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Quality Improvement

Find out how the Cystic Fibrosis Trust’s new Quality Improvement Team is working to improve quality of care in CF centres across the UK.


What is Quality Improvement (QI)?

Quality improvement is about trying to make the health care you receive more:

Safe – trying to ensure the care you receive makes you better, not worse

Timely – do you receive the care and information you need, when you need it?

Effective – are the treatments and advice you’re receiving evidence-based? Do they work?

Efficient – helping your centre understand and use their resources to ensure optimal care

People-centred – ensuring your opinions on your care are listened to and acted upon

Equitable – reducing unnecessary differences in how care is provided across the UK

What does the Trust’s Quality Improvement Team do?

The QI team was established in 2018 to provide resources that help to support CF centres across the UK to improve the quality of the care they provide.

Current projects

Patient Reported Experience Measures (PREMs) Survey

Our UK-wide patient experience survey will give participating CF centres insights into what their patients and families think about the health care they receive. Results of the survey will be compared to the UK average for each question, to allow centres to benchmark their performance. This will help CF teams identify potential areas for change. Running the PREMs survey every three years will track how patients’ feelings about their care change over time and help CF teams measure if their QI projects have had a positive impact.

Staffing tool

This online tool, completed by the centres, aims to give a yearly snapshot of staffing resources in participating UK CF centres. Centre-level and UK reports will be available in March 2020 and will show centres how their staffing and vacancy levels compare to UK averages. We are happy to say that 75% of centres have participated and we would like to thank them for their contribution.

How can you get involved?

Quality Improvement Working Group

Join our new Quality Improvement working group, made up of people with CF, their families, CF professionals and members of the Trust, and help to form our QI strategy and develop key projects that improve CF care and services.

We want everyone in the CF community to have an equal say in which care issues we focus on and how we support CF centres.

What will I have to do?

The group will meet online at least four times a year using collaborative platforms to share documents and ideas. We will use something called ‘co-design’, meaning that everybody involved has an equal level of power within the process. People with CF and their carers’ lived experience can provide insight, wisdom and ideas. Combining their knowledge with the on-the-ground pragmatism of clinicians and the Trust’s Quality Improvement team ensures that the changes taking place are patient-centred and helps support modern healthcare teams with an emphasis on better care and health outcomes.

Co-design has been used with great success by other healthcare charities, such as Mind, Diabetes UK, the Cystic Fibrosis Foundation in the USA, and the Trust’s Clinical Trials Accelerator Platform.

You’ll receive training, and no prior experience is necessary, just a fiery determination to make CF care the best it can be!

Please feel free to contact us with any questions you may have by emailing QI@cysticfibrosis.org.uk.

Patient Reported Experience Measures update

Due to the COVID-19 pandemic, we have decided to close this version of the paediatric PREMs survey. This is in acknowledgement of the fact that CF centres have drastically changed how they are providing care, so that care experiences pre and during the pandemic are not directly comparable.

The paediatric PREMs survey ran for over seven months and offered patients and parents the opportunity to tell us how they feel about the care they receive in their CF centre. Twenty-five paediatric centres participated, and we are thrilled to say that we have received nearly 700 surveys, exceeding our 20% response target. We would like to thank the participating centres, parents and patients for contributing to the success of this project. We aim to have the centre and UK PREMs reports available by the end of this year.

Adults with cystic fibrosis will have the opportunity to complete a modified survey in late 2020/early 2021.

Participating centres

  • Addenbrookes Hospital, Cambridge
  • Alder Hey NHS Children’s Hospital, Liverpool
  • Birmingham Children's Hospital
  • Bristol Royal Hospital for Children
  • Crosshouse Hospital, Ayr
  • Derriford Hospital, Devon
  • Great North Children's Hospital, Royal Victoria Infirmary, Newcastle Upon Tyne
  • Hull and East Yorkshire Teaching Hospital
  • James Cook University Hospital, Middlesbrough
  • John Radcliffe Hospital, Oxford
  • Leicester Royal Infirmary
  • Noah's Ark Children's Hospital for Wales
  • Norfolk and Norwich University Hospital (Jenny Lind Children's Hospital)
  • North West Midlands CF Centre, Royal Stoke University Hospital
  • Nottingham Children's Hospital (Queen's Medical Centre)
  • Royal Brompton Hospital, London
  • Royal Cornwall Hospital
  • Royal Devon and Exeter Hospital
  • Royal Hospital for Children, Glasgow
  • Royal Hospital for Sick Children, Edinburgh
  • Royal London Children’s Hospital
  • Royal Manchester Children's Hospital
  • Sheffield Children's Hospital
  • Southampton Children's Hospital
  • University Hospital Wishaw, Lanarkshire



UK CF Registry

The Registry is an anonymised database of people with CF in the UK - a powerful tool for monitoring and auditing the care that people receive.

Resources for professionals

Explore the resources, programmes and awards that we offer to CF professionals to help them provide the best support they possible can to people with cystic fibrosis.

Helpline

Contact our wonderful helpline team by telephone or email, Monday to Friday, for answers to your questions.