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单项数字线性模拟自评(LASA)量表的规范数据及具有临床意义的效应量

Normative data and clinically significant effect sizes for single-item numerical linear analogue self-assessment (LASA) scales.

作者信息

Singh Jasvinder A, Satele Daniel, Pattabasavaiah Suneetha, Buckner Jan C, Sloan Jeff A

机构信息

Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.

Medicine Service, Veterans Affairs Medical Center, Birmingham, AL, USA.

出版信息

Health Qual Life Outcomes. 2014 Dec 18;12:187. doi: 10.1186/s12955-014-0187-z.

Abstract

BACKGROUND

Single-item assessments have been the most often-used measures in National Cancer Institute (NCI) cancer control clinical trials, but normative data are not available. Our objective was to examine the normative data and clinically significant effect sizes for single-item numerical linear analogue self-assessment (LASA) scale for overall quality of life (QOL).

METHODS

We analyzed baseline data from 36 clinical trials and 6 observational studies with various populations, including healthy volunteers, cancer trial patients (patients with advanced incurable cancer or patients receiving treatment with curative intent) and hospice patients as well as their caregivers. The overall QOL LASA was rated 0 (as bad as it can be) to 10 (as good as it can be). We calculated the summary statistics and the proportion of patients reporting a clinically meaningful deficit (CMD) of a score equal to 5 or less on the 0-10 scale.

RESULTS

In total, for the collective sample of 9,295 individuals, the average overall QOL reported was 7.39 (SD = 2.11) with a markedly skewed distribution with roughly 17% reporting a score of 5 or below indicating a clinically significant deficit in overall QOL. Hospice patients report a much worse average score of 5.7 upon entry to hospice; hospice caregivers average 7.4. Cancer patients vary within these two extremes with most patients averaging in the 7's on the 0-10 scale (range, 0 to 10 p-value < 0.0001). Men and women's QOL distributions were virtually identical (with average of 7.6 vs. 7.5, p-value = 0.046). Overall QOL was weakly related to performance status with a Spearman correlation coefficient of -0.29 (p-value < 0.0001). Overall QOL was related to tumor response (p-value = 0.0094), i.e. patients with a full or partial response reported a CMD in 11.4% of cases compared to 14.4% among those with stable disease and 18.5% among those with disease progression. Data missingness was high for performance status and tumor response associations.

CONCLUSIONS

This study provides the normative data for cancer patients and healthy volunteers for overall QOL using the LASA. These can serve as benchmarks for future studies and inform clinical practice decision-making.

摘要

背景

单项评估一直是美国国立癌症研究所(NCI)癌症控制临床试验中最常用的测量方法,但尚无规范数据。我们的目的是研究单项数字线性模拟自我评估(LASA)量表用于总体生活质量(QOL)的规范数据和具有临床意义的效应量。

方法

我们分析了来自36项临床试验和6项观察性研究的基线数据,这些研究涉及不同人群,包括健康志愿者、癌症试验患者(晚期无法治愈的癌症患者或接受根治性治疗的患者)、临终关怀患者及其护理人员。总体生活质量LASA的评分范围为0(尽可能差)至10(尽可能好)。我们计算了汇总统计数据以及在0至10分制中报告得分等于或低于5分的具有临床意义缺陷(CMD)的患者比例。

结果

总共,在9295名个体的总体样本中,报告的总体生活质量平均分为7.39(标准差=2.11),分布明显偏态,约17%的人报告得分在5分或以下,表明总体生活质量存在临床意义上的缺陷。临终关怀患者入院时报告的平均得分低得多,为5.7分;临终关怀护理人员的平均分为7.4分。癌症患者的得分在这两个极端之间变化,大多数患者在0至10分制中的平均得分在7分左右(范围为0至10,p值<0.0001)。男性和女性的生活质量分布几乎相同(平均分为7.6对7.5,p值=0.046)。总体生活质量与体能状态弱相关,Spearman相关系数为-0.29(p值<0.0001)。总体生活质量与肿瘤反应相关(p值=0.0094);即完全或部分缓解的患者中有11.4%的病例报告有CMD,而病情稳定的患者中这一比例为14.4%,疾病进展的患者中为18.5%。体能状态和肿瘤反应关联的数据缺失率很高。

结论

本研究提供了使用LASA量表对癌症患者和健康志愿者总体生活质量的规范数据。这些数据可作为未来研究的基准,并为临床实践决策提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3617/4302440/104e3bcbf1b2/12955_2014_187_Fig1_HTML.jpg

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