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Transplant Testing

HLA Pretransplant Workup Sensitized Recipient Panel 4 Test

This test assesses compatibility for kidney and liver transplant recipients, particularly those identified as sensitized. It helps identify potential donor-recipient incompatibilities to improve transplant success.

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
6 mL (3 mL min.) whole blood in 1 Yellow Top (ACD) tube, 9 mL (6 mL min.) serum from 3 SST's, 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube, 4 mL (2 mL min.) whole blood in 1 Green Top (Sodium Heparin) tube.
Results
Confirm with the laboratory before booking.
Preparation
Specimens should preferably be collected 48 hours after dialysis. A doctor's prescription on letterhead, along with one photograph each of the recipient and donor (duly stamped), and a consent form for HLA Typing for Solid organ transplant (Form 33) are mandatory. Confirm with the laboratory before booking.
Test priceKSh 137,358

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 HLA Pretransplant Workup Sensitized Recipient Panel 4 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.

  • ✓Individuals awaiting a kidney or liver transplant.
  • ✓Patients identified as sensitized recipients.
  • ✓Individuals with a history of previous transplants.
  • ✓Patients experiencing complications related to organ transplantation.
02

In plain language

What this test helps you understand

This test is used to determine the compatibility between a potential kidney or liver transplant recipient and potential donors, especially for individuals who are sensitized or have a history of transplants. It helps predict the risk of transplant rejection and guides donor selection.
The HLA Pretransplant Workup Sensitized Recipient Panel 4 Test is a critical diagnostic procedure designed to evaluate potential transplant recipients for kidney and liver transplants. This test assesses the compatibility between the recipient and potential donors, which is essential for the success of solid organ transplants.

This test measures various components essential for transplant compatibility, including HLA DNA Typing, High resolution NGS, HLA T & B cell lymphocyte crossmatch vs potential donor, HLA Panel Reactive IgG antibodies (PRA) Screen Luminex, and Single antigen bead (SAB) IgG Class I & II Luminex.

Taking this test offers numerous benefits, including identifying compatible donors, reducing the risk of transplant rejection, providing detailed insights into the recipient's immune response, guiding nephrologists in making informed decisions about transplant options, and enhancing the overall success rate of kidney and liver transplants.

Results from the HLA Pretransplant Workup Sensitized Recipient Panel 4 Test will indicate the level of compatibility between the recipient and potential donors. It is crucial to discuss these results with your nephrologist, who will provide guidance on the next steps in the transplant process.
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 →
PreparationSpecimens should preferably be collected 48 hours after dialysis. A doctor's prescription on letterhead, along with one photograph each of the recipient and donor (duly stamped), and a consent form for HLA Typing for Solid organ transplant (Form 33) are mandatory. Confirm with the laboratory before booking.
Sample6 mL (3 mL min.) whole blood in 1 Yellow Top (ACD) tube, 9 mL (6 mL min.) serum from 3 SST's, 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube, 4 mL (2 mL min.) whole blood in 1 Green Top (Sodium Heparin) tube.
MethodologyThis test utilizes multiple methodologies including HLA DNA Typing, High resolution NGS, HLA T & B cell lymphocyte crossmatch, HLA Panel Reactive IgG antibodies (PRA) Screen Luminex, and Single antigen bead (SAB) IgG Class I & II Luminex.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test assesses specific HLA compatibility markers. Other factors can influence transplant success. Results must be interpreted in the context of the patient's overall clinical picture by a qualified physician.
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 involves analyzing blood and serum samples to assess HLA compatibility between the recipient and potential donors using various techniques like DNA typing, crossmatching, and antibody screening.
This test is primarily for individuals preparing for a kidney or liver transplant, especially those considered 'sensitized' due to previous transplants, blood transfusions, or pregnancies.
Multiple blood and serum samples are required, collected in specific tubes (Yellow Top, SST, Lavender Top, Green Top). Please refer to the specimen requirements section for details.
The results indicate the level of compatibility between the recipient and potential donors based on HLA markers and antibodies. Your doctor will interpret these results in detail.
Turnaround time varies. Please contact the laboratory for the most current estimate.
A doctor's prescription, photographs of the recipient and donor, and a signed consent form (Form 33) are required.
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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