Your body needs a certain amount of oxygen for its organs to function properly. But as idiopathic pulmonary fibrosis (IPF) progresses, the fibrosis prevents enough oxygen from being transferred into your bloodstream. This is why your doctor may prescribe supplemental oxygen therapy as part of your care. (Learn how your lungs work.)

Learn about getting started on oxygen therapy.

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“If low oxygen levels are assessed while resting, during sleep, or with activity—oxygen therapy will be prescribed by your doctor. Your prescription will include how much to use and when. Generally, oxygen therapy is adjusted to support an oxygen level of at least 90 percent. Guidelines include starting oxygen therapy when levels are 88 percent or below.”

Trina Limberg, Director of Pulmonary Rehabilitation at UC SD Medical Center

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Your doctor will use tests, such as an arterial blood gas test and a pulse oximetry test, to determine whether you need oxygen therapy and, if so, how often and how much. These tests measure how much oxygen is in your blood. A low level of oxygen is a sign that you need oxygen therapy. The tests should be obtained when resting, during activity such as walking, and—in some instances—during sleep as oxygen levels can vary depending on what you are doing. Some people with IPF may have relatively normal oxygen levels while resting or when seated, but low oxygen levels when walking or doing other physically exerting activities. That’s because many muscle groups are used with these particular activities.

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“To assess your needs, your doctor will measure your blood oxygen level using a small device that fits on your finger called a pulse oximeter. If it is below 88%, oxygen therapy is often normally recommended.”

Chris Garvey, FNP, MSN, MPA, MAACVPR University of California San Francisco

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How Oxygen Is Delivered

Oxygen therapy is provided in a metal cylinder or other container. It flows through a tube and is delivered to your lungs in one of the following ways:

	Nasal cannula	Two small plastic tubes, or prongs, that fit within both of your nostrils
	Face mask	Fits over your nose and mouth and straps onto your head For those needing high flow oxygen, specialized cannula such as the Oxymizer© may be available, but require continuous oxygen and monitoring to assure adequate oxygen saturation is present at rest and with exercise. Face masks are not recommended unless the flow setting is 6 LPM or above to wash out carbon dioxide

Your doctor will work with you to determine which type of oxygen delivery device you should use, as well as how much oxygen you need and how often.

Learn tips for living and traveling with supplemental oxygen

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The Possible Benefits and Risks of Oxygen Therapy

The use of supplemental oxygen in people with IPF who have low oxygen levels at rest has been shown to:

In addition to reducing breathlessness, in studies of people using oxygen therapy to treat COPD, patients reported that oxygen therapy improved their ability to perform everyday activities such as cleaning, reading, and shaving.

However, it’s important to note that there are a number of risks that come along with using oxygen therapy, including a number of possible complications and side effects, such as:

Tell your doctor if these problems persist. Your doctor may be able to help relieve some or all of these issues.

If you start using home oxygen therapy, you should ask your home equipment provider to give you a complete list of safety steps you'll need to follow.

The Importance of Sticking with Your Therapy

Remember to use oxygen therapy as prescribed by your doctor. While some people may feel embarrassed by having to use oxygen therapy in public, remember that it’s an important medical therapy. Low blood oxygen levels can lead to additional health problems. Your need to use oxygen therapy shouldn’t prevent you from taking part in social activities.

Lung transplantation is an option for certain people with idiopathic pulmonary fibrosis (IPF). It is one form of treatment currently available for IPF, but not everyone is eligible, and finding a donor lung isn’t guaranteed. Lung transplants have been shown to improve both life expectancy and quality of life in people with IPF, but there are serious risks involved.

In order to qualify for a lung transplant, you must meet certain criteria. For one, you must have no other significant health problems, such as cancer; heart, liver, or kidney disease; or chronic incurable infections. This can be a challenge in people with IPF, as many suffer from other lung conditions, coronary artery disease, or other problems that make them ineligible to receive a transplant. Your doctor will be able to tell you if you are eligible for a transplant based on your overall health status.

In the past, individuals over the age of 65 rarely received transplants. However, because surgical techniques and results have improved, more centers are performing transplants in older patients.

Risks of Lung Transplantation

Lung transplantation is a highly risky procedure and there is no guarantee that it will be successful. Risks include:

Only your doctor can say whether or not you are a possible candidate for a lung transplant. Medical guidelines recommend that the option of lung transplant be brought up at the time IPF is diagnosed if the patient meets all the criteria for transplant. Before pursuing the option of a lung transplant, you should discuss all the potential risks and benefits with your doctor.

Waiting is Now Reduced for Eligible Patients

The new lung allocation system (LAS) used by the United Network for Organ Sharing (UNOS, www.unos.org) has set new standards for how they evaluate transplant candidates. LAS is now based on the severity of lung disease. As a result, wait times have been reduced considerably for patients with severe lung function issues, including people with IPF.

If you’ve been diagnosed with IPF, your doctor will likely use tests to track how the disease progresses over time. Knowing how your condition is changing over time can help you and your doctor make informed treatment decisions.

You can find a list below of some of the tests your doctor may use. Note that this is just for your information. Your doctor may not use all of these. They may even employ tests not listed here.

Medical Tests Used to Track the Progression of IPF

Looking to learn about an FDA-approved treatment for IPF?

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You can also take part in tracking your IPF by keeping a record of your symptoms over time. Use our Symptom Tracker to document how you’re feeling each day to be shared with your doctor.

There are things you can do to help manage idiopathic pulmonary fibrosis (IPF) symptoms and try to sustain your ability to perform daily activities for as long as possible.

53% of patients and 55% of caregivers believe a better understanding of managing IPF symptoms can help improve overall well-being

The approaches used to manage the symptoms of IPF are designed to meet each patient’s unique needs. Every person’s medical history is different. In addition, people with IPF frequently suffer from other medical conditions. These other conditions may have an impact on the course of IPF. (See "Managing other conditions" below.)

It’s also important to remember that each patient experiences IPF differently, and while some people with IPF don’t live long after getting their diagnosis, others may live longer than the often-quoted averages. Working together, you and your doctor can develop a plan to help you manage your symptoms in an effort to sustain your ability to participate in daily activities for as long as possible. Common approaches to managing IPF symptoms are listed below.

Summary of Options for Managing IPF Symptoms

Managing Other Conditions

As mentioned above, it is common for people with IPF to also have other medical conditions (called “comorbidities”). These may include obesity, diabetes, pulmonary hypertension, obstructive sleep apnea, coronary artery disease, and emphysema.

These conditions will often require their own treatments and medicines. They may even have an impact on the course of IPF. Remember to always take your medicines as prescribed by your doctor.

If you have any questions about other health conditions you have, or the medicines you are taking for them, be sure to talk to your doctor.

Call IPFandYou^TM to get personalized support and questions answered.

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If you've been diagnosed with idiopathic pulmonary fibrosis (IPF), then you're sure to have a lot of questions. People with IPF can experience a variety of physical and emotional challenges throughout the day, ranging from fatigue to powerful emotions and frustration. Understanding how IPF affects you as an individual will help you to better manage your symptoms and anticipate what lies ahead. The good news? People with IPF can play a big role in managing their IPF symptoms.

Customizing a Plan That Works For You

Because IPF disease affects each person differently and progresses at different rates, prescribed treatment plans are tailored to meet each person’s individual needs.

Create a personal action plan and set daily goals

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Getting Involved in Your Own Treatment Makes a Difference

You are the biggest factor in managing your IPF treatment. As with all diseases, it is important to live a healthy lifestyle. Activities such as physical conditioning, breathing exercises, nutritional counseling, and anxiety, stress, and depression management may all be a part of your personal disease treatment plan your doctor may create for you.

There Are a Number of Things You Can Do to Help Manage Your IPF Symptoms:

Quit Smoking	If you're still smoking, the most important thing you can do is to seek help and stop smoking as soon as possible. Remember, additional potential benefits to quitting include: increased oxygen levels in your blood, lowered blood pressure, and improved circulation.
Eat Well	A healthy diet plays an essential role in your overall physical and mental health. A diet rich in nutrients and low in saturated fat, trans fat, cholesterol, salt, and added sugar, along with a healthy balance of fruits, vegetables, whole grains, lean meats, poultry, fish, beans, and fat-free or low-fat dairy products, will help you get the fuel you need throughout the day. Remember, eating several smaller meals (rather than a few large meals) may prevent feeling too full, which can make it hard to breathe.
Exercise	A lack of exercise can work against people who have IPF, as inactivity weakens the muscles, making even the simplest activities more difficult. Developing an active lifestyle is often key in decreasing ‘air hunger' and strengthening the muscles to make them more resistant to fatigue. Regular exercise can help you develop the energy you need to accomplish daily tasks with less shortness of breath, and also help you to ease feelings of anxiety and depression.
Oxygen Therapy	Supplemental oxygen can make a substantial difference in a person’s ability to manage many of the lifestyle-altering effects that can accompany IPF. Oxygen therapy may provide the additional oxygen the body needs to help people with IPF maintain an active lifestyle, and can also decrease shortness of breath and the additional strain on the heart due to low oxygen saturation levels.
Get Rest	Getting at least eight hours of sleep every night can boost your overall sense of well-being. Rest can also help you deal with the stress of living with IPF.
Connect with Others	Whether it's friends and family or support and advocacy groups, staying connected to others who can provide good company and a positive outlet for what you're going through can make a powerful difference in adding meaning to your life and helping you cope with living with IPF.
Manage Emotions	Psychological and spiritual support is often an important factor in keeping a positive outlook, reducing fears, and enhancing the daily lives of people with IPF. Keeping a positive attitude and staying relaxed may conserve valuable oxygen by avoiding its excessive use that can come with tension.

Create a personal action plan and set daily goals

Download Tip Sheet