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测量液体摄入量类型和尿失禁类型的问卷的结构效度。

Construct validity of a questionnaire to measure the type of fluid intake and type of urinary incontinence.

机构信息

Division of Urogynecology and Reconstructive Pelvic Surgery, Department of Obstetrics and Gynecology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

出版信息

Neurourol Urodyn. 2011 Nov;30(8):1597-602. doi: 10.1002/nau.21091. Epub 2011 Apr 1.

Abstract

OBJECTIVE

To determine the reproducibility and construct validity of the Questionnaire Based Voiding Diary (QVD) for measuring the type and volume of fluid intake and the type of urinary incontinence.

METHODS

250 women completed the QVD, a 48-hour bladder diary and underwent complete urogynecologic evaluation to determine a final clinical diagnosis. The questionnaire was re-administered after a 2-week period with no change in treatment, and 2-3 months later following treatment of urinary symptoms.

RESULTS

The reproducibility of the fluid intake, output, fluid intake behavior and urinary symptom subscales of the QVD was 0.68-0.92. Correlation of the fluid intake scale of the QVD with the 48-hour voiding diary for determining the type and volume of fluid intake was high (r = 0.65-0.83, P < 0.01). High correlations were noted between the fluid intake behavior scale and urinary frequency (r = 0.82, P < .01), urgency (r = 0.77, P < .01) and urge incontinence (r = 0.71, P < .01). The median total fluid intake and mean urinary symptom score was significantly lower in responders (2074 mL, 10.2 ± 3.3) than non-responders (2347 mL, 18.5 ± 4.6). As compared to the final clinical diagnosis, the sensitivity, specificity and positive likelihood ratio of the QVD for the diagnosis of predominant stress urinary incontinence are 86%, 66% and 2.6 and for predominant urge incontinence 82%, 79% and 4.0 respectively.

CONCLUSION

The QVD provides clinically meaningful information on the type and volume of fluid intake and the type of urinary incontinence at the initial office visit.

摘要

目的

确定基于问卷的排尿日记(QVD)测量液体摄入类型和量以及尿失禁类型的可重复性和结构效度。

方法

250 名女性完成了 QVD、48 小时膀胱日记,并接受了完整的泌尿妇科评估,以确定最终的临床诊断。在没有改变治疗的情况下,2 周后重新进行了问卷调查,并且在治疗尿症状后 2-3 个月进行了随访。

结果

QVD 的液体摄入、输出、液体摄入行为和尿症状分量表的可重复性为 0.68-0.92。QVD 的液体摄入量表与 48 小时排尿日记用于确定液体摄入类型和量的相关性很高(r=0.65-0.83,P<0.01)。QVD 的液体摄入行为量表与尿频率(r=0.82,P<.01)、紧迫性(r=0.77,P<.01)和急迫性尿失禁(r=0.71,P<.01)之间存在高度相关性。在有反应者(2074 mL,10.2±3.3)中,中位数总液体摄入量和平均尿症状评分明显低于无反应者(2347 mL,18.5±4.6)。与最终临床诊断相比,QVD 对主要压力性尿失禁的诊断的敏感性、特异性和阳性似然比分别为 86%、66%和 2.6,对主要急迫性尿失禁的诊断的敏感性、特异性和阳性似然比分别为 82%、79%和 4.0。

结论

QVD 在初始就诊时提供了关于液体摄入类型和量以及尿失禁类型的有临床意义的信息。

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