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Medical information Clinical review pending

Infection Testing

Sepsis Panel Test

The Sepsis Panel Test helps detect infections early, potentially preventing sepsis, a life-threatening condition. It measures key biomarkers like Procalcitonin and C-Reactive Protein.

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
Serum (5 mL minimum from 1 SST tube), Blood for Aerobic Culture (8-10 mL in 2 special Plus Aerobic bottles, or 2 mL each in 2 Special Paeds Plus bottles for children under 12). Blood must be collected from two different sites.
Results
Confirm with the laboratory before booking.
Preparation
No special preparation is required for this test.
Test priceKSh 10,000

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 Sepsis Panel 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 sepsis or severe infection
  • ✓Fever, chills, rapid heart rate, confusion
  • ✓Monitoring infection severity
  • ✓Guiding antibiotic therapy
  • ✓Patients with weakened immune systems
  • ✓Patients with chronic illnesses
  • ✓Post-surgery or invasive procedure monitoring
02

In plain language

What this test helps you understand

This test aids healthcare providers in the early detection and management of sepsis by identifying potential bacterial infections and guiding treatment decisions.
The Sepsis Panel Test is a vital diagnostic tool used to detect infections that may lead to sepsis, a severe and potentially life-threatening condition. Early detection is crucial for effective treatment, making this test an essential component of patient care in clinical settings. This test measures key biomarkers that indicate the presence of infection, including Procalcitonin, C-Reactive Protein, and blood cultures to identify specific bacteria. Individuals showing symptoms of severe infection, such as fever, chills, rapid heart rate, or confusion, may benefit from this test. It is particularly important for those with weakened immune systems, chronic illnesses, recent surgeries, or those currently hospitalized. Taking this test allows for early detection of infections, timely intervention, monitoring of treatment effectiveness, and guidance for appropriate antibiotic selection, ultimately improving patient outcomes.
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 special preparation is required for this test.
SampleSerum (5 mL minimum from 1 SST tube), Blood for Aerobic Culture (8-10 mL in 2 special Plus Aerobic bottles, or 2 mL each in 2 Special Paeds Plus bottles for children under 12). Blood must be collected from two different sites.
MethodologyThe test involves measuring Procalcitonin and C-Reactive Protein levels using laboratory assays and performing aerobic blood cultures to identify bacteria.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects biomarkers associated with infection and sepsis but does not definitively diagnose sepsis on its own. Results must be interpreted in the context of the patient's clinical presentation. Blood cultures may take additional time for results.
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

Sepsis is a life-threatening condition that arises when the body's response to an infection causes damage to its own tissues and organs.
Early detection and treatment of sepsis significantly improve patient outcomes and reduce the risk of complications or death.
These are biomarkers, substances found in the blood that indicate the presence of inflammation or infection, particularly bacterial infections.
No, no special preparation is required for the Sepsis Panel Test.
The test requires a blood sample for serum analysis and blood cultures. Blood should be drawn from two different sites.
Yes, home sample collection services are available for your convenience. Please contact us to arrange.
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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