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Medical information Clinical review pending

Genetic Testing

Mycoplasma Pneumonia RNA Detection Qualitative Test

Detects the presence of Mycoplasma pneumoniae RNA to diagnose respiratory infections. Uses Real Time PCR for accurate results.

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
Bronchoalveolar lavage fluids, throat swabs, endocervical swabs, blood, urine, cerebrospinal fluid (CSF), serum, or plasma.
Results
Results are typically available within 24 hours via phone and 36 hours via email. Confirm with the laboratory before booking.
Preparation
Patients must sign a consent document and provide relevant clinical history before the test.
Test priceKSh 12,240

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 Mycoplasma Pneumonia RNA Detection Qualitative 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.

  • ✓Persistent cough
  • ✓Fever
  • ✓Chest pain
  • ✓Shortness of breath
  • ✓Fatigue
  • ✓Suspected atypical pneumonia
  • ✓Diagnosis in patients with respiratory symptoms
  • ✓Monitoring treatment response
02

In plain language

What this test helps you understand

This test helps confirm an active Mycoplasma pneumoniae infection by detecting its RNA, aiding in the diagnosis of respiratory illnesses.
The Mycoplasma Pneumonia RNA Detection Qualitative Test is a diagnostic tool used to identify infections caused by Mycoplasma pneumoniae, a common cause of respiratory illnesses. This test uses the Real Time PCR method to detect the RNA of the pathogen in various biological samples, helping healthcare providers confirm an active infection and differentiate it from other respiratory pathogens.

This test specifically measures the presence of Mycoplasma pneumonia RNA in the sample provided. Detecting the RNA allows for an accurate diagnosis of an active infection.

Individuals experiencing symptoms such as persistent cough, fever, chest pain, shortness of breath, or fatigue should consider this test. Those with risk factors like weakened immune systems or chronic respiratory conditions may also benefit from testing.

Taking this test offers advantages including early and accurate diagnosis, guidance for appropriate treatment, monitoring treatment effectiveness, and reducing the risk of complications from untreated infections.

Results are typically available within 36 hours via email and 24 hours via phone. A positive result indicates an active infection, while a negative result suggests the absence of Mycoplasma pneumonia RNA. Discuss your results with your healthcare provider for interpretation and next steps.
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 sign a consent document and provide relevant clinical history before the test.
SampleBronchoalveolar lavage fluids, throat swabs, endocervical swabs, blood, urine, cerebrospinal fluid (CSF), serum, or plasma.
MethodologyReal Time PCR (Polymerase Chain Reaction) is used to detect Mycoplasma pneumoniae RNA.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects the presence of Mycoplasma pneumoniae RNA. A negative result does not completely rule out infection, especially if the sample was collected late in the illness or if the viral load is low. Confirm with the laboratory before booking.
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 detects the RNA of Mycoplasma pneumoniae, the bacteria that causes Mycoplasma pneumonia.
Symptoms like persistent cough, fever, chest pain, shortness of breath, and fatigue may indicate a need for this test.
Samples can include throat swabs, blood, urine, sputum, or other fluids as specified by your doctor. Please confirm the required sample type with the laboratory.
Results are typically available within 24 hours via phone and 36 hours via email. Confirm with the laboratory before booking.
A positive result indicates the presence of Mycoplasma pneumoniae RNA, suggesting an active infection. Discuss the results with your healthcare provider.
We have branches in major cities across Kenya and offer home sample collection services. Please contact us for details.
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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