Khetsuriani Nino, Lamonte Ashley, Oberste M Steven, Pallansch Mark
Epidemiology Branch, Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.
Pediatr Infect Dis J. 2006 Oct;25(10):889-93. doi: 10.1097/01.inf.0000237798.07462.32.
Neonatal enterovirus (EV) infections lead to a wide range of clinical manifestations, from mild febrile illness to severe, sometimes fatal, sepsislike disease.
To determine the relationship of EV serotypes with the risk of neonatal infection and its fatal outcome, we analyzed data reported to the National Enterovirus Surveillance System (NESS) during 1983-2003.
Of the 26,737 EV detections reported during this period, neonates accounted for 2544 (11.4% of those with known age). Serotypes most commonly isolated from neonates included echovirus (E) 11 (14.0% of EV with known serotype), coxsackievirus (CV) B2 (8.9%), CVB5 (7.5%), E6, E9 and CVB4 (6.8% each). CVB1-4, E11, and E25 were significantly more common, whereas CVA16, E4, E9, E21, E30, and human parechovirus 1 (formerly E22) were less common among neonates than among persons aged > or =1 month. Fatal outcome was noted for 3.3% of reports, with neonates at a higher risk of death than persons aged > or =1 month (11.5% versus 2.5%; odds ratio [OR] 5.1; 95% confidence interval [CI] = 3.3-7.8). Neonates infected with CVB4 were at a higher risk of death (OR 6.5; 95% CI = 2.4-17.7) than those infected with other EV.
EV are important neonatal pathogens associated with high risk of infection and death. Because of the limitations of the NESS (incomplete reporting, limited clinical data, bias towards more severe and younger cases), additional studies are needed to better evaluate the role of different EV in neonatal infections.
新生儿肠道病毒(EV)感染可导致广泛的临床表现,从轻度发热疾病到严重的、有时致命的败血症样疾病。
为了确定EV血清型与新生儿感染风险及其致命结局之间的关系,我们分析了1983年至2003年期间向国家肠道病毒监测系统(NESS)报告的数据。
在此期间报告的26737例EV检测中,新生儿占2544例(占已知年龄者的11.4%)。最常从新生儿中分离出的血清型包括埃可病毒(E)11型(占已知血清型EV的14.0%)、柯萨奇病毒(CV)B2型(8.9%)、CVB5型(7.5%)、E6型、E9型和CVB4型(各占6.8%)。CVB1 - 4型、E11型和E25型在新生儿中明显更常见,而CVA16型、E4型、E9型、E21型、E30型和人细小病毒1型(原E22型)在新生儿中比在年龄≥1个月的人群中更少见。3.3%的报告出现致命结局,新生儿的死亡风险高于年龄≥1个月的人群(11.5%对2.5%;比值比[OR]5.1;95%置信区间[CI]=3.3 - 7.8)。感染CVB4型的新生儿比感染其他EV的新生儿死亡风险更高(OR 6.5;95% CI = 2.4 - 17.7)。
EV是与感染和死亡高风险相关的重要新生儿病原体。由于NESS存在局限性(报告不完整、临床数据有限、偏向于更严重和更年幼的病例),需要进行更多研究以更好地评估不同EV在新生儿感染中的作用。