Nitin Sample: Collected On:

Nasal & throat Swab Jun 12 2021 10:00 AM

Patient ID: 1906144322 Received
2 On:
Age: 29 Y 9 Gender: Male Jun 12 2021 11:21 AM
Refer Doctor: Self Reported on:
SRF ID: 0707800630002 Jun 12 2021 11:29 AM
3

Investigation Observed Value Unit Biological Ref. Interval

MOLECULAR
BIOLOGY
SARS COV -2 REAL TIME

RT-PCR NEGATIVE Please refer the table below

CT Value: E Gene/ORF1ab(RdRp Gene) 0.00/30.48*
PCR SARS-CoV-2 (COVID-
19) 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 SARSCoV-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.
*******************End Of The Report*******************
CONDITIONS OF LABORATORY TESTING & REPORTING
1. It is presumed that the test sample belongs to the patient named or 4. The results of a laboratory test are dependent on the
identified in the test requisition form quality of the sample as well as the assay technology.
. 5. Result delays could be because of uncontrolled
2. Hindustan Wellness confirms that all tests have been performed or circumstances. e.g. assay run failure.
assaye d with highest qualitystandards, clinical safety & technical integrity. 6. Laboratory results should be correlated with clinical
3. A requested test might not be performed if: information to determine Final diagnosis.
a. Specimen received is insufficient or inappropriate specimen quality is 7. Test results are not valid for Medico legal purposes. 8.
unsatisfactory b.Incorrect specimen type In case of queries or unexpected test results please call at
c. Request for testing is withdrawn by the ordering doctor or patient d. There is a customer care (9810981073/83).
discrepancy between the label on the specimen container and the name on the e-
test requisition form