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Clinical features and prognostic analysis of posterior reversible encephalopathy syndrome in children
Ting Deng1,2, Xinyu Zhang1, Xiaoling Peng3
1Department of Neurology Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing, China.
Insights
Posterior reversible encephalopathy syndrome (PRES) in children often results from renal or hematological disorders and hypertension. While most pediatric PRES cases show good prognosis, MRI severity and hospital stay length are key risk factors for adverse outcomes.
Area of Science:
- Pediatric Neurology
- Radiology
- Internal Medicine
Background:
- Posterior Reversible Encephalopathy Syndrome (PRES) is a neurological condition affecting children.
- Understanding its clinical features and prognosis is crucial for effective management.
Purpose of the Study:
- To investigate the clinical characteristics of pediatric PRES.
- To determine the prognostic factors influencing outcomes in children with PRES.
Main Methods:
- Retrospective analysis of clinical data from 47 children diagnosed with PRES.
- Data collected from June 2015 to May 2019 at a children's hospital.
- Follow-up assessment using the modified Rankin Scale.
Main Results:
- Common PRES causes included renal disorders (62%), hematological diseases (28%), and hypertension (11%).
- Seizures (91%), hypertension (98%), and parietal-occipital lobe involvement on MRI (89%) were frequent findings.
- Most patients (87%) showed symptom relief within 1-2 weeks; however, 32% experienced adverse outcomes, including epilepsy and mental decline.
Conclusions:
- Pediatric PRES is a syndrome with diverse etiologies and characteristic clinical and radiographic features.
- While many children recover well, MRI severity and prolonged hospital stay are independent predictors of poor outcomes.
Background:
We aimed to investigate the clinical features and prognosis of posterior reversible encephalopathy syndrome (PRES) in children.
Methods:
Clinical data of children with PRES diagnosed at the Children's Hospital of Chongqing Medical University from June 2015 to May 2019 were retrospectively analyzed.
Results:
The study enrolled 47 patients with a mean age at diagnosis of 8.79 ± 3.72 years (range, 2-15 years). PRES causes included renal disorder (29/47), hematological disease (13/47), and hypertension (5/47). PRES manifested as seizure (43/47), headache (28/47), visual impairment (18/47), dizziness (18/47), vomiting (18/47), and mental and behavioral abnormalities (17/47). Forty-six children had hypertension (46/47) at PRES onset. Magnetic resonance imaging (MRI) mainly involved the parietal and occipital lobes (42/47), 38 cases were mild (38/47), seven were moderate (7/47), and two were severe (2/47). The clinical symptoms of 41 patients (41/47) were relieved within 1-2 weeks. Thirty-seven children were followed up for 7-54 months (modified Rankin Scale). Twenty-five children had favorable outcomes (25/37). Twelve children had adverse outcomes (12/37), including epilepsy, disorders of consciousness, visual impairment, and mental decline. Analysis of single factors revealed that severity on MRI, length of in-hospital stay, and mental and behavioral abnormalities were related to adverse outcomes after PRES. Analysis of multiple factors revealed that severity on MRI and length of in-hospital stay were independent risk factors for PRES.
Conclusion:
Pediatric PRES is a clinical radiographic syndrome with multiple etiologies. Most patients have a good prognosis. Severity on MRI and length of in-hospital stay are independent risk factors.
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