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Neurodevelopmental long-term outcome in children after hemolytic uremic syndrome
Kathrin Buder1, Beatrice Latal, Samuel Nef
1Pediatric Nephrology Unit, University Children's Hospital, Zurich, Steinwiesstrasse 75, 8032, Zurich, Switzerland.
Insights
Children with hemolytic uremic syndrome (HUS) show normal cognitive function long-term. However, neuromotor skills are impaired, regardless of central nervous system (CNS) involvement during HUS.
Area of Science:
- Pediatric Neurology
- Nephrology
- Neurodevelopmental Disorders
Background:
- Hemolytic uremic syndrome (HUS) is a serious condition affecting children.
- Long-term neurodevelopmental outcomes after HUS require further investigation.
- Understanding the impact of central nervous system (CNS) involvement during HUS is crucial.
Purpose of the Study:
- To assess the long-term neurodevelopmental outcomes in children following HUS.
- To compare neurodevelopmental outcomes based on the presence of CNS involvement during the acute phase of HUS.
Main Methods:
- Retrospective cohort study of 47 children with a history of HUS.
- Neurodevelopmental assessment included cognitive (Wechsler Intelligence Scale) and neuromotor (Zurich Neuromotor Assessment) evaluations.
- Evaluation of neurological symptoms during the acute phase of HUS.
Main Results:
- The study population exhibited normal mean full-scale IQ scores.
- Significant impairments were observed in adaptive fine motor, gross motor, static balance, and associated movements.
- No significant difference in neurodevelopmental outcomes was found between children with and without CNS involvement during HUS.
Conclusions:
- Children recovering from HUS demonstrate favorable cognitive outcomes.
- Neuromotor deficits are a common long-term consequence of HUS in children.
- Acute CNS involvement during HUS does not predict long-term neurodevelopmental outcomes.
Background:
To investigate the long-term neurodevelopmental outcome in children after hemolytic uremic syndrome (HUS) and to compare outcome dependent on central nervous system (CNS) involvement during HUS.
Methods:
A single-center retrospective cohort of 47 children was examined at a median age of 10.6 (range 6-16.9) years and a median follow-up of 7.8 (range 0.4-15.3) years after having had HUS. Intellectual performance was assessed with the German version of the Wechsler Intelligence Scale 4th version and neuromotor performance with the Zurich Neuromotor Assessment (ZNA). The occurrence of neurological symptoms during the acute phase of HUS was evaluated retrospectively.
Results:
Mean IQ of the whole study population fell within the normal range (median full scale IQ 104, range 54-127). Neuromotor performance was significantly poorer in the domains "adaptive fine," "gross motor," "static balance" (all p < 0.05) and "associated movements" (p < 0.001); only the "pure motor" domain was within the normal reference range. Neurological findings occurred in 16/47 patients (34 %) during acute HUS. Neurodevelopmental outcome was not significantly different between children with or without CNS involvement.
Conclusions:
Our follow-up of children after HUS showed a favorable cognitive outcome. However, neuromotor outcome was impaired in all study participants. Neurological impairment during acute HUS was not predictive of outcome.
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