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   <subfield code="a">10.1007/s00167-013-2785-4</subfield>
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   <subfield code="a">Effect of VEGF-A165 addition on the integration of a cortical allograft in a tibial segmental defect in rabbits</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Miguel Ruiz-Ibán, Fausto Gonzalez-Lizán, Jorge Diaz-Heredia, Maria Elías-Martin, Carlos Correa Gorospe]</subfield>
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   <subfield code="a">Purpose: Long-bone segmental defects caused by infection, fracture, or tumour are a challenge for orthopaedic surgeons. Structural allografts are sometimes used in their treatment but their poor biological characteristics are a liability. The objective of this study was to determine whether the addition of recombinant vascular endothelial growth factor-A (VEGF) to a structural allograft improved its integration into a rabbit tibial segmental defect in a non-union model. Methods: Tibial segmental defects were filled with heat sterilized allogenic tubular tibiae sections and then stabilized with a screw plate. In the VEGF treatment group (n=6 tibiae), 2μg of VEGF added to a 50μl matrigel solution was inserted into the allograft cavity. In the control group (n=6 tibiae), only matrigel was added. After 12weeks, macroscopic and microscopic analysis, radiographs, and computerized micro-tomography (micro-CT) were performed. If allograft consolidation was present, a torsional resistance analysis was performed. Results: Addition of VEGF to the allograft decreased the rate of osteosynthesis failure compared with the control group (1/6 vs. 5/6, p=0.08), increased trabecular continuity evaluated by micro-CT in the bone-allograft interphases (8/12 vs. 2/12, p=0.036) and histological trabecular continuity (7/12 vs. 0/12, p=0.0046). Full consolidation was observed in three tibiae of the VEGF group and one in the control group (differences not significant); however, torsional resistance showed no significant differences (n.s.). Conclusion: Addition of VEGF to a structural allograph inserted into a rabbit tibial segmental defect increased allograft integration rate. Further research in this direction might help clinicians in dealing with large bone defects.</subfield>
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   <subfield code="a">Springer-Verlag Berlin Heidelberg, 2013</subfield>
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   <subfield code="a">Tibia</subfield>
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   <subfield code="a">Allograft</subfield>
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   <subfield code="a">Rabbit</subfield>
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   <subfield code="a">Ruiz-Ibán</subfield>
   <subfield code="D">Miguel</subfield>
   <subfield code="u">Department of Orthopaedic Surgery and Trauma, Hospital Universitario Ramón y Cajal, Cta Colmenar Km 9.100, 28034, Madrid, Spain</subfield>
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   <subfield code="a">Gonzalez-Lizán</subfield>
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   <subfield code="u">Department of Orthopaedic Surgery and Trauma, Hospital Universitario Ramón y Cajal, Cta Colmenar Km 9.100, 28034, Madrid, Spain</subfield>
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   <subfield code="a">Diaz-Heredia</subfield>
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   <subfield code="u">Department of Orthopaedic Surgery and Trauma, Hospital Universitario Ramón y Cajal, Cta Colmenar Km 9.100, 28034, Madrid, Spain</subfield>
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   <subfield code="a">Elías-Martin</subfield>
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   <subfield code="u">Department of Anesthesiology and Reanimation, Hospital Universitario Ramón y Cajal, Cta Colmenar Km 9.100, 28034, Madrid, Spain</subfield>
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   <subfield code="a">Correa Gorospe</subfield>
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   <subfield code="t">Knee Surgery, Sports Traumatology, Arthroscopy</subfield>
   <subfield code="d">Springer Berlin Heidelberg</subfield>
   <subfield code="g">23/5(2015-05-01), 1393-1400</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
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