Retrospective screening for congenital cytomegalovirus infection in the Survey of Neonates in Pomerania shows very low disease burden.

IF 4.1 Q1 PEDIATRICS
Jan Baier, Chiara Konrad, Maximilian Groffmann, Till Ittermann, Heike Allenberg, Maria Asmus, Friedrich Ihler, Chia-Jung Busch, Kathrin Lehmann, Karsten Becker, Anja Lange, Matthias Heckmann
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Abstract

BACKGROUND: Congenital cytomegalovirus (cCMV) infection is considered one of the most common infectious pathologies in neonates, showing a wide range of clinical manifestations, ranging from completely asymptomatic to critically ill newborns. Primary infection during the first trimester of pregnancy carries the highest risk of severe fetal involvement. However, the majority of infected fetuses show an asymptomatic or mild course of disease. The most common long-term sequela is sensorineural hearing loss, which is detected in only about 50% of affected children during newborn hearing screenings. Furthermore, epidemiological data on disease burden remain limited and show considerable variability. The aim of this study was to investigate the prevalence of cCMV and its associated disease burden at follow-up, particular sensorineural hearing loss, in a population-based birth cohort. RESULTS: We conducted a retrospective analysis for cCMV in n = 1995 newborns using urine and plasma biosamples from the second baseline cohort of the Survey of Neonates in Pomerania (SNiP-II). Four participants (prevalence rate 0.2%) were tested positive. Two of these cases had already been identified shortly after birth, having been screened for cCMV due to clinical suspicion. The seroprevalence of IgG antibodies among pregnant women was 47.6%. For follow-up, the patient database of our Department of Otolaryngology, Head and Neck Surgery (ENT) was reviewed for hearing pathologies in all children born during the SNiP-II recruitment period (2013–2017). Twelve out of n = 1138 SNiP-II participants (1.1%) showed confirmed sensorineural hearing loss (SNHL), none of which were associated with cCMV. A complete clinical follow-up of the cCMV-positive cases revealed no sequelae related to the infection. CONCLUSIONS: By using a population-based retrospective analysis approach, we demonstrated a very low prevalence and disease burden of cCMV in our region. Our data supports the current guideline recommendations of a risk factor-based screening strategy.

波美拉尼亚新生儿先天性巨细胞病毒感染的回顾性筛查显示疾病负担非常低。
背景:先天性巨细胞病毒(cCMV)感染被认为是新生儿最常见的感染性疾病之一,其临床表现广泛,从完全无症状到新生儿危重症不等。在妊娠头三个月期间的原发性感染携带严重的胎儿受累的最高风险。然而,大多数受感染的胎儿表现出无症状或轻微的病程。最常见的长期后遗症是感觉神经性听力损失,在新生儿听力筛查期间,只有约50%的受影响儿童发现这种情况。此外,关于疾病负担的流行病学数据仍然有限,并显示出相当大的差异。本研究的目的是在以人口为基础的出生队列中调查cCMV的患病率及其相关疾病负担,特别是感音神经性听力损失。结果:我们使用来自波美拉尼亚新生儿调查(snipi)第二基线队列的尿液和血浆生物样本对n = 1995名新生儿的cCMV进行了回顾性分析。4名参与者(患病率0.2%)检测呈阳性。其中两例在出生后不久就已确诊,由于临床怀疑已进行了cCMV筛查。孕妇血清IgG抗体阳性率为47.6%。为了进行随访,我们对我院耳鼻喉头颈外科(ENT)患者数据库进行了回顾,以了解在snap - ii招募期间(2013-2017)出生的所有儿童的听力病理。1138名snap - ii参与者中有12人(1.1%)确诊为感音神经性听力损失(SNHL),没有一例与cCMV相关。对ccmv阳性病例进行完整的临床随访,未发现与感染相关的后遗症。结论:通过基于人群的回顾性分析方法,我们证实了本地区cCMV的患病率和疾病负担非常低。我们的数据支持当前基于风险因素的筛查策略的指南建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
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