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Evaluation of Pediatric Posterior Glottic Diastasis Using Dynamic Voice Computed Tomography
Anisha R Noble1, Robert J Fleck2, Matthew T Maksimoski1
1Division of Pediatric Otolaryngology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, U.S.A.
Pediatric patients with posterior glottic diastasis (PGD) and dysphonia have larger posterior glottic gaps. Endoscopic posterior cricoid reduction (ePCR) effectively improved voice quality by reducing the glottic gap.
Area of Science:
- Laryngology
- Pediatric Otolaryngology
- Voice Disorders
Background:
- Posterior glottic diastasis (PGD) is a significant cause of dysphonia in children with a history of airway reconstruction or prolonged intubation.
- Endoscopic posterior cricoid reduction (ePCR) is a surgical technique to address PGD by reducing the posterior glottic gap.
Purpose of the Study:
- To describe pediatric PGD using dynamic voice computed tomography (DVCT).
- To establish surgical parameters for ePCR by comparing posterior glottic gaps in dysphonic and non-dysphonic children.
- To evaluate the efficacy of ePCR in improving voice function.
Main Methods:
- Retrospective review of DVCTs from 2014-2023 in pediatric patients undergoing ePCR and non-dysphonic controls.
- Analysis of ePCR operative reports, pre- and postoperative Pediatric Voice Handicap Index (pVHI) and Consensus Auditory-Perceptual Evaluation of Voice (CAPE-V) scores, and aerodynamic measures.
Main Results:
- Dysphonic patients (n=17) had significantly larger posterior glottic gaps (median 2.4 mm) compared to non-dysphonic controls (n=19, median 1.3 mm).
- The average width of cricoid removed during ePCR was 1.6 mm.
- Significant improvements were observed in pVHI (55.5 to 34.6) and CAPE-V (52.7 to 36.5) scores post-ePCR.
Conclusions:
- A posterior glottic gap of 1.3 mm is tolerated in children without dysphonia.
- Pediatric patients with PGD present with a median gap of 2.4 mm, which was effectively reduced by 1.6 mm via ePCR.
- ePCR demonstrated significant improvement in dysphonia, optimizing management for pediatric PGD.
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