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Test Code CEA Carcinoembryonic Antigen

EHR Test Codes

  Test Code Test Name
Atlas CEA CEA
Cerner CEA Carcinoembryonic Antigen

 

Specimen Requirements

Preparation of Patient: 

None

 

Container Type: 

Gold Top SST Gel & Clot Activator Tube

Specimen Type:

Serum

 

Specimen Volume: 

1.0 mL of Serum minimum .5 mL of Serum

 

Specimen Handling/Transport:

Separate serum from cells within 2 hours of collection.

Transport refrigerated 2-8°C

 

Specimen Stability/Storage:

2 days refrigerated 2-8°C

Performing Laboratory

Munson Medical Center Laboratories

Chemistry Department

Priority, Frequency, & Turnaround

Priority:

Non-Emergent

 

Frequency:

24 hours 7 days a week

 

Turnaround:

0 - 1 days

Methodology

Chemiluminescent Immunoassay

Reporting

Reference Range

0 - 3 ng/mL

 

Interpretive Data:

Smoking may elevate CEA results. Testing performed by chemiluminescence on a Beckman Coulter DXI/Access platform. Results may not be comparable with tests performed on other manufacturer's methods or platforms.

 

Critical Decision: 

None

Clinical Significance

Patients with confirmed carcinoma frequently have a pretreatment CEA level in the same range as healthy individuals. Elevations in circulating CEA levels may be observed in smokers as well as in patients nonmalignant disease. For these reasons a CEA level, regardless of value, should not be interpreted as absolute evidence for the presence or absence of malignant disease. The CEA level should be used in conjunction with information available from clinical evaluation and other diagnostic procedures. The CEA Assay Should NOT Be Used As A Cancer Screening Test.

 

Causes of increased CEA values include acute pancreatitis, regional enteritis, malignancy, liver disease, smoking, and pulmonary tuberculosis. Clinical relevance of CEA values are shown in management of patients with colorectal, breast, lung, prostatic, pancreatic and ovarian carcinoma.

CPT Code

82378