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土耳其人群中脊柱关节病的Amor和ESSG分类标准评估。

Evaluation of the Amor and ESSG classification criteria for spondylarthropathies in a Turkish population.

作者信息

Ertürk M, Alaca R, Tosun E, Duruöz M T

机构信息

Physical Medicine and Rehabilitation Department, GATA Haydarpasa Training Hospital, Istanbul, Turkey.

出版信息

Rev Rhum Engl Ed. 1997 May;64(5):293-300.

PMID:9190002
Abstract

This study evaluated the Amor and European Spondylarthropathy Study Group (ESSG) classification criteria for spondyloarthropathies in Turkish patients seen from October 1990 to August 1993 at the Physical Medicine and Rehabilitation Department of the GATA Haydarpasa Training Hospital. The Amor and ESSG criteria were evaluated in 157 patients with spondylarthropathies and in 124 controls with a variety of other rheumatic diseases. The sensitivity, specificity, positive predictive value, and negative predictive value of each criteria set were calculated, as well as the sensitivity and specificity of each of the 24 criteria used in these sets. For Amor's criteria, sensitivity was 88.5%, specificity was 91.9%, positive predictive value was 93.3% and negative predictive value was 86.4%. For the ESSG criteria, sensitivity was 86.6%, specificity was 91.1%, positive predictive value was 92.5% and negative predictive value was 84.3%. No significant differences were found between the two criteria sets. Our data show that the Amor and ESSG criteria are of similar value for the classification of spondylarthropathies and are comparable in terms of sensitivity and specificity. They also demonstrate the need for monitoring patients with equivocal clinical patterns using both sets of criteria as tools that complement each other.

摘要

本研究评估了1990年10月至1993年8月间在加齐安泰普培训医院物理医学与康复科就诊的土耳其患者中,用于脊柱关节病分类的阿莫尔标准和欧洲脊柱关节病研究组(ESSG)标准。对157例脊柱关节病患者和124例患有各种其他风湿性疾病的对照者进行了阿莫尔标准和ESSG标准评估。计算了每组标准的敏感性、特异性、阳性预测值和阴性预测值,以及这些标准中使用的24项标准各自的敏感性和特异性。对于阿莫尔标准,敏感性为88.5%,特异性为91.9%,阳性预测值为93.3%,阴性预测值为86.4%。对于ESSG标准,敏感性为86.6%,特异性为91.1%,阳性预测值为92.5%,阴性预测值为84.3%。两组标准之间未发现显著差异。我们的数据表明,阿莫尔标准和ESSG标准在脊柱关节病分类方面具有相似价值,在敏感性和特异性方面具有可比性。它们还表明,需要使用这两组相互补充的标准作为工具,对临床症状不明确的患者进行监测。

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