Suppr超能文献

先天性巨细胞病毒新生儿听力筛查未通过的脑磁共振成像。

Brain Magnetic Resonance Imaging in Congenital Cytomegalovirus With Failed Newborn Hearing Screen.

机构信息

Division of Pediatric Neurology, University of Utah, Salt Lake City, Utah.

Division of Otolaryngology-Head and Neck Surgery, University of Utah, Salt Lake City, Utah.

出版信息

Pediatr Neurol. 2020 Sep;110:55-58. doi: 10.1016/j.pediatrneurol.2020.05.006. Epub 2020 May 20.

Abstract

BACKGROUND

In 2013, Utah enacted legislation requiring that infants failing newborn hearing screening be tested for cytomegalovirus infection. As a result, cytomegalovirus-infected infants are being identified because of hearing deficits. The neuroimaging findings in this population have not been characterized.

METHODS

Retrospective medical record review was used to identify patients seen at the University of Utah and Primary Children's Hospitals in Salt Lake City, Utah, who failed newborn hearing screening. A cohort of patients with congenital cytomegalovirus infection, brain magnetic resonance imaging (MRI), and sedated auditory brainstem response testing was studied.

RESULTS

Seventeen patients were identified; 11 (65%) were female. Confirmatory auditory brainstem response testing, performed at a median age 29 days, showed profound hearing loss in 8 (47%) subjects, severe loss in two (12%), moderate loss in two (12%), and mild loss in three (18%); two (12%) subjects had normal hearing. The diagnosis of cytomegalovirus infection was made at a median age 23 days. Brain imaging was performed at a median age 65 days. Ten (59%) subjects had one or more neuroimaging abnormality. White matter lesions were found in eight (47%) subjects, cysts in three (18%), and stroke in two (12%). Polymicrogyria was identified in two (12%) subjects. Seven (41%) subjects had normal brain MRIs.

CONCLUSIONS

These results indicate that most infants whose cytomegalovirus infections were identified after failing newborn hearing screening had abnormal brain MRIs. Our results suggest that brain MRIs should be considered in infants with congenital cytomegalovirus infections who are identified through hearing screening programs.

摘要

背景

2013 年,犹他州颁布法规,要求对未能通过新生儿听力筛查的婴儿进行巨细胞病毒感染检测。因此,由于听力缺陷,正在发现巨细胞病毒感染的婴儿。该人群的神经影像学发现尚未得到描述。

方法

回顾性病历审查用于确定在犹他州盐湖城的犹他大学和主要儿童医院就诊的未能通过新生儿听力筛查的患者。研究了一组患有先天性巨细胞病毒感染、脑磁共振成像(MRI)和镇静听觉脑干反应测试的患者。

结果

确定了 17 名患者;11 名(65%)为女性。在中位数为 29 天的时间进行的确认性听觉脑干反应测试显示,8 名(47%)患者存在严重听力损失,2 名(12%)患者存在严重听力损失,2 名(12%)患者存在中度听力损失,3 名(18%)患者存在轻度听力损失;2 名(12%)患者听力正常。巨细胞病毒感染的诊断在中位数年龄 23 天做出。中位数年龄 65 天进行脑成像。10 名(59%)患者有一项或多项神经影像学异常。8 名(47%)患者发现白质病变,3 名(18%)患者发现囊肿,2 名(12%)患者发现中风。2 名(12%)患者发现多微小脑回。7 名(41%)患者的 MRI 脑部正常。

结论

这些结果表明,在新生儿听力筛查后发现巨细胞病毒感染的大多数婴儿的脑部 MRI 异常。我们的结果表明,对于通过听力筛查计划发现的先天性巨细胞病毒感染婴儿,应考虑进行脑部 MRI。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2573/8856767/96c6456e9a44/nihms-1615317-f0001.jpg

相似文献

引用本文的文献

1
Hemorrhagic stroke in children.儿童出血性中风
J Cent Nerv Syst Dis. 2024 Nov 1;16:11795735241289913. doi: 10.1177/11795735241289913. eCollection 2024.

本文引用的文献

9
Congenital cytomegalovirus infection and brain clefting.先天性巨细胞病毒感染与脑裂畸形。
Pediatr Neurol. 2014 Mar;50(3):218-23. doi: 10.1016/j.pediatrneurol.2013.11.005. Epub 2013 Nov 16.
10
Congenital cytomegalovirus infection: clinical outcome.先天性巨细胞病毒感染:临床结果。
Clin Infect Dis. 2013 Dec;57 Suppl 4(Suppl 4):S178-81. doi: 10.1093/cid/cit629.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验