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Critical care

Tracheostomy in intensive care: what it is, how it works and recovery

A tracheostomy is a hole made at the front of the neck with a tube inserted into the windpipe to help someone breathe. In intensive care it is commonly used to connect a person to a ventilator and clear secretions. This guide explains why it is done, what the procedure and tube involve, how speaking and eating are affected, how long it stays in, and when to seek help.

Last checked: 2026-10-10

Key facts

At a glance.

  • What it is

    The NHS says a tracheostomy is a procedure where a hole is made at the front of the neck and a tube is inserted through the opening into the windpipe (trachea) to help you breathe.

  • Why it is done

    Reasons include helping you breathe if your throat is blocked, removing excess fluid and mucus from the lungs, and delivering oxygen from a ventilator to the lungs.

  • Often planned, sometimes urgent

    The NHS says a tracheostomy is often planned in advance but sometimes needs to be done as soon as possible in an emergency.

  • Temporary for many

    Some people only need a tracheostomy for a few days, while others need it for much longer; the tube is removed when you no longer need help breathing.

  • ICU context

    The NHS lists a ventilator tube placed in the mouth, nose or through a small cut in the throat (tracheostomy) among the equipment that may be used on an intensive care unit.

What a tracheostomy is

The windpipe carries air from the nose and mouth to the lungs. A tracheostomy creates a new opening to it through the front of the neck. The NHS explains that the surgeon makes a cut in the skin at the front of the neck and creates a small hole in the windpipe, a tracheostomy tube is inserted through the hole, and it is held in place by a piece of tape around the neck. You breathe through the tube rather than through your nose and mouth.

In intensive care units (ICUs), which the NHS describes as specialist hospital wards providing treatment and monitoring for people who are very ill, most patients have problems with one or more organs, for example being unable to breathe on their own. A ventilator is a machine that helps with breathing, and the NHS says the tube may be placed in the mouth, in the nose, or through a small cut in the throat, which is a tracheostomy.

Why it is done in intensive care

The NHS lists three reasons for a tracheostomy: to help you breathe if your throat is blocked, to remove excess fluid and mucus from your lungs, and to deliver oxygen from a ventilator to your lungs.

The NHS says a tracheostomy is usually done under general anaesthetic, so you are asleep and feel no pain, but if it needs to be done in an emergency you will have a local anaesthetic, where you are awake but your neck is numb. If you need a tracheostomy but cannot give your consent, it will be discussed with your family; the NHS adds that ICU staff will usually decide on what they feel is in the person’s best interests and talk things over with the family whenever possible.

Living with a tracheostomy tube

The NHS says it may take a while to get used to having a tracheostomy. The tube often has an air-filled cuff around it, and you will not be able to speak when the cuff is inflated, so at first you may need to communicate using writing and gestures. As you recover, air is gradually removed from the cuff and you can start to speak, and a speaking valve is sometimes fitted to make the voice stronger.

For eating and drinking, the NHS says you may be able to eat and drink with a tracheostomy, but if you cannot swallow you may need a thin feeding tube passed through your nose down to your stomach to give liquid food and fluids. It adds that the tube may need to be changed if it has been in for 28 days or you need a different tube to help with breathing and talking, and that changing it is a quick and simple procedure usually done in hospital.

Everyday issues with a tracheostomy, according to the NHS
IssueWhat the NHS says
SpeakingNot possible while the cuff is inflated; air is gradually removed as you recover; a speaking valve can help
Eating and drinkingPossible for some people; a feeding tube through the nose may be needed if you cannot swallow
Tube changesMay be needed if the tube has been in 28 days or a different tube is needed; quick and usually done in hospital
Going homeIf able to go home with a tracheostomy, you or your carer are shown how to clean and care for it and given help afterwards

Weaning and removal

The NHS says the tracheostomy tube is removed when you no longer need help breathing, which might be a few days or weeks but for some people longer. A dressing is put over the hole after the tube is removed, the hole usually takes about 7 to 10 days to heal, and you may have some pain or discomfort where the tube was that improves as the hole heals. There will be a small scar on the neck, which fades over time.

The NHS says that once a person no longer needs intensive care they can be transferred to another ward to continue their recovery before going home, and that many people who leave an ICU make a good recovery.

Risks and complications

The NHS says a tracheostomy is a common procedure but, as with any surgery, there are risks and possible complications that your doctor will discuss with you before you agree to a planned tracheostomy.

  • Bleeding in or around the tracheostomy.

  • Damage to the windpipe or the area around it.

  • The tube becoming blocked or moving out of place.

  • Problems with the hole healing after the tube is removed, such as infection.

  • A build-up of air between the lungs and chest wall, which can cause pain, breathing difficulty or, in severe cases, a collapsed lung.

When to get help

The NHS says to call NHS 111 or get an urgent GP appointment if you are at home after a tracheostomy and have problems swallowing, cough or are sick after eating or drinking, have noisy breathing during the day or night including snoring, have a raised or uncomfortable scar, have pain or discomfort around the tracheostomy particularly when swallowing, or have a hoarse or weak voice for more than a week. You may be referred to a specialist.

It says to call 999 if you have had a tracheostomy and have difficulty breathing. The NHS also notes that after intensive care some people have lingering problems such as weakness and stiffness, extreme tiredness, sleep problems, depression, anxiety or post-traumatic stress, and problems with memory or thinking that can last several months; it advises seeking medical advice if they persist and says some people need ongoing rehabilitation.

For families and visitors

The NHS notes that an ICU can be overwhelming. Patients may be connected to tubes, wires and cables and may be drowsy, appear swollen or have injuries, but staff ensure they are as comfortable as possible. You will normally be free to touch, comfort and talk to the person, and it may help them to hear familiar voices even if they do not appear to respond.

It signposts the ICUsteps charity and the Intensive Care Society for information and support for patients and relatives. Intensive care is provided through the NHS, with private hospitals offering critical care in general terms for their own patients, but the principles and equipment described here are the same.

Frequently asked

Questions people ask.

Quick, plain-English answers to the questions we hear most.

  • What is a tracheostomy?

    A hole made at the front of the neck with a tube inserted into the windpipe to help you breathe, according to the NHS. It is also called a tracheotomy.

  • Why do people in intensive care have one?

    To help breathing if the throat is blocked, to remove excess fluid and mucus from the lungs, and to deliver oxygen from a ventilator to the lungs, according to the NHS.

  • Is it painful?

    It is usually done under general anaesthetic so you feel no pain, according to the NHS. In an emergency a local anaesthetic is used, so you are awake but your neck is numb.

  • Can the person talk with a tracheostomy?

    Not while the cuff is inflated. The NHS says air is gradually removed as you recover and a speaking valve is sometimes fitted to help make the voice stronger.

  • Can they eat and drink?

    Some people can. If swallowing is not possible, a thin feeding tube through the nose into the stomach may be needed, according to the NHS.

  • How long does the tube stay in?

    Some people only need it for a few days, while others need it for much longer, according to the NHS. It is removed when you no longer need help breathing.

  • Will there be a scar?

    There will be a small scar on the neck that fades over time. The NHS says the hole usually takes about 7 to 10 days to heal after the tube is removed.

  • What are the risks?

    Bleeding, damage to the windpipe or nearby tissue, the tube blocking or moving out of place, infection at the site and a build-up of air around the lungs, according to the NHS.

  • Who decides if the person cannot consent?

    The NHS says it will be discussed with the family. If this is not possible in an emergency, ICU staff usually decide what they feel is in the person’s best interests, talking things over with relatives when possible.

  • What should I do if breathing becomes difficult at home?

    Call 999, according to the NHS, if you have had a tracheostomy and are having difficulty breathing. Call 111 for noisy breathing, swallowing problems or a hoarse voice that lasts more than a week.

Where this comes from

Sources and checking.

This guide is for information, not medical advice.

Your GP or consultant knows your history and can tell you which parts apply to you. If your symptoms are severe, rapidly worsening, or come with red-flag features, seek urgent medical care. Figures and availability change, so treat them as a guide and confirm with the provider.

Published 2026-10-10, next review 2027-10-10.