TY - JOUR
T1 - ERS statement on standardisation of cardiopulmonary exercise testing in chronic lung diseases
AU - Radtke, Thomas
AU - Crook, Sarah
AU - Kaltsakas, Georgios
AU - Louvaris, Zafeiris
AU - Berton, Danilo
AU - Urquhart, Don S.
AU - Kampouras, Asterios
AU - Rabinovich, Roberto A.
AU - Verges, Samuel
AU - Kontopidis, Dimitris
AU - Boyd, Jeanette
AU - Tonia, Thomy
AU - Langer, Daniel
AU - De Brandt, Jana
AU - Goertz, Yvonne M. J.
AU - Burtin, Chris
AU - Spruit, Martijn A.
AU - Braeken, Dionne C. W.
AU - Dacha, Sauwaluk
AU - Franssen, Frits M. E.
AU - Laveneziana, Pierantonio
AU - Eber, Ernst
AU - Troosters, Thierry
AU - Neder, J. Alberto
AU - Puhan, Milo A.
AU - Casaburi, Richard
AU - Vogiatzis, Ioannis
AU - Hebestreit, Helge
N1 - Funding Information:
Support statement: Funding was received from the European Respiratory Society, grant number TF-2016-12. The research of Jana De Brandt is financially supported by FWO (grant #11B4718N) and the research of Chris Burtin is partially sponsored by Limburg Kankerfonds. Funding information for this article has been deposited with the Crossref Funder Registry.
Funding Information:
Conflict of interest: T. Radtke reports personal fees for registration and travel/accomodation for conferences from Vifor Pharma, outside of the submitted work. S. Crook has nothing to disclose. G. Kaltsakas has nothing to disclose. G. Louvaris has nothing to disclose. D. Berton has nothing to disclose. D.S. Urquhart has nothing to disclose. A. Kampouras has nothing to disclose. R.A. Rabinovich has nothing to disclose. S. Verges has nothing to disclose. D. Kontopidis is President of the Hellenic Cystic Fibrosis Association. J. Boyd reports is an employee of the European Lung Foundation. T. Tonia reports acting as ERS Methodologist. D. Langer has nothing to disclose. J. De Brandt has nothing to disclose. Y.M.J. Goërtz has nothing to disclose. C. Burton has nothing to disclose. M.A. Spruit reports grants and personal fees from Boehringer-Ingelheim and AstraZeneca, personal fees from GSK and Novartis, congress travel support from TEVA, and grants from the Netherlands Lung Foundation, outside the submitted work. D.C.W. Braeken has nothing to disclose. S. Dacha has nothing to disclose. F.M.E. Franssen reports personal fees from AstraZeneca, Boehringer Ingelheim, Chiesi, GlaxoSmithKline and TEVA, and grants and personal fees from Novartis, outside the submitted work. P. Laveneziana reports personal fees from Novartis France and Boehringer France, outside the submitted work. E. Eber has nothing to disclose. T. Troosters has nothing to disclose. J.A Neder has nothing to disclose. M.A. Puhan has nothing to disclose. R. Casaburi reports that he shares patent US 7927251 B1, relating to a linear treadmill testing protocol, issued to Los Angeles Biomedical Research Institute. I. Vogiatzis has nothing to disclose. H. Hebestreit reports grants and personal fees from Vertex Pharmaceuticals, grants from Mukoviszidose e.V. (German CF Organization), outside the submitted work; and is the Coordinator of the European Cystic Fibrosis Society Exercise Working Group who discuss exercise testing and organise respective symposia.
Funding Information:
The ERS Task Force was formed in October 2016, composed primarily of experts from the ERS Rehabilitation and Chronic Care Group, the Clinical Respiratory Physiology, Exercise and Functional Imaging group, the Paediatric Assembly, the Physiotherapists Group, and an ERS methodologist. Task Force members were clinical scientists and (exercise) physiologists with experience in CPET in a broad range of paediatric and adult lung diseases. The Task Force received support from the European Lung Foundation (ELF) throughout the project.
Publisher Copyright:
© ERS 2019.
PY - 2019/12/31
Y1 - 2019/12/31
N2 - The objective of this document was to standardise published cardiopulmonary exercise testing (CPET) protocols for improved interpretation in clinical settings and multicentre research projects. This document: 1) summarises the protocols and procedures used in published studies focusing on incremental CPET in chronic lung conditions; 2) presents standard incremental protocols for CPET on a stationary cycle ergometer and a treadmill; and 3) provides patients' perspectives on CPET obtained through an online survey supported by the European Lung Foundation. We systematically reviewed published studies obtained from EMBASE, Medline, Scopus, Web of Science and the Cochrane Library from inception to January 2017. Of 7914 identified studies, 595 studies with 26 523 subjects were included. The literature supports a test protocol with a resting phase lasting at least 3 min, a 3-min unloaded phase, and an 8- to 12-min incremental phase with work rate increased linearly at least every minute, followed by a recovery phase of at least 2-3 min. Patients responding to the survey (n=295) perceived CPET as highly beneficial for their diagnostic assessment and informed the Task Force consensus. Future research should focus on the individualised estimation of optimal work rate increments across different lung diseases, and the collection of robust normative data.
AB - The objective of this document was to standardise published cardiopulmonary exercise testing (CPET) protocols for improved interpretation in clinical settings and multicentre research projects. This document: 1) summarises the protocols and procedures used in published studies focusing on incremental CPET in chronic lung conditions; 2) presents standard incremental protocols for CPET on a stationary cycle ergometer and a treadmill; and 3) provides patients' perspectives on CPET obtained through an online survey supported by the European Lung Foundation. We systematically reviewed published studies obtained from EMBASE, Medline, Scopus, Web of Science and the Cochrane Library from inception to January 2017. Of 7914 identified studies, 595 studies with 26 523 subjects were included. The literature supports a test protocol with a resting phase lasting at least 3 min, a 3-min unloaded phase, and an 8- to 12-min incremental phase with work rate increased linearly at least every minute, followed by a recovery phase of at least 2-3 min. Patients responding to the survey (n=295) perceived CPET as highly beneficial for their diagnostic assessment and informed the Task Force consensus. Future research should focus on the individualised estimation of optimal work rate increments across different lung diseases, and the collection of robust normative data.
KW - MAXIMAL VOLUNTARY VENTILATION
KW - OBSTRUCTIVE PULMONARY-DISEASE
KW - RESPIRATORY GAS-EXCHANGE
KW - VISUAL ANALOG SCALES
KW - HEART-RATE RECOVERY
KW - SCIENTIFIC STATEMENT
KW - PULSE-OXIMETRY
KW - OXYGEN-UPTAKE
KW - PHYSIOLOGICAL-RESPONSES
KW - NONINVASIVE ASSESSMENT
U2 - 10.1183/16000617.0101-2018
DO - 10.1183/16000617.0101-2018
M3 - Article
SN - 0905-9180
VL - 28
JO - European Respiratory Review
JF - European Respiratory Review
IS - 154
M1 - 1901441
ER -