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Magnetic Resonance Imaging Detects Chronic Rhinosinusitis in Infants and Preschool Children with Cystic Fibrosis
Olaf Sommerburg1,2,3, Mark O Wielpütz2,3,4, Jan-Philipp Trame2,3,4
1Division of Pediatric Pulmonology & Allergy and Cystic Fibrosis Center, Department of Pediatrics.
Insights
Magnetic resonance imaging (MRI) revealed high rates of chronic rhinosinusitis (CRS) in young children with cystic fibrosis (CF). This non-invasive method can aid in diagnosing and monitoring CRS in this vulnerable population.
Area of Science:
- Pediatric Pulmonology
- Medical Imaging
- Otolaryngology
Background:
- Chronic rhinosinusitis (CRS) significantly impacts patients with cystic fibrosis (CF).
- The early onset and progression of CRS in infants and preschool-aged children with CF are not well understood.
- Understanding CRS in young CF patients is crucial for managing disease burden.
Purpose of the Study:
- To investigate the prevalence and extent of CRS in young children with CF.
- To utilize magnetic resonance imaging (MRI) for assessing sinonasal abnormalities in CF.
- To establish a baseline for CRS diagnosis and monitoring in pediatric CF patients.
Main Methods:
- 67 infants and preschool children with CF and 30 non-CF controls underwent MRI under sedation.
- A dedicated CRS MRI scoring system evaluated paranasal sinus dimensions and structural abnormalities.
- Abnormalities assessed included mucosal swelling, mucopyoceles, nasal polyps, and maxillary sinus wall deformation.
Main Results:
- Paranasal sinus dimensions were similar between CF and control groups.
- MRI showed significantly higher prevalence of mucosal swelling (83% vs. 17%), mucopyoceles (75% vs. 2%), polyps (26% vs. 7%), and maxillary sinus wall deformation (68% vs. 2%) in CF patients.
- The MRI sum score for CRS abnormalities was substantially higher in CF patients (22.9 ± 10.9) compared to controls (4.5 ± 7.6).
Conclusions:
- MRI demonstrated normal paranasal sinus dimensions but a high prevalence and severity of CRS-related abnormalities in young CF patients.
- This study supports MRI as a sensitive, non-invasive tool for diagnosing and monitoring CRS in infants and preschool children with CF.
- MRI findings can serve as valuable outcome measures in clinical trials for pediatric CF patients with CRS.
Abstract:
Rationale: Chronic rhinosinusitis (CRS) contributes to disease burden of patients with cystic fibrosis (CF). However, its onset and progression in infants and preschool children with CF remain poorly understood.Objectives: To determine the prevalence and extent of CRS in young children with CF using magnetic resonance imaging (MRI).Methods: MRI was performed in sedation in 67 infants and preschool children with CF (mean age 2.3 ± 2.1 yr; range 0-6 yr) and 30 non-CF control subjects (3.5 ± 2.0 yr; range 0-6 yr). Paranasal sinus dimensions and structural abnormalities, including mucosal swelling; mucopyoceles; and nasal polyps of the maxillary, frontal, sphenoid, and ethmoid sinuses; and, in addition, medial maxillary sinus wall deformation, were assessed using a dedicated CRS MRI scoring system.Results: Pneumatization and dimensions of paranasal sinuses did not differ between the two groups. MRI detected an increased prevalence of mucosal swelling (83% vs. 17%; P < 0.001), mucopyoceles (75% vs. 2%; P < 0.001), polyps (26% vs. 7%; P < 0.001), and maxillary sinus wall deformation (68% vs. 2%; P < 0.001) in infants and preschool children with CF compared with age-matched control subjects. Furthermore, the extent of these abnormalities was also increased with a MRI sum score of 22.9 ± 10.9 in CF compared with 4.5 ± 7.6 in non-CF control subjects (P < 0.001).Conclusions: MRI detected normal dimensions of paranasal sinuses, and a high prevalence and severity of paranasal sinus abnormalities due to CRS in infants and preschool children with CF without radiation exposure. Our results support the development of MRI for sensitive noninvasive diagnosis and monitoring of CRS in young children with CF, and as outcome measures for clinical trials.Clinical trial registered with www.clinicaltrials.gov (NCT00760071).
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