Prevalence of pulmonary arterial hypertension in post-tuberculosis lung fibrosis patients: A cross-sectional observational study

Introduction: Post-tuberculosis (TB) lung fibrosis is an infrequently reported cause of Pulmonary arterial hypertension (PAH). Pulmonary TB still being an important global health problem, especially in developing countries, PAH developing after pulmonary TB deserves attention. This study was underta...

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Main Authors: Rupak Chatterjee, Priyanka Ghosh, Kumkum Sarkar, Shambo Samrat Samajdar, Shatavisa Mukherjee, Alex George, Netai Pramanik
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2023-12-01
Series:The Journal of Association of Chest Physicians
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Online Access:https://journals.lww.com/10.4103/jacp.jacp_11_23
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author Rupak Chatterjee
Priyanka Ghosh
Kumkum Sarkar
Shambo Samrat Samajdar
Shatavisa Mukherjee
Alex George
Netai Pramanik
author_facet Rupak Chatterjee
Priyanka Ghosh
Kumkum Sarkar
Shambo Samrat Samajdar
Shatavisa Mukherjee
Alex George
Netai Pramanik
author_sort Rupak Chatterjee
collection DOAJ
description Introduction: Post-tuberculosis (TB) lung fibrosis is an infrequently reported cause of Pulmonary arterial hypertension (PAH). Pulmonary TB still being an important global health problem, especially in developing countries, PAH developing after pulmonary TB deserves attention. This study was undertaken to know the prevalence of PAH among patients with post-TB lung fibrosis. Methods: A cross-sectional observational study was carried out in two tertiary care hospitals in Kolkata over a period of 1 year. Sixty adult post-TB lung fibrosis patients without any cardiovascular or other pulmonary comorbidities were included in this study. Results: Out of the 60 patients with varying degrees of lung fibrosis confirmed radiologically, eight patients were found to have PAH (13.33% of the study population). Among the eight cases, six were males and two were females. Five of the males were smokers with a mean of 17.6 pack years of smoking. Out of the eight diagnosed PAH cases, three were mild PAH, four were moderate, and one case had severe PAH (grading based on 2D echocardiography findings). Pulmonary function test (PFT) revealed obstructive pattern in three cases, restrictive pattern in three cases, and mixed in two cases. On PFT, smokers with PAH exhibited obstructive pattern and mixed pattern, whereas the nonsmoker PAH cases exhibited restrictive pattern. Conclusion: All post-TB lung fibrosis cases must be followed up at regular intervals and screened to rule out PAH. Early diagnosis and prompt treatment of the cases will help to reduce morbidity and mortality of the disease which otherwise has a poor prognosis.
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spelling doaj-art-d67b116ab599418797e75f54df97186f2025-01-20T07:26:04ZengWolters Kluwer Medknow PublicationsThe Journal of Association of Chest Physicians2320-87752023-12-0111419820110.4103/jacp.jacp_11_23Prevalence of pulmonary arterial hypertension in post-tuberculosis lung fibrosis patients: A cross-sectional observational studyRupak ChatterjeePriyanka GhoshKumkum SarkarShambo Samrat SamajdarShatavisa MukherjeeAlex GeorgeNetai PramanikIntroduction: Post-tuberculosis (TB) lung fibrosis is an infrequently reported cause of Pulmonary arterial hypertension (PAH). Pulmonary TB still being an important global health problem, especially in developing countries, PAH developing after pulmonary TB deserves attention. This study was undertaken to know the prevalence of PAH among patients with post-TB lung fibrosis. Methods: A cross-sectional observational study was carried out in two tertiary care hospitals in Kolkata over a period of 1 year. Sixty adult post-TB lung fibrosis patients without any cardiovascular or other pulmonary comorbidities were included in this study. Results: Out of the 60 patients with varying degrees of lung fibrosis confirmed radiologically, eight patients were found to have PAH (13.33% of the study population). Among the eight cases, six were males and two were females. Five of the males were smokers with a mean of 17.6 pack years of smoking. Out of the eight diagnosed PAH cases, three were mild PAH, four were moderate, and one case had severe PAH (grading based on 2D echocardiography findings). Pulmonary function test (PFT) revealed obstructive pattern in three cases, restrictive pattern in three cases, and mixed in two cases. On PFT, smokers with PAH exhibited obstructive pattern and mixed pattern, whereas the nonsmoker PAH cases exhibited restrictive pattern. Conclusion: All post-TB lung fibrosis cases must be followed up at regular intervals and screened to rule out PAH. Early diagnosis and prompt treatment of the cases will help to reduce morbidity and mortality of the disease which otherwise has a poor prognosis.https://journals.lww.com/10.4103/jacp.jacp_11_23pulmonary arterial hypertensionpulmonary tuberculosislung fibrosis
spellingShingle Rupak Chatterjee
Priyanka Ghosh
Kumkum Sarkar
Shambo Samrat Samajdar
Shatavisa Mukherjee
Alex George
Netai Pramanik
Prevalence of pulmonary arterial hypertension in post-tuberculosis lung fibrosis patients: A cross-sectional observational study
The Journal of Association of Chest Physicians
pulmonary arterial hypertension
pulmonary tuberculosis
lung fibrosis
title Prevalence of pulmonary arterial hypertension in post-tuberculosis lung fibrosis patients: A cross-sectional observational study
title_full Prevalence of pulmonary arterial hypertension in post-tuberculosis lung fibrosis patients: A cross-sectional observational study
title_fullStr Prevalence of pulmonary arterial hypertension in post-tuberculosis lung fibrosis patients: A cross-sectional observational study
title_full_unstemmed Prevalence of pulmonary arterial hypertension in post-tuberculosis lung fibrosis patients: A cross-sectional observational study
title_short Prevalence of pulmonary arterial hypertension in post-tuberculosis lung fibrosis patients: A cross-sectional observational study
title_sort prevalence of pulmonary arterial hypertension in post tuberculosis lung fibrosis patients a cross sectional observational study
topic pulmonary arterial hypertension
pulmonary tuberculosis
lung fibrosis
url https://journals.lww.com/10.4103/jacp.jacp_11_23
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