No registrations found.
ID
Source
Brief title
Health condition
Heart failure
Sponsors and support
Intervention
Outcome measures
Primary outcome
All cause mortality and a composite of all-cause mortality and/or first readmission for cardiovascular reasons within 6 months after discharge.
Secondary outcome
Cause specific mortality
Quality of life score
Background summary
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.
Study objective
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.
Study design
Shortly after discharge (one to two weeks)
6 months after discharge
Intervention
None
Inclusion criteria
- Undergo treatment for acute decompensated heart failure
- Aged 18 or above and mentally competent.
- Capable of understanding the Dutch language.
- Must sign informed consent.
Exclusion criteria
- Patients where follow-up is not possible (e.g. in-hospital mortality or follow-up not
taking place at the study center).
Design
Recruitment
Followed up by the following (possibly more current) registration
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL6774 |
NTR-old | NTR7643 |
CCMO | NL65323.100.18 |
OMON | NL-OMON46619 |