Lab Serial No. : 0192308000434 SIN No.

, Date : 19013944 25-Aug-23 02:29 PM

Patient Name : Mr. AKASH Sample collection date : 25-Aug-2023 02:30PM
Referred by : Dr. SELF SRA Date : 25-Aug-2023 02:39PM
Age/Gender : 20 Y 7 M 22 D / M Report Date : 25-Aug-2023 02:52PM
Source By : Report printed on : 25-Aug-2023 03:05PM
Franchise - Neemrana Center-
Collected at : Document No. : -
19

HAEMATOLOGY
Test Name Observation Unit Biological Ref. interval

COMPLETE BLOOD COUNT(CBC/HAEMOGRAM) (EDTA Blood)

Haemoglobin by SLS method 14.2 g/dL 13.0-17.0
Haematocrit (HCT) by RBC Pulse High detection method 43.2 % 40-50
Red Blood Cell Count (RBC) by DC detection method 5.10 million/mm3 4.5-5.5
Mean Corposcular Volume (MCV) by Calculated 84.7 fL 83-101
method
Mean Corposcular Haemoglobin (MCH) by 27.9 pg 27-32
Calculated method
Mean Corposcular Haemoglobin Conc.(MCHC) 32.9 g/dL 31.5-34.5
by Calculated method
Red Cell Distribution Width (RDWcv) by Calculated 14.4 % 11.8-14.5
method
Total Leucocyte Count (TLC) by Flow Cytometry 8.70 1000/mm3 4.0-10.0
method
Differential Leucocyte Count
Segmented Neutrophils by Flow Cytometry method 77 % 42-72
Lymphocytes by Flow Cytometry method 12 % 25-45
Eosinophils by Flow Cytometry method 6 % 1-6
Monocytes by Flow Cytometry method 5 % 2-10
Basophils by Flow Cytometry method 00 % 0-2
Absolute Leucocyte Count
Neutrophils by Flow Cytometry method 6 1000/mm3 2.0-7.0
Lymphocytes. by Flow Cytometry method 1 1000/mm3 1.0-3.0
Eosinophils. by Flow Cytometry method 0.5 1000/mm3 0.05-0.50
Monocytes. by Flow Cytometry method 0.4 1000/mm3 0.2-1.0
Basophils. by Flow Cytometry method 00 1000/mm3 0.02-0.2
ITDOSE INFOSYSTEMS PVT. LTD.

Platelet count by DC detection method 2.34 Lakhs/cumm 1.5-4.0

Mean Platelet Volume (MPV) by Calculated method 8.5 fL 7.8-11.0
Remark:As per the recommendation of International Council for Standardization in Hematology,the differential leucocyte counts are additionally
being reported as absolute numbers of each cell in per unit volume of blood.

Page 1 of 4
The test has been processed at -
 Lab Serial No. : 0192308000434 SIN No., Date : 19013944 25-Aug-23 02:29 PM
Patient Name : Mr. AKASH Sample collection date : 25-Aug-2023 02:30PM
Referred by : Dr. SELF SRA Date : 25-Aug-2023 02:39PM
Age/Gender : 20 Y 7 M 22 D / M Report Date : 25-Aug-2023 02:52PM
Source By : Report printed on : 25-Aug-2023 03:05PM
Franchise - Neemrana Center-
Collected at : Document No. : -
19

HAEMATOLOGY

MALARIA PARASITE BY RAPID CARD

Malaria Parasite, EDTA Blood by pLDH Method

Result : Negative
Indicative of Plasmodium falciparum infection.
Indicative of Plasmodium other than P.falciparum infection.

Note:- In India, Plasmodium vivax is most common. Plasmodium malariae

also responsible for approx 1% cases of malaria in india.

Remarks :-

1. P.f/Pan Ag Test is an immunochromatographic assay for the differential detection between

Plasmodium falciparum Histidine-Rich (HRP-II) and Plasmodium species (Plasmodium falciparum,
P.vivax, P.ovale and P.malariae) lactate dehydrogenase (pLDH) in human whole blood.
2. Relative Sensitivity with 98.72%.
3. Relative Specificity with 96.76%.
ITDOSE INFOSYSTEMS PVT. LTD.

Page 2 of 4
The test has been processed at -
 Lab Serial No. : 0192308000434 SIN No., Date : 19013944 25-Aug-23 02:29 PM
Patient Name : Mr. AKASH Sample collection date : 25-Aug-2023 02:30PM
Referred by : Dr. SELF SRA Date : 25-Aug-2023 02:39PM
Age/Gender : 20 Y 7 M 22 D / M Report Date : 25-Aug-2023 02:52PM
Source By : Report printed on : 25-Aug-2023 03:05PM
Franchise - Neemrana Center-
Collected at : Document No. : -
19

SEROLOGY

Typhoid Antibodies (IgG & IgM)

Serum by Rapid Chromatographic Immunoassay

Test Name Result

Anti S.typhi / paratyphi Antibodies (IgG) NEGATIVE

Anti S.typhi / paratyphi Antibodies (IgM) NEGATIVE

Conclusion :-
Negative
Positive - (Indicative of Current Infection)
Positive - (Indicative of Previous or Latent or Late stage of infection)

Remarks :-
1. The Typhoid IgG/IgM Combo Rapid Test is screening test based on lateral flow
chromatographic immunoassay. The test qualitatively detects and differentiates IgG and IgM
antibodies to S. typhi and S. paratyphi in serum, plasma or whole blood specimens thus aiding
in the determination of either current or previous exposure to S. typhi and S.paratyphi.
2. IgM positive or IgM/IgG both positive suggest Current infection, while only IgG positive
ITDOSE INFOSYSTEMS PVT. LTD.

suggests previous infection, Latent infection or Late stage of infection.

Limitation :-
1. The Typhoid IgG/IgM Combo Rapid Test is limited to the qualitative detection of
antibodies to S. typhi or S. paratyphi in human serum, plasma or whole blood.
2. A negative result for an individual subject indicates absence of detectable anti-S. typhi or
anti- S. paratyphi antibodies. However, a negative test result does not precludes the possibility

Page 3 of 4
The test has been processed at -
 Lab Serial No. : 0192308000434 SIN No., Date : 19013944 25-Aug-23 02:29 PM
Patient Name : Mr. AKASH Sample collection date : 25-Aug-2023 02:30PM
Referred by : Dr. SELF SRA Date : 25-Aug-2023 02:39PM
Age/Gender : 20 Y 7 M 22 D / M Report Date : 25-Aug-2023 02:52PM
Source By : Report printed on : 25-Aug-2023 03:05PM
Franchise - Neemrana Center-
Collected at : Document No. : -
19

SEROLOGY
of exposure to S. typhi or S. paratyphi.
3. A negative result can occur if the quantity of anti-S. typhi or paratyphi antibodies present
in the specimen is below the detection limits of the assay or the antibodies that are detected
are not present during the stage of disease in which a sample is collected.
4. Some specimens containing unusually high titers of heterophile antibodies or rheumatoid factor
may affect expected results.
5. False positive cases may occur in the patients suffering with Dengue fever. (Reference: Cross Reactivity
of Rapid Salmonella Typhi IgM Immunoassay in Dengue Fever without co-existing infection by Adnan et al).
6. If the symptoms persist while the result from FastVue Typhoid IgG/IgM Combo Rapid Test
is negative or nonreactive result, it is recommended to re-sample the patient a few days later
or test with an alternative test method such as bacterial culture method via blood, bone marrow or Widal test.
7. The results obtained with this test should only be interpreted in conjunction with other
diagnostic procedures and clinical findings.

*** End of report ***

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