Cargando…

Autologous matrix-induced chondrogenesis is effective for focal chondral defects of the knee

Focal chondral defects of the knee are common and their management is challenging. This study investigated the efficacy and safety of Autologous Matrix-Induced Chondrogenesis (AMIC) for focal chondral defects of the knee. A systematic review and meta-analysis was conducted (according to the 2020 PRI...

Descripción completa

Detalles Bibliográficos
Autores principales: Migliorini, Filippo, Maffulli, Nicola, Baroncini, Alice, Bell, Andreas, Hildebrand, Frank, Schenker, Hanno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9167289/
https://www.ncbi.nlm.nih.gov/pubmed/35661147
http://dx.doi.org/10.1038/s41598-022-13591-6
_version_ 1784720784234643456
author Migliorini, Filippo
Maffulli, Nicola
Baroncini, Alice
Bell, Andreas
Hildebrand, Frank
Schenker, Hanno
author_facet Migliorini, Filippo
Maffulli, Nicola
Baroncini, Alice
Bell, Andreas
Hildebrand, Frank
Schenker, Hanno
author_sort Migliorini, Filippo
collection PubMed
description Focal chondral defects of the knee are common and their management is challenging. This study investigated the efficacy and safety of Autologous Matrix-Induced Chondrogenesis (AMIC) for focal chondral defects of the knee. A systematic review and meta-analysis was conducted (according to the 2020 PRISMA statement) to investigate the efficacy of AMIC in improving symptoms and to compare AMIC versus microfracture (MFx). In January 2022, the following databases were accessed: Pubmed, Web of Science, Google Scholar, Embase. No time constrain was used for the search. All the clinical trials investigating AMIC and/or those comparing AMIC versus MFx for focal chondral defects of the knee were accessed. Only studies published in peer reviewed journals were considered. Studies which investigated other locations of the defects rather than knee were not eligible, nor those reporting data form mixed locations. Studies which reported data on revision settings, as well as those investigating efficacy on kissing lesions or multiple locations, were not suitable. The mean difference (MD) and odd ratio (OR) effect measure were used for continuous and binary data, respectively. Data from 18 studies (548 patients) were retrieved with a mean follow-up of 39.9 ± 26.5 months. The mean defect size was 3.2 ± 1.0 cm(2). The visual analogue scale (VAS) decreased of − 3.9/10 (95% confidence interval (CI) − 4.0874 to -3.7126), the Tegner Activity Scale increased of + 0.8/10 (95% CI 0.6595 to 0.9405). The Lysholm Knee Scoring System increased of + 28.9/100 (95% CI 26.8716 to 29.1284), as did the International Knee Documentation Committee (IKDC) + 33.6/100 (95% CI 32.5800 to 34.6200). At last follow-up no patient showed signs of hypertrophy. 4.3% (9 of 210) of patients underwent revision procedures. The rate of failure was 3.8% (9 of 236). Compared to MFx, AMIC demonstrated lower VAS score (MD: − 1.01; 95% CI − 1.97 to 0.05), greater IKDC (MD: 11.80; 95% CI 6.65 to 16.94), and lower rate of revision (OR: 0.16; 95% CI 0.06 to 0.44). AMIC is effective for focal chondral defects of the knee. Furthermore, AMIC evidenced greater IKDC, along with a lower value of VAS and rate of revision compared to MFx.
format Online
Article
Text
id pubmed-9167289
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-91672892022-06-06 Autologous matrix-induced chondrogenesis is effective for focal chondral defects of the knee Migliorini, Filippo Maffulli, Nicola Baroncini, Alice Bell, Andreas Hildebrand, Frank Schenker, Hanno Sci Rep Article Focal chondral defects of the knee are common and their management is challenging. This study investigated the efficacy and safety of Autologous Matrix-Induced Chondrogenesis (AMIC) for focal chondral defects of the knee. A systematic review and meta-analysis was conducted (according to the 2020 PRISMA statement) to investigate the efficacy of AMIC in improving symptoms and to compare AMIC versus microfracture (MFx). In January 2022, the following databases were accessed: Pubmed, Web of Science, Google Scholar, Embase. No time constrain was used for the search. All the clinical trials investigating AMIC and/or those comparing AMIC versus MFx for focal chondral defects of the knee were accessed. Only studies published in peer reviewed journals were considered. Studies which investigated other locations of the defects rather than knee were not eligible, nor those reporting data form mixed locations. Studies which reported data on revision settings, as well as those investigating efficacy on kissing lesions or multiple locations, were not suitable. The mean difference (MD) and odd ratio (OR) effect measure were used for continuous and binary data, respectively. Data from 18 studies (548 patients) were retrieved with a mean follow-up of 39.9 ± 26.5 months. The mean defect size was 3.2 ± 1.0 cm(2). The visual analogue scale (VAS) decreased of − 3.9/10 (95% confidence interval (CI) − 4.0874 to -3.7126), the Tegner Activity Scale increased of + 0.8/10 (95% CI 0.6595 to 0.9405). The Lysholm Knee Scoring System increased of + 28.9/100 (95% CI 26.8716 to 29.1284), as did the International Knee Documentation Committee (IKDC) + 33.6/100 (95% CI 32.5800 to 34.6200). At last follow-up no patient showed signs of hypertrophy. 4.3% (9 of 210) of patients underwent revision procedures. The rate of failure was 3.8% (9 of 236). Compared to MFx, AMIC demonstrated lower VAS score (MD: − 1.01; 95% CI − 1.97 to 0.05), greater IKDC (MD: 11.80; 95% CI 6.65 to 16.94), and lower rate of revision (OR: 0.16; 95% CI 0.06 to 0.44). AMIC is effective for focal chondral defects of the knee. Furthermore, AMIC evidenced greater IKDC, along with a lower value of VAS and rate of revision compared to MFx. Nature Publishing Group UK 2022-06-04 /pmc/articles/PMC9167289/ /pubmed/35661147 http://dx.doi.org/10.1038/s41598-022-13591-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Migliorini, Filippo
Maffulli, Nicola
Baroncini, Alice
Bell, Andreas
Hildebrand, Frank
Schenker, Hanno
Autologous matrix-induced chondrogenesis is effective for focal chondral defects of the knee
title Autologous matrix-induced chondrogenesis is effective for focal chondral defects of the knee
title_full Autologous matrix-induced chondrogenesis is effective for focal chondral defects of the knee
title_fullStr Autologous matrix-induced chondrogenesis is effective for focal chondral defects of the knee
title_full_unstemmed Autologous matrix-induced chondrogenesis is effective for focal chondral defects of the knee
title_short Autologous matrix-induced chondrogenesis is effective for focal chondral defects of the knee
title_sort autologous matrix-induced chondrogenesis is effective for focal chondral defects of the knee
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9167289/
https://www.ncbi.nlm.nih.gov/pubmed/35661147
http://dx.doi.org/10.1038/s41598-022-13591-6
work_keys_str_mv AT migliorinifilippo autologousmatrixinducedchondrogenesisiseffectiveforfocalchondraldefectsoftheknee
AT maffullinicola autologousmatrixinducedchondrogenesisiseffectiveforfocalchondraldefectsoftheknee
AT baroncinialice autologousmatrixinducedchondrogenesisiseffectiveforfocalchondraldefectsoftheknee
AT bellandreas autologousmatrixinducedchondrogenesisiseffectiveforfocalchondraldefectsoftheknee
AT hildebrandfrank autologousmatrixinducedchondrogenesisiseffectiveforfocalchondraldefectsoftheknee
AT schenkerhanno autologousmatrixinducedchondrogenesisiseffectiveforfocalchondraldefectsoftheknee