Multicentre chest computed tomography standardisation in children and adolescents with cystic fibrosis: the way
Wieying Kuo1, Mariette P C Kemner-van de Corput2, Adria Perez-Rovira3
1Dept of Pediatric Pulmonology, Erasmus MC - Sophia Children's Hospital, Rotterdam, The Netherlands Dept of Radiology, Erasmus MC, Rotterdam, The Netherlands.
Insights
Standardizing chest CT protocols for pediatric cystic fibrosis (CF) patients is crucial for early disease monitoring. The SCIFI CF initiative found that despite protocol variations, CT scanner performance is similar across centers, enabling multicenter standardization for clinical trials.
Area of Science:
- Medical Imaging
- Pulmonology
- Pediatrics
Background:
- Progressive cystic fibrosis (CF) lung disease is a primary cause of mortality in CF patients, beginning in early childhood.
- Current care standards show normal respiratory function in children, necessitating sensitive measures for early CF lung disease detection.
- Chest CT is the most sensitive imaging technique for monitoring pulmonary structural changes in pediatric and adolescent CF patients.
Purpose of the Study:
- To standardize chest CT protocols for reliable quantification of structural lung disease across multiple centers.
- To optimize CT protocols for children and adolescents with CF in a multicenter setting.
- To assess chest CT image quality and radiation doses within the SCIFI CF framework.
Main Methods:
- The SCIFI CF (Standardised Chest Imaging Framework for Interventions and Personalised Medicine in CF) initiative involved 16 European CF centers across 10 countries.
- Characterization of chest CT image quality and radiation doses was performed.
- Analysis focused on optimizing CT protocols for pediatric and adolescent CF patients.
Main Results:
- A wide variation in CT protocols, image quality, and radiation dose usage was observed among participating centers.
- Despite variations, the performance of all CT scanners was found to be highly similar when considering spatial resolution and radiation dose.
- The study demonstrated the feasibility of multicenter standardization for chest CT in pediatric and adolescent CF patients.
Conclusions:
- Multicenter standardization of chest CT protocols in children and adolescents with CF is achievable.
- Standardized protocols are essential for reliable data in future clinical trials and personalized medicine approaches.
- This standardization will enhance the ability to monitor early CF lung disease and evaluate interventions effectively.
Abstract:
Progressive cystic fibrosis (CF) lung disease is the main cause of mortality in CF patients. CF lung disease starts in early childhood. With current standards of care, respiratory function remains largely normal in children and more sensitive outcome measures are needed to monitor early CF lung disease. Chest CT is currently the most sensitive imaging modality to monitor pulmonary structural changes in children and adolescents with CF. To quantify structural lung disease reliably among multiple centres, standardisation of chest CT protocols is needed. SCIFI CF (Standardised Chest Imaging Framework for Interventions and Personalised Medicine in CF) was founded to characterise chest CT image quality and radiation doses among 16 participating European CF centres in 10 different countries. We aimed to optimise CT protocols in children and adolescents among several CF centres. A large variety was found in CT protocols, image quality and radiation dose usage among the centres. However, the performance of all CT scanners was found to be very similar, when taking spatial resolution and radiation dose into account. We conclude that multicentre standardisation of chest CT in children and adolescents with CF can be achieved for future clinical trials.
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