About this trial
The goal of this observational study is to learn how changes in urinary sodium and chloride levels relate to fluid overload and short-term outcomes in patients hospitalized with acute heart failure (AHF). The main questions it aims to answer are:
* Do changes over time in urinary sodium and chloride reflect how well excess fluid is being removed during hospitalization? * Are these changes associated with residual congestion at discharge and with the risk of worsening heart failure or death after discharge?
Participants hospitalized for AHF and treated with intravenous diuretics as part of their usual care will have clinical assessments, blood and urine tests, and echocardiographic evaluations collected at several time points during their hospital stay. Researchers will also record clinical outcomes, including worsening heart failure or death, at 30 days and 3 months after discharge.
Eligibility criteria
Qualifiers
Provision of written informed consent prior to any study-related procedures;
Age ≥ 18 years;
Episode of AHF requiring hospital admission and treatment with intravenous furosemide;
New York Heart Association (NYHA) functional class II-IV;
Disqualifiers
Symptomatic hyponatremia or plasma sodium level ≤125 mmol/L;
Hemoglobin <9 g/dL;
Hypokalemia: serum potassium <3 mEq/L;
Chronic kidney disease with estimated glomerular filtration rate (eGFR) <15 mL/min/1.73 m²;
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal
Lead sponsor
Carlos III Health Institute
Collaborator