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Objective cough frequency in Idiopathic Pulmonary Fibrosis 英文参考文献
Key et al. Cough 2010, 6:4
/content/6/1/4
Cough
RESEARCH
Open Access
Objective cough frequency in Idiopathic Research
Pulmonary Fibrosis
Angela L Key?1,3, Kimberley Holt?1,3, Andrew Hamilton?2, Jaclyn A Smith?2 and John E Earis*?1,3
Abstract
Background: Cough is a common presenting symptom in patients with Idiopathic Pulmonary Fibrosis (IPF). This study
measured cough rates in IPF patients and investigated the association between cough and measures of health related
quality of life and subjective cough assessments. In addition, IPF cough rates were related to measures of physiological
disease severity and compared to cough rates in health and other respiratory conditions.
Methods: Nineteen IPF patients, mean age 70.8 years ± 8.6 , five female (26 .3%) were studied. Subjects performed full
pulmonary function testing, 24 hour ambulatory cough recordings, completed a cough related quality of life
questionnaire (Leicester Cough Questionnaire) and subjectively scored cough severity with a visual analogue scale.
Ambulatory cough recordings were manually counted and reported as number of coughs per hour.
Results: The 24hr cough rates were high (median 9.4, range 1.5-39.4), with day time rates much higher than night time
(median 14.6 , range 1.9-56 .6 compared to 1.9, range 0-19.2, p = 0.003). Strong correlations were found between
objective cough frequency and both the VAS (day r = 0.80, p 0.001, night r = 0.71, p = 0.001) and LCQ (r = -0.80, p
0.001), but not with measures of pulmonary function. Cough rates in IPF were higher than healthy subjects (p 0.001)
and asthma patients (p 0.001) but similar to patients with chronic cough (p = 0.33).
Conclusions: This study confirms objectively that cough is a major, very distressing and disabling symptom in IPF
patients. The strong correlations between objective cough counts and cough related quality of life measures suggest
that in IPF patients, perception of cough frequency is very accurate.
Background
Idi
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