Heart Failure
Conditions
Brief summary
The investigators will determine the feasibility of identifying and quantifying changes in interstitial and intravascular congestion by imaging in participants with heart failure. The investigators will either continue or temporarily suspend both loop diuretics and mineralo-corticoid antagonists (MRA) for 48 hours in participants with heart failure that is both stable and mild and compare measurements of interstitial (B-lines) and intra-vascular fluids (IVC and JV diameter and renal venous flow) by ultrasound and, in a subset of participants without contra-indications, by cardiac MRI.
Interventions
OTHERDiuretics
As per group descriptions
Sponsors
NHS Greater Glasgow and Clyde
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
19 Years to 100 Years
Healthy volunteers
No
Inclusion criteria
* Clinical diagnosis of heart failure * Plasma NT-proBNP \>125ng/L or BNP \>35 ng/l * Left ventricular ejection fraction (LVEF) \<50% on prior imaging test * Treated routinely with a daily dose of loop diuretic * Receiving other guideline-indicated therapy for heart failure * Willing to sign the informed consent form * Greater than 18 years of age
Exclusion criteria
* Chronic Kidney Disease Stage 4 or worse (eGFR \<30 mL/min/1.73 m²) * Atrial fibrillation * Significant valve disease (investigators opinion) * Breathlessness or chest pain at rest or minor exertion * Patients unable to lie flat * Patients deemed too unstable to miss treatment with diuretics for 48 hours * Patients taking part in another interventional trial * Any other concomitant condition that in the opinion of the investigator would not allow a safe participation in the study (ie:-pregnancy, significant frailty) * Patients unwilling or unable to consent * For patients willing to undergo MRI; contraindication to MRI including claustrophobia, metalworkers, and intra-orbital or intracranial metal (eg:- stents), and non-MRI compliant device.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Differences in ultrasound markers or congestion following continuation or suspension of diuretics for 48 hours. | at baseline | Differences in interstitial (B-lines) and intravascular (IVC and JV diameter, and renal venous flow) congestion by ultrasound in patients with heart failure following continuation or suspension of diuretics for 48 hours. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| The acute variation in interstitial and intravascular congestion on imaging tests following administration of diuretics. | up to 3 hours | The acute variation in interstitial (B-lines) and intravascular (inferior vena cava, jugular vein diameter and renal venous flow) congestion on imaging tests following administration of diuretics. |
| The acute variation in biomarkers of congestion, inflammation and myocardial injury following administration of diuretics. | at 3 hours | The acute variation in biomarkers of congestion (NT-proBNP), inflammation (HsCRP) and myocardial injury (Troponin) following administration of diuretics. |
Countries
United Kingdom
Contacts
Primary ContactPierpaolo Pellicori, MD, FESC
Outcome results
None listed