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Fractional Excretion of Urea for the Differential Diagnosis of Acute Kidney Injury in Liver Cirrhosis

A

Assiut University

Status

Unknown

Conditions

Liver Cirrhosis

Treatments

Diagnostic Test: FEUrea

Study type

Observational

Funder types

Other

Identifiers

NCT03675633
FEUrea in liver cirrhosis

Details and patient eligibility

About

The aim of this study is to evaluate the diagnostic performance of FEUrea for the differential diagnosis of AKI in patients with cirrhosis and ascites Specifically, the ability of FEUrea to distinguish between ATN versus Pre renal azotemia and HRS.

Full description

AKI according to KDIGO guidelines is defined as the followings:

  • An increase in serum creatinine by ≥0.3 mg/dl (≥26.5 µmol/l) within 48 h
  • An increase in serum creatinine to ≥1.5 times baseline within the previous 7 days
  • Urine volume ≤0.5 ml/kg/h for 6 h Serum creatinine overestimates renal function in cirrhotic patients due to a number of factors: Creatinine production in patients with cirrhosis is reduced due to muscle wasting, there is an increased secretion of creatinine in the renal tubules, sCr may be diluted due to an increased volume of distribution, and finally, high bilirubin levels may interfere with the assays to measure its level. Recently, the International Club of Ascites (ICA) has adopted the concept of AKI which was developed originally to be used in general critically-ill patients. AKI is defined as the increase of at least 0.3 mg/dL (26 μmol/L) and/or ≥ 50% from baseline, within 48 hours Since urea absorption is largely modulated in the proximal tubules, it is not affected by diuretics acting more distally. The investigators therefore hypothesized that the fractional excretion of urea (FEUrea) could serve as a clinical aid in making an early distinction between ATN versus Pre renal azotemia and HRS type 1 in patients with cirrhosis and ascites presenting with AKI Fractional excretion of urea (FEUrea) ([urine urea nitrogen/ blood urea nitrogen)/(urine creatinine/plasma creatinine)] X 100) < 35% is specific for prerenal azotemia, and > 50% is specific for ATN

Enrollment

100 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Liver cirrhosis of any etiology diagnosed by clinical parameters involving laboratory tests, endoscopic or radiologic evidence of cirrhosis,
  • History of decompensation (hepatic encephalopathy, ascites, variceal bleeding, jaundice)
  • Age greater than 18 years
  • Presence of moderate or severe ascites

Exclusion criteria

Patients excluded from analysis were those who did not meet inclusion criteria as well as the following

  • Prior liver or kidney transplant,
  • Advanced chronic kidney disease G4(GFR category grade 4) according to KDIGO guidelines.
  • Patients on acute or chronic renal replacement therapy,
  • Ambiguous diagnosis of AKI and phenotype of AKI,
  • Patients with hepatocellular carcinoma.

Trial design

100 participants in 1 patient group

FEUrea in decompensated liver cirrhosis
Description:
FEUrea for the differential diagnosis of AKI in patients with cirrhosis and ascites Specifically, the ability of FEUrea to distinguish between ATN versus Pre renal azotemia and HRS
Treatment:
Diagnostic Test: FEUrea

Trial contacts and locations

0

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Central trial contact

Nermeen Mobarez, specialist; Essam Abdel Aziz, lecturer

Data sourced from clinicaltrials.gov

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