External validation of discharge risk score for patients admitted with acute decompensated heart failure (ADHF). Determine added value of biomarkers in multimarker panel for discharge risk stratification of ADHF patients. Determine added value of…
ID
Bron
Verkorte titel
Aandoening
Heart failure
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
All cause mortality and a composite of all-cause mortality and/or first readmission for cardiovascular reasons within 6 months after discharge.
Achtergrond van het onderzoek
Patients admitted with acute decompensated HF (ADHF) have poor short- and long-term prognosis, after discharge ≈ 20% of patients are
readmitted within 30 days and up to 50% by 6 months. A reduction in HF readmissions simultaneously improves the
quality of care and reduces costs. To reduce HF readmission rates a comprehensive characterization of predictors of
readmission in patients with HF is imperative. Multivariable risk scores can predict risk for adverse events such as
readmission or mortality in patients admitted with ADHF. Next to natriuretic peptide levels, other biomarkers have emerged that allow prognostication of patients admitted with
ADHF. Recent studies have shown that combining multiple biomarkers in a multimarker panel, substantially improves
prediction of adverse events beyond current metrics. The primary objective of this study is to
perform an external validation of the ELAN-HF score in a cohort of patients admitted with ADHF at the Catharina
Hospital. A second primary objective is to serially measure a multimarker panel in this cohort and combine these
measurements with clinical data from multiple sources (e.g. prescribed medication, medical history, physiological
measurements etc.) to capture the heterogeneous nature of HF in a novel discharge risk score.
Doel van het onderzoek
External validation of discharge risk score for patients admitted with acute decompensated heart failure (ADHF).
Determine added value of biomarkers in multimarker panel for discharge risk stratification of ADHF patients.
Determine added value of wrist-based PPG measurements after discharge in predicting readmission and/or mortality of ADHF patients.
Determine association between biomarkers and quality of life in patients with ADHF.
External validation of a Bayesian hemodynamics model in patients with ADHF.
Onderzoeksopzet
Shortly after discharge (one to two weeks)
6 months after discharge
Onderzoeksproduct en/of interventie
None
Algemeen / deelnemers
Wetenschappers
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- Undergo treatment for acute decompensated heart failure
- Aged 18 or above and mentally competent.
- Capable of understanding the Dutch language.
- Must sign informed consent.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Patients where follow-up is not possible (e.g. in-hospital mortality or follow-up not
taking place at the study center).
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL6774 |
NTR-old | NTR7643 |
CCMO | NL65323.100.18 |
OMON | NL-OMON46619 |