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ERS technical standard on bronchial challenge testing : General considerations and performance of methacholine challenge tests

Coates, Allan L. (author)
Hospital for Sick Children, Toronto
Wanger, Jack (author)
Cockcroft, Donald W. (author)
Royal University Hospital, Saskatoon
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Culver, Bruce H. (author)
University of Washington
Carlsen, Kai-Håkon (author)
University of Oslo
Diamant, Zuzana (author)
Lund University,Lunds universitet,Lungmedicin, allergologi och palliativ medicin,Sektion II,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Respiratory Medicine, Allergology, and Palliative Medicine,Section II,Department of Clinical Sciences, Lund,Faculty of Medicine,University of Groningen
Gauvreau, Gail M (author)
McMaster University
Hall, Graham L. (author)
Curtin University
Hallstrand, Teal S. (author)
University of Washington
Horvath, Ildiko Fanny (author)
Semmelweis University
de Jongh, Frans H C (author)
Joos, Guy (author)
Ghent University
Kaminsky, David A. (author)
University of Vermont
Laube, Beth L. (author)
Johns Hopkins University School of Medicine
Leuppi, Joerg D. (author)
University Hospital Basel
Sterk, Peter J (author)
Academic Medical Center of University of Amsterdam (AMC)
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 (creator_code:org_t)
2017-05-01
2017
English.
In: European Respiratory Journal. - : European Respiratory Society (ERS). - 0903-1936 .- 1399-3003. ; 49:5
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • This international task force report updates general considerations for bronchial challenge testing and the performance of the methacholine challenge test. There are notable changes from prior recommendations in order to accommodate newer delivery devices. Rather than basing the test result upon a methacholine concentration (provocative concentration (PC20) causing a 20% fall in forced expiratory volume in 1 s (FEV1)), the new recommendations base the result upon the delivered dose of methacholine causing a 20% fall in FEV1 (provocative dose (PD20)). This end-point allows comparable results from different devices or protocols, thus any suitable nebuliser or dosimeter may be used, so long as the delivery characteristics are known. Inhalation may be by tidal breathing using a breath-actuated or continuous nebuliser for 1 min (or more), or by a dosimeter with a suitable breath count. Tests requiring maximal inhalations to total lung capacity are not recommended because the bronchoprotective effect of a deep breath reduces the sensitivity of the test.

Subject headings

TEKNIK OCH TEKNOLOGIER  -- Medicinteknik -- Medicinsk apparatteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Medical Engineering -- Medical Equipment Engineering (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Lungmedicin och allergi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Respiratory Medicine and Allergy (hsv//eng)

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