Local Soft Tissue and Bone Displacements Following Midfacial Bipartition Distraction in Apert Syndrome - Quantification Using a Semi-Automated Method.


Journal

The Journal of craniofacial surgery
ISSN: 1536-3732
Titre abrégé: J Craniofac Surg
Pays: United States
ID NLM: 9010410

Informations de publication

Date de publication:
Historique:
pubmed: 15 7 2021
medline: 5 11 2021
entrez: 14 7 2021
Statut: ppublish

Résumé

Patients with Apert syndrome experience midfacial hypoplasia, hypertelorism, and downslanting palpebral fissures which can be corrected by midfacial bipartition distraction with rigid external distraction device. Quantitative studies typically focus on quantifying rigid advancement and rotation postdistraction, but intrinsic shape changes of bone and soft tissue remain unknown. This study presents a method to quantify these changes. Pre- and post-operative computed tomography scans from patients with Apert syndrome undergoing midfacial bipartition distraction with rigid external distraction device were collected. Digital Imaging and Communications in Medicine files were converted to three-dimensional bone and soft tissue reconstructions. Postoperative reconstructions were aligned on the preoperative maxilla, followed by nonrigid iterative closest point transformation to determine local shape changes. Anatomical point-to-point displacements were calculated and visualized using a heatmap and arrow map. Nine patients were included.Zygomatic arches and frontal bone demonstrated the largest changes. Mid-lateral to supra-orbital rim showed an upward, inward motion. Mean bone displacements ranged from 3.3 to 12.8 mm. Soft tissue displacements were relatively smaller, with greatest changes at the lateral canthi. Midfacial bipartition distraction with rigid external distraction device results in upward, inward rotation of the orbits, upward rotation of the zygomatic arch, and relative posterior motion of the frontal bone. Local movements were successfully quantified using a novel method, which can be applied to other surgical techniques/syndromes.

Identifiants

pubmed: 34260460
doi: 10.1097/SCS.0000000000007875
pii: 00001665-202112000-00021
doi:

Types de publication

Journal Article

Langues

eng

Pagination

2646-2650

Informations de copyright

Copyright © 2021 by Mutaz B. Habal, MD.

Déclaration de conflit d'intérêts

The authors report no conflicts of interest.

Références

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Auteurs

Lara S van de Lande (LS)

UCL Great Ormond Street Institute of Child Health; Craniofacial Unit, Great Ormond Street Hospital for Children.

Eimear O'Sullivan (E)

UCL Great Ormond Street Institute of Child Health; Craniofacial Unit, Great Ormond Street Hospital for Children.
Department of Computing, Imperial College London, London, UK.

Paul G M Knoops (PGM)

UCL Great Ormond Street Institute of Child Health; Craniofacial Unit, Great Ormond Street Hospital for Children.

Athanasios Papaioannou (A)

UCL Great Ormond Street Institute of Child Health; Craniofacial Unit, Great Ormond Street Hospital for Children.
Department of Computing, Imperial College London, London, UK.

Juling Ong (J)

UCL Great Ormond Street Institute of Child Health; Craniofacial Unit, Great Ormond Street Hospital for Children.

Greg James (G)

UCL Great Ormond Street Institute of Child Health; Craniofacial Unit, Great Ormond Street Hospital for Children.

N Owase Jeelani (NO)

UCL Great Ormond Street Institute of Child Health; Craniofacial Unit, Great Ormond Street Hospital for Children.

Silvia Schievano (S)

UCL Great Ormond Street Institute of Child Health; Craniofacial Unit, Great Ormond Street Hospital for Children.

David J Dunaway (DJ)

UCL Great Ormond Street Institute of Child Health; Craniofacial Unit, Great Ormond Street Hospital for Children.

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