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Published on: September 25, 2012
Progression from first symptom to diagnosis in childhood brain tumours
Sophie Wilne1, Jacqueline Collier, Colin Kennedy
1Department of Paediatric Oncology, Nottingham University Hospitals' NHS Trust Queen's Medical Centre, Nottingham, UK. sophie.wilne@nuh.nhs.uk
Insights
Diagnosing pediatric brain tumors often involves a median of six symptoms, a significant increase from symptom onset. Reducing the 3.3-month diagnostic interval is crucial for timely intervention in children with brain tumors.
Area of Science:
- Pediatric Neuro-oncology
- Clinical Neurology
- Childhood Cancer Research
Background:
- Delayed diagnosis of pediatric brain tumors impacts patient outcomes.
- Understanding the progression of clinical features is vital for early detection.
Purpose of the Study:
- To investigate the evolution of clinical features from symptom onset to diagnosis in children with brain tumors.
- To identify factors contributing to the delay in diagnosis and suggest methods for shortening this interval.
Main Methods:
- Retrospective analysis of 139 children diagnosed with brain tumors across four UK pediatric neuro-oncology centers.
- Detailed documentation of symptoms at onset and diagnosis, and the time interval between them.
Main Results:
- The median number of symptoms increased from one at onset to six at diagnosis.
- The median time from symptom onset to diagnosis was 3.3 months.
- Headache, nausea/vomiting, motor and visual abnormalities, and behavioral changes significantly increased from onset to diagnosis.
Conclusions:
- A significant evolution of clinical features occurs between symptom onset and diagnosis in pediatric brain tumors.
- Longer diagnostic delays were associated with specific symptoms like head tilt and cranial nerve palsies.
- Interventions aimed at recognizing and addressing these evolving symptoms are needed to shorten the time to diagnosis.
Abstract:
This study was undertaken to investigate the evolution of clinical features between onset of symptoms and diagnosis in children with brain tumours and to identify ways of shortening the time to diagnosis. One hundred and thirty-nine children with a brain tumour were recruited from four UK paediatric neuro-oncology centres. Children had a median of one symptom or sign at symptom onset and six by diagnosis. The symptoms and/or signs experienced at symptom onset and at diagnosis were as follows: headache in 55 and 81 children, nausea and vomiting in 39 and 88 children, motor system abnormalities in 31 and 93 children, cranial nerve palsies in 24 and 75 children, visual system abnormalities in 23 and 96 children, endocrine or growth abnormalities in 10 and 35 children and behavioural change in 4 and 55 children. The median time between symptom onset and diagnosis (symptom interval) was 3.3 months. A longer symptom interval was associated with head tilt, cranial nerve palsies, endocrine and growth abnormalities and reduced visual acuity. More than half of children with brain tumours developed problems with vision and more than a third developed motor problems, cranial nerve palsies, behavioural change, or nausea and vomiting between symptom onset and diagnosis.
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