Interstitial pulmonary fibrosis is more severe, with limited treatment and a poor prognosis.
Interstitial fibrosis refers to the end-stage lung pathological changes of interstitial lung disease, and patients may experience a variety of symptoms such as dry cough and dyspnea. With this disease will cause obvious damage to lung function, and the disease is more serious because the current treatment effect is limited and the prognosis is poor.
Interstitial pulmonary fibrosis is a hidden underlying primary disease, and the lungs may have been significantly damaged after the disease is clarified. At this time, you should go to the hospital in time to do the appropriate examination, for the primary disease treatment, can to a certain extent slow down the progress of pulmonary fibrosis.
Patients with interstitial fibrosis should consult a specialist in a timely manner to determine the cause of the disease, and should pay attention to follow the doctor’s instructions during treatment.