Comparison of Biodegradable and Titanium Fixation Systems in Maxillofacial Surgery

Author:

van Bakelen N.B.1,Buijs G.J.1,Jansma J.1,de Visscher J.G.A.M.2,Hoppenreijs Th.J.M.3,Bergsma J.E.4,Stegenga B.15,Bos R.R.M.1

Affiliation:

1. Department of Oral and Maxillofacial Surgery, University Medical Centre Groningen, University of Groningen, P.O. Box 30.001, 9700 RB Groningen, The Netherlands

2. Department of Oral and Maxillofacial Surgery, Medical Centre Leeuwarden, P.O. Box 888, 8901 BR Leeuwarden, The Netherlands

3. Department of Oral and Maxillofacial Surgery, Rijnstate Hospital Arnhem, 6800 TA Arnhem, P.O. Box 9555, The Netherlands

4. Department of Oral and Maxillofacial Surgery, Amphia Hospital Breda, Postbus 90.158, 4800 RK Breda, The Netherlands

5. UMCG Centre for Dentistry and Oral Hygiene, Department of Oral Health Care & Clinical Epidemiology, University Medical Centre Groningen, University of Groningen, P.O. Box 30.001, 9700 RB Groningen, The Netherlands

Abstract

Biodegradable osteosynthesis could reduce/delete the problems associated with titanium plate removal. The aim of the present study was to compare the clinical performance in the first 2 post-operative years between a biodegradable and a titanium system in oral and maxillofacial surgery. The multicenter randomized controlled trial (RCT) was performed in the Netherlands from December 2006 to July 2009. Included were 230 patients who underwent a bilateral sagittal split osteotomy (BSSO) and/or a Le Fort-I osteotomy and those treated for fractures of the mandible, maxilla, or zygoma. The patients were randomly assigned to a titanium group (KLS Martin) or to a biodegradable group (Inion CPS). Plate removal was necessary in 16 of the 134 patients (11.9%) treated with titanium and in 21 of the 87 patients (24.1%) treated with the biodegradable system within the first 2 post-operative years [ p = .016, HR biodegradable (95% CI) = 2.2 (1.1-4.2), HR titanium = 1]. Occlusion, VAS, and MFIQ scores showed that both groups had good mandibular function and were (almost) free of pain 1 and 2 years post-operatively ( http://controlled-trials.com ISRCTN 44212338).

Publisher

SAGE Publications

Subject

General Dentistry

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