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A lot of cancer care has moved into people's homes. Pumps that used to hang from a pole in a ward now travel in a shoulder bag. Drains, ports and oxygen concentrators arrive with a leaflet 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. And knowing who to call when it isn't.
Central lines and ports
Treatment over months usually means you will be offered a device that gives reliable access to a large vein. That may be a port under the skin of the chest, a PICC line threaded from the upper arm, or a tunneled catheter. These spare your veins and make infusions and blood draws easier.
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 you. It also advises asking about the pros and cons of a central line if one is needed, and avoiding touching the tubing and the place where it exits the skin as much as possible.
Practical habits that matter:
- Wash your hands before touching the dressing or tubing, and ask visitors to do the same
- Watch anyone who accesses the line clean the hub or port site first — it is reasonable to ask them to
- Keep the dressing clean, dry and intact, and report it if it lifts, gets wet or looks soiled
- Know your flushing and dressing-change schedule, and who does it
- Call about redness, swelling, pain, oozing, a bad smell at the site, or fever — see cancer emergencies
Infusion pumps at home
Some chemotherapy is given continuously over a day or more, through a small battery-powered pump worn in a pouch. Others deliver pain medicine or nutrition. They beep. Learning what each alarm means before you leave is worth more than the leaflet.
Before you go home, make sure you know several things. 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. 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 them, record the amount and note the color. That record determines when the drain comes out, so keep the log even on days that feel routine.
Ostomies are a bigger adjustment. The most useful resource is a wound, ostomy and continence nurse, so ask for a referral if you have not been given one. Skin around the stoma should look like skin elsewhere. Soreness, itching or leaking usually means the appliance fit needs adjusting, not that you are doing it wrong. With an ileostomy, output that turns high and watery can dehydrate you quickly, so ask what output should prompt a call.
Report promptly: a drain that suddenly stops draining or drains far more, fluid that turns cloudy or smells bad, a stoma that turns dusky or pulls inward, no output at all with cramping and vomiting, or a wound that opens.
Home oxygen
Oxygen is a drug, and it is prescribed at a set rate. Do not turn it up because you feel breathless — call and ask, because breathlessness has causes that more oxygen will not fix.
The safety issues are mostly about fire. Oxygen makes anything that is burning burn much faster. No smoking in the house, and none by visitors. Keep tubing well away from stoves, gas heaters, candles and open flames. Avoid petroleum-based products on the face. Long tubing is a real trip hazard, so plan where it runs. Ask the supplier what happens in a power outage. Ask whether you have backup cylinders, and whether your utility company should know there is medical equipment at the address.
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

Common questions
Why do I need a port or a line at all?
Treatment over months usually means being offered a device that gives reliable access to a large vein: a port under the skin of the chest, a PICC line threaded from the upper arm, or a tunneled catheter. These spare your veins and make infusions and blood draws easier. The main risk is infection, because the line is a direct path into the bloodstream.
How do I lower the infection risk at home?
Wash your hands before touching the dressing or tubing, and ask visitors to do the same. Watch anyone who accesses the line clean the hub or port site first, and it is reasonable to ask them to. Keep the dressing clean, dry and intact, report it if it lifts, gets wet or looks soiled, and call about redness, swelling, pain, oozing, a bad smell at the site, or fever.
What should I know about the pump before I go home?
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. Learning what each alarm means before you leave is worth more than the leaflet, and if you are receiving chemotherapy, ask for the spill and body-fluid precautions in writing.
The skin around my stoma is sore. Am I doing it wrong?
Probably not. Skin around the stoma should look like skin elsewhere, and soreness, itching or leaking usually means the appliance fit needs 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. Report a stoma that turns dusky or pulls inward, no output at all with cramping and vomiting, or a wound that opens.
Can I turn my oxygen up when I feel breathless?
No. Oxygen is a drug and it is prescribed at a set rate, so call and ask, because breathlessness has causes that more oxygen will not fix. The other risks are mostly about fire: no smoking in the house and none by visitors, keep tubing well away from stoves, gas heaters, candles and open flames, and avoid petroleum-based products on the face. Long tubing is also a real trip hazard, so plan where it runs.
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Sources last checked: 2026-08-11 what this meansLast updated: 2026-08-11Next planned review: 2028-07-26
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How this page was created
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. We do not employ clinicians and do not intend to — our work 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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