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Sirolimus Test -
Measures sirolimus levels to monitor transplant therapy, preventing rejection
Synonym Sirolimus Test
Test Code BIOT26040116
Test Type Biochemistry
Pre-Test Condition No special
Report Availability 1–2 D(s)
# Test(s) 1
Test details Sample Report
Sirolimus Test Sample Report Cowin-PathLab
Synonym Sirolimus Test
Test Code BIOT26040116
Test Category Transplant Rejection
Pre-Test Condition No special
Medical History Share & see Updates
Report Availability 1–2 D(s)
Specimen/Sample Refer Updates
Stability @21-26 deg. C 24 H(s)
Stability @ 2-8 deg. C 48 H(s)
Stability @ Frozen Not frozen
# Test(s) 1
Processing Method Biochemistry
Overview: Sirolimus Test
Introduction: The Sirolimus Test measures sirolimus levels to monitor transplant therapy, preventing rejection. Aligned with 2023 AST guidelines, it uses biochemical methods for high specificity, supporting drug monitoring. This test is critical for guiding therapy adjustments and improving outcomes in biochemistry for transplant patients.
Other Names: Rapamycin Assay, Sirolimus Level Test.
FDA Status: Laboratory-developed test (LDT), meeting biochemistry standards for therapeutic drug monitoring.
Historical Milestone: Sirolimus monitoring began in the 1990s with transplant therapy. Biochemical methods improved in the 2000s, enhancing precision.
Purpose: Measures sirolimus levels to monitor transplant therapy, guides dosing, and prevents rejection.
Test Parameters: 1. Sirolimus Level
Pretest Condition: No fasting required. Collect whole blood. Report history of transplant or immunosuppressive therapy.
Specimen: Whole Blood (EDTA, 2-5 mL). Transport in a biohazard container.
Sample Stability at Room Temperature: 24 hours
Sample Stability at Refrigeration: 48 hours
Sample Stability at Frozen: Not frozen
Medical History: Document transplant history, rejection episodes, or immunosuppressive therapy. Include current medications, especially sirolimus.
Consent: Written consent required, detailing the tests purpose, transplant therapy implications, and risks of sample collection.
Procedural Considerations: Uses liquid chromatography-mass spectrometry (LC-MS) to measure sirolimus levels. Results are available in 1-2 days, supporting clinical decisions. Performed in laboratories, often for transplant monitoring.
Factors Affecting Result Accuracy: Improper sample storage or timing of collection relative to dosing can affect results. Drug interactions may alter levels.
Clinical Significance: Therapeutic sirolimus levels confirm effective immunosuppression, guiding dose adjustments. Suboptimal levels may indicate risk of rejection or toxicity.
Specialist Consultation: Consult a transplant specialist or pharmacologist for result interpretation and dosing adjustments.
Additional Supporting Tests: Kidney function tests, tacrolimus levels, or rejection biomarkers to monitor transplant health.
Test Limitations: Non-specific for rejection causes; clinical correlation is needed. Sample timing affects accuracy.
References: AST Transplant Guidelines, 2023; Transplantation, Kahan BD, 2022.

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