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美国对剑桥肺动脉高压结局评估(CAMPHOR)的验证。

United States validation of the Cambridge Pulmonary Hypertension Outcome Review (CAMPHOR).

作者信息

Gomberg-Maitland Mardi, Thenappan Thenappan, Rizvi Kamran, Chandra Sonal, Meads David M, McKenna Stephen P

机构信息

University of Chicago Medical Center, Chicago, Illinois 60637, USA.

出版信息

J Heart Lung Transplant. 2008 Jan;27(1):124-30. doi: 10.1016/j.healun.2007.10.004.

Abstract

BACKGROUND

The Cambridge Pulmonary Hypertension Outcome Review (CAMPHOR) is the first pulmonary hypertension-specific instrument for assessing patient-reported symptoms, functioning, and quality of life. To enable use in the United States, this study adapted, field-tested, and evaluated its reliability and validity at a single center in Chicago.

METHODS

A lay panel confirmed appropriate wording of CAMPHOR for United States patients, and 15 patients with pulmonary hypertension field-tested the CAMPHOR for face and content validity. A postal validation study, with the Medical Outcomes Study Short Form 36 (SF-36) Health Survey as a comparator, was sent to patients on 2 occasions, 2 weeks apart. World Health Organization (WHO) functional class and 6-minute walk test data were obtained.

RESULTS

Field-test interviews found the CAMPHOR relevant and comprehensible. A total of 147 patients (84.0% women) with a mean of 50 +/- 14.6 years participated in the validation study. The new scales had good test-retest reliability (range, 0.80-0.95) and internal consistency (range, 0.78-0.95). The CAMPHOR scales correlated with the SF-36 and 6-minute walk test. Patients in WHO functional class III had worse scores than those in class II (p = 0.02), as did patients who rated their health worse (p < 0.001).

CONCLUSIONS

The US CAMPHOR is a reliable and valid measure of quality of life and health status in pulmonary hypertension and can be recommended for use in clinical practice and trials in the United States.

摘要

背景

剑桥肺动脉高压结局评估量表(CAMPHOR)是首个用于评估患者报告的症状、功能及生活质量的肺动脉高压专用工具。为使其能在美国使用,本研究在芝加哥的一个中心对其进行了改编、现场测试,并评估了其信度和效度。

方法

一个外行小组确认了CAMPHOR对美国患者的措辞恰当,15名肺动脉高压患者对CAMPHOR进行了表面效度和内容效度的现场测试。一项邮寄验证研究,以医学结局研究简表36(SF - 36)健康调查作为对照,分两次寄给患者,间隔2周。获取了世界卫生组织(WHO)功能分级和6分钟步行试验数据。

结果

现场测试访谈发现CAMPHOR相关且易于理解。共有147名患者(84.0%为女性)参与了验证研究,平均年龄50±14.6岁。新量表具有良好的重测信度(范围为0.80 - 0.95)和内部一致性(范围为0.78 - 0.95)。CAMPHOR量表与SF - 36及6分钟步行试验相关。WHO功能分级为Ⅲ级的患者得分低于Ⅱ级患者(p = 0.02),自我评估健康状况较差的患者得分也较低(p < 0.001)。

结论

美国版CAMPHOR是一种可靠且有效的肺动脉高压生活质量和健康状况测量工具,可推荐用于美国的临床实践和试验。

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