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针对听力筛查未通过的新生儿进行先天性巨细胞病毒相关听力损失的靶向唾液筛查的作用。

Contribution of targeted saliva screening for congenital CMV-related hearing loss in newborns who fail hearing screening.

作者信息

Ari-Even Roth Daphne, Lubin Daniel, Kuint Jacob, Teperberg-Oikawa Michal, Mendelson Ella, Strauss Tzipora, Barkai Galia

机构信息

Hearing, Speech and Language Center, Chaim Sheba Medical Center, Ramat Gan, Israel.

Department of Communication Disorders, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

出版信息

Arch Dis Child Fetal Neonatal Ed. 2017 Nov;102(6):F519-F524. doi: 10.1136/archdischild-2016-311859. Epub 2017 May 3.

Abstract

BACKGROUND

We previously reported a 2.2% rate of infants born with sensorineural hearing loss (SNHL) due to congenital cytomegalovirus (cCMV) infection identified by universal neonatal screen for cCMV using saliva.

OBJECTIVE

To evaluate the contribution of targeted saliva screening for cCMV to the detection of infants born with cCMV-related SNHL who failed universal newborn hearing screening (UNHS).

METHODS

We retrospectively reviewed the audiological and medical records of infants who failed UNHS and were tested for cCMV using saliva sample prior to discharge at Sheba Medical Center between 2014 and 2015. Positive cases were confirmed by urine sample.

RESULTS

Two hundred (1%) of the 19 830 infants tested during the study period failed in-hospital hearing screening. A saliva specimen was obtained prior to discharge in 187 infants (93.5% of those who failed UNHS). In 178 infants saliva testing was performed at ≤21 days of chronological age and yielded results. cCMV infection was identified in 4/178 tested infants (2.25%, 95% CI 0.8% to 5.3%), of whom three were diagnosed with SNHL (1.7%, 95% CI 0.5% to 4.4%) and offered antiviral treatment. Two of the tested infants (1.12%, 95% CI 0.2% to 3.6%) were diagnosed with cCMV solely due to failure in UNHS. Occult central nervous system (CNS) symptoms of cCMV infection were detected in 2/4 infants following targeted investigation.

CONCLUSIONS

Targeted cCMV screening in newborns who failed UNHS contributed to the early detection of infants born with cCMV-related isolated SNHL or with occult CNS symptoms who could potentially benefit from antiviral treatment.

摘要

背景

我们之前报道过,通过使用唾液对先天性巨细胞病毒(cCMV)进行普遍新生儿筛查,发现因先天性巨细胞病毒感染而患有感音神经性听力损失(SNHL)的婴儿比例为2.2%。

目的

评估针对cCMV的靶向唾液筛查对检测出患有cCMV相关SNHL且未通过新生儿听力普遍筛查(UNHS)的婴儿的贡献。

方法

我们回顾性分析了2014年至2015年期间在舍巴医疗中心未通过UNHS且在出院前使用唾液样本进行cCMV检测的婴儿的听力和医疗记录。阳性病例通过尿液样本进行确认。

结果

在研究期间接受检测的19830名婴儿中,有200名(1%)未通过住院听力筛查。187名婴儿(占未通过UNHS婴儿的93.5%)在出院前采集了唾液样本。178名婴儿在实际年龄≤21天时进行了唾液检测并得出结果。在178名接受检测的婴儿中,有4名(2.25%,95%CI为0.8%至5.3%)被确诊为cCMV感染,其中3名被诊断为SNHL(1.7%,95%CI为0.5%至4.4%)并接受了抗病毒治疗。2名接受检测的婴儿(1.12%,95%CI为0.2%至3.6%)仅因未通过UNHS而被诊断为cCMV感染。在进行靶向调查后,4名婴儿中有2名检测出cCMV感染的隐匿性中枢神经系统(CNS)症状。

结论

对未通过UNHS的新生儿进行靶向cCMV筛查有助于早期发现患有cCMV相关孤立性SNHL或隐匿性CNS症状且可能从抗病毒治疗中获益的婴儿。

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