Initial development and pilot testing of observer-reported outcomes (ObsROs) for children with cystic fibrosis ages 0-11 years

被引:10
作者
Edwards, T. C. [1 ]
Emerson, J. [2 ]
Genatossio, A. [2 ]
McNamara, S. [2 ]
Goss, C. [3 ]
Patrick, D. L. [1 ]
Onchiri, F. [4 ,5 ]
Rosenfeld, M. [6 ]
机构
[1] Univ Washington, Dept Hlth Serv, 1208 NE 43rd St Campus Box 359455, Seattle, WA 98195 USA
[2] Seattle Childrens Hosp, Div Pulm Med, Seattle, WA USA
[3] Univ Washington, Dept Med & Pediat, Div Pulm & Crit Care Med, Seattle, WA 98195 USA
[4] Seattle Childrens Res Inst, Ctr Biomed Stat, Seattle, WA USA
[5] Seattle Childrens Res Inst, Ctr Clin & Translat Res, Seattle, WA USA
[6] Univ Washington, Dept Pediat, Div Pulm Med, Seattle Childrens Hosp, Seattle, WA 98195 USA
关键词
Children; Cystic fibrosis; Signs; Observation; Diary; Outcome; QUALITY-OF-LIFE; SYMPTOMS;
D O I
10.1016/j.jcf.2017.12.008
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Purpose: Patient-reported outcomes are important clinical trial endpoints. Young children may not be able to reliably report on how they feel or function, so observer-reported outcomes (ObsROs) may be more appropriate for them. The purpose of this study was to develop and pilot field test electronic parent-reported observational instruments for children with cystic fibrosis (CF) 0-6 and 7-11 years of age. Methods: We performed concept elicitation interviews with parents of children with CF <= 11 years of age to elicit the respiratory signs they could observe at baseline and during an acute respiratory illness. The resulting instruments were refined based on interviews with parents and clinicians. We conducted a pilot field test to evaluate test-retest reliability and the ability of items to distinguish well and sick periods. Results: The instruments consist of 17 items assessing respiratory signs and observable CF-related impacts. Test-retest reliability was acceptable for both age groups but discrimination was low for ages 7-11, likely reflecting less direct observation of older children by their parents. Conclusions: An ObsRO for children with CF ages 0-6 appears promising, while self-report may be more appropriate for children >6 years of age. Next steps for the 0-6 year old instrument will be utilizing it as an exploratory endpoint in clinical trials to enable item reduction, scale development, and further reliability and validity testing. Ultimately, this ObsRO could be a promising endpoint for early intervention trials in young children with CF. (C) 2018 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:680 / 686
页数:7
相关论文
共 18 条
  • [1] [Anonymous], N AM CYST FIBR C
  • [2] [Anonymous], GUID IND QUAL PROC D
  • [3] [Anonymous], FDA CLIN TRIAL OUTC
  • [4] [Anonymous], 2009, GUID IND PAT REP OUT
  • [5] Comparison of 7-day and repeated 24-hour recall of symptoms of cystic fibrosis
    Bennett, Antonia V.
    Patrick, Donald L.
    Lymp, James F.
    Edwards, Todd C.
    Goss, Christopher H.
    [J]. JOURNAL OF CYSTIC FIBROSIS, 2010, 9 (06) : 419 - 424
  • [6] Fowler FJ, 2012, Survey research methods, V4th, DOI [DOI 10.4135/9781452230184, 10.4135/9781452230184]
  • [7] Patient-reported respiratory symptoms in cystic fibrosis
    Goss, C. H.
    Edwards, T. C.
    Ramsey, B. W.
    Aitken, M. L.
    Patrick, D. L.
    [J]. JOURNAL OF CYSTIC FIBROSIS, 2009, 8 (04) : 245 - 252
  • [8] MEASURING HEALTH-RELATED QUALITY-OF-LIFE
    GUYATT, GH
    FEENY, DH
    PATRICK, DL
    [J]. ANNALS OF INTERNAL MEDICINE, 1993, 118 (08) : 622 - 629
  • [9] Hays R.D., 2005, Assessing quality of life in clinical trials, V2nd, P3
  • [10] Keller Vicki E Clarkson, 2006, Pediatr Nurs, V32, P420