Key result
Non-polio enteroviruses detected in ~11% of acute flaccid paralysis cases and linked to residual weakness.
Why the study?
To determine the prevalence, epidemiologic trends, and clinical features of non-polio enteroviruses among children with acute flaccid paralysis in Iraq to improve surveillance sensitivity and guide public health measures.
Observational (n=5,662)
Yes
Non-polio enteroviruses are a significant cause of acute flaccid paralysis in Iraqi children, particularly those aged 1-2 years, and are associated with residual weakness but lower mortality compared to NPEV-negative cases.
Answers are grounded in this paper and cite their sources.
AFP surveillance detects ongoing NPEV circulation; leaves open serotype-specific risks and interventions.
Background: Acute flaccid paralysis surveillance, forms the basis for poliovirus eradication efforts and provides useful data on non-polio enteroviruses, which are significant causes of acute flaccid paralysis in polio-free countries. Non polio enteroviruses were the most common isolates from acute flaccid paralysis cases at this time, indicating sensitivity of surveillance and continued circulation of enteroviruses. Objectives: This study aimed to determine the prevalence, epidemiologic trends and clinical features of non- polio enteroviruses among children with acute flaccid paralysis in Iraq, from 2018 to 2024, for improving surveillance sensitivity and complementary evidence-based public health measures. Methods: The data was gathered from the acute flaccid paralysis surveillance system in Iraq. Stool specimens were analyzed at the National Polio Laboratory according to the World Health Organization guidelines. Suspensions of stool were prepared and inoculated into the Rhabdomyosarcoma cell line and genetically modified mouse L cells expressing the human poliovirus receptor. Isolates were subjected for real-time polymerase chain reaction, whereas cultures were checked for cytopathic effect. Isolates negative for poliovirus but positive in Rhabdomyosarcoma cells were classified as non-polio enteroviruses. Demographics and clinical findings were analyzed using appropriate statistical tests. Results: Non-polio enteroviruses were reported in 10.5% of the cases; the prevalence being highest in children 1 to 2 years. They appeared to be two peaks; one in January and another in May, and cases were particularly low in September. Non-polio enteroviruses were associated with residual weakness and lower mortality. Conclusions: Non-polio enteroviruses detection declined during 2020–2023 with recovery in 2024. Positivity was significantly higher in younger children, and demonstrated clear seasonal peaks. Non-polio enteroviruses infection was associated with residual weakness but not with gender, fever, or mortality.
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Nasir et al. (2026) conducted an observational in Acute Flaccid Paralysis (n=5,662). Non-polio enteroviruses (NPEV) vs. NPEV-negative acute flaccid paralysis cases was evaluated on Prevalence of non-polio enteroviruses in acute flaccid paralysis cases. Non-polio enteroviruses were detected in 10.5% of acute flaccid paralysis cases in Iraqi children under 15 years, with significantly higher positivity in younger children and an association with residual weakness.
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