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Comprehensive Endovascular and Open Surgical Management of Cerebral Arteriovenous Malformations
Published on: October 20, 2017
Results of the surgical treatment in children with Chiari malformation type I
Paweł Jarski1, Mikołaj Zimny1, Michał Linart1
1Department of Pediatric Neurosurgery, Medical University of Silesia in Katowice, ul. Medykow 16, 40-752, Katowice, Poland.
Insights
Surgery for Chiari malformation type 1 (CM-1) in pediatric patients significantly improves quality of life. Most patients experienced positive outcomes, with no reported worsening after surgical intervention.
Area of Science:
- Pediatric Neurosurgery
- Neurology
- Quality of Life Research
Background:
- Chiari malformation type 1 (CM-1) is a complex neurological condition requiring careful surgical consideration in pediatric patients.
- Evaluating the long-term impact of surgical interventions on patient well-being is crucial for treatment optimization.
Purpose of the Study:
- To assess the quality of life in pediatric patients following surgical treatment for Chiari malformation type 1 (CM-1).
- To analyze the effectiveness of surgical intervention in improving patient outcomes using a standardized scale.
Main Methods:
- Retrospective analysis of 11 pediatric patients with CM-1 treated between 2007 and 2016.
- Short-term evaluation involved symptom and radiological assessment pre- and post-surgery.
- Long-term follow-up utilized the Chicago Chiari Outcome Scale (CCOS) survey questionnaires.
Main Results:
- 55% of patients (6/11) showed improvement in quality of life based on CCOS scores.
- 45% of patients (5/11) remained unchanged; no patients worsened post-surgery.
- A significant negative correlation was observed between CCOS score and age at surgery (R = -0.85, p = 0.0009).
Conclusions:
- Surgical intervention in symptomatic pediatric CM-1 patients leads to improved quality of life.
- The Chicago Chiari Outcome Scale (CCOS) is an effective tool for measuring long-term outcomes.
- Careful consideration of surgical indications is essential for pediatric CM-1 management.
Purpose:
Our study aimed to evaluate the quality of life of the patients operated due to Chiari malformation type 1 (CM-1) in the Department of Pediatric Neurosurgery, Medical University of Silesia in Katowice.
Methods:
We performed a retrospective analysis of 11 patients diagnosed with CM-1 who were treated in our center in the years 2007 to 2016. There were 6 female and 5 male individuals. Short-term evaluation of the outcome was based on comparison of the presenting symptoms and radiological images before and after the surgical treatment. Long-term follow-up was carried out using survey questionnaires based on the Chicago Chiari Outcome Scale (CCOS) devised originally by Aliaga et al. RESULTS: Patients, based on their CCOS score were divided into three groups marked as "improved," "unchanged," and "worse," depending on a range of CCOS score: 13-16, 9-12, 4-8, respectively. The outcome of patients was as follows: 6 patients (55%) were evaluated as improved, and 5 (45%) as unchanged. No patient was classified as worse after surgery. Significant negative Spearman's correlation was found between the CCOS score and patients' age at the time of surgery (R = - 0.85, p = 0.0009).
Conclusions:
The decision of whether to operate pediatric patients with CM-1 should be considered very carefully. In our department, the main indication for surgery was the occurrence of clinical symptoms. Our study revealed that in the symptomatic patients, surgery improves their quality of life measured with CCOS.
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