Diagnostic Report: Patient Name: Krishna Buddhiraj Kaushik KRISM1511769A 0009TK039957

DIAGNOSTIC REPORT
CLIENT CODE : C000103537
CLIENT'S NAME AND ADDRESS :

GETWELL DIAGNOSTICS SRL LIMITED
SHOP NO. 126, HUDA MARKET, SECTOR-37, SRL,REFERENCE LAB, GP-26, MARUTI INDUSTRIAL ESTATE,UDYOG
VIHAR,SECTOR-18,
FARIDABAD 121001 GURGAON, 122015
HARYANA INDIA HARYANA, INDIA
9990002512 9891555451 Tel : 1800-222-000, Fax : CIN - U74899PB1995PLC045956
Email : [email protected]
PATIENT NAME : KRISHNA BUDDHIRAJ KAUSHIK PATIENT ID : KRISM1511769A
ACCESSION NO : 0009TK039957 AGE : 44 Years SEX : Male DATE OF BIRTH :
DRAWN : RECEIVED : 15/11/2020 19:03 REPORTED : 15/11/2020 21:25
REFERRING DOCTOR : SELF CLIENT PATIENT ID :
CLINICAL INFORMATION :
ICMR Registration No: SRLRL001

SRF- 0606000127886
Test Report Status Final Results Biological Reference Interval Units
MOLECULAR BIOLOGY
SARS COV -2 REAL TIME PCR
SARS-COV-2 RNA POSITIVE

Comments
NOTE: CONFIRMATORY GENE CT VALUE=25
Interpretation(s)
SARS COV -2 REAL TIME PCR-
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 and complications.
Positive result indicates that RNA from SARS-CoV-2 was detected in the specimen, and the patient is considered infected with the virus and presumed to be contagious.
Negative test result for this test means that SARS-CoV-2 RNA was not detected in the specimen above the limit of detection of the assay.
Limitations:
• 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.
• Positive results do not rule out bacterial infection or co-infection with other viruses.
• 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.
• Follow-up testing may particularly be important if patient has a clinical picture of viral pneumonia, a potential exposure history, and/or radiographic findings (chest CT or
MRI scan) consistent with COVID -19 pneumonia. However repeat testing in the near-term after clearance (within 90 days) should be avoided as prolonged shedding of
non-viable virus is not uncommon
• Ct values generated from different assay systems within the same laboratory, or from different laboratories, are not directly comparable and do not necessarily reflect the
same viral load due to inter-assay and inter-laboratory variability.
• Variation in timing of sample collection, fluctuations in virus shedding, and difference between detection limit of different testing methods within same or different labs could
lead to variation in results particularly during initial phase of infection.
• 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.
• The performance of this test has not been established for monitoring treatment of 2019-nCoV infection.
Note: Test is performed using ICMR approved Kit.
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
**End Of Report**
Please visit www.srlworld.com for related Test Information for this accession
Dr. Rashmi Talwar, PhD Dr. Yoginder Pal Singh, Ph.D Dr. Anurag Bansal
Section Head- Genetics Molecular Biologist LAB DIRECTOR
Page 1 Of 2
DIAGNOSTIC REPORT
CLIENT CODE : C000103537
CLIENT'S NAME AND ADDRESS :

GETWELL DIAGNOSTICS SRL LIMITED
SHOP NO. 126, HUDA MARKET, SECTOR-37, SRL,REFERENCE LAB, GP-26, MARUTI INDUSTRIAL ESTATE,UDYOG
VIHAR,SECTOR-18,
FARIDABAD 121001 GURGAON, 122015
HARYANA INDIA HARYANA, INDIA
9990002512 9891555451 Tel : 1800-222-000, Fax : CIN - U74899PB1995PLC045956
Email : [email protected]
PATIENT NAME : KRISHNA BUDDHIRAJ KAUSHIK PATIENT ID : KRISM1511769A
ACCESSION NO : 0009TK039957 AGE : 44 Years SEX : Male DATE OF BIRTH :
DRAWN : RECEIVED : 15/11/2020 19:03 REPORTED : 15/11/2020 21:25
REFERRING DOCTOR : SELF CLIENT PATIENT ID :
CLINICAL INFORMATION :
ICMR Registration No: SRLRL001

SRF- 0606000127886
Test Report Status Final Results Biological Reference Interval Units
CONDITIONS OF LABORATORY TESTING & REPORTING

1. It is presumed that the test sample belongs to the patient 5. The results of a laboratory test are dependent on the
named or identified in the test requisition form. quality of the sample as well as the assay technology.
2. All Tests are performed and reported as per the 6. Result delays could be because of uncontrolled
turnaround time stated in the SRL Directory of services circumstances. e.g. assay run failure.
(DOS). 7. Tests parameters marked by asterisks are excluded from
3. SRL confirms that all tests have been performed or the “scope" of NABL accredited tests. (If laboratory is
assayed with highest quality standards, clinical safety & accredited).
technical integrity. 8. Laboratory results should be correlated with clinical
4. A requested test might not be performed if: information to determine Final diagnosis.
a. Specimen received is insufficient or inappropriate 9. Test results are not valid for Medico- legal purposes.
specimen quality is unsatisfactory 10. In case of queries or unexpected test results please call
b. Incorrect specimen type at SRL customer care (Toll free: 1800-222-000). Post proper
c. Request for testing is withdrawn by the ordering doctor investigation repeat analysis may be carried out.
or patient
d. There is a discrepancy between the label on the
specimen container and the name on the test requisition
form
SRL Limited
Fortis Hospital, Sector 62, Phase VIII,
Mohali 160062
Page 2 Of 2

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DIAGNOSTIC REPORT

CLIENT CODE : C000103537

CLIENT'S NAME AND ADDRESS :

PATIENT NAME : KRISHNA BUDDHIRAJ KAUSHIK PATIENT ID : KRISM1511769A

ACCESSION NO : 0009TK039957 AGE : 44 Years SEX : Male DATE OF BIRTH :

DRAWN : RECEIVED : 15/11/2020 19:03 REPORTED : 15/11/2020 21:25

REFERRING DOCTOR : SELF CLIENT PATIENT ID :

ICMR Registration No: SRLRL001

Test Report Status Final Results Biological Reference Interval Units

SARS-COV-2 RNA POSITIVE

NOTE: CONFIRMATORY GENE CT VALUE=25

Note: Test is performed using ICMR approved Kit.

CLIENT CODE : C000103537

CLIENT'S NAME AND ADDRESS :

PATIENT NAME : KRISHNA BUDDHIRAJ KAUSHIK PATIENT ID : KRISM1511769A

ACCESSION NO : 0009TK039957 AGE : 44 Years SEX : Male DATE OF BIRTH :

DRAWN : RECEIVED : 15/11/2020 19:03 REPORTED : 15/11/2020 21:25

REFERRING DOCTOR : SELF CLIENT PATIENT ID :

ICMR Registration No: SRLRL001

Test Report Status Final Results Biological Reference Interval Units

CONDITIONS OF LABORATORY TESTING & REPORTING

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