Long-Term Outcomes After External Maxillary Distraction Surgery in Patients With Down Syndrome

Patients with Down syndrome have severe facial deformities that can precipitate functional consequences and social stigmatization. Craniofacial surgical intervention can play a role in improving these symptoms and patient quality of life. The objective of this study was to investigate the long-term...

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Published inThe Journal of craniofacial surgery Vol. 34; no. 3; p. 1045
Main Authors Arnold, Sydney H, Figueroa, Alvaro A, Wiegmann, Aaron L, Lee, Jugyeong, Padala, Soumya, Hamati, Fadi, Hansdorfer, Marek A, Tragos, Christina
Format Journal Article
LanguageEnglish
Published United States 01.05.2023
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Abstract Patients with Down syndrome have severe facial deformities that can precipitate functional consequences and social stigmatization. Craniofacial surgical intervention can play a role in improving these symptoms and patient quality of life. The objective of this study was to investigate the long-term outcomes of distraction osteogenesis and orthognathic surgical intervention in patients with Down syndrome. Charts of 3 patients with Down syndrome who were treated with external maxillary distraction osteogenesis were retrospectively reviewed. The patients' caregivers were prospectively interviewed between 10 and 15 years after surgery to determine surgical stability, long-term function, and quality of life status. All patients and their caregivers reported excellent results with improvements in function and quality of life. Facial skeletal changes have been stable over time. The cephalometric analysis demonstrated significant maxillary advancement in all 3 patients and mandibular changes to correct mandibular prognathism and asymmetry in the patient who underwent finishing orthognathic surgery. External maxillary distraction osteogenesis and orthognathic surgery may be considered in select patients with Down syndrome as part of their multidisciplinary health care. These interventions can result in long-term improvements in patient function and quality of life.
AbstractList Patients with Down syndrome have severe facial deformities that can precipitate functional consequences and social stigmatization. Craniofacial surgical intervention can play a role in improving these symptoms and patient quality of life. The objective of this study was to investigate the long-term outcomes of distraction osteogenesis and orthognathic surgical intervention in patients with Down syndrome. Charts of 3 patients with Down syndrome who were treated with external maxillary distraction osteogenesis were retrospectively reviewed. The patients' caregivers were prospectively interviewed between 10 and 15 years after surgery to determine surgical stability, long-term function, and quality of life status. All patients and their caregivers reported excellent results with improvements in function and quality of life. Facial skeletal changes have been stable over time. The cephalometric analysis demonstrated significant maxillary advancement in all 3 patients and mandibular changes to correct mandibular prognathism and asymmetry in the patient who underwent finishing orthognathic surgery. External maxillary distraction osteogenesis and orthognathic surgery may be considered in select patients with Down syndrome as part of their multidisciplinary health care. These interventions can result in long-term improvements in patient function and quality of life.
Author Wiegmann, Aaron L
Hamati, Fadi
Padala, Soumya
Figueroa, Alvaro A
Hansdorfer, Marek A
Arnold, Sydney H
Lee, Jugyeong
Tragos, Christina
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Snippet Patients with Down syndrome have severe facial deformities that can precipitate functional consequences and social stigmatization. Craniofacial surgical...
SourceID pubmed
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StartPage 1045
SubjectTerms Cephalometry
Down Syndrome - complications
Humans
Maxilla - abnormalities
Maxilla - surgery
Osteogenesis, Distraction - methods
Quality of Life
Retrospective Studies
Skull
Treatment Outcome
Title Long-Term Outcomes After External Maxillary Distraction Surgery in Patients With Down Syndrome
URI https://www.ncbi.nlm.nih.gov/pubmed/36882912
Volume 34
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