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

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 reliabil...

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Veröffentlicht in:The Journal of heart and lung transplantation 2008, Vol.27 (1), p.124-130
Hauptverfasser: Gomberg-Maitland, Mardi, MD, MSc, Thenappan, Thenappan, MD, Rizvi, Kamran, MD, Chandra, Sonal, MD, Meads, David M., MSc, McKenna, Stephen P., PhD
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Sprache:eng
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Zusammenfassung: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.
ISSN:1053-2498
1557-3117
DOI:10.1016/j.healun.2007.10.004