Sirolimus (Rapamycin), Whole Blood

Specimen requirement

Adult patient:

 

EDTA tube

 

Minimum blood volume: 3 mL

Paediatric patient:

Paediatric EDTA tube

Number of vials: 1

Minimum blood volume: 1.3 mL

Authorisation code required

No

24 Hr available service

No

Precaution Trough level monitoring (pre-dose)

Method

Liquid chromatography-tandem mass spectrometry

Reference interval

Trough level: 5 - 15 µg/L

 

(Source: Clinical Therapeutics (2000) 22 Suppl B: B101)

Clinical indication

Therapeutic drug monitoring in patients receiving sirolimus therapy to avoid rejection of organ transplants and to detect toxic levels.

Result interpretation

An elevated result provides an early indication of the possibility of toxicity.

 

The use of sirolimus together with other immunosuppressants (e.g. cyclosporin A) can be associated with serious toxic side effects, primarily nephrotoxicity. Their adverse side effects include hypertriglyceridaemia, thrombocytopenia and leucopenia.

Measurement of uncertainty

See table.

Frequency of measurement

Weekly