Welcome to the Royal College of Emergency Medicine’s Safety Resources hub. Here you will find information and resources about alerts, safety resources, safety in the Emergency Department and safety events.
Patient Safety
What is Patient Safety?
Patient Safety is the avoidance of unintended or unexpected harm to people during the provision of healthcare.
What is the Royal College of Emergency Medicine doing about patient safety?
The College has established a Safer Care Committee which is undertaking the following:
- Developing and disseminating patient safety and risk management strategies for the speciality of Emergency Medicine
- Advising and collaborating with NHS England Patient Safety Team, NHS Resolution, HSSIB, the UK Clinical Pharmacy Association, NCEPOD, the Royal Colleges and other national bodies who have an interest in risk management and patient safety in Emergency Departments
- Developing and identifying resources for patient safety
- Informing Fellows and Members of patient safety research, key publications and resources
- Reviewing of significant incident reports in emergency medicine
To see the terms of reference and committee members e-mail safety@rcem.ac.uk
Safety Flashes & News Alerts
RCEM Safety Flashes
Click on the links below for the latest information.
- Glucocorticoid Steroid Dependency (June 2025 Update)
- Glycerol Toxicity from Slushies (Updated June 2025)
- Euglycaemic DKA with SGLT-2 Inhibitor (-flozin) (April 2025)
- Water Beads and Bowel Obstruction (December 2024)
- Ingestion of super strong magnets in children (Updated December 2024)
- Undetected button and coin cell battery ingestion in children (Updated December 2024)
- Handlebar Injuries in Children (November 2024)
- Glycerol Toxicity from Slushies (September 2024)
- MPox Outbreak (September 2024)
- Pabrinex Shortage (August 2024)
- Cortico Steroid Dependency (December 2023)
- Time Critical Medications (November 2023)
- World Safety Day - Engaging patients for patients safety (September 2023)
- Nitrous Oxide Associated Neuropathy (December 2022)
- Shortages of Alteplase and Tenecteplase (September 2022)
- Monkey Pox Evolving Situation - (May 2022)
- Wearable Diabetes Technology - (March 2022)
- Meningitis - (November 2021)
- Drug errors in high-pressure or infrequent situations (August 2021)
- Communication errors with PPE (Update March 2021)
- Think Ectopic (February 2021)
- Appropriate PPE and risk assessment (December 2020)
- NEWS2 and oxygen requirement (December 2020)
- PPE Importance (November 2020)
- Localised cutaneous argyria after nasal cautery (August 2020)
- Children & COVID-19 Clinical Brief (June 2020)
- Airway management in COVID-19 Pandemic (May 2020)
- All that glitters… Things to remember during the COVID pandemic (May 2020)
- Salbutamol, peak flow and nebulisation advice during Covid-19 (April 2020)
- People with diabetes and COVID-19 (April 2020)
- Buddy System (April 2020)
- Anorexia Nervosa (January 2020)
- Silver Trauma (September 2019)
- Silver Nitrate: Spot the difference (May 2019
- Take your breaks and stay safe (March 2019)
- Absconding (June 2018)
- Aortic Dissection poster and podcast (April 2018)
- Pressure Ulcers (April 2018)
- Fascia Iliaca Block (FIB) and RCEM statement (February 2018 revised)
- Time critical medicines (November 2017)
- Abnormal results (October 2017)
- Retained guidewires (August 2017)
- IV administration of Oramorph (July 2017)
- Insulin errors in the ED (May 2017)
- Missed hip fractures (Jan 2017)
- Phenytoin toxicity (Nov 2016)
- Oral dentures (Sept 2016)
- Inadvertent injection of solutions intended for topical use (Aug 2015)
Clinical Learning Case
Click on the link below for the latest information.
- Cocaine Induced Bowel Ischaemia (August, 2018)
Legal Learning Case
Click on the link below for the latest information.
- Accurate waiting time information (December, 2018)
Health Services Safety Investigations Body (HSSIB) Reports
The Healthcare Safety Investigation Branch (HSIB) conducts independent investigations of patient safety concerns in NHS-funded care across England. HSIB aims to improve safety through effective and independent investigations that don't apportion blame or liability. Investigations identify the contributory factors that have led to harm or have the potential to cause harm to patients. The recommendations aim to improve healthcare systems and processes in order to reduce risk and improve safety.
- Assessment of risk during the maternity pathway | HSIB
- HSIB focus group - investigation into the diagnosis of non-accidental injuries in infants
- Clinical decision making: diagnosis of pulmonary embolism in emergency departments | HSIB
- Local integrated investigation pilot 3:Transfer of a patient who had suffered a stroke to emergency care | HSIB
- Weight-based medication errors in children | HSIB
- Treating COVID-19 patients using Continuous Positive Airway Pressure - Report (HSIB, November 2021)
- Treating COVID-19 patients using Continuous Positive Airway Pressure - Summary (HSIB, November 2021)
- Surgical Care of NHS Patients in Independent Hospitals (HSIB, October 2021)
- Missed detection of lung cancer on chest x-rays of patients being seen in primary care (HSIB, October 2021)
- Intrapartum Stillbirth Report - Final (HSIB, September 2021)
- Intrapartum Stillbirth Supplement (HSIB, September 2021)
- A thematic analysis of HSIB's first 22 national investigations (HSIB, September 2021)
- Timely detection and treatment of cauda equina syndrome (HSIB, August 2021)
- Oxygen issues during the Covid-19 pandemic - Report (HSIB, June 2021)
- Oxygen issues during the Covid-19 pandemic - Summary (HSIB, June 2021)
- Wrong site surgery – wrong tooth extraction (HSIB, Apr 2021)
- Placement of nasogastric tubes, summary (HSIB, Dec 2020)
- Placement of nasogastric tubes, full report (HSIB, Dec 2020)
- Procurement, usability and adoption of ‘smart’ infusion pumps , full report (HSIB, Dec 2020)
- Procurement, usability and adoption of ‘smart’ infusion pumps, summary (HSIB, Dec 2020)
- Delays to intrapartum intervention once fetal compromise is suspected, full report (HSIB, Nov 2020)
- Delays to intrapartum intervention once fetal compromise is suspected, Summary (HSIB, Nov 2020)
- Early warning scores to detect deterioration in Covid-19 inpatients (HSIB, Jul 2020)
- Investigation into electronic prescribing and medicines administration systems and safe discharge (HSIB, Oct 2019)
- Wrong patient details on blood sample, full report (HSIB, 2019)
- Wrong patient details on blood sample, summary (HSIB, 2019)
- Management of acute onset testicular pain (HSIB, Sept 2019)
- Failures in communication or follow-up of unexpected significant radiological findings (HSIB, Jul 2019)
- Undetected button/coin cell battery ingestion in children (HSIB, June 2019)
- Recognising and responding to critically unwell patients (HSIB, May 2019)
- Provision of mental health care to patients presenting at the emergency department (HSIB, Nov 2018)
National Patient Safety Alerts
This page has links to recent flashes on equipment faults, high risk procedures etc, as well as other safety organisations.
Please contact safety@rcem.ac.uk if you hear of additional topics that should be on this page.
See all RCEM issued safety newsflashes in the tab below.
Central Alerting System
The Central Alerting System (CAS) is a web-based cascading system for issuing patient safety alerts, important public health messages and other safety critical information and guidance to the NHS and others, including independent providers of health and social care.
Patient Safety Alerts
Links to NHS England, MHRA and Public Health England patient safety alerts can be found below:
2023
- Patient Synthetic Opioids Implicated in Heroin Overdoses and Deaths (July 2023)
- Potential risk of underdosing with calcium gluconate in severe hyperkalaemia
2021
- Eliminating the risk of inadvertent connection to medical air via a flowmeter - 16 June 2021
- Updated Publication of Remdesivir guidance for patients hospitalised with Covid-19 (adults and children aged 12 years and older) - 14 June 2021
- Personal protective equipment and heat: risk of heat stress - 9 June 2021
- Urgent assessment/treatment following ingestion of 'super strong' magnets - 19 May 2021
- Medicine Supply Notification: Acetylcysteine 2g/10ml solution for injection - 25 March 2021
2020
- Steroid Emergency Card to support early recognition and treatment of adrenal crisis in adults - 13 Aug 2020
- Blood control safety cannula and needle thoracostomy for tension pneumothorax - 2 April 2020
Medical Device Alerts
All Medical Device Alerts (MDA) can be viewed on the MHRA website here. Selected MDAs sent by the MHRA for circulation to RCEM members are-- listed below:
2021
- Becton Dickinson (BD) is recalling all ethylene oxide (EtO) sterilised BD Venflon Pro Safety (VPS) and Venflon Pro IV Cannulae after identifying an increase in reports of leakage from the injection port - 4 May 2021
- Total parenteral (TPN) and enteral nutrition bags manufactured by Diffuplast: Sterilisation issue - 20 April 2021
- Dexcom G6 Sensor: untested barrier methods to reduce skin reactions - 6 April 2021
- Medoject sterile hypodermic and blunt fill needles manufactured by Chirana T. Injecta – discontinue use - 29 March 2021
2019
- Arjo Minstrel passove floor lift (portable hoist) - risk of spreader bar detachment from lifts without a scale (MDA/2019/004)
- Recall of certain batches of Eurotrol haemoglobin controls due to microbial contamination (MDA/2019/005)
- Ophthalmic implant Raindrop Near Vision Inlay - risk of corneal haze (MDA/2019/007)
- Implantable cardiac pacemakers: specific brands of dual chamber pacemakers - risk of syncope due to pause in pacing therapy (MDA/2019/008)
- Professional use monitor/defibrillator: LIFEPAK 15 – risk of device failure during patient treatment and possible failure to deliver therapy (MDA/2019/010)
- Multi parameter patient monitors: Carescape B450, B650, B850, B20, B40, B20i, B40i, B125, B105, Dash 3000,4000,5000, Solar 8000M/i, 9500 – risk of loss of patient monitoring (MDA/2019/011)
- Potentially breached sterile packaging of: rectal tubes, Unoversal drainage systems, SimpaVac, sterile suction connecting tubes, sterile connecting pieces, suction handles/sets (FilterFlow™/Deltaflo), oxygen catheters, sterile nasal oxygen cannulas, sterile oxygen connecting tubes, and sterile forceps (MDA/2019/012)
- enFlow® IV fluid and blood warmer - risk of unsafe levels of aluminium leaching from the device (MDA/2019/015)
- enFlow® IV fluid and blood warmer - risk of unsafe levels of aluminium leaching from the device – updated safety advice from manufacturer (MDA/2019/016)
- Pagewriter Cardiographs (TC20/30/50/70) manufactured before 20 November 2018 and Efficia Monitors (CM10/12/100/120/150) manufactured before 25 October 2018 – risk of batteries overheating or igniting (MDA/2019/017)
2018
- Suction catheters, gastro-enteral tubes, intermittent urology catheters and sterile urine drainage bags - potential breach in sterile barrier packaging (MDA/2018/34)
- CoaguChek Test Strips for Point of Care and Home use - risk of false high results (MDA/2018/033)
- Various trauma guide wires - risk of infection due to packaging failure (MDA/2018/032)
- SureSigns VS & VM patient monitors and Viewing stations manufactured before May 2018: risk of batteries overheating or igniting (MDA/2018/031)
- Flex connectors in Halyard Closed Suction Kits - risk of interruption of ventilation (MDA/2018/030)
- Novaline haemodialysis bloodlines used with Baxter/Gambro haemodialysis machines – Recall of specific products due to various problems encountered during clinical use (MDA/2018/025R)
- All Alaris™ and Asena™ GS, GH, CC, TIVA, PK, enteral syringe pumps – risk of uncontrolled bolus of medicine(MDA/2018/024R)
- SAM XT Extremity Tourniquet - Recall due to the risk of tourniquet failing in use (MDA/2018/022)
- Alaris Smartsite Add-On Bag Access device – removal and destruction of specific batches due to risk of disconnection or leakage (MDA/2018/021)
- Smiths Medical CADD® Non Flow-Stop Medication Cassette Reservoirs – recall of specific lots due to risk of under delivery of medication (MDA/2018/020)
- JM103 and JM105 Jaundice Meters – risk of misinterpretation of measurement in hyperbilirubinemia cases (MDA/2018/019)
- Various Arrow Critical Care devices – recall due to incomplete packaging seals (MDA/2018/018)
- Home use and Point of Care blood glucose monitoring system: Accu-Chek Aviva, Accu-Chek Performa and Accu-Chek Inform II test strips – risk of strip error messages and false high and low blood glucose results (MDA/2018/16)
- Infinity Acute Care System and M540 Patient Monitors software versions VG2.2-VG6.0 – risk that alarms are not activated (MDA/2018/014)
- Medical device alert: cobas b 221 instruments with AutoQC module – software limitation affecting automatic QC measurements(MDA/2018/013)
- BD Vacutainer® EDTA & BD Vacutainer® Lithium Heparin Tubes – risk of incorrect results for lead testing or other assays using ASV methodology (MDA/2018/012)
- All T34 ambulatory syringe pumps - risk of unintended pump shutdown and delay to treatment (MDA/2018/010)
- Aquilon series of nebulisers - CE mark withdrawn and supply ceased(MDA/2018/008)
- Plum 360 infusion pumps - user actions required to prevent risk of interrupted or delay to treatment (MDA/2018/006)
- All Philips HeartStart MRx monitors/defibrillators - significant delay in the supply of batteries (MDA/2018/002)
- Pacemakers and CRT - overseeing of minute ventilation sensor signal leading to risk of syncope and pre-syncope (MDA/2018/001)
2017
- Syringe pumps - required user actions in the event of PL3 alarm to prevent risk of interrupted infusion (MDA/2017/027)
- Intra-aortic balloon pump (IABP): CS100, CS100i and CS300 – risk of haemodynamic instability to patients with critical conditions due to a delay in or sudden interruption of therapy (MDA/2017/027)
- DePuy Synthes Impactor for PFNA (Proximal Femoral Nail Anti-rotation) Blade: risk of infection (MDA/2017/022)
- Unomedical high concentration oxygen masks (specific lots) - risk of hypoxia as the tubing can disconnect from the oxygen mask (MDA/2017/19)
- BVM (Bag-Valve-Mask) manual resuscitation systems – risk of delay to emergency treatment (MDA/2017/017)
- Solus Flexible Wire Reinforced Laryngeal Mask Airway – risk of hypoxia due to partial or total occlusion of the airway tube after inflating the cuff(MDA/2017/015)
- All HeartStart MRx defibrillators – possible failure to deliver a shock, cardioversion, pacing or monitoring (MDA/2017/14)
- All LIFEPAK 1000 automatic external defibrillators (AEDs) - risk of device shutting down unexpectedly during patient treatment and possible failure to deliver therapy(MDA/2017/013)
- V60 ventilator – potential for unexpected shutdown (MDA/2017/012)
- BD Plastipak 100ml catheter tip syringe with Luer slip adaptor, specific lots – risk of leakage and delayed therapy (MDA/2017/009)
- CARDIOSAVE Hybrid intra-aortic balloon pump (IABP) and CARDIOSAVE Rescue IABP – damaged lithium ion batteries may give off smoke, a bad smell or produce sparks (MDA/2017/004)
- Reflection® dead blow mallet (all batches) – risk of exposure to lead particles (MDA/2017/002)
- Oxylog 3000 and Oxylog 3000 plus ventilator – risk of failure (MDA/2017/001)
- Shortages of Alteplase and Tenecteplase (September 2022)
- Monkey Pox Evolving Situation – (May 2022)
- Absconding (June 2018)
Labelling blood transfusion samples from unknown patients – 29 july 2015
Is your organisation compliant with national guidance for the labelling of blood transfusion samples from unknown patients?
Unidentified patients in the ED are at high risk of transfusion errors due to misidentification. The British Committee for Standards in Haematology recommend that as a minimum, in an unknown patient requiring a blood sample for transfusion the following should be used.
- A unique identification number, ideally using non-sequential numbers
- The gender of the patient
- A second, independent sample (taken at different time) be sent
The Safer Care Committee ask that senior teams in the ED review their local policies to ensure they are compliant and the appropriate steps have been taken to minimise the risk of incorrect transfusion in unknown patients.
Insertion of chest drains (26 September 2014)
The College is issuing a safety alert following an inquest into the death of a patient after a chest drain was inserted into the wrong side. A number of factors specific to the ED were shown to have contributed to this never event; failure to identify an incorrectly labelled chest x-ray, a failure to examine the patient prior to the procedure, a failure to review all chest x-rays and misinterpretation of the chest x-ray reviewed.
Senior teams within EDs are asked to reflect on the possibility of such an event occurring in their own department and ensure they have done all that is possible to reduce the risks associated with this procedure. The safer care committee has previously prepared guidance regarding never events but also refer you to the NRLS Rapid Response Report of May 2008 which addresses the risks associated with chest drain insertion.
Button batteries as a cause of haematemesis in children
Would you consider ingestion of a button battery if a child were to present with a haematemesis?
The modern family home is likely to be littered with multiple devices and toys using button batteries. These are liable to be swallowed by small children and can present in a variety of ways including haematemesis.
Following a recent adverse event a Coroner has issued a regulation 28 notice which highlights the need for staff to be aware of the need to exclude ingestion of a button battery as a cause for upper GI bleeding in young children. This should occur even in the absence of a history of ingestion. Being aware of this presentation and undertaking the appropriate imaging is critical in ensuring the right management of such patients.
Further information is available at the Toxbase website (for health professionals only).
Summary of Reports to Prevent Future Deaths (Regulation 28)
For more information, please contact safety@rcem.ac.uk
Guidance & Resources
The resources have been produced to help local clinical governance and safety teams in creating a framework for addressing patient safety. The templates can be adapted as necessary.
Never Events are incidents which are considered unacceptable and eminently preventable. The Safer Care Committee has prepared a guide which highlights Never Events that could occur within your Emergency Department. It proposes examples of how to mitigate the risk of these happening and relevant NPSA Alerts and resources.
- Download the Never Events document.
If you have implemented any other mitigation not included in this guide please do let us know by emailing: safety@rcem.ac.uk
For further information about Never Events please visit the Department of Health and NHS England websites:
The following organisations have key responsibilities relating to the promotion of patient safety.
Emergency Medicine doctors may wish to consult these to keep up to date with developments in safer emergency care.
Care Quality Commission (CQC) - CQC is the health and social care regulator for England.
Centre for Patient Safety and Service Quality (CPSSQ) - CPSSQ comprises a highly specialised set of research groups, working together to improve patient safety and the quality of healthcare services. CPSSQ is part of the National Institute for Health Research.
Institute of Health Improvement (IHI) - an independent not-for-profit organization helping to lead the improvement of health care throughout the world. Founded in 1991 and based in Cambridge, Massachusetts.
National Health Service Resolution (NHSR) - handles negligence claims and works to improve risk management practices in the NHS.
National Institute for Health and Clinical Excellence (NICE) - is an independent organisation responsible for providing national guidance on promoting good health and preventing and treating ill health.
National Patient Safety Agency (NPSA) - leads and contributes to improved, safe patient care by informing, supporting and influencing the health sector.
They have 3 divisions:
- National Reporting and Learning Service (NRLS) - collects and analyses errors across England and Wales
- National Clinical Assessment Service (NCAS)
- National Research Ethics Service (NRES)
Scottish Patient Safety Alliance (SPSA) - The Scottish Patient Safety Alliance has been established by NHS Scotland to oversee the development of the Scottish Patient Safety Programme, which aims to steadily improve the safety of hospital care by using evidence-based tools and techniques to improve the reliability and safety of everyday health care systems and processes www.patientsafetyalliance.scot.nhs.uk
World Health Organisation (WHO) Patient Safety – a programme which aims to coordinate, disseminate and accelerate improvements in patient safety worldwide. Each year, WHO Patient Safety delivers a number of programmes covering systemic and technical aspects to improve patient safety around the world.
Second victims are health care providers who are involved in an unanticipated adverse patient event, in a medical error and/or become victims in the sense that they are traumatised by the event. The Safer Care Sub-committee has prepared a guidance document for supporting Emergency Department colleagues who experience such events. This guide advocates key recommendations for individuals and the senior team within the Emergency Department:
- Download ’Supporting the Second Victim’
- Download our summary of recommendations.
The Safer Care Sub-Committee promotes training materials which address patient safety. Within this page you can find training materials which address safer patient care.
Essential Reading
Francis Report
The Francis Report is essential reading for all clinicians working in Emergency Departments and has important recommendations for patient safety.
The Safer Care team have developed the following resources to support safety in the wake of the Francis review.
Francis report: a call to arms
The Francis Report is mandatory reading for all clinicians working in Emergency Departments. Drs Ruth Brown and Sue Robinson have written ‘The Francis Report: a call to arms,’ published within the Emergency Medicine Journal. In this article they advocate that the Francis report serves as a call to arms for ED staff to stop normalising the abnormal and tolerating substandard care, to respect and protect our patients and hold our leaders, and ourselves, to account.
View the Francis Report
Francis Report Recommendations – a Checklist for Senior Teams in Emergency Departments
The Francis report has many recommendations for organisations as a result of the enquiry. The College has developed this checklist for Clinical Directors of the Emergency Department – taking the most relevant recommendations and identifying key actions for clinical leaders of emergency departments. While the list is not exhaustive it is meant as a handy guide to action that might usefully be taken in the first instance.
View the Francis Report recommendations.
Francis Report – Statement for Fellows and Members
The College has prepared a statement for Fellows and Members on the Francis Inquiry Report outlining what the report is and why it is important for Emergency Medicine. This document also acts a guide to challenging occurrences of poor care.
View the Statement for Fellows & Members on the Francis Inquiry Report
Berwick Report
The Berwick report is essential reading for emergency medicine practitioners. It identifies changes that could help the English NHS become safer and more patient-centered whilst making numerous recommendations to help protect patients.
Read the recommendations from Professor Don Berwick and the National Advisory Group on the Safety of Patients in England – Berwick review into patient safety.
Non-technical Skills
Non-technical skills (NTS) have a vital role to play in Emergency Medicine practice. There is increasing awareness that a clinician must not only possess good technical skills but should also be proficient in a variety of interpersonal and cognitive skills in order to optimise patient care. Non-technical skills reduce the opportunity for human error and enhance risk management both of which are known to improve patient care. The College has prepared a Non-technical Skills-Top 10 Tips as a guide on how to maximise emergency physician’s non-technical skills for the benefit of patients and staff.
Integrating Safety Checklist
The Safer Care Committee has developed a new checklist for integrating safety into your Emergency Department. This allows you to assess how well you integrate and consider safety in your departmental activities and makes suggestions for which staff need to be involved.
Radiology Processes
There have been cases that were the subject of a Coroner’s rule 43 report to the Secretary of State. Both of these involved the system for reporting serious and potentially fatal unexpected findings on radiological imaging. The Safer Care team have prepared guidance for Emergency Teams on reviewing radiological imaging.
Tools Resources and Systems
The Safer Care Team recommend that Emergency Medicine doctors utilise these tools, resources and systems when considering patient safety.
Crisis Resource Management (CRM)
CRM can be defined as a management system which makes optimum use of all available resources – equipment, procedures and people – to promote safety and enhance efficiency. Originally used in aviation but increasingly utilised in healthcare.
Clinical Negligence Scheme for Trusts (CNST)
The Clinical Negligence Scheme for Trusts handles all clinical negligence claims against member NHS bodies where the incident in question took place on or after 1 April 1995 (or when the body joined the scheme, if that is later). Membership of the scheme is voluntary.
Essentials of Patient Safety
Written by Prof Charles Vincent, a short version is available to download for free. The topics addressed include the evolution of patient safety; the research that underpins the area, understanding how things go wrong, and the practical action needed to reduce error and harm and, when harm does occur, to help those involved. The main book covers these topics in more depth and a number of additional topics such as measurement, safety culture, design, safety campaigns and safe organisations.
See Essentials of Patient Safety.
FMEA: A model for reducing medical errors
Failure Mode and Effects Analysis (FMEA) – a methodology for analysing potential reliability problems. See:
M Chiozza, C Ponzetti
Clinica Chimica Acta
Volume 404, Issue 1, 6 June 2009, Pages 75-78
Global Trigger Tool (GTT)
An easy to use tool that supports a structured case note review to identify harm events. Tracking adverse events over time is a useful way to tell if changes being made are improving the safety of the care processes. The Trigger Tool methodology includes a retrospective review of a random sample of patient records using triggers to identify possible adverse events. It is important to note, however, that the IHI Global Trigger Tool is not meant to identify every single adverse event in a patient record. See:
Griffin FA, Resar RK. IHI Global Trigger Tool for Measuring Adverse Events (Second Edition). IHI Innovation Series white paper. Cambridge, MA: Institute for Healthcare Improvement; 2009 (Available on www.IHI.org)
NHS Evidence
Provided by NICE, NHS Evidence is a new service which will develop, enhance and expand the services that were previously provided by the National Library for Health (NLH).
National Service Frameworks (NSF)
The National Service Frameworks cover some of the high priority conditions and key patient groups. They work to:
- set clear quality requirements for care based on the best available evidence of what treatments and services work most effectively for patients, and
- offer strategies and support to help organisations achieve these
See more in the National Archives.
Patient Safety – 10 things NHS Trusts should already be doing
This document from the Centre for Reviews and Dissemination of the NIHR and University of York highlights 10 key things which should be undertaken by Trusts to promote patient safety.
Patient Safety First
Patient Safety First is a national campaign that aims:
- to ensure the safety of patients is everyone’s highest priority
- to reduce harm by changing in specific areas.
It is sponsored by the NHS Institute for Innovation and Improvement, the NPSA and the Health Foundation.
Plan, Do, Study, Act (PDSA)
The PDSA cycle tests a change by developing a plan to test the change (Plan), carrying out the test (Do), observing and learning from the consequences (Study), and determining what modifications should be made to the test (Act).
Patient Safety Alert (PSA)
Through analysis of reports of patient safety incidents, and safety information from other sources, the National Reporting and Learning Service (NRLS) develops advice for the NHS that can help to ensure the safety of patients.
Advice is issued to the NHS as and when issues arise, via the Central Alerting System in England and directly to NHS organisations in Wales. Alerts cover a wide range of topics. Types of alerts include Rapid Response Reports, Patient Safety Alerts, and Safer Practice Notices. See more here
Reporting incidents
From 1 April 2010 it became mandatory for NHS trusts in England to report all serious patient safety incidents to the Care Quality Commission as part of the Care Quality Commission registration process. To avoid duplication of reporting, all incidents resulting in death or severe harm should be reported to the National Reporting and Learning Service (NRLS), who will then report them to the Care Quality Commission. Report a patient safety incident here.
Staff Care, How to engage staff in NHS and why it matters
This report from the Point of Care Foundation shows that the way healthcare staff feel about their work has a direct impact on the quality of patient care as well as on an organisation’s efficiency and financial performance. This report is available here.
Royal College of Emergency Medicine – Top tips for patient safety
The RCEM Safer Care committee had produced a poster that lists simple steps that everyone can take to improve patient safety and raise awareness of patient safety. Please download and display in your ED. See here.