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A Single-Center Retrospective Analysis of a Standardized Sedation Protocol for MRI in Children with Achondroplasia:
Barbora Nedomová1,2, Lucia Babulicová1, Ľubica Tichá3
1Department of Pediatric Anesthesiology and Intensive Medicine, Faculty of Medicine, Comenius University and National Institute of Children's Diseases, 83340 Bratislava, Slovakia.
Insights
A standardized sedation protocol using midazolam and propofol is safe and effective for pediatric achondroplasia patients undergoing MRI, yielding high-quality images with minimal complications.
Area of Science:
- Pediatric Anesthesiology
- Medical Imaging
- Skeletal Dysplasias
Background:
- Achondroplasia presents unique challenges for procedural sedation in children.
- Distinct anatomical and physiological features require specialized approaches for sedation.
Purpose of the Study:
- To evaluate a standardized sedation protocol for magnetic resonance imaging (MRI) in pediatric achondroplasia patients.
- Assess the safety, effectiveness, and imaging quality of the protocol.
Main Methods:
- Retrospective analysis of 22 MRI procedures in 12 pediatric patients.
- Utilized intravenous midazolam and propofol with continuous monitoring and standardized dosing.
- Compared sedation parameters between age groups (<1 year and ≥1 year).
Main Results:
- High-quality MRI images were obtained in all cases.
- Sedation was safe and effective, with one instance of self-limited desaturation (4.5%) and no other complications.
- No significant differences in sedative doses or infusion rates were observed between age groups, indicating protocol consistency.
Conclusions:
- The standardized sedation protocol is safe, effective, and reproducible for pediatric achondroplasia patients undergoing MRI.
- This approach ensures high-quality diagnostic imaging with a low incidence of adverse events.
- The protocol demonstrates consistency across different age groups within the pediatric population.
Abstract:
Background/Objectives: Achondroplasia, the most common form of skeletal dysplasia, poses significant challenges for procedural sedation due to distinct anatomical and physiological features. This study evaluated the safety, effectiveness, and imaging quality of a standardized sedation protocol for magnetic resonance imaging (MRI) in children with achondroplasia. Methods: We conducted a single-center, retrospective analysis of 22 MRI procedures in 12 pediatric patients. Intravenous midazolam and propofol were used as primary sedatives, with continuous monitoring and standardized dosing. Sedation parameters were compared between children aged <1 year and children aged ≥1 year. Results: The median sedation duration was 35 (25-65) min, and the median recovery time was 9 (5-14) min. No significant differences were found between age groups in midazolam dose (<1 year: 0.15 ± 0.05 mg/kg vs. ≥1 year: 0.13 ± 0.04 mg/kg; p = 0.238), propofol induction (2.26 ± 1.14 vs. 1.80 ± 0.52 mg/kg; p = 0.375), or infusion rate (3.18 ± 2.74 vs. 5.13 ± 2.65 mg/kg/h; p = 0.203), indicating protocol consistency. High-quality images were obtained in all cases. In one case (4.5%), self-limited desaturation to 92% occurred, with no intervention required. No airway instrumentation or other complications were reported. Conclusions: This protocol provides safe, effective, and reproducible sedation in children with achondroplasia, ensuring high-quality MRI with minimal adverse events.
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