From the *Regional Neonatal Unit, St. Michael's Hospital, University Hospitals Bristol Foundation Trust, Bristol; †Microbiology, Belfast Health and Social Services Trust; ‡Royal Jubilee Maternity Hospital; §Royal Belfast Hospital for Sick Children, Belfast Health and Social Services Trust; and ¶Centre for Infection and Immunity, Queens University of Belfast, Belfast, United Kingdom.
Pediatr Infect Dis J. 2015 Feb;34(2):121-4. doi: 10.1097/INF.0000000000000510.
Approximately 5-6% of all infective episodes in neonatal intensive care unit (NICU) are of viral origin. Previous studies suggest that human parechovirus (HPeV) infection presents most commonly in term infants, as a sepsis-like syndrome in which meningoencephalitis is prominent. Our aim was to study the infection rate and associated features of HPeV.
Blood samples were taken from NICU babies older than 48 hours, who were being investigated for late onset sepsis. Clinical and laboratory data were collected at the time of the suspected sepsis episode. Samples were tested using universal primers and probe directed at the 5'-untranslated region of the HPeV genome by reverse transcriptase polymerase chain reaction (RT-PCR). Results were confirmed by electrophoresis and DNA sequencing.
HPeV was detected in 11 of 84 samples (13%). These infants had a mean [interquartile range (IQR)] gestational age of 28.9 (26.9-30.6) weeks and mean birth weight of 1.26 (SD = 0.72) kg. The median day of presentation was 16 (IQR: 11-27). These characteristics were similar to the infants without positive viral detection. Six infants presented with respiratory signs. One infant presented with signs of meningitis. Six of the 11 episodes of HPeV infection occurred during the winter months (December to February). No HPeV positive infants had abnormal findings on their 28-day cranial ultrasound examination.
We found an HPeV infection rate of 13% in infants being tested for late onset sepsis. HPeV should be considered as a possible cause of sepsis-like symptoms in preterm infants.
新生儿重症监护病房(NICU)中约有 5-6%的感染发作是由病毒引起的。先前的研究表明,人类肠道病毒(HPeV)感染最常见于足月婴儿,表现为类似于败血症的综合征,其中脑膜脑炎较为突出。我们的目的是研究 HPeV 的感染率和相关特征。
从 NICU 中大于 48 小时的婴儿采集血液样本,这些婴儿正在接受迟发性败血症的检查。在疑似败血症发作时收集临床和实验室数据。使用针对 HPeV 基因组 5'-非翻译区的通用引物和探针通过逆转录聚合酶链反应(RT-PCR)对样本进行检测。结果通过电泳和 DNA 测序进行确认。
在 84 个样本中的 11 个(13%)中检测到 HPeV。这些婴儿的平均[四分位间距(IQR)]胎龄为 28.9(26.9-30.6)周,平均出生体重为 1.26(SD=0.72)kg。中位表现日为 16(IQR:11-27)。这些特征与未检测到病毒的婴儿相似。6 名婴儿出现呼吸迹象。1 名婴儿出现脑膜炎迹象。11 例 HPeV 感染中有 6 例发生在冬季(12 月至 2 月)。没有 HPeV 阳性婴儿在 28 天头颅超声检查中发现异常。
我们发现正在接受迟发性败血症检查的婴儿中 HPeV 感染率为 13%。HPeV 应被视为早产儿类似败血症症状的可能原因。