The Role of Adrenomedullin on the Outcome of Severe Heart Failure: a Clinical Randomized Study
Heart Failure

About this trial
This is an interventional treatment trial for Heart Failure focused on measuring adrenomedullin, heart failure, ultrafiltration, hemofiltration
Eligibility Criteria
Inclusion Criteria:
more than two item:
- more than eighteen years of age
- orthopnea
- Chest Rx with cardiomegaly and pulmonary infiltration
- edema
- diuretic resistance
Exclusion Criteria:
- insulin dependent diabetes
- hepatic cirrhosis
- vascular access problems
- creatinine more than 2,5 mg/dl before acute heart failure
- systemic infection
- aortic stenosis and heart transplantation
- radiologic contrast up to 72 hours prior randomization
- advanced neoplasia
Sites / Locations
- Instituto de Cardiologia
Arms of the Study
Arm 1
Arm 2
Arm 3
Other
Experimental
Experimental
clinical treatment
ultrafiltration
isovolumetric hemofiltration
Patients with previous diagnosis of decompensated III and IV Heart Failure will be included. The clinical treatment will be optimized. Clinical assessment, Adrenomedullin, Angiotensin II, Brain Natriuretic Peptide, oxydative stress, sympathetic nervous system activity will be evaluated at the beginning, at discharge and 90 days after randomization(plus or minus3).
ultrafiltration will be done on decompensated patients III and IV acute heart failure on Intensive Care Unit. This patients will have biochemical analysis, adrenomedullin, angiotensin II,Brain Natriuretic Peptide, oxydative stress measurements,sympathetic nervous system activity evaluated and clinical outcome analyzed at the beginning,at discharge and 90 days after randomization(plus or minus 3). Diuretic will be withdrawn during ultrafiltration.
Patients randomized to this group will have isovolumetric hemofiltration on Intensive Care Unit. They will have biochemical analysis, Adrenomedullin plasmatic level, Brain Natriuretic Peptide Level, Angiotensin II level, Oxydative stress measurement,sympathetic nervous system, and clinical outcome evaluated at the study beginning,at discharge and 90 days after randomization(plus or minus 3).