Diagnostics & Screening
- Appropriate screenings for unhealthy alcohol use, binge drinking, and alcohol use disorder
- Alcohol Use Disorders Inventory Test (AUDIT)
- AUDIT-C (questions 1-3 of AUDIT)
- Biomarkers of alcohol use can be found in urine, hair, or blood
- NOT recommended to use as tools to “catch” people à open the floor for discussion
- Patients should always consent to testing
Laboratory Values
Liver Related Enzymes | ||
Laboratory Test | Description | Key Points |
Aminotransferases
(AST/ALT) | -Produced in hepatocytes
-Indicates hepatocellular injury -Rapidly changing | -Inadequate to establish alcohol use
-AST:ALT ratio > 1 may indicate cirrhosis 2/2 alcohol |
Gamma-glutamyl transferase
(GGT) | -Enzyme found in cell membranes in spleen and liver tissues
– | -Frequently elevated in heavy drinking
-Greater sensitivity than AST for cirrhosis -Not specific for alcohol use |
Bilirubin | -Created through degradation of several heme-containing proteins
-Non-specific to liver disease | -Elevations occur in 1later disease, and may indicate more severe cirrhosis
– |
Additional Labs | ||
Laboratory Test | Description | Key Points |
Albumin | -Produced by the liver in hepatocytes, accounts for 10% of liver protein production daily
-Provides oncotic pressure in plasma -Indicator of nutritional status | -Lower albumin carries an overall negative prognosis (cirrhosis + other disease states)
-Should not be supplemented externally (ALBIOS, ATTIRE) for sake of repletion |
INR | -Prothrombin time compared to a laboratory normative prothrombin time
-Designed with vitamin-k antagonists in mind | -NOT an indication of bleed risk
-Patients may be in a hypercoagulable state despite elevated INR |
Platelets | -Synthesized by the liver
-Improved prognostic factor for bleeding when compared to INR | -Can be used as a biomarker for cirrhosis severity, not validated, taking trend and baseline into account |