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The effect of HIV-associated tuberculosis, tuberculosis-IRIS and prednisone on lung function

Residual pulmonary impairment is common after treatment for tuberculosis (TB). Lung function data in patients with HIV-associated TB are scarce, especially in the context of paradoxical TB-associated immune reconstitution inflammatory syndrome (TB-IRIS) and prophylactic prednisone. We aimed to deter...

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Autores principales: Stek, Cari, Allwood, Brian, Du Bruyn, Elsa, Buyze, Jozefien, Schutz, Charlotte, Thienemann, Friedrich, Lombard, Adele, Wilkinson, Robert J., Meintjes, Graeme, Lynen, Lutgarde
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066470/
https://www.ncbi.nlm.nih.gov/pubmed/31862762
http://dx.doi.org/10.1183/13993003.01692-2019
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author Stek, Cari
Allwood, Brian
Du Bruyn, Elsa
Buyze, Jozefien
Schutz, Charlotte
Thienemann, Friedrich
Lombard, Adele
Wilkinson, Robert J.
Meintjes, Graeme
Lynen, Lutgarde
author_facet Stek, Cari
Allwood, Brian
Du Bruyn, Elsa
Buyze, Jozefien
Schutz, Charlotte
Thienemann, Friedrich
Lombard, Adele
Wilkinson, Robert J.
Meintjes, Graeme
Lynen, Lutgarde
author_sort Stek, Cari
collection PubMed
description Residual pulmonary impairment is common after treatment for tuberculosis (TB). Lung function data in patients with HIV-associated TB are scarce, especially in the context of paradoxical TB-associated immune reconstitution inflammatory syndrome (TB-IRIS) and prophylactic prednisone. We aimed to determine the prevalence of lung function abnormalities in patients with HIV-associated TB and CD4 counts ≤100 cells·μL(−1) and assess the effect of prophylactic prednisone and the development of paradoxical TB-IRIS on pulmonary impairment. We performed spirometry, 6-min walk test (6MWT) and chest radiography at baseline (week 0) and at weeks 4, 12 and 28 in participants of the PredART trial, which evaluated a 28-day course of prednisone to prevent TB-IRIS in patients with HIV-associated TB commencing antiretroviral therapy. 153 participants underwent spirometry and/or 6MWT at one or more time points. Abnormal spirometry measurements were present in 66% of participants at week 0 and 50% at week 28; low forced vital capacity was the commonest abnormality. Chest radiographs showed little or no abnormalities in the majority of participants. Prednisone use resulted in a 42 m greater 6-min walk distance and a 4.9% higher percentage of predicted forced expiratory volume in 1 s at week 4; these differences were no longer significantly different from week 12 onwards. TB-IRIS did not significantly impair lung function outcome. Residual pulmonary impairment is common in HIV-associated TB. In patients with low CD4 counts, neither prophylactic prednisone as used in our study nor the development of TB-IRIS significantly affected week-28 pulmonary outcome.
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spelling pubmed-70664702020-03-18 The effect of HIV-associated tuberculosis, tuberculosis-IRIS and prednisone on lung function Stek, Cari Allwood, Brian Du Bruyn, Elsa Buyze, Jozefien Schutz, Charlotte Thienemann, Friedrich Lombard, Adele Wilkinson, Robert J. Meintjes, Graeme Lynen, Lutgarde Eur Respir J Original Articles Residual pulmonary impairment is common after treatment for tuberculosis (TB). Lung function data in patients with HIV-associated TB are scarce, especially in the context of paradoxical TB-associated immune reconstitution inflammatory syndrome (TB-IRIS) and prophylactic prednisone. We aimed to determine the prevalence of lung function abnormalities in patients with HIV-associated TB and CD4 counts ≤100 cells·μL(−1) and assess the effect of prophylactic prednisone and the development of paradoxical TB-IRIS on pulmonary impairment. We performed spirometry, 6-min walk test (6MWT) and chest radiography at baseline (week 0) and at weeks 4, 12 and 28 in participants of the PredART trial, which evaluated a 28-day course of prednisone to prevent TB-IRIS in patients with HIV-associated TB commencing antiretroviral therapy. 153 participants underwent spirometry and/or 6MWT at one or more time points. Abnormal spirometry measurements were present in 66% of participants at week 0 and 50% at week 28; low forced vital capacity was the commonest abnormality. Chest radiographs showed little or no abnormalities in the majority of participants. Prednisone use resulted in a 42 m greater 6-min walk distance and a 4.9% higher percentage of predicted forced expiratory volume in 1 s at week 4; these differences were no longer significantly different from week 12 onwards. TB-IRIS did not significantly impair lung function outcome. Residual pulmonary impairment is common in HIV-associated TB. In patients with low CD4 counts, neither prophylactic prednisone as used in our study nor the development of TB-IRIS significantly affected week-28 pulmonary outcome. European Respiratory Society 2020-03-12 /pmc/articles/PMC7066470/ /pubmed/31862762 http://dx.doi.org/10.1183/13993003.01692-2019 Text en Copyright ©ERS 2020 http://creativecommons.org/licenses/by/4.0/This version is distributed under the terms of the Creative Commons Attribution Licence 4.0.
spellingShingle Original Articles
Stek, Cari
Allwood, Brian
Du Bruyn, Elsa
Buyze, Jozefien
Schutz, Charlotte
Thienemann, Friedrich
Lombard, Adele
Wilkinson, Robert J.
Meintjes, Graeme
Lynen, Lutgarde
The effect of HIV-associated tuberculosis, tuberculosis-IRIS and prednisone on lung function
title The effect of HIV-associated tuberculosis, tuberculosis-IRIS and prednisone on lung function
title_full The effect of HIV-associated tuberculosis, tuberculosis-IRIS and prednisone on lung function
title_fullStr The effect of HIV-associated tuberculosis, tuberculosis-IRIS and prednisone on lung function
title_full_unstemmed The effect of HIV-associated tuberculosis, tuberculosis-IRIS and prednisone on lung function
title_short The effect of HIV-associated tuberculosis, tuberculosis-IRIS and prednisone on lung function
title_sort effect of hiv-associated tuberculosis, tuberculosis-iris and prednisone on lung function
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066470/
https://www.ncbi.nlm.nih.gov/pubmed/31862762
http://dx.doi.org/10.1183/13993003.01692-2019
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