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Print View Attached Docs: | | Methodology: | Enzyme-Linked Immunosorbent Assay (ELISA) / Chemiluminescent Immunoassay (CLIA) | | Edit Date: | 4/6/2009 | | Components: | Alpha Fetoprotein (AFP) / /Human Chorionic Gonadotropin (hCG) / Inhibin A / Unconjugated Estriol (uE3) / Risk for Down Syndrome and Neural Tube Defect / Trisomy 18 / Calculation of AFP, MoM, hCG MoM, uE3 MoM, Inhibin A MoM / Interpretations | | Performed: | Monday-Friday | | Released: | 48-72 hours of receipt | | CPT Code: | 82105 / 82677 / 84702 / 86336 | | Specimen Collection Details | | Collection: | These requirements are for the second trimester draw for the Sequential Integrated Screen and can be performed only on individuals between 15 weeks, 0 days and 21 weeks, 6 days gestation, and who have had the Sequential Integrated Screen, 1st Trimester (41990). Order on a PeaceHealth Laboratories Obstetric requisition or electronically, and include any change from 1st Trimester test in patient’s weight or number of fetuses. Collect one 7.5 mL serum separator tube (SST). Also acceptable: One 5 mL red top tube. | | Handling: | Allow to clot, centrifuge and separate serum from cells immediately. | | Stability: | 7 days refrigerated at 2-8° C, or frozen at -2-8° C. | | Standard Volume: | 3 mL serum | | Minimum Volume: | 1.5 mL serum | | Transport: | Refrigerated, or frozen on dry ice. | | Rejection Criteria: | Gross hemolysis or lipemia. |
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PeaceHealth Laboratories, formerly Oregon Medical Laboratories & Northwest Regional Laboratory. All rights reserved.
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