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Home Medical Devices in Cancer Care

Managing IV pumps, drain tubes, ostomy care, and oxygen safely at home.

Source:Centers for Disease Control and Prevention

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This page is for patients and caregivers looking after a medical device at home during cancer care. It covers central lines and ports, infusion pumps, drains and ostomies, and home oxygen.

A lot of cancer care has moved into people's homes. Pumps that used to hang from a pole in a hospital room now travel in a shoulder bag. Drains, ports and oxygen concentrators arrive with a handout and, if you are lucky, an unhurried nurse. Most people manage these devices well. Three things make the difference:

  • Being taught properly.
  • Knowing what normal looks like.
  • Knowing who to call when something isn't normal.

Central lines and ports

Some people have a central line for treatment. It may be a port, a PICC line or a tunneled catheter. Ask your team which kind you have and why.

The main risk is infection, because the line is a direct path into the bloodstream. The CDC calls these central line-associated bloodstream infections. It advises patients to speak up and ask providers what they are doing to protect them. It also advises asking about the options and the pros and cons of a central line if one is needed, and touching the tubing and the place where it exits the skin as little as possible.

Practical habits that matter:

  • Touch the tubing and the place where it exits the skin as little as possible.
  • Ask your team what they are doing to protect you from infection. It is reasonable to ask them.
  • Ask how to keep the dressing clean, dry and intact, and what to do if it lifts, gets wet or looks soiled.
  • Know your flushing and dressing-change schedule, and who does it.
  • Call right away, at any hour, about redness, swelling, pain, oozing, a bad smell at the site, or fever (CDC) — see cancer emergencies

Infusion pumps at home

Some people go home with a portable infusion pump. Ask your team to teach you how it works before you leave, including what each alarm means.

Before you go home, ask about:

  • How to tell it is still running.
  • What the alarms mean, and which ones you can reset yourself.
  • What to do if it stops.
  • Whether it can get wet.
  • When and where it gets disconnected.
  • What to do if the line leaks or comes apart.

If you are receiving chemotherapy, ask for the spill and body-fluid precautions in writing rather than guessing at them.

Drains and ostomies

Surgical drains are usually temporary. You will be asked to empty the drain regularly, and to write down the amount of fluid, the date and the time. Keep the log even on days that feel routine, and bring it to your appointments.

Contact your surgeon if the drainage is cloudy or smells bad, if it stops suddenly after steady output, if it increases for more than 2 days in a row, if the tube comes out or the stitches come loose, or if you have signs of infection such as fever, spreading redness or pus (MedlinePlus).

Ostomies are a bigger adjustment. An ostomy is an opening made in the belly, called a stoma, that lets waste leave the body into a pouch. The most useful resource is a wound, ostomy and continence nurse, so ask for a referral if you have not been given one. A healthy stoma is pink or red, moist and a little shiny. Stool is irritating to skin, so a pouch that fits well matters. Redness, rash, raw areas or itching around the stoma are reasons to ask your team or ostomy nurse for help. With an ileostomy, very high output, ongoing diarrhea, a dry mouth or light-headedness can mean dehydration, so ask what output should prompt a call.

Call your team right away, at any hour, for:

  • A stoma that turns purple, black or white, or pulls inward below the skin.
  • Much less output than usual, or none at all with cramping and vomiting.

Call your team the same day for:

  • A drain that suddenly stops draining or drains far more.
  • Fluid that turns cloudy or smells bad.
  • A wound that starts to open.

If an incision splits open, go to an emergency department. Do not drive yourself.

Home oxygen

Oxygen is available only by prescription. If you feel more breathless, call your team before changing the flow.

The safety issues are mostly about fire. Oxygen makes things burn much faster. No one should smoke in a room where oxygen is in use, and a NO SMOKING sign helps. Keep oxygen at least 6 feet from stoves, candles, fireplaces, space heaters and electric blankets. Ask your team before using petroleum-based creams on your face or upper body. Secure the tubing so no one trips. Also ask your supplier about backup supply and what to do in a power cut.

Ask for the training, twice

Nobody absorbs device teaching well on discharge day. Ask for written instructions. Ask for the demonstration to be repeated with whoever will actually be doing it at home. Get the supplier's number as well as the clinic's, because equipment faults and clinical problems often go to different places.

Caring for someone with several devices is a real workload, and caregiver burnout is worth reading before you hit it. If something about a device feels wrong and you cannot say why, that is still a reason to call. Getting a nurse to look at a dressing costs very little. Waiting can cost far more.

Sources

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Common questions

What is a central line, and what is the main risk?

Some people have a central line, such as a port, a PICC line or a tunneled catheter, for treatment. Ask your team which kind you have and why. The main risk is infection, because the line is a direct path into the bloodstream.

How do I lower the infection risk at home?

Touch the tubing and exit site as little as you can, and ask your team how to keep the dressing clean, dry and intact. Ask how to care for it, who flushes the line and when. Call right away, at any hour, about redness, swelling, pain, oozing, a bad smell at the site, or fever ([CDC](https://www.cdc.gov/cancer-preventing-infections/patients/symptoms.html)).

What should I ask about a home pump before I go?

How to tell it is still running. What the alarms mean, and which ones you can reset yourself. What to do if it stops, whether it can get wet, when and where it gets disconnected, and what to do if the line leaks or comes apart. Ask your team to teach you what each alarm means before you leave. If you are receiving chemotherapy, ask whether you need spill and body-fluid precautions, and get them in writing.

The skin around my stoma is sore. Am I doing it wrong?

Not necessarily. Stool irritates skin, so a poorly fitting pouch can cause redness, itching or leaks. Tell your team, because the fit may need adjusting. A wound, ostomy and continence nurse is the most useful resource here, so ask for a referral if you have not been given one. Call your team right away, at any hour, for a stoma that turns purple, black or white, or pulls inward below the skin, or for much less output than usual, or none at all with cramping and vomiting. Call the same day for a drain that suddenly stops, drainage that is cloudy or smells bad, or a wound that starts to open. If an incision splits open, go to an emergency department. Do not drive yourself.

Can I turn my oxygen up when I feel breathless?

No. Oxygen is available only by prescription, so call your team before changing the flow. The other risks are mostly about fire: oxygen makes things burn much faster, so no one should smoke in a room where it is used, and tubing and the tank should stay at least 6 feet from stoves, candles, heaters and other heat sources. Ask your team before putting petroleum-based creams on your face or upper body. Secure tubing so it does not become a trip hazard.

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Sources last checked: 2026-08-11 what this meansLast updated: 2026-10-02Next planned review: 2028-07-26

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Cancer Explained does not originate medical claims. Every page restates guidance already published by the National Cancer Institute, the CDC, the USPSTF and the FDA, in plain language, with the source cited so you can check the original yourself. AI does the translating and organizing; automated checks test claims, citations, clarity and safety before anything publishes, and this is translation and navigation, not clinical judgment. Nothing here is personal medical advice, and no page can account for your particular situation.

Human medical review: not completed. Pages here are not signed off by a clinician before they publish. That is not an oversight we are quietly working around: we restate published guidance and cite it, so the authority belongs to the source rather than to us, and every page names where its claims come from — you can verify us instead of trusting us. Where a volunteer clinician has reviewed a page, their name and credentials appear on it; where no name appears, no clinician has checked it. We are glad to have reviewers and are recruiting them, and we do not hold pages back waiting for one. Use this site to understand your situation and to ask better questions of the people treating you.

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