Rivera Lisa B, Boppana Suresh B, Fowler Karen B, Britt William J, Stagno Sergio, Pass Robert F
Department of Pediatrics, University of Alabama School of Medicine, Birmingham, Alabama 35233, USA.
Pediatrics. 2002 Oct;110(4):762-7. doi: 10.1542/peds.110.4.762.
Congenital cytomegalovirus (CMV) infection is a major cause of sensorineural hearing loss (SNHL) and neurologic impairment in children. Although the majority of children with symptomatic congenital CMV infection develop hearing loss, many symptomatic infants have normal hearing. The purpose of this study was to identify indicators present in the newborn period that have predictive value for the development of hearing loss in children with symptomatic congenital CMV infection.
Of the 190 children who had symptomatic congenital CMV infection and were born between 1966 and 1997 and enrolled in a follow-up study, hearing outcome was known for 180 children. Follow-up data were analyzed using univariate and multivariate logistic regression analyses to determine the specific demographic, newborn clinical, and laboratory findings predictive of hearing loss. The amount of infectious CMV in urine was quantified in a subset of 21 children who were born between 1994 and 1998.
The presence of intrauterine growth retardation, petechiae, hepatosplenomegaly, hepatitis, thrombocytopenia, and intracerebral calcifications was associated with the development of hearing loss on univariate analysis. The presence of microcephaly and other neurologic abnormalities was not predictive of hearing loss. Logistic regression analysis revealed that only petechiae and intrauterine growth retardation independently predicted hearing loss. None of the demographic and other newborn findings predicted progressive hearing loss. The children who developed hearing loss had higher urine CMV titers during infancy than those with normal hearing.
In children with symptomatic congenital CMV infection, evidence of disseminated infection with or without the presence of neurologic involvement at birth was predictive of the development of hearing loss. However, it was not possible to identify factors that are independently predictive of the development of progressive hearing loss.
先天性巨细胞病毒(CMV)感染是儿童感音神经性听力损失(SNHL)和神经功能损害的主要原因。虽然大多数有症状的先天性CMV感染儿童会出现听力损失,但许多有症状的婴儿听力正常。本研究的目的是确定新生儿期存在的、对有症状的先天性CMV感染儿童听力损失发展具有预测价值的指标。
在1966年至1997年出生且参加随访研究的190例有症状的先天性CMV感染儿童中,180例儿童的听力结局已知。采用单因素和多因素逻辑回归分析对随访数据进行分析,以确定预测听力损失的具体人口统计学、新生儿临床和实验室检查结果。对1994年至1998年出生的21例儿童的子集进行尿中感染性CMV定量分析。
单因素分析显示,宫内生长迟缓、瘀点、肝脾肿大、肝炎、血小板减少和脑内钙化与听力损失的发生有关。小头畸形和其他神经异常的存在不能预测听力损失。逻辑回归分析显示,只有瘀点和宫内生长迟缓能独立预测听力损失。人口统计学和其他新生儿检查结果均不能预测进行性听力损失。发生听力损失的儿童在婴儿期的尿CMV滴度高于听力正常的儿童。
在有症状的先天性CMV感染儿童中,出生时有无神经系统受累的播散性感染证据可预测听力损失的发生。然而,无法确定独立预测进行性听力损失发展的因素。