Background There is very little evidence of the utility of the exhaled fraction of NO (FeNO) for the diagnosis of interstitial lung disease and nearly all of it is related with connective tissue disease. Some authors have suggested that in patients with hypersensitivity pneumonitis (HP), evolution to pulmonary fibrosis may be mediated by a Th2 mechanism, which could redound in a potential utility of FeNO. The aim of this study was to investigate the values of FeNO before and after antigenic exposure with the specific inhalation challenge (SIC) and to analyze its potential utility for the diagnosis of HP. MethodsIt was a prospective, cross-sectional study of all patients older than 18 years referred to our center for suspected chronic HP between May 2012 and May 2014 and who underwent a SIC. FeNO was collected before and after SIC. ResultsThe study sample comprised 25 patients. Eleven were diagnosed with chronic HP; six had been exposed to avian proteins and five to fungal agents. Of these 11 patients, seven had positive SICs. In the 14 patients with diagnoses other than HP, all the SICs were negative. No significant differences in baseline characteristics were observed according to HP diagnosis, except in the BAL lymphocyte count. No differences were found after the test in patients diagnosed with HP; nor were there differences in baseline FeNO in patients diagnosed with HP and those who received alternative diagnoses. ConclusionsThe results suggest that FeNO measurement is not useful for the diagnosis of chronic HP.
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[1]
Alving K, 2010, EUR RESPIR MONOGR, P1, DOI 10.1183/1025448x.00028509
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Cleveland Clin Fdn, Div Pulm, Dept Med, Cleveland, OH 44195 USAUniv London Imperial Coll Sci Technol & Med, Airway Dis Sect, Natl Heart & Lung Inst, London, England
Dweik, Raed A.
Gelb, Arthur F.
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Lakewood Reg Med Ctr, Div Pulm, Dept Med, Lakewood, CA USA
UCLA Med Ctr, Geffen Sch Med, Los Angeles, CA USAUniv London Imperial Coll Sci Technol & Med, Airway Dis Sect, Natl Heart & Lung Inst, London, England
Gelb, Arthur F.
Gibson, Peter G.
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John Hunter Hosp, Woolcock Inst Med Res, Dept Resp & Sleep Med, New Lambton, NSW, AustraliaUniv London Imperial Coll Sci Technol & Med, Airway Dis Sect, Natl Heart & Lung Inst, London, England
Gibson, Peter G.
George, Steven C.
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Univ Calif Irvine, Dept Biomed Engn & Chem Engn & Mat Sci, Irvine, CA USAUniv London Imperial Coll Sci Technol & Med, Airway Dis Sect, Natl Heart & Lung Inst, London, England
George, Steven C.
Grasemann, Hartmut
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Hosp Sick Children, Div Resp Med, Dept Pediat & Physiol, Toronto, ON M5G 1X8, CanadaUniv London Imperial Coll Sci Technol & Med, Airway Dis Sect, Natl Heart & Lung Inst, London, England
机构:
Cleveland Clin Fdn, Div Pulm, Dept Med, Cleveland, OH 44195 USAUniv London Imperial Coll Sci Technol & Med, Airway Dis Sect, Natl Heart & Lung Inst, London, England
Dweik, Raed A.
Gelb, Arthur F.
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Lakewood Reg Med Ctr, Div Pulm, Dept Med, Lakewood, CA USA
UCLA Med Ctr, Geffen Sch Med, Los Angeles, CA USAUniv London Imperial Coll Sci Technol & Med, Airway Dis Sect, Natl Heart & Lung Inst, London, England
Gelb, Arthur F.
Gibson, Peter G.
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h-index: 0
机构:
John Hunter Hosp, Woolcock Inst Med Res, Dept Resp & Sleep Med, New Lambton, NSW, AustraliaUniv London Imperial Coll Sci Technol & Med, Airway Dis Sect, Natl Heart & Lung Inst, London, England
Gibson, Peter G.
George, Steven C.
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Univ Calif Irvine, Dept Biomed Engn & Chem Engn & Mat Sci, Irvine, CA USAUniv London Imperial Coll Sci Technol & Med, Airway Dis Sect, Natl Heart & Lung Inst, London, England
George, Steven C.
Grasemann, Hartmut
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Hosp Sick Children, Div Resp Med, Dept Pediat & Physiol, Toronto, ON M5G 1X8, CanadaUniv London Imperial Coll Sci Technol & Med, Airway Dis Sect, Natl Heart & Lung Inst, London, England