Methodology
Flow cytometry
Test Description and clinical significance
Probes/Genes
CD2, CD3, CD4, CD5, CD7, CD8, CD10, CD11c, CD16, CD19, CD20, CD23, CD25, CD38, CD45, CD56, CD57, CD103, CD123, Kappa, Lambda
Disease:
Anemia, leukopenia, leukocytosis, pancytopenia, lymphoma, non-Hodgkin lymphoma, multiple myeloma, plasma cell neoplasm, leukemia, acute leukemia, chronic leukemia
Multiparameter flow cytometry plays an important role in the diagnosis, staging, and monitoring of patients with a suspected hematological malignancy.
Markers run evaluate lymphocytes to identify presence/absence of malignant cells.
Specimen Requirements
Collection:
Peripheral blood: 2-5 mL in Green top (sodium heparin) tube preferred, OR purple top (EDTA) tube
Bone marrow aspirate: 1-2mL in Green top (sodium heparin) tube preferred, OR purple top (EDTA) tube
Fresh tissue: 1 cm3 marble-sized piece of tissue in RPMI or sterile saline
Fluid: 10mL fluid in RPMI
Stability:
Peripheral blood: 48 hours
Bone marrow aspirate: 48 hours
Fresh tissue: 24 hours
Fluid: 24 hours
Unacceptable Conditions:
Specimen submitted is in the incorrect anticoagulant. Specimen received after the stability date. Gross hemolysis. Frozen specimen. Insufficient specimen. Unlabeled. Left un-refrigerated for an extended period.
Storage & Transport
If testing is expected to occur in less than eight hours, specimens must be transported between 18°C and 25°C
If testing is expected to occur in greater than eight hours, specimens must be transported with cold packs to maintain specimens between 2-8°C prior to testing
CPT(s)
88184x1, 88185x20, 88189x1
New York Approved
Yes
TAT
24 hours from specimen receipt
Levels of Service
Global, technical only, professional only
*The CPT codes provided are for informational purposes only and are based on AMA guidelines The billing party is solely responsible for correct CPT coding.
With core values rooted in service and integrity, our leadership team sets the bar high.
We consistently strive to set the model for exactly how a reference laboratory should engage with both physicians and patients.
siParadigm is accredited by CLIA (Clinical Laboratory Improvement Amendments) and certified by CAP (College of American Pathologists).
We also hold select state licensure where required.