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TPMT Phenotype+/- Genotype

Alternative Names:Thiopurine Methyl Transferase
Laboratory:Clinical Biochemistry
Test Code:TPMT
Specimen Types:Blood
Container Types:
EDTA 10 mL
Collection & Request Instructions:

Used for the identification of patients at risk of myelosuppression prior to initiation of thiopurine drug therapy (e.g. azothioprine, 6-mercaptopurine, thioguanine). We are now sending TPMT tests to PathWest (QEII Medical Centre, WA) who offer a comprehensive, sequential TPMT testing service. TPMT Phenotype, which measures thiopurine methyltransferase activity, is the first-line test and if it is normal no further testing is indicated. If TPMT Phenotype is abnormal, it is automatically followed by the TPMT Genotype test which screens for the common TPMT mutations. There are rare mutations not detected by this Genotype test. An abnormal Phenotype which is not associated with common mutations will prompt sequencing of the entire coding region of the TPMT gene to detect rare mutations.

Processing Instructions:Do Not Centrifuge
Store at 4'C
Transport Instructions between Sites and/or Laboratories:Room Temperature
Assay Frequency:Weekly
External Laboratory:PathWest QEII Medical Centre
External Transport Instructions:Send at 4'C with Ice Pack

Specimens are usually transported to W.A. Tuesday and Thursdays.

Sample stability: 7 days.

Send sample chilled

AVOID FREEZING SAMPLE DURING TRANSPORT TO EXTERNAL LAB