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Medical information Clinical review pending

Cytogenetics

Homovanillic Acid (HVA) 24 Hour Urine Test

The Homovanillic Acid (HVA) 24 Hour Urine Test measures HVA levels in urine collected over 24 hours. This test helps in the detection and monitoring of certain cancers, particularly neuroblastoma. Confirm with the laboratory before booking.

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
A 24-hour urine collection is required. A minimum volume of 50 mL is needed.
Results
Confirm with the laboratory before booking.
Preparation
Patients must avoid taking L-Dopa at least 72 hours before and during the 24-hour collection period. Follow specific collection instructions provided by the laboratory.
Test priceKSh 11,000

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 Homovanillic Acid (HVA) 24 Hour Urine 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 neuroblastoma
  • ✓Monitoring response to cancer treatment
  • ✓Investigating neuroendocrine tumors
  • ✓Evaluating symptoms like abdominal pain or unexplained weight loss
  • ✓Screening individuals with risk factors for neuroblastoma
02

In plain language

What this test helps you understand

This test is used to help detect and monitor certain types of cancer, particularly neuroblastoma, by measuring levels of homovanillic acid (HVA), a metabolite of dopamine, in a 24-hour urine sample.
The Homovanillic Acid (HVA) 24 Hour Urine Test is a diagnostic tool used to measure the levels of homovanillic acid in urine over a 24-hour period. This test is particularly important in the field of oncology, as elevated levels of HVA can indicate the presence of neuroblastoma and other types of cancer. Early detection through this test can significantly improve treatment outcomes and patient prognosis.

This test quantifies the amount of homovanillic acid, a metabolite of dopamine, in the urine. Abnormal levels may suggest neuroendocrine tumors, particularly neuroblastoma, which is most commonly found in children.

Individuals experiencing symptoms such as unexplained weight loss, abdominal pain, bone pain, fatigue, or swelling in the abdomen or neck may be advised to take this test. Patients with risk factors for cancer, particularly neuroblastoma, should also consider this test. If you have a family history of cancer or have been exposed to certain environmental factors, this test may be recommended by your healthcare provider.

Benefits of taking the test include early detection of cancer, monitoring treatment effectiveness, providing information for personalized treatment plans, and using a non-invasive collection method.

Results are typically available within a few days after sample collection. Normal ranges may vary, and it is essential to discuss your results with your healthcare provider to understand their significance fully. Elevated levels of HVA may require further investigation or additional tests.
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 →
PreparationPatients must avoid taking L-Dopa at least 72 hours before and during the 24-hour collection period. Follow specific collection instructions provided by the laboratory.
SampleA 24-hour urine collection is required. A minimum volume of 50 mL is needed.
MethodologyThe test involves measuring the concentration of homovanillic acid in a 24-hour urine sample using laboratory techniques.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test measures HVA levels, which can be elevated in conditions other than neuroblastoma. False positives or negatives can occur. Results must be interpreted by a qualified healthcare professional in conjunction with other clinical information.
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

Homovanillic acid (HVA) is a substance produced when the body breaks down dopamine. Measuring its levels in urine can help detect certain medical conditions.
Collecting urine over 24 hours provides a more accurate measurement of HVA levels compared to a single sample, as levels can fluctuate throughout the day.
Elevated HVA levels can indicate the presence of certain tumors, particularly neuroblastoma. However, other conditions can also cause elevated levels. Your doctor will interpret the results in context.
You will need to collect all urine produced over a 24-hour period. It is crucial to avoid L-Dopa medication for at least 72 hours before starting the collection. Specific instructions will be provided.
No, the test involves collecting urine, which is a non-invasive process.
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.

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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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