Functional features in interstitial lung diseases
Background: Interstitial lung diseases (ILD) are a group of disorders that are generally thought to commonly share a restrictive ventilatory defect and reduced diffusing capacity for carbon monoxide (DLCO). The aim was to find distinctive features of the pulmonary function tests (PFT) results in dif...
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Scientific Medical Association of Moldova
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doaj-e710a6ad2e4749638dc63bcd9753c1fc2020-11-25T03:37:17ZengScientific Medical Association of MoldovaThe Moldovan Medical Journal2537-63732537-63812020-10-0163591410.5281/zenodo.4018896Functional features in interstitial lung diseasesDiana Calaras0https://orcid.org/0000-0002-8963-459XDoina Rusu1https://orcid.org/0000-0003-3029-5025Aliona David2https://orcid.org/0000-0002-7143-6800Victor Botnaru3https://orcid.org/0000-0002-0863-5268Discipline of Pneumology and Allergology, Nicolae Testemitanu State University of Medicine and Pharmacy Chisinau, the Republic of MoldovaDiscipline of Pneumology and Allergology, Nicolae Testemitanu State University of Medicine and Pharmacy Chisinau, the Republic of MoldovaChiril Draganiuc Institute of Phthisiopneumology, Chisinau, the Republic of MoldovaDiscipline of Pneumology and Allergology, Nicolae Testemitanu State University of Medicine and Pharmacy Chisinau, the Republic of MoldovaBackground: Interstitial lung diseases (ILD) are a group of disorders that are generally thought to commonly share a restrictive ventilatory defect and reduced diffusing capacity for carbon monoxide (DLCO). The aim was to find distinctive features of the pulmonary function tests (PFT) results in different types of ILD. Material and methods: We conducted a retrospective study of 40 consecutive patients with ILD admitted to the Institute of Pthisiopneumology, Chisinau, the Republic of Moldova, during January 2019 – February 2020. The cohort included 10 cases of sarcoidosis patients, 8 cases of idiopathic pulmonary fibrosis (IPF) patients, 7 patients with nonspecific idiopathic interstitial pneumonia, 9 cases with hypersensitivity pneumonitis (HP) and 6 histiocytosis cases. All patients have been evaluated by pulmonary function tests (PFT), 6 minutes walk test, Medical Research Council scale for dyspnea, etc. Results: Overall, we found normal mean spirometry parameters, a slightly increased mean residual volume (127.5±42.1), a mildly decreased mean total lung capacity (88.8±22.3) and moderately reduced DLCO (52.6±21.5). We found a dominant restrictive pattern in 75% of patients, and obstruction only in 7.5% when we used spirometry parameters. When we applied the bodyplethismographic values, we have found that an air-trapping pattern was identified in 32.5% cases of patients. This pattern has been identified in 1/3 of HP patients and in 10% of sarcoidosis patients. Conclusions: PFT can help identifying individual features of different types of ILD being able to show even obstructive changes in a group of diseases thought to be strictly restrictive.http://moldmedjournal.md/wp-content/uploads/2020/09/moldovan-med-j-2020-63-5-calaras-et-al-full-text.pdfinterstitial lung diseasespulmonary function testsobstructionrestriction |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Diana Calaras Doina Rusu Aliona David Victor Botnaru |
spellingShingle |
Diana Calaras Doina Rusu Aliona David Victor Botnaru Functional features in interstitial lung diseases The Moldovan Medical Journal interstitial lung diseases pulmonary function tests obstruction restriction |
author_facet |
Diana Calaras Doina Rusu Aliona David Victor Botnaru |
author_sort |
Diana Calaras |
title |
Functional features in interstitial lung diseases |
title_short |
Functional features in interstitial lung diseases |
title_full |
Functional features in interstitial lung diseases |
title_fullStr |
Functional features in interstitial lung diseases |
title_full_unstemmed |
Functional features in interstitial lung diseases |
title_sort |
functional features in interstitial lung diseases |
publisher |
Scientific Medical Association of Moldova |
series |
The Moldovan Medical Journal |
issn |
2537-6373 2537-6381 |
publishDate |
2020-10-01 |
description |
Background: Interstitial lung diseases (ILD) are a group of disorders that are generally thought to commonly share a restrictive ventilatory defect and reduced diffusing capacity for carbon monoxide (DLCO). The aim was to find distinctive features of the pulmonary function tests (PFT) results in different types of ILD. Material and methods: We conducted a retrospective study of 40 consecutive patients with ILD admitted to the Institute of Pthisiopneumology, Chisinau, the Republic of Moldova, during January 2019 – February 2020. The cohort included 10 cases of sarcoidosis patients, 8 cases of idiopathic pulmonary fibrosis (IPF) patients, 7 patients with nonspecific idiopathic interstitial pneumonia, 9 cases with hypersensitivity pneumonitis (HP) and 6 histiocytosis cases. All patients have been evaluated by pulmonary function tests (PFT), 6 minutes walk test, Medical Research Council scale for dyspnea, etc. Results: Overall, we found normal mean spirometry parameters, a slightly increased mean residual volume (127.5±42.1), a mildly decreased mean total lung capacity (88.8±22.3) and moderately reduced DLCO (52.6±21.5). We found a dominant restrictive pattern in 75% of patients, and obstruction only in 7.5% when we used spirometry parameters. When we applied the bodyplethismographic values, we have found that an air-trapping pattern was identified in 32.5% cases of patients. This pattern has been identified in 1/3 of HP patients and in 10% of sarcoidosis patients. Conclusions: PFT can help identifying individual features of different types of ILD being able to show even obstructive changes in a group of diseases thought to be strictly restrictive. |
topic |
interstitial lung diseases pulmonary function tests obstruction restriction |
url |
http://moldmedjournal.md/wp-content/uploads/2020/09/moldovan-med-j-2020-63-5-calaras-et-al-full-text.pdf |
work_keys_str_mv |
AT dianacalaras functionalfeaturesininterstitiallungdiseases AT doinarusu functionalfeaturesininterstitiallungdiseases AT alionadavid functionalfeaturesininterstitiallungdiseases AT victorbotnaru functionalfeaturesininterstitiallungdiseases |
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