Samuel Alban-Stanley
PFD Report
All Responded
Ref: 2022-0082
Child Death (from 2015)
Hospital Death (Clinical Procedures and medical management) related deaths
Mental Health related deaths
Other related deaths
All 3 responses received
· Deadline: 11 Apr 2022
Coroner's Concerns (AI summary)
Inadequate support and psychosocial interventions were provided for a child with Prader Willi syndrome and high-risk behaviours. Poor communication between agencies also prevented coordinated care.
View full coroner's concerns
(1) Evidence given at the inquest by Professor from Great Ormond Street made it clear that the episodes of behavioural difficulties experienced by Sammy were inherently a part of his Prader Willi syndrome. He also indicated that it was not uncommon for the parents of children with behavioural difficulties associated with their underlying disease to inform him that they did not have adequate support. He opined that whilst the risk cannot be eliminated it could be managed through a combination of psychosocial intervention, sometimes with medication and care. He told the court that more support should be available to the families of children with rare diseases such as Prader Willi syndrome.
(2) Evidence was given at the inquest that the social workers from Kent County Council were fully aware of Sammy’s high-risk behaviour and had on several occasions referred him to their Children with Disabilities team who refused to assess him. Sammy’s behaviour was also having an adverse impact on his three younger siblings. His mother had repeatedly reported that she could not keep Sammy safe without support and had sought assistance from state agencies, Charites and done as much as she possibly could herself. Social workers took steps to try to access support for his family to enable them to care for him but the way services were managed meant those involved had little knowledge of what was available. One social worker gave evidence that Sammy’s behaviour had escalated between August 2019 and January 2020 when he did not have access to support in the home. However, despite being aware that Sammy needed more support to provide wrap around care before and after the school day only very limited support was funded from the end of January 2020. When the advice was given for him to shield in March 2020, due to the Covid 19 pandemic, he now had to isolate and was without the supportive school environment yet no replacement support was provided despite the need being obvious.
(3) There was evidence given that the mental health team at North East London Foundation Trust were also aware of Sammy’s high-risk behaviours. Support had been provided by a psychology student in the past and he had reportedly responded well to mindfulness therapy and the de-escalation techniques employed by his family. Psychosocial interventions were not offered by the Mental Health Trust and a Care Education and Treatment Review was suggested but not implemented before Sammy’s death. The court heard that such interventions may not have been successful but, in any event, North East London Foundation Trust had not been commissioned to provide anything other than a diagnostic service to children presenting with autism and learning disabilities rather than an overt mental health diagnosis.
(4) The evidence at the inquest also revealed that communication between agencies involved in his short life was inadequate. It is possible that had information been shared in a timely manner and actions taken as a result then more support could have been provided to Sammy and his family. Had he, and his family, had more practical help and support this may have made a difference to his high-risk behaviour and ultimately his death.
(5) It was clear at the hearing that locally Kent County Council had taken steps to change the way their services were delivered following Sammy’s death but it is predictable that a similar incident may arise in other areas if children with complex neurodevelopmental needs are excluded from accessing the care and treatment they require to keep them safe.
(2) Evidence was given at the inquest that the social workers from Kent County Council were fully aware of Sammy’s high-risk behaviour and had on several occasions referred him to their Children with Disabilities team who refused to assess him. Sammy’s behaviour was also having an adverse impact on his three younger siblings. His mother had repeatedly reported that she could not keep Sammy safe without support and had sought assistance from state agencies, Charites and done as much as she possibly could herself. Social workers took steps to try to access support for his family to enable them to care for him but the way services were managed meant those involved had little knowledge of what was available. One social worker gave evidence that Sammy’s behaviour had escalated between August 2019 and January 2020 when he did not have access to support in the home. However, despite being aware that Sammy needed more support to provide wrap around care before and after the school day only very limited support was funded from the end of January 2020. When the advice was given for him to shield in March 2020, due to the Covid 19 pandemic, he now had to isolate and was without the supportive school environment yet no replacement support was provided despite the need being obvious.
(3) There was evidence given that the mental health team at North East London Foundation Trust were also aware of Sammy’s high-risk behaviours. Support had been provided by a psychology student in the past and he had reportedly responded well to mindfulness therapy and the de-escalation techniques employed by his family. Psychosocial interventions were not offered by the Mental Health Trust and a Care Education and Treatment Review was suggested but not implemented before Sammy’s death. The court heard that such interventions may not have been successful but, in any event, North East London Foundation Trust had not been commissioned to provide anything other than a diagnostic service to children presenting with autism and learning disabilities rather than an overt mental health diagnosis.
(4) The evidence at the inquest also revealed that communication between agencies involved in his short life was inadequate. It is possible that had information been shared in a timely manner and actions taken as a result then more support could have been provided to Sammy and his family. Had he, and his family, had more practical help and support this may have made a difference to his high-risk behaviour and ultimately his death.
(5) It was clear at the hearing that locally Kent County Council had taken steps to change the way their services were delivered following Sammy’s death but it is predictable that a similar incident may arise in other areas if children with complex neurodevelopmental needs are excluded from accessing the care and treatment they require to keep them safe.
Responses
Action Taken
North East London Foundation Trust is working with the Kent and Medway ICS and the local authority to learn lessons from the report, and has put training in place for all relevant staff on the signs and impacts of the relevant condition, and introduced reviews for high complexity cases. (AI summary)
North East London Foundation Trust is working with the Kent and Medway ICS and the local authority to learn lessons from the report, and has put training in place for all relevant staff on the signs and impacts of the relevant condition, and introduced reviews for high complexity cases. (AI summary)
View full response
Dear Ms Wood,
Thank you for your letter of 12 March 2022, to the then Secretary of State for Health and Social Care, Sajid Javid, about the death of Samuel Alban-Stanley. I am replying as Minister with responsibility for Care and Mental Health and thank you for the additional time provided.
I would like to begin by offering my deepest condolences to the family of Samuel. It is, of course, vital that we take learnings, where they are identified, to improve NHS care, and I am grateful to you for bringing these matters to my attention.
In preparing this response, my officials made enquiries with NHS England and NHS Improvement and the Care Quality Commission. I am further advised that the NHS Kent and Medway Integrated Care System has also provided a detailed response to your report.
At the start of the Covid-19 pandemic, people with serious underlying health conditions, such as Samuel, were advised to follow shielding measures. We recognise that such measures had an impact on many people’s mental health and wellbeing. However, urgent action was needed at the time to suppress the Covid-19 virus, prevent the NHS from becoming overwhelmed, and ultimately save lives. These measures were kept under constant review and were removed as soon as it was considered safe to do so.
I am sorry to hear that Samuel was not offered the care and treatment that he needed to keep him safe, and for the poor communication between the agencies that were supposed to provide this care. The North East London Foundation Trust is now working with the Kent and Medway ICS and the local authority to learn lessons from this report and what happened to Samuel. Training has been put in place for all relevant staff so that they are aware of the signs and impacts of Samuel’s condition. They have also introduced reviews for high complexity cases that may not meet the criteria for neurodevelopmental services, to ensure the needs of patients in the future are addressed.
You may wish to know that under the Equality Act (2010), health and social care organisations must make reasonable adjustments to ensure that disabled people are not disadvantaged. Commissioners are responsible for ensuring the provision of services based on the local needs of their population, including for people with learning disabilities, mental health problems and complex physical needs. Commissioners should take into consideration any relevant guidance, such as those published by the National Institute for Health and Care Excellence in designing their local services.
More broadly, the NHS Long Term Plan, published in 2019, includes a commitment that by 2023/24 children and young people with a learning disability and/or who are autistic with the most complex needs will have a designated keyworker. As a result, the Children and Young People's keyworker programme, a four-year multi-million-pound investment by NHS England and NHS Improvement, and full coverage of the key-working service across England, is expected by 2024. Keyworkers will ensure that these children and their families get the right support at the right time. They will also ensure that local systems are responsive to fully meeting the young people’s needs in a joined-up way and that, whenever it is possible to provide care and treatment in the community with the right support, this becomes the norm.
I understand from your report that a Care (Education) and Treatment Review (C(E)TR) was suggested locally, however, not implemented in Samuel’s case. You may wish to note that the C(E)TR policy, which sets out when a C(E)TR should be offered, relates to people of all ages with learning disabilities, autism, or both, that are facing potential admission to, or are patients in, any specialist learning disability or mental health hospital, and who are the commissioning responsibility of NHS England or the Integrated Care Systems.
Finally, I would add that this Department is not able to comment on issues relating to school support or children’s social care. You may, therefore, also wish to raise your concerns directly with the Department for Education, at the below address:
Department for Education Sanctuary Buildings Great Smith Street London SW1P 3BT
I hope this response is helpful. Thank you for bringing these concerns to my attention.
GILLIAN KEEGAN
Thank you for your letter of 12 March 2022, to the then Secretary of State for Health and Social Care, Sajid Javid, about the death of Samuel Alban-Stanley. I am replying as Minister with responsibility for Care and Mental Health and thank you for the additional time provided.
I would like to begin by offering my deepest condolences to the family of Samuel. It is, of course, vital that we take learnings, where they are identified, to improve NHS care, and I am grateful to you for bringing these matters to my attention.
In preparing this response, my officials made enquiries with NHS England and NHS Improvement and the Care Quality Commission. I am further advised that the NHS Kent and Medway Integrated Care System has also provided a detailed response to your report.
At the start of the Covid-19 pandemic, people with serious underlying health conditions, such as Samuel, were advised to follow shielding measures. We recognise that such measures had an impact on many people’s mental health and wellbeing. However, urgent action was needed at the time to suppress the Covid-19 virus, prevent the NHS from becoming overwhelmed, and ultimately save lives. These measures were kept under constant review and were removed as soon as it was considered safe to do so.
I am sorry to hear that Samuel was not offered the care and treatment that he needed to keep him safe, and for the poor communication between the agencies that were supposed to provide this care. The North East London Foundation Trust is now working with the Kent and Medway ICS and the local authority to learn lessons from this report and what happened to Samuel. Training has been put in place for all relevant staff so that they are aware of the signs and impacts of Samuel’s condition. They have also introduced reviews for high complexity cases that may not meet the criteria for neurodevelopmental services, to ensure the needs of patients in the future are addressed.
You may wish to know that under the Equality Act (2010), health and social care organisations must make reasonable adjustments to ensure that disabled people are not disadvantaged. Commissioners are responsible for ensuring the provision of services based on the local needs of their population, including for people with learning disabilities, mental health problems and complex physical needs. Commissioners should take into consideration any relevant guidance, such as those published by the National Institute for Health and Care Excellence in designing their local services.
More broadly, the NHS Long Term Plan, published in 2019, includes a commitment that by 2023/24 children and young people with a learning disability and/or who are autistic with the most complex needs will have a designated keyworker. As a result, the Children and Young People's keyworker programme, a four-year multi-million-pound investment by NHS England and NHS Improvement, and full coverage of the key-working service across England, is expected by 2024. Keyworkers will ensure that these children and their families get the right support at the right time. They will also ensure that local systems are responsive to fully meeting the young people’s needs in a joined-up way and that, whenever it is possible to provide care and treatment in the community with the right support, this becomes the norm.
I understand from your report that a Care (Education) and Treatment Review (C(E)TR) was suggested locally, however, not implemented in Samuel’s case. You may wish to note that the C(E)TR policy, which sets out when a C(E)TR should be offered, relates to people of all ages with learning disabilities, autism, or both, that are facing potential admission to, or are patients in, any specialist learning disability or mental health hospital, and who are the commissioning responsibility of NHS England or the Integrated Care Systems.
Finally, I would add that this Department is not able to comment on issues relating to school support or children’s social care. You may, therefore, also wish to raise your concerns directly with the Department for Education, at the below address:
Department for Education Sanctuary Buildings Great Smith Street London SW1P 3BT
I hope this response is helpful. Thank you for bringing these concerns to my attention.
GILLIAN KEEGAN
Action Taken
Training on Prader-Willi syndrome has been provided to CYPMHS staff at NELFT, and joint posts have been created across the Local Authority and Primary Care to identify children with additional needs early. Kent has also mobilised the National NHS England Designated Key Worker Early Adopter programme and continues to develop programmes for early intervention and support. (AI summary)
Training on Prader-Willi syndrome has been provided to CYPMHS staff at NELFT, and joint posts have been created across the Local Authority and Primary Care to identify children with additional needs early. Kent has also mobilised the National NHS England Designated Key Worker Early Adopter programme and continues to develop programmes for early intervention and support. (AI summary)
View full response
Dear Ms Wood,
Nursing and Quality Team Kent House 81 Station Road Ashford Kent TN23 1PP
Response to Regulation 28 Report to Prevent Future Deaths, dated 12th March 2022 Re. Samuel Alban Stanley
Following the Inquest opened on the 14th of May 2020, the NHS Kent and Medway Clinical Commissioning Group (CCG) received the Regulation 28 Report touching on the death of Samuel Alban Stanley.
The CCG while not in attendance at the Inquest would like to take this opportunity to extend their condolences to the family and friends of Sammy following his tragic death.
Clinical commissioning groups were established as part of the Health and Social Care Act in 2012 and are responsible for commissioning healthcare services for their local populations. They are also system leaders with a key role to play in improving the quality of care and their role does not sit in isolation. However, they are not directly responsible for the provision of services and nor are they responsible for the commissioning of social care services, which in Kent is the responsibility of Kent County Council.
Notwithstanding this and recognising the coroner’s comments regarding the need for closer communication between agencies, the CCG acting in good faith, has liaised with both Northeast London NHS Foundation Trust (NELFT), Kent County Council (KCC) in order to respond to the concerns cited.
1. Concerns that more support should have been available to Sammy and his family for the rare nature of conditions such as Prader-Willi syndrome.
The Kent and Medway health and care system (the system) has taken steps to learn and embed changes from this case to improve the experience of patients in the future.
Training has been provided to staff within the Children’s and Young Person’s Mental Health Services (CYPMHS) at NELFT, specifically on Prader-Willi syndrome. NELFT has reported that training was received by 400 staff from February 2021.
Due to the rarity of the condition, reviews have been put in place to consider high complexity cases that may not meet the criteria for Neurodevelopmental Services. In future, where these very complex cases present, joint assessments will take place between the CYPMHS and the Neurodevelopmental (ND) and Learning Disabilities (LD) services, to combine the expertise of the services and generate a joint working arrangement to address the needs of the patient. NELFT have stated that this process will ensure that joint working is fully embedded and that the assessments fully include a holistic view of the young person’s needs, risks, and presentation.
Clinical harm reviews on the highest risk and most vulnerable patients have also been introduced across social care and NELFT, as a way of ensuring that patients are identified as early as possible and given additional support if required.
Further training has also been designed to support staff in the CYPMHS to provide more support of a combined psychological and medical nature to people suffering with Autistic Spectrum Disorders (ASD): the senior clinical leads for the service completed this training in December 2021.
2. Concerns that the local authority Kent County Council (KCC), were aware of the high- risk situation at Sammy’s home but did not have adequate knowledge on what support could be accessed by the family and did not robustly respond to the change in needs during the pandemic when the support available became more limited.
KCC have taken several steps to ensure better engagement with the local mental health resources. The working protocol between teams at the local authority and NELFT has fundamentally changed to ensure that they are now party to one another’s multidisciplinary meetings as a matter of course. This allows for improved information sharing between agencies, rapid and accurate decision making and enabling access to resources
Also, working with the wider healthcare system, KCC have taken steps to ensure that they are improving services for children and young people. The criteria for services have been reviewed specifically with regards to neurodiversity, which has already led to several children and young people being transferred to services that better meet their needs.
A large amount of work has also been undertaken regarding the suicide prevention strategy for young people since the death of Sammy. This includes the lead for KCC actively working with healthcare providers and the CCG to identify high-risk cases and provide support in the home to avoid admission where this is safe to do; and to ensure that families have access to the services they need. Meetings in relation to these cases have representation from the relevant stakeholders across the system. They proactively discuss any placement breakdown and consider how best to support and deliver potential solutions.
The CCG has also established a ‘Dynamic Support Database’, which has been developed to enable all statutory partners to better understand the needs of children and young people with Learning Disability and Autism. Consent to details being added to the database is given and the CCG holds this list to ensure it can support patients who may need additional services or help in future. It is a way of helping managing system risk for patients with complex needs and helps facilitate system ownership of all these cases, to ensure provision of the right help and support at the right time, in collaboration with the patient and their family.
During the Inquest, it was highlighted that there was a lack of knowledge and understanding of the rights of parent carers of a disabled child to request a separate assessment of their needs; how to carry out the assessment and where the information is held and how needs may be met through Direct Payments. In response to this, KCC has delivered training to families, covering the rights of parents of disabled children to request a Parent Carer assessment, separate to their child’s assessment. They have also introduced new Parent Carer Assessment forms so that social work staff consider and consult with parents of disabled children as to whether a separate assessment of their needs is required, or the parents/carers are content for their needs to be included in the Child and Family Assessment (majority).
3. Concern that there was a lack of psychosocial and psychological therapies offered in this case. This was compounded by the information shared that NELFT may not have been commissioned to provide anything other than a diagnostic service for those presenting with autism and learning disabilities rather than an overt mental health issue.
In terms of the commissioning of services, the CCG actively works with partners across the health system to ensure gaps do not exist and that pathways are in place to cater for the presentations and needs of the local communities it serves. NELFT are commissioned to provide more than just diagnostic services including psychological and psychosocial interventions, but the CCG acknowledge that mental health services are under extreme pressure, with increasing referrals that have significantly peaked during and post pandemic. Therefore, the CCG is actively working with NELFT to ensure that services are developed to meet the needs of all children and young people and to identify areas where the service offer can be strengthened and have increased significant levels of investment to help address this.
Since 2019/20 additional investment of £2.1 million has been made into local Neurodevelopmental services. Whilst unfortunately this did not prevent the tragic death of Sammy, it has subsequently generated improvements to services provided.
This investment includes the commissioning of Nurture UK to deliver an ‘inclusion’ programme in schools to improve educational outcomes for children with Special Educational Needs and Disabilities (SEND). Inclusive schools contain the following elements:
• a belief that all children have the potential to learn and grow
• the ability to respond to the cultural and/or socio-economic needs of the students
• the ability to support positive behaviour in and out of the classroom
• a dedication to seeing each child as an individual
• the modification of curriculum and activities to include all students
“Together with Parents’ is another service which is being jointly funded between the CCG and KCC to provide better support to families in the community. The service was co-produced with parents, carers and professional partners and delivers local support to parents and carers whose child has either received a diagnosis or are awaiting diagnosis for a neurodevelopmental condition. The new service is to ensure parents can access support and information in a timely way before reaching crisis point.
With regard to the psychological treatment offered in this specific case during the episode prior to Sammy’s sad death, the CCG has been assured that NELFT undertook an assessment of need. Sammy’s escalation of need occurred at onset of the pandemic, when statutory services were severely limited in terms of the care they could provide, and the guidance around the management of clinically vulnerable children during the pandemic was in an embryonic stage. Sammy was under the care of a consultant psychiatrist who regularly reviewed and monitored the prescribing of medications. KMCCG understanding of the clinical opinion and expertise of Sammy’s needs was that the psychological intervention of cognitive behavioural therapy would not have been appropriate or effective to meet his needs and hence the more psychosocial intervention of Non Violent Resistance was offered. NVR is an evidence-based psychosocial intervention to support parents in responding to their child’s more challenging needs.
4. Concern that the communications between agencies in this case were inadequate.
As detailed above, several new processes have been put in place to improve the way in which the relevant agencies communicate in a timely manner. Multidisciplinary meetings between agencies are now a matter of course and fundamentally the standard operating procedure for CYPMHS has been amended to ensure that the communication and sharing of expertise is embedded as a business-as-usual activity. This has been emphasised with regards to LD cases specifically, due to the complexity of these, as has the need to involve numerous agencies as standard practice.
KMCCG have worked with NELFT, acute and community trusts, KCC, NHS England and wider partners to improve communications regarding children and young people who have the most complex presentations and are considered at risk. KMCCG has invested in new strategic leadership posts whose role is to drive improved dialogue across agencies and to provide a route for rapid escalation and resolution. Since Sammy’s death, KMCCG have worked in collaboration with system partners to develop and implement shared Kent and Medway escalation policy and protocols. This enables rapid identification of children and young people who need senior leader oversight to ensure appropriate care.
5. Concern that children in other areas with neurodevelopmental needs may be excluded from accessing the care and treatment they need to keep them safe.
Since Sammy’s death, KMCCG has made investments in posts and mechanisms to improve the offer for children and young people with neurodevelopmental presentation. A number of joint posts have been created across the Local Authority and Primary Care so that children and young people with additional needs are identified early and care is coordinated rapidly around the child and family.
Kent partners have been successful in bidding for and mobilising the National NHS England Designated Key Worker Early Adopter programme. This team is based in KCC and is a partnership project across health, the Local Authority and NHSE. The Designated Key Workers provide practice consultancy to multi agency partners/networks and case coordination for children and young people with complex neurodevelopment. The team work in conjunction with the KMCCG Learning Disability and Autism team to ensure referrals to the Dynamic Support Database and CETR processes has better supported the needs of children and young people to avoid placement breakdown and admission to T4 services.
There continues to be developments and innovation focussed on earlier intervention and support for families who have children and young people with neurodevelopment needs. Examples of which include new programmes within schools across Kent to promote inclusive practice and reduce exclusions. Piloting early identification and support of children and young people through a Primary Care multi-disciplinary approach utilising Care Navigators to support meeting the holistic needs of a family.
As a health and care system we are determined to ensure we learn from Serious Incidents such as this tragic case and continue to take appropriate action, as outlined above, to prevent similar occurrences from happening in the future.
From July 2022, Integrated Care Boards will succeed CCGs across the country. The Boards of these organisations will include Partner Members from Local Authorities and NHS Providers, with a focus on greater collaboration and more seamless joint decision making
Nursing and Quality Team Kent House 81 Station Road Ashford Kent TN23 1PP
Response to Regulation 28 Report to Prevent Future Deaths, dated 12th March 2022 Re. Samuel Alban Stanley
Following the Inquest opened on the 14th of May 2020, the NHS Kent and Medway Clinical Commissioning Group (CCG) received the Regulation 28 Report touching on the death of Samuel Alban Stanley.
The CCG while not in attendance at the Inquest would like to take this opportunity to extend their condolences to the family and friends of Sammy following his tragic death.
Clinical commissioning groups were established as part of the Health and Social Care Act in 2012 and are responsible for commissioning healthcare services for their local populations. They are also system leaders with a key role to play in improving the quality of care and their role does not sit in isolation. However, they are not directly responsible for the provision of services and nor are they responsible for the commissioning of social care services, which in Kent is the responsibility of Kent County Council.
Notwithstanding this and recognising the coroner’s comments regarding the need for closer communication between agencies, the CCG acting in good faith, has liaised with both Northeast London NHS Foundation Trust (NELFT), Kent County Council (KCC) in order to respond to the concerns cited.
1. Concerns that more support should have been available to Sammy and his family for the rare nature of conditions such as Prader-Willi syndrome.
The Kent and Medway health and care system (the system) has taken steps to learn and embed changes from this case to improve the experience of patients in the future.
Training has been provided to staff within the Children’s and Young Person’s Mental Health Services (CYPMHS) at NELFT, specifically on Prader-Willi syndrome. NELFT has reported that training was received by 400 staff from February 2021.
Due to the rarity of the condition, reviews have been put in place to consider high complexity cases that may not meet the criteria for Neurodevelopmental Services. In future, where these very complex cases present, joint assessments will take place between the CYPMHS and the Neurodevelopmental (ND) and Learning Disabilities (LD) services, to combine the expertise of the services and generate a joint working arrangement to address the needs of the patient. NELFT have stated that this process will ensure that joint working is fully embedded and that the assessments fully include a holistic view of the young person’s needs, risks, and presentation.
Clinical harm reviews on the highest risk and most vulnerable patients have also been introduced across social care and NELFT, as a way of ensuring that patients are identified as early as possible and given additional support if required.
Further training has also been designed to support staff in the CYPMHS to provide more support of a combined psychological and medical nature to people suffering with Autistic Spectrum Disorders (ASD): the senior clinical leads for the service completed this training in December 2021.
2. Concerns that the local authority Kent County Council (KCC), were aware of the high- risk situation at Sammy’s home but did not have adequate knowledge on what support could be accessed by the family and did not robustly respond to the change in needs during the pandemic when the support available became more limited.
KCC have taken several steps to ensure better engagement with the local mental health resources. The working protocol between teams at the local authority and NELFT has fundamentally changed to ensure that they are now party to one another’s multidisciplinary meetings as a matter of course. This allows for improved information sharing between agencies, rapid and accurate decision making and enabling access to resources
Also, working with the wider healthcare system, KCC have taken steps to ensure that they are improving services for children and young people. The criteria for services have been reviewed specifically with regards to neurodiversity, which has already led to several children and young people being transferred to services that better meet their needs.
A large amount of work has also been undertaken regarding the suicide prevention strategy for young people since the death of Sammy. This includes the lead for KCC actively working with healthcare providers and the CCG to identify high-risk cases and provide support in the home to avoid admission where this is safe to do; and to ensure that families have access to the services they need. Meetings in relation to these cases have representation from the relevant stakeholders across the system. They proactively discuss any placement breakdown and consider how best to support and deliver potential solutions.
The CCG has also established a ‘Dynamic Support Database’, which has been developed to enable all statutory partners to better understand the needs of children and young people with Learning Disability and Autism. Consent to details being added to the database is given and the CCG holds this list to ensure it can support patients who may need additional services or help in future. It is a way of helping managing system risk for patients with complex needs and helps facilitate system ownership of all these cases, to ensure provision of the right help and support at the right time, in collaboration with the patient and their family.
During the Inquest, it was highlighted that there was a lack of knowledge and understanding of the rights of parent carers of a disabled child to request a separate assessment of their needs; how to carry out the assessment and where the information is held and how needs may be met through Direct Payments. In response to this, KCC has delivered training to families, covering the rights of parents of disabled children to request a Parent Carer assessment, separate to their child’s assessment. They have also introduced new Parent Carer Assessment forms so that social work staff consider and consult with parents of disabled children as to whether a separate assessment of their needs is required, or the parents/carers are content for their needs to be included in the Child and Family Assessment (majority).
3. Concern that there was a lack of psychosocial and psychological therapies offered in this case. This was compounded by the information shared that NELFT may not have been commissioned to provide anything other than a diagnostic service for those presenting with autism and learning disabilities rather than an overt mental health issue.
In terms of the commissioning of services, the CCG actively works with partners across the health system to ensure gaps do not exist and that pathways are in place to cater for the presentations and needs of the local communities it serves. NELFT are commissioned to provide more than just diagnostic services including psychological and psychosocial interventions, but the CCG acknowledge that mental health services are under extreme pressure, with increasing referrals that have significantly peaked during and post pandemic. Therefore, the CCG is actively working with NELFT to ensure that services are developed to meet the needs of all children and young people and to identify areas where the service offer can be strengthened and have increased significant levels of investment to help address this.
Since 2019/20 additional investment of £2.1 million has been made into local Neurodevelopmental services. Whilst unfortunately this did not prevent the tragic death of Sammy, it has subsequently generated improvements to services provided.
This investment includes the commissioning of Nurture UK to deliver an ‘inclusion’ programme in schools to improve educational outcomes for children with Special Educational Needs and Disabilities (SEND). Inclusive schools contain the following elements:
• a belief that all children have the potential to learn and grow
• the ability to respond to the cultural and/or socio-economic needs of the students
• the ability to support positive behaviour in and out of the classroom
• a dedication to seeing each child as an individual
• the modification of curriculum and activities to include all students
“Together with Parents’ is another service which is being jointly funded between the CCG and KCC to provide better support to families in the community. The service was co-produced with parents, carers and professional partners and delivers local support to parents and carers whose child has either received a diagnosis or are awaiting diagnosis for a neurodevelopmental condition. The new service is to ensure parents can access support and information in a timely way before reaching crisis point.
With regard to the psychological treatment offered in this specific case during the episode prior to Sammy’s sad death, the CCG has been assured that NELFT undertook an assessment of need. Sammy’s escalation of need occurred at onset of the pandemic, when statutory services were severely limited in terms of the care they could provide, and the guidance around the management of clinically vulnerable children during the pandemic was in an embryonic stage. Sammy was under the care of a consultant psychiatrist who regularly reviewed and monitored the prescribing of medications. KMCCG understanding of the clinical opinion and expertise of Sammy’s needs was that the psychological intervention of cognitive behavioural therapy would not have been appropriate or effective to meet his needs and hence the more psychosocial intervention of Non Violent Resistance was offered. NVR is an evidence-based psychosocial intervention to support parents in responding to their child’s more challenging needs.
4. Concern that the communications between agencies in this case were inadequate.
As detailed above, several new processes have been put in place to improve the way in which the relevant agencies communicate in a timely manner. Multidisciplinary meetings between agencies are now a matter of course and fundamentally the standard operating procedure for CYPMHS has been amended to ensure that the communication and sharing of expertise is embedded as a business-as-usual activity. This has been emphasised with regards to LD cases specifically, due to the complexity of these, as has the need to involve numerous agencies as standard practice.
KMCCG have worked with NELFT, acute and community trusts, KCC, NHS England and wider partners to improve communications regarding children and young people who have the most complex presentations and are considered at risk. KMCCG has invested in new strategic leadership posts whose role is to drive improved dialogue across agencies and to provide a route for rapid escalation and resolution. Since Sammy’s death, KMCCG have worked in collaboration with system partners to develop and implement shared Kent and Medway escalation policy and protocols. This enables rapid identification of children and young people who need senior leader oversight to ensure appropriate care.
5. Concern that children in other areas with neurodevelopmental needs may be excluded from accessing the care and treatment they need to keep them safe.
Since Sammy’s death, KMCCG has made investments in posts and mechanisms to improve the offer for children and young people with neurodevelopmental presentation. A number of joint posts have been created across the Local Authority and Primary Care so that children and young people with additional needs are identified early and care is coordinated rapidly around the child and family.
Kent partners have been successful in bidding for and mobilising the National NHS England Designated Key Worker Early Adopter programme. This team is based in KCC and is a partnership project across health, the Local Authority and NHSE. The Designated Key Workers provide practice consultancy to multi agency partners/networks and case coordination for children and young people with complex neurodevelopment. The team work in conjunction with the KMCCG Learning Disability and Autism team to ensure referrals to the Dynamic Support Database and CETR processes has better supported the needs of children and young people to avoid placement breakdown and admission to T4 services.
There continues to be developments and innovation focussed on earlier intervention and support for families who have children and young people with neurodevelopment needs. Examples of which include new programmes within schools across Kent to promote inclusive practice and reduce exclusions. Piloting early identification and support of children and young people through a Primary Care multi-disciplinary approach utilising Care Navigators to support meeting the holistic needs of a family.
As a health and care system we are determined to ensure we learn from Serious Incidents such as this tragic case and continue to take appropriate action, as outlined above, to prevent similar occurrences from happening in the future.
From July 2022, Integrated Care Boards will succeed CCGs across the country. The Boards of these organisations will include Partner Members from Local Authorities and NHS Providers, with a focus on greater collaboration and more seamless joint decision making
Action Planned
The Department for Education is working with the Children’s Commissioner’s Office and the Information Commissioner’s Office (ICO) to identify ways to better improve data sharing in child safeguarding cases. They have also committed to publishing an ambitious implementation strategy later this year. (AI summary)
The Department for Education is working with the Children’s Commissioner’s Office and the Information Commissioner’s Office (ICO) to identify ways to better improve data sharing in child safeguarding cases. They have also committed to publishing an ambitious implementation strategy later this year. (AI summary)
View full response
Dear Ms Wood, Thank you for your letter of 9 August 2022, to the Department for Education, about the death of Samuel Alban-Stanley. I am replying as the Minister responsible for Special Educational Needs and Children’s Social Care at the Department for Education. I would like to begin by expressing my deepest condolences to Samuel’s family. This is a tragic case and I agree entirely with my colleague, the former Minister of State for Care and Mental Health, who made clear in her response to you that it is imperative that we learn lessons to improve services to safeguard and prevent harm to vulnerable children and young people. As the former Minister of State for Care and Mental Health set out in her response, at the start of the Covid-1 9 pandemic in March 2020, people with serious underlying health conditions, such as Samuel, were advised to follow shielding measures. This included advice not to attend school, even though education and care settings remained open for vulnerable children (including those with Education, Health and Care (EHC) plans) and children of critical workers. We recognise that such measures had a significant impact on many children’s mental health and wellbeing, which is why the Government prioritised opening education and care settings for all pupils as soon as it was possible. These measures were kept under constant review and advice on shielding was relaxed as soon as it was considered safe to do so. This situation was unprecedented and presented new and unfamiliar demands on local authorities, schools, and other services. The department and local authorities developed and improved processes throughout the response to the pandemic, adapting and learning from the latest scientific and medical advice.
During this time, children and young people with EHC plans were a particular concern for us. The guidance the department issued in March 2020 advised local authorities to undertake an individual assessment of all children and young people for whom they maintained EHC plans, to consider the balance of risk between contracting Covid-19 and the risk of disruption to education and support. We expect that Kent County Council and Samuel’s parents will have taken account of this guidance and the medical advice and wider government guidance that Samuel should follow shielding measures in deciding that he should not continue to attend Laleham Gap special school. am sorry to hear that Samuel was not offered the care and treatment that he needed to keep him safe, and for the poor communication between the agencies that were supposed to provide this care. Local authorities have a duty under s17 of the Children Act 1989 to carry out an assessment of children in need and to provide services to them for the purpose of safeguarding and promoting their welfare. Working together to safeguard children (2018), sets out that safeguarding partners should agree with their relevant agencies the levels for the different types of assessment and services to be delivered, including services for disabled children. Safeguarding partners should then publish a threshold document setting out local criteria for action, including procedures and processes for cases relating to disabled children. It would therefore be for Kent local authority to undertake this. Working together to safeguard children (2018), is clear that local areas should have a comprehensive range of effective, evidence-based services in place to address needs, and that effective sharing of information between practitioners and local organisations and agencies is key. We agree that missed opportunities to share information in a timely manner can have severe consequences for the safety and welfare of children and young people. On the 23 May 2022, the Department for Education made a statement in Parliament about the final report arising from the review of Children’s Social Care. To support delivery of recommended changes, the department are already working with the Children’s Commissioner’s Office and the Information Commissioner’s Office (ICO) to identify ways to better improve data sharing in child safeguarding cases. I understand from your report that Kent County Council has taken steps to reflect on the way its services were delivered during this case. I was pleased to see that more recently, Ofsted rated Kent County Council’s children’s services as outstanding’ in its most recent inspection report, published in July 2022. The report noted the Council’s improvements in areas identified in previous visits and its work to improve services throughout the pandemic. There is nothing more important than protecting children from harm and having a strong and robust system in place to safeguard children and promote their welfare is a key priority for this Government. We have also announced ambitious reforms through publication of the Special Educational Needs and DisabWties and Alternative Provision Green Paper and in response to the Independent Review of Children’s Social Care we have set out actions we are undertaking now to improve support for families and children’s social care and have committed to publishing an ambitious implementation strategy later
this year. I hope this response is helpful. Thank you for bringing these concerns to my attention.
During this time, children and young people with EHC plans were a particular concern for us. The guidance the department issued in March 2020 advised local authorities to undertake an individual assessment of all children and young people for whom they maintained EHC plans, to consider the balance of risk between contracting Covid-19 and the risk of disruption to education and support. We expect that Kent County Council and Samuel’s parents will have taken account of this guidance and the medical advice and wider government guidance that Samuel should follow shielding measures in deciding that he should not continue to attend Laleham Gap special school. am sorry to hear that Samuel was not offered the care and treatment that he needed to keep him safe, and for the poor communication between the agencies that were supposed to provide this care. Local authorities have a duty under s17 of the Children Act 1989 to carry out an assessment of children in need and to provide services to them for the purpose of safeguarding and promoting their welfare. Working together to safeguard children (2018), sets out that safeguarding partners should agree with their relevant agencies the levels for the different types of assessment and services to be delivered, including services for disabled children. Safeguarding partners should then publish a threshold document setting out local criteria for action, including procedures and processes for cases relating to disabled children. It would therefore be for Kent local authority to undertake this. Working together to safeguard children (2018), is clear that local areas should have a comprehensive range of effective, evidence-based services in place to address needs, and that effective sharing of information between practitioners and local organisations and agencies is key. We agree that missed opportunities to share information in a timely manner can have severe consequences for the safety and welfare of children and young people. On the 23 May 2022, the Department for Education made a statement in Parliament about the final report arising from the review of Children’s Social Care. To support delivery of recommended changes, the department are already working with the Children’s Commissioner’s Office and the Information Commissioner’s Office (ICO) to identify ways to better improve data sharing in child safeguarding cases. I understand from your report that Kent County Council has taken steps to reflect on the way its services were delivered during this case. I was pleased to see that more recently, Ofsted rated Kent County Council’s children’s services as outstanding’ in its most recent inspection report, published in July 2022. The report noted the Council’s improvements in areas identified in previous visits and its work to improve services throughout the pandemic. There is nothing more important than protecting children from harm and having a strong and robust system in place to safeguard children and promote their welfare is a key priority for this Government. We have also announced ambitious reforms through publication of the Special Educational Needs and DisabWties and Alternative Provision Green Paper and in response to the Independent Review of Children’s Social Care we have set out actions we are undertaking now to improve support for families and children’s social care and have committed to publishing an ambitious implementation strategy later
this year. I hope this response is helpful. Thank you for bringing these concerns to my attention.
Sent To
- Department of Health and Social Care
- NHS Kent and Medway Clinical Commissioning Group
Response Status
Linked responses
3 of 2
56-Day Deadline
11 Apr 2022
All responses received
About PFD responses
Organisations named in PFD reports must respond within 56 days explaining what actions they are taking.
Source: Courts and Tribunals Judiciary
Report Sections
Investigation and Inquest
On the 14th May 2020 I opened an inquest into the death of Samuel Alban Stanley. At the inquest, which lasted nine days and heard from many of those involved in Sammy’s short life, I concluded on 29th November 2021 with a narrative conclusion “Samuel Alban-Stanley died as a consequence of injuries sustained during an episode of high-risk behaviour, related to his Prader-Willi syndrome, on a background of inadequate support from the Local Authority and Mental Health Services.”
Circumstances of the Death
(1) Samuel Alban Stanley was the eldest of four children and a loving caring little boy who was cared for by a dedicated family. Unfortunately, he suffered from Prader-Willi syndrome, a rare genetic condition with a known association with behavioural problems which often increase with age. Not unexpectedly as Sammy got older his behavioural problems increased and at times these were incredibly high risk including trying to jump out of moving cars, building windows and into the sea. Police intervention was required, at times, to assist the family in managing his behaviour. (2) In 2018 he and his family moved to Kent and after a prolonged period, including appeals against decisions to place him in a mainstream school, he was placed in Laleham Gap school in March 2019 and he thrived in the supportive environment provided by the school. Concerns about his behaviour remained and he was at risk of significant harm when he was in a distressed and emotional state. His family struggled to manage his high risk behaviours in particular at times such as the school holidays and they had repeatedly requested assistance from social services. (3) In March 2020 he was deemed to be vulnerable to the effects of Covid 19 and advised to shield which meant he no longer had access to the supportive school environment. A child in need meeting was held on 17 April 2020 to discuss support for the increased risks of Sammy being at home but no support was provided. (4) On 22 April 2020 Sammy left his house early in the morning and was seen to and despite prompt treatment and attention he died in Kings College hospital on 26 April 2020 as a consequence of his injuries.
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Data sourced from Courts and Tribunals Judiciary under the Open Government Licence.