Cardio-Renal Syndrome
Conditions
Brief summary
The purpose of this study is to investigate whether hemodynamic data obtained by a noninvasive bio-impedance system (NICAS) sampled from patients with cardiorenal syndrome type I (CRS1) improve clinical outcomes. We hypothesize that hemodynamic data provided to the caring physician will improve management of CRS1 patients.
Detailed description
Patients admitted to the hospital due to acute decompensation of heart failure (ADHF) may manifest some deterioration in their renal function. The latter is associated with unfavorable outcomes: prolonged hospitalization and death. Cardiorenal syndrome type 1 (CRS1) is defined as a deterioration in renal function manifested by an increase in serum creatinine level by \>0.3 mg% compared to patient's baseline level. The etiology of CRS1 is not clear and may be related to body fluid overload congesting the kidneys or dehydration reducing perfusion to the kidneys. Body fluid status is affected by diuretics. Presently, the practitioner has no objective data to assess whether CRS1 resulted from fluid overload or dehydration. In this study investigators plan to measure hemodynamic parameters from all patients admitted with CRS1 to our department. Parameters will be measured using the noninvasive bio-impedance system (NICAS). Randomly, patients will be allocated to either a study or control group. In the study group, the hemodynamic variables of the NICAS system will be available to the caring physicians. The physicians will use the data according to their discretion. The hemodynamic system is a decision making supporting system and therefore the physician may use the data according to his/her understanding. In the control group, the hemodynamic variables of the NICAS system will not be available to the caring physicians. We hypothesize that using the NICAS system as a decision making supporting system will improve patient management by decreasing length of hospitalization, and shortening the time interval to reverse creatinine to its baseline level.
Interventions
OTHERProviding caring physicians with hemodynamic variables
NICAS electrodes are applied to the skin of the forearm bilaterally (similar to EKG electrodes). Conductors, attached to the electrodes, connect the patient with the measuring system.
Sponsors
HaEmek Medical Center, Israel
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
40 Years to 90 Years
Healthy volunteers
No
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Mean hospitalization duration (in days) | 2 months | Time of hospitalization is defined from time of recruitment till the time patient is ready for discharge. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Time from maximum serum creatinine level to patient's discharge | 2 months | Time from maximum serum creatinine level to time when patient is ready for discharge |
| Maximum difference in serum creatinine level | 2 months | This outcome is defined by the maximum serum creatinine level obtained during the followup of the patient minus patient's mean serum creatinine level |
Outcome results
None listed