Allahabad Customer Care
Resume:
HOME COLLECTION SRL LTD ALLAHABAD LAB
SRL LIMITED, 43/1, SARDAR PATEL MARG,
CIVIL LINES,
ALLAHABAD 211001
UTTAR PRADESH INDIA
Patient Ref. No. 201************
CLIENT CODE :
CLIENT'S NAME AND ADDRESS :
DIAGNOSTIC REPORT
SRL Ltd
43/1,Sardar Patel Marg, Civil Lines,
Allahabad, 211001
Uttar Pradesh, INDIA
Tel : 911*******, Fax : CIN - U74899PB1995PLC045956 PATIENT NAME : SARFRAZ PASSPORT NO. M1628763 PATIENT ID : SARFM0101940 ACCESSION NO : 0201VA001174 AGE : 28 Years SEX : Male DRAWN : 05/01/2022 15:33 RECEIVED : 05/01/2022 17:17 REPORTED : 05/01/2022 19:04 REFERRING DOCTOR : SELF CLIENT PATIENT ID :
ICMR NO.: SRLPRUP
DOB.: 15/01/1993
CLINICAL INFORMATION :
Test Report Status Final Results Biological Reference Interval Units SARS COV -2 REAL TIME PCR
SARS-COV-2 RNA NEGATIVE
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. SARS-CoV-2 transmission occurs primarily via respiratory droplets. SARS-CoV-2 is likely to be at the highest concentrations in the nasopharynx during the first 3 to 5 days of symptomatic illness. Real Time PCR assay targets specific genes and can be used for diagnosis of SARS-CoV-2 virus infection.
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 Limitations:
• Negative results do not preclude COVID-19 and must be correlated with clinical observations, patient history, and epidemiological information.
• Positive results do not rule out bacterial infection or co-infection with other viruses.
• The sensitivity of the assay is dependent on the timing of the specimen collection (in relation to symptom onset/stage of infection), quality, and type of the specimen submitted for testing
• 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 targeting any of these genes – E/RDRP/N/ORF1AB References:
1. Euro Surveill 2020;25, 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.Yugank Anand
Consultant Pathologist
Dr. Asvene Kr. Sharma
Microbiologist
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C000057382
HOME COLLECTION SRL LTD ALLAHABAD LAB
SRL LIMITED, 43/1, SARDAR PATEL MARG,
CIVIL LINES,
ALLAHABAD 211001
UTTAR PRADESH INDIA
Patient Ref. No. 201************
CLIENT CODE :
CLIENT'S NAME AND ADDRESS :
DIAGNOSTIC REPORT
SRL Ltd
43/1,Sardar Patel Marg, Civil Lines,
Allahabad, 211001
Uttar Pradesh, INDIA
Tel : 911*******, Fax : CIN - U74899PB1995PLC045956 PATIENT NAME : SARFRAZ PASSPORT NO. M1628763 PATIENT ID : SARFM0101940 ACCESSION NO : 0201VA001174 AGE : 28 Years SEX : Male DRAWN : 05/01/2022 15:33 RECEIVED : 05/01/2022 17:17 REPORTED : 05/01/2022 19:04 REFERRING DOCTOR : SELF CLIENT PATIENT ID :
ICMR NO.: SRLPRUP
DOB.: 15/01/1993
CLINICAL INFORMATION :
Test Report Status Final Results Biological Reference Interval Units 5. The results of a laboratory test are dependent on the quality of the sample as well as the assay technology. 6. Result delays could be because of uncontrolled
circumstances. e.g. assay run failure.
7. Tests parameters marked by asterisks are excluded from the “scope" of NABL accredited tests. (If laboratory is accredited).
8. Laboratory results should be correlated with clinical information to determine Final diagnosis.
9. Test results are not valid for Medico- legal purposes. 10. In case of queries or unexpected test results please call at SRL customer care (Toll free: 180*-***-***). Post proper investigation repeat analysis may be carried out.
1. It is presumed that the test sample belongs to the patient named or identified in the test requisition form.
2. All Tests are performed and reported as per the turnaround time stated in the SRL Directory of services
(DOS).
3. SRL confirms that all tests have been performed or assayed with highest quality standards, clinical safety & technical integrity.
4. A requested test might not be performed if:
a. Specimen received is insufficient or inappropriate specimen quality is unsatisfactory
b. Incorrect specimen type
c. Request for testing is withdrawn by the ordering doctor or patient
d. There is a discrepancy between the label on the specimen container and the name on the test requisition form
CONDITIONS OF LABORATORY TESTING & REPORTING
SRL Limited
Fortis Hospital, Sector 62, Phase VIII,
Mohali 160062
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