Skip to content

Mental Health Crisis in Children and Young People with SEND

Mental health crisis

The Mental Health Act Code of Practice highlights that behaviours perceived as “challenging” (including self harm) in children and young people with SEND, are often a communication of unmet need, sensory distress, or emotional overwhelm, not a sign of mental illness that requires hospitalisation. 

This is why for children and young people with SEND:

  • Admission to hospital for a mental health crisis should be avoided wherever possible.
  • The child’s environment, support, and unmet needs must be explored first before an admission.
  • Whenever possible effective community‑based care should be put in place instead of an admission.

There are strong preventative processes designed to step in early, coordinate services, and reduce the need for inpatient care wherever safely possible.

Two of the most important tools are:

  • The Dynamic Support Register (DSR)
  • Care, Education and Treatment Reviews (CETRs)

The Dynamic Register and CETR's are a way of ensuring children and young people with unmet needs, sensory distress, or emotional overwhelm do not end up in hospital.

A Dynamic Support Register is a local health and social care list that helps identify children and young people with learning disabilities, autism, or both who may be at risk of crisis or potential admission to a mental health hospital. This includes young people whose behaviour or distress may escalate without the right help.

Every area in England keeps one. This register is used to keep track of who needs extra support, who is at growing risk, and what actions agencies must take.

A Dynamic Support Register is a local health and social care list that helps identify children and young people with learning disabilities, autism, or both who may be at risk of crisis or potential admission to a mental health hospital. This includes young people whose behaviour or distress may escalate without the right help.

Every area in England keeps one. This register is used to keep track of who needs extra support, who is at growing risk, and what actions agencies must take.

Being on the register means:

  • Your child is visible to senior NHS and local authority teams who meet regularly to plan and coordinate support.
  • It allows professionals to spot early signs of escalation and intervene sooner.
  • It makes it easier to prioritise access to services, including more intensive community support.
  • It triggers discussion about whether a Care, Education and Treatment Review (CETR) is needed to help prevent admission.

Being on the register means:

  • Your child is visible to senior NHS and local authority teams who meet regularly to plan and coordinate support.
  • It allows professionals to spot early signs of escalation and intervene sooner.
  • It makes it easier to prioritise access to services, including more intensive community support.
  • It triggers discussion about whether a Care, Education and Treatment Review (CETR) is needed to help prevent admission.

A child or young person can be added to the DSR with:

  • Parent/carer consent
  • Young person’s consent, if appropriate

If you believe your child is at risk of crisis, you can ask your CAMHS lead professional or social worker whether they are on the register and request that they are added if they are not.

A child or young person can be added to the DSR with:

  • Parent/carer consent
  • Young person’s consent, if appropriate

If you believe your child is at risk of crisis, you can ask your CAMHS lead professional or social worker whether they are on the register and request that they are added if they are not.

A CETR is a structured meeting that brings together:

  • You and your child
  • Health professionals (CAMHS, paediatrics, learning disability nurses, etc.)
  • Education services
  • Social care
  • Two independent experts:
    • A clinical expert
    • An “expert by experience” (usually a parent of a child with similar needs or someone with lived experience)

The purpose of the meeting is to stop unnecessary admissions and ensure your child gets the right help in the community wherever possible.

A CETR is a structured meeting that brings together:

  • You and your child
  • Health professionals (CAMHS, paediatrics, learning disability nurses, etc.)
  • Education services
  • Social care
  • Two independent experts:
    • A clinical expert
    • An “expert by experience” (usually a parent of a child with similar needs or someone with lived experience)

The purpose of the meeting is to stop unnecessary admissions and ensure your child gets the right help in the community wherever possible.

A CETR should take place when:

  • A child or young person with learning disabilities or autism is at risk of admission to hospital, or
  • They are already in hospital and need regular review

If things are deteriorating quickly a Local Area Emergency Protocol Review, also called a 'Blue Light meeting', can be used to create a rapid, temporary plan instead.

The Local Area Emergency Protocol Review is triggered when a CETR cannot take place due to not enough time, extreme risk, or the need for immediate action.

It functions as a crisis management system, aiming to identify alternative community-based care to prevent admission.

A CETR should take place when:

  • A child or young person with learning disabilities or autism is at risk of admission to hospital, or
  • They are already in hospital and need regular review

If things are deteriorating quickly a Local Area Emergency Protocol Review, also called a 'Blue Light meeting', can be used to create a rapid, temporary plan instead.

The Local Area Emergency Protocol Review is triggered when a CETR cannot take place due to not enough time, extreme risk, or the need for immediate action.

It functions as a crisis management system, aiming to identify alternative community-based care to prevent admission.

The panel must consider three key questions:

  1. Is the person safe?
  2. Are they getting good support now?
  3. What are the plans for the future—and can this be done in the community?

The panel must consider three key questions:

  1. Is the person safe?
  2. Are they getting good support now?
  3. What are the plans for the future—and can this be done in the community?

A CETR will help:

  • Identify unmet needs (e.g., unrecognised anxiety, sensory overload, lack of support at school).
  • Recommend reasonable adjustments at home, school, or in services.
  • Bring agencies together to form a single, coordinated plan, rather than families being left to chase professionals separately.
  • Hold local services to account if timely support hasn’t been put in place.
  • Explore alternatives to hospital, such as crisis outreach, respite, extra school support, or adjustments to the child’s environment.

Every recommendation is written down, and services are expected to act on them.

A CETR will help:

  • Identify unmet needs (e.g., unrecognised anxiety, sensory overload, lack of support at school).
  • Recommend reasonable adjustments at home, school, or in services.
  • Bring agencies together to form a single, coordinated plan, rather than families being left to chase professionals separately.
  • Hold local services to account if timely support hasn’t been put in place.
  • Explore alternatives to hospital, such as crisis outreach, respite, extra school support, or adjustments to the child’s environment.

Every recommendation is written down, and services are expected to act on them.

Being on the DSR leads to earlier action

The DSR flags your child as needing monitoring and possibly urgent help. It ensures your child’s situation is regularly discussed at a strategic level, not only in their usual appointments.

A CETR creates a concrete prevention plan

If risks increase, a CETR gathers everyone needed to put preventative support in place—quickly, clearly and collaboratively.

Together, these measures mean the focus is:

  • Early recognition of crisis signs
  • Better planning and joined‑up support
  • Rapid response when things start to deteriorate
  • Avoiding the distress, disruption, and trauma of hospital admission where possible

Being on the DSR leads to earlier action

The DSR flags your child as needing monitoring and possibly urgent help. It ensures your child’s situation is regularly discussed at a strategic level, not only in their usual appointments.

A CETR creates a concrete prevention plan

If risks increase, a CETR gathers everyone needed to put preventative support in place—quickly, clearly and collaboratively.

Together, these measures mean the focus is:

  • Early recognition of crisis signs
  • Better planning and joined‑up support
  • Rapid response when things start to deteriorate
  • Avoiding the distress, disruption, and trauma of hospital admission where possible

You can request:

  • To have your child added to the Dynamic Support Register
  • A CETR, if you believe your child is at risk of hospital admission

Who to ask

  • Your child’s CAMHS clinician
  • Your social worker, if involved
  • Your SENCO
  • Your GP

If things are escalating and you are not getting a response, families can also contact the Integrated Care Board for your area.

You can request:

  • To have your child added to the Dynamic Support Register
  • A CETR, if you believe your child is at risk of hospital admission

Who to ask

  • Your child’s CAMHS clinician
  • Your social worker, if involved
  • Your SENCO
  • Your GP

If things are escalating and you are not getting a response, families can also contact the Integrated Care Board for your area.

What if my child or young people needs to be admitted to hospital?

Children and young people with severe mental health needs may sometimes require admission to a specialist mental health hospital. This happens when community support can no longer keep a child safe or well because they are in crisis, pose a danger to themselves or others, or require urgent, 24/7 specialist care that cannot be managed in the community. It is a last resort, aimed at providing a safe environment when outpatient treatment is insufficient.

Having a child in hospital – or preparing for them to be admitted – can bring up a lot of emotions. You might feel extremely worried or distressed, but you may also feel some relief knowing they’re in the right place to get the care they need. Whatever you’re experiencing, it’s important to remember that for many young people, spending time in hospital is an important part of their recovery.

Hospitals can be busy places, and it’s normal to feel overwhelmed by the environment and the number of professionals involved in your child’s care. This information aims to answer common questions about what to expect on the ward, where to find guidance, how to raise concerns, and how you can continue to support your child during their stay.

Informal (Voluntary) Admission

A child/young person can be admitted voluntarily to a mental health hospital if give consent. A young person can consent to being admitted if:

  • Over 16 and have been assessed under the Mental Capacity Act as having capacity to give consent.
  • Under 16 and “Gillick Competent”.

Gillick Competence means that the child or young person under 16 years old has enough intelligence, competence and understanding to fully appreciate what's involved in their treatment so can can consent to it.

More information on voluntary admission from Mind

Sectioned (Detained) Under the Mental Health Act

This happens when a young person cannot be kept safe otherwise. The two main sections are:

  • Section 2 – assessment for up to 28 days
  • Section 3 – treatment for up to 6 months (renewable)

A specially trained professional (an AMHP) and two doctors must agree on the decision. Parents may have rights as the “nearest relative”, including the power to object to some sections.

More information on being sectioned by Mind

Informal (Voluntary) Admission

A child/young person can be admitted voluntarily to a mental health hospital if give consent. A young person can consent to being admitted if:

  • Over 16 and have been assessed under the Mental Capacity Act as having capacity to give consent.
  • Under 16 and “Gillick Competent”.

Gillick Competence means that the child or young person under 16 years old has enough intelligence, competence and understanding to fully appreciate what's involved in their treatment so can can consent to it.

More information on voluntary admission from Mind

Sectioned (Detained) Under the Mental Health Act

This happens when a young person cannot be kept safe otherwise. The two main sections are:

  • Section 2 – assessment for up to 28 days
  • Section 3 – treatment for up to 6 months (renewable)

A specially trained professional (an AMHP) and two doctors must agree on the decision. Parents may have rights as the “nearest relative”, including the power to object to some sections.

More information on being sectioned by Mind

Young people are usually admitted to an Assessment and Treatment Unit (ATU) or occasionally a A Psychiatric Intensive Care Unit (PICU) if there is very high risk.

Assessment and Treatment Units (ATU) are specialist inpatient units designed to assess and treat autistic people, learning disabled people and people with mental health challenges.

A Psychiatric Intensive Care Unit (PICU) is a secure, locked, high-staffed, and often single-sex ward that provides short-term, intensive care for individuals (usually adults aged 18-65) in the most acute, disturbed phase of a mental illness. These units focus on stabilizing severe symptoms like extreme aggression, risk of self-harm, or suicide, aiming for a quick, safe, and positive transition to less restrictive care.

The first days in both a ATU or PICU usually include:

  • A physical health check
  • Assessment by a range of professionals (psychiatry, psychology, education staff, therapists)
  • A personalised care plan
  • Allocation of a key worker

Families should receive:

  • A welcome pack
  • Ward rules and visiting information
  • Contact details for staff

Young people have the right to an Independent Mental Health Advocate (IMHA) if they are detained.

Young people are usually admitted to an Assessment and Treatment Unit (ATU) or occasionally a A Psychiatric Intensive Care Unit (PICU) if there is very high risk.

Assessment and Treatment Units (ATU) are specialist inpatient units designed to assess and treat autistic people, learning disabled people and people with mental health challenges.

A Psychiatric Intensive Care Unit (PICU) is a secure, locked, high-staffed, and often single-sex ward that provides short-term, intensive care for individuals (usually adults aged 18-65) in the most acute, disturbed phase of a mental illness. These units focus on stabilizing severe symptoms like extreme aggression, risk of self-harm, or suicide, aiming for a quick, safe, and positive transition to less restrictive care.

The first days in both a ATU or PICU usually include:

  • A physical health check
  • Assessment by a range of professionals (psychiatry, psychology, education staff, therapists)
  • A personalised care plan
  • Allocation of a key worker

Families should receive:

  • A welcome pack
  • Ward rules and visiting information
  • Contact details for staff

Young people have the right to an Independent Mental Health Advocate (IMHA) if they are detained.

Young people admitted to hospital—voluntarily or under section—have the right to:

  • Safe, high‑quality care
  • Information in a format they understand
  • Respect, dignity and privacy
  • Age‑appropriate facilities
  • Family contact
  • Advocacy to help them understand decisions
  • Least restrictive interventions (e.g., separation from family should be minimised)

Parents with parental responsibility have rights to be involved unless a competent young person refuses information sharing and there is no safeguarding risk.

Young people admitted to hospital—voluntarily or under section—have the right to:

  • Safe, high‑quality care
  • Information in a format they understand
  • Respect, dignity and privacy
  • Age‑appropriate facilities
  • Family contact
  • Advocacy to help them understand decisions
  • Least restrictive interventions (e.g., separation from family should be minimised)

Parents with parental responsibility have rights to be involved unless a competent young person refuses information sharing and there is no safeguarding risk.

Welcome Meeting

Within the first week there will be an introduction to the team and a care plan will be created or updated if one already exists.

CETR (Care, Education and Treatment Review)

  • This is mandatory for children with autism and/or learning disability when they become an inpatient.
  • It must be held within 2 weeks of admission and every 3 months there after.
  • An independent panel checks the care is appropriate and considers whether community alternatives exist.

CPA (Care Programme Approach) Meetings

This meeting coordinates care, risk and discharge planning. It will be held at least every 6 months.

Welcome Meeting

Within the first week there will be an introduction to the team and a care plan will be created or updated if one already exists.

CETR (Care, Education and Treatment Review)

  • This is mandatory for children with autism and/or learning disability when they become an inpatient.
  • It must be held within 2 weeks of admission and every 3 months there after.
  • An independent panel checks the care is appropriate and considers whether community alternatives exist.

CPA (Care Programme Approach) Meetings

This meeting coordinates care, risk and discharge planning. It will be held at least every 6 months.

Young people may access:

  • Medication (prescribed carefully under NICE guidance, with monitoring)
  • Psychology / talking therapies
  • Occupational therapy
  • Speech and language therapy
  • Dietetic support for eating issues

Stopping Over Medication of People (STOMP) is a plan from the NHS to help stop people with a learning disability or autistic people being given too much medicine, or the wrong kind of medicine, for behaviour or mental health. It tries to make sure people only get medicine when they really need it.

Supporting Treatment and Appropriate Medication in Paediatrics (STAMP) is a similar plan for children and young people. It makes sure autistic children and those with a learning disability get the right medicine, in the right amount, and only for as short a time as needed.

More information about the STOMP‑STAMP programme.

Young people may access:

  • Medication (prescribed carefully under NICE guidance, with monitoring)
  • Psychology / talking therapies
  • Occupational therapy
  • Speech and language therapy
  • Dietetic support for eating issues

Stopping Over Medication of People (STOMP) is a plan from the NHS to help stop people with a learning disability or autistic people being given too much medicine, or the wrong kind of medicine, for behaviour or mental health. It tries to make sure people only get medicine when they really need it.

Supporting Treatment and Appropriate Medication in Paediatrics (STAMP) is a similar plan for children and young people. It makes sure autistic children and those with a learning disability get the right medicine, in the right amount, and only for as short a time as needed.

More information about the STOMP‑STAMP programme.

Sometimes, for safety, staff may use:

  • Enhanced observation
  • Physical restraint
  • Seclusion
  • Chemical or mechanical restraint

These must be:

  • Proportionate
  • For the shortest possible time
  • Clearly recorded
  • Discussed with you afterwards

Families should be involved in developing Positive Behaviour Support Plans to reduce the need for restrictive practices.

Sometimes, for safety, staff may use:

  • Enhanced observation
  • Physical restraint
  • Seclusion
  • Chemical or mechanical restraint

These must be:

  • Proportionate
  • For the shortest possible time
  • Clearly recorded
  • Discussed with you afterwards

Families should be involved in developing Positive Behaviour Support Plans to reduce the need for restrictive practices.

Discharge planning starts early. If your child was detained under certain sections (e.g., Section 3), they are legally entitled to free Section 117 aftercare, which may include:

  • Mental health support
  • Support with education
  • Social care support
  • Accommodation support

Young people should not be discharged until:

  • A safe community plan is in place
  • Relevant services agree to support
  • You and your child have been involved in planning

Discharge planning starts early. If your child was detained under certain sections (e.g., Section 3), they are legally entitled to free Section 117 aftercare, which may include:

  • Mental health support
  • Support with education
  • Social care support
  • Accommodation support

Young people should not be discharged until:

  • A safe community plan is in place
  • Relevant services agree to support
  • You and your child have been involved in planning

Start by raising concerns informally with the ward. You can then:

Families are encouraged to keep written records of concerns.
Downloadable Carer’s Monitoring Form

Start by raising concerns informally with the ward. You can then:

Families are encouraged to keep written records of concerns.
Downloadable Carer’s Monitoring Form