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Test Code ACETA Acetaminophen

Specimen Type

Blood

Preferred Collection Container

GRN-PST

Collection Instructions

Routine venipuncture, When evaluating possible toxicity, 4-hour post ingestion sample should be drawn.

Collection Volume

3 mL

Minimum Collection Volume

1 mL

Testing Volume

0.2 mL (200 ul)

Rejection Criteria

Specimen not stored properly, grossly lipemic, hemolyzed and icteric specimens, Inadequate labeling, improper collection.

Specimen Storage and Stability

Separate serum and refrigerate.

Day(s) and Time(s) Performed

Monday through Sunday, 24 hours

Alias

Acetaminophen, Serum; Datril; Liquiprin; Paracetamol; Tempra; Tylenol; Anacin-3; Panadol; Panex;

EPIC Code

LAB43

Acceptable Collection Container

GRN-PST, SST, R-NoGel, G-NoGel

Patient Preparation

Therapeutic monitoring should be drawn 30-60 minutes post oral dose. (Peak), (Trough): Prior to next dose.

Additional Information

Acetaminophen is rapidly absorbed from the gastrointestinal tract, with peak levels occurring 1-3 hours after ingestion. Serum levels drawn less than 4 hours after ingestion may not represent peak levels.The normal half-life of the drug is approximately 3 hours. A half-life of greater than 4 hours indicates impaired metabolism and potential for hepatic injury. Toxicity due to acetaminophen should be monitored by determining both serum concentration and rate of clearance (half-life). An elevated serum acetaminophen with a half life of greater than 4 hours indicates a high likelihood of hepatic injury. The hepatic toxicity of acetaminophen is related to the formation of one or more highly reactive metabolites in the liver. Orally administered N-acetylcysteine (Mucomyst) has been shown to provide protection against acetaminophen toxicity. The patient’s condition should be monitored clinically for hepatotoxicity. Liver function tests may be indicated

Turn Around Time

24 hours; Stats – 2 hours

Lab Department

Chemistry

LOINC

3298-7

CPT

80143