Bioimpedance and Hand-held Echocardiographay for Clinical Decision-making in Treatment of Cardio-renal Syndrome Type I
Cardio-Renal Syndrome
About this trial
This is an interventional treatment trial for Cardio-Renal Syndrome
Eligibility Criteria
Inclusion Criteria:
- Patient admitted for acute decompensation of heart failure and developed cardiorenal syndrome (all three criteria below are required):
A. Evidence of heart failure defined by either (i) or (ii) and (iii), where:
(i) is clinical complaints of dyspnea or leg swelling or fatigue (ii) is clinical findings of pulmonary rales, leg edema, or congestion on chest film (iii) is recent (within 1 year of admission) echocardiographic examination demonstrating heart failure B. Patient as in A (above) whos serum creatinine level on admission is 0.3 mg% greater than patient's baseline.
C. Patient capable of submitting informed consent
Exclusion Criteria:
- Other causes for dyspnea or leg edema (e.g. exacerbation of COPD, pneumonia, liver cirrhosis, hypoalbuminemia, nephrotic syndrome)
- other causes for acute renal failure (e.g. contrast media nephropathy 10 days prior to admission, use of NSAIDS or antibiotics (aminoglycosides, quinolones), diarrhea, vomiting, rhabdomyolysis, seizures, sepsis.
- Anemia (Hb<8 gr%)
- significant bleeding (upper or lower GI, hemoptysis)
- BMI>40, or BMI<18
- Signs of a new myocardial infarction by EKG, and increase in troponin levels to levels 1.5 above baseline levels.
- Hypothyroidism
- Addison's disease
- patient on Hemo- or peritoneal dialysis
- Mechanical ventillation
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Hemodynamic data available
Hemodynamic data not available
Providing caring physicians with hemodynamic variables measured using the NICAS system.
Hemodynamic variables measured using the NICAS system will not be provided to the caring physicians.