Tracheostomy living
Informed by recognized medical guidance
Overview
A tracheostomy is a surgical opening made in the front of your neck and into your windpipe (trachea). A thin plastic tube is placed through this opening to help you breathe. This tube is called a tracheostomy tube. The opening itself is called a stoma. A tracheostomy can be temporary, while you heal or recover from an illness, or permanent, if you need long-term breathing support.
Key facts
- A tracheostomy bypasses your nose and mouth, so air goes directly into your windpipe and lungs.
- You may not be able to speak normally while the tube is in place, but there are ways to communicate and even speak with a special valve.
- With proper care and support, most people can go home and live a full, active life with a tracheostomy.
- You and your caregivers will receive training on how to clean, suction, and manage the tracheostomy safely.
A tracheostomy is a fairly common procedure in hospitals, especially for people who need help breathing for a long time or have a blocked airway. Many thousands of people have a tracheostomy each year across the world.
A tracheostomy can affect people of all ages – from newborn babies to older adults. It may be needed after a serious injury, major surgery, or because of a long-term illness that weakens breathing, such as a nerve or muscle condition or cancer in the throat.
Symptoms
- Sudden trouble breathing or gasping for air
- The tracheostomy tube comes completely out and you cannot put it back
- Blue or grey lips, face, or fingernails
- Bleeding from the stoma that will not stop
- Feeling that the airway is blocked and you cannot pass air
- ⚠Fever or chills
- ⚠Yellow, green, or foul-smelling discharge from the stoma
- ⚠Redness, swelling, or pain spreading around the stoma
- ⚠The tube is clogged and suctioning does not help
- ⚠Difficulty swallowing or pain with swallowing
Common symptoms
- Increased mucus or secretions from the stoma or tube
- A wet-sounding cough
- Mild soreness or irritation around the stoma
- Difficulty speaking or making sounds
- The need to occasionally clear or suction the tube
Symptoms in children
- Extra fussiness or irritability
- Difficulty feeding or swallowing
- Skin redness or breakdown around the stoma
- Frequent crying without sound
- The tube may come out more easily than in adults, so parents need extra training
Symptoms in older adults
- Higher risk of chest infections, such as pneumonia
- Dry mouth or thick secretions due to multiple medicines
- Confusion or agitation caused by low oxygen or infection
- Skin fragility around the stoma
- Needing more help with daily care and swallowing
Causes
Main causes
- Prolonged need for a breathing machine (ventilator) to support weak or failing lungs
- Blockage of the upper airway due to swelling, injury, or a growth
- Severe infection or inflammation that narrows the windpipe
- Nerve or muscle disorders that make it hard to breathe or protect the airway
- Major surgery on the head, neck, or chest that affects breathing
Risk factors
- Being on a ventilator for a long time in the hospital
- Serious injury to the neck, face, or chest
- Neurologic conditions such as spinal cord injury or stroke
- Cancer of the throat or vocal cords
- Severe weight loss or frailty that weakens breathing muscles
When to see a doctor
See a doctor urgently if:
- If you have any of the emergency signs listed above, call your local emergency number immediately.
- Contact your healthcare team the same day if your tube feels blocked, suctioning does not work, or you have signs of infection.
- If your stoma is bleeding or the skin looks badly damaged, get urgent care.
Book a routine appointment if:
- See your specialist team regularly to check the stoma and the tube.
- Attend all planned appointments with your doctor or tracheostomy nurse.
- Have your tube changed on the schedule your team recommends.
- Ask about seeing a speech and language therapist and a dietitian if you have trouble swallowing or eating.
Diagnosis
A tracheostomy is created by a surgeon, so there is no 'diagnosis' in the usual sense. However, after the procedure, you will need regular check-ups to confirm the stoma is healing well, the tube is in the right position, and your lungs are receiving enough air.
Tests that may be done
- Chest X-ray – often done after surgery to check the tube position
- Arterial blood gas – measures oxygen and carbon dioxide levels in your blood
- Stoma and skin assessment – your nurse checks for signs of infection or irritation
- Airflow checks – your team may measure breathing while you are on the ventilator or breathing on your own
- Swallowing tests – if you are eating or drinking, a speech therapist may help assess your risk
What to expect at your appointment
You will be seen by a team that may include doctors, nurses, speech and language therapists, dietitians, and physiotherapists. They will teach you and your family how to clean the stoma, suction the tube, change the dressing, and recognise signs of trouble. You may have a trial of speaking valves or other devices to help you communicate.
Treatment
There is no pill that treats a tracheostomy itself. Treatment focuses on keeping the opening clean, the tube clear, and the lungs healthy. Your care team will create a personal plan based on why you have the tracheostomy, whether it is temporary or permanent, and your overall health.
Self-care at home
- Clean the stoma area gently every day as shown by your nurse, using clean supplies.
- Use a humidifier or saline drops to keep mucus moist and prevent blockage.
- Suction the tube whenever you feel or hear mucus, but not too often – ask your team for guidance.
- Drink plenty of fluids (if safe for you) to keep secretions thin.
- Protect the stoma from water when showering – ask about special waterproof guards.
- Avoid smoke, dust, and strong fumes that can irritate your airways.
Medical treatments
Treatment may include inhaled medicines to keep the airways open or to thin mucus, given as a mist through a nebuliser. If you have an infection, your doctor may prescribe antibiotics. For people with too much saliva or mucus, there are medicines that help reduce secretions. Your team may also use a humidified breathing tube (heat and moisture exchanger) to keep the air you breathe moist. Always ask your healthcare provider before using any new medicine or device.
When is surgery considered?
If your tracheostomy was temporary, a minor surgery or procedure may be done later to remove the tube and close the stoma, allowing you to breathe normally again. If it is permanent, you may occasionally need surgery to revise the stoma or treat scar tissue that narrows the airway.
Living with this condition
Your daily routine will include cleaning the stoma area, checking the tube, and suctioning as needed. You may learn to talk using a speaking valve or by covering the tube with a finger. Showering can be done with special waterproof covers, and you can usually sleep normally after a short adjustment period. It is important to always keep emergency suction or a spare tube with you, and to tell close family and friends what to do in an emergency.
Lifestyle tips
- Wear a medical alert bracelet that says you have a tracheostomy.
- Carry a small emergency kit with a spare tube, suction catheters, scissors, and a copy of your care plan.
- Avoid swimming or being under water – even a small splash can enter the stoma.
- If you smoke, ask your healthcare team about support to quit – smoking seriously increases risks.
- When going outside, wear a loose soft collar or scarf to cover the stoma and filter the air.
Diet and exercise
You may need to adjust your diet if swallowing is affected. A speech and language therapist or dietitian can help you find safe textures and positions to eat. Regular gentle exercise, as advised by your physiotherapist, can keep your lungs and body strong. Avoid exercise that involves heavy straining or lifting that could shift the tube.
Mental health and emotional wellbeing
Living with a tracheostomy can feel isolating, frustrating, or scary at first. Changes to your voice and appearance may affect your confidence and mood. It is very common to feel anxious or depressed. It is important to talk openly with your care team, family, and friends. If you are struggling, ask your doctor or nurse about counselling or support. If you have thoughts of harming yourself, please reach out to a mental health crisis line – help is available.
Prevention
A tracheostomy itself is usually a life-saving treatment, so it cannot be 'prevented' when it is needed. However, you can prevent many complications – like infections and tube blockages – by carefully following your care plan, keeping the stoma clean and dry, and washing your hands before touching the tube.
Vaccines
It is strongly recommended to stay up to date on vaccines, especially against the flu, pneumonia, and COVID-19, because a tracheostomy increases your risk of chest infections. Ask your healthcare provider about which vaccines are right for you.
Screening programmes
Your team will regularly check the stoma and lungs for early signs of problems. If you had a tracheostomy because of throat cancer, you will have regular follow-up appointments as part of your cancer care.
Complications
If left untreated
- Serious infection of the stoma or lungs (pneumonia)
- Blockage of the tube by dried mucus, which can stop breathing
- Bleeding from small blood vessels in the windpipe
- Scar tissue or narrowing of the windpipe over time
- Damage to the skin around the stoma from constant moisture or rubbing
Long-term outlook
The outlook for people living with a tracheostomy is generally very good, especially with proper training and support. Many people go on to live full, productive lives – working, travelling, and enjoying family time. For some, the tracheostomy is temporary and can be reversed. For others, it is a permanent but manageable part of life. You are not alone, and your healthcare team will be with you every step of the way.
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Always verify with your doctor
Health guidelines vary by country and region. The information in this article is based on international clinical guidelines but may not reflect the specific guidelines, medications, or practices in your country. Always discuss your health concerns with your own doctor or healthcare provider, and refer to your local national health guidelines where available.
Important notice This information is for educational purposes only. It does not replace professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider about your specific situation. If you are experiencing a medical emergency, call your local emergency services immediately.
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Sources and guidance
This article is educational and is prepared with reference to recognized health information and clinical guidance sources where available. Specific source links may vary by topic.
Last updated: July 31, 2026
Educational note: This information is for education only and is not a diagnosis.
Use it to support, not replace, advice from a licensed clinician.
If symptoms are severe, worsening, or urgent, call your local emergency number or seek emergency care.