在山羊模型中,宏观ICRS与O - Driscoll组织软骨修复评估相关性较差

Kok Ac, van Bergen Cj, Tuijthof Gjm, Klinkenbijl Mn, van Noorden Cjf, van Dijk Cn, G. Kerkhoffs
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引用次数: 4

摘要

背景:本研究的目的是评价用ICRS评分对山羊距骨软骨缺损修复软骨质量的宏观评价是否与O’driscoll组织学评分的组织学评价一致。方法:对32例山羊6mm骨软骨缺损经微骨折治疗后6个月的高分辨率数字图像进行分析。两名观察员使用ICRS(0-12分)独立对缺陷进行评分。1名组织学专家对5 μm的Masson Goldner和Safranin O染色切片进行组织学分析,采用O 'Driscoll评分(0-24分)。采用Spearman相关系数比较ICRS总分和O 'Driscoll评分及各单项评分(p0.05)。结论:本动物实验提示,软骨修复组织的孤立宏观ICRS评价与组织学评价相关性不强。可能的解释是,与深入组织分析相比,表面评估存在局限性,需要更详细的宏观评估,包括肥大、颜色、病变大小、位置和关节退行性状态。更准确、精确和可靠的技术,如组织学、dGEMERIC和T2成像MRI、对比增强CT或光学相干断层扫描(OCT),应被视为替代或至少作为补充方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Macroscopic ICRS Poorly Correlates with O Driscoll Histological CartilageRepair Assessment in a Goat Model
Background: The purpose of this research was to evaluate whether the macroscopic assessment of repair cartilage quality of talar osteochondral defects in a goat model using the ICRS score is in correspondence with histological assessment using the O’Driscoll histology score. Methods: 32 caprine samples with six mm osteochondral defects treated with microfracture were analyzed six months postoperatively using high-resolution digital images. Two observers independently scored the defects using the ICRS (0-12 points). Histological analysis was performed by one expert histologist using the O’Driscoll Score (0-24 points) on 5 μm slices stained with Masson Goldner and Safranin O. Total ICRS and O’Driscoll scores as well as sub items were compared using a Spearman correlation coefficient (p<0.05). Results: The median ICRS for Observer 1 and 2 were 6.5 (range: 4-11) and 6.5 (range: 3-11). The median O’Driscoll score was 11.5 (range: 3-20). The correlation of the total ICRS scores and the O’Driscoll score was not significant, nor was the correlation of sub items (p>0.05). Conclusion: This animal study suggests that isolated macroscopic ICRS assessment of cartilage repair tissue does not correlate well with histological assessment. Possible explanations may be limitations of surface assessment compared to analysis deeper into the tissue and the necessity of more elaborate macroscopic assessment including hypertrophy, colour, lesion size, location and degenerative status of the joint. Techniques that are more accurate, precise and reliable, such as histology, dGEMERIC and T2 mapping MRI, contrast enhanced CT or optical coherence tomography (OCT), should be considered as alternatives or at least as complimentary methods.
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