Pearl Avery in Dorset explains how being part of the IBD Registry and using the PMS has impacted her practice. Since joining she’s noticed a positive impact on her patients’ confidence in the IBD service and has used local data to achieve funding for additional IBD nurse resource.
Clinical Nurse Specialist Pearl Avery reports on how being part of the IBD Registry is helping the Dorset IBD team provide a better service to patients.
Responding to patients
The patient management system is giving us the ability to respond to patient queries effectively, since you have access to all the information right there and then. When I get a call on the helpline it’s quick and easy to see the patient’s history as well as colleagues’ comments. This helps us see the whole picture and provide better continuity of care for the patient. You need to remember that often, people have been symptomatic for a while before they contact you for help. Having all the information at your fingertips when they do call boosts patients’ confidence in the IBD service.
In the past when patients phoned we’d sometimes have to arrange to phone back if it was a complex case, to give us time to go through the paper notes.
It also impacts on patient safety as it helps us make the right medication choices, and reduces the chance of our making silly mistakes.
Working more efficiently
The IBD Registry patient management system is easy to use in clinic, and can be adapted to local needs, which is a bonus.
Previously we recorded information in the notes, then had to enter data onto the hospital PAS, as well as write a GP letter, which was time consuming for us, and inefficient for the Trust.
Being able to generate GP letters and patient summaries is a big benefit. We copy and paste these into our local document system, and it’s made our letter production much quicker, so the patient and GP aren’t having to wait weeks to hear about any change to the clinical management of patients.
Being able to update patient records from different locations allows us to be more efficient. The robust infrastructure also helps with continuity when colleagues are away, but also gives us a great way to demonstrate our work; for example we can easily report on the number of helpline calls received, the time it took to respond, and the number of clinic appointments or A&E visits saved.
Planning and resourcing the service
Once we’ve registered all our patients we’ll have a clear picture of our population, which will allow us to resource effectively; for example, by making sure we’ve got sufficient nurse specialists to meet the IBD Standards. Up to now we’ve made an estimate based on our catchment population and the average incidence of IBD in the population to corroborate the data laboriously recorded in a spreadsheet. Being part of the Registry will not only allow us to define our population more accurately but also compare our incidence and outcomes with services in other parts of the UK.
Pearl used Registry data to track the number of IBD patients in her local catchment population. She then used this to make a business case to the CCG which has given them the necessary funding to take on an extra 0.6 whole time equivalent IBD nurse and to achieve funding for the helpline for the first time in 20 years.
I can see benefits for the local health economy too: care is less expensive when patients are well managed, and you can only do that with a well-run service. The Registry has helped us to streamline the service, freeing up time from audit for care.
The Central University Manchester Hospital NHS Foundation Trust failed to meet IBDQIP criteria for having a real time database in 2014. They used this to make a case to hospital management for a means to collect better data for quality improvement. Karen and the team also have some advice on how to approach the data entry challenge of the IBD Registry in order to reap benefits in the long term.
Dr Karen Kemp PhD, MPhil, BSc (Hons), RGN, is Consultant Nurse IBD at Central Manchester University Hospitals NHS Foundation Trust, where she runs a service with around 4,000 IBD patients.
The Manchester Gastroenterology and Hepatobiliary Centre’s goal is to provide excellent care for patients, but the IBD service failed to meet IBDQIP standards in 2014, due to the fact that they had no real time database. They kept track of their patients on a number of different spreadsheets (for steroids, azathioprine, biologics etc) as well as putting information into the IBD Audit web tool; all of which was not only time consuming and difficult to manage, but also meant considerable duplication of effort.
The IBD team presented the IBDQIP results to the Trust Board and within this the case for the InfoFlex PMS was included, which would allow them to have a comprehensive view of the whole service for the first time and provide them with an efficient management tool. The Trust managers approved the funding for the PMS and as additional two more full time IBD nurses in order to improve performance against IBDQIP.
The main barrier was finding time for the clinical team to plan the implementation; but Karen was able to find a champion in the IT department, and this colleague was one of the key people who drove the implementation process internally and made it easy. Although the process ran smoothly as a result of the informatics support, it did take some time from start to finish, due to competing demands on staff time across the Trust and other constraints. At one point, for example, training was delayed due to the junior doctors’ strike.
The main benefit for Karen is not having multiple databases, so not having to double up on work. An example of this is the biologics audit, which used to take a lot of time to complete each year, but now the team will save time by having put the information in as they go along, and they have a good feeling about working towards something together, now that they have one single database for all their patients.
Every team will have their own approach to data entry. At Central Manchester the patients complete disease scoring questions on clinic forms in the waiting area. Consent forms and disease scoring forms are included with the infusion paperwork, and then an administrator enter the scores and the consent into the database.
In terms of clinical information, what works for Karen and her team is to enter data during their virtual biologics clinic; most of the information needed is included in the clinic letter so it’s quite straightforward and not too time-consuming to get the minimum data entered on people being treated with biologics or biosimilars, and they find the system easier than the old biologics tool. They estimate each patient takes around ten minutes to enter.
Karen feels it’s important not to try and get all the information on in one go, but to do it incrementally. Accept that it will take time; it will be really useful to you in the long run.
“When we think of the cancer registries and the impact they’ve had on patient care and outcomes over the years it’s really exciting to consider how the IBD Registry will undoubtedly improve the care of our patients; building on the success of the IBD audit, before too long we’ll have the data to prove what works and to demonstrate the need for better resources.”