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@article{Chung:2022:10.1007/s00408-022-00589-0,
author = {Chung, KF and Birring, SS and Morice, AH and McGarvey, LP and Mazzone, SB and Maher, TM and Dicpinigaitis, PV},
doi = {10.1007/s00408-022-00589-0},
journal = {Lung: an international journal on lungs, airways and breathing},
pages = {673--675},
title = {Tackling the neuropathic cough of idiopathic pulmonary fibrosis (IPF): more needs to be done},
url = {http://dx.doi.org/10.1007/s00408-022-00589-0},
volume = {200},
year = {2022}
}

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TY  - JOUR
AB  - Up to 80% of patients with idiopathic pulmonary fibrosis (IPF) suffer from a chronic cough, which may be the first symptom of the disease. Cough has been reported to be an independent predictor of disease progression [1] and is associated with reduced quality of life (QoL), because from the patients’ point of view, it causes physical and emotional distress with chest pain, hoarse voice, incontinence, and sleep disturbance [2, 3]. In addition, cough QoL scores have been independently associated with a higher risk of hospitalisation, lung transplantation and death at 1 year [4]. Therefore, control of cough in IPF remains an important priority.
AU  - Chung,KF
AU  - Birring,SS
AU  - Morice,AH
AU  - McGarvey,LP
AU  - Mazzone,SB
AU  - Maher,TM
AU  - Dicpinigaitis,PV
DO  - 10.1007/s00408-022-00589-0
EP  - 675
PY  - 2022///
SN  - 0341-2040
SP  - 673
TI  - Tackling the neuropathic cough of idiopathic pulmonary fibrosis (IPF): more needs to be done
T2  - Lung: an international journal on lungs, airways and breathing
UR  - http://dx.doi.org/10.1007/s00408-022-00589-0
UR  - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000880269900002&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=a2bf6146997ec60c407a63945d4e92bb
UR  - http://hdl.handle.net/10044/1/101430
VL  - 200
ER  -

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