31-Aug-2021-08_10pm-37961-291791

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DIAGNOSTIC REPORT

Patient Ref. No. 777000001549326

CLIENT CODE : C000082254


Cert. No. MC-2010
CLIENT'S NAME AND ADDRESS :
CALLHEALTH SERVICES PVT LTD SRL DIAGNOSTICS
10th FLOOR,RAMKY TOWERS, SURVEY No:136/2 & 4GA CHIBOWLI, PRIME SQUARE BUILDING,PLOT NO 1,GAIWADI INDUSTRIAL
MIND SPACE ROAD, DIST:-RANAGREDDY, ESTATE,S.V. ROAD,GOREGAON (W)
HYDERABAD 500032 MUMBAI, 400062
TELANGANA INDIA MAHARASHTRA, INDIA
40-33557799 Tel : 9111591115, Fax : 022 - 67801212
CIN - U74899PB1995PLC045956

PATIENT NAME : GAURAV MUTHA PATIENT ID : GAURM29087942

ACCESSION NO : 0042UH007184 AGE : 42 Years SEX : Male

DRAWN : 29/08/2021 00:00 RECEIVED : 29/08/2021 15:52 REPORTED : 31/08/2021 15:52

REFERRING DOCTOR : SELF CLIENT PATIENT ID : 291791

Test Report Status Final Results Units

HBV VIRAL LOAD BY REAL TIME PCR


HBV VIRAL LOAD 4311 IU/ml

Comments

***** KINDLY NOTE: THE HBV VIRAL LOAD CAN BE EXPRESSED AS LOG 3.63 AND THE CALCULATED VALUE
IS 35393 CPS/ML (CONVERSION FACTOR: 1 IU/ML= 8.21 CPS/ML).

Interpretation(s)
HBV VIRAL LOAD BY REAL TIME PCR-
Clinical Utility: The viral load provides the direct and reliable estimate of the level of HBV replication. Quantitation of HBV DNA level is important as it serves to be a
prognostic marker of HBV infection. It is used for establishing baseline levels in patients before initiation of the therapy and for monitoring therapeutic response and disease
progression. A sudden rise in the viral load may indicate emergence of resistant strains during the therapy.

Interpretation: HBV viral load is expressed as IU/ml. For conversion to WHO International Units (IU): 1 IU corresponds to approximately 8.21 copies/ml. The lower limit of
detection of this assay is 32 IU/mL. Values below 32 IU/ml does not exclude the possibility of an infection. It may reflect a viral load below the detection limit of the assay.
An increase or decrease of more than threefold may be considered clinically significant. Follow up viral load values below the detectable limit may indicate resolution of the
infection after therapy. Reappearance or increasing viral load may indicate relapse or resistance to the therapy. All viral load results should be interpreted in conjunction
with the clinical history, clinical status of the patient and other diagnostic parameters.

Recommendations: Viral load is a monitoring test and hence should not be used for screening or diagnostic purpose. Wide variations in viral load have been observed due to
following reasons:
a) Use of different technologies/ platforms for follow up testing. Hence, it is recommended to monitor patients using same technology.
b) Non adherence to specimen collection protocol. Hence, it is recommended to immediately freeze the serum/EDTA plasma after collection and separation.

Limitations: PCR is a highly sensitive technique common reasons for paradoxical results are contamination during specimen collection, selection of inappropriate specimens
and inherent PCR inhibitors in the specimen.

References
1. Hepatology (1989) 10: 198202
2. New England Journal of Medicine (1990) 323:295301.
3. Hepatology (1997) 25: 241244.
4. Antiviral Res (1997) 35: 65 82.
5. WHO: Blood Safety & Clinical Technology (2002) 19.

Note: The performance of this assay has been evaluated at SRL Limited.
**End Of Report**
Please visit www.srlworld.com for related Test Information for this accession

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DIAGNOSTIC REPORT
Patient Ref. No. 777000001549326

CLIENT CODE : C000082254


Cert. No. MC-2010
CLIENT'S NAME AND ADDRESS :
CALLHEALTH SERVICES PVT LTD SRL DIAGNOSTICS
10th FLOOR,RAMKY TOWERS, SURVEY No:136/2 & 4GA CHIBOWLI, PRIME SQUARE BUILDING,PLOT NO 1,GAIWADI INDUSTRIAL
MIND SPACE ROAD, DIST:-RANAGREDDY, ESTATE,S.V. ROAD,GOREGAON (W)
HYDERABAD 500032 MUMBAI, 400062
TELANGANA INDIA MAHARASHTRA, INDIA
40-33557799 Tel : 9111591115, Fax : 022 - 67801212
CIN - U74899PB1995PLC045956

PATIENT NAME : GAURAV MUTHA PATIENT ID : GAURM29087942

ACCESSION NO : 0042UH007184 AGE : 42 Years SEX : Male

DRAWN : 29/08/2021 00:00 RECEIVED : 29/08/2021 15:52 REPORTED : 31/08/2021 15:52

REFERRING DOCTOR : SELF CLIENT PATIENT ID : 291791

Test Report Status Final Results Units

Dr. Rashmi Khadapkar Dr. Sunita Polampalli,MD Path


Senior Research Scientist Head -R&D, Molecular
Genomics

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 (91115 91115). 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

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