TY - JOUR
T1 - Predicting Severe Short-Term Neurologic Outcomes in Human Parechovirus Meningoencephalitis
AU - Shah, Nisha
AU - Katragkou, Aspasia
AU - Fortin, Olivier
AU - Tomatis Souverbielle, Cristina
AU - Santos Oren, Marina
AU - Sheth, Avni
AU - Calardo, Sarah
AU - Hauger, Sarmistha B.
AU - Angelis, Dimitrios
AU - Gagliardo, Christina
AU - Solaiman, Adil
AU - Erdem, Guliz
AU - Harik, Nada
AU - Mulkey, Sarah B.
AU - Downey, Rachel
AU - Ansusinha, Emily
AU - Chalak, Lina
AU - Chiu, Stephanie
AU - Di Pentima, M. Cecilia
AU - Sánchez, Pablo J.
AU - Teran, Paul R.
N1 - Copyright © 2025 by the American Academy of Pediatrics.
PY - 2025/10/1
Y1 - 2025/10/1
N2 - BACKGROUND AND OBJECTIVES: Human parechovirus (PeV) is an increasingly recognized cause of meningoencephalitis (ME) in infants. The US 2022 outbreak provided opportunity to analyze the clinical presentation and predictors of severe disease in affected infants. METHODS: We conducted a multicenter retrospective review of infants diagnosed with PeV ME during the outbreak. We examined demographics, clinical features, laboratory findings, and neuroimaging results. Logistic regression was used to identify predictors of complicated disease and abnormal brain magnetic resonance imaging (MRI). Complicated disease was defined as requiring intensive care or findings of an abnormal brain MRI or electroencephalogram. RESULTS: 139 infants had PeV ME. The median age was 19 days. Fever was the most common presenting symptom (89.2%) and was associated with uncomplicated disease and normal MRI. A total of 42 (30.2%) infants had complicated disease. Hypothermia (36.5% vs 5.1%), somnolence (38.1% vs 13.4%), poor feeding (76.1% vs 47.4%), hemodynamic instability (28.5% vs 3%), seizures (57.1% vs 4.1%), apnea (40.4% vs 0%), hypoglycemia (16.6% vs 1%), mechanical ventilation (23.8% vs 0%), and inotropic support (11.9% vs 0%) were associated with complicated disease. Younger age and seizures were predictors of abnormal MRI on multivariable analysis (adjusted odds ratio, 0.92 [0.48-0.99] and 40.1 [3.49-460.7], respectively). Laboratory findings, including cerebrospinal fluid indices, were rarely abnormal. CONCLUSION: Despite nonspecific symptoms on presentation and normal laboratory values, PeV can cause complicated disease, requiring clinicians to maintain high suspicion for this infection. We suggest PeV evaluation in workup of infant sepsis cases, neuroimaging in patients at high risk, and long-term developmental follow-up.
AB - BACKGROUND AND OBJECTIVES: Human parechovirus (PeV) is an increasingly recognized cause of meningoencephalitis (ME) in infants. The US 2022 outbreak provided opportunity to analyze the clinical presentation and predictors of severe disease in affected infants. METHODS: We conducted a multicenter retrospective review of infants diagnosed with PeV ME during the outbreak. We examined demographics, clinical features, laboratory findings, and neuroimaging results. Logistic regression was used to identify predictors of complicated disease and abnormal brain magnetic resonance imaging (MRI). Complicated disease was defined as requiring intensive care or findings of an abnormal brain MRI or electroencephalogram. RESULTS: 139 infants had PeV ME. The median age was 19 days. Fever was the most common presenting symptom (89.2%) and was associated with uncomplicated disease and normal MRI. A total of 42 (30.2%) infants had complicated disease. Hypothermia (36.5% vs 5.1%), somnolence (38.1% vs 13.4%), poor feeding (76.1% vs 47.4%), hemodynamic instability (28.5% vs 3%), seizures (57.1% vs 4.1%), apnea (40.4% vs 0%), hypoglycemia (16.6% vs 1%), mechanical ventilation (23.8% vs 0%), and inotropic support (11.9% vs 0%) were associated with complicated disease. Younger age and seizures were predictors of abnormal MRI on multivariable analysis (adjusted odds ratio, 0.92 [0.48-0.99] and 40.1 [3.49-460.7], respectively). Laboratory findings, including cerebrospinal fluid indices, were rarely abnormal. CONCLUSION: Despite nonspecific symptoms on presentation and normal laboratory values, PeV can cause complicated disease, requiring clinicians to maintain high suspicion for this infection. We suggest PeV evaluation in workup of infant sepsis cases, neuroimaging in patients at high risk, and long-term developmental follow-up.
KW - Disease Outbreaks
KW - Electroencephalography
KW - Female
KW - Humans
KW - Infant
KW - Infant, Newborn
KW - Magnetic Resonance Imaging
KW - Male
KW - Meningoencephalitis/epidemiology
KW - Parechovirus
KW - Picornaviridae Infections/complications
KW - Prognosis
KW - Retrospective Studies
KW - Severity of Illness Index
UR - https://www.scopus.com/pages/publications/105017772653
U2 - 10.1542/peds.2025-071878
DO - 10.1542/peds.2025-071878
M3 - Article
C2 - 40935385
AN - SCOPUS:105017772653
SN - 0031-4005
VL - 156
JO - Pediatrics
JF - Pediatrics
IS - 4
M1 - e2025071878
ER -