A longitudinal assessment of acute cough.
RATIONALE: Cough can be assessed with visual analog scales (VAS), health status measures, and 24-hour cough frequency monitors (CF(24)). Evidence for their measurement properties in acute cough caused by upper respiratory tract infection (URTI) and longitudinal data is limited. OBJECTIVES: To asses...
Auteurs principaux: | , , , , , |
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Format: | Journal article |
Langue: | English |
Publié: |
2013
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_version_ | 1826301784353669120 |
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author | Lee, K Matos, S Evans, D White, P Pavord, I Birring, S |
author_facet | Lee, K Matos, S Evans, D White, P Pavord, I Birring, S |
author_sort | Lee, K |
collection | OXFORD |
description | RATIONALE: Cough can be assessed with visual analog scales (VAS), health status measures, and 24-hour cough frequency monitors (CF(24)). Evidence for their measurement properties in acute cough caused by upper respiratory tract infection (URTI) and longitudinal data is limited. OBJECTIVES: To assess cough longitudinally in URTI with subjective and objective outcome measures and determine sample size for future studies. METHODS: Thirty-three previously healthy subjects with URTI completed cough VAS, Leicester Cough Questionnaire (LCQ-acute), and CF(24) monitoring (Leicester Cough Monitor) on three occasions, 4 days apart. Changes in subjects' condition were assessed with a global rating of change questionnaire. The potential for baseline first-hour cough frequency (CF(1)), VAS, and LCQ to identify low CF(24) was assessed. MEASUREMENTS AND MAIN RESULTS: Mean ± SD duration of cough at visit 1 was 4.1 ± 2.5 days. Geometric mean ± log SD baseline CF(24) and median (interquartile range) cough bouts were high (14.9 ± 0.4 coughs/h and 85 [39-195] bouts/24 h). Health status was severely impaired. There was a significant reduction in CF(24) and VAS, and improvement in LCQ, from visits 1-3. At visit 3, CF(24) remained above normal limits in 52% of subjects. The smallest changes in CF(24), LCQ, and VAS that subjects perceived important were 54%, 2- and 17-mm change from baseline, respectively. The sample sizes required for parallel group studies to detect these changes are 27, 51, and 25 subjects per group, respectively. CF(1) (<20.5 coughs/h) was predictive of low CF(24). CONCLUSIONS: CF(24), VAS, and LCQ are responsive outcome tools for the assessment of acute cough. The smallest change in cough frequency perceived important by subjects is 54%. The sample sizes required for future studies are modest and achievable. |
first_indexed | 2024-03-07T05:37:36Z |
format | Journal article |
id | oxford-uuid:e47239c9-c90f-4acd-97d5-52cfe8b192fc |
institution | University of Oxford |
language | English |
last_indexed | 2024-03-07T05:37:36Z |
publishDate | 2013 |
record_format | dspace |
spelling | oxford-uuid:e47239c9-c90f-4acd-97d5-52cfe8b192fc2022-03-27T10:16:43ZA longitudinal assessment of acute cough.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:e47239c9-c90f-4acd-97d5-52cfe8b192fcEnglishSymplectic Elements at Oxford2013Lee, KMatos, SEvans, DWhite, PPavord, IBirring, S RATIONALE: Cough can be assessed with visual analog scales (VAS), health status measures, and 24-hour cough frequency monitors (CF(24)). Evidence for their measurement properties in acute cough caused by upper respiratory tract infection (URTI) and longitudinal data is limited. OBJECTIVES: To assess cough longitudinally in URTI with subjective and objective outcome measures and determine sample size for future studies. METHODS: Thirty-three previously healthy subjects with URTI completed cough VAS, Leicester Cough Questionnaire (LCQ-acute), and CF(24) monitoring (Leicester Cough Monitor) on three occasions, 4 days apart. Changes in subjects' condition were assessed with a global rating of change questionnaire. The potential for baseline first-hour cough frequency (CF(1)), VAS, and LCQ to identify low CF(24) was assessed. MEASUREMENTS AND MAIN RESULTS: Mean ± SD duration of cough at visit 1 was 4.1 ± 2.5 days. Geometric mean ± log SD baseline CF(24) and median (interquartile range) cough bouts were high (14.9 ± 0.4 coughs/h and 85 [39-195] bouts/24 h). Health status was severely impaired. There was a significant reduction in CF(24) and VAS, and improvement in LCQ, from visits 1-3. At visit 3, CF(24) remained above normal limits in 52% of subjects. The smallest changes in CF(24), LCQ, and VAS that subjects perceived important were 54%, 2- and 17-mm change from baseline, respectively. The sample sizes required for parallel group studies to detect these changes are 27, 51, and 25 subjects per group, respectively. CF(1) (<20.5 coughs/h) was predictive of low CF(24). CONCLUSIONS: CF(24), VAS, and LCQ are responsive outcome tools for the assessment of acute cough. The smallest change in cough frequency perceived important by subjects is 54%. The sample sizes required for future studies are modest and achievable. |
spellingShingle | Lee, K Matos, S Evans, D White, P Pavord, I Birring, S A longitudinal assessment of acute cough. |
title | A longitudinal assessment of acute cough. |
title_full | A longitudinal assessment of acute cough. |
title_fullStr | A longitudinal assessment of acute cough. |
title_full_unstemmed | A longitudinal assessment of acute cough. |
title_short | A longitudinal assessment of acute cough. |
title_sort | longitudinal assessment of acute cough |
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