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PROMIS Pediatrics 大规模调查的抽样计划和患者特征。

Sampling plan and patient characteristics of the PROMIS pediatrics large-scale survey.

机构信息

Department of Epidemiology, University of North Carolina at Chapel Hill, CB #7294, Chapel Hill, NC 27599, USA.

出版信息

Qual Life Res. 2010 May;19(4):585-94. doi: 10.1007/s11136-010-9618-4. Epub 2010 Mar 5.

Abstract

PURPOSE

This paper describes a large-scale administration of the Patient-Reported Outcomes Measurement Information System (PROMIS) pediatric items to evaluate measurement characteristics.

METHODS

Each child completed one of seven test forms containing items from a pool of 293 PROMIS items and four legacy scales. PROMIS items covered six domains (physical function, emotional distress, social role relationship, fatigue, pain, and asthma).

RESULTS

From January 2007 to May 2008, 4,129 children aged 8-17 were enrolled. The sample was 51% female, 55% aged 8-12, 42% minority race and 17% were Hispanic ethnicity. Approximately, 35% of the children participating in the survey consulted a clinician for a chronic illness diagnosis or treatment within 6 months prior to study enrollment.

CONCLUSIONS

The final PROMIS pediatric item banks include physical function (n = 52 items), emotional distress (n = 35 items), social role relationships (n = 15 items), fatigue (n = 34 items), pain (n = 13 items), and asthma (n = 17 items). The initial calibration data were provided by a diverse set of children with varying health states (e.g., children with a variety of common chronic illnesses) and racial/ethnic backgrounds.

摘要

目的

本文描述了对患者报告结局测量信息系统(PROMIS)儿科项目进行大规模管理,以评估测量特性。

方法

每个孩子完成了七个测试表单中的一个,这些表单包含了 293 个 PROMIS 项目和四个传统量表的项目。PROMIS 项目涵盖了六个领域(身体机能、情绪困扰、社会角色关系、疲劳、疼痛和哮喘)。

结果

2007 年 1 月至 2008 年 5 月,共有 4129 名 8-17 岁的儿童参与了研究。样本中 51%为女性,55%为 8-12 岁,42%为少数族裔,17%为西班牙裔。大约 35%的参与调查的儿童在研究入组前 6 个月内曾因慢性病就诊接受过诊断或治疗。

结论

最终的 PROMIS 儿科项目库包括身体机能(n = 52 项)、情绪困扰(n = 35 项)、社会角色关系(n = 15 项)、疲劳(n = 34 项)、疼痛(n = 13 项)和哮喘(n = 17 项)。初始校准数据由具有不同健康状况(例如,患有各种常见慢性病的儿童)和种族/族裔背景的多样化儿童提供。

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