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   <subfield code="a">Paediatric cranial defect reconstruction using bioactive fibre-reinforced composite implant: early outcomes</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Jaakko Piitulainen, Jussi Posti, Kalle Aitasalo, Ville Vuorinen, Pekka Vallittu, Willy Serlo]</subfield>
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   <subfield code="a">Background: In children, approximately half of cryopreserved allograft bone flaps fail due to infection and resorption. Synthetic materials offer a solution for allograft bone flap resorption. Fibre-reinforced composite with a bioactive glass particulate filling is a new synthetic material for bone reconstruction. Bioactive glass is capable of chemically bonding with bone and is osteoinductive, osteoconductive and bacteriostatic. Fibre-reinforced composite allows for fabricating thin (0.8mm) margins for implant, which are designed as onlays on the existing bone. Bioactive glass is dissolved over time, whereas the fibre-reinforced composite serves as a biostable part of the implant, and these have been tested in preclinical and adult clinical trials. In this study, we tested the safety and other required properties of this composite material in large skull bone reconstruction with children. Method: Eight cranioplasties were performed on seven patients, aged 2.5-16years and having large (&gt;16cm2) skull bone defects. The implant used in this study was a patient-specific, glass-fibre-reinforced composite, which contained a bioactive glass particulate compound, S53P4. Results: During follow-up (average 35.1months), one minor complication was observed and three patients needed revision surgery. Two surgical site infections were observed. After treatment of complications, a good functional and cosmetic outcome was observed in all patients. The implants had an onlay design and fitted the defect well. In clinical and imaging examinations, the implants were in the original position with no signs of implant migration, degradation or mechanical breakage. Conclusions: Here, we found that early cranioplasty outcomes with the fibre-reinforced composite implant were promising. However, a longer follow-up time and a larger group of patients are needed to draw firmer conclusions regarding the long-term benefits of the proposed novel biomaterial and implant design. The glass-fibre-reinforced composite implant incorporated by particles of bioactive glass may offer an original, non-metallic and bioactive alternative for reconstruction of large skull bone defects in a paediatric population.</subfield>
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   <subfield code="a">Springer-Verlag Wien, 2015</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Cranioplasty</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Craniectomy</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Craniofacial bone reconstruction</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Fibre-reinforced composite</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">FRC</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Bioactive glass</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Paediatric</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Skull bone defect</subfield>
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   <subfield code="a">Piitulainen</subfield>
   <subfield code="D">Jaakko</subfield>
   <subfield code="u">Division of Surgery and Cancer Diseases, Department of Otorhinolaryngology - Head and Neck Surgery, Turku University Hospital, PO Box 52, 20521, Turku, Finland</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="a">Posti</subfield>
   <subfield code="D">Jussi</subfield>
   <subfield code="u">Division of Clinical Neurosciences, Department of Neurosurgery, Turku University Hospital, Turku, Finland</subfield>
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   <subfield code="a">Aitasalo</subfield>
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   <subfield code="u">Division of Surgery and Cancer Diseases, Department of Otorhinolaryngology - Head and Neck Surgery, Turku University Hospital, PO Box 52, 20521, Turku, Finland</subfield>
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   <subfield code="a">Vuorinen</subfield>
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   <subfield code="u">Division of Clinical Neurosciences, Department of Neurosurgery, Turku University Hospital, Turku, Finland</subfield>
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   <subfield code="a">Vallittu</subfield>
   <subfield code="D">Pekka</subfield>
   <subfield code="u">Department of Biomaterials Science and Turku Clinical Biomaterials Centre - TCBC, Institute of Dentistry, University of Turku, Turku, Finland</subfield>
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   <subfield code="a">Serlo</subfield>
   <subfield code="D">Willy</subfield>
   <subfield code="u">Department of Children and Adolescents, Oulu University Hospital, Oulu, Finland</subfield>
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  <datafield tag="773" ind1="0" ind2=" ">
   <subfield code="t">Acta Neurochirurgica</subfield>
   <subfield code="d">Springer Vienna</subfield>
   <subfield code="g">157/4(2015-04-01), 681-687</subfield>
   <subfield code="x">0001-6268</subfield>
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   <subfield code="a">BK010053</subfield>
   <subfield code="b">XK010053</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
   <subfield code="2">nationallicence</subfield>
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