When mpox outbreaks happen, a pressing question is how they affect children. A new global review of existing studies and case reports offers some initial answers, but also shows how much we still need to learn. The analysis found that the rate of positive PCR tests for mpox in kids ranged widely—from about 7% in regions where the virus isn't common to over 35% in areas where it is endemic. The research, which looked at data from paediatric populations worldwide, suggests younger children may be more susceptible to severe complications. Common symptoms included progressive skin lesions and fever. The review also pointed to potential risk factors like close household contact and having other infections at the same time. It's important to understand this isn't a new experiment or clinical trial. The findings come from pulling together and analyzing many different existing reports, which means the exact numbers might not apply everywhere. The review didn't establish cause-and-effect for the risk factors, only associations. Its main value is in painting a clearer picture of how mpox manifests in children globally, which public health officials can use to craft better, age-specific guidelines and improve diagnostic efforts.
Paediatric mpox PCR positivity rates range from 6.95% to 35.6% in global systematic reviewHow does mpox affect children? New review finds wide range in positive tests
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This systematic review and meta-analysis examined the epidemiology, clinical manifestations, and management of mpox in paediatric populations globally, synthesizing data from 22 studies. The analysis included 1414 records from databases and 24 from gray literature, covering both endemic and non-endemic regions. No specific intervention or comparator was reported, as the review focused on descriptive outcomes including pooled positivity rates, risk factors, and clinical features.
The main results showed PCR positivity rates for paediatric mpox cases ranging from 6.95% to 35.6%. Specifically, positivity was 6.95% in non-endemic regions and 35.6% in endemic areas. Clinical manifestations commonly included progressive skin lesions and fever. The review identified younger children as more susceptible to severe complications and noted key risk factors including close household contact, coinfections, and socioeconomic factors. Safety and tolerability data were not reported.
Key limitations include the observational nature of the included studies and case reports, which precludes establishing causality for identified risk factors. The review reports ranges rather than precise pooled estimates, and generalizability of exact positivity rates beyond these ranges is uncertain. Funding and conflicts of interest were not reported. For practice, the findings underscore a need for age-specific public health interventions, improved diagnostic capabilities, and harmonized clinical guidelines, but should be interpreted with caution given the evidence base.