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中文版苏黎世间歇性跛行问卷的信度、效度及最小临床重要差异

Reliability, validity and minimum clinical importance difference of the Chinese version of the Zurich claudication questionnaire.

作者信息

Gao Yi-Xuan, Weng Zhi-Wen, Shao Hui, Bo Han, Chen Zhi-Hui, Song Meng, Liu Lu-Ping, Zhang Ling-Yun, Liu Jia-Yu, Wang Yu-Han, Zhang Meng-Meng, Wang Xi-You, Sun Ya-Nan, Yu Chang-He, Wang Xi-You, Sun Ya-Nan, Yu Chang-He

机构信息

First clinical college, Beijing University of Chinese Medicine, Beijing, China.

Tuina and pain management department, Beijing University of Chinese Medicine Affiliated Dongzhimen Hospital, Beijing, China.

出版信息

Sci Rep. 2025 May 13;15(1):16654. doi: 10.1038/s41598-025-01380-w.

DOI:10.1038/s41598-025-01380-w
PMID:40360606
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12075636/
Abstract

The Zurich Claudication Questionnaire (ZCQ) has been translated and validated in multiple languages but few people have verified the measurement performance of the Chinese version of Zurich Claudication Questionnaire (Ch-ZCQ). The purpose of this study is to assess the performance of the Ch-ZCQ in lumbar spinal stenosis (LSS) patients undergoing non-surgical treatment. It includes the reliability, validity, responsiveness and minimally clinical important difference (MCID) of the two dimensions of symptom severity (SS) and physical function (PF). The results shows that the internal consistency and test-retest reliability were good. The content validity index was 0.764. The structural validity was good and moderate suitability. The correlation between the two dimensions of ZCQ is good, which is strongly correlated with Oswestry Disability Index (ODI) and moderately correlated with 12-item Short Form Health Survey Version 2(SF-12v2). Discriminative validity had significant differences in the degree of classification. The ZCQ's SS and PF dimensions demonstrated a moderate Effect Size (ES) of 0.46 and 0.35. The Standardized Response Mean (SRM) was low, with values of 0.34 and 0.25. Additionally, the Change Rate (CR) was 10% for both, indicating a low level of change. MCID SS= -0.21[95% CI (-0.36, -0.05)]; MCID PF= -0.16[95% CI (-0.36, -0.03)]. This study demonstrates the Ch-ZCQ to be a reliable and valid tool, which can effectively evaluate the effectiveness of nonsurgical treatments for patients with LSS. However, to optimize its application for the Chinese population, further refinement is needed to address the ceiling/floor effects of some items.

摘要

苏黎世跛行问卷(ZCQ)已被翻译成多种语言并进行了验证,但很少有人验证过中文版苏黎世跛行问卷(Ch-ZCQ)的测量性能。本研究的目的是评估Ch-ZCQ在接受非手术治疗的腰椎管狭窄症(LSS)患者中的性能。它包括症状严重程度(SS)和身体功能(PF)两个维度的可靠性、有效性、反应性和最小临床重要差异(MCID)。结果表明,内部一致性和重测信度良好。内容效度指数为0.764。结构效度良好且适度适宜。ZCQ两个维度之间的相关性良好,与奥斯威斯利功能障碍指数(ODI)呈强相关,与12项简短健康调查问卷第2版(SF-12v2)呈中度相关。区分效度在分类程度上有显著差异。ZCQ的SS和PF维度显示出中等效应量(ES),分别为0.46和0.35。标准化反应均值(SRM)较低,分别为0.34和0.25。此外,两者的变化率(CR)均为10%,表明变化水平较低。MCID SS = -0.21[95%置信区间(-0.36,-0.05)];MCID PF = -0.16[95%置信区间(-0.36,-0.03)]。本研究表明Ch-ZCQ是一种可靠且有效的工具,可有效评估LSS患者非手术治疗的效果。然而,为了优化其在中国人群中的应用,需要进一步改进以解决某些项目的天花板/地板效应。