• Health Qual Life Out · Jan 2012

    Randomized Controlled Trial Comparative Study

    The validity and precision of the Leicester Cough Questionnaire in COPD patients with chronic cough.

    • Farida F Berkhof, Lisenka N Boom, Nynke E ten Hertog, Steven M Uil, Huib A M Kerstjens, and Jan W K van den Berg.
    • Isala klinieken, department of pulmonary diseases, Zwolle, The Netherlands. f.f.berkhof@isala.nl
    • Health Qual Life Out. 2012 Jan 1; 10: 4.

    BackgroundA validated instrument to assess the effects of chronic cough on health status in patients with chronic obstructive pulmonary disease (COPD) is currently not available. The Leicester Cough Questionnaire (LCQ) is a cough-specific health status questionnaire which is originally validated for a population of general patients presenting with chronic cough. We examined the psychometric performance of the LCQ in patients with COPD and chronic productive cough.MethodsConcurrent validity, internal consistency, reproducibility and responsiveness were determined. The St. George's Respiratory Questionnaire (SGRQ) and the Short Form-36 (SF-36) were used as external criteria. Questionnaires were completed at the start of the study. After 2 and 12 weeks the LCQ was repeated, together with a global rating of change.ResultsIn total 54 patients were included. Concurrent validity analysis showed significant correlations between corresponding domains of the LCQ and the SGRQ (r(s) -0.31 to -0.60). Corresponding domains of the LCQ and the SF-36 showed weaker correlations (r(s) 0.04 to 0.41). Internal consistency was adequate for two of the three domains (Cronbach's α 0.74 - 0.86). Test-retest reliability in stable patients was high (intraclass correlation coefficients 0.79 - 0.93). The mean difference after two weeks was 0.73 (± 1.75). Responsiveness analysis indicated that the LCQ was able to detect changes after 12 weeks.ConclusionThe LCQ is a valid, reliable, responsive instrument to measure health status in COPD patients with chronic productive cough.Trial RegistrationClinicalTrials.gov: NCT01071161.© 2012 Berkhof et al; licensee BioMed Central Ltd.

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