Apert Syndrome Type III Hand: Prevalence and Outcomes

Author:

Raposo-Amaral Cassio E.12,Medeiros Lucas L.1,Raposo-Amaral Cesar A.1

Affiliation:

1. Institute of Plastic and Craniofacial Surgery, SOBRAPAR Hospital, Campinas

2. Department of Neurology, University of Campinas (UNICAMP), São Paulo, Brazil

Abstract

Background: The Upton type III hand, which represents the most severe hand type among Apert syndrome patients, has been considered the least prevalent hand type. The objective of this study is to address type III Apert hand prevalence and describe treatment strategies that will result in a 5 digit hand. Methods: The authors retrospectively reviewed 15 years of Apert syndrome hand practice at our hospital. Demographic (patient sex and age at the time of the operation), surgical (eg, techniques used for webspace release, osteotomy, and various aspects of soft-tissue reconstruction), and outcome (perioperative and long-term complication and need for revision operation) data was verified through medical records, clinical photographs, radiographic images, and interviews with patients’ families. Patients who had incomplete medical records and/or postoperative follow up <6 months in length were excluded from this study. Results: A total of 93 Apert patients [50 male (56.1%) and 43 female (43.9%)] were treated at our hospital from 2007 to 2021. Stratification of Apert hand severity using Upton’s classification system identified 34 patients with type I hands (36.4%), 19 patients with type II hands (20.6%), and 40 patients with type III hands (43%). Of the 40 patients with type III hands a 5 digit hand was achieved for 35 patients (87%), with an average of 3.37 operations per patient. Conclusions: The Upton type III hand is the most prevalent hand type among Apert syndrome patients. Following a three stage protocol, a surgical team can consistently achieve a 5 digit hand for the majority of Apert syndrome patients with type III hands.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine,Otorhinolaryngology,Surgery

Reference17 articles.

1. Paternal age as a contributing factor in Apert syndrome;Raposo-Amaral;J Craniofac Surg,2020

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3. What’s new in syndromic craniosynostosis surgery?;Taylor;Plast Reconstr Surg,2017

4. Apert syndrome management: changing treatment algorithm;Raposo-Amaral;J Craniofac Surg,2020

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