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将患者报告的结局指标纳入临床实践:炎症性关节炎问卷的制定和验证。

Incorporating patient reported outcome measures in clinical practice: development and validation of a questionnaire for inflammatory arthritis.

机构信息

Rheumatology Department, Darent Valley Hospital, Kent, UK.

出版信息

Clin Exp Rheumatol. 2010 Sep-Oct;28(5):734-44. Epub 2010 Oct 22.

Abstract

BACKGROUND

Rheumatology is embarking on a fundamental redesign of rheumatic disease care. It has become mandatory not only to recognise disease activity core set data, but also the risks for other co-morbidities associated with inflammatory arthritis. Measurement of patient reported outcomes have become critical in both standard clinical practice and long term observational studies.

OBJECTIVES

To assess validity, reliability and responsiveness to change of a patient self-reported questionnaire which can assess construct outcome measures of patients with inflammatory arthritis.

METHODS

Four hundred and sixty-two patients with inflammatory arthritis were included in this work. The questionnaire was developed by integrating information obtained from patients suffering from inflammatory arthritis based on the Rasch model for ordered response options. The questionnaire includes assessment for functional disability, quality of life, VAS for joint pain, global status, fatigue, duration of morning stiffness, review of the systems, falls and cardiovascular risks, self-helplessness, as well as self reported joint pain.

RESULTS

The questionnaire was reliable as demonstrated by a high-standardised alpha (0.891-0.992). The questionnaire items correlated significantly (p<0.01) with clinical parameters of disease activity. RA patient reported tender joints correlated significantly with the physician's scores (0.842). Changes in functional disability, quality of life as well as self-helplessness scores showed significant (p<0.01) variation with disease activity status. The PROMs questionnaire also showed a high degree of comprehensibility.(9.4).

CONCLUSIONS

Integrating patient reported outcome measures into standard clinical practice is feasible and applicable. This version of a multidimensional questionnaire was found to be valid and reliable. It provides informative quantitative measures for the disease activity core set data, and in the mean time, facilitates assessing the patients' health related quality of life measure, cardiovascular and falls risks on an individual basis.

摘要

背景

风湿病学正在对风湿病治疗进行根本性的重新设计。不仅要识别疾病活动核心数据集,还要识别与炎症性关节炎相关的其他合并症风险,这已成为强制性要求。患者报告的结果测量在标准临床实践和长期观察研究中都变得至关重要。

目的

评估一种患者自我报告问卷的有效性、可靠性和对变化的反应能力,该问卷可评估炎症性关节炎患者的结构结局测量。

方法

本研究纳入了 462 例炎症性关节炎患者。该问卷是通过整合基于有序反应选项的 Rasch 模型从炎症性关节炎患者那里获得的信息而开发的。问卷包括功能障碍、生活质量、关节疼痛视觉模拟评分、总体状况、疲劳、晨僵持续时间、系统回顾、跌倒和心血管风险、无助感以及自我报告的关节疼痛评估。

结果

该问卷具有高度可靠性,标准化α值为 0.891-0.992。问卷项目与疾病活动的临床参数显著相关(p<0.01)。类风湿关节炎患者报告的压痛关节与医生评分显著相关(0.842)。功能障碍、生活质量和无助感评分的变化与疾病活动状态有显著(p<0.01)的变化。PROMs 问卷也表现出高度的可理解性(9.4)。

结论

将患者报告的结局措施纳入标准临床实践是可行和适用的。这种多维问卷版本被发现具有有效性和可靠性。它为疾病活动核心数据集提供了有信息的定量测量,同时有助于对患者的健康相关生活质量测量、心血管和跌倒风险进行个体化评估。

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