Patient Name : MASTER. E.

SAI KARTHIK Organization : DIRECT

Age / Gender : 14 years / Male Collection Time : Oct 17, 2021, 12:12 p.m.
Patient ID : 14104 Receiving Time : Oct 17, 2021, 12:57 p.m.
Referral : SELF Reporting Time : Oct 17, 2021, 03:35 p.m.
Sample ID :
212900009

Test Description Value(s) Unit(s) Reference Range

COVID-19
Sample Type : Nasopharyngeal/Oropharyngeal Swabs

* N-Gene (N1-Region) (Covid-19) NOT DETECTED

* N-Gene (N2-Region) (Covid-19) NOT DETECTED

Method Real Time PCR(RT-PCR)

Results Interpretation : NOT DETECTED : NEGATIVE FOR

SARS-COV-2(COVID-19)
in the submitted specimen
NOTE :
• Test conducted on Nasopharyngeal-Oropharyngeal swabs in viral transport media
• Clinical correlation with patient history and other diagnostic information is necessary to determine patient infection status.
• Negative results must be combined with clinical observations, patient history and epidemiological information as number of
factors could lead to a negative result in an infected individual, including but not limited to the following limitations: poor
quality of the specimen, specimen was collected late or very early in the infection, technical reasons inherent in the test, e.g.
Virus mutuation or PCR inhibition.
• Biological Reference Ct value Range : <35 : +Ve, >35: -Ve (ICMR D.O.NO VIR/4/2021/ECD-1)
• Ct value : Cycle number at which detectable signal is achieved
• Positive results indicates the Presence of SARS CoV-2 in the submitted specimen
• Negative results indicates the Absence of SARS CoV-2 in the sumitted specimen
• Kindly consult Refering Physician/Authorized Government Hospital for appropriate follow up
• LAB INFORMATION:
• ICMR-Registration Number for COVID-19 is UCRLUPHT.
• COVID-19 test conducted with kit approved by ICMR/CE-IVD/US-FDA.

**END OF REPORT**

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 Patient Name : MASTER. E. SAI KARTHIK Organization : DIRECT
Age / Gender : 14 years / Male Collection Time : Oct 17, 2021, 12:12 p.m.
Patient ID : 14104 Receiving Time : Oct 17, 2021, 12:57 p.m.
Referral : SELF Reporting Time : Oct 17, 2021, 03:35 p.m.
Sample ID :
212900009

Test Description Value(s) Unit(s) Reference Range

Scan to Validate
 Patient Name : MASTER. E. SAI KARTHIK Organization : DIRECT
Age / Gender : 14 years / Male Collection Time : Oct 17, 2021, 12:12 p.m.
Patient ID : 14104 Receiving Time : Oct 17, 2021, 12:57 p.m.
Referral : SELF Reporting Time : Oct 17, 2021, 03:35 p.m.
Sample ID :
212900009

Test Description Value(s) Unit(s) Reference Range

Widal Slide Agglutination Test* (Serum, Agglutination)

Salmonella Typhi - 'O' Antigen No Agglutination Agglutination titre <(or)= 1:80
Salmonella Typhi - 'H' Antigen No Agglutination Agglutination titre <(or)= 1:80
Salmonella Paratyphi - 'AH' Antigen No Agglutination Agglutination titre <(or)= 1:80
Salmonella Paratyphi - 'BH' Antigen No Agglutination Agglutination titre <(or)= 1:80
Interpretation and Remarks:
• The Widal test is applied for the diagnosis of enteric fever that includes typhoid and paratyphoid caused by Salmonella? typhi
and Salmonella paratyphi respectively.
• For the slide agglutination test, stained Salmonella antigens are used to detect the presence of specific agglutinin in the
patient's serum.
• The slide agglutination test is used as a primary screening procedure.
• Widal test measures somatic O and flagellar H antibodies against Typhoid and Paratyphoid bacilli. The Agglutinins appears
usually at the end of the first week of infection and increases steadily till third / fourth week after which the decline starts. A
positive Widal test may occur because of typhoid vaccination or past typhoid infection and in certain autoimmune diseases.
Nonspecific febrile disease may cause titre to increase. The test may be falsely negative in cases of Enteric fever treated with
antibiotics in the early stages.

**END OF REPORT**

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 Patient Name : MASTER. E. SAI KARTHIK Organization : DIRECT
Age / Gender : 14 years / Male Collection Time : Oct 17, 2021, 12:12 p.m.
Patient ID : 14104 Receiving Time : Oct 17, 2021, 12:57 p.m.
Referral : SELF Reporting Time : Oct 17, 2021, 03:35 p.m.
Sample ID :
212900009

Test Description Value(s) Unit(s) Reference Range

COMPLETE BLOOD COUNT(CBC)

Hemoglobin (Hb)* 14.6 gm/dL 13.5 - 18.0
Method : Cynmeth Photometric Measurement

Erythrocyte (RBC) Count* 5.27 mil/cu.mm 4.7 - 6.0

Method : Electrical Impedence

Packed Cell Volume (PCV)* 43.1 % 42 - 52

Method : Calculated

Mean Cell Volume (MCV)* 81.78 fL 78 - 100

Method : Electrical Impedence

Mean Cell Haemoglobin (MCH)* 27.70 pg 27 - 31

Method : Calculated

Mean Corpuscular Hb Concn. (MCHC)* 33.87 gm/dL 32 - 36

Method : Calculated

Red Cell Distribution Width (RDW)* 12.2 % 11.5 - 14.0

Method : Electrical Impedence

Total Leucocytes (WBC) Count* 5.93 *10^3/ul 4.0-10.0

Method : Electrical Impedence

Neutrophils* 52 % 40 - 80
Method : VCSn Technology

Lymphocytes* 37.3 % 20 - 40
Method : VCSn Technology

Monocytes* 8.9 % 2 - 10
Method : VCSn Technology

Eosinophils* 1 % 1-6
Method : VCSn Technology

Basophils* 0.80 % 0-1

Method : VCSn Technology

Absolute Neutrophil Count* 3.08 * 10^9/L 2.0 - 7.0

Method : Calculated

Absolute Lymphocyte Count* 2.21 * 10^9/L 1-3

Method : Calculated

Scan to Validate
 Patient Name : MASTER. E. SAI KARTHIK Organization : DIRECT
Age / Gender : 14 years / Male Collection Time : Oct 17, 2021, 12:12 p.m.
Patient ID : 14104 Receiving Time : Oct 17, 2021, 12:57 p.m.
Referral : SELF Reporting Time : Oct 17, 2021, 03:35 p.m.
Sample ID :
212900009

Test Description Value(s) Unit(s) Reference Range

Absolute Eosinophil Count* 0.06 * 10^9/L 0.0-0.5

Method : Calculated

Absolute Monocyte Count* 0.53 * 10^9/L 0.2-1.0

Method : Calculated

Absolute Basophils Count* 0.05 * 10^9/L 1-2

Method : Calculated

Platelet Count* 295 *10^3/ul 150 - 450

Method : Electrical Impedence

Mean Platelet Volume (MPV)* 9.1 fL 7.2 - 11.7

Method : Electrical Impedence

PDW* 9.9 % 9.0 - 17.0

Method : Calculated

RBC NORMOCYTIC NORMOCHROMIC

WBC WITH IN NORMAL LIMITS
Platelet NORMAL AND ADEQUATE

Tests done on Automated Five Part Cell Counter. (WBC, RBC,Platelet count by impedance method, colorimetric method for Hemoglobin, WBC differential by flow

cytometry using laser technology other parameters are calculated). All Abnormal Haemograms are reviewed confirmed microscopically.

**END OF REPORT**

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