CARRESS - Duke University
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CARRESS
Cardiorenal Rescue Study in
Acute Decompensated Heart
Failure
Duke Heart Failure Research
Pager: 970-0736
Purpose
Randomized, controlled, multi-center clinical
trial to test the hypothesis that ultrafiltration
compared to a stepped pharmacological care
approach will result in improved renal
function and relief of congestion in patients
hospitalized with acute decompensated heart
failure (ADHF) and cardiorenal syndrome.
Inclusion Criteria
Patients admitted with
ADHF who develop
cardiorenal syndrome
Cardiorenal
syndrome:
serum creatinine
concentration >0.3
mg/dL in setting of
persistent congestion
Interventions
Randomized to
1 of 2
treatments
Slow continuous
venous
ultrafiltration
Stepped pharmacologic
care
Interventions
ULTRAFILTRATION (UF)
GROUP
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Loop diuretics d/c’d during UF
Receive Heparin; goal PTT
2-2.5x normal
UF fluid removal 200cc/hr;
continue until signs/symptoms
of congestion optimized
Patients randomized to UF
group must be transferred to
7300 unit to receive treatment
STEPPED
PHARMACOLOGIC GROUP
–
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IV diuretics used to address
signs/symptoms of
congestion
Completed when volume
status optimized
Algorithm by Heart Failure
Network provided;
addresses intensification of
diuretics and use of
vasodilators and inotropes
Nursing Roles
Ensure fluid restriction and 2gm Na diet as ordered
Weigh patients before treatment and daily qAM
Record I&O
Administer study drugs according to CPOE orders
Nursing Roles
For patients randomized to UF arm:
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ELC* + 18 gauge IV
Heparin protocol; start when PTT 50-75
Hold diuretics
UF removal rate 200cc/hr
VS q15 min x1 hr, q 30-60 min x4 hr, q 4 hrs
Secure and flush post treatment policy
*ELC = extended-length catheter
Outcomes
Why is this study being done?
To look at the safety and efficacy of UF for treatment
of persistent congestion and cardiorenal syndrome
as measured by:
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Change in serum creatinine AND weight
Treatment failure
Change in electrolytes
% achieving clinical decongestion
Total net fluid loss