AKSELERASI GRAFT TUNNEL HEALING PADA REKONSTRUKSI ANTERIOR CRUCIATE LIGAMENT MENGGUNAKAN AUTOGRAF TENDON HAMSTRING DENGAN TRANSPLANTASI ALLOGENIC BM-MSCs – VEGF SECARA INTRATUNNEL PENELITIAN EKSPERIMENTAL LABORATORIS
Background : Anterior cruciate ligament (ACL) injury is one of the most common knee injuries that occurs as a result of sport or physical exercise. ACL reconstruction is the gold standard of treatment for ACL injury using tendon graft. The process of tissue formation between the tendon graft and...
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id-langga.582422017-06-19T16:25:00Z http://repository.unair.ac.id/58242/ AKSELERASI GRAFT TUNNEL HEALING PADA REKONSTRUKSI ANTERIOR CRUCIATE LIGAMENT MENGGUNAKAN AUTOGRAF TENDON HAMSTRING DENGAN TRANSPLANTASI ALLOGENIC BM-MSCs – VEGF SECARA INTRATUNNEL PENELITIAN EKSPERIMENTAL LABORATORIS ROSY SETIAWATI, NIM011317017315 RA1-1270 Public aspects of medicine Background : Anterior cruciate ligament (ACL) injury is one of the most common knee injuries that occurs as a result of sport or physical exercise. ACL reconstruction is the gold standard of treatment for ACL injury using tendon graft. The process of tissue formation between the tendon graft and the bone is an important link at the early stage of healing process. The combination of intratunnel allogenic Bone Marrow-Mesenschymal Stem Cells (BM-MSCs) and Vascular Endothelial Growth Factor (VEGF) is able to improve the microenviroment, as well as stimulate cell proliferation, differentiation and matrix deposition by enhancing angiogenesis and osteogenesis of the graft in the tunnel. Objective : The objective of this study is to prove the transplantation of Intratunnel Allogenic BM-MSCs and VEGF is able to enhance the early graft tunnel healing in ACL reconstruction by using autograft hamstring tendon. Methods : A controlled animal study was promoted by using four group of rabbits which underwent bilateral ACL reconstruction with semitendinosus tendon, then transplanted with intratunnel allogenic BM-MSCs and VEGF. The treatment was divided into two groups which based on the time of healing process evaluation, in 3 and 6 weeks. Then the graft tunnel healing was analyzed by evaluating the number of capillaries, the surface area of cells expressing ALP, collagen type I and collagen type III, the number of Sharpey like fiber, signal intensity of tendon graft, the width of tendon bone interface and pullout strength test. Results : All parameters have indicated to increase more in the treated groups with intratunnel allogenic BM-MSCs and VEGF than the control groups without. There were significant differences of the surface area of cells in expressing ALP, collagen type I and type III, tendon graft signal intensity, and pullout strength, as well as bone tendon interface between treated and control groups. However, there were no significant differences in the number of capillaries (p=0,275) as well as Sharpey like fiber (p=0,052). The two treated groups has showed no differences in all variables studied. Conclusion : The transplantation of intratunnel allogenic BM-MSC and VEGF after ACL reconstruction has accelerated the graft tunnel healing as early as 3 weeks after surgery. Key words : Graft tunnel healing, Anterior cruciate ligament, Bone marrow mesenchymal stem cells, Vascular endothelial growth factor. 2016 Thesis NonPeerReviewed text id http://repository.unair.ac.id/58242/1/Dis%20K.%2023-16%20Set%20a%20abstrak.pdf text id http://repository.unair.ac.id/58242/2/Dis%20K.%2023-16%20Set%20a.pdf ROSY SETIAWATI, NIM011317017315 (2016) AKSELERASI GRAFT TUNNEL HEALING PADA REKONSTRUKSI ANTERIOR CRUCIATE LIGAMENT MENGGUNAKAN AUTOGRAF TENDON HAMSTRING DENGAN TRANSPLANTASI ALLOGENIC BM-MSCs – VEGF SECARA INTRATUNNEL PENELITIAN EKSPERIMENTAL LABORATORIS. Disertasi thesis, Universitas Airlangga. http://lib.unair.ac.id |
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RA1-1270 Public aspects of medicine ROSY SETIAWATI, NIM011317017315 AKSELERASI GRAFT TUNNEL HEALING PADA REKONSTRUKSI ANTERIOR CRUCIATE LIGAMENT MENGGUNAKAN AUTOGRAF TENDON HAMSTRING DENGAN TRANSPLANTASI ALLOGENIC BM-MSCs – VEGF SECARA INTRATUNNEL PENELITIAN EKSPERIMENTAL LABORATORIS |
description |
Background : Anterior cruciate ligament (ACL) injury is one of the most
common knee injuries that occurs as a result of sport or physical exercise. ACL
reconstruction is the gold standard of treatment for ACL injury using tendon graft.
The process of tissue formation between the tendon graft and the bone is an
important link at the early stage of healing process. The combination of
intratunnel allogenic Bone Marrow-Mesenschymal Stem Cells (BM-MSCs) and
Vascular Endothelial Growth Factor (VEGF) is able to improve the
microenviroment, as well as stimulate cell proliferation, differentiation and matrix
deposition by enhancing angiogenesis and osteogenesis of the graft in the tunnel.
Objective : The objective of this study is to prove the transplantation of
Intratunnel Allogenic BM-MSCs and VEGF is able to enhance the early graft
tunnel healing in ACL reconstruction by using autograft hamstring tendon.
Methods : A controlled animal study was promoted by using four group of
rabbits which underwent bilateral ACL reconstruction with semitendinosus
tendon, then transplanted with intratunnel allogenic BM-MSCs and VEGF. The
treatment was divided into two groups which based on the time of healing process
evaluation, in 3 and 6 weeks. Then the graft tunnel healing was analyzed by
evaluating the number of capillaries, the surface area of cells expressing ALP,
collagen type I and collagen type III, the number of Sharpey like fiber, signal
intensity of tendon graft, the width of tendon bone interface and pullout strength
test.
Results : All parameters have indicated to increase more in the treated groups
with intratunnel allogenic BM-MSCs and VEGF than the control groups without.
There were significant differences of the surface area of cells in expressing ALP,
collagen type I and type III, tendon graft signal intensity, and pullout strength, as
well as bone tendon interface between treated and control groups. However,
there were no significant differences in the number of capillaries (p=0,275) as
well as Sharpey like fiber (p=0,052). The two treated groups has showed no
differences in all variables studied.
Conclusion : The transplantation of intratunnel allogenic BM-MSC and VEGF
after ACL reconstruction has accelerated the graft tunnel healing as early as 3
weeks after surgery.
Key words : Graft tunnel healing, Anterior cruciate ligament, Bone marrow
mesenchymal stem cells, Vascular endothelial growth factor. |
format |
Theses and Dissertations NonPeerReviewed |
author |
ROSY SETIAWATI, NIM011317017315 |
author_facet |
ROSY SETIAWATI, NIM011317017315 |
author_sort |
ROSY SETIAWATI, NIM011317017315 |
title |
AKSELERASI GRAFT TUNNEL HEALING PADA REKONSTRUKSI ANTERIOR CRUCIATE LIGAMENT MENGGUNAKAN AUTOGRAF TENDON HAMSTRING DENGAN TRANSPLANTASI ALLOGENIC BM-MSCs – VEGF SECARA INTRATUNNEL PENELITIAN EKSPERIMENTAL LABORATORIS |
title_short |
AKSELERASI GRAFT TUNNEL HEALING PADA REKONSTRUKSI ANTERIOR CRUCIATE LIGAMENT MENGGUNAKAN AUTOGRAF TENDON HAMSTRING DENGAN TRANSPLANTASI ALLOGENIC BM-MSCs – VEGF SECARA INTRATUNNEL PENELITIAN EKSPERIMENTAL LABORATORIS |
title_full |
AKSELERASI GRAFT TUNNEL HEALING PADA REKONSTRUKSI ANTERIOR CRUCIATE LIGAMENT MENGGUNAKAN AUTOGRAF TENDON HAMSTRING DENGAN TRANSPLANTASI ALLOGENIC BM-MSCs – VEGF SECARA INTRATUNNEL PENELITIAN EKSPERIMENTAL LABORATORIS |
title_fullStr |
AKSELERASI GRAFT TUNNEL HEALING PADA REKONSTRUKSI ANTERIOR CRUCIATE LIGAMENT MENGGUNAKAN AUTOGRAF TENDON HAMSTRING DENGAN TRANSPLANTASI ALLOGENIC BM-MSCs – VEGF SECARA INTRATUNNEL PENELITIAN EKSPERIMENTAL LABORATORIS |
title_full_unstemmed |
AKSELERASI GRAFT TUNNEL HEALING PADA REKONSTRUKSI ANTERIOR CRUCIATE LIGAMENT MENGGUNAKAN AUTOGRAF TENDON HAMSTRING DENGAN TRANSPLANTASI ALLOGENIC BM-MSCs – VEGF SECARA INTRATUNNEL PENELITIAN EKSPERIMENTAL LABORATORIS |
title_sort |
akselerasi graft tunnel healing pada rekonstruksi anterior cruciate ligament menggunakan autograf tendon hamstring dengan transplantasi allogenic bm-mscs – vegf secara intratunnel penelitian eksperimental laboratoris |
publishDate |
2016 |
url |
http://repository.unair.ac.id/58242/1/Dis%20K.%2023-16%20Set%20a%20abstrak.pdf http://repository.unair.ac.id/58242/2/Dis%20K.%2023-16%20Set%20a.pdf http://repository.unair.ac.id/58242/ http://lib.unair.ac.id |
_version_ |
1681147721528901632 |