MYTHOS-HF: Furosemide-induced Diuresis With Matched Dehydration Compared to Standard Diuretic Therapy in Patients With Acute Heart Failure and Overt Fluid Overload
Study Details
Study Description
Brief Summary
Acute decompensated heart failure (ADHF) is a complex clinical syndrome caused by cardiac abnormalities compromising the ability of the heart to provide a blood supply adequate to the metabolic needs of peripheral tissues. ADHF is characterized by systemic and pulmonary fluid retention, with weight gain, peripheral edema, needing diuretic therapy. Moreover, ADHF is associated with neurohormonal hyper-activation with enhanced sympathetic nervous and renin-angiotensin-aldosterone systems stimulation, that sustain the vicious circle of cardiac dysfunction and fluid retention.
The administration of high doses of diuretics, usually required in ADHF treatment, can induce hypovolemia-induced neurohormonal activation and transient deterioration of kidney function, that, in turn, counteracts the effect of diuretics and limits recovery from fluid overload.
The investigators hypothesized that, in patients with ADHF, a more controlled and physiologically-oriented dehydration may blunt diuretic-associated neurohormonal activation, thus providing a safer and more sustained clinical benefit. This controlled dehydration can be achieved by combining furosemide with the RenalGuard System (see The RenalGuard™ System Operator's Manual for specific instructions in setting up and running the device). To date, no data have been provided regarding the potential beneficial effect of this therapeutic strategy in patients with ADHF and fluid overload. Much of the evidences on the use of the RenalGuard system comes from the clinical setting of acute kidney injury (AKI) prevention in patients undergoing intravascular contrast exposure. In this specific field, furosemide-induced high-volume diuresis with concurrent maintenance of intravascular volume through matched hydration, by the RenalGuard System, is now considered by current Guidelines a recommended strategy for AKI prevention in patients with chronic renal failure undergoing coronary interventional procedures. Based on this experience, the investigators will assess the safety and efficacy of this known system capable of delivering intravenous fluid in an amount exactly pre-determined, considering the volume of urine produced by the patient and precisely weighed by the system. This could prevent hypovolemia that may occur in response to high-volume diuresis induced by furosemide. The researchers will perform a spontaneous, prospective, randomized trial aiming at investigating the effect of combined furosemide-induced diuresis and automated matched dehydration, compared with standard furosemide administration in ADHF patients with fluid overload.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| No Intervention: Control Group Furosemide infusion (standard treatment) |
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| Experimental: RenalGuard group Furosemide infusion with matched de-hydration |
Device: RenalGuard device
Patients will be given an intravenous loading dose of 40 mg of furosemide and continuous infusion of furosemide based on baseline eGFR. An additional bolus of 40 mg of furosemide will be administered and the infusion rate increased according to the same protocol of the control group (Figure 1). The venous peripheral cannula will be connected with the extracorporeal circuit of the RenalGuard System (PLC Medical Systems Inc., MA) for fluid infusion. The RenalGuard System is capable of delivering sterile replacement solution to a patient in an amount matched, or higher or lower, to the volume of urine produced by the patient. Thus, in the RenalGuard group, estimated daily targeted negative fluid balance will be utilized to define, for each patient, hourly negative fluid balance to be set in the RenalGuard system display.
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Outcome Measures
Primary Outcome Measures
- Daily serum creatinine measurement during study treatment for assessment of acute kidney injury occurrence [Daily, up to 72 hours]
Blood sample for creatinine evaluation will be performed daily
Secondary Outcome Measures
- Daily weight decrease during study treatment [Daily, up to 72 hours]
Weight evaluation will be performed daily
Eligibility Criteria
Criteria
Inclusion Criteria:
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18 years of age
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New York Heart Association (NYHA) functional class III or IV
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estimated weight gain due to peripheral fluid overload >4 kg
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admission BNP values >400 pg/ml if in sinus rhythm and >600 pg/ml if in atrial fibrillation
Exclusion Criteria:
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inability to provide informed consent
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acute pulmonary edema, cardiogenic shock
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end-stage renal disease (Stage V) or need for renal replacement therapy
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ongoing treatment with Entresto (BNP not reliable)
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need for inotropic/vasopressor drug support
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contraindications to placement of a Foley catheter.
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Known hypersensitivity to furosemide
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Centro Cardiologico Monzino, Irccs | Milano | Italy | 20138 |
Sponsors and Collaborators
- Centro Cardiologico Monzino
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- CCM 964