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  • Prenatal Screening Services
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  • Test of Perinatal Risk Evaluation of Pre-eclampsia

Test of Perinatal Risk Evaluation of Pre-eclampsia

Test of Perinatal Risk Evaluation of Pre-eclampsia
Test code: PE
Test Inquiry
Test code: PE
Test Inquiry

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.
View test information
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.
Test code: PE
Download PDF Version
This test is not available in your region Japan, please select your nearest laboratory to request more information.
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Test information

  • Test description
  • Indications for testing
  • Condition description
  • Test methods and limitations
  • Detailed sample requirements

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
Test Details Page
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.

Learn More

1. Build Your Custom Panel

Complete the Genomics Gene Tool Form, and a unique test code will be generated for you.

 

2. Complete and print the test requisition

Complete & print the test requisition.

Ensure that:

  • You entered your unique test code from the Genomics Gene Tool
  • All sections are complete
  • Your patient has signed an informed consent
     

3. Collect and Send Patient Sample

Collect patient sample.

  1. Obtain a sample for testing from the patient and confirm that the sample is correctly labeled with the patient's name and date of birth.
  2. Note: if you do not have a Revvity Omics kit available in your office, please email or call us at 1-866-354-2910.

Send patient sample.

Ship your test kit back using the pre-paid shipping label. Remember to include:

✔   Patient sample

✔   Completed informed consent

✔   Test requisition form

✔   Any applicable medical records or clinical notes
 

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