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首页> 外文期刊>Frontiers in Veterinary Science >Comparison of Serum Amyloid A Measurements in Equine Synovial Fluid With Routine Diagnostic Methods to Detect Synovial Infection in a Clinical Environment
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Comparison of Serum Amyloid A Measurements in Equine Synovial Fluid With Routine Diagnostic Methods to Detect Synovial Infection in a Clinical Environment

机译:马滑膜液中血清淀粉样蛋白A测定与常规诊断方法在临床环境中检测滑膜感染的比较

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摘要

Synovial fluid analysis is utilized to diagnose septic synovitis. However, not all cases are clearly and rapidly discernible with the diagnostic tools available in the laboratory. Serum amyloid A (SAA), an acute phase protein, has been shown to be elevated in synovial fluid from inflamed synovial structures. The goal of this study is to describe the correlation between two diagnostic tests measuring equine SAA levels in septic and non-septic synovial structures and to understand the correlation between an elevated SAA result and synovial sepsis. Prospective estimation of sensitivity (Se) and specificity (Sp) of two tests, handheld and ELISA, measuring SAA in synovial fluid was completed in 62 horses presented with injured synovial structures. The comparison was made to a reference diagnosis based on white cell count, percentage of neutrophils, intracellular bacteria and bacterial culture on synovial fluid. Handheld test levels were classified as: 4 lines visible - SAA level negative; 3 lines visible - SAA level mild; 2 lines visible - SAA level moderate; and 1 line visible - SAA level severe and compared to the numerical value obtained with ELISA test. The ELISA SAA test had an area under the curve of 0.88 (0.78 - 0.98). An ELISA cut-off of 23.95 μg/mL maximized Se and Sp. This cutoff gave a Se of 0.93 (0.66-1.00) and Sp of 0.77 (0.63 – 0.88). The handheld test was highly correlated with the ELISA SAA test (Spearman rank correlation 0.96) and at a cutoff of moderate or higher for positive results gave identical Se and Sp. Se and Sp of synovial fluid SAA hand held test are very reliable when clinical signs of synovitis are present for 6 hours. This test, in conjunction with traditional methods, can assist practitioners to rapidly diagnose and expedite appropriate intervention of synovial sepsis.
机译:滑液分析用于诊断败血性滑膜炎。但是,并不是所有的情况都可以通过实验室中可用的诊断工具清晰,快速地辨别出来。血清淀粉样蛋白A(SAA)是一种急性期蛋白,已被证明在发炎的滑膜结构的滑液中升高。这项研究的目的是描述两种在化脓性和非化脓性滑膜结构中测量马SAA水平的诊断测试之间的相关性,并了解SAA结果升高与滑膜败血症之间的相关性。对62例滑膜结构受损的马进行了前瞻性估计,即手持和ELISA检测滑液中SAA的两项检测的敏感性(Se)和特异性(Sp)。根据白细胞计数,中性粒细胞百分比,细胞内细菌和滑液上细菌培养,与参考诊断进行比较。手持式测试等级分为:4条可见线-SAA等级阴性;可见3条线-SAA水平温和;可见2行-SAA级别适中; 1条线可见-SAA水平严重,并与ELISA试验获得的数值进行比较。 ELISA SAA测试的曲线下面积为0.88(0.78-0.98)。最大Se和Sp的ELISA临界值为23.95μg/ mL。该截止值给出了0.93(0.66-1.00)的Se和0.77(0.63 – 0.88)的Sp。手持式测试与ELISA SAA测试高度相关(Spearman等级相关系数0.96),对于阳性结果,在中等或更高的临界值下,Se和Sp相同。当滑膜炎的临床体征持续超过6小时时,滑液SAA的Se和Sp值非常可靠。该测试与传统方法相结合,可以帮助从业人员快速诊断并加速滑膜败血症的适当干预。

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