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International cross-cultural field validation of an European Organization for Research and Treatment of Cancer questionnaire module for patients with primary liver cancer, the European Organization for Research and Treatment of Cancer quality-of-life questionnaire HCC18

机译:欧洲癌症研究和治疗组织针对原发性肝癌患者的问卷调查模块的国际跨文化领域验证,欧洲癌症研究和治疗组织生活质量问卷HCC18

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摘要

This international field validation study examined the psychometric properties and clinical validity of the European Organization for Research and Treatment of Cancer (EORTC) questionnaire module for hepatocellular carcinoma (HCC), the EORTC quality-of-life questionnaire (QLQ)-HCC18. The EORTC QLQ-HCC18 was administered with the core questionnaire, the EORTC QLQ-C30, to 272 patients from seven centers in 6 countries. Patient acceptability of the module was examined with a debriefing questionnaire, and psychometric and clinical properties were assessed. Multitrait scaling analyses confirmed the hypothesized scale structure without any scaling error, and the fatigue scale demonstrated satisfactory internal consistency. The test-retest reliability scores were high for all scales, except abdominal swelling and sexual interest. The correlations between all scales of the QLQ-HCC18 and the QLQ-C30 were low or moderate, and many scales could distinguish patients with different clinical conditions. The module demonstrated responsiveness to clinical change in pain before and after surgery and some borderline change in patients undergoing systemic treatment. Conclusion: The EORTC QLQ-HCC18 can be used as a supplementary module for the EORTC QLQ-C30 in clinical trials for patients with HCC. (HEPATOLOGY 2012)
机译:这项国际现场验证研究检查了欧洲癌症研究和治疗组织(EORTC)肝细胞癌(HCC)问卷模块,EORTC生活质量问卷(QLQ)-HCC18的心理计量学特性和临床有效性。 EORTC QLQ-HCC18随核心问卷EORTC QLQ-C30一起接受了来自6个国家/地区七个中心的272名患者的治疗。通过汇报调查表检查了该模块的患者可接受性,并评估了心理和临床特征。多特征尺度分析证实了假设的尺度结构,没有任何尺度误差,疲劳尺度显示出令人满意的内部一致性。除腹部肿胀和性兴趣外,所有范围的重测信度得分都很高。 QLQ-HCC18和QLQ-C30的所有量表之间的相关性均较低或中等,许多量表可以区分具有不同临床状况的患者。该模块展示了对手术前后疼痛的临床变化的反应能力,以及接受全身治疗的患者的一些临界变化。结论:EORTC QLQ-HCC18可以作为EORTC QLQ-C30在HCC患者临床试验中的补充模块。 (2012年肝病)

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