Related Experiment Video
Updated: May 15, 2026

Endoscopic Septoplasty with Limited Two-line Resection: Minimally Invasive Surgery for Septal Deviation
Published on: June 20, 2018
Restricting indications for sinonasal computed tomography in children with cystic fibrosis
Oren Cavel1, Marie-Claude Quintal, Jacques-Édouard Marcotte
1Departments of Otorhinolaryngology, Sainte-Justine University Hospital, University of Montreal, Montreal, Quebec, Canada. orencavel@gmail.com
Insights
Strict criteria for sinonasal computed tomographic (CT) scans in children with cystic fibrosis (CF) can significantly lower radiation exposure. Preoperative planning is the primary valid indication for CT scans in this pediatric population.
Area of Science:
- Pediatric Radiology
- Otolaryngology
- Pulmonology
Background:
- Children with cystic fibrosis (CF) face increased risks of sinonasal disease.
- Longer life expectancy in CF patients necessitates minimizing cumulative radiation exposure.
- Sinonasal computed tomographic (CT) scans are often used in CF care but carry radiation risks.
Purpose of the Study:
- To determine if strict criteria can limit sinonasal CT scan use in pediatric CF patients.
- To assess the effectiveness of CT scans in guiding treatment for CF-related sinonasal issues.
- To highlight the importance of radiation dose reduction in this growing patient population.
Main Methods:
- Retrospective chart review of 277 children with CF over 11 years.
- Analysis of 39 sinonasal CT scans performed on 33 patients.
- Evaluation of scan indications, ordering physician, treatment modifications, and time to surgery.
Main Results:
- Only 12% of CF patients underwent sinonasal CT scans (0.018 scans/patient/year).
- Preoperative planning accounted for 74% of scans, identifying disease extent and obstruction.
- Non-preoperative scans (26%) did not alter patient management.
Conclusions:
- Stringent criteria effectively reduce sinonasal CT scan exposure in children with CF.
- Preoperative planning is the optimal indication for sinonasal CT in this group.
- CT scans for general disease evaluation in CF patients may be unnecessary and avoidable.
Abstract:
OBJECTIVES To evaluate whether a low rate of exposure to sinonasal computed tomographic (CT) scans can be achieved when strict criteria are applied for their use in children with cystic fibrosis (CF) and to emphasize the importance of limiting radiation exposure in the context of the current longer life expectancy in this group of patients. DESIGN Retrospective chart review. SETTING Tertiary care children's hospital. PATIENTS The study included 277 children who were regularly followed up in the CF clinic in the last 11 years (mean duration of follow up, 7.87 years), 33 of whom underwent sinonasal CT. MAIN OUTCOME MEASURES Indications used for scanning, health professional (ear, nose, and throat specialist or pulmonologist) ordering the test, eventual modifications of ongoing treatment according to CT results, and time lapse between CT scanning and surgery. RESULTS Of 277 children with CF, 33 (12%) underwent a total of 39 sinonasal CT scans during the follow-up period (0.018 scans per patient per year of follow-up). Twenty-nine of the CT scans (74% of all cases, 90% of CT scans ordered by the ear, nose, and throat surgeon) were performed in the preoperative context and demonstrated the extent of the polypoid disease whenever present (26 cases [90%]) and the cause of nasal obstruction (20 cases [69%]). The mean period between the scanning and the surgery was 57 days (range, 0.10-173 days). Computed tomographic scans that were not meant for preoperative planning were performed in 10 cases (26%). The indications were disease evaluation (10%), ruling out a mucocele (5%); pre-lung transplantation status (5%), ruling out an intraorbital complication (3%); and headache investigation (3%). The results of the scans did not modify the management of the disease in those patients. CONCLUSIONS With the use of stringent criteria, it is possible to achieve a low rate of exposure to sinonasal CT scans in the population of children with CF. The main indication should be the preoperative planning regarding anatomy, extent of disease, and sites of nasal obstruction. The use of CT scans for disease evaluation does not seem to appreciably modify the treatment course and could be avoided.
Related Concept Videos
Cystic Fibrosis: Management
Sinus disease and chronic sinusitis...
Imaging Studies I: CT and MRI
Description of the Procedures
Computed Tomography (CT) scan:
Computed Tomography (CT) scans use X-ray technology to generate detailed images of bones, organs, and tissues. During the scan, the patient lies on a moving table...
Radiological Investigation I: X-ray and CT
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation, but...
Imaging Studies III: Computed Tomography
Imaging Studies for Cardiovascular System V: CT
