Department of Otolaryngology, National Taiwan University Hospital, Address: 7, Chung-Shan S. Rd., 10002, Taipei, Taiwan, ROC.
Department of Otolaryngology, National Taiwan University Biomedical Park Hospital, Hsinchu, Taiwan.
Sci Rep. 2022 Mar 25;12(1):5219. doi: 10.1038/s41598-022-08392-w.
Congenital cytomegalovirus (cCMV) infection is the most prevalent cause of non-genetic sensorineural hearing loss (SNHL) in children. However, the prognostic determinants of SNHL remain unclear. Children with cCMV infection in a tertiary hospital were enrolled. The presence of cCMV-related symptoms at birth, the newborn hearing screening (NHS) results, and the blood viral loads were ascertained. Audiologic outcomes and initial blood viral loads were compared between different groups. Of the 39 children enrolled, 16 developed SNHL. SNHL developed in 60% of children who were initially symptomatic, and in 34.5% of those who were initially asymptomatic with normal hearing or isolated hearing loss, respectively. Failuire in NHS was a reliable tool for early detection of SNHL. The initial viral loads were higher in children who were symptomatic at birth, those who failed NHS, and those who developed SNHL. We observed SNHL deterioration in a patient after CMV DNAemia clearance was achieved, and in another patient with the flare-up of viral load. The presence of cCMV-related symptoms at birth, failure in NHS, and blood viral load might be the prognostic factors for hearing outcomes. Regular audiologic examinations are necessary in all children with cCMV infection even after CMV DNAemia clearance.
先天性巨细胞病毒(cCMV)感染是儿童非遗传性感觉神经性听力损失(SNHL)的最常见原因。然而,SNHL 的预后决定因素仍不清楚。我们招募了一家三级医院的 cCMV 感染患儿。确定了出生时是否存在 cCMV 相关症状、新生儿听力筛查(NHS)结果和血液病毒载量。比较了不同组之间的听力结果和初始血液病毒载量。在 39 名入组的患儿中,有 16 名出现了 SNHL。最初有症状的患儿中,有 60%出现 SNHL,而最初无症状、听力正常或孤立性听力损失的患儿中,分别有 34.5%出现 SNHL。NHS 失败是早期发现 SNHL 的可靠工具。在出生时即有症状、NHS 失败和出现 SNHL 的患儿中,初始病毒载量较高。我们观察到一名患者在 CMV DNA 血症清除后出现 SNHL 恶化,另一名患者出现病毒载量反弹。出生时存在 cCMV 相关症状、NHS 失败和血液病毒载量可能是听力结果的预后因素。即使在 CMV DNA 血症清除后,所有 cCMV 感染的患儿都需要定期进行听力检查。