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Medical information Clinical review pending

Infection Testing

Influenza Group A & B Viral Load Quantitative Test

The Influenza Group A & B Viral Load Quantitative Test detects and measures the amount of influenza virus in respiratory samples using Real-Time PCR. This helps in diagnosing infection severity and guiding treatment.

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
Respiratory sample (e.g., nasopharyngeal swab, throat swab, sputum). Confirm specific sample type with the laboratory before booking.
Results
Confirm with the laboratory before booking. Results typically available within 24-36 hours.
Preparation
No specific patient preparation is required. Inform the laboratory about any current medications or relevant medical history.
Test priceKSh 11,900

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 Influenza Group A & B Viral Load Quantitative 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.

  • ✓Suspected influenza infection
  • ✓Flu-like symptoms (fever, cough, sore throat, body aches)
  • ✓Monitoring treatment response
  • ✓Assessing infection severity
  • ✓Patients at high risk for complications
  • ✓Epidemiological surveillance
02

In plain language

What this test helps you understand

This test helps diagnose influenza infections, assess the severity of the infection by quantifying the viral load, and monitor the effectiveness of antiviral treatment.
The Influenza Group A & B Viral Load Quantitative Test is a diagnostic tool used to detect and quantify the presence of influenza viruses (Group A and B) in the body. This test is particularly useful during periods of high flu activity. Understanding the viral load can assist healthcare providers in making informed decisions about treatment and managing the infection.

This test measures the quantity of influenza virus present in a respiratory sample. It uses Real-Time PCR technology to provide accurate results, which are important for effective patient care.

Individuals experiencing flu-like symptoms such as fever, cough, sore throat, body aches, and fatigue may benefit from this test. People with underlying health conditions or weakened immune systems, who are at higher risk for severe flu complications, should also consider testing.

Benefits of this test include accurate diagnosis, monitoring of viral load to assess treatment effectiveness, and providing information to guide clinical decisions. Early detection can contribute to better management and outcomes.

Results are typically available within 36 hours via email or 24 hours via phone. Discuss your results with your healthcare provider for proper interpretation and management. A higher viral load may suggest a more severe infection, while lower levels might indicate recovery.
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 →
PreparationNo specific patient preparation is required. Inform the laboratory about any current medications or relevant medical history.
SampleRespiratory sample (e.g., nasopharyngeal swab, throat swab, sputum). Confirm specific sample type with the laboratory before booking.
MethodologyReal-Time Polymerase Chain Reaction (PCR)
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects Influenza A and B viruses. It may not detect other respiratory viruses causing similar symptoms. Results are dependent on proper sample collection and handling. Viral load may not always correlate perfectly with clinical severity.
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

Viral load refers to the amount of virus present in a sample, in this case, the influenza virus in your respiratory tract.
Quantifying the viral load can help assess the severity of the infection and monitor how well treatment is working.
The sample is typically collected as a swab from the nose or throat, or sometimes as sputum. Please confirm the required sample type with the lab.
Results are typically available within 24-36 hours. Confirm the exact turnaround time with the laboratory.
Consult your healthcare provider. They can advise if testing is necessary and recommend appropriate treatment.
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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