In this pilot, investigator-initiated multi-centre, multinational, observational study the investigators would like to examine the impact of therapy optimization on the level of biomarkers in patients with acute decompensated and decompensated chronic heart failure. The primary objective is to determine the best time point for measuring biomarker levels during therapy optimization in patients with decompensation to predict clinical outcomes such as mortality, hospitalisation, and quality of life. Secondary objectives are: 1. To evaluate the impact of guideline-recommended medication on biomarker levels during and following recompensation. 2. To evaluate whether the trajectory of relevant biomarkers (MR-proANP, MR-proADM) is of relevance to guide medical therapy following decompensation. 3. To evaluate whether the degree of biomarker change (e.g. slow versus rapid change) is of relevance with regard to hemodynamic stability and cardiovascular events such as hospitalisation. 4. To evaluate whether the trajectory of relevant biomarkers (copeptin, CT-pro-ET1) is of relevance to guide medical therapy following decompensation.
Study Type
OBSERVATIONAL
Enrollment
150
Charité Campus Virchow Klinikum-Medizinische Klinik mit Schwerpunkt Kardiologie
Berlin, Germany
Time to first event - all cause death - cardiovascular death - all cause hospitalisation - cardiovascular hospitalisation - hospitalization for heart failure
Time to first event * all cause death * cardiovascular death * all cause hospitalisation * cardiovascular hospitalisation * hospitalization for heart failure
Time frame: from study start (day 1) during hosptialisation until second year of follow up
quality of life
The EuroQoL EQ-5D quality of life scale consists of 5 items scaled 1 to 3 reflecting different dimensions of quality of life and a visual analog scale measuring overall self-rated health. The Short Form 36 Health Survey. The Hospital Anxiety and Depression Scale (HADS) consists of 14 items measuring symptoms of anxiety and depression in physically ill patients. The ENRICHD Social Support Instrument (ESSI) has been developed as a brief tool for measuring perceived social support in the large randomized ENRICHD study.
Time frame: from study start (day 1) during hosptialisation until second year of follow up
Six-minute walk test distance
Six-minute walk test distance will be performed at Visit 1-6 a s well as Follow-up after first and second year.
Time frame: from study start (day 1) during hosptialisation until second year of follow up
Echocardiographic parameters
Echocardiography (done within the first seven days from the day of entering the study): dimensions of the left ventricle, wall thickness and EF per Simpson (if it is not possible to determine EF per Simpson in particular cases due to very limited sound conditions, then it could be visually assessed by an experienced echocardiographer), diastolic function of the left ventricle per the American Society of Echocardiography (ASE): mitral Doppler, tissue Doppler, pulmonary vein Doppler.
Time frame: from study start (day 1) during hosptialisation until second year of follow up
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