OPTIMISation of Cardio-renal-metabolic-pulmonary Disease Guideline Adherence in High Risk Community Dwelling Individuals
- Conditions
- Cardiovascular DiseasesRenal DiseaseMetabolic DiseasePulmonary Disease
- Interventions
- Other: NICE guidance
- Registration Number
- NCT06444711
- Lead Sponsor
- University of Leeds
- Brief Summary
Cardiovascular disease (CVD) causes a quarter of all deaths in the United Kingdom (UK). This is the single biggest area where the National Health Service (NHS) can save lives by detecting and treating risk factors early.
Improvements in control of blood pressure, cholesterol, diabetes, kidney disease, as well as weight loss in individuals who are obese, have been shown to reduce the risk of CVD and death. The NHS has guidelines for investigations and treatments for risk factors recommended by the National Institute for Health and Care Excellence (NICE).
Though it is known that better control of risk factors will reduce the risk of CVD the investigators do not know whether having extra appointments in primary care with heart specialists can lead to better treatment and better control of risk factors.
The OPTIMISE trial (OPTIMISation of Cardio-renal-metabolic-pulmonary Disease Guideline Adherence in High Risk Community Dwelling Individuals) will compare patients who have consultations at a local General Practitioner (GP) practice by a cardiology professional to optimise the treatment of their risk factors (OPTIMISE) with those patients who receive standard care (Standard care). Standard care is patients being seen by their GP at routine care appointments.
Participants in the OPTIMISE arm will be reviewed by the cardiology professional and recommended treatment in line with current NICE guidance. They will be seen at 3 months to review their treatment and potentially adjusted to ensure it meets NICE guidelines.
Participants in the standard arm will have data related to their cardiovascular, renal, metabolic and pulmonary risk factors collected through their Electronic Health Record (EHR).
At 6 months, all participants will be seen to find out changes to their prescribed medication and the effect of this on their blood pressure, cholesterol, blood sugar level, and body mass index (BMI).
All participants will also complete a quality of life questionnaire prior to randomisation study and at 6 months to identify any differences between the arms and time points.
- Detailed Description
Cardiovascular disease (CVD) causes a quarter of all deaths in the UK and is the largest cause of premature mortality in deprived areas. The National Health Service (NHS) Long Term Plan emphasises that this is the single biggest area where the NHS can save lives and that better detection and treatment of cardiovascular, renal, metabolic and pulmonary risk factors is a priority.
Treatment of blood pressure, cholesterol, diabetes, kidney disease, as well as weight loss in individuals who are obese, have been shown in randomised clinical trials (RCT) to reduce the risk of CVD and cardiovascular death.
Many risk factors for patients with CVD do not occur in isolation, but often co-exist in clusters and increase the risk of other risk factors such as obesity, high blood pressure and diabetes.
In the NHS CVD risk factors identification and improvement is through contact with a healthcare professional in primary care. It is from primary care that the prescription of medications and monitoring to control cardio-renal-metabolic-pulmonary risk factors is delivered.
Research has demonstrated that, especially during the Coronavirus disease 2019 (COVID-19) pandemic, the management of cardio-renal-metabolic-pulmonary risk factors, through monitoring of observations and blood tests and prescription of medications, deteriorated. That is, patients in the community may not be receiving the full extent of NICE guideline directed care and prescriptions of medications for cardiovascular, renal, metabolic and pulmonary risk factors to reduce their risk of future cardiovascular events like heart attack, stroke and death.
The investigator's research has demonstrated that individuals identified as at higher predicted risk of Atrial Fibrillation (AF) are also at increased risk of other conditions such as chronic kidney disease, heart failure, diabetes mellitus, stroke/transient ischaemic attack, myocardial infarction and peripheral vascular disease. The investigators have also shown in their study Future Innovations in Novel Detection of Atrial Fibrillation (FIND AF) that high FIND-AF predicted risk individuals are also at higher risk of death, the majority of which are of cardiovascular cause during 10 years of follow up. Accordingly, individuals at higher FIND-AF predicted risk may have comorbidities and cardiovascular risk factors that are undiagnosed or under-treated during routine practice that may be potential targets for guideline directed treatment to reduce the risk of future adverse events.
The study will take advantage of the FIND AF Primary Care network and processes by recruiting from the FIND AF participants who have already been identified as having a high FIND AF predicted risk score. OPTIMISE (OPTIMISation of Cardio-renal-metabolic-pulmonary Disease Guideline Adherence in High Risk Community Dwelling Individuals) will compare General Practitioner (GP) based clinic appointments with a cardiovascular healthcare professional compared to usual care on therapeutic interventions for cardio-renal-metabolic-pulmonary disease and risk factors. It will determine the effect of the differing approaches over a follow up of six months to find out if GP based clinic appointments with a cardiovascular healthcare provides better outcomes for patients than standard care.
OPTIMISE is a multicentre pragmatic prospective randomised open-label blinded-endpoint strategy trial (PROBE).
Eligible patients will have consented to take part in the FIND AF pilot study and be assessed as at high risk of developing Atrial Fibrillation in the next 6 months by the FIND AF algorithm.
For patients who have consented to the optional follow up visit for the FIND AF pilot study, prior to their visit they will be posted the OPTIMISE patient information sheet. At the visit the patient will have the opportunity to ask questions, provide consent and complete a questionnaire. They will then undergo randomisation into either the standard care arm or the Optimisation arm. The aim is to recruit 1:1 between the two arms. If the participant is randomised to the Optimisation arm, the patient will undergo the Optimise baseline appointment at the same time as the FIND AF pilot study optional visit. Combining the visits will reduce the overall time required by the participant as it will avoid duplication of any clinical observations.
For patients who have consented to further contact from the research team and have either already undergone the FIND AF pilot study optional visit or have declined to attend the visit, they will be sent the patient information sheet, consent, questionnaire and a reply paid envelope. They will be supplied with the study team's contact information so if they have any questions they can contact the team. Upon receipt of the consent and questionnaire, the study team will randomise the participant. The study team will then contact the participant with the results of the randomisation and if the patient has been randomised to the Optimisation arm, arrange the baseline appointment.
It will be clearly stated that the participant has the right to refuse participation without giving a reason and can withdraw from the study at any time without prejudicing their further treatment or their legal rights. The participant will be allowed as much time as wished to consider the information, and the opportunity to question the research team, their GP, or family and friends to decide whether they will participate in the study.
For the baseline assessment, the research team cardiology doctor will review the data stored in the participant's GP records with relation to previous cardiovascular disease, hypertension, dyslipidaemia, chronic kidney disease, diabetes, Body Mass Index (BMI), Chronic obstructive pulmonary disease (COPD) and smoking history. At the baseline appointment they will conduct observations and blood tests that are recommended in National Institute for Health and Care Excellence (NICE) guidance if the results are not already available in the GP medical records. They will also carry out an ambulatory lung test (to screen for risk of pulmonary diseases).
For patients in the Optimisation arm, the research team cardiology doctor will recommend changes to treatment if the treatment the patient is currently on does not adhere to NICE guidelines. The research team will not directly initiate treatment, but will provide a letter and verbal communication with the participant's GP of the recommendations.
Patients in the standard arm will have consented to their data being reviewed in their GP's record as per the Optimisation arm however they will not undergo an appointment with the research team cardiology doctor and no recommendations for changes to treatment will be identified.
For patients in the Optimisation arm, at three months following their baseline appointment, they will attend their second visit and undergo the same tests as at the baseline appointment and again, will recommend changes in line with NICE guidance.
At six months both participants in the Optimisation arm and the standard arm will have their observations (e.g. blood pressure, BMI) and an ambulatory lung test taken during an appointment by a research team suitably qualified health professional, as well as any blood tests that are indicated by the patient's known comorbidities (e.g. HBA1c if known to have diabetes), as well as completing a patient-reported outcome measure (EQ-5D-5L).
All visits will take place at the participant's primary care site.
An endpoint adjudication committee, blinded to allocation, will review observations, laboratory measures and GP medical records data for the participant to establish adherence of care to guidelines.
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 138
- Consented participants in the FIND-AF study
- Higher predicted FIND-AF risk according to the FIND-AF score
- Unable to give written informed consent for participation in the study
- Unable to adhere to the study requirements
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Optimisation arm NICE guidance Participants in the intervention arm will attend a baseline visit and two further research appointments at three months and six months from time of randomisation, For baseline assessment, the research cardiology doctor will review the participant's GP records with relation to previous cardiovascular disease, hypertension, dyslipidaemia, chronic kidney disease, diabetes, BMI, COPD and smoking history. They will conduct observations and blood tests that are recommended in NICE guidance if the results are not already available. They will carry out an ambulatory lung test (to screen for risk of pulmonary diseases). They will recommend changes to treatment if the treatment the patient is currently on does not adhere to guidelines. The research team will provide a letter and verbal communication with the participant's GP of the recommendations. For the second visit at three months after randomisation, the research team doctor will conduct the same review as undertaken at the first visit.
- Primary Outcome Measures
Name Time Method The proportion of patients with any of the following therapeutic intervention to optimise cardio-renal-metabolic-pulmonary risk factor management 6 months The proportion of patients with any of the following therapeutic intervention to optimise cardio-renal-metabolic-pulmonary risk factor management including initiation or increase in dose regimen of:
* Angiotensin converting enzyme inhibitor / angiotensin 2 receptor blocker
* Calcium channel blocker / thiazide-like diuretic / spironolactone / alpha blocker / beta blocker
* SGLT2 inhibitor
* Glucagon-like peptide (GLP) -1 receptor agonist
* Metformin / Dipeptidyl peptidase 4 (DPP4) inhibitor / pioglitazone / sulphonylurea / insulin
* Statin / ezetimibe / icosapent ethyl / bempedoic acid / PCSK9 inhibitor
* Orlistat
* Nicotine replacement therapy / bupropion
* Inhaler therapy
- Secondary Outcome Measures
Name Time Method Number of participants developing a new cardio-renal-metabolic-pulmonary risk factor 6 months Number of patients receiving a diagnosis of new cardio-renal-metabolic-pulmonary risk factor (hypertension, diabetes, chronic kidney disease, obesity, current smoking, COPD) between randomisation and six months.
Time to diagnosis of a new cardio-renal-metabolic-pulmonary risk factor 6 months Time to diagnosis of a new cardio-renal-metabolic-pulmonary risk factor
Change in EuroQol five dimensional descriptive system (EQ-5D-5L) questionnaire score 6 months A comparison of the two arms of the change in EuroQol five dimensional descriptive system (EQ-5D-5L) questionnaire score between randomisation and six months follow-up with a large change indicating a better outcome. Analysis will be carried out as per the EuroQoL guidance and will incorporate both questions and scale participant responses.
The EQ-5D-5L has a maximum index value of 1, representing full health, and a minimum index value of -0.59, which corresponds to the worst health state. The instrument includes five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression with each dimension having five levels. We will be measuring the change in index value between baseline and 6 months.Components of primary endpoint 6 months The proportion of participants who have experienced any of the individual components of primary endpoint which are an initiation or increase in the dose regimen of each of the following:
* Angiotensin converting enzyme inhibitor / angiotensin 2 receptor blocker
* Calcium channel blocker / thiazide-like diuretic / spironolactone / alpha blocker / beta blocker
* SGLT2 inhibitor
* Glucagon-like peptide (GLP) -1 receptor agonist
* Metformin / Dipeptidyl peptidase 4 (DPP4) inhibitor / pioglitazone / sulphonylurea / insulin
* Statin / ezetimibe / icosapent ethyl / bempedoic acid / PCSK9 inhibitor
* Orlistat
* Nicotine replacement therapy / bupropion
* Inhaler therapyTime to primary endpoint 6 months The median time to primary endpoint from randomisation reported in days eg the date of initiation or increase in the dose regimen of one of the following:
* Angiotensin converting enzyme inhibitor / angiotensin 2 receptor blocker
* Calcium channel blocker / thiazide-like diuretic / spironolactone / alpha blocker / beta blocker
* SGLT2 inhibitor
* Glucagon-like peptide (GLP) -1 receptor agonist
* Metformin / Dipeptidyl peptidase 4 (DPP4) inhibitor / pioglitazone / sulphonylurea / insulin
* Statin / ezetimibe / icosapent ethyl / bempedoic acid / PCSK9 inhibitor
* Orlistat
* Nicotine replacement therapy / bupropion
* Inhaler therapyNumber of participants with a new uptake of guideline directed risk factor management 6 months Number of participants with a new uptake of guideline directed risk factor management in those with recorded cardio-renal-metabolic-pulmonary risk factors (hypertension, lipid modification, diabetes, chronic kidney disease, obesity, current smoking, COPD), between randomisation and six months