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Stem cell therapy for the treatment of early stage avascular necrosis of the femoral head: a systematic review

BACKGROUND: Avascular necrosis (AVN) of the femoral head (FH) is believed to be caused by a multitude of etiologic factors and is associated with significant morbidity in younger populations. Eventually, the disease progresses and results in FH collapse. Thus, a focus on early disease management aim...

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Autores principales: Lau, Rick L, Perruccio, Anthony V, Evans, Heather MK, Mahomed, Safiyyah R, Mahomed, Nizar N, Gandhi, Rajiv
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4038713/
https://www.ncbi.nlm.nih.gov/pubmed/24886648
http://dx.doi.org/10.1186/1471-2474-15-156
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author Lau, Rick L
Perruccio, Anthony V
Evans, Heather MK
Mahomed, Safiyyah R
Mahomed, Nizar N
Gandhi, Rajiv
author_facet Lau, Rick L
Perruccio, Anthony V
Evans, Heather MK
Mahomed, Safiyyah R
Mahomed, Nizar N
Gandhi, Rajiv
author_sort Lau, Rick L
collection PubMed
description BACKGROUND: Avascular necrosis (AVN) of the femoral head (FH) is believed to be caused by a multitude of etiologic factors and is associated with significant morbidity in younger populations. Eventually, the disease progresses and results in FH collapse. Thus, a focus on early disease management aimed at joint preservation by preventing or delaying progression is key. The use of stem cells (SC) for the treatment of AVN of the FH has been proposed. We undertook a systematic review of the medical literature examining the use of SC for the treatment of early stage (precollapse) AVN of the FH, in both pre-clinical and clinical studies. METHODS: Data collected included: Pre-clinical studies – model of AVN, variety and dosage of SC, histologic and imaging analyses. Clinical studies – study design, classification and etiology of AVN, SC dosage and treatment protocol, incidence of disease progression, patient reported outcomes, volume of necrotic lesion and hip survivorship. RESULTS: In pre-clinical studies, the use of SC uniformly demonstrated improvements in osteogenesis and angiogenesis, yet source of implanted SC was variable. In clinical studies, groups treated with SC showed significant improvements in patient reported outcomes; however hip survivorship was not affected. Discrepancies regarding dose of SC, AVN etiology and disease severity were present. CONCLUSIONS: Routine use of this treatment method will first require further research into dose and quality optimization as well as confirmed improvements in hip survivorship.
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spelling pubmed-40387132014-05-31 Stem cell therapy for the treatment of early stage avascular necrosis of the femoral head: a systematic review Lau, Rick L Perruccio, Anthony V Evans, Heather MK Mahomed, Safiyyah R Mahomed, Nizar N Gandhi, Rajiv BMC Musculoskelet Disord Research Article BACKGROUND: Avascular necrosis (AVN) of the femoral head (FH) is believed to be caused by a multitude of etiologic factors and is associated with significant morbidity in younger populations. Eventually, the disease progresses and results in FH collapse. Thus, a focus on early disease management aimed at joint preservation by preventing or delaying progression is key. The use of stem cells (SC) for the treatment of AVN of the FH has been proposed. We undertook a systematic review of the medical literature examining the use of SC for the treatment of early stage (precollapse) AVN of the FH, in both pre-clinical and clinical studies. METHODS: Data collected included: Pre-clinical studies – model of AVN, variety and dosage of SC, histologic and imaging analyses. Clinical studies – study design, classification and etiology of AVN, SC dosage and treatment protocol, incidence of disease progression, patient reported outcomes, volume of necrotic lesion and hip survivorship. RESULTS: In pre-clinical studies, the use of SC uniformly demonstrated improvements in osteogenesis and angiogenesis, yet source of implanted SC was variable. In clinical studies, groups treated with SC showed significant improvements in patient reported outcomes; however hip survivorship was not affected. Discrepancies regarding dose of SC, AVN etiology and disease severity were present. CONCLUSIONS: Routine use of this treatment method will first require further research into dose and quality optimization as well as confirmed improvements in hip survivorship. BioMed Central 2014-05-16 /pmc/articles/PMC4038713/ /pubmed/24886648 http://dx.doi.org/10.1186/1471-2474-15-156 Text en Copyright © 2014 Lau et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Lau, Rick L
Perruccio, Anthony V
Evans, Heather MK
Mahomed, Safiyyah R
Mahomed, Nizar N
Gandhi, Rajiv
Stem cell therapy for the treatment of early stage avascular necrosis of the femoral head: a systematic review
title Stem cell therapy for the treatment of early stage avascular necrosis of the femoral head: a systematic review
title_full Stem cell therapy for the treatment of early stage avascular necrosis of the femoral head: a systematic review
title_fullStr Stem cell therapy for the treatment of early stage avascular necrosis of the femoral head: a systematic review
title_full_unstemmed Stem cell therapy for the treatment of early stage avascular necrosis of the femoral head: a systematic review
title_short Stem cell therapy for the treatment of early stage avascular necrosis of the femoral head: a systematic review
title_sort stem cell therapy for the treatment of early stage avascular necrosis of the femoral head: a systematic review
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4038713/
https://www.ncbi.nlm.nih.gov/pubmed/24886648
http://dx.doi.org/10.1186/1471-2474-15-156
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