Treatment Options for Idiopathic Pulmonary Fibrosis (IPF)
Idiopathic pulmonary fibrosis is the scarring of the lung tissue that leads to shortness in breath. Excessive scarring can cause damage to the lungs and make it difficult to breathe. There is no specific cause that is identified for this condition. There are various treatment options for idiopathic pulmonary fibrosis (IPF) as listed below. Medication Currently, there are no medicines that can cure the condition. Medicines like azathioprine, prednisone, and N-acetylcysteine can help. There is no evidence that supports its use. Prednisone This is an anti-inflammatory medicine that can be taken orally every day. It can also be administered through a needle or tube into the vein. It can cause strong side effects; hence, the doctor may only prescribe it for three to six months initially. If it works, the dosage can be reduced over time. Azathioprine Azathioprine will suppress your immune system. It can be taken orally, but it has serious side effects. N-acetylcysteine This is an antioxidant that may prevent the lung damage. It can be taken orally several times a day. A combination of all the three medicines is a common treatment for IPF. However, it is harmful and not advisable for the long term. Patients should start and stop the medication after consulting a doctor.