Prevention of Future Deaths reports · 2026
Regulation 28 report to prevent future deaths, reference 2026-0302, written 15 Jun 2026. A coroner writes one of these when an inquest reveals a risk that could cause further deaths unless something changes.
| Date of report | 15 Jun 2026 |
|---|---|
| Reference | 2026-0302 |
| Deceased | Alex Ganski |
| Coroner | Joseph Turner |
| Coroner area | West Sussex, Brighton and Hove |
| Organisation named | Sussex Partnership NHS Foundation Trust · South East Coast Ambulance Service NHS Foundation Trust |
| Source | judiciary.uk record |
| Responses published | 1 |
Text extracted from the PDF text layer. Reproduced verbatim, including the scan's own layout.
REPORT TO PREVENT FUTURE DEATHS REGULATION 28 OF THE CORONERS (INVESTIGATIONS) REGULATIONS 2013 Please do not include any living persons’ names in this document, in accordance with the Chief Coroner’s PFD Publication Policy (2026). 1. 2. 3. CORONER I am Joseph TURNER, Area Coroner, for the coroner area of West Sussex, Brighton and Hove. DATE OF REPORT 15 June 2026 CORONER’S LEGAL POWERS I make this report under paragraph 7, Schedule 5, of the Coroners and Justice Act 2009 and regulations 28 and 29 of the Coroners (Investigations) Regulations 2013. 4. THIS REPORT IS BEING SENT TO 1. (Secretary of State for Health and Social Care – response already received) 2. NHS England You are under a duty to respond to this report within 56 days of the date of this report, namely by August 10, 2026. I, the coroner, may extend the period if an appropriate application is made. 5. YOUR RESPONSE Your response must contain details of action taken or proposed to be taken, setting out the timetable for action. Otherwise, you must explain why no action is proposed. I have a duty to send a copy of your response to the Chief Coroner. In accordance with the Chief Coroner’s Publication Policy, you should send me any representations regarding publication of your response. These representations should be made at the same time as the response is provided. I will pass any representations received to the Chief Coroner for a decision. Please note any links to webpages included in the response will not be checked for sensitive information prior to publication, as the information is already online. The names of those who do not respond to PFD reports are regularly published on the Chief Coroner’s webpages Non-responses to Prevention of Future Death (PFD) reports - Courts and Tribunals Judiciary. SUMMARY OF CORONER’S CONCERN 6. The principal concern on which I now seek comment from NHS England is as to the apparent absence of any national guidance/advice to frontline emergency crews who may be called to patients with complex and overlapping clinical, behavioural and addiction issues, but who may be unaware of the full extent of these and/or of partner agencies’ involvement. Whilst I understand the need for ambulance services to triage patients according to their immediate presentation, this is currently a missed opportunity to update and refer them to partner agencies. 7. ACTION SHOULD BE TAKEN In my opinion unless action is taken to address the above concerns then there is a significant risk of future deaths and I believe each of you have the power to take such action. 8. INVESTIGATION AND INQUEST Alex Ganski sadly died from injuries sustained when he jumped from a bridge on 20th July 2024. This was the fifth occasion in three years he had visited the same location with thoughts of self harm. His death was referred to the Coroner Service by Sussex Police and an investigation under s.1 Coroners and Justice Act 2009 was opened on 22nd July 2024. The inquest was held on 19th March 2026. The inquest concluded that Alex took his own life following traumatic events earlier in his life causing depression and long-term suicidal thoughts, leading to the use of illicit drugs. He had suddenly absconded from home that evening whilst under the influence of ketamine and diazepam, having relapsed following a period of addiction support. He was receiving specialist care for his mental health but there had not been fully shared information between the services supporting him, or a clear overall lead, creating a missed opportunity to more closely address the confluence of poor mental health, drug misuse, and resulting risk of self-harm. 9. CIRCUMSTANCES OF DEATH Alex was 19 but had undergone traumatic events in his teens which led to long term mental health struggles and suicidality. At the time he died he was under the care of the local Trust’s Mental Health Assessment and Treatment service, with a Registered Mental Health Nurse as his lead practitioner. Contact had been consistent. He had been misusing cannabis, ketamine and diazepam intermittently for some years, although had latterly ceased the latter two drugs whilst receiving support from the local Drug and Alcohol Wellbeing Network. He had been formally diagnosed with suicidal thoughts, anxiety and depression and his GP had prescribed medication although Alex had ceased taking this some weeks prior to death, with the GP’s knowledge. Although he had undergone assistance to reduce drug misuse, he had several relapses. Two weeks before he died thishad resulted in the ambulance service attending to him, although he declined to be taken to hospital, contrary to paramedic advice. His drug support network was unaware of and not alerted to this incident. The week before he died he had overdosed on tablets bought on the internet. He appeared to have made a physical recovery but was granted mental health leave by his employer that week. He spent the week at home or on family day trips. His mood was low but there were no immediate concerns. However, he purchased several combined packs of despite family attempts to intervene. On the Saturday evening he had indicated willingness to consider a rehabilitation facility in his native Poland but he also made a further drug purchase. Suddenly at around 9.20 he burst out of the house and proceeded to a nearby bridge jumped sustaining fatal injuries. This was the fifth occasion in three years he had visited the same location with thoughts of self harm. and diazepam from a local dealer on the Friday and Saturday, , from which he 10. CORONER’S CONCERNS During the course of the inquest I heard evidence giving rise to concern. In my opinion there is a risk that future deaths could occur unless action is taken. In the circumstances it is my statutory duty to report to you. The MATTERS OF CONCERN are as follows: The evidence disclosed that whilst there were multiple agencies, organisations and healthcare providers who had been treating or triaging Alex’s mental and physical health conditions, including his misuse of illicit drugs: a. There was no – and nationally there appears to be no - policy, guidance or structure which would enable a designated lead, or ‘single point of contact’ with full oversight of, and (more importantly) authority over, Alex’s care – taking particular account of his young age. b. This represents a ‘care gap’ and missed opportunity whereby a nominated lead could ensure that each incident, attendance, relapse or overdose was alerted to those other agencies, organisations or providers who would need to know or who may benefit from knowing of the occurrence. And then – critically - directing and assuring the right treatment or long-term intervention to follow. c. The sharing and updating of information regarding Alex’s multiple health and drug issues was fragmented, in the absence of clear, national protocols and requirements as to the informing and alerting of new incidents, treatment, or other change in mental or physical health or addiction. d. I was encouraged to learn of the Plexus Care Record initiative in this local area (Plexus Care Record) but the evidence was that this is voluntary, and that not all providers or agencies are able or willing to connect or provide their records and share information. Moreover, I heard evidence that this is a local but not national initiative and hence information and record sharing elsewhere may be worse. As such the situation is ameliorated by local changes but appears to be a wider and national issue. I found that these factors were exacerbated in Alex’s case as a vulnerable 19 year old who had clearly been suffering with poor mental health and drug misuse whilst, and since, a child, noting that he lacked the experience and knowledge to successfully advocate for himself, or insight into his own needs. My further concern is that there was no simple mechanism or designation across thevarious patient record systems for those who may become involved with Alex, to know of the significant wider and historical health and drug misuse issues, in the absence of his own willingness or ability to fully disclose these at each turn. Especially when he may have been under the influence of substances. This meant repeated opportunities to better address Alex’s serious underlying conditions and issues were not taken. This lack of an easily recognised national designator, shown across systems and records,such as ‘person at [serious] risk’ gives rise to an incomplete understanding of, and risks a failure to sufficiently enquire into, someone’s full condition as and when services become intermittently involved, and creates a risk of further similar deaths. I add that I am very conscious of the Chief Coroner’s guidance to consider what can practically be achieved and not to engage with ‘ideal world’ scenarios, as well as considering the realistic prospect, including on resource grounds, that this report will be acted upon. I respectfully see no such barriers as regards the ‘lead point of contact’. I recognise information sharing will be subject to data protection and handling, consent, privacy and confidentiality issues, but progress has been made locally within existing resource and I consider that these issues need to be better addressed in the national healthcare context, else they will continue to be barriers to preventing deaths, rather than enablers to save lives. 11. COPIES AND PUBLICATION OF THIS REPORT I have a duty to send a copy of my report to every Interested Person who in my opinion should receive it. I also may send a copy of the report to any other person who I believe may find it useful or of interest. I can confirm I have sent the report to: [please do not use individual’s names, but instead roles/titles] Alex Ganski’s Mother Sussex Partnership NHS Foundation Trust Change Grow Live (West Sussex) South East Coast Ambulance Service NHS Foundation Trust Chief CORONER (REG 28) I also have a duty to send a copy of the report to the Chief Coroner. You may make representations to me, the coroner, about the publication of the contents of this report in line with Chief Coroner’s PFD Publication Policy (2026). Any representations will be sent to the Chief Coroner alongside the report. Please refer to box 4 above for additional information relating to the publication of reports and responses. 12. SIGNATURE Joseph TURNER Area Coroner for West Sussex, Brighton and Hove
1 response published against this report on judiciary.uk. A response is a body's written reply to the coroner's concerns; publication is at the discretion of the Chief Coroner's office, so an absent response does not mean nobody replied.
Mr Joseph Turner
HM Area Coroner
West Sussex, Brighton and Hove
The Coroner’s Office
Woodvale
Lewes Road
Brighton
BN2 3QB
National Medical Director
NHS England
Wellington House
133-155 Waterloo Road
London
SE1 8UG
3 August 2026
Dear Mr Turner,
Re: Regulation 28 Report to Prevent Future Deaths – Alex Ganski who died on
20 July 2024.
Thank you for your Report to Prevent Future Deaths (hereafter “Report”) dated 15
June 2026 concerning the death of Alex Ganski on 20 July 2024. In advance of
responding to the specific concerns raised in your Report, I would like to express my
deep condolences to Alex’s family and loved ones. NHS England is keen to assure
the family and yourself that the concerns raised about Alex’s care have been listened
to and reflected upon.
Your Report raised the following concerns:
1. There is a lack of national policy, guidance or structure to enable there to be a
designated lead or ‘single point of contact’ with full oversight of, and authority
over a patient’s care in the community and who could alert all agencies involved
in providing care of any changes with the patient.
2. A lack of national protocols means the sharing and updating of information
relating to physical and mental health changes and addiction was fragmented.
3. There is no national initiative to share records and information across agencies
and currently depends on voluntary local arrangements.
4. There is an absence of guidance or advice to frontline emergency crews who
are called to patients with complex and overlapping clinical, behaviour and
addiction issues, when such crews may be unaware of the extent of partner
agency involvement. This creates a missed opportunity to update and refer
them to partner agencies.
1. National policy to enable a designated lead for care
As part of a national pilot to transform mental health care, six new neighbourhood
mental health hubs are being developed across England.
These hubs are designed to bring services closer to home, offering round-the-clock
support in local settings. They provide walk-in access, co-located support teams, and
in some cases, short-stay beds — all helping to reduce hospital admissions and
provide earlier, more joined-up care.
The 24/7 Neighbourhood Mental Health Centre (NMHC) model represents a
fundamental shift in how mental health care is organised, addressing long-standing
issues of fragmented provision and poor continuity of care. Traditional systems often
require people to navigate multiple services, repeat their story, and experience unclear
thresholds and disjointed support. NMHCs respond directly to this by offering an open-
access, neighbourhood-based model that simplifies pathways and centres care
around the person.
A key strength of the model is its focus on continuity of care. Rather than being passed
between different teams such as community, crisis, and inpatient services, individuals
are supported by one consistent team across their whole journey. This reduces
duplication, avoids repeated assessments, and enables staff to build strong, trusting
relationships. These relationships are critical in mental health care, supporting better
engagement, earlier identification of deterioration, and more personalised care.
This integrated approach improves oversight of care. With shared information
systems, joint working, and a clear sense of responsibility for a defined neighbourhood
population, teams are better able to understand an individual’s needs and respond
proactively. The model supports improved information sharing and real-time
coordination, meaning risks can be identified earlier and care can be adjusted quickly.
As a result, people are less likely to fall through gaps or experience crisis escalation
due to disconnected services.
NHS England has piloted the approach over the past two years, with an independent
evaluation. Further roll-out is currently underway.
2. National protocols for sharing information about changes to a person’s
health
NHS England is committed to supporting the sharing of critical clinical information
across NHS organisations. This is discussed in more detail at point 3below.
The Connecting Care Records (ConCR) programme facilitated the extensive and
collaborative sharing of patient data and information across care settings and
geographic boundaries to enable the delivery of more patient-centred care, in line with
the NHS 10 Year Health Plan and Long Term Plan.
The NMHC model detailed above, supports improved information sharing and real-
time coordination, meaning risks can be identified earlier and care can be adjusted
quickly. As a result, people are less likely to fall through gaps or experience crisis
escalation due to disconnected services.
3. Lack of a national initiative to share records and information
The National Care Records Service (NCRS) provides a quick, secure way to access
national patient information to improve clinical decision making and healthcare
outcomes, and it is free to use. NCRS is internet based, accessible via a web browser.
NHS England’s national digital team have advised that they would expect the local
Mental Health Trust, and the local Drug and Alcohol treatment service to have access
to patient’s summary care records via NCRS however utilisation of this resource will
vary according to the local business processes. Further information on NCRS can be
available here: National Care Records Service - NHS England Digital.
The NCRS provides access to a patient’s Summary Care Records (SCR). The SCR is
a national database that holds electronic records of important information such as a
current medication, allergies and details of any previous bad reactions to medicines.
It is created from GP medical records – whenever a GP record is updated, the changes
are synchronized to SCR. It can be seen and used by authorised staff in other areas
of the health and care system who are involved in the patient’s direct care but do not
need access to the patient’s full record. As such, the SCR is intended to provide a
summary to patient’s during an unscheduled care encounter.
As a minimum, the SCR contains important information about:
• Current medication
• Allergies and details of any previous reactions to medicines
• The name, address, date of birth and NHS number of the patient
In addition, details of long-term conditions, significant medical history, or specific
communications needs, are now included by default with an SCR, unless the client
has previously told the NHS that they did not want this information to be shared.
Further information, and to illustrate the type of content included in an SCR, an
example of SCR is available here: Additional Information in SCR - NHS England Digital
Additional information in the SCR includes the active problems and significant past
problems (from Optum/TPP/Medicus provider systems) for a patient as recorded by
their registered GP practice.
The SCR can also include more information in addition to the patient’s current
medication, allergies and adverse reactions to medicines which is referred to as
‘Additional Information’. This ‘Additional Information’ may include significant medical
history, anticipatory care information (such as information about the management of
long-term conditions), immunisations or specific communication needs. This is now
included by default for patients with an SCR, unless they have previously told the NHS
that they did not want this information to be shared. This can include, for example, any
history of deliberate self harm, suicide attempts or suicidal ideation. The SCR is not
intended to include the full detail of a patient’s care plan and the design/format of the
SCR does not support this. However, the SCR can include a signpost to the existence
of a care plan, either by a relevant code such as:
• Emergency health care plan
• Emergency medicine care plan
• Liaison psychiatry care plan
• Mental health crisis plan
• Crisis plan
• Treatment escalation plan
• Vulnerable adult care plan
• Community mental health care plan
• Or via a text free entry
Regarding SCR, as of 29 June 2026, 88% of the population of England (approx. 60
million patients) have an SCR with Additional Information, 7.3% have a Core Only
SCR (Allergies and Medications only) and 1.5% have Opted Out of SCR. Furthermore,
where possible, patient’s need to provide their Permission to View before their SCR
can be accessed. However, an Emergency Access option is available for scenarios
where a patient is not able to provide their Permission to View e.g. the patient is
unconscious.
NHS England’s National Record Locator (NRL) service allows health or social care
workers to find and access patient information shared by other health and social care
organisations across England, to support the direct care of a patient. It does this by
recording the location of digital (and paper) records within the NHS and provides an
index of pointers/bookmarks that contain the information required to retrieve key
patient information from the source. The vision is to improve cross-border
interoperability and help make data sharing possible by allowing healthcare
professionals, such as Care Coordinators within a Mental Health Trust to securely and
remotely retrieve information from source at the point of need so that they can get a
longitudinal view of a patient’s records and an indication of their treatment history. The
National Record Locator (NRL) removes the need for organisations to create duplicate
copies of information across systems and organisations, by facilitating access to up-
to-date information directly from the source. It will also provide users with an indication
of the organisations with which a patient currently has a care relationship to enable a
user to contact the service responsible for a plan to support the individual in the event
of a crisis.
Mental Health Crisis plans are one of the pointer types supported by the NRL Service.
NRL does not store any of the Mental Health data but points users to where they can
find it. NRL Information can be consumed from source through the National Care
Records Service (NCRS). In instances where multiple pointers are returned, users
have the ability to sort results by creation date.
With regards to the sharing of care plans, the NHS tends to share those Care Plans
that need to be viewed by multiple different healthcare professionals and organisations
with those organisations that are involved with creating, managing and updating these
care plans (as well as the patient). However, those care plans which are more service
specific that detail how a patient should be cared for by a specific service are less
likely to be shared with multiple other healthcare providers that may be involved in the
patient’s care.
Connecting Care Records
The NCRS complements Connecting Care Records (ConCR), also known as Shared
Care Records. Every Integrated Care Board (ICB) has a shared care record (ShCR)
in place, which provides, through different suppliers, a mechanism to access shared
information between NHS Trusts and general practice. Shared Care Records will
include prescribed medications and will typically hold more information about an
individual than a Summary Care Record.
A number of primary care networks, local authorities and other community
organisations are also accessing information from the ShCR and providing information
into their local ShCR.
Responsibility for delivering shared care records sits with local Integrated Care Boards
(ICBs). Each ICB’s shared care records are developed in response to the health and
care needs of the local area, existing systems, and future planning. This means some
of their shared care records are available to neighbouring ICBs, while others are only
supported within their own ICB. Future plans include making shared care records link
together regardless of where you live or receive care in England.
The interoperability programme of work supports the provision of interoperable
records across England, sharing patient data across health and social care providers
through ShCRs. National interoperability is needed as circa 20% of patients have care
provided outside of their home ICB boundary. This work is evolving into the Single
Patient Record, which will bring together a patient’s health information so that it is
joined up across all health and care settings.
We note that ‘Plexus’ provides the shared care record for Sussex, and they are already
connected to the National Record Locator (NRL). They are sharing patient pointers to
Mental Health Crisis Plans from Sussex Partnership NHS FT, and they went live on 3
November 2025. However, the PDF documents they are sharing do not currently
contain any clinical information specific to the patient – it’s a generic document that
contains the SPFT team contact information.
Further information should be sought with regards to the actual content of the SCR
and information held on ConCR in addition to accessed clinical information which may
help assist with the identification of the ‘Care Gaps’ to which the Coroner refers.
Your Report indicates that Alex had formally been diagnosed with suicidal thoughts,
anxiety and depression and drug misuse so it would be reasonable to expect that
these diagnoses and medications prescribed for anxiety and depression (including the
‘Last Issued’ dates) would be visible in Alex’s SCR provided the patient had not ‘opted
out’. Brief further clinical details, for example, regarding the history of suicidal thoughts,
previous overdoses or acts of deliberate self-harm, and the use of illicit drugs
(cannabis, ketamine and diazepam) may also have been included in Alex’s SCR
where this information had been coded into Alex’s GP record. The SCR would have
been available to paramedics / front line emergency staff.
Furthermore, SCR can include signposting (and possibly contact details) for other
healthcare services and professionals that are involved in the patient’s care for
example, the local Trust Mental Health assessment and treatment service, the
patient’s registered Mental Health Nurse, the local Drug and Alcohol Wellbeing
network key worker, the emergency contact details of a specialist support team, where
this information had been recorded and coded into the patient’s GP record. However
the SCR does not contain correspondence, so would not include information regarding
the correspondence between the local Mental Health Trust and patient’s registered
GP or other services involved.
The local drug and alcohol service are currently commissioned by the Local Authority
and not the NHS and as such they run on different systems. However, the NHS
England South East Region advises us that the two services work together where they
can.
As noted above, NHS England and DHSC have published Fit for the Future: 10 Year
Health Plan for England, which sets out the government’s plan for healthcare in
England over the next decade. The Plan includes a commitment to give patients ‘a
single, secure and authoritative account of their data – a single patient record’ to
support more coordinated, personalised and predictive care.
4. Absence of guidance or advice to frontline emergency crews
Ambulance clinicians are primarily responsible for assessing and managing the
patient's immediate clinical needs and determining the most appropriate course of
action based on the information available at the time.
Ambulance clinicians may have access to additional patient information through
systems such as the Summary Care Record and other locally available shared care
records, where these are available and appropriate to access. Access to information-
sharing systems and the extent of information available varies between local areas.
National policy and professional guidance are clear that appropriate information
sharing is a fundamental part of delivering safe and effective care across the NHS.
Clinicians are also able to share relevant information for the purposes of direct care in
accordance with established information governance principles.
Where a patient consents, or where information sharing is otherwise justified for direct
care, ambulance clinicians may contact other healthcare professionals or specialist
services involved in a patient's care. However, the availability of referral routes,
specialist services and information-sharing arrangements is determined locally and is
not subject to a single nationally mandated model.
National policy and professional guidance are clear that appropriate information
sharing is a fundamental part of delivering safe and effective care across the NHS.
NHS England continues to support improvements in interoperability and the
development of shared care records to enable safer, more joined up care. This under
pins the approach of moving from analogue to digital, hospital to community and
treatment to prevention as outlined in the 10 Year Health Plan. These developments
aim to improve information flow while ensuring that data is shared with appropriate
clinical context and in line with professional standards, so that information generated
in one care setting is not misinterpreted or used inappropriately in another.
I would also like to provide further assurances on the national NHS England work
taking place around the Reports to Prevent Future Deaths. All reports received are
discussed by the Regulation 28 Working Group, comprising Regional Medical
Directors, and other clinical and quality colleagues from across the regions. This
ensures that key learnings and insights around events, such as the sad death of Alex,
are shared across the NHS at both a national and regional level and helps us to pay
close attention to any emerging trends that may require further review and action.
Thank you for bringing these important patient safety issues to my attention and please
do not hesitate to contact me should you need any further information.
Yours sincerely,
National Medical Director
NHS England
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