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Updated: Jun 6, 2026

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Measuring Maxillary Posterior Tooth Movement: A Model Assessment using Palatal and Dental Superimposition
Published on: February 23, 2024
Five years experience with a new intraoral maxillary distraction device (RID)
Arnaud Picard1, Patrick A Diner, Eva Galliani
1AP-HP, Hôpital d'enfants Armand-Trousseau, Service de Chirurgie Maxillo-Faciale et Chirurgie Plastique, Paris, F-75012, France. a.picard@trs.aphp.fr
The British Journal of Oral & Maxillofacial Surgery
|December 15, 2010
Summary
A new intraoral device for maxillary distraction osteogenesis successfully treated severe retromaxilla in 19 patients. This innovative device improved surgical control and patient comfort while achieving significant maxillary advancement.
Area of Science:
- Oral and Maxillofacial Surgery
- Orthodontics
- Craniofacial Surgery
Background:
- Severe retromaxilla requires effective treatment modalities.
- Maxillary distraction osteogenesis is a recognized surgical technique.
- Existing devices may have limitations in surgical exposure and patient comfort.
Purpose of the Study:
- To evaluate the efficacy and patient experience of a novel intraoral maxillary distraction device.
- To assess the degree of maxillary advancement achieved with the new device.
- To compare the new device with existing maxillary distraction systems.
Main Methods:
- Retrospective case series of 19 patients treated since 2004.
- Utilized a new intraoral device for maxillary distraction osteogenesis.
- Measured maxillary advancement using lateral cephalograms.
Main Results:
- Successful maxillary advancement in all 19 patients.
- Mean advancement of 9.6mm (range 4-17mm).
- The new device demonstrated reduced surgical exposure, fewer implanted materials, and enhanced control during distraction.
Conclusions:
- The novel intraoral device is effective for treating severe retromaxilla.
- This device offers improved surgical outcomes and patient comfort compared to traditional methods.
- The device is psychologically well-accepted and comfortable for patients undergoing maxillary advancement.
