The primary objective of this study is to explore the correlation between invasive and non-invasive haemodynamic variables and monitor the effect of treatment during admission for acute decompensated heart failure. In particular to investigate…
ID
Bron
Aandoening
Heart Failure, Acute Heart Failure
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
The ability of the device data to detect improvements in haemodynamic status.
Doel van het onderzoek
The primary objective of this study is to explore the correlation between invasive and non-invasive haemodynamic variables and monitor the effect of treatment during admission for acute decompensated heart failure. In particular to investigate correlations between device data (trans-thoracic impedance) and invasive measures of pulmonary capillary wedge pressures.
The secondary objective is to investigate the relationship between device data at discharge and risk of readmission/death at 6 months.
Onderzoeksproduct en/of interventie
N/A
Publiek
Riet
Dierckx
Moorselbaan 164
9300
Wetenschappelijk
Riet
Dierckx
Moorselbaan 164
9300
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- Age ≥ 18 years
- Presence of an impedance-enabled CRT and/or ICD device > 2 months
- Hospitalized because of symptoms/ signs of decompensation
- Objective evidence of cardiac dysfunction
- NTproBNP on admission > 450 pg/ml
- Follow-up exclusively in the OLV Hospital of Aalst
- Need for treatment with diuretics (IV or oral), in higher dose than maintenance dose
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Severe pulmonary disease (one minute forced expiratory volume below 1.0L/s)
- Poor echo window
- Anticoagulant therapy
- Need for ventilation
- Prisoners
- Pregnancy
Opzet
Deelname
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In overige registers
| Register | ID |
|---|---|
| NTR-new | NL5207 |
| NTR-old | NTR5356 |
| Ander register | : B1260201523663 |