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Test of Perinatal Risk Evaluation of Pre-eclampsia
Test of Perinatal Risk Evaluation of Pre-eclampsia
Test code:
PE
Test of Perinatal Risk Evaluation of Pre-eclampsia
The level of pregnance-associated plasma protein A (PAPP-A) in human serum is detected by AutoDELFIA®1235 automatic time-resolved fluorescence immunoassay system.
| Test Code | PE |
|---|---|
| Test Summary | The level of pregnance-associated plasma protein A (PAPP-A) in human serum is detected by AutoDELFIA®1235 automatic time-resolved fluorescence immunoassay system. |
| Turn Around Time | 2 - 3 days |
| Acceptable Sample Types | Serum |
| NY Approved | No |
| Accreditations | EQA |
*TAT starts after the sample and all required sample information is received at the processing laboratory.
**The CPT codes listed are in accordance with Current Procedural Terminology, a publication of the American Medical Association, and are provided for informational purposes only. CPT coding is the sole responsibility of the billing party.
This testing service has not been cleared or approved by the U.S. Food and Drug Administration. Testing services may not be licensed in accordance with the laws in all countries. The availability of specific test offerings is dependent upon laboratory location.
**The CPT codes listed are in accordance with Current Procedural Terminology, a publication of the American Medical Association, and are provided for informational purposes only. CPT coding is the sole responsibility of the billing party.
This testing service has not been cleared or approved by the U.S. Food and Drug Administration. Testing services may not be licensed in accordance with the laws in all countries. The availability of specific test offerings is dependent upon laboratory location.
Test code:
PE
This test is not available in your region United States, please select your nearest laboratory to request more information.
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Test information
Test description
Perinatal preeclampsia risk assessment for pregnant women who are in the first trimester (11 to 13+6 weeks of pregnancy) and who are in the second and third trimesters.
Indications for testing
- Pregnant women who are in the first trimester (11 to 13+6 weeks of pregnancy) .
- Pregnant women who are in the second and third trimesters.
Condition description
Preeclampsia is a serious condition that can happen after the 20th week of pregnancy or after giving birth (called postpartum preeclampsia). In addition to causing high blood pressure, it can cause organs, like the kidneys and liver, to not work normally. Blood pressure is the force of blood that pushes against the walls of your arteries. High blood pressure (also called hypertension) is when the force of blood against the walls of the blood vessels is too high. Arteries are blood vessels that carry blood away from your heart to other parts of the body. Having high blood pressure can stress your heart and cause problems during pregnancy.
Test methods and limitations
MEIA/AutoDELFIA
Detailed sample requirements
Serum
| Collection Container(s) |
Serum tubes (red top) |
|---|---|
| Collection |
Collect blood by venipuncture, allow it to clot, and separate the serum by centrifugation as quickly as possible. |
| Sample Condition |
Serum samples can be stored for at least 30 days at +2 – +8 degrees Celsius |
| Shipping |
Ship overnight at +2 – +8 degrees Celsius ensuring receipt within 2 days of collection. |
How To Order
Step 1
Choose Your Test
Select the correct test for your patient, and download and fill out the Clinical Genomics test requisition form.
Step 2
Collect Sample
Obtain a sample for testing from the patient using one of the provided Revvity Omics test packs.
Step 3
Send Samples
Send samples and all required forms back to Revvity for processing using pre-paid shipping label.
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