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MR - Kuldeep Pandya PDF

Mr. Kuldeep Pandya, a 24-year-old male, tested positive for SARS-CoV-2 (COVID-19) via a real-time RT-PCR test of a throat and nasal swab. The positive result indicates the presence of SARS-CoV-2 RNA and clinical correlation is needed. The test was performed at Pune Haveli by Atharva Healthcare Services and reported on July 8, 2020.

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0% found this document useful (0 votes)
266 views1 page

MR - Kuldeep Pandya PDF

Mr. Kuldeep Pandya, a 24-year-old male, tested positive for SARS-CoV-2 (COVID-19) via a real-time RT-PCR test of a throat and nasal swab. The positive result indicates the presence of SARS-CoV-2 RNA and clinical correlation is needed. The test was performed at Pune Haveli by Atharva Healthcare Services and reported on July 8, 2020.

Uploaded by

abhishek mayekar
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd

CID : 2018907791 SID : 177801725810 R

Name : MR.KULDEEP PANDYA Registered : 07-Jul-2020 / 16:46 E


P
Age / Gender : 24 Years / Male Collected : 07-Jul-2020 / 18:10 O
Dr. : AMOL DANGE Reported : 08-Jul-2020 / 16:58 R
T
Reg. Location : Pune Haveli, Atharva Healthcare Services Printed : 10-Jul-2020 / 17:07

Real time Qualitative RT-PCR detection of 2019-nCOV RNA / COVID-19 RNA


PARAMETER RESULT
Result SARS-CoV-2: DETECTED

‡ ICMR Registration No. SUBUR001

Specimen: Throat swab + Nasal swab in VTM

Method: Real time RT-PCR

Note:

ƕ The result relates only to the specimen received in the lab.


ƕ All the positive cases will be notified to ICMR for further surveillance.
ƕ Positive results are indicative of the presence of SARS-CoV-2 RNA; clinical correlation with patient history and
other diagnostic information is necessary to determine patient infection status.
ƕ Results do not rule out bacterial infection or co-infection with other viruses as little is known about co-
infection.
ƕ RT PCR kits used are RUO approved for use by ICMR recommended for government and private laboratories.
ƕ The internal validation is done at Molecular Diagnostics Department, Suburban Diagnostics, Mumbai.

Limitations:

ƕ Optimum specimen types and timing of peak viral levels during infections caused by 2019-nCOV have not been
determined. Collection of multiple specimens (Types & Time points) may be necessary in view of suspected
clinical history. The repeat specimen may be considered after a gap of 2-4 days after the collection of first
specimen for additional testing if required. (other respiratory pathogens)
ƕ Negative results do not preclude SARS - CoV - 2 infection and should not be used as the sole basis for patient
management decisions.

References:

i. Diagnostic detection of 2019-nCoV by real-time RT-PCR, Berlin Jan 17th, 2020


ii. Labcorp COVID-19 RT-PCR test EUA Summary. Accelerated Emergency Use Authorization (EUA) summary covid-
1 RT-PCR test (laboratory corporation of America).
* Sample processed at Molecular Diagnostics Laboratory, CPL, Andheri West
*** End Of Report ***

HEENA SATAM. Dr.SHWETA NAIK


Ph.D. M.D D.N.B
MOLECULAR BIOLOGIST MICROBIOLOGIST
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