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Published on: July 6, 2013
Neurodevelopmental outcomes of children with congenital cytomegalovirus: a systematic scoping review
Megan H Pesch1, Clare S Lauer2,3, Jason B Weinberg4,5
1Division of Developmental and Behavioral Pediatrics, Department of Pediatrics, University of Michigan and CS Mott Children's Hospital, Ann Arbor, MI, USA. pesch@umich.edu.
Insights
Neurodevelopmental delays are common in children with congenital cytomegalovirus (cCMV), but inconsistent definitions of disease severity and outcome measures hinder precise quantification. Standardized approaches are needed for better understanding and clinical utility.
Area of Science:
- Pediatric Neurology
- Developmental Pediatrics
- Infectious Diseases
Background:
- Newborn screening for congenital cytomegalovirus (cCMV) is increasing, leading to more diagnosed infants requiring long-term monitoring.
- Understanding neurodevelopmental outcomes in children with cCMV is crucial for effective follow-up and intervention.
Purpose of the Study:
- To systematically review and summarize existing literature on neurodevelopmental outcomes in children with cCMV.
- To analyze how study-specific definitions of disease severity (symptomatic vs. asymptomatic) influence reported outcomes.
Main Methods:
- A systematic scoping review was conducted following PRISMA guidelines.
- Searched PubMed, PsychInfo, and Embase databases for studies on children (≤18 years) with cCMV measuring neurodevelopment.
- Included studies assessed global, motor, speech/language, or cognitive/intellectual domains.
Main Results:
- 33 studies met inclusion criteria; global development was most frequently assessed (n=21).
- Most studies (31/33) differentiated by cCMV severity, but definitions varied widely.
- Children with cCMV generally showed equivalent or lower neurodevelopmental scores compared to controls.
Conclusions:
- Inconsistent definitions of cCMV severity and the use of broad categorical outcomes limit the generalizability of findings.
- Standardized definitions and in-depth neurodevelopmental outcome reporting are recommended for future research in cCMV.
- Neurodevelopmental delays are prevalent in cCMV, but current literature gaps challenge precise quantification.
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.
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