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Beginner 8 min readEditorial review complete

Tracheostomy Care After Cancer

Patient and caregiver planning for tracheostomy care after cancer: warning changes, questions, safety limits, and care-team instructions.

This is general education — it cannot tell you what to do in your situation.

Instructions and urgent-contact thresholds vary by treatment and care team. If you are in treatment, follow the instructions your oncology team gave you, and contact them about any new or worsening symptom. If you think you may be having a medical emergency, call your local emergency number.

Source

MedlinePlus (National Library of Medicine)

An older man and woman walk arm in arm together outdoors
An older man and woman walk arm in arm together outdoors

Key fact

The goal is to organize tracheostomy supplies, humidification, communication, suction teaching, and emergency preparation.

The short answer

This medically held draft helps readers organize tracheostomy supplies, humidification, communication, suction teaching, and emergency preparation. It cannot set a personal emergency threshold or replace an action plan.

  • The goal is to organize tracheostomy supplies, humidification, communication, suction teaching, and emergency preparation.

  • Identify the tube type, size, cuff status, and reason for the tracheostomy.

  • Practice routine care and emergency steps with the specialist before discharge.

  • Keep prescribed spare equipment and emergency contacts together.

Choose how you want to understand this

The full explanation.

An opening in the neck, and a tube to keep it open

A tracheostomy is a surgical opening through the front of the neck into the windpipe. The opening itself is called a stoma. MedlinePlus describes what follows: "After the hole is made, a plastic tube is placed in the hole to keep it open. A ribbon is tied around the neck to keep the tube in place."

In cancer care there are two common reasons for one. MedlinePlus lists "cancer of the neck, which can restrict breathing by pressing on the airway." The other is surgery in or around the voice box, where the airway needs protecting while things heal.

Most of what follows applies to anyone with a tracheostomy. One distinction comes first, because it changes what happens in an emergency.

Tracheostomy or laryngectomy: know which you are

These are not the same, and mixing them up can kill someone.

With many tracheostomies, the mouth and nose still connect to the lungs. Air can travel the old way as well as the new one.

A total laryngectomy removes that option permanently. StatPearls explains that after the operation "the entirety of the trachea is diverted to a stoma in the anterior neck, and the pharyngeal remnant is closed on itself." The consequence is absolute: "All respiration, including any needed oxygen supplementation or intubation, is via the anterior neck stoma." MedlinePlus says the same in plainer words. "After surgery you will breathe through your stoma." That stoma is permanent and "will never be removed."

So a person after total laryngectomy cannot breathe through the nose or mouth at all. Rescue breaths given to the face do nothing. StatPearls records the hospital practice: "Signs should be placed at the head of the bed and the room door indicating that the patient is a permanent neck breather and cannot be intubated orally or nasally."

Outside hospital, that sign is you. Carry a medical alert card and wear a bracelet that says permanent neck breather. Make sure the people you live with can say that sentence to a paramedic.

Get help now

If the tube comes out, or blocks, or breathing becomes difficult, call 911 straight away. Make the call first, or have someone else make it while you act. MedlinePlus says to call 911 if the tube comes out and you cannot put it back in, but do not read that as a reason to wait: a blocked or displaced tube is a blocked airway. Only put a tube back in if your own team has trained you or your carer to do it, and only following the plan they wrote for this tube. A stoma that is only days old, a cuffed or specialist tube, or a person who depends on a ventilator all change what is safe to attempt, and forcing a tube in can make things much worse. That written airway plan and the spare tube MedlinePlus tells you to carry, "in case your tube gets plugged", should travel with you.

Call your team the same day for any of these, which MedlinePlus lists for tracheostomy care:

  • Fever or chills. CDC's threshold for people with cancer is a temperature of "100.4ºF (38ºC) or higher." CDC adds that "fever may be the only sign that you have an infection."
  • Redness, swelling or pain around the stoma that is getting worse.
  • Bleeding or drainage from the hole, especially drainage that is thick, colored or smells bad.
  • A sudden increase in mucus, or mucus that turns thick and hard to clear.
  • A cough that will not settle, or shortness of breath.
  • Nausea, or anything else that is simply not usual for you.

For comparison, the American Cancer Society notes a healthy stoma "should look pink or red. It's warm, moist, and produces mucus." That is your baseline.

The parts, and why the names matter

Nursing Skills, an NIH-hosted teaching text, sets out the components.

The outer cannula is the tube itself, sitting through the stoma. The inner cannula slides inside it and comes out for cleaning. It exists precisely because it "becomes occluded with secretions and must be cleaned or replaced frequently." The obturator is a solid plug used to guide the tube in during insertion. The flange is the plate at the neck that the ties attach to. Some tubes have a cuff, a small balloon inflated through a pilot balloon to seal the airway.

Some tubes are fenestrated, meaning they have an opening that lets air reach the voice box for speech. These carry a specific hazard. Nursing Skills warns that "suctioning should never be performed through a fenestrated tube without first inserting a nonfenestrated inner cannula, or severe tracheal damage can occur."

Write down four things and keep them with you: the make, the size, whether it is cuffed, and whether it is fenestrated.

What has to stay within reach

Nursing Skills lists the emergency kit: spare tracheostomy tubes in the same size and one size smaller, the obturator, a bag valve mask, lubricant, and a syringe for the cuff.

The smaller spare is the part people skip. If the stoma starts to close, the usual size may no longer fit.

MedlinePlus is blunt about leaving the house: "You should always carry an extra tube with you in case your tube gets plugged."

Cleaning, day by day

Nursing Skills sets the minimum for the inner cannula: cleaning "should be performed every 12-24 hours at a minimum." The method is sterile technique, a brush in saline, a rinse, and drying with pipe cleaners before it goes back in.

For the stoma itself, MedlinePlus says that once the area is no longer sore from surgery, "clean the hole with a cotton swab or a cotton ball at least once a day." Change bandages and ties whenever they are soiled. Nursing Skills adds a warning: avoid hydrogen peroxide, because it "can impair healing."

Check the skin for redness, drainage and swelling every time you clean.

Suctioning, with real numbers

Ask your team to write your own instructions down. These are the general limits Nursing Skills gives.

Depth: shallow suctioning goes to the length of the tube. Deep suctioning goes in until you meet resistance, then withdraws 1 cm before suction is applied.

Time: no more than 15 seconds per pass, to avoid dropping oxygen levels. Allow 30 to 60 seconds between passes.

Pressure for adults: 100 to 150 mm Hg. Lower for children and infants.

Extra oxygen before and during suctioning may be needed for some people.

Before reaching for the catheter, MedlinePlus offers a gentler first step: "A few drops of salt water (saline) will loosen a plug of thick mucus. Put a few drops in your tube and windpipe, then take a deep breath and cough."

Do not change your depth or pressure on your own.

Humidity is not optional

MedlinePlus explains the problem in one line: "Your nose will no longer keep the air you breathe moist."

Your nose used to warm and humidify every breath. Now air goes straight to the windpipe, dry. Dry air thickens mucus, thick mucus forms plugs, and plugs are what block tubes. Most tracheostomy emergencies start here.

MedlinePlus suggests humidifiers and keeping gauze moist over the tube opening. Ask what your team wants you using, and use it overnight too.

Water, dust and everyday life

MedlinePlus is specific: "Do not breathe in water, food, powder, or dust. When you take a shower, cover the hole with a tracheostomy cover. You will not be able to go swimming."

That rules out aerosol sprays, talcum powder and sanding dust. Showers are fine with the cover on and the water aimed away.

Speaking and eating again

MedlinePlus says most people need "1 to 3 days to adapt to breathing through a tracheostomy tube," and that speech usually returns with training and a speaking valve.

After a total laryngectomy the route is different. StatPearls notes that a tracheoesophageal puncture may be made during the operation, which later allows speech through a voice prosthesis. MedlinePlus says speech rehabilitation with a speech therapist helps you relearn how to speak, and that about two weeks after the procedure you will most likely be able to return to eating by mouth.

Ask for the speech and language therapist by name before you leave hospital.

Sources

Words to know

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Common questions

What should I know about the tube itself?

Identify the tube type, size, cuff status, and the reason the tracheostomy was done, and keep that written down. Practice routine care and the emergency steps with the specialist before discharge, not afterward. Keep prescribed spare equipment and emergency contacts together in one place.

Can I change the tube, suction depth, oxygen or cuff settings myself?

No. Do not change any of those unless you have been trained and instructed to. The safest next step depends on severity, speed, diagnosis, recent treatment, medicines, devices, and the person's baseline, and other conditions can cause similar changes.

How do I know when something is urgent?

Ask the treating team to write three separate levels: what can be discussed at a routine visit, what requires an urgent same-day call, and what requires emergency services. Record the exact contact numbers and instructions alongside them. Do not wait for a portal response when someone may be in immediate danger — contact local emergency services.

What information should be kept together?

Keep the diagnosis, recent treatments and dates, medicines and last doses, allergies, devices, recent laboratory or imaging information, the symptom timeline, any measurements the team requested, location, transport plan, and advance directives in one place. That is what makes an urgent call fast instead of frantic.

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Where to get help with this, by name

A hospital social worker or financial navigator is the best first call if you have one. If you do not, these organisations help at no cost to you.

  • Patient Advocate Foundation(800) 532-5274. Case managers take on insurance appeals, denials and medical debt with you. Free.
  • TotalAssist (Patient Advocate Foundation's copay programme, merged with the PAN Foundation in 2026)866-512-3861. Help with medication copays, coinsurance and deductibles, insurance premiums, and office-visit and administration charges on the day of treatment, across nearly 150 conditions.
  • CancerCare800-813-HOPE (4673). Oncology social workers, free counselling and support groups. Limited financial help with transport, home care, child care and lodging for people in active treatment who meet their income guidelines — funding is first-come, first-served, so call to ask what is open.
  • Triage Cancer424-258-4628. Free legal and financial navigation: insurance, employment rights, disability.
  • Blood Cancer United (formerly the Leukemia & Lymphoma Society)(800) 955-4572. Information Specialists answer questions on treatment, insurance and financial problems.
  • HealthCare.gov1-800-318-2596. For questions about the external review process — the independent review your insurer is required by law to accept.

Your state Department of Insurance regulates insurers and takes consumer complaints. On Medicare, your State Health Insurance Assistance Program (SHIP) gives free one-to-one counselling. If a specific drug is the problem, ask the manufacturer about its patient assistance programme.

Phone numbers checked 31 July 2026. Programmes and eligibility change — if a number has moved, please tell us.

Plain-language explanation of the published sources cited on this page. AI-assisted, source-checked, not clinician-reviewed.

Sources last checked: 2026-08-11 what this meansLast updated: 2026-08-19Next planned review: 2027-01-22

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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. 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.

Editorial status — Editorial review complete. This page completed Cancer Explained's editorial checks (sources, safety, plain language, duplication). It has not been reviewed by a physician or other healthcare professional.

High-risk topic — talk to your care team. This topic can involve urgent, individual medical decisions. This page is general education only: it cannot tell you whether your situation is an emergency or what you personally should do. Follow your oncology team's instructions and contact them for individual guidance.

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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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.

Editorial status: Editorial review complete This page completed Cancer Explained's editorial checks (sources, safety, plain language, duplication). It has not been reviewed by a physician or other healthcare professional.

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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