HealthFirst

Rare among lung diseases, pulmonary fibrosis is characterized by the thickening and scarring of lung tissues. Fibrosis refers to these lesions. “Pulmonary fibrosis” is referred to as “idiopathic” because the etiology of this condition remains undetermined. It is therefore referred to as idiopathic pulmonary fibrosis. This condition is critical in nature and can impact individuals of any stage of life. Respiratory failure, pulmonary embolism (development of blood clots in the arteries supplying nutrients to the lungs), lung cancer, cardiac failure, and pulmonary hypertension may result from improper IPF treatment. In contrast to women, males aged 50 years and above exhibit a higher incidence of IPF infection. Pulmonary idiopathic fibrosis symptoms According to the severity of the disease, the manifestation of symptoms in individuals with idiopathic pulmonary fibrosis may differ. IPF patients frequently exhibit the following indications and symptoms: Dry cough that persists Severe respir