Bone defect filling with a novel rattan-wood based not-sintered hydroxyapatite and beta-tricalcium phosphate material (b.Bone™) after tricortical bone graft harvesting - A consecutive clinical case series of 9 patients.

Biomaterial Bone defect Hydroxyapatite Iliac crest beta-tricalcium phosphate

Journal

Trauma case reports
ISSN: 2352-6440
Titre abrégé: Trauma Case Rep
Pays: Netherlands
ID NLM: 101711730

Informations de publication

Date de publication:
Apr 2023
Historique:
accepted: 17 02 2023
entrez: 28 2 2023
pubmed: 1 3 2023
medline: 1 3 2023
Statut: epublish

Résumé

Harvesting of tricortical bone graft from the iliac crest is an integral part of bone defect reconstruction in orthopaedic surgery. There are several options for filling the iliac crest defect area to avoid hematoma, pain, hernias and cosmetic issues, including different gelatin-based and other alternative biomaterials. Recently, a novel rattan-wood based not-sintered hydroxyapatite and beta-tricalcium phosphate material (b.Bone™, GreenBone ORTHO S.p.A Faenza, Italy) was shown to promote bone healing in an experimental setting. The goal of the current work is to report clinical and radiographical outcomes of a consecutive case series of 9 patients with defect filling at the iliac crest with this novel scaffold biomaterial after tricortical bone graft harvesting with a minimum follow-up of 6 months. All 9 patients (8 male, 1 female) with an average age of 42.7 years (range: 18-76 years) had tricortical bone graft harvesting from the iliac crest for different reconstructive procedures at the extremities and received blocks of the biomaterial with an average size of 26.3 × 16.8 × 10 mm (length, height, width; range: 15 × 15 × 10 to 40 × 20 × 10 mm). Intraoperative handling of the biomaterial was easy and the blocks could be customized to the individual size of the defect with standard surgical instruments and were press-fitted into the defect. All 9 patients showed uneventful wound healing at the iliac crest and 7 patients reported no pain (VAS: 0) and two patients only mild pain (VAS:1 and VAS:3) after an average follow-up of 9.8 months (range: 6-16 months). There was no post-operative hematoma, surgical revision or other implant-related complications at the iliac crest. In all patients, good radiographical integration without dislocation of the implant and good bony integration was observed. The use of this novel biomaterial for iliac crest defect filling was associated with good clinical and radiographical outcomes after an average follow-up of 9.8 months.

Identifiants

pubmed: 36851907
doi: 10.1016/j.tcr.2023.100805
pii: S2352-6440(23)00053-5
pmc: PMC9958041
doi:

Types de publication

Case Reports

Langues

eng

Pagination

100805

Informations de copyright

© 2023 The Authors. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

VA, TB and MP are paid consultants for GREENBONE ORTHO S.p.A., 48018 Faenza (RA), Italy.

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Auteurs

Volker Alt (V)

Department of Trauma Surgery, University Hospital Regensburg, Germany.

Nike Walter (N)

Department of Trauma Surgery, University Hospital Regensburg, Germany.

Markus Rupp (M)

Department of Trauma Surgery, University Hospital Regensburg, Germany.

Thierry Begué (T)

Department of Orthopedics and Trauma Surgery, Antoine Beclere Hospital, University Paris-Saclay, France.

Michael Plecko (M)

AUVA - Trauma Center Styria (UKH) Hospital Graz, Austria.

Classifications MeSH