Drossman D A, Patrick D L, Whitehead W E, Toner B B, Diamant N E, Hu Y, Jia H, Bangdiwala S I
UNC Center for Functional GI and Motility Disorders, Division of Digestive Diseases, University of North Carolina, Chapel Hill 27599-7080, USA.
Am J Gastroenterol. 2000 Apr;95(4):999-1007. doi: 10.1111/j.1572-0241.2000.01941.x.
There has been growing interest in the investigation of health-related quality of life (HRQOL) among patients with gastrointestinal (GI) disorders. We recently reported on the development and preliminary validation of the IBS-QOL, a specific quality-of-life measure for irritable bowel syndrome (IBS). The aim of this study was to determine the longitudinal construct validity (responsiveness) of the IBS-QOL.
Female patients enrolled in a multicenter treatment trial for functional bowel disorders were studied pre- and posttreatment with the IBS-QOL and other health status measures. Based on the response to treatment for several variables (pain/14-day score, daily function, and days in bed/3 months), patients were stratified into Responders, Partial Responders, and Nonresponders. Change scores in the IBS-QOL were then statistically compared with changes in the other variables to determine their correlation and whether Responders were significantly different from non- and Partial Responders on the IBS-QOL.
There was a significant correlation between change scores on the IBS-QOL and the other measures of treatment effect (Pain/14 days, r = 0.25, p < 0.002; Sickness Impact Profile [SIP] Total Score, r = 0.28, p < 0.0004). In addition, the IBS-QOL scores significantly differentiated Responders from Nonresponders for most of the variables tested (regression trend test for Pain/14 days, p < 0.04; SIP Total, p < 0.0001; SIP Physical, p < 0.0001; SIP Psychosocial, p < 0.002, and SIP Eating, p < 0.04).
The IBS-QOL is responsive to treatment in a referral-based clinical population of patients with functional bowel disorders.
胃肠道(GI)疾病患者的健康相关生活质量(HRQOL)调查越来越受到关注。我们最近报告了肠易激综合征(IBS)特异性生活质量测量工具IBS-QOL的开发及初步验证情况。本研究旨在确定IBS-QOL的纵向结构效度(反应性)。
参加功能性肠病多中心治疗试验的女性患者在治疗前后接受IBS-QOL及其他健康状况测量。根据对几个变量(疼痛/14天评分、日常功能、卧床天数/3个月)的治疗反应,将患者分为反应者、部分反应者和无反应者。然后对IBS-QOL的变化分数与其他变量的变化进行统计学比较,以确定它们之间的相关性,以及反应者在IBS-QOL上是否与无反应者和部分反应者有显著差异。
IBS-QOL的变化分数与其他治疗效果测量指标之间存在显著相关性(疼痛/14天,r = 0.25,p < 0.002;疾病影响量表[SIP]总分,r = 0.28,p < 0.0004)。此外,对于大多数测试变量,IBS-QOL分数能显著区分反应者和无反应者(疼痛/14天的回归趋势检验,p < 0.04;SIP总分,p < 0.0001;SIP身体方面,p < 0.0001;SIP心理社会方面,p < 0.002,以及SIP饮食方面,p < 0.04)。
在基于转诊的功能性肠病临床患者群体中,IBS-QOL对治疗有反应。