TO STUDY THE CHANGES IN SERIAL LUNG FUNCTIONS IN INTERSTITIAL LUNG DISEASE (ILD) PATIENTS
DOI:
https://doi.org/10.48047/Keywords:
Interstitial lung disease (ILD), Idiopathic Pulmonary Fibrosis, Spirometry, Pulmonary Fibrosis, Connective tissue disease, Chronic obstructive pulmonary disease.Abstract
Background: The assessment of lung function, particularly lung volumes and gas transfer,
recorded initially upon patient presentation and subsequent follow-up evaluations, along with
high-resolution computed tomography (HRCT) of the chest, can facilitate the evaluation of the
natural history of the disease or provide insights to guide therapy in interstitial lung disease
(ILD). The utilization of available data related to connective tissue-related ILD (CTD-ILD),
gastroesophageal reflux disease (GERD), smoke exposure, as well as any potential correlation
of treatment with changes in lung functions, can offer valuable insights