S. Pneumoniae, H. Influenzae, Chl. Pneumoniae, N. Meningitis RG Multiplex RNA Detection Qualitative Test
The S. Pneumoniae, H. Influenzae, Chl. Pneumoniae, N. Meningitis RG Multiplex RNA Detection Qualitative Test is a cutting-edge diagnostic tool designed to detect multiple bacterial pathogens responsible for serious respiratory infections. Understanding these infections is crucial for prompt treatment and management, especially in vulnerable populations such as children and the elderly.
What the Test Measures/Detects
This test utilizes advanced Real Time PCR technology to qualitatively detect RNA from:
- S. Pneumoniae (Streptococcus pneumoniae)
- H. Influenzae (Haemophilus influenzae)
- Chl. Pneumoniae (Chlamydia pneumoniae)
- N. Meningitis (Neisseria meningitidis)
Who Should Consider This Test?
Individuals exhibiting the following symptoms or risk factors should consider this test:
- Persistent cough
- Fever and chills
- Shortness of breath
- Chest pain
- History of respiratory infections
- Weakened immune system
Benefits of Taking the Test
- Early detection of serious bacterial pathogens
- Facilitates timely and appropriate treatment
- Helps in managing outbreaks in community settings
- Reduces the risk of complications associated with delayed diagnosis
Understanding Your Results
Results from the S. Pneumoniae, H. Influenzae, Chl. Pneumoniae, N. Meningitis RG Multiplex RNA Detection Qualitative Test will provide information on the presence or absence of the detected pathogens. A positive result indicates the presence of the pathogen, which may require immediate medical intervention. Always discuss your results with your healthcare provider for proper interpretation and next steps.
Test Name and Price
| Discount Price | Regular Price |
|---|---|
| 170,000 NGN | 200,000 NGN |
Book the Test
To book the S. Pneumoniae, H. Influenzae, Chl. Pneumoniae, N. Meningitis RG Multiplex RNA Detection Qualitative Test, please contact us:
Phone/WhatsApp: +2348077798758
Turnaround time for results is 3rd working day via email (36 hours) or 24 hours via phone.
Pre-Test Instructions: Please sign the consent document and bring any clinical history of the patient for the test.
