Neurodevelopmental outcomes of children with congenital cytomegalovirus: a systematic scoping review

• Published in: Pediatric research 2024-01, Vol.95 (2), p.418-435
• Main Authors: Pesch, Megan H., Lauer, Clare S., Weinberg, Jason B.
• Format: Article
• Language: English
• Subjects: Asymptomatic; Childrens health; Clinical outcomes; Congenital diseases; Cytomegalovirus; Medical screening; Medicine; Medicine & Public Health; Neurodevelopmental disorders; Pediatric Surgery; Pediatrics; Systematic Review
• ISSN: 0031-3998; 1530-0447; 1530-0447
• DOI: 10.1038/s41390-023-02639-6

Background With the emergence of newborn congenital cytomegalovirus (cCMV) screening programs, more infants are being diagnosed and require long-term follow-up. The objective of the study was to summarize the literature to date on neurodevelopmental outcomes in children with cCMV with attention to study-specific definitions of disease severity (symptomatic vs. asymptomatic). Methods This systematic scoping review included studies of children with cCMV (≤18 years-old) measuring neurodevelopment in ≥1 domain: global, gross motor, fine motor, speech/language, and intellectual/cognitive. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines were followed. PubMed, PsychInfo, and Embase databases were searched. Results 33 studies met inclusion criteria. Global development most frequently measured ( n  = 21), followed by cognitive/intellectual ( n  = 16) and speech/language ( n  = 8). Most (31/33) studies differentiated children by cCMV severity (symptomatic vs. asymptomatic), definitions of which ranged broadly. 15/21 studies described global development categorically (e.g., normal vs. abnormal). Across studies and domains, children with cCMV generally had equivalent or lower scores (vs. controls or normed measures). Conclusions Variation in definitions of cCMV severity and blunt categorical outcomes may limit the generalizability of findings. Future studies should utilize standardized definitions of disease severity and in-depth measurement and reporting of neurodevelopmental outcomes in children with cCMV. Impact Neurodevelopmental delays are common among children with cCMV, although gaps in the literature to have made quantification of such delays challenging. Variation in definitions of asymptomatic and symptomatic cCMV as well as the use of categorical outcomes of neurodevelopment (e.g., normal vs. abnormal) limits the generalizability and clinical utility of findings.