Test Directory
| Test Code | ||
| TPOSE | ||
| Test Name | ||
| Thrombopoietin (TPO) | ||
| CPT Codes | ||
| 83520 | ||
| Expected Turnaround Time | ||
| 7 - 28 days | ||
| Clinical Utility | ||
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This test will be used to measure serum TPO level in patients with thrombocytopenia of unknown cause. ITP (Idiopathic Thrombocytopenia purpura) is a common cause of thrombocytopenia. The diagnosis is based on exclusion criteria. Serum TPO levels are normal or only slightly elevated in ITP so that if TPO level is markedly elevated the diagnosis of ITP is strongly in doubt. Markedly elevated TPO levels may occur in individuals with genetic mutations of CD110. New Drugs, non peptide thrombopoietin receptor agonist (CD110) are becoming increasingly used in patients with thrombocytopenia of ITP. The cost of these new drugs is very high. That is why it is important to know levels of TPO. Patients with elevated TPO levels do not respond to treatment with thrombopoietin receptor agonist. Knowing levels of TPO may help in predicting efficacy of response to an extremely expensive stimulating drug used in a wide variety of hematologic disorders. May reduce the need for platelet transfusions with all known complications and reduced cost of blood products by hospital. |
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| Specimen and Container Info | ||
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Specimen Type: Serum
Collection Container: Red Top, Plain Alternate Collection Container: Gold Top, Serum Separator Desired Specimen Volume: 1 mL |
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| Collection Instructions | ||
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| Processing and Submission Instructions | ||
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| Patient Preparation | ||
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Cytokine levels may demonstrate diurnal variation. Recommend cytokine levels be determined at the same time of day for improved longitudinal comparison. |
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| Transport Instructions | ||
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Transport to the laboratory frozen. |
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| Stability Requirements | ||
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| Causes for Rejection | ||
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| Methodology | ||
| Immunoassay | ||
| Reference Intervals | ||
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See patient report. |
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| Limitations | ||
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This test was performed using a kit that has not been cleared or approved by the FDA. The analytical performance characteristics of this test have been determined by Quest Diagnostics. This test should not be used for diagnosis without confirmation by other medically established means. |
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| Reference Lab | ||
| Quest Diagnostics Nichols Institute | ||
| Testing Schedule | ||
| Varies | ||
The American Medical Association (AMA) Current Procedural Terminology (CPT) codes published by HNL Lab Medicine are guidelines and are intended for informational purposes only. CPT coding is the exclusive responsibility of the billing entity. View the Terms.
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