SCD for CRS in Congestive Heart Failure (CHF) (No Left Ventricular Assist Device)

Inclusion Criteria:

Primary hospitalization for acute decompensated chronic systolic heart failure as defined:

Left ventricular ejection fraction ≤35% as confirmed by baseline imaging procedure.
New York Heart Association (NYHA) class III or IV chronic (≤ 90 days) systolic heart failure, with failure to respond to optimal medical therapy (beta blocker, Angiotensin-converting enzyme (ACE) inhibitor or angiotensin receptor blockers (ARB) or valsartan/sacubitril, aldosterone antagonist, unless not tolerated or contraindicated, and loop diuretic, as needed) for 45 of the last 60 days.
Baseline Estimated Glomerular Filtration Rate (eGFR)** ≥ 40 ml/min/1.73 m2 (baseline defined as the highest known eGFR within 90 days of study enrollment)
Worsening renal failure (WRF), defined for the purposes of this study as increase serum creatinine ≥ 0.5 mg/dL from baseline (baseline defined as the lowest known serum creatinine within 90 days of study enrollment)
Cardiorenal syndrome is the most likely explanation for WRF

Persistent signs and /or symptoms of congestion (peripheral edema, dyspnea, pulmonary rales, neck vein distension) despite optimal medical therapy including intravenous diuretic therapy and an estimated need for greater than 5 kg. of fluid removal. For the purposes of this study, optimal intravenous diuretic therapy is defined as:

Furosemide equivalent total daily dose of 240 mg (furosemide 40mg=1mg bumetanide)
Furosemide equivalent dose given either as a single or multiple intravenous bolus or continuous infusion
A furosemide equivalent total daily dose <240 mg if the dose has resulted in >3000 ml urine output/24 hours

Exclusion Criteria:

Prior sensitivity to dialysis device components
Individual with known hypersensitivity to citrate
Bacteremia or possible infection, as evidence by fever, white blood cell count > 10,000/microliter, or any other signs of acute or chronic infection, and any patient receiving antibiotic or antiviral therapy.
Active malignancy requiring chemotherapy, biological therapy or radiation therapy.
The use of intravenous iodinated contrast agent within the prior 72 hours or the anticipated use of such an agent during SCD therapy.
Need for intravenous vasopressor (i.e., phenylephrine, vasopressin), intravenous. vasoconstricting inotrope (i.e., norepinephrine or epinephrine) or dopamine > 3 mcg/kg/min. (Note: use of vasodilating inotropes [i.e., dobutamine and milrinone] or dopamine at ≤ 3 mcg/kg/min will not preclude study inclusion).
Persistent systolic blood pressure (SBP) < 80 mmHg.
White blood cell (WBC)<4000/microliter.
Platelets < 50,000/microliter.
Serum creatinine > 4 mg/dL or receiving dialysis / continuous renal replacement therapy (CRRT)
Acute coronary syndrome within the past month.
Women who are pregnant, breastfeeding a child, or trying to become pregnant.
Subject not able to sign informed consent.
Use of any other investigational drug or device within the previous 30 days
Concurrent enrollment in another interventional clinical trial. Patients enrolled in clinical studies where only measurements and/or samples are taken (i.e., no test device or test drug used) are allowed to participate.