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Medical information Clinical review pending

Gynecological Testing

First Trimester Triple Marker Test

A prenatal screening test performed between 10-13 weeks of pregnancy to assess the risk of certain chromosomal abnormalities and pre-eclampsia.

General information only: This page is not a diagnosis or personal medical advice. A qualified clinician should decide whether testing is appropriate and interpret results in context.

Review status: No completed medical review is recorded for this page.

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Counselor guidance included Confidential handling Kenya-wide coordination

At a glance

Plan your test

Sample
3 ml (1.5 ml minimum) of maternal serum collected in a Serum Separator Tube (SST).
Results
Confirm with the laboratory before booking.
Preparation
The test must be performed between 10 and 13 weeks of gestation. Ensure the Maternal Serum Screen requisition form (Form 11) and Preeclampsia screening form (Form 13) are completed accurately.
Test priceKSh 8,400

Payment: M-Pesa and card options can be confirmed during booking.

Insurance & government schemes

Is this test covered for you?

We help you verify whether the First Trimester Triple Marker Test test can be claimed against your insurer, employer scheme or a Kenyan government health scheme — before you book. Coverage depends on your plan, clinical indication and your provider's rules; final approval always rests with them.

Talk to a claims advisor

Providers & schemes we can help you check

Government & public schemes

SHIF — Social Health Insurance Fund Linda Mama EduAfya NHIF (legacy cards)

Eligibility and benefits follow the current rules of the Social Health Authority (SHA) and applicable government programmes.

Private insurers & employer schemes

Jubilee Health AAR APA Britam CIC Madison Resolution Pioneer Minet Old Mutual GA Life Heritage + other licensed insurers

Names shown for identification only — listing does not imply partnership or guarantee of coverage.

Have these ready when we check

  • Insurer or scheme name & policy / member number
  • A clinician's request / prescription for the test
  • Pre-authorisation letter, if your plan requires one

Free coverage check

Ask us to verify your cover

Send your details and our claims team confirms what documents you need and whether pre-authorisation applies — usually the same working day.

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Used only to process your coverage check — see our Privacy Policy. Verification support is free and does not guarantee your provider will pay.

01

Start with fit

Is this the right test for you?

The best test starts with a clear clinical question. These are common reasons a clinician or family may consider this test.

  • ✓Pregnant women between 10 and 13 weeks gestation.
  • ✓Screening for risk of trisomy 13, 18, and 21.
  • ✓Screening for risk of early and late onset pre-eclampsia.
  • ✓Women with risk factors such as advanced maternal age.
  • ✓Women with a history of pre-eclampsia or previous trisomy pregnancies.
  • ✓Women with pre-existing conditions like diabetes or hypertension.
02

In plain language

What this test helps you understand

This test screens for potential risks associated with pregnancy, including certain chromosomal abnormalities (trisomy 13, 18, 21) and pre-eclampsia. It helps healthcare providers identify pregnancies that may require further investigation or closer monitoring.
The First Trimester Triple Marker Test is a screening test for pregnant women, typically performed between 10 and 13 weeks of gestation. It helps assess the risk of certain genetic conditions and potential pregnancy complications like pre-eclampsia. This test is an important part of early prenatal care, providing valuable information to guide further management if needed.

This test measures levels of three specific substances in the mother's blood: Free Beta HCG, Pregnancy Associated Plasma Protein A (PAPP-A), and Placental Growth Factor (PlGF). These levels, combined with maternal age and other factors, are used to calculate the risk for conditions such as trisomy 13, trisomy 18, trisomy 21, and early and late onset pre-eclampsia.

Discussing this test with your healthcare provider is essential to understand if it's appropriate for your individual circumstances, especially if you have specific risk factors.
03

Medical review status

Clinical review pending

A completed medical review is not recorded for this page. No clinician has endorsed the information shown here. Please discuss testing decisions with a qualified healthcare professional.

Meet the DNA Labs Kenya medical team →
04

A simple process

What happens next?

You do not have to navigate the test alone. We help you move from question to next step.

1

Speak with us

We check the test and answer your questions before collection.

2

Give your sample

Choose home collection or a coordinated hub visit in Kenya. We explain whether this test uses a cheek swab or blood draw.

3

Understand your report

A counselor helps you understand the result and the next steps.

05

Choose your collection

Home collection or a lab visit

We will explain the sample, preparation, and next steps before anything is collected.

Home collection

Choose a coordinated visit at home or another convenient location. Our team confirms the appointment and sample requirements in advance.

Lab or hub visit

Prefer to visit a coordinated location? We can guide you to the right hub and explain what to expect when you arrive.

Ask about locations →
PreparationThe test must be performed between 10 and 13 weeks of gestation. Ensure the Maternal Serum Screen requisition form (Form 11) and Preeclampsia screening form (Form 13) are completed accurately.
Sample3 ml (1.5 ml minimum) of maternal serum collected in a Serum Separator Tube (SST).
MethodologyThe test involves measuring the levels of Free Beta HCG, PAPP-A, and PlGF in maternal serum using laboratory assays. The results are then combined with maternal age and other relevant factors to calculate risk scores.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This is a screening test, not a diagnostic test. A high-risk result does not confirm a diagnosis but indicates the need for further diagnostic testing. False positives and false negatives can occur. Accuracy is dependent on correct gestational dating.
06

Read your report

What common result terms mean

PositiveA finding was identified. Your clinician or counselor will explain what it means for your care.
NegativeThe specific finding tested for was not identified. It does not rule out every possible cause.
VUSA variant was found, but current evidence is not enough to classify it. Your counselor can explain follow-up.
07

Questions people ask

Frequently asked questions

This test is typically performed between 10 and 13 weeks of pregnancy.
It screens for the risk of certain chromosomal abnormalities (trisomy 13, 18, 21) and pre-eclampsia.
No, this is a screening test. It assesses risk, and further diagnostic tests may be needed to confirm results.
A blood sample (maternal serum) is required.
Ensure the test is done within the correct gestational age window (10-13 weeks) and that the necessary requisition forms are completed.
Results indicate risk levels. It is essential to discuss the results with your doctor for proper interpretation and guidance.
08

Collaboration

Open for partnership with hospitals, clinics, doctors & researchers

Whether you are referring patients, building a research programme or supporting students, we work as an extension of your team — with responsive communication and clear scientific standards.

Hospitals & clinics

Referral pathways, coordinated sample logistics and shared reporting that fits your clinical workflow.

Doctors & specialists

LOINC-coded reports, ACMG-based variant classification and a direct scientific line for complex cases.

Research institutions

Sanger sequencing, NGS panels and custom assays — with project design support, batch pricing and agreed turnaround commitments.

Students & academic projects

Discounted laboratory services for college, master's and PhD research projects — including proposal guidance and cost-effective batch testing.

Explore partnerships
09

Trust & transparency

Sources, standards & how this page is maintained

Standards & references

  • ACMG/AMP technical standards for sequence variant interpretation
  • ClinGen curation and gene–disease validity frameworks where applicable
  • LOINC-coded reporting for interoperable results
  • ISO 9001:2015 quality management; ISO 15189 accreditation in progress

Page provenance

  • Last updated: September 27, 2026
  • Medical review: not yet completed
  • Written for patients & clinicians in Kenya; reviewed periodically against current guidance

Medical disclaimer: this page is general information, not a diagnosis or personal medical advice. Testing decisions and result interpretation should be made with a qualified healthcare professional.

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