SARS-CoV-2 Monitoring Panel Test
Short Name: SARS-CoV-2 Monitoring Panel
Also known as: SARS-CoV-2 Monitoring Panel, COVID-19 Monitoring Panel
SARS-CoV-2 Monitoring Panel Test test available at DNA Labs India for ₹5,499. Uses Real Time RT-PCR, Immunoturbidimetry, Electrical Impedance, VCS, Spectrophotometry, Indirect ISE on Oropharyngeal and Nasopharyngeal Swabs / ET secretions / BAL / Sputum in VTM; Serum (SST); Whole Blood (EDTA) samples. Results in Samples received by 11 am are generally processed, and reports are delivered within 2 days (48 hours).. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
The purpose of the SARS-CoV-2 Monitoring Panel is to provide a single integrated assessment of active SARS-CoV-2 infection and the body's inflammatory/organ-function response. It assists in confirming the diagnosis, triaging symptomatic individuals, detecting variant-associated mutations, and identifying complications such as hepatic, renal, or haematological involvement. It is not intended to replace clinical judgement but to complement it with objective laboratory data.
- Test Code
- 3625
- Price
- ₹5,499
- Sample Type
- Oropharyngeal and Nasopharyngeal Swabs / ET secretions / BAL / Sputum in VTM; Serum (SST); Whole Blood (EDTA)
- Result Time
- Samples received by 11 am are generally processed, and reports are delivered within 2 days (48 hours).
- Fasting Required
- Yes (10 hours)
- Method
- Real Time RT-PCR, Immunoturbidimetry, Electrical Impedance, VCS, Spectrophotometry, Indirect ISE
Sample Collection
Overnight fasting is preferred. Please carry the duly filled Covid-19 Clinical Information Form (Form 44) / SRF ID as mandated by GOI. Inform your physician about current symptoms and medications.
Method: Nasopharyngeal/oropharyngeal swab, respiratory secretions, BAL, sputum; venipuncture
Laboratory Analysis
A trained phlebotomist will collect blood from a vein in your arm, and a qualified professional will collect the respiratory specimen using appropriate PPE. The swab may cause mild discomfort or gagging.
Report Delivery
You may resume normal activities after sample collection unless advised otherwise. Slight soreness or redness at the blood draw site can occur; apply gentle pressure and keep the site clean.
Timeline: Samples received by 11 am are generally processed, and reports are delivered within 2 days (48 hours).
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the SARS-CoV-2 Monitoring Panel is to provide a single integrated assessment of active SARS-CoV-2 infection and the body's inflammatory/organ-function response. It assists in confirming the diagnosis, triaging symptomatic individuals, detecting variant-associated mutations, and identifying complications such as hepatic, renal, or haematological involvement. It is not intended to replace clinical judgement but to complement it with objective laboratory data.
How to Prepare
- Duly filled Covid-19 Clinical Information Form (Form 44) / SRF ID is mandatory.
- Submit oropharyngeal and nasopharyngeal swabs / ET secretions / BAL / sputum in a special viral transport medium (VTM) from DNA Labs India.
- Ship swab samples refrigerated in a special transport box. Do not freeze.
- Collect 3 mL of serum (min 2 mL) in one SST and 3 mL of whole blood (min 2 mL) in one lavender top EDTA tube. Ship refrigerated. Do not freeze.
- Overnight fasting is preferred before blood collection.
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"This monitoring panel provides a more complete clinical picture by combining a molecular COVID-19 test with haematological and biochemical markers used to assess severity and organ involvement."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Missing or incomplete Covid-19 Clinical Information Form (Form 44) / SRF ID.
- Unlabeled or mismatched patient identification.
- Swab submitted without proper viral transport medium (VTM).
- Blood samples received frozen or grossly haemolysed.
- Samples stored beyond recommended stability time.
Understanding Your Results
SARS-CoV-2 RT-PCR: Not Detected / Negative
No SARS-CoV-2 RNA was detected in the submitted respiratory specimen. It does not exclude infection if sample collection timing was very early or sample quality was suboptimal.
SARS-CoV-2 RT-PCR: Detected / Positive
SARS-CoV-2 RNA is present, indicating current or recent infection. Clinical correlation is required.
CRP > 6.0 mg/L
Elevated acute-phase inflammation may be present; serial monitoring helps track disease severity.
NLR elevated above reference
Neutrophil-lymphocyte imbalance may reflect inflammation and has been used in COVID-19 severity assessment.
Abnormal liver/kidney markers
May indicate hepatic or renal involvement, medication effect, or pre-existing disease; requires physician review.
Consult your doctor immediately if you develop breathing difficulty, persistent chest pain, confusion, drowsiness, bluish lips/face, inability to drink fluids, or worsening fever. If your test is positive, follow state and national isolation guidelines and contact your physician.
Limitations
- ⚠RT-PCR detects current infection and may remain positive after the infectious period in some individuals.
- ⚠Variant detection is dependent on viral load, sample quality, and current assay design.
- ⚠The panel does not provide immunity status; antibody testing is a separate test.
- ⚠Reference ranges may vary by age, sex, and laboratory, so clinical correlation is required.
Risks & Considerations
- ●Minimal bleeding, bruising, or soreness at the venipuncture site.
- ●Dizziness/fainting during or after blood draw.
- ●Nasopharyngeal swab may cause mild pain, tearing, or gagging.
- ●Rare risk of infection at the puncture site (standard precautions minimize it).
Interfering Factors
- ●Haemolysed, lipaemic or icteric blood samples may affect spectrophotometric and ISE measurements.
- ●Food intake before blood collection can influence liver function and some biochemical parameters.
- ●Improper transport or storage may compromise swab sample integrity.
- ●Medications, recent transfusions and concurrent conditions may affect CBC and inflammatory markers.
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Frequently Asked Questions
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Can this test detect COVID-19 variants?
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Why are LFT, KFT and CRP included in this panel?
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