A Comparison of Two Albumin Administration Schedules for Spontaneous Bacterial Peritonitis
Status: | Completed |
---|---|
Conditions: | Gastrointestinal |
Therapuetic Areas: | Gastroenterology |
Healthy: | No |
Age Range: | 18 - 75 |
Updated: | 4/21/2016 |
Start Date: | September 2010 |
End Date: | January 2015 |
A Randomized Comparison of Two Albumin Administration Schedules for Spontaneous Bacterial Peritonitis
Spontaneous bacterial peritonitis (SBP) is a common and frequently fatal complication of
end-stage liver disease with a mortality of up to 10% primarily due to the development of
kidney failure. Current standard practice is to treat this infection with broad spectrum
antibiotics and salt-poor albumin administration on day one and three of treatment. In this
study the investigators test the hypothesis that the administration of a second dose of
albumin at 48 hours only to patients with renal insufficiency is as effective at preventing
kidney failure as administering the second dose to all patients at 72 hours. In addition, a
kidney function determined approach to albumin dosing may lead to substantial cost and
resource saving from decreased albumin use without compromising treatment efficacy.
end-stage liver disease with a mortality of up to 10% primarily due to the development of
kidney failure. Current standard practice is to treat this infection with broad spectrum
antibiotics and salt-poor albumin administration on day one and three of treatment. In this
study the investigators test the hypothesis that the administration of a second dose of
albumin at 48 hours only to patients with renal insufficiency is as effective at preventing
kidney failure as administering the second dose to all patients at 72 hours. In addition, a
kidney function determined approach to albumin dosing may lead to substantial cost and
resource saving from decreased albumin use without compromising treatment efficacy.
Inclusion Criteria:
- Age 18 to 75
- Evidence of end stage liver disease / cirrhosis
- Documented SBP (ANC > 250 or positive ascites culture
- Ability to provide informed consent
- Serum Creatinine > 1.0 mg/dL and/or Total Bilirubin > 4.0 mg/dL
Exclusion Criteria:
- Nonportal hypertensive ascites (i.e. malignancy)
We found this trial at
1
site
Click here to add this to my saved trials