Department of Pediatrics, School of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Centers for Disease Control and Prevention, Atlanta, United States of America.
PLoS One. 2019 Apr 10;14(4):e0214077. doi: 10.1371/journal.pone.0214077. eCollection 2019.
Globally, over 400,000 neonatal deaths in 2015 were attributed to sepsis, however, the incidence and etiologies of these infections are largely unknown in low-middle income countries. We aimed to determine incidence and etiology of community-acquired early-onset (<72 hours age) sepsis (EOS) using culture and molecular diagnostics.
This was a prospective observational study, in which we conducted a surveillance for pathogens using a combination of blood culture and a polymerase chain reaction (PCR)-based test. Blood culture was performed on all neonates with suspected EOS. Among the subset fulfilling criteria for protocol-defined EOS, blood and nasopharyngeal (NP) respiratory swabs were tested by quantitative real-time reverse-transcriptase PCR using a Taqman Array Card (TAC) with 15 bacterial and 12 viral targets. Blood and NP samples from 312 healthy newborns were also tested by TAC to estimate background positivity rates. We used variant latent-class methods to attribute etiologies and calculate pathogen-specific proportions and incidence rates.
We enrolled 2,624 neonates with suspected EOS and from these 1,231 newborns met criteria for protocol-defined EOS (incidence- 39.3/1,000 live-births). Using the partially latent-class modelling, only 26.7% cases with protocol-defined EOS had attributable etiology, and the largest pathogen proportion were Ureaplasma spp. (5.4%; 95%CI: 3.6-8.0) and group B Streptococcus (GBS) (4.8%; 95%CI: 4.1-5.8), and no etiology was attributable for 73.3% of cases. Blood cultures were positive in 99/1,231 (8.0%) with protocol-defined EOS (incidence- 3.2/1,000 live-births). Leading pathogens on blood culture included GBS (35%) and viridans streptococci (24%). Ureaplasma spp. was the most common organism identified on TAC among cases with protocol-defined EOS.
Using a combination of blood culture and a PCR-based test the common pathogens isolated in neonates with sepsis were Ureaplasma spp. and GBS. Despite documenting higher rates of protocol-defined EOS and using a combination of tests, the etiology for EOS remains elusive.
2015 年,全球有超过 40 万新生儿死于败血症,但中低收入国家对这些感染的发病率和病因知之甚少。我们旨在通过培养和分子诊断来确定社区获得性早发性(<72 小时龄)败血症(EOS)的发病率和病因。
这是一项前瞻性观察研究,我们使用血液培养和聚合酶链反应(PCR)为基础的检测相结合来进行病原体监测。对所有疑似 EOS 的新生儿进行血液培养。在符合方案定义的 EOS 标准的亚组中,对血液和鼻咽(NP)呼吸道拭子进行定量实时逆转录酶-PCR 检测,使用带有 15 种细菌和 12 种病毒靶标的 Taqman 阵列卡(TAC)。还使用 TAC 检测 312 名健康新生儿的血液和 NP 样本,以估计背景阳性率。我们使用变异潜伏类方法来确定病因,并计算病原体特异性比例和发病率。
我们共纳入了 2624 例疑似 EOS 的新生儿,其中 1231 例新生儿符合方案定义的 EOS 标准(发病率为 39.3/1000 活产儿)。使用部分潜伏类模型,只有 26.7%的符合方案定义的 EOS 病例有可归因病因,最大的病原体比例是脲原体属(5.4%;95%CI:3.6-8.0)和 B 群链球菌(GBS)(4.8%;95%CI:4.1-5.8),73.3%的病例无病因可归因。在 1231 例符合方案定义的 EOS 新生儿中,有 99 例血液培养阳性(发病率为 3.2/1000 活产儿)。血液培养的主要病原体包括 GBS(35%)和草绿色链球菌(24%)。在符合方案定义的 EOS 病例中,TAC 最常见的病原体是脲原体属。
使用血液培养和 PCR 为基础的检测相结合,败血症新生儿分离的常见病原体是脲原体属和 GBS。尽管记录了更高的协议定义的 EOS 发生率,并使用了多种检测方法,但 EOS 的病因仍然难以确定。