From Birth to Maturity: Midline Tessier 0–14 Craniofacial Cleft Patients who have Completed Protocol Management at a Single Craniofacial Unit

Author:

Pidgeon Thomas E.1,Flapper Walter J.2,David David J.3,Anderson Peter J.3

Affiliation:

1. University Hospital Coventry and Warwickshire NHS Trust, Coventry, West Midlands, United Kingdom.

2. Australian Craniofacial Unit, Women's and Children's Hospital, Adelaide, Australia.

3. Faculty of Health Sciences, University of Adelaide, Adelaide, Australia.

Abstract

Introduction The rare craniofacial clefts form an important component of craniofacial pathology, but little has been written regarding the definitive management of affected patients. This report describes the presentation, management, and outcomes in a group of patients who have completed their protocol management for treatment of midline Tessier 0–14 clefts. Methods A retrospective review of the clinical, photographic, and radiographic records of all midline cleft patients treated at a single center was performed. Data describing each patient's presenting features, surgical management, and final outcomes are presented. Results Four patients were identified as having completed protocol management for Tessier 0–14 midline clefting at the unit. The age range at the most recent follow-up was 19.3 to 36.3 years. Three patients had entered protocol management during infancy, and the remaining patient presented to the unit at 13.8 years of age. The surgical management regimen is described in detail. Outcomes for development, hearing, speech, and vision at maturity were all acceptable. Three patients attained a respectable educational and social status. With respect to facial aesthetics scores, the only significant difference after management was a significant worsening of deformity in the region of the orbits. The Whitaker grade for repeat surgery improved after management (3.25 before to 2.63 postmanagement), but this improvement was not statistically significant. Conclusion Presented are the results of the first cohort of midline Tessier 0–14 cleft patients to have completed protocol management at a single craniofacial unit. As more patients complete their management in the future, further refinements to the protocol could be made.

Publisher

SAGE Publications

Subject

Otorhinolaryngology,Oral Surgery

Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Rare craniofacial clefts: Surgical management protocols;Journal of Plastic, Reconstructive & Aesthetic Surgery;2024-10

2. Introducing A Family With Tens of Rare Craniofacial Clefts;Journal of Craniofacial Surgery;2019

3. The Rare Facial Cleft;Cleft Lip and Palate Treatment;2017-09-20

4. Tessier Clefts and Hypertelorism;Facial Plastic Surgery Clinics of North America;2016-11

5. Functional Analysis of SPECC1L in Craniofacial Development and Oblique Facial Cleft Pathogenesis;Plastic and Reconstructive Surgery;2014-10

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