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Validity and reliability of an interviewer-administered questionnaire to measure the severity of lower urinary tract symptoms of storage abnormality: the Leicester Urinary Symptom Questionnaire.

机译:由访调员管理的调查问卷的有效性和可靠性,该调查问卷用于衡量存储异常的下尿路症状的严重性:莱斯特泌尿系统症状调查表。

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Objective To develop a valid and reliable interviewer-administered questionnaire to measure the presence and severity of storage abnormality symptoms of incontinence, urgency, frequency and nocturia. Subjects and methods Subjects were 930 men and women aged >/=40 years, taking part in a randomized controlled trial of a continence nurse practitioner (CNP) service. Criterion validity was tested by comparing questionnaire responses to 24-h pad test and 3-day urinary diary. Responsiveness was assessed by comparing questionnaire responses before and after treatment. Questions about urgency were investigated for construct validity in patients taking part in the trial who underwent urodynamic investigation (243). Test-retest and inter-rater reliability was measured at approximately 6 days in subjects recruited to an associated epidemiological study (104 and 102, respectively). Results The questionnaire responses showed significant associations with pad-test and diary measures. Questions about the severity of daytime incontinence performed better than those measuring night-time incontinence. The response categories of soaked, wet, damp and almost dry had better associations with the pad test than other measures of the severity of incontinence. Test-retest and inter-rater reliability was good for all questions, and all were responsive to change in symptoms, showing significant differences before and after treatment. Conclusion There is a clear need for standardization of measurement using well-validated instruments. This interviewer-administered questionnaire is valid, reliable and sensitive to change in a wide range of severity of symptoms, and in both men and women aged >/=40 years. The questionnaire provides a useful assessment tool for primary and secondary care in research and clinical settings.
机译:目的建立由访调员管理的有效,可靠的问卷,以衡量尿失禁,尿急,尿频和夜尿的存储异常症状的存在和严重程度。受试者和方法受试者为930岁以上40岁以下的男性和女性,参加了一项自控护士执业(CNP)服务的随机对照试验。通过比较问卷调查表对24小时便笺本测试和3天泌尿日记的反应,来检验标准的有效性。通过比较治疗前后的问卷回答来评估反应性。调查了参与尿液动力学检查的患者的尿急性问题,以验证其结构的有效性(243)。在招募参加相关流行病学研究的受试者中,大约6天后进行了重测和评定者间信度(分别为104和102)。结果问卷调查结果显示与便签测试和日记措施之间存在显着关联。关于白天尿失禁的严重性的问题要比测量夜间尿失禁的问题表现得更好。与尿失禁严重程度的其他指标相比,浸泡,湿润,潮湿和几乎干燥的反应类别与垫试验的关联性更好。重测和评分者间的信度对所有问题都很好,并且所有人都对症状的变化有反应,显示出治疗前后的显着差异。结论显然需要使用经过充分验证的仪器对测量进行标准化。这份由访调员管理的问卷对于年龄在40岁以上的男性和女性,在各种严重程度的症状变化中均有效,可靠且敏感。问卷为研究和临床环境中的初级和二级保健提供了有用的评估工具。

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