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在 COPD 临床试验中测量呼吸症状:日常日记的可靠性和有效性。

Measuring respiratory symptoms in clinical trials of COPD: reliability and validity of a daily diary.

机构信息

Evidera, , Bethesda, Maryland, USA.

出版信息

Thorax. 2014 May;69(5):443-9. doi: 10.1136/thoraxjnl-2013-204428. Epub 2014 Mar 4.

Abstract

BACKGROUND

Although respiratory symptoms are characteristic features of COPD, there is no standardised method for quantifying their severity in stable disease.

OBJECTIVE

To evaluate the EXACT-Respiratory Symptom (E-RS) measure, a daily diary comprising 11 of the 14 items in the Exacerbations of Chronic Pulmonary Disease Tool (EXACT).

METHODS

Qualitative: patient focus group and interviews to address content validity. Quantitative: secondary data analyses to test reliability and validity.

RESULTS

Qualitative: n=84; mean (SD) age 65 (10) years, FEV1 1.2(0.4) L; 44% male. Subject descriptions of their respiratory symptoms were consistent with E-RS content and structure. Quantitative: n=188; mean (SD) age 66 (10) years, FEV1 1.2(0.5) L; 50% male. Factor analysis (FA) showed 3 subscales: RS-Breathlessness, RS-Cough & Sputum, and RS-Chest Symptoms; second-order FA supported a general factor and total score. Reliability (total and subscales): 0.88, 0.86, 0.73, 0.81; 2-day test-retest ICC: 0.90, 0.86, 0.87, 0.82, respectively.

VALIDITY

Total scores correlated significantly (p < 0.0001) with SGRQ Total (r=0.75), Symptoms (r=0.66), Activity (r=0.57), Impact (r=0.70) scores; subscale correlations were also significant (r=0.26, p < 0.05 (RS-Chest Symptoms with Activity) to r=0.69, p < 0.0001 (RS-Cough & Sputum with Symptoms). RS-Breathlessness correlated with rescue medication use (r=0.32, p < 0.0001), clinician-reported mMRC (r=0.33, p < 0.0001), and FEV1% predicted (r=-0.17, p < 0.05). E-RS scores differentiated groups based on chronic bronchitis diagnosis (p < 0.01-0.001), smoking status (p < 0.05-0.001), and rescue medication use (p < 0.05-0.0001).

CONCLUSIONS

Results suggest the RS-Total is a reliable and valid instrument for evaluating respiratory symptom severity in stable COPD. Further study of sensitivity to change is warranted.

摘要

背景

尽管呼吸症状是 COPD 的特征性表现,但目前尚无用于量化稳定期疾病严重程度的标准化方法。

目的

评估 EXACT-Respiratory Symptom(E-RS)量表,该量表是慢性肺部疾病加重工具(EXACT)的 14 个项目中的 11 个项目组成的日常日记。

方法

定性:患者焦点小组和访谈以解决内容有效性。定量:二次数据分析以测试可靠性和有效性。

结果

定性:n=84;平均(SD)年龄 65(10)岁,FEV1 1.2(0.4)L;44%为男性。患者对呼吸症状的描述与 E-RS 的内容和结构一致。定量:n=188;平均(SD)年龄 66(10)岁,FEV1 1.2(0.5)L;50%为男性。因子分析(FA)显示 3 个分量表:RS-呼吸困难、RS-咳嗽和咳痰、RS-胸部症状;二阶 FA 支持一个一般因子和总分。可靠性(总分和分量表):0.88、0.86、0.73、0.81;2 天测试-重测 ICC:0.90、0.86、0.87、0.82,分别。

有效性

总分与 SGRQ 总分(r=0.75)、症状(r=0.66)、活动(r=0.57)、影响(r=0.70)显著相关(p<0.0001);分量表相关性也显著(r=0.26,p<0.05(RS-胸部症状与活动)至 r=0.69,p<0.0001(RS-咳嗽和咳痰与症状)。RS-呼吸困难与急救药物使用(r=0.32,p<0.0001)、临床医生报告的 mMRC(r=0.33,p<0.0001)和 FEV1%预测值(r=-0.17,p<0.05)相关。E-RS 评分根据慢性支气管炎诊断(p<0.01-0.001)、吸烟状况(p<0.05-0.001)和急救药物使用(p<0.05-0.0001)区分了不同的组别。

结论

结果表明,RS 总分是评估稳定期 COPD 呼吸症状严重程度的可靠和有效的工具。需要进一步研究其对变化的敏感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91fb/3995276/ced281969e90/thoraxjnl-2013-204428f01.jpg

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