Impact of Azathioprine use in chronic hypersensitivity pneumonitis patients

Systemic corticosteroids are widely used in chronic hypersensitivity pneumonitis (CHP); however, there is not much evidence to support their use, besides being associated with significant side effects. Azathioprine (AZA) use is common in CHP, although not prospectively tested in randomized controlle...

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Published inPulmonary pharmacology & therapeutics Vol. 60; p. 101878
Main Authors Terras Alexandre, André, Martins, Natália, Raimundo, Sara, Melo, Natália, Catetano Mota, Patrícia, Novais e Bastos, Hélder, Pereira, José Miguel, Cunha, Rui, Guimarães, Susana, Souto Moura, Conceição, Morais, António
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.02.2020
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Summary:Systemic corticosteroids are widely used in chronic hypersensitivity pneumonitis (CHP); however, there is not much evidence to support their use, besides being associated with significant side effects. Azathioprine (AZA) use is common in CHP, although not prospectively tested in randomized controlled trials. Our objective was to evaluate the lung function trajectory of CHP patients after AZA initiation, as well as to assess the safety profile of this drug. Retrospective analysis of patients initiated on AZA following a multidisciplinary team diagnosis of CHP. The longitudinal trajectory of lung function in the first 2 years of treatment was assessed. Thirty-five out of 62 patients (56.5%) remained on treatment after 2 years. AZA treatment was associated with a significant improvement in forced vital capacity (FVC) at 12 and 24 months (p = 0.015 and p < 0.001, respectively). A slight increase in total lung capacity (TLC) and 6-min walking test (6MWT) were also reported, although it did not reach statistical differences at the end of 2 years. No changes in diffusion capacity for carbon monoxide (DLCO) were observed. This is the first study identifying an improvement in lung function (FVC) of CHP patients on AZA treatment for 2 years. Prospective studies are needed to confirm these results and to more adequately select CHP patients who may benefit from AZA.
ISSN:1094-5539
1522-9629
DOI:10.1016/j.pupt.2019.101878