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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 and this leads to marked shortness of breath.  The steps below apply to such patients.

Options to Improve Oxygen Flow for Pulmonary Fibrosis Patients

1.      Oxygen Concentrator

Obtain an oxygen concentrator from your Durable Medical Equipment supplier (this will require your doctor to send an order to the company) that can deliver at least 10 liters per minute.

2.    Oximizer Cannula

Switch from regular nasal cannula to an oximizer cannula or a high flow cannula.  The oximizer cannula has a reservoir that holds oxygen so that when you breathe in through your nose, you are pulling additional oxygen from the reservoir.  The high flow cannula is bigger and as a result there is less resistance to the movement of oxygen from the concentrator.

3.    Increase the Flow

Increase the flow on the concentrator until you are at the maximum.

4.    Face-Mask Oxygen

For patients that are not adequately supported using an oximizer cannula and flow rates of 10 -15 liters per minute, you may add face-mask oxygen delivered from a portable “E” tank.  Many patients use both nasal cannula and face mask oxygen when they are exerting themselves or are particularly short of breath.

5.    High Flow Oxygen

In the hospital we have another option—high flow oxygen.  This system delivers up to 80 liters per minute of heated, humidified oxygen via very large cannula.  Patients find this system very comfortable and an emerging body of literature supports high flow use in the hospital setting.  We are starting to see home high flow systems slowly becoming available.  Not every insurance is willing to pay for the device.

6.    Trans-Tracheal Oxygen

In a very select group of patients we may consider trans-tracheal oxygen delivery.  This was more popular in the 1990’s and early 2000’s.  This involves cutting a small hole in your neck (trachea) and inserting an oxygen catheter.  The direct delivery of oxygen into the trachea provides comfortable support at lower flow levels.  The problem with this system is that it requires an invasive procedure in our patients least able to handle invasive procedures.  Furthermore, cough may be a frustrating side effect.  Patients that have large amounts of mucous are not good candidates.  I very rarely use trans-tracheal oxygen.

Filed Under: IPF Tips

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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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