Consent to treatment (2024)

Consent to treatment means a person must give permissionbefore they receive any type of medical treatment, testor examination.

This must be doneon the basis ofan explanation by a clinician.

Consent from a patient is needed regardless ofthe procedure, whether it's a physical examination or something else.

The principle of consent is an important part of medical ethics and international human rights law.

Defining consent

For consent to be valid, it must be voluntary and informed, and the person consenting must have the capacity to make the decision.

The meaning of these terms are:

  • voluntary–the decision to either consent or not to consent to treatment must be made by the person, and must not be influenced by pressure from medical staff, friends or family
  • informed–the person must be given all of the information about what the treatment involves, including the benefits and risks, whether there are reasonable alternative treatments, and what will happen if treatment does not go ahead
  • capacity –the person must be capable of giving consent, which means they understand the information given to them and can use it to make an informed decision

If an adult has the capacity to make a voluntary and informed decision to consent to or refuse a particular treatment, their decision must be respected.

This is still the case even if refusing treatment would result in their death, or the death of their unborn child.

If a person does not have the capacity to make a decision about their treatment and they have not appointed a lasting power of attorney (LPA), the healthcare professionals treating them can go ahead and give treatment if they believe it's in the person's best interests.

But clinicians must take reasonable steps to discuss the situation with the person's friends or relatives before making these decisions.

Read more about assessing the capacity to consent, which explains what someone can do if they know their capacity to consent may be affected in the future.

How consent is given

Consentcan be given:

  • verbally –for example, a person saying they're happy to have an X-ray
  • in writing –for example, signing a consent form for surgery

Someone could also give non-verbal consent, as long as they understand the treatment or examination about to take place– for example,holding out an armfor ablood test.

Consent should be given to the healthcare professional responsible for the person's treatment.

This could be a:

  • nurse arranging a blood test
  • GP prescribing new medication
  • surgeon planning an operation

If someone's going to have a major procedure, such as an operation, their consent should be secured well in advance so they have plenty of time to understand the procedure and ask questions.

If they change their mind at any point before the procedure, they're entitled to withdraw their previous consent.

Consent from children and young people

If they're able to, consent is usually given by patients themselves.

But someone with parental responsibility may need to give consent for a child up to the age of 16 to have treatment.

Find out more about how the rules of consent apply to children and young people

When consent is not needed

There are some exceptions when treatment may be able to go ahead without the person's consent, even if they're capable of giving their permission.

It may not be necessary to obtain consent if a person:

  • needs emergency treatment to save their life, but they're incapacitated (for example, they're unconscious)–the reasons why treatment was necessary should be fully explained once they have recovered
  • immediately needs an additional emergencyprocedure during an operation– there has to be a clear medical reason why it would be unsafe to wait to obtain consent
  • with a severe mental health condition,such as schizophrenia, bipolar disorder or dementia, lacks the capacity to consent to the treatment of their mental health (under theMental Health Act)– in these cases, treatment for unrelated physical conditions still requires consent, which the patient may be able to provide, despite their mental health condition
  • needshospital treatmentfor a severe mental health condition, but self-harmed or attempted suicide while competent and is refusing treatment (under theMental Health Act)–the person's nearest relative or an approved social worker must make an application for the person to be forcibly kept in hospital, and 2 doctors must assess the person's condition
  • is severely ill and living in unhygienic conditions (under the National Assistance Act 1948)– a person who's severely ill or infirm and living in unsanitary conditions can be taken to a place of care without their consent

Consent and life support

Apersonmay be being kept alive with supportive treatments, such as lung ventilation,without having made anadvance decision,which outlines the care they'd refuse to receive.

In these cases, a decision about continuing or stopping treatment needs to be made based on what that person's best interests are believed to be.

To help reach a decision, healthcare professionals should discuss the issue with the relatives and friends of the person receiving the treatment.

They should consider:

  • what the person's quality of life will be if treatment is continued
  • how long the person may live if treatment is continued
  • whether there's any chance of the person recovering

Treatment can be stopped if there's an agreement that continuing treatment is not in the person's best interests.

The case will be referred to the courts before further action is taken if:

  • an agreement cannot be reached
  • a decision has to be made on whether to stop treatment for someone who's been in astate of impaired consciousnessfor a long time (usually at least 12 months)

It's important to note the difference between stopping a person's life support and taking a deliberate action to make them die.

For example, injecting a lethal medicine would beillegal.

Complaints

If you believe you have received treatment you did not consent to, you can make an official complaint.

Find out more about how to make a complaint

Page last reviewed: 08 December 2022
Next review due: 08 December 2025

Consent to treatment (2024)

FAQs

How do you ensure that patient has given consent for treatment? ›

Obtaining informed consent in medicine is process that should include: (1) describing the proposed intervention, (2) emphasizing the patient's role in decision-making, (3) discussing alternatives to the proposed intervention, (4) discussing the risks of the proposed intervention and (5) eliciting the patient's ...

What are the three 3 criteria for a valid informed consent? ›

The informed consent process involves three key features: (1) disclosing to potential research subjects information needed to make an informed decision; (2) facilitating the understanding of what has been disclosed; and (3) promoting the voluntariness of the decision about whether or not to participate in the research.

What is an example of consent to treat? ›

I have the right to discuss any treatment with my provider. I am encouraged to ask questions about any concerns I have. I understand that if additional testing or invasive procedures are needed, I will be asked to read and sign additional consent forms. This consent is valid until I revoke it in writing.

What is the consent given by a patient who has enough information to make a decision called? ›

Defining consent

informed – the person must be given all of the information about what the treatment involves, including the benefits and risks, whether there are reasonable alternative treatments, and what will happen if treatment does not go ahead.

What are the three things a patient must have to give informed consent? ›

  • patient must have the capacity/competency to make an informed decision.
  • pt must be given sufficient info and alternatives available.
  • pt must voluntarily give consent.

How do you ensure valid consent? ›

You must clearly explain to people what they are consenting to in a way they can easily understand. The request for consent needs to be prominent, concise, separate from other terms and conditions, and in plain language. If the request for consent is vague, sweeping or difficult to understand, then it will be invalid.

What are the two exceptions to informed consent? ›

There are two well-recognized exceptions to the need for informed consent to medical treatment. The more common is a medical emergency, in which an unconscious or delirious patient cannot consent. The second is rare and involves certain court-ordered treatments or treatments and tests mandated by law.

What are the 4 pillars of consent? ›

There are 4 components of informed consent including decision capacity, documentation of consent, disclosure, and competency. Doctors will give you information about a particular treatment or test in order for you to decide whether or not you wish to undergo a treatment or test.

What are three key points about consent? ›

5 core concepts of consent
  • 1 - Free and voluntary. Consent must be free and voluntary. ...
  • 2 - Specific and informed. Consent must be specific and informed. ...
  • 3 - Affirmative and communicated. ...
  • 4 - Ongoing and mutual. ...
  • 5 - Reflects capacity.
Jan 20, 2024

What is a bad example of consent? ›

Consent does NOT look like this:

Someone being under the legal age of consent, as defined by the state. Someone being incapacitated because of drugs or alcohol Pressuring someone into sexual activity by using fear or intimidation. Assuming you have permission to engage in a sexual act because you've done it in the past.

What are the 4 rules of consent? ›

Consent requires voluntary, informed, mutual, honest, and verbal or non-verbal agreement. Consent is ongoing and must be asked for every step of the way. If you want to move to the next level of sexual intimacy, just ask.

Is consent to treat the same as informed consent? ›

Informed Consent is specific to a medication or procedure after Consent to Treat is provided. CD/FCCM is not required to have a specific form that you sign for this purpose at this time.

What is adequate informed consent? ›

Ensure that informed consent is truly informed by making sure that the patient understands what they are consenting to undergo. Do not assume that patients understand the medical terms in the consent form. A consent form alone is not sufficient for informed consent.

What are the 5 requirements of consent? ›

The 5 Requirements for Consent under the GDPR
  • The consent is freely given. Under the EU's GDPR, the individual to whom the personal data belongs, aka the data subject, must give their consent freely. ...
  • The consent is informed. ...
  • The consent is specific. ...
  • The consent is unambiguous. ...
  • The consent is verifiable.

When questions arise as to whether adequate consent has been given? ›

When questions arise as to whether adequate consent has been given, some courts take into consideration the information that is ordinarily provided by other physicians. A physician must: disclose to the patient the potential for death associated with a particular procedure.

How do you ensure consent is given? ›

the patient giving consent must have capacity • the consent must be freely given • the consent must be sufficiently specific to the procedure or treatment proposed • the consent must be informed. The four criteria for a valid consent must be met irrespective of whether the consent is in writing or oral.

How do you ensure participants have given informed consent? ›

Obtaining Written or Verbal Informed Consent. Obtaining consent involves explaining the research and assessing participant comprehension using a consent document, usually a written consent form or information sheet, as a guide for the verbal explanation of the study.

What is the only way to ensure you have consent? ›

Consent should be clearly and freely communicated. A verbal and affirmative expression of consent can help both you and your partner to understand and respect each other's boundaries. Consent cannot be given by individuals who are underage, intoxicated or incapacitated by drugs or alcohol, or asleep or unconscious.

How do you know if a patient is able to give informed consent? ›

Informed Consent
  1. Assess the patient's ability to understand relevant medical information and the implications of treatment alternatives and to make an independent, voluntary decision.
  2. Present relevant information accurately and sensitively, in keeping with the patient's preferences for receiving medical information.

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