Effects of tranexamic acid on the recovery of osteochondral defects treated by microfracture and acellular matrix scaffold: an experimental study
Microfracture and scaffold application in the treatment of osteochondral defects is still one of the most frequently used methods in the clinic. The most important step in this treatment method is the stabilization of fibrin clot. Tranexamic acid (TA) is an antifibrinolytic agent commonly used in or...
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Published in | Journal of orthopaedic surgery and research Vol. 14; no. 1; pp. 105 - 8 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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England
BioMed Central Ltd
15.04.2019
BioMed Central BMC |
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Abstract | Microfracture and scaffold application in the treatment of osteochondral defects is still one of the most frequently used methods in the clinic. The most important step in this treatment method is the stabilization of fibrin clot. Tranexamic acid (TA) is an antifibrinolytic agent commonly used in orthopedic surgery in recent years. This study evaluated the effect of local TA application on healing of experimentally induced osteochondral defects on rabbits.
This paper contains an animal in vivo data and histological outcomes on the effect of TA. Eighteen New Zealand white rabbits were treated unilaterally and cylindrical defects having a width of 4 mm and depth of 5 mm were created in the weight-bearing surfaces of the medial and lateral condyles of the right femur. They were divided into two groups, as group 1 study and group 2 control groups, respectively. One milliliter (ml) of TA was injected into the knee joints of the subjects in group 1. All animals were sacrificed for the extraction of the femur condyles for histologic study at the fourth and eighth weeks after surgery. Histological evaluations were performed by Brittberg and O'Driscoll scores to all samples. Data were organized in a Standard Statistical Package System v.22 software package (SPSS/PC Inc., Chicago, IL.) and reported as mean and median (min-max). Repeated measures ANOVA test was used to compare groups and condyle effects together for each week. p values below 0.05 were considered as statistically significant.
Samples were taken in the fourth and eighth weeks. The regularity of the surface in group 1 was smoother, and the tissue stability was more robust. Mean Brittberg scores in both weeks were statistically higher in group 1 when compared with group 2. In the microscopic evaluation, it was observed that the regeneration of subchondral and cartilage tissues were more rapid and organized in group 1, and the mean O' Driscoll scores in both weeks were statistically higher in group 1.
Application of TA improves the healing time and tissue stability in osteochondral defects which are implanted a-cellular scaffold after microfracture and should be applicable to humans for the treatment of osteochondral defects. |
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AbstractList | Microfracture and scaffold application in the treatment of osteochondral defects is still one of the most frequently used methods in the clinic. The most important step in this treatment method is the stabilization of fibrin clot. Tranexamic acid (TA) is an antifibrinolytic agent commonly used in orthopedic surgery in recent years. This study evaluated the effect of local TA application on healing of experimentally induced osteochondral defects on rabbits. This paper contains an animal in vivo data and histological outcomes on the effect of TA. Eighteen New Zealand white rabbits were treated unilaterally and cylindrical defects having a width of 4 mm and depth of 5 mm were created in the weight-bearing surfaces of the medial and lateral condyles of the right femur. They were divided into two groups, as group 1 study and group 2 control groups, respectively. One milliliter (ml) of TA was injected into the knee joints of the subjects in group 1. All animals were sacrificed for the extraction of the femur condyles for histologic study at the fourth and eighth weeks after surgery. Histological evaluations were performed by Brittberg and O'Driscoll scores to all samples. Data were organized in a Standard Statistical Package System v.22 software package (SPSS/PC Inc., Chicago, IL.) and reported as mean and median (min-max). Repeated measures ANOVA test was used to compare groups and condyle effects together for each week. p values below 0.05 were considered as statistically significant. Application of TA improves the healing time and tissue stability in osteochondral defects which are implanted a-cellular scaffold after microfracture and should be applicable to humans for the treatment of osteochondral defects. Microfracture and scaffold application in the treatment of osteochondral defects is still one of the most frequently used methods in the clinic. The most important step in this treatment method is the stabilization of fibrin clot. Tranexamic acid (TA) is an antifibrinolytic agent commonly used in orthopedic surgery in recent years. This study evaluated the effect of local TA application on healing of experimentally induced osteochondral defects on rabbits. This paper contains an animal in vivo data and histological outcomes on the effect of TA. Eighteen New Zealand white rabbits were treated unilaterally and cylindrical defects having a width of 4 mm and depth of 5 mm were created in the weight-bearing surfaces of the medial and lateral condyles of the right femur. They were divided into two groups, as group 1 study and group 2 control groups, respectively. One milliliter (ml) of TA was injected into the knee joints of the subjects in group 1. All animals were sacrificed for the extraction of the femur condyles for histologic study at the fourth and eighth weeks after surgery. Histological evaluations were performed by Brittberg and O'Driscoll scores to all samples. Data were organized in a Standard Statistical Package System v.22 software package (SPSS/PC Inc., Chicago, IL.) and reported as mean and median (min-max). Repeated measures ANOVA test was used to compare groups and condyle effects together for each week. p values below 0.05 were considered as statistically significant. Samples were taken in the fourth and eighth weeks. The regularity of the surface in group 1 was smoother, and the tissue stability was more robust. Mean Brittberg scores in both weeks were statistically higher in group 1 when compared with group 2. In the microscopic evaluation, it was observed that the regeneration of subchondral and cartilage tissues were more rapid and organized in group 1, and the mean O' Driscoll scores in both weeks were statistically higher in group 1. Application of TA improves the healing time and tissue stability in osteochondral defects which are implanted a-cellular scaffold after microfracture and should be applicable to humans for the treatment of osteochondral defects. Background Microfracture and scaffold application in the treatment of osteochondral defects is still one of the most frequently used methods in the clinic. The most important step in this treatment method is the stabilization of fibrin clot. Tranexamic acid (TA) is an antifibrinolytic agent commonly used in orthopedic surgery in recent years. This study evaluated the effect of local TA application on healing of experimentally induced osteochondral defects on rabbits. Methods This paper contains an animal in vivo data and histological outcomes on the effect of TA. Eighteen New Zealand white rabbits were treated unilaterally and cylindrical defects having a width of 4 mm and depth of 5 mm were created in the weight-bearing surfaces of the medial and lateral condyles of the right femur. They were divided into two groups, as group 1 study and group 2 control groups, respectively. One milliliter (ml) of TA was injected into the knee joints of the subjects in group 1. All animals were sacrificed for the extraction of the femur condyles for histologic study at the fourth and eighth weeks after surgery. Histological evaluations were performed by Brittberg and O’Driscoll scores to all samples. Data were organized in a Standard Statistical Package System v.22 software package (SPSS/PC Inc., Chicago, IL.) and reported as mean and median (min-max). Repeated measures ANOVA test was used to compare groups and condyle effects together for each week. p values below 0.05 were considered as statistically significant. Results Samples were taken in the fourth and eighth weeks. The regularity of the surface in group 1 was smoother, and the tissue stability was more robust. Mean Brittberg scores in both weeks were statistically higher in group 1 when compared with group 2. In the microscopic evaluation, it was observed that the regeneration of subchondral and cartilage tissues were more rapid and organized in group 1, and the mean O’ Driscoll scores in both weeks were statistically higher in group 1. Conclusions Application of TA improves the healing time and tissue stability in osteochondral defects which are implanted a-cellular scaffold after microfracture and should be applicable to humans for the treatment of osteochondral defects. Abstract Background Microfracture and scaffold application in the treatment of osteochondral defects is still one of the most frequently used methods in the clinic. The most important step in this treatment method is the stabilization of fibrin clot. Tranexamic acid (TA) is an antifibrinolytic agent commonly used in orthopedic surgery in recent years. This study evaluated the effect of local TA application on healing of experimentally induced osteochondral defects on rabbits. Methods This paper contains an animal in vivo data and histological outcomes on the effect of TA. Eighteen New Zealand white rabbits were treated unilaterally and cylindrical defects having a width of 4 mm and depth of 5 mm were created in the weight-bearing surfaces of the medial and lateral condyles of the right femur. They were divided into two groups, as group 1 study and group 2 control groups, respectively. One milliliter (ml) of TA was injected into the knee joints of the subjects in group 1. All animals were sacrificed for the extraction of the femur condyles for histologic study at the fourth and eighth weeks after surgery. Histological evaluations were performed by Brittberg and O’Driscoll scores to all samples. Data were organized in a Standard Statistical Package System v.22 software package (SPSS/PC Inc., Chicago, IL.) and reported as mean and median (min-max). Repeated measures ANOVA test was used to compare groups and condyle effects together for each week. p values below 0.05 were considered as statistically significant. Results Samples were taken in the fourth and eighth weeks. The regularity of the surface in group 1 was smoother, and the tissue stability was more robust. Mean Brittberg scores in both weeks were statistically higher in group 1 when compared with group 2. In the microscopic evaluation, it was observed that the regeneration of subchondral and cartilage tissues were more rapid and organized in group 1, and the mean O’ Driscoll scores in both weeks were statistically higher in group 1. Conclusions Application of TA improves the healing time and tissue stability in osteochondral defects which are implanted a-cellular scaffold after microfracture and should be applicable to humans for the treatment of osteochondral defects. Microfracture and scaffold application in the treatment of osteochondral defects is still one of the most frequently used methods in the clinic. The most important step in this treatment method is the stabilization of fibrin clot. Tranexamic acid (TA) is an antifibrinolytic agent commonly used in orthopedic surgery in recent years. This study evaluated the effect of local TA application on healing of experimentally induced osteochondral defects on rabbits.BACKGROUNDMicrofracture and scaffold application in the treatment of osteochondral defects is still one of the most frequently used methods in the clinic. The most important step in this treatment method is the stabilization of fibrin clot. Tranexamic acid (TA) is an antifibrinolytic agent commonly used in orthopedic surgery in recent years. This study evaluated the effect of local TA application on healing of experimentally induced osteochondral defects on rabbits.This paper contains an animal in vivo data and histological outcomes on the effect of TA. Eighteen New Zealand white rabbits were treated unilaterally and cylindrical defects having a width of 4 mm and depth of 5 mm were created in the weight-bearing surfaces of the medial and lateral condyles of the right femur. They were divided into two groups, as group 1 study and group 2 control groups, respectively. One milliliter (ml) of TA was injected into the knee joints of the subjects in group 1. All animals were sacrificed for the extraction of the femur condyles for histologic study at the fourth and eighth weeks after surgery. Histological evaluations were performed by Brittberg and O'Driscoll scores to all samples. Data were organized in a Standard Statistical Package System v.22 software package (SPSS/PC Inc., Chicago, IL.) and reported as mean and median (min-max). Repeated measures ANOVA test was used to compare groups and condyle effects together for each week. p values below 0.05 were considered as statistically significant.METHODSThis paper contains an animal in vivo data and histological outcomes on the effect of TA. Eighteen New Zealand white rabbits were treated unilaterally and cylindrical defects having a width of 4 mm and depth of 5 mm were created in the weight-bearing surfaces of the medial and lateral condyles of the right femur. They were divided into two groups, as group 1 study and group 2 control groups, respectively. One milliliter (ml) of TA was injected into the knee joints of the subjects in group 1. All animals were sacrificed for the extraction of the femur condyles for histologic study at the fourth and eighth weeks after surgery. Histological evaluations were performed by Brittberg and O'Driscoll scores to all samples. Data were organized in a Standard Statistical Package System v.22 software package (SPSS/PC Inc., Chicago, IL.) and reported as mean and median (min-max). Repeated measures ANOVA test was used to compare groups and condyle effects together for each week. p values below 0.05 were considered as statistically significant.Samples were taken in the fourth and eighth weeks. The regularity of the surface in group 1 was smoother, and the tissue stability was more robust. Mean Brittberg scores in both weeks were statistically higher in group 1 when compared with group 2. In the microscopic evaluation, it was observed that the regeneration of subchondral and cartilage tissues were more rapid and organized in group 1, and the mean O' Driscoll scores in both weeks were statistically higher in group 1.RESULTSSamples were taken in the fourth and eighth weeks. The regularity of the surface in group 1 was smoother, and the tissue stability was more robust. Mean Brittberg scores in both weeks were statistically higher in group 1 when compared with group 2. In the microscopic evaluation, it was observed that the regeneration of subchondral and cartilage tissues were more rapid and organized in group 1, and the mean O' Driscoll scores in both weeks were statistically higher in group 1.Application of TA improves the healing time and tissue stability in osteochondral defects which are implanted a-cellular scaffold after microfracture and should be applicable to humans for the treatment of osteochondral defects.CONCLUSIONSApplication of TA improves the healing time and tissue stability in osteochondral defects which are implanted a-cellular scaffold after microfracture and should be applicable to humans for the treatment of osteochondral defects. Background Microfracture and scaffold application in the treatment of osteochondral defects is still one of the most frequently used methods in the clinic. The most important step in this treatment method is the stabilization of fibrin clot. Tranexamic acid (TA) is an antifibrinolytic agent commonly used in orthopedic surgery in recent years. This study evaluated the effect of local TA application on healing of experimentally induced osteochondral defects on rabbits. Methods This paper contains an animal in vivo data and histological outcomes on the effect of TA. Eighteen New Zealand white rabbits were treated unilaterally and cylindrical defects having a width of 4 mm and depth of 5 mm were created in the weight-bearing surfaces of the medial and lateral condyles of the right femur. They were divided into two groups, as group 1 study and group 2 control groups, respectively. One milliliter (ml) of TA was injected into the knee joints of the subjects in group 1. All animals were sacrificed for the extraction of the femur condyles for histologic study at the fourth and eighth weeks after surgery. Histological evaluations were performed by Brittberg and O'Driscoll scores to all samples. Data were organized in a Standard Statistical Package System v.22 software package (SPSS/PC Inc., Chicago, IL.) and reported as mean and median (min-max). Repeated measures ANOVA test was used to compare groups and condyle effects together for each week. p values below 0.05 were considered as statistically significant. Results Samples were taken in the fourth and eighth weeks. The regularity of the surface in group 1 was smoother, and the tissue stability was more robust. Mean Brittberg scores in both weeks were statistically higher in group 1 when compared with group 2. In the microscopic evaluation, it was observed that the regeneration of subchondral and cartilage tissues were more rapid and organized in group 1, and the mean O' Driscoll scores in both weeks were statistically higher in group 1. Conclusions Application of TA improves the healing time and tissue stability in osteochondral defects which are implanted a-cellular scaffold after microfracture and should be applicable to humans for the treatment of osteochondral defects. Keywords: Osteochondral defect, Microfracture, A-cellular scaffold, Tranexamic acid |
ArticleNumber | 105 |
Audience | Academic |
Author | Kaya, Yasin Emre Sahin, Abdullah Alper Yilmaz, Fahri Degirmenci, Erdem Ozturan, Kutay Engin |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30992060$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1007_s00167_020_06219_7 crossref_primary_10_1016_j_arthro_2023_08_019 crossref_primary_10_3389_fbioe_2021_812383 crossref_primary_10_5312_wjo_v13_i6_555 crossref_primary_10_1177_03635465231220855 crossref_primary_10_3390_polym13203470 crossref_primary_10_1016_j_injury_2020_09_008 crossref_primary_10_1097_PRS_0000000000008884 crossref_primary_10_7759_cureus_14873 crossref_primary_10_3389_fmed_2024_1352967 crossref_primary_10_3390_ph17121576 |
Cites_doi | 10.3109/17453679608994664 10.2106/JBJS.15.01208 10.1016/j.injury.2008.01.042 10.2106/00004623-198870040-00017 10.1007/s00167-011-1777-5 10.1016/j.arth.2018.04.043 10.1016/j.biomaterials.2011.06.018 10.5312/wjo.v5.i4.444 10.1016/j.biomaterials.2007.09.005 10.1007/s10561-011-9290-0 10.1177/0363546516629434 10.1177/036354659702500624 10.1016/j.joca.2011.07.004 10.1007/s11999-011-2107-4 10.1007/s00167-010-1042-3 10.1053/jars.2003.50112 10.1002/jor.20879 10.1177/1947603515611949 10.1016/j.joca.2004.12.016 10.1016/j.arthro.2005.06.018 10.1007/s00402-012-1621-5 10.1016/j.arthro.2013.05.027 10.2106/00004623-200710000-00002 10.2106/JBJS.RVW.17.00103 10.1089/ten.teb.2009.0452 10.1007/s00167-013-2747-x 10.2147/DDDT.S175407 10.1177/0363546514528093 10.1016/0142-9612(93)90160-4 10.1242/jcs.00912 10.1177/0363546508328414 10.1302/0301-620X.100B3.BJJ-2017-1135.R1 10.1007/s12306-013-0242-7 10.2165/00003495-198529030-00003 10.1016/j.arthro.2016.06.035 |
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Keywords | A-cellular scaffold Tranexamic acid Microfracture Osteochondral defect |
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References | K Midhoefer (1144_CR29) 2009; 37 1144_CR34 JR Tuttle (1144_CR42) 2015; 44 JL Cook (1144_CR7) 2016; 44 JA Buckwalter (1144_CR2) 1997; 25 LA Solchaga (1144_CR9) 2005; 13 C Erggelet (1144_CR12) 2007; 28 A Rastrelli (1144_CR5) 1990; 9 CC Wang (1144_CR8) 2011; 32 JD Parker (1144_CR41) 2018; 100-B P Sitek (1144_CR20) 2013; 14 GP Dowthwaite (1144_CR3) 2004; 117 1144_CR18 J Insall (1144_CR27) 1974; 101 S Bark (1144_CR25) 2014; 5 D Goyal (1144_CR35) 2013; 29 YA Fillingham (1144_CR39) 2018; 33 K Messner (1144_CR1) 1996; 67 C Albrecht (1144_CR10) 2011; 19 J Gille (1144_CR26) 2010; 18 L Benedetti (1144_CR6) 1993; 14 G Knutsen (1144_CR36) 2007; 89 J Gille (1144_CR24) 2013; 133 1144_CR22 E Cholewinski (1144_CR14) 2009; 15 LF Ambra (1144_CR19) 2017; Nov 8 1144_CR40 A Siclari (1144_CR11) 2012; 470 SW O’Driscoll (1144_CR23) 1988; 70A A Marmotti (1144_CR16) 2016; 30 CR Chu (1144_CR17) 2010; 16 M Verstraete (1144_CR21) 1985; 3 MR Steinwachs (1144_CR4) 2008; 39 KF Schuttler (1144_CR32) 2014; 22 G Knutsen (1144_CR37) 2016; 98 C Bauer (1144_CR13) 2016; 7 C Erggelet (1144_CR31) 2009; 27 D Saris (1144_CR38) 2014; 42 FC Kuo (1144_CR15) 2018; 12 JR Steadman (1144_CR28) 2003; 19 R Gudas (1144_CR30) 2005; 21 H Sofu (1144_CR33) 2017; 33 |
References_xml | – volume: 67 start-page: 165 year: 1996 ident: 1144_CR1 publication-title: Acta Orthop Scand doi: 10.3109/17453679608994664 – volume: 98 start-page: 1332 year: 2016 ident: 1144_CR37 publication-title: J Bone Joint Surg Am doi: 10.2106/JBJS.15.01208 – volume: 39 start-page: 26 year: 2008 ident: 1144_CR4 publication-title: Injury doi: 10.1016/j.injury.2008.01.042 – volume: 15 start-page: 1 year: 2009 ident: 1144_CR14 publication-title: Tissue Eng – volume: 9 start-page: 199 year: 1990 ident: 1144_CR5 publication-title: Clin Implant Mater – volume: 70A start-page: 595 year: 1988 ident: 1144_CR23 publication-title: J Bone Joint Surg doi: 10.2106/00004623-198870040-00017 – ident: 1144_CR34 doi: 10.1007/s00167-011-1777-5 – volume: 33 start-page: 3090 issue: 10 year: 2018 ident: 1144_CR39 publication-title: J Arthroplasty doi: 10.1016/j.arth.2018.04.043 – volume: 32 start-page: 7118 year: 2011 ident: 1144_CR8 publication-title: Biomaterials doi: 10.1016/j.biomaterials.2011.06.018 – volume: 5 start-page: 444 issue: 4 year: 2014 ident: 1144_CR25 publication-title: World J Orthop doi: 10.5312/wjo.v5.i4.444 – volume: 28 start-page: 5570 year: 2007 ident: 1144_CR12 publication-title: Biomaterials doi: 10.1016/j.biomaterials.2007.09.005 – volume: 14 start-page: 133 year: 2013 ident: 1144_CR20 publication-title: Cell Tissue Bank doi: 10.1007/s10561-011-9290-0 – volume: 44 start-page: 1260 year: 2016 ident: 1144_CR7 publication-title: Am J Sports Med doi: 10.1177/0363546516629434 – volume: 25 start-page: 873 year: 1997 ident: 1144_CR2 publication-title: Am J Sports Med doi: 10.1177/036354659702500624 – volume: 44 start-page: 497 year: 2015 ident: 1144_CR42 publication-title: Am J Orthop – volume: 19 start-page: 1219 year: 2011 ident: 1144_CR10 publication-title: Osteoarthr Cartil doi: 10.1016/j.joca.2011.07.004 – volume: 470 start-page: 910 year: 2012 ident: 1144_CR11 publication-title: Clin Orthop Relat Res doi: 10.1007/s11999-011-2107-4 – volume: 101 start-page: 61 year: 1974 ident: 1144_CR27 publication-title: Clin Orthop Relat Res – volume: 18 start-page: 1456 issue: 11 year: 2010 ident: 1144_CR26 publication-title: Knee Surg Sports Traumatol Arthrosc doi: 10.1007/s00167-010-1042-3 – volume: 19 start-page: 477 issue: 5 year: 2003 ident: 1144_CR28 publication-title: Arthroscopy doi: 10.1053/jars.2003.50112 – volume: 27 start-page: 1353 year: 2009 ident: 1144_CR31 publication-title: Inc J Orthop Res doi: 10.1002/jor.20879 – volume: 7 start-page: 265 year: 2016 ident: 1144_CR13 publication-title: Cartilage doi: 10.1177/1947603515611949 – volume: 13 start-page: 297 year: 2005 ident: 1144_CR9 publication-title: Osteoarthr Cartil doi: 10.1016/j.joca.2004.12.016 – volume: 21 start-page: 1066 year: 2005 ident: 1144_CR30 publication-title: Arthroscopy doi: 10.1016/j.arthro.2005.06.018 – volume: 133 start-page: 87 year: 2013 ident: 1144_CR24 publication-title: Arch Orthop Trauma Surg doi: 10.1007/s00402-012-1621-5 – volume: 29 start-page: 1579 issue: 9 year: 2013 ident: 1144_CR35 publication-title: Arthroscopy doi: 10.1016/j.arthro.2013.05.027 – volume: 89 start-page: 2105 year: 2007 ident: 1144_CR36 publication-title: J Bone Joint Surg Am. doi: 10.2106/00004623-200710000-00002 – ident: 1144_CR40 doi: 10.2106/JBJS.RVW.17.00103 – volume: 16 start-page: 105 year: 2010 ident: 1144_CR17 publication-title: Tissue Eng Part B Rev doi: 10.1089/ten.teb.2009.0452 – volume: 22 start-page: 1270 year: 2014 ident: 1144_CR32 publication-title: Knee Surg Sports Traumatol Arthrosc doi: 10.1007/s00167-013-2747-x – volume: 12 start-page: 3163 year: 2018 ident: 1144_CR15 publication-title: Drug Des Devel Ther doi: 10.2147/DDDT.S175407 – ident: 1144_CR18 – volume: Nov 8 start-page: 4746 year: 2017 ident: 1144_CR19 publication-title: Knee Surg Sports Traumatol Arthrosc – volume: 42 start-page: 1384 issue: 6 year: 2014 ident: 1144_CR38 publication-title: Am J Sports Med doi: 10.1177/0363546514528093 – volume: 14 start-page: 1135 issue: 15 year: 1993 ident: 1144_CR6 publication-title: Biomaterials doi: 10.1016/0142-9612(93)90160-4 – volume: 117 start-page: 889 year: 2004 ident: 1144_CR3 publication-title: J Cell Sci doi: 10.1242/jcs.00912 – volume: 37 start-page: 2053 year: 2009 ident: 1144_CR29 publication-title: Am J Sports Med doi: 10.1177/0363546508328414 – volume: 100-B start-page: 404 issue: 3 year: 2018 ident: 1144_CR41 publication-title: Bone Joint J doi: 10.1302/0301-620X.100B3.BJJ-2017-1135.R1 – ident: 1144_CR22 doi: 10.1007/s12306-013-0242-7 – volume: 3 start-page: 236 year: 1985 ident: 1144_CR21 publication-title: Drugs doi: 10.2165/00003495-198529030-00003 – volume: 30 start-page: 33 year: 2016 ident: 1144_CR16 publication-title: J Biol Regul Homeost Agents – volume: 33 start-page: 209 year: 2017 ident: 1144_CR33 publication-title: J Arthroscopic and Related Surg doi: 10.1016/j.arthro.2016.06.035 |
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Snippet | Microfracture and scaffold application in the treatment of osteochondral defects is still one of the most frequently used methods in the clinic. The most... Background Microfracture and scaffold application in the treatment of osteochondral defects is still one of the most frequently used methods in the clinic. The... Abstract Background Microfracture and scaffold application in the treatment of osteochondral defects is still one of the most frequently used methods in the... |
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SubjectTerms | A-cellular scaffold Analysis Antifibrinolytic agents Biomedical materials Bone surgery Cartilage Collagen Data processing Defects Femur Fibrin Hemostatic agents Joint surgery Knee Microfracture NMR Nuclear magnetic resonance Orthopedic surgery Orthopedics Osteochondral defect Rabbits Statistical analysis Studies Surgery Systematic review Tranexamic acid Transplants & implants |
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Title | Effects of tranexamic acid on the recovery of osteochondral defects treated by microfracture and acellular matrix scaffold: an experimental study |
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