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Published on: October 20, 2017
[Cerebrovascular accidents in paediatric care. Our experience gained over an 18-year period]
Ignacio Ruiz del Olmo-Izuzquiza1, Antonio de Arriba-Muñoz, Javier López-Pisón
1Unidad de Neuropediatría, Hospital Universitario Miguel Servet, 50009 Zaragoza, España.
Insights
Pediatric non-hemorrhagic cerebrovascular accidents (CVA) are rare, especially without prior pathology. This study reviewed 41 cases, identifying various causes and outcomes, highlighting the need for collaborative specialist care.
Area of Science:
- Neurology
- Pediatrics
- Vascular Medicine
Context:
- Non-hemorrhagic cerebrovascular accidents (CVA) in children are uncommon.
- This study focuses on post-natal CVA cases in pediatric patients without pre-existing conditions.
- A 18-year review (1990-2008) of 10,270 children identified 41 cases of post-natal non-hemorrhagic CVA.
Purpose:
- To review the experience with pediatric non-hemorrhagic cerebrovascular accidents (CVA) occurring after the perinatal period.
- To analyze cases with no previous pathology.
- To understand the causes, treatments, and outcomes of these rare pediatric events.
Summary:
- The study identified 41 pediatric non-hemorrhagic CVA cases, with 13 having no known prior pathology.
- Causes included ischemic CVA (ICVA), venous sinus thrombosis, and hemorrhagic infarction, with identified triggers like fibromuscular dysplasia and infections.
- Outcomes varied, with some patients experiencing no sequelae, others hemiparesis, and two fatalities (one ICVA, one thrombosis).
Impact:
- Highlights the diverse etiologies of pediatric non-hemorrhagic CVA.
- Underscores the challenges in establishing clear treatment guidelines due to limited research and trials in pediatric populations.
- Emphasizes the critical need for multidisciplinary collaboration among specialists for optimal patient management.
Patients And Methods:
This study reviews our experience over the last 18 years with paediatric patients diagnosed with non-haemorrhagic cerebrovascular accidents (CVA) after the perinatal period. Data were collected for the period between May 1990 and May 2008 (n = 10 270 children) and special attention was given to cases with no previous pathology.
Results:
We found 41 cases that were diagnosed with post-natal non-haemorrhagic CVA, of which 13 did not present any known pathology at the onset of the symptoms. Nine patients were diagnosed as having ischaemic CVA (ICVA), three cases had thrombosis of the venous sinuses and there was one case of haemorrhagic infarction (HI). No causation was found in five cases, three of which were heterozygotic for the C677T mutation of methylenetetrahydrofolate reductase. ICVA was caused by fibromuscular dysplasia, aneurysm of the auricular septum and patent foramen ovale, homocystinuria and chickenpox. A recent ear infection and diminished levels of protein C were noted in two cases of venous thrombosis. Five patients with ICVA and the case of HI were treated with oral antiaggregants, anticoagulants were administered in two of the thromboses, and the remaining cases did not receive any treatment. Seven patients (four ICVA, two thromboses and the HI) did not present any kind of sequelae, four ICVA presented different degrees of hemiparesis and two died (one ICVA and one thrombosis).
Conclusions:
The scarcity of studies and therapeutic clinical trials in the paediatric age makes it difficult to lay down clear guidelines of conduct, especially from the therapeutic point of view. The different specialists involved must collaborate with each other.
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