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MMG2021W015052

This document contains the results of a COVID-19 RT-PCR test for a patient. The test was negative and did not detect the SARS-CoV-2 virus. Some additional information is provided about the test methodology and limitations.

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Karthikeya Puttagunta
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38 views1 page

MMG2021W015052

This document contains the results of a COVID-19 RT-PCR test for a patient. The test was negative and did not detect the SARS-CoV-2 virus. Some additional information is provided about the test methodology and limitations.

Uploaded by

Karthikeya Puttagunta
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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ICMR Rgd. Nos.

: MMGIPHT / MAPMGILSRRT

AMARESH NUKALA

Sample ID MMG2021W015052 Sample Type Oropharyngeal/Nasopharyngeal


Gender Male Sample Collected On Dec 03, 2021 : 11:16
Age / DOB 43 Report Date Dec 03, 2021 : 18:57
Aadhar Number 4873 1184 4806 Mobile Number 9866284545
Referred By Hospital

RT-PCR test for COVID-19 (NOVEL CORONA VIRUS)

Result
Investigation CT Value Result

SARS-CoV-2 virus detection (N Gene) Undetermined Not Detected (Negative)


Method: Qualitative Real Time Polymerase Chain Reaction (RT-PCR)

Intrepretation of Results
• Detection of Nucleocapsid (N) gene of virus indicates the presence of SARS-CoV-2 virus in the specimen tested.
• Clinical correlation with patient history and other diagnostic information is necessary to determine patient infection status.
• CT Value is the cycle time needed to detect the virus. It is inversely proportional to the viral load. Lower CT indicates higher viral load.
Limitations of Assay
Performance of 2019-nCoV Real-Time RT-PCR Diagnostic Panel has only been established in upper and lower respiratory specimens
(nasopharyngeal or oropharyngeal swabs, sputum, lower respiratory tract aspirates, bronchoalveolar lavage, and nasopharyngeal
wash/aspirate or nasal aspirate).

Negative results do not preclude 2019-nCoV infection and should not be used as the sole basis for treatment or other patient
management decisions. Optimum specimen types and timing for peak viral levels during infections caused by 2019-nCoV have not
been determined. Collection of multiple specimens (types and time points) from the same patient may be necessary to detect the
virus.

Note
• COVID test is conducted by ICMR/NABL/USFDA approved Kit.
• Kindly consult referring Physician / Authorized hospitals for appropriate follow up.

Please scan QR
code to verify the
Dr. M Aravind Kumar
report online
Head of Molecular Testing Laboratory

Report will be available online for 30 days from the date of sample collection.
Reach us if you need the report after 30 days.
(1800-102-4595 (toll-free), +91-8688310052)

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