Longitudinal Assessment of Health-Related Quality of Life in an Observational Cohort of Patients With Cystic Fibrosis

被引:78
|
作者
Sawicki, Gregory S. [1 ]
Rasouliyan, Lawrence [2 ]
McMullen, Ann H. [3 ]
Wagener, Jeffrey S. [4 ]
McColley, Susanna A. [5 ]
Pasta, David J. [2 ]
Quittner, Alexandra L. [6 ]
机构
[1] Childrens Hosp, Div Resp Dis, Boston, MA 02115 USA
[2] ICON Clin Res, San Francisco, CA USA
[3] Univ Rochester, Rochester, NY USA
[4] Univ Colorado, Sch Med, Denver, CO USA
[5] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA
[6] Univ Miami, Miami, FL USA
关键词
national database; patient-reported outcomes; minority status; PSEUDOMONAS-AERUGINOSA; AZTREONAM LYSINE; CHRONIC ILLNESS; CHILDREN; ADULTS; QUESTIONNAIRE; ADOLESCENTS; VALIDATION; INHALATION; PARENTS;
D O I
10.1002/ppul.21325
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Patient-reported outcomes (PROs) are increasingly used to evaluate the efficacy of new treatments and the progression of chronic diseases. The Cystic Fibrosis Questionnaire-Revised (CFQ-R) is a disease-specific, PRO measure of health-related quality of life (HRQOL). We evaluated associations between changes in health status over time and HRQOL in a national CF database. Methods: Using the Epidemiologic Study of Cystic Fibrosis (ESCF) data, we identified participants who had completed age-appropriate CFQ-R assessments on two occasions separated by 9-15 months. Next, we developed multivariate regression models to test whether associations existed between (1) changes in respiratory signs/symptoms and changes in the respiratory health domains of the CFQ-R, (2) changes in nutritional health status and changes in the nutritional health domains of the CFQ-R, and (3) changes in treatment complexity and changes in the Treatment Burden scale of the CFQ-R. Results: We analyzed 1,947 pairs of assessments: 337 child (mean age 8.9, range 6-13 years), 581 parent (mean age of child 8.8, range 6-13 years), 398 adolescent (mean age 15.3, range 14-17 years), and 631 adult (mean age 26.9, range 18-73 years). On average, we found little change in both health status indicators and CFQ-R domain scores over 1 year. Significant associations over time, however, were found between increases in respiratory symptoms and worse CFQ-R Respiratory Symptom scores, declining weight and worsening scores on CFQ-R nutritional health domains, and increases in treatment complexity and worsening CFQ-R Treatment Burden scores for parent respondents. Conclusion: Health status and HRQOL changes were small over a 1-year period in this CF population. However, changes in respiratory symptoms and weight were associated with significant changes on relevant CFQ-R scores, indicating that this PRO is sensitive to changes in health status over time. Pediatr Pulmonol. 2011; 46: 36-44. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:36 / 44
页数:9
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