Literature DB >> 11391207

Distraction osteogenesis of the craniofacial skeleton.

J G McCarthy1, E J Stelnicki, B J Mehrara, M T Longaker.   

Abstract

Distraction osteogenesis is becoming the treatment of choice for the surgical correction of hypoplasias of the craniofacial skeleton. Its principle is based on the studies of Ilizarov, who showed that osteogenesis can be induced if bone is expanded (distracted) along its long axis at the rate of 1 mm per day. This process induces new bone formation along the vector of pull without requiring the use of a bone graft. The technique also provides the added benefit of expanding the overlying soft tissues, which are frequently deficient in these patients. This article reviews the authors' 11-year clinical and research experience with mandibular distraction osteogenesis. It highlights the indications and contraindications of the technique and emphasizes the critical role that basic science research has played in its evolution.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11391207     DOI: 10.1097/00006534-200106000-00029

Source DB:  PubMed          Journal:  Plast Reconstr Surg        ISSN: 0032-1052            Impact factor:   4.730


  28 in total

1.  Masticatory mechanics of a mandibular distraction osteogenesis site: interfragmentary micromovement.

Authors:  Zongyang Sun; Katherine L Rafferty; Mark A Egbert; Susan W Herring
Journal:  Bone       Date:  2007-04-25       Impact factor: 4.398

2.  Mandibular mechanics after osteotomy and distraction appliance placement I: Postoperative mobility of the osteotomy site.

Authors:  Zongyang Sun; Katherine L Rafferty; Mark A Egbert; Susan W Herring
Journal:  J Oral Maxillofac Surg       Date:  2006-04       Impact factor: 1.895

Review 3.  The Effect of Photobiomodulation on Distraction Osteogenesis.

Authors:  Sarvin Sarmadi; Behrad Tanbakuchi; Arian Hesam Arefi; Nasim Chiniforush
Journal:  J Lasers Med Sci       Date:  2019-10-01

4.  Articular surface remodeling of the hip after periacetabular osteotomy.

Authors:  Brian J Rasquinha; Junaid Sayani; John F Rudan; Gavin C A Wood; Randy E Ellis
Journal:  Int J Comput Assist Radiol Surg       Date:  2011-07-08       Impact factor: 2.924

Review 5.  A review of reconstructive materials for use in craniofacial surgery bone fixation materials, bone substitutes, and distractors.

Authors:  James Tait Goodrich; Adam L Sandler; Oren Tepper
Journal:  Childs Nerv Syst       Date:  2012-08-08       Impact factor: 1.475

6.  Maxillary distraction osteogenesis versus orthognathic surgery for cleft lip and palate patients.

Authors:  Dimitrios Kloukos; Piotr Fudalej; Patrick Sequeira-Byron; Christos Katsaros
Journal:  Cochrane Database Syst Rev       Date:  2018-08-10

7.  An Update on Midface Advancement Using Le Fort II and III Distraction Osteogenesis.

Authors:  Youssef Tahiri; Jesse Taylor
Journal:  Semin Plast Surg       Date:  2014-11       Impact factor: 2.314

Review 8.  The role of 3D printing in treating craniomaxillofacial congenital anomalies.

Authors:  Christopher D Lopez; Lukasz Witek; Andrea Torroni; Roberto L Flores; David B Demissie; Simon Young; Bruce N Cronstein; Paulo G Coelho
Journal:  Birth Defects Res       Date:  2018-05-20       Impact factor: 2.344

9.  Pierre Robin sequence and Treacher Collins hypoplastic mandible comparison using three-dimensional morphometric analysis.

Authors:  Michael T Chung; Benjamin Levi; Jeong S Hyun; David D Lo; Daniel T Montoro; Jeffrey Lisiecki; James P Bradley; Steven R Buchman; Michael T Longaker; Derrick C Wan
Journal:  J Craniofac Surg       Date:  2012-11       Impact factor: 1.046

10.  Role of parathyroid hormone therapy in reversing radiation-induced nonunion and normalization of radiomorphometrics in a murine mandibular model of distraction osteogenesis.

Authors:  K Kelly Gallagher; Sagar Deshpande; Catherine N Tchanque-Fossuo; Alexis Donneys; Deniz Sarhaddi; Noah S Nelson; Douglas B Chepeha; Steven R Buchman
Journal:  Head Neck       Date:  2013-01-17       Impact factor: 3.147

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.