Corona Report

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SRF ID :0707904780529

PO No :PO1151670408-986

Name : Mr.SURINDER SINGH KOHLI :


Age/Gender : 40/Male Registration Date : 07-Aug-22 11:26 AM
Patient ID : MLM119295 Collection Date : 07/Aug/2022 09:48AM
Barcode ID / Order ID : A7924011 / 5337037 Sample Receive Date : 07/Aug/2022 02:56PM
Referred By : Dr. Report Status : Final Report
Sample Type : ORAL AND NASOPHARYNGEAL SWAB Report Date : 07/Aug/2022 06:21PM

Molecular Biology
Test Name Result Unit Bio. Ref. Range Method

SARS-CoV-2 RT PCR (Qualitative)


SARS-CoV2 RT PCR NEGATIVE NEGATIVE RT PCR

Comment:

ICMR Registration Number : 1MGTPLGH

Methodology -
Qualitative RT PCR.

Clinical Significance:
This test is used for the detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a positive-sense, single-stranded RNA virus that causes coronavirus
disease 2019 (COVID-19). SARS-CoV-2 transmission occurs primarily via respiratory droplets.
The most common symptoms of COVID-19 are fever, tiredness, and dry cough. Some patients may have aches and pains, nasal congestion,
runny nose, sore throat or diarrhea. These symptoms are usually mild and begin gradually. Some people become infected but don’t develop
any symptoms and don't feel unwell. Most people recover from the disease without needing special treatment. Few people who gets COVID-
19 becomes seriously ill and develops difficulty breathing. Older people, and those with underlying medical problems like high blood pressure,
heart problems or diabetes,are more likely to develop serious illness.

Upper respiratory specimens ( e.g., Nasopharynx, oropharynx) are usually adequate for testing early-stage infections, especially in
asymptomatic or mild cases.
Lower respiratory specimens (eg, sputum, tracheal aspirate, bronchoalveolar fluid) are advised if collected later in the course of the COVID-
19 disease or in patients with a negative upper respiratory tract sampling and there is a strong clinical suspicion of COVID-19.

Limitations :
Improper collection, storage or transport of specimens may lead to false negative or invalid results.
Test results should be interpreted in conjunction with the patient’s medical history, clinical signs and symptoms, and the results of other
diagnostic tests performed.
Negative results do not rule out SARS-CoV-2 infections and should not be used as the sole basis for patient management decisions.
Detection of SARS-CoV-2 RNA may be affected by sample collection methods, patient factors (e.g., presence of symptoms), and/or stage of
infection.
False negative or invalid results may occur due to interference or the presence of inhibitors. The Internal Control is included to help identify
the specimens containing interfering substances or inhibitors.
This is a qualitative test and is not indicative of the quantity of virus in the sample.
False negative results may occur if viruses are present at levels below the test’s limit of detection.
False negative results may occur if mutations are present in the regions targeted by the test.
A potentialy reduced sensitivity may occur when viral concentrations are at or near the limit of detection of the assay.
Analyte targets (viral nucleic acid) may persist in vivo, independent of virus viability. Detection of analyte targets does not imply that the
corresponding viruses are infectious, or are the causative agents for clinical symptoms.

Page 1 of 2
SRF ID :0707904780529
PO No :PO1151670408-986

Name : Mr.SURINDER SINGH KOHLI :


Age/Gender : 40/Male Registration Date : 07-Aug-22 11:26 AM
Patient ID : MLM119295 Collection Date : 07/Aug/2022 09:48AM
Barcode ID / Order ID : A7924011 / 5337037 Sample Receive Date : 07/Aug/2022 02:56PM
Referred By : Dr. Report Status : Final Report
Sample Type : ORAL AND NASOPHARYNGEAL SWAB Report Date : 07/Aug/2022 06:21PM

Molecular Biology
Test Name Result Unit Bio. Ref. Range Method
Interpretation Guidelines:
E Gene - It is common for Serbecovirus family of viruses, it’s detection in absence of RdRp/N Gene requires further testing.
RdRp and N Gene - These genes are confirmatory for SARS-CoV-2.

Note: It is not recommended to rely on numerical Ct values for determining infectiousness of COVID-19 patients and deciding patient
management protocols

*** End Of Report ***

Page 2 of 2
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2. We ensure that all tests are carried out with


utmost care, in accordance with the
accepted national and international norms
and clinical safety standards such as good
laboratory practices by WHO and ICMR.

3.

Our lab test reports undergo multiple levels
of meticulous processing and detailed
verification. Every single report goes

through a 3-step review process and is
verified by a doctor holding a postgraduate
degree in Pathology or Microbiology.

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Conditions of Laboratory Testing & Reporting:


*Test results released pertain to the sample,as received *Laboratory investigations are only a tool to facilitate in arriving at
a diagnosis and should be clinically correlated by the interpreting clinician.*Result delays may happen because of
unforeseen or uncontrollable circumstances.*Test report may vary depending on the assay method used *Test results may
show inter-laboratory variations *Test results are not valid for medico-legal purposes *Please mail your queries related to
test results to Customer Care mail ID cs.labs@1mg.com

Disclaimer: Results relate only to the sample received. Test results marked “BOLD” indicate abnormal results i.e., higher or
lower than normal. All lab test results are subject to clinical interpretation by a qualified medical professional. This report
cannot be used for any medico-legal purposes. Partial reproduction of the test results is not permitted. Also, TATA 1mg
Labs is not responsible for any misinterpretation or misuse of the information. The test reports alone may not be conclusive
of the disease/condition, hence clinical correlation is necessary. Reports should be vetted by a qualified doctor only.

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