Key result
Ongoing trial evaluates whether IVC ultrasound-guided therapy improves decongestion in acute decompensated heart failure.
Why the study?
Optimal guidance of decongesting therapy and treatment targets in acute decompensated heart failure presenting with volume overload are not well defined.
Does ultrasound assessment of the IVC in addition to clinical assessment improve decongestion in patients with acute decompensated heart failure?
RCT (n=388)
Single-blind
Permuted blocks of random sizes, stratified by trial site and NYHA class
Yes
Does ultrasound assessment of the IVC in addition to clinical assessment improve decongestion in patients with acute decompensated heart failure?
The CAVA-ADHF-DZHK10 trial will determine if adding IVC ultrasound to clinical assessment improves decongestion (measured by NT-proBNP reduction) in patients with acute decompensated heart failure.
AIMS: Treating patients with acute decompensated heart failure (ADHF) presenting with volume overload is a common task. However, optimal guidance of decongesting therapy and treatment targets are not well defined. The inferior vena cava (IVC) diameter and its collapsibility can be used to estimate right atrial pressure, which is a measure of right-sided haemodynamic congestion. The CAVA-ADHF-DZHK10 trial is designed to test the hypothesis that ultrasound assessment of the IVC in addition to clinical assessment improves decongestion as compared with clinical assessment alone. METHODS AND RESULTS: CAVA-ADHF-DZHK10 is a randomized, controlled, patient-blinded, multicentre, parallel-group trial randomly assigning 388 patients with ADHF to either decongesting therapy guided by ultrasound assessment of the IVC in addition to clinical assessment or clinical assessment alone. IVC ultrasound will be performed daily between baseline and hospital discharge in all patients. However, ultrasound results will only be reported to treating physicians in the intervention group. Treatment target is relief of congestion-related signs and symptoms in both groups with the additional goal to reduce the IVC diameter ≤21 mm and increase IVC collapsibility >50% in the intervention group. The primary endpoint is change in N-terminal pro-brain natriuretic peptide from baseline to hospital discharge. Secondary endpoints evaluate feasibility, efficacy of decongestion on other scales, and the impact of the intervention on clinical endpoints. CONCLUSIONS: CAVA-ADHF-DZHK10 will investigate whether IVC ultrasound supplementing clinical assessment improves decongestion in patients admitted for ADHF.
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Jobs et al. (2020) conducted an RCT in Acute Decompensated Heart Failure (n=388). Decongestion therapy guided by IVC ultrasound in addition to clinical assessment vs. Clinical assessment alone was evaluated on Change in N-terminal pro-brain natriuretic peptide (NT-proBNP) from baseline to hospital discharge (ratio of NT-proBNP at discharge to baseline). This design rationale describes an ongoing trial investigating whether supplementing clinical assessment with inferior vena cava ultrasound improves decongestion in acute decompensated heart failure.
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