TY - JOUR
T1 - ERS guidelines on the diagnosis and treatment of chronic cough in adults and children
AU - Morice, Alyn H.
AU - Millqvist, Eva
AU - Bieksiene, Kristina
AU - Birring, Surinder S.
AU - Dicpinigaitis, Peter
AU - Ribas, Christian Domingo
AU - Boon, Michele Hilton
AU - Kantar, Ahmad
AU - Lai, Kefang
AU - McGarvey, Lorcan
AU - Rigau, David
AU - Satia, Imran
AU - Smith, Jacky
AU - Song, Woo Jung
AU - Tonia, Thomy
AU - van den Berg, Jan W.K.
AU - van Manen, Mirjam J.G.
AU - Zacharasiewicz, Angela
N1 - Funding Information:
an unlicensed product (Merck Sharp & Dohme, USA); advisor for study design of an over-the-counter product (Sanofi, Germany) and (Infirst, UK). No financial or intellectual conflicts of interest regarding the content of this manuscript. K. Lai reports grants and personal fees from AstraZeneca, GlaxoSmithKline, Merck, Daiyichi Sankyo and Novartis, outside the submitted work. L. McGarvey reports personal fees from Merck & Co., Inc. and AstraZeneca, grants, personal fees and non-financial support from Chiesi, personal fees and non-financial support from Boehringer Ingelheim, grants and non-financial support from GlaxoSmithKline, grants and personal fees from Almirall, grants from NC3R, during the conduct of the study; grants from European Union Interreg VA Health & Life Science Programme, outside the submitted work. D. Rigau acts as methodologist for the ERS. I. Satia is currently supported by ERS Marie Curie Respire 3 Global Fellowship programme (713406), and reports grants from BMA James Trust Award, grants from North West Lung Centre Charity Grant, personal fees for lectures from GSK and AstraZeneca, travel Awards for attending conferences from GSK and Chiesi, outside the submitted work. J. Smith reports grants and personal fees for consultancy and advisory board work from GlaxoSmithKline, grants and personal fees for consultancy from NeRRe Pharmaceuticals, Menlo, Bayer, Axalbion and Merck, personal fees for consultancy from Boehringer Ingelheim, Genentech, Neomed, Chiesi and Bellus, non-financial support (provision of cough monitoring equipment) from Vitalograph, grants and personal fees from Afferent, personal fees for consultancy and non-financial support (scientific collaboration support in kind) from AstraZeneca, outside the submitted work; and has a patented method for generating output data licensed. W-J. Song has nothing to disclose. T. Tonia acts as ERS methodologist. J.W.K. van den Berg reports personal fees for advisory board work from MSD, grants from Bayer, outside the submitted work. M.J.G. van Manen has nothing to disclose. A. Zacharasiewicz reports payment for consultancy work for Vertex, Novartis, Abbvie and Loewenstein, travel sponsorship from Mylan, Chiesi and Teva, support for research from Abbvie.
Funding Information:
Conflict of interest: A.H. Morice reports grants, personal fees, non-financial support and other (advisory board participation) from Merck Sharp & Dohme Corp., Bayer AG Research & Development, Bayer US, Sanofi and Phillips Respironics, personal fees, non-financial support and other (advisory board participation) from Bellus Health, personal fees and non-financial support from AstraZeneca, Chiesi Ltd and Boehringer Ingelheim, grants, personal fees and non-financial support from GlaxoSmithKline and Respivant Sciences, Inc., grants, personal fees and other (advisory board participation) from NeRRe Therapeutics, grants from Menlo Therapeutics, during the conduct of the study. E. Millqvist filed an international patent application (PCT application) for the use of capsaicin as a cough-reducing product on January 3, 2014. There is a pending patent application in the USA, Canada and the EU. In Australia a patent was issued on August 17 2017. However, this treatment method is not described, recommended or emphasised in any way in the guidelines. K. Bieksiene has nothing to disclose. S.S. Birring reports grants from Merck, personal fees for advisory board work from Merck, Bayer, GSK, Menlo and Sanofi, travel expenses reimbursement from Boehringer Ingleheim, outside the submitted work. P. Dicpinigaitis has nothing to disclose. C. Domingo Ribas reports personal fees for lectures and advisory board participation from MSD, AstraZeneca, ALK and Sanofi-Aventis, personal fees for lectures, advisory board participation and non-financial support (study collaboration) from Novartis and Teva, personal fees for meeting attendance from Allergy Therapeutics, Immunotek, Esteve and Menarini, personal fees from Chiesi, personal fees for lectures from Ferrer, non-financial support (study collaboration) from GSK, outside the submitted work. M. Hilton Boon reports grants from Medical Research Council (UK) (MC_UU_12017/15), and from Scottish Government Chief Scientist Office (SPHSU15), during the conduct of the study. A. Kantar is advisor for study design of
Funding Information:
Support statement: This work was funded by the European Respiratory Society. Funding information for this article has been deposited with the Crossref Funder Registry.
Publisher Copyright:
Copyright © ERS 2020
PY - 2020/1/1
Y1 - 2020/1/1
N2 - These guidelines incorporate the recent advances in chronic cough pathophysiology, diagnosis and treatment. The concept of cough hypersensitivity has allowed an umbrella term that explains the exquisite sensitivity of patients to external stimuli such a cold air, perfumes, smoke and bleach. Thus, adults with chronic cough now have a firm physical explanation for their symptoms based on vagal afferent hypersensitivity. Different treatable traits exist with cough variant asthma (CVA)/eosinophilic bronchitis responding to anti-inflammatory treatment and non-acid reflux being treated with promotility agents rather the anti-acid drugs. An alternative antitussive strategy is to reduce hypersensitivity by neuromodulation. Low-dose morphine is highly effective in a subset of patients with cough resistant to other treatments. Gabapentin and pregabalin are also advocated, but in clinical experience they are limited by adverse events. Perhaps the most promising future developments in pharmacotherapy are drugs which tackle neuronal hypersensitivity by blocking excitability of afferent nerves by inhibiting targets such as the ATP receptor (P2X3). Finally, cough suppression therapy when performed by competent practitioners can be highly effective. Children are not small adults and a pursuit of an underlying cause for cough is advocated. Thus, in toddlers, inhalation of a foreign body is common. Persistent bacterial bronchitis is a common and previously unrecognised cause of wet cough in children. Antibiotics (drug, dose and duration need to be determined) can be curative. A paediatric-specific algorithm should be used.
AB - These guidelines incorporate the recent advances in chronic cough pathophysiology, diagnosis and treatment. The concept of cough hypersensitivity has allowed an umbrella term that explains the exquisite sensitivity of patients to external stimuli such a cold air, perfumes, smoke and bleach. Thus, adults with chronic cough now have a firm physical explanation for their symptoms based on vagal afferent hypersensitivity. Different treatable traits exist with cough variant asthma (CVA)/eosinophilic bronchitis responding to anti-inflammatory treatment and non-acid reflux being treated with promotility agents rather the anti-acid drugs. An alternative antitussive strategy is to reduce hypersensitivity by neuromodulation. Low-dose morphine is highly effective in a subset of patients with cough resistant to other treatments. Gabapentin and pregabalin are also advocated, but in clinical experience they are limited by adverse events. Perhaps the most promising future developments in pharmacotherapy are drugs which tackle neuronal hypersensitivity by blocking excitability of afferent nerves by inhibiting targets such as the ATP receptor (P2X3). Finally, cough suppression therapy when performed by competent practitioners can be highly effective. Children are not small adults and a pursuit of an underlying cause for cough is advocated. Thus, in toddlers, inhalation of a foreign body is common. Persistent bacterial bronchitis is a common and previously unrecognised cause of wet cough in children. Antibiotics (drug, dose and duration need to be determined) can be curative. A paediatric-specific algorithm should be used.
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U2 - 10.1183/13993003.01136-2019
DO - 10.1183/13993003.01136-2019
M3 - Article
C2 - 31515408
AN - SCOPUS:85075547665
SN - 0903-1936
VL - 55
JO - Scandinavian Journal of Respiratory Diseases
JF - Scandinavian Journal of Respiratory Diseases
IS - 1
M1 - 1901136
ER -