Induction of a barrier membrane to facilitate reconstruction of massive segmental diaphyseal bone defects: An ovine model

被引:108
作者
Viateau, Veronique [1 ]
Guillemin, Genevieve
Calando, Yolande
Logeart, Delphine
Oudina, Karim
Sedel, Laurent
Hannouche, Didier
Bousson, Valerie
Petite, Herve
机构
[1] Univ Paris 07, Fac Med Lariboisiere St Louis, Unite Pedagog Pathol Chirurg,Ctr Natl Rech Sci Sc, Ecole Natl Vet Alfort,Lab Rech Orthoped, Paris, France
[2] Univ Paris 07, Fac Med Lariboisiere St Louis, UMR 7052, Expt Radiol Lab, Paris, France
关键词
D O I
10.1111/j.1532-950X.2006.00173.x
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Objectives-To report an ovine model that can be used to evaluate the efficacy of bone substitutes for repair of segmental diaphyseal bone defects. Study Design-Experimental study. Animals-Eleven 2-year-old Pre-Alpes Sheep. Methods-Mid-diaphyseal metatarsal bone defects (25 mm long) were stabilized by a dynamic compression plate over a polymethylmethacrylate (PMMA) cement spacer, and by external coaptation. The PMMA spacer was removed at 6 weeks by incising the encapsulating membrane. The defect remained unfilled (Group 1; n=5) or was filled with morselized autologous corticocancellous graft (Group 2; n=6), the membrane sutured closed, and external coaptation applied for 6 months, when healing was evaluated. Results-Radiographic, computed tomographic, and histologic examinations at 6 months after the 2nd surgery revealed non-union in ungrafted defects whereas grafted defects showed bone healing. The induced membrane had blood vessels, CBFA1+ cells, and very few macrophages entrapped in a collagenous tissue positive for type I collagen. Conclusion-This ovine metatarsal defect model resulted in a critical-size defect (non-union) that healed when grafted. The PMMA-induced membrane constrained the graft, was well vascularized, and may have osteogenic properties. Clinical Relevance-This model may be useful to evaluate new strategies in bone tissue engineering because the PMMA-induced membrane may help confine bone morphogenetic proteins, skeletal stem cells, or other agents to the defect cavity where they could be useful to enhance bone formation.
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页码:445 / 452
页数:8
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