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Randomized Controlled Trial
. 2012 Mar;18(3):176-82.
doi: 10.1016/j.cardfail.2011.12.009. Epub 2012 Feb 2.

Cardiorenal rescue study in acute decompensated heart failure: rationale and design of CARRESS-HF, for the Heart Failure Clinical Research Network

Affiliations
Randomized Controlled Trial

Cardiorenal rescue study in acute decompensated heart failure: rationale and design of CARRESS-HF, for the Heart Failure Clinical Research Network

Bradley A Bart et al. J Card Fail. 2012 Mar.

Abstract

Background: Worsening renal function is common among patients hospitalized for acute decompensated heart failure (ADHF). When this occurs, subsequent management decisions often pit the desire for effective decongestion against concerns about further worsening renal function. There are no evidence-based treatments or guidelines to assist in these difficult management decisions. Ultrafiltration is a potentially attractive alternative to loop diuretics for the management of fluid overload in patients with ADHF and worsening renal function.

Methods and results: The National Heart, Lung, and Blood Institute Heart Failure Clinical Research Network designed a clinical trial to determine if ultrafiltration results in improved renal function and relief of congestion compared with stepped pharmacologic care when assessed 96 hours after randomization in patients with ADHF and cardiorenal syndrome. Enrollment began in June 2008. This paper describes the rationale and design of the Cardiorenal Rescue Study in Acute Decompensated Heart Failure (CARRESS-HF).

Conclusions: Treating the signs and symptoms of congestion in ADHF is often complicated by worsening renal function. CARRESS-HF compares treatment strategies (ultrafiltration vs stepped pharmacologic care) for the management of worsening renal function in patients with ADHF. The results of the CARRESS-HF trial are expected to provide information and evidence as to the most appropriate approaches for treating this challenging patient population.

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Figures

Fig. 1
Fig. 1
Two-dimensional grid for the primary end point of change in weight and change in creatinine 96 hours after enrollment. Each study subject's change in weight and change in creatinine will be plotted on the figure such that subjects in quadrant I will represent those with increased weight and increased creatinine and subjects in quadrant III will represent those with weight loss and a reduction in creatinine.

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