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Conventional rotator cuff repair complemented by the aid of mononuclear autologous stem cells

PURPOSE: To investigate the behavior of rotator cuff tears treated with conventional repair technique with the aid of autologous bone marrow mononuclear cells (BMMC). METHODS: Fourteen consecutive patients (9 women, 5 men, mean age of 59.2 years) with complete rotator cuff tears (mean preoperative U...

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Autores principales: Ellera Gomes, João L., da Silva, Ricardo Canquerini, Silla, Lúcia M. R., Abreu, Marcelo R., Pellanda, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262133/
https://www.ncbi.nlm.nih.gov/pubmed/21773831
http://dx.doi.org/10.1007/s00167-011-1607-9
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author Ellera Gomes, João L.
da Silva, Ricardo Canquerini
Silla, Lúcia M. R.
Abreu, Marcelo R.
Pellanda, Roberto
author_facet Ellera Gomes, João L.
da Silva, Ricardo Canquerini
Silla, Lúcia M. R.
Abreu, Marcelo R.
Pellanda, Roberto
author_sort Ellera Gomes, João L.
collection PubMed
description PURPOSE: To investigate the behavior of rotator cuff tears treated with conventional repair technique with the aid of autologous bone marrow mononuclear cells (BMMC). METHODS: Fourteen consecutive patients (9 women, 5 men, mean age of 59.2 years) with complete rotator cuff tears (mean preoperative UCLA score of 12 ± 3.0) were fixed by transosseous stitches through mini-open incision, with subsequent injection of BMMC into the tendon borders, obtained from the iliac crest just prior to surgery. Magnetic resonance images (MRI) were acquired before and after surgery and evaluated by two musculoskeletal radiologists regarding new postoperative findings of patients treated with BMMC. RESULTS: After a minimum 12-month follow-up period, the UCLA score increased from 12 ± 3.0 to 31 ± 3.2. Clinical findings remained unaltered in the following year in all but one patient (13/14). MRI analysis after a 12-month follow-up period demonstrated tendon integrity in all cases (14/14), presence of low-signal intensity areas along the supraspinatus tendon and distal muscle belly in 8 cases (8/14), and high-intensity blooming small round artifact at the bursal and tendon topography in 11 cases (11/14). Six patients (6/14) showed formation of a high-signal intensity zone at the critical zone. Clinical findings remained unaltered in the following year in all but one patient, who relapsed into loss of strength and pain, being considered a bad result. CONCLUSION: Implantation of BMMC in rotator cuff sutures appears to be a safe and promising alternative to other biological approaches currently used to enhance tissue quality in affected tendons. LEVEL OF EVIDENCE: IV.
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spelling pubmed-32621332012-02-03 Conventional rotator cuff repair complemented by the aid of mononuclear autologous stem cells Ellera Gomes, João L. da Silva, Ricardo Canquerini Silla, Lúcia M. R. Abreu, Marcelo R. Pellanda, Roberto Knee Surg Sports Traumatol Arthrosc Shoulder PURPOSE: To investigate the behavior of rotator cuff tears treated with conventional repair technique with the aid of autologous bone marrow mononuclear cells (BMMC). METHODS: Fourteen consecutive patients (9 women, 5 men, mean age of 59.2 years) with complete rotator cuff tears (mean preoperative UCLA score of 12 ± 3.0) were fixed by transosseous stitches through mini-open incision, with subsequent injection of BMMC into the tendon borders, obtained from the iliac crest just prior to surgery. Magnetic resonance images (MRI) were acquired before and after surgery and evaluated by two musculoskeletal radiologists regarding new postoperative findings of patients treated with BMMC. RESULTS: After a minimum 12-month follow-up period, the UCLA score increased from 12 ± 3.0 to 31 ± 3.2. Clinical findings remained unaltered in the following year in all but one patient (13/14). MRI analysis after a 12-month follow-up period demonstrated tendon integrity in all cases (14/14), presence of low-signal intensity areas along the supraspinatus tendon and distal muscle belly in 8 cases (8/14), and high-intensity blooming small round artifact at the bursal and tendon topography in 11 cases (11/14). Six patients (6/14) showed formation of a high-signal intensity zone at the critical zone. Clinical findings remained unaltered in the following year in all but one patient, who relapsed into loss of strength and pain, being considered a bad result. CONCLUSION: Implantation of BMMC in rotator cuff sutures appears to be a safe and promising alternative to other biological approaches currently used to enhance tissue quality in affected tendons. LEVEL OF EVIDENCE: IV. Springer-Verlag 2011-07-20 2012 /pmc/articles/PMC3262133/ /pubmed/21773831 http://dx.doi.org/10.1007/s00167-011-1607-9 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Shoulder
Ellera Gomes, João L.
da Silva, Ricardo Canquerini
Silla, Lúcia M. R.
Abreu, Marcelo R.
Pellanda, Roberto
Conventional rotator cuff repair complemented by the aid of mononuclear autologous stem cells
title Conventional rotator cuff repair complemented by the aid of mononuclear autologous stem cells
title_full Conventional rotator cuff repair complemented by the aid of mononuclear autologous stem cells
title_fullStr Conventional rotator cuff repair complemented by the aid of mononuclear autologous stem cells
title_full_unstemmed Conventional rotator cuff repair complemented by the aid of mononuclear autologous stem cells
title_short Conventional rotator cuff repair complemented by the aid of mononuclear autologous stem cells
title_sort conventional rotator cuff repair complemented by the aid of mononuclear autologous stem cells
topic Shoulder
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262133/
https://www.ncbi.nlm.nih.gov/pubmed/21773831
http://dx.doi.org/10.1007/s00167-011-1607-9
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