Prevention of Future Deaths reports · 2026
Regulation 28 report to prevent future deaths, reference 2026-0188, written 1 Apr 2026. A coroner writes one of these when an inquest reveals a risk that could cause further deaths unless something changes.
| Date of report | 1 Apr 2026 |
|---|---|
| Reference | 2026-0188 |
| Deceased | Colin Foley |
| Coroner | Paul Marks |
| Coroner area | East Riding and Hull |
| Category | Hospital Death (Clinical Procedures and medical management) related deaths |
| Organisation named | Hull University Teaching Hospitals NHS Trust |
| Source | judiciary.uk record · original PDF |
| Responses published | 1 |
Text extracted from the PDF text layer. Reproduced verbatim, including the scan's own layout.
ANNEX A REGULATION 28: REPORT TO PREVENT FUTURE DEATHS (1) NOTE: This form is to be used after an inquest. REGULATION 28 REPORT TO PREVENT FUTURE DEATHS THIS REPORT IS BEING SENT TO: 1. Chief Executive N.H.S. England 2. 3. 4. 5. 6. 7. 8. 9. 10. 1 CORONER I am Professor Paul Marks, Senior Coroner, for the Coroner Area of City of Kingston Upon Hull and the County of the East Riding of Yorkshire. 2 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. 3 INVESTIGATION and INQUEST On 10th October 2025, I commenced an investigation into the death of Colin Foley, aged 84 years. The investigation concluded at the end of the inquest on 11th March 2026, the narrative conclusion of the inquest was:- Colin Foley was admitted to Hull Royal Infirmary on the 8th June 2025 with decompensated cardiac failure. He received treatment with intravenous frusemide according to standard practice. The intravenous cannula in his right forearm became painful, failed, and had to be removed. It subsequently became infected and this developed into cellulitis, sepsis, which caused multiorgan failure and Mr Foley's death on the 28th June 2025. Whilst the infection could have been picked up earlier and antibiotics commenced, it cannot be said on the evidence heard, that earlier treatment would have prevented his death. 1 4 CIRCUMSTANCES OF THE DEATH The findings of fact are attached. 5 CORONER’S CONCERNS During the course of the inquest the evidence revealed matters giving rise to concern. In my opinion there is a risk that future deaths will occur unless action is taken. In the circumstances it is my statutory duty to report to you. The MATTERS OF CONCERN are as follows. – Evidence was heard at inquest that the insertion of intravenous access devices are frequently performed procedures in clinical practice which require meticulous attention to detail, not only in their insertion and maintenance, but also in the documentation surrounding them, as well as awareness of associated complications, some of which may be life threatening, that may occur. Whilst the Hull University Teaching Hospitals have instituted on-going training which will continue in perpetuity, I believe that the NHS at large should be aware of issues that relate to these commonly performed procedures. 6 ACTION SHOULD BE TAKEN In my opinion action should be taken to prevent future deaths and I believe you and your organisation has the power to take such action. This may include, for example, providing on-going training and audit relating to the use of these ubiquitous medical devices. YOUR RESPONSE 7 You are under a duty to respond to this report within 56 days of the date of this report, namely by 27th May 2026. However, if you are able to comply with this, I, the coroner, may extend the period. 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. 8 COPIES and PUBLICATION I have sent a copy of my report to the Chief Coroner and to the following Interested (Son); Hull University Teaching Hospitals NHS Trust; I am also Persons sending a copy to the Department of Health and equivalent organisations in the other countries of the United Kingdom. I am also under a duty to send the Chief Coroner a copy of your response. The Chief Coroner may publish either or both in a complete or redacted or summary form. He may send a copy of this report to any person who he believes may find it useful or of interest. You may make representations to me, the coroner, at the time of your response, about the release or the publication of your response by the Chief Coroner. 9 2 1st April 2026 3
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.
Professor Paul Marks
Senior Coroner for City of Kingston Upon Hull
and the County of the East Riding of Yorkshire
Coroner’s Service
The Guildhall
Alfred Gelder Street
Hull
HU1 2AA
National Medical Director
NHS England
Wellington House
133-155 Waterloo Road
London
SE1 8UG
8th May 2026
Dear Coroner,
Re: Regulation 28 Report to Prevent Future Deaths – Colin Foley who died on
28th June 2025.
Thank you for your Report to Prevent Future Deaths (hereafter “Report”) dated 1st April
2026 concerning the death of Colin Foley on 28th June 2025. In advance of
responding to the specific concerns raised in your Report, I would like to express my
deep condolences to Mr Foley’s family and loved ones. NHS England is keen to assure
the family and yourself that the concerns raised about Mr Foley’s care have been
listened to and reflected upon.
Your Report raises concerns regarding the insertion of intravenous access devices,
their maintenance and the documentation surrounding them. You were concerned that
awareness needed raising to the NHS at large of their associated complications, which
may be life threatening.
Infection Prevention Control
The NHS recognises that the insertion and management of intravenous (IV) access
devices are among the most commonly performed clinical procedures but are not
without risk. These procedures require a high level of technical competence, careful
clinical decision-making, and accurate documentation. Complications associated with
vascular access devices, including infection and device failure, can in some cases be
serious or life-threatening.
At a national level, established guidance already supports safe and standardised
practice. The UK Vessel Health and Preservation (VHP) Framework (2020)promotes
a proactive, evidence-based approach to vascular access. This includes early
assessment of patients, appropriate device selection using the “Right Line” approach,
daily review of device necessity, and prompt recognition and management of
complications. The Framework also emphasises consideration of alternative routes of
treatment where clinically appropriate.
In addition, national infection prevention standards, including NICE Quality statement
5: Vascular access devices and High Impact Intervention (HII) care bundles, set out
the essential elements required during insertion and maintenance of vascular access
devices. These measures are designed to reduce the risk of harm, particularly device-
related infection, and rely on consistent application in all care settings.
The Device-Related Infection Prevention Practice (DRIPP) improvement collaborative
(2019) has further supported this work at a national level by developing and promoting
evidence-based resources and shared learning to strengthen practice across
organisations.
The concerns raised in Mr Foley’s case reinforce the importance of a continued
national focus on vascular access safety, including education, training, and the
consistent application of existing guidance. Work will continue across the NHS to
support organisations in embedding these principles and auditing compliance to
reduce avoidable harm associated with these commonly performed procedures.
In addition, there is specific learning supported by NHS England through the NHS
Learning Hub and the e-Learning for Health site which both contain a training package
known as the IV Therapy Passport. The passport contains several parts to support
best practice for intravenous access including:
•
•
•
•
•
•
•
An introduction to IV therapy
The intravenous route
Vascular access devices
Risks and complications of intravenous therapy
Fluids and electrolytes in intravenous therapy
Preparation and administration of intravenous medicines
Drug calculations in intravenous therapy
There is also a portal option to provide feedback on the content which was last updated
in October 2025.
We trust this response provides assurance that this area is recognised and addressed
at a national level.
Nursing
Nursing staff responsibilities for patients with IV access devices include daily
inspection before each access or whenever the patient reports pain or discomfort,
maintaining clean, dry, intact dressings, use of aseptic non touch technique for access
and flushing and prompt escalation and removal if concerns identified. The cannula
should be changed only when clinically indicated and includes checking for: pain,
redness, swelling, exudate, signs of infection or phlebitis and secure dressing and
patency. This should be clearly documented in the patient’s medical records.
Insertion bundles emphasise the use of aseptic non touch technique (ANTT), effective
hand hygiene, appropriate skin antisepsis (chlorhexidine alcohol preparation with
sufficient drying
time), correct site and device selection, securement, and
comprehensive documentation of insertion details. The evidence base shows that
omission or inconsistent application of any individual element increases the risk of
local infection and treatment failure, particularly in frail older adults.
From a nursing perspective, peripheral intravenous cannula (PIVC) care is best
understood as an intervention, requiring structured systems and a consistent
application of evidence-based practice. National guidance describes this as a safety
critical nursing activity requiring meticulous attention to detail throughout the full life
cycle of the device: insertion, ongoing assessment, maintenance, and timely removal.
National frameworks recognise that safe IV care is influenced not only by individual
competence, but by organisational systems, including education, competency
assessment, audit, staffing, and leadership oversight. In high acuity areas caring for
frail older adults, nurses must frequently manage multiple intravenous devices
alongside competing clinical priorities. Standardised bundles, supported by ongoing
training and audit, are therefore essential to safeguard quality and reduce reliance on
informal practice variation.
The Royal College of Nursing’s Standards for Infusion Therapy states that nurses are
professionally accountable for safe management of intravenous therapy, including
assessment, documentation, escalation and removal, while also recognising that
organisations hold responsibility for ensuring staff are trained, competent and
supported by clear policies.
The Nursing and Midwifery Council (NMC) reinforces that employers must provide
systems, staffing, education and resources that enable nurses to practise safely, and
that failures in care often arise from system pressures rather than individual error.
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 Mr
Foley, 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 Director of Patient Safety
NHS England
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