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Idiopathic Pulmonary Fibrosis

Jeremy Feldman, MD

  • What is Idiopathic Pulmonary Fibrosis?
    • Idiopathic Pulmonary Fibrosis Definition
    • Symptoms of Idiopathic Pulmonary Fibrosis
    • Causes of Idiopathic Pulmonary Fibrosis
    • Who Gets Idiopathic Pulmonary Fibrosis
    • Gastro-Esophageal Reflux (GER) and Idiopathic Pulmonary Fibrosis
    • Interstitial Lung Disease vs. Idiopathic Pulmonary Fibrosis
    • Is Pulmonary Fibrosis Hereditary?
    • Research, Life Expectancy and Prognosis for Idiopathic Pulmonary Fibrosis
  • Diagnosing & Monitoring PF
    • Monitoring Progress of IPF
    • Idiopathic Pulmonary Fibrosis Diagnosis
    • Chest X-rays Used in IPF
    • CPET used in IPF
    • HRCT Scans Used to Evaluate IPF
    • Lung Biopsy To Diagnose IPF
    • Pulmonary Function Tests (PFTS)
    • Six Minute Walk Test To Monitor IPF
    • Stages of Idiopathic Pulmonary Fibrosis
    • Complications of Idiopathic Pulmonary Fibrosis
  • PF Treatment Options
    • Esbriet (pirfenidone) Used to Treat IPF
    • OFEV (nintedanib) Used to Treat IPF
    • Pulmonary Rehab for IPF Patients
    • Lung Transplantation for Pulmonary Fibrosis
    • Oxygen Used to Treat IPF
      • Update on Oxygen Use
    • Clinical Trials in Idiopathic Pulmonary Fibrosis
    • IPF & Leg Swelling
    • Pulmonary Hypertension and Idiopathic Pulmonary Fibrosis
    • IPF Exacerbation
  • PF Advocacy & News
  • FAQ’s
    • Respiratory failure, NSIP, diet
    • Leg swelling, lung biopsy, side effects & pets
    • FAQ’s Enzyme Therapy, Progression of IPF & Oxygen
    • FAQ: Diarrhea, Fibrosis Reversal, IPF Symptoms
    • FAQ: Oxygen Flow, Anesthesia & Genetics
    • FAQ: Contagious Cough? Stem Cells, Familial IPF, Flying
    • FAQ: GERD, Fatigue & Environmental Exposure
    • FAQ: How to Travel to Your Doctor’s Office with Oxygen
    • FAQ: Lung Biopsy with Pulmonary Fibrosis
    • FAQ’s: Alcohol, Clinical Trials, Pulmonary Function Testing
    • FAQs: Emphysema, Exercise & Lung Biopsy

Update on Oxygen Use for IPF Patients

April 18, 2016 By Dr. Jeremy Feldman

Oxygen for pulmonary fibrosis.

Typical oxygen flow rates are between 2 and 5 liters per minute.  For most patients that require supplemental oxygen this provides adequate support.  However, some patients require higher flow rates to meet their needs.  My approach is a stepwise algorithm to address my patient’s oxygen needs.  Some patients with very advanced pulmonary fibrosis have severely low oxygen levels … [Read more...]

Your FAQ’s: Abrupt Respiratory Failure, Non-Specific Interstitial Pneumonia, Diet & IPF

April 2, 2016 By Dr. Jeremy Feldman

GERD may contribute to IPF

Your Pulmonary Fibrosis Questions Answered Our readers have submitted some great questions.  We value your questions and encourage you to continue to tell us about your interests and questions. What can be expected when a patient develops abrupt respiratory failure on a background of Idiopathic Pulmonary Fibrosis? IPF is an unpredictable disease.  There can be long periods … [Read more...]

Your IPF Questions Answered

March 10, 2016 By Dr. Jeremy Feldman

Pulmonary Fibrosis FAQ

We appreciate our readers submitting questions. Why Does Leg Swelling Develop in Patients with Idiopathic Pulmonary Fibrosis? Early in IPF, common symptoms are cough and shortness of breath with vigorous exercise or walking up inclines.  As IPF progresses, there is progressive loss of lung tissue including blood vessels in the lungs.  Over time, this leads to increased work … [Read more...]

Don’t Be Discouraged

February 29, 2016 By Dr. Jeremy Feldman

Phase 2 Study for Simtuzumab as IPF Treatment Stopped Gilead Sciences recently announced that their large phase 2 study of Simtuzumab (identified by the acronym RAINIER) was stopped at the mid-term analysis for lack of efficacy.  We were all saddened by the news.  The IPF community was riding high after two successful molecules were approved (Esbriet and OFEV).  However, we … [Read more...]

Alternative Medicines and IPF

January 26, 2016 By Dr. Jeremy Feldman

Until last year, the IPF community had no FDA approved medications to treat Idiopathic Pulmonary Fibrosis.  Today we have two medications (OFEV and Esbriet).  Both probably improve survival by slowing disease progression and decreasing the frequency of dangerous flares of the disease.  Unfortunately, these medications do nothing to decrease some of the most troubling symptoms … [Read more...]

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Popular Articles

IPF patient with doctor

Idiopathic Pulmonary Fibrosis Treatment Options

What is IPF?

  • What is Idiopathic Pulmonary Fibrosis?
    • Symptoms of Idiopathic Pulmonary Fibrosis
    • Causes of Idiopathic Pulmonary Fibrosis
    • Who Gets Idiopathic Pulmonary Fibrosis
    • Gastro-Esophageal Reflux (GER) and IPF
    • Interstitial Lung Disease vs. Idiopathic Pulmonary Fibrosis
    • Is Pulmonary Fibrosis Hereditary?
    • Research, Life Expectancy & Prognosis for Pulmonary Fibrosis

Diagnosing IPF

  • Idiopathic Pulmonary Fibrosis Diagnosis
    • Chest X-rays Used in IPF
    • CPET used in IPF
    • HRCT Scans Used to Evaluate IPF
    • Lung Biopsy To Diagnose IPF
    • Pulmonary Function Tests (PFTS)
    • Six Minute Walk Test To Monitor IPF
    • Stages of Idiopathic Pulmonary Fibrosis
    • Complications of Idiopathic Pulmonary Fibrosis

Treating IPF

  • Pulmonary Fibrosis Treatment Options
    • Esbriet (pirfenidone) Used to Treat IPF
    • OFEV (nintedanib) Used to Treat IPF
    • Pulmonary Rehab for IPF Patients
    • Lung Transplantation for Pulmonary Fibrosis
    • Oxygen Used to Treat IPF
    • Clinical Trials in Idiopathic Pulmonary Fibrosis
    • IPF & Leg Swelling
    • Pulmonary Hypertension and Idiopathic Pulmonary Fibrosis
    • IPF Exacerbation

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