Mr.

DESH DEEPAK Sample: Collected On:

Nasal & throat Swab May 13 2021 9:00AM
Patient ID: 21052279333 Received On:
Age : 66 Y Gender : Male May 13 2021 2:30PM
ReferDoctor : Self Reported on:
SRF ID: 0707800652053 May 14 2021 12:20PM

Investigation Observed Value Unit Biological Ref.Interval

MOLECULAR BIOLOGY

SARS COV -2 REAL TIME PCR

SARS-CoV-2 (COVID-19)
POSITIVE Please refer the table below
RT-PCR
CT Value: E Gene/ORF1ab(RdRp Gene) 17.25/17.79*
Clinical Significance:
Result Remarks
Positive RNA specific to SARS-CoV-2 Detected.
Negative RNA specific to SARS-CoV-2 NOT detected.
Inconclusive A repeat testing on fresh sample is recommended.

ICMR Covid - 19 lab Registration number is HIWEPLGH.

Test conducted on Nasal & Throat Swab Samples.
Lower respiratory tract samples like Sputum, BAL, ET aspirate are appropriate samples especially in severe and progressive lung disease.
Kindly consult referring Physician / Authorized hospitals for appropriate follow up.
Covid-19 Test conducted as per kits approved by ICMR / CE-IVD / USFDA.

Limitations:
1. Negative results do not preclude COVID-19 and should not be used as the sole basis for patient management decisions. Negative results must be combined with
clinical observations, patient history, and epidemiological information.
2. Presence of inhibitors, mutations or insufficient RNA Specific to SARS-CoV-2 can influence the test result. Kindly correlate the results with clinical findings.
3. Positive results but do not rule out bacterial infection or co-infection with other viruses.
4. 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.
5. If the virus mutates in the rRT-PCR target region, 2019-nCoV may not be detected or may be detected less predictably. Inhibitors or other types of interference may
produce a false negative result.
6. The performance of this test has not been established for monitoring treatment of 2019-nCoV infection.

Comments: SARS-CoV-2, formerly known as 2019-nCoV, is the causative agent of the coronavirus disease 2019 (COVID-19). Main symptoms of the disease include fever,
cough and shortness of breath. The virus is spread via person-to-person contact through respiratory droplets produced when a person coughs or sneezes. The SARS-
CoV-2 RNA is generally detectable in nasopharyngeal/oropharyngeal swabs during the acute phase of infection. Positive results are indicative of active infection. Real
Time PCR assay targets specific genes and can be used for diagnosis of SARS-CoV-2 virus infection which contributes to severe upper respiratory distress,
complications

References:
1. Laboratory testing for coronavirus disease 2019 (COVID-19) in suspected human cases. Interim guidance. World Health Organization.
2. Druce et al. JCM. 2011
3. N. Engl. J. Med. 2020, 382, 929–936
*Disclaimer:Low Viral Load may indicate early incubation or late incubation phase. Two different samples taken at two different times
and different conditions shall not be liable for the same results.
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CONDITIONS OF LABORATORY TESTING & REPORTING
1. It is presumed that the test sample belongs to the patient named or identified in the test requisition form 4. The results of a laboratory test are dependent on the quality of the sample as well
.
2. Hindustan Wellness confirms that all tests have been performed or assaye d with highest quality as the assay technology.
standards, clinical safety & technical integrity. 5. Result delays could be because of uncontrolled circumstances. e.g. assay run
3. A requested test might not be performed if: failure.
a. Specimen received is insufficient or inappropriate specimen quality is unsatisfactory 6. Laboratory results should be correlated with clinical information to determine Final
b.Incorrect specimen type diagnosis.
c. Request for testing is withdrawn by the ordering doctor or patient d. There is a discrepancy between 7. Test results are not valid for Medicolegal purposes. 8. In case of queries or
the label on the specimen container and the name on the e-test requisition form unexpected test results please call at customer care (9810981073/83).