GBS 败血症病例可能会对这一负担产生相当大的影响,而未来的 GBS 疫苗可能会预防这些病例。