Naturally Controlled Decongestion Using Renal Independent System in ADHF Patients, a European Registry

Exclusion Criteria

• •Subject is enrolled to another clinical investigation that might interfere with this study.
• •Baseline systolic blood pressure \<100 mm Hg
• •Subject considered to be in the acute worsening of the heart failure: Requiring ventilation, mechanical support or is clinically unstable requiring pressors, deterioration triggered by arrythmia, infection or other medical condition unrelated to fluid overload.
• •Subject has any known lower body skin problems (open wounds, ulcers)
• •Subject with severe peripheral arterial disease
• •Subject is pregnant or planning to become pregnant within the study period, or lactating mothers.
• •End-stage renal disease (eGFR\<15 ml/min/1.73 m2) or requiring dialysis.
• •Inability or unwillingness to comply with the study requirements.
• •History of heart transplant or actively listed for heart transplant or Left Ventricular Assist Device (LVAD).
• •Implanted left ventricular assist device or implant anticipated \<3 months.
• •Malignancy or other noncardiac condition limiting life expectancy to \<12 months.