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Development of AOSpine BOnE (Bone Osteobiologics and Evidence) Classification
STUDY DESIGN: Classification development. OBJECTIVES: The aim of our study was to develop a 3-tier classification for the levels of evidence for osteobiologics and provide a description of the principles by which osteobiologics can be evaluated. BOnE (Bone Osteobiologics and Evidence) classification...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7485069/ https://www.ncbi.nlm.nih.gov/pubmed/32905732 http://dx.doi.org/10.1177/2192568219880176 |
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author | Wang, Jeffrey C. Yoon, S. Tim Brodke, Darrel S. Park, Jong-Beom Hsieh, Patrick Meisel, Hans-Joerg Buser, Zorica |
author_facet | Wang, Jeffrey C. Yoon, S. Tim Brodke, Darrel S. Park, Jong-Beom Hsieh, Patrick Meisel, Hans-Joerg Buser, Zorica |
author_sort | Wang, Jeffrey C. |
collection | PubMed |
description | STUDY DESIGN: Classification development. OBJECTIVES: The aim of our study was to develop a 3-tier classification for the levels of evidence for osteobiologics and provide a description of the principles by which osteobiologics can be evaluated. BOnE (Bone Osteobiologics and Evidence) classification evaluates each osteobiologic based on the available evidence, and if the published evidence is based on clinical, in vivo or in vitro studies. METHODS: The process of establishing the BOnE classification included 5 face-to-face meetings and 2 web calls among members of the AOSpine Knowledge Forum Degenerative. RESULTS: The 3 levels of evidence were determined based on the type of data on osteobiologics: level A for human studies, level B for animal studies, and level C for in vitro studies, with level A being the highest level of evidence. Each level was organized into 4 subgroups (eg, A1, A2, A3, and A4). CONCLUSIONS: The use and the variety of osteobiologics for spine fusion has dramatically increased over the past few decades; however, literature on their effectiveness is inconclusive. Several prior systematic reviews developed by AOSpine Knowledge Forum Degenerative reported low level of evidence primarily due to the high risk of bias, small sample size, lack of control groups, and limited patient-reported outcomes. BOnE classification will provide a universal platform for research studies and journal publications to classify a new or an existing product and will allow for creating decision-making algorithms for surgical planning. |
format | Online Article Text |
id | pubmed-7485069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-74850692020-09-17 Development of AOSpine BOnE (Bone Osteobiologics and Evidence) Classification Wang, Jeffrey C. Yoon, S. Tim Brodke, Darrel S. Park, Jong-Beom Hsieh, Patrick Meisel, Hans-Joerg Buser, Zorica Global Spine J Original Articles STUDY DESIGN: Classification development. OBJECTIVES: The aim of our study was to develop a 3-tier classification for the levels of evidence for osteobiologics and provide a description of the principles by which osteobiologics can be evaluated. BOnE (Bone Osteobiologics and Evidence) classification evaluates each osteobiologic based on the available evidence, and if the published evidence is based on clinical, in vivo or in vitro studies. METHODS: The process of establishing the BOnE classification included 5 face-to-face meetings and 2 web calls among members of the AOSpine Knowledge Forum Degenerative. RESULTS: The 3 levels of evidence were determined based on the type of data on osteobiologics: level A for human studies, level B for animal studies, and level C for in vitro studies, with level A being the highest level of evidence. Each level was organized into 4 subgroups (eg, A1, A2, A3, and A4). CONCLUSIONS: The use and the variety of osteobiologics for spine fusion has dramatically increased over the past few decades; however, literature on their effectiveness is inconclusive. Several prior systematic reviews developed by AOSpine Knowledge Forum Degenerative reported low level of evidence primarily due to the high risk of bias, small sample size, lack of control groups, and limited patient-reported outcomes. BOnE classification will provide a universal platform for research studies and journal publications to classify a new or an existing product and will allow for creating decision-making algorithms for surgical planning. SAGE Publications 2019-10-23 2020-10 /pmc/articles/PMC7485069/ /pubmed/32905732 http://dx.doi.org/10.1177/2192568219880176 Text en © The Author(s) 2019 https://creativecommons.org/licenses/by-nc-nd/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 License (https://creativecommons.org/licenses/by-nc-nd/4.0/) which permits non-commercial use, reproduction and distribution of the work as published without adaptation or alteration, without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Articles Wang, Jeffrey C. Yoon, S. Tim Brodke, Darrel S. Park, Jong-Beom Hsieh, Patrick Meisel, Hans-Joerg Buser, Zorica Development of AOSpine BOnE (Bone Osteobiologics and Evidence) Classification |
title | Development of AOSpine BOnE (Bone Osteobiologics and Evidence) Classification |
title_full | Development of AOSpine BOnE (Bone Osteobiologics and Evidence) Classification |
title_fullStr | Development of AOSpine BOnE (Bone Osteobiologics and Evidence) Classification |
title_full_unstemmed | Development of AOSpine BOnE (Bone Osteobiologics and Evidence) Classification |
title_short | Development of AOSpine BOnE (Bone Osteobiologics and Evidence) Classification |
title_sort | development of aospine bone (bone osteobiologics and evidence) classification |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7485069/ https://www.ncbi.nlm.nih.gov/pubmed/32905732 http://dx.doi.org/10.1177/2192568219880176 |
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