Heart Failure with Reduced Ejection Fraction, Hyperkalaemia, Left Ventricular Systolic Dysfunction
Conditions
Keywords
Hyperkalaemia, Heart failure with reduced ejection fraction, Renin-angiotensin-aldosterone system inhibitors, Left Ventricular Systolic Dysfunction, Decision making process, Hyperkalaemia due to RAASi
Brief summary
Renin-angiotensin-aldosterone system inhibitors (RAASi) have transformed prognosis of patients with heart failure with reduced ejection fraction, diabetic nephropathy and chronic kidney disease. However, in everyday clinical practice patients often receive suboptimal doses of RAASi. The development of hyperkalaemia is one of the reasons for dose reduction or complete withdrawal of RAASi and this in turn is likely to have an adverse impact on patient outcomes. Yet it remains unknown precisely how often hyperkalaemia leads to changes to RAASi doses, if it is the sole reason, or whether this occurs in combination with other clinical situations such as worsened renal function and hypotension. It is also unclear what influences the decision-making process of healthcare professionals in managing patients with hyperkalaemia who take RAASi and if this is influenced by specialty, experience or indications for RAASi. In order to improve our understanding of the problem we are taking forward a research study (made up of 3 complimentary studies). These data are needed to help achieve our ultimate goal of improving the care of patients with prognostic indication for RAASi.
Detailed description
The study aims to answer the following research questions: 1. What is the incidence of hyperkalaemia following RAASi therapy initiation and uptitration in patients with a new diagnosis of HFrEF including those with a new diagnosis of post myocardial infarction (MI) left ventricular systolic dysfunction? 2. How does it impact on RAASi prescription? 3. How does hyperkalaemia impact on RAASi therapy according to the clinical indication for the drug(s) in an adult population of patients who are hospitalised or attending the emergency department (and not receiving dialysis) with hyperkalaemia and receiving RAASi? 4. At what level of hyperkalaemia do healthcare professionals consider making changes to RAASi and does it vary according to the clinical indication for the drug(s)?
Interventions
None listed
Sponsors
Vifor Pharma
Portsmouth Hospitals NHS Trust
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
For patients with heart failure Inclusion criteria 1. Patients with newly diagnosed HFrEF (within 4 weeks of diagnosis, including those with post MI LVSD, identified as outpatients or during hospital admission, typically for decompensated heart failure or post myocardial infarction) who are initiated on RAASi or have a clinical indication for uptitration of current RAASi (in patients already receiving RAASi for other indications). 2. Able to provide informed consent. 3. Age 18 and above.
Exclusion criteria
1. Patients receiving dialysis. For patients with hyperkalaemia Inclusion criteria 1. Patients in ED or inpatients who already receive RAASi and who have at least 1 blood test with a potassium level of ≥5.5 mmol/l. 2. Able to provide informed consent. 3. Age 18 and above.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Incidence of hyperkalaemia in patients with new diagnosis of HFrEF | 12 months | Incidence of hyperkalaemia in patients with new heart failure with reduced ejection fraction started on renin-angiotensin-aldosterone receptor inhibitor(s) |
| Frequency of dose reduction/withdrawal for RAASi after hyperkalaemia in patients with HFrEF | 12 months | Proportion of patients with new HFrEF started on RAASi who experienced RAASi dose reduction/withdrawal/prevention of dose uptitration due to hyperkalaemia. |
| Proportion of patients with hyperkalaemia (hospitalised or attending ED) who experienced changes to RAASi after episodes of hyperkalaemia | 12 months | 3\. Proportion of hospitalised patients/ED attenders with documented hyperkalaemia, receiving RAASi for prognostic benefit who experience RAASi dose reduction/withdrawal, assessed at discharge |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Hospitalisations | 12 months | Number and causes (all cause, cardiovascular or HF) of hospitalisation at 12 months. |
| Hyperkalaemia level at which healthcare professionals make changes to RAASi | 12 months | Level of hyperkalaemia at which healthcare professionals reduce/stop RAASi in patients with and without clear prognostic indications for RAASi. |
| Incidence of repeated episodes of hyperkalaemia | 12 months | Incidence of repeated episodes of hyperkalaemia after initial episode. |
| Awareness of RAASi benefits and target doses for patients with HFrEF | 12 months | Proportion of different grades and specialties of healthcare professionals who are aware of RAASi target doses and benefits in HFrEF. |
| Description of healthcare professionals making changes to RAASi after episodes of hyperkalaemia | 12 months | Proportion of different grades and specialties of healthcare professionals reducing dose/stopping RAASi in hyperkalaemic patients. |
| RAASi discontinuation due to other causes rather than hyperkalaemia | 12 months | Proportion of patients discontinuing RAASi due to other causes than hyperkalaemia (hypotension, worsening renal function, other). |
| Mortality | 12 months | Number and causes (all cause, cardiovascular or HF) of mortality at 12 months. |
Countries
United Kingdom
Outcome results
None listed