不同新生儿先天性巨细胞病毒筛查算法的敏感性和特异性比较

IF 4 Q1 GENETICS & HEREDITY
Mark R Schleiss, Lori Panther, Sandeep Basnet, Meklit Workneh, John Diaz-Decaro
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引用次数: 1

摘要

筛查新生儿先天性巨细胞病毒(cCMV)感染对于早期发现和及时诊断感染的相关长期后果至关重要,如感音神经性听力损失和神经发育迟缓。本研究的目的是描述不同新生儿cCMV感染筛查方法的有效性,并比较在靶向和通用筛查算法中检测到的cCMV病例的预期数量。需要听觉脑干反应失败和瞬态诱发耳声发射(TOAE)的靶向筛选算法的总体灵敏度(OSn);在使用唾液和尿液PCR检测诊断巨细胞病毒之前,两次失败连续检测或仅TOAE(一次失败连续检测)分别为79%和88%。用干血斑(DBS)诊断巨细胞病毒(CMV)检测的两次失败串联检测的OSn为75%。相比之下,通用筛查(唾液和尿液PCR检测)的OSn为90%,单独使用DBS检测的通用筛查的OSn为86%。总的来说,所有算法的特异性都是100%。与两次失败的连续检测相比,使用DBS检测和使用唾液和尿液检测进行普遍筛查,每10万活产婴儿中分别可能多发现312例和373例cCMV病例。总体而言,实施普遍的新生儿cCMV筛查将改善cCMV的检测,最终带来更好的健康结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparison of Overall Sensitivity and Specificity across Different Newborn Screening Algorithms for Congenital Cytomegalovirus.

Comparison of Overall Sensitivity and Specificity across Different Newborn Screening Algorithms for Congenital Cytomegalovirus.

Comparison of Overall Sensitivity and Specificity across Different Newborn Screening Algorithms for Congenital Cytomegalovirus.

Comparison of Overall Sensitivity and Specificity across Different Newborn Screening Algorithms for Congenital Cytomegalovirus.

Screening newborns for congenital cytomegalovirus (cCMV) infection is critical for early detection and prompt diagnosis of related long-term consequences of infection, such as sensorineural hearing loss and neurodevelopmental delays. The objective of this study was to describe the validity of different newborn cCMV infection screening approaches and compare the expected number of cCMV cases detected across targeted and universal screening algorithms. The overall sensitivity (OSn) of targeted screening algorithms that required failure of auditory brain stem response and transient evoked otoacoustic emissions (TOAE; two-fail serial testing) or TOAE only (one-fail serial testing) before diagnostic CMV testing using saliva and urine PCR tests was 79% and 88%, respectively. The OSn for two-fail serial testing with diagnostic CMV testing using dried blood spot (DBS) was 75%. In contrast, OSn was 90% for universal screening (saliva and urine PCR tests) and 86% for universal screening with DBS testing alone. Overall, specificities were 100% across all algorithms. Universal screening using DBS testing and universal screening using saliva and urine testing can potentially detect 312 and 373 more cCMV cases per 100,000 live births, respectively, than two-fail serial testing. Overall, implementing universal cCMV newborn screening would improve cCMV detection, ultimately leading to better health outcomes.

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来源期刊
International Journal of Neonatal Screening
International Journal of Neonatal Screening Medicine-Pediatrics, Perinatology and Child Health
CiteScore
6.70
自引率
20.00%
发文量
56
审稿时长
11 weeks
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