Comparison of 7-day and repeated 24-hour recall of symptoms of cystic fibrosis
- PMID: 20817624
- PMCID: PMC12414477
- DOI: 10.1016/j.jcf.2010.08.008
Comparison of 7-day and repeated 24-hour recall of symptoms of cystic fibrosis
Abstract
Background: Patient reporting of symptoms in a questionnaire with a 7-day recall period is expected to differ from reporting in daily symptom diaries.
Methods: 38 patients with cystic fibrosis (CF) completed 77 week-long symptom diaries. Each diary day comprised 13 symptom items with 5-point response scales. Days 1-6 of the diary had a 24-hour recall period. Day 7 had a 7-day recall period. Concordance of 7-day recall with summary descriptors of daily reports (e.g. mean, maximum) was examined and ability of 7-day recall and mean of daily reports to discriminate between well and ill periods of health compared.
Results: The average difference in scores was less than 0.25 response scale points. 7-day recall was most concordant with the mean of daily reports. Discriminant ability was comparable.
Conclusions: In this study sample, a questionnaire with 7-day recall provided information similar to a daily diary about the week-long experience of CF symptoms.
Copyright © 2010 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.
Conflict of interest statement
Conflict of interest statement
The authors report no financial or personal relationships which could inappropriately influence this study
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References
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- Gibson R, Burns J, Ramsey B. Pathophysiology and management of pulmonary infections in cystic fibrosis. Am J Respir Crit Care Med 2003;168:918–51. - PubMed
-
- Goss CH, Edwards TC, Ramsey BW, Aitken ML, Patrick DL. Patient-reported respiratory symptoms in cystic fibrosis. J Cyst Fibros 2009. Jul;8(4):245–52. - PubMed
-
- Revicki DA, Osoba D, Fairclough D, Barofsky I, Berzon R, Leidy NK, et al. Recommendations on health-related quality of life research to support labeling and promotional claims in the United States. Qual Life Res 2000;9(8):887–900. - PubMed
-
- FDA. Patient Reported Outcome (PRO) Measures: Use in Medical Product Development to Support Labeling Claims. Federal Register. 2009;74(235).
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