Key result
Doraya catheter safely lowers CVP by ~6 mm Hg in acute heart failure.
Why the study?
Lowering elevated central venous pressure may reduce renal dysfunction in acute heart failure patients, but the safety and feasibility of the Doraya catheter had not been tested in humans.
Does transient Doraya catheter deployment safely improve hemodynamics and diuresis in acute heart failure patients with poor diuretic response?
Does transient Doraya catheter deployment safely improve hemodynamics and diuresis in acute heart failure patients with poor diuretic response?
In a first-in-human study, the Doraya catheter safely and effectively lowered central venous pressure and improved diuresis in acute heart failure patients with poor diuretic response.
May support Doraya feasibility in diuretic-resistant acute HF; hypothesis-generating and should not yet change practice.
Lowering elevated central venous pressure may reduce renal dysfunction in acute heart failure (AHF) patients. The Doraya catheter lowers renal venous pressure by creating a gradient in the inferior vena cava below the renal veins. Here, we present a first-in-human feasibility study of the Doraya catheter performed on 9 AHF patients. We assessed the safety, feasibility, and acute clinical (hemodynamic and renal) effects of transient Doraya catheter deployment when added to the standard diuretic-based regimen in AHF patients with a poor diuretic response. The procedures decreased central venous pressure from 18.4 ± 3.8 mm Hg to 12.4 ± 4.7 mm Hg (P < 0.001) and improved mean diuresis and clinical signs of congestion. No device-related serious adverse events were observed. Thus, Doraya catheter deployment was safe and feasible in AHF patients. (First In Human Study of the Doraya Catheter for the Treatment of AHF Patients; NCT03234647)
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Zymliński et al. (2023) studied Acute heart failure (n=9). Doraya catheter vs. Baseline was evaluated on Central venous pressure (p=<0.001). Doraya catheter deployment in acute heart failure patients safely decreased central venous pressure from 18.4 to 12.4 mm Hg (P<0.001) with no device-related serious adverse events.
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