D-37/1, TTC MIDC, Turbhe, Navi Mumbai-400 703: Name Ref. by Test Asked::: Patientid: Home Collection

PROCESSED AT :
Thyrocare
D-37/1,TTC MIDC,Turbhe,
Navi Mumbai-400 703
NAME : MOHAMMED KHAJA FAIYAZUDDIN (31Y/M) HOME COLLECTION :

REF. BY 302 NS RESIDENCY,FATHIMA NAGAR, ,
: SELF
HYDERABAD - 500008
TEST ASKED : DENGUE NS1 ANTIGEN,DENGUE-IgM
PATIENTID : MF17481494
TEST NAME TECHNOLOGY VALUE UNITS
DENGUE-IGM E.L.I.S.A 2.8 OD Ratio

Reference Range :
Negative : < 9
Equivocal: 9 - 11
Positive : > 11
Clinical Significance
Diagnosis of an infectious disease should not be established on the basis of a single test result. A precise diagnosis should take into
consideration clinical history, symptomatology as well as serological data. The Flaviviridae family includes the serotypes of Dengue
virus as well as yellow fever and Japanese encephalitis viruses. There is a cross reactivity among flaviviruses, due to the presence of
common antigenic determinants.
Reference: Pinheiro FP, CorberSJ : Global situation of Dengue and Dengue haemorrhagic fever and its emergence in the Americas.
World Health Stat ! 50(3/4):161-169, 1997
Method : SOLID PHASE CAPTURE ENZYME IMMUNOASSAY
Please correlate with clinical conditions.
Sample Collected on (SCT) : 25 Aug 2021 14:00
Sample Received on (SRT) : 26 Aug 2021 12:19

Report Released on (RRT) : 26 Aug 2021 20:08
Sample Type : SERUM
Labcode : 2608005432/SP201 Dr.Prachi Sinkar MD(Path)
Barcode : V6890510
Page : 1 of 4
PROCESSED AT :
Thyrocare
Navi Mumbai-400 703

REF. BY : SELF 302 NS RESIDENCY,FATHIMA NAGAR, , HYDERABAD
- 500008
TEST ASKED : DENGUE NS1 ANTIGEN,DENGUE-IgM
TEST NAME TECHNOLOGY VALUE UNITS
DENGUE NS1 ANTIGEN E.L.I.S.A 4.59 Ag Units
Reference Range :-
Negative : < 9
Equivocal : 9 - 11
Positive : > 11
Clinical Significance
The detection of highly specific dengue NS1 antigen is possible in the serum of dengue virus infected individuals from the onset of
clinical symptoms in primary as well as secondary infections. Therefore this antigen detection is an important tool for diagnosis of
acute dengue virus infection. It allows rapid detection on the first day of fever, before antibodies appear some 5 or more days
late.
Specifications:
Sensitivity: 99.5% & Specificity:100%
Please correlate with clinical conditions.
Method:- SOLID PHASE ENZYME IMMUNOASSAY

Sample Type : SERUM
Dr.Prachi Sinkar MD(Path)
Labcode : 2608005432/SP201
Barcode : V6890510 Page : 2 of 4
PROCESSED AT :
Thyrocare
Navi Mumbai-400 703

REF. BY : SELF 302 NS RESIDENCY,FATHIMA NAGAR, ,
HYDERABAD - 500008
TEST ASKED : HEMOGRAM
TEST NAME VALUE UNITS REFERENCE RANGE
TOTAL LEUCOCYTES COUNT 4.08 X 10³ / µL 4.0-10.0
NEUTROPHILS 52 % 40-80
LYMPHOCYTE PERCENTAGE 43.4 % 20-40
MONOCYTES 3.7 % 0-10
EOSINOPHILS 0.5 % 0.0-6.0
BASOPHILS 0.2 % <2
IMMATURE GRANULOCYTE PERCENTAGE(IG%) 0.2 % 0-0.5
NEUTROPHILS - ABSOLUTE COUNT 2.12 X 10³ / µL 2.0-7.0
LYMPHOCYTES - ABSOLUTE COUNT 1.77 X 10³ / µL 1.0-3.0
MONOCYTES - ABSOLUTE COUNT 0.15 X 10³ / µL 0.2-1
BASOPHILS - ABSOLUTE COUNT 0.01 X 10³ / µL 0-0.1
EOSINOPHILS - ABSOLUTE COUNT 0.02 X 10³ / µL 0-0.5
IMMATURE GRANULOCYTES(IG) 0.01 X 10³ / µL 0-0.3
TOTAL RBC 5.94 X 10^6/µL 4.5-5.5
NUCLEATED RED BLOOD CELLS Nil X 10³ / µL <0.01
NUCLEATED RED BLOOD CELLS % Nil % <0.01
HEMOGLOBIN 15.2 g/dL 13-17
HEMATOCRIT(PCV) 42.56 % 40-50
MEAN CORPUSCULAR VOLUME(MCV) 86.9 fL 83-101
MEAN CORPUSCULAR HEMOGLOBIN(MCH) 25.6 pq 27-32
MEAN CORP.HEMO.CONC(MCHC) 29.5 g/dL 31.5-34.5
RED CELL DISTRIBUTION WIDTH - SD(RDW-SD) 52.3 fL 39-46
RED CELL DISTRIBUTION WIDTH (RDW-CV) 16.5 % 11.6-14
PLATELET DISTRIBUTION WIDTH(PDW) 11 fL 9.6-15.2
MEAN PLATELET VOLUME(MPV) 9.9 fL 6.5-12
PLATELET COUNT 205 X 10³ / µL 150-400
PLATELET TO LARGE CELL RATIO(PLCR) 23.9 % 19.7-42.4
PLATELETCRIT(PCT) 0.2 % 0.19-0.39
Please Correlate with clinical conditions.
Method : Fully automated bidirectional analyser (6 Part Differential SYSMEX XN-1000)
(This device performs hematology analyses according to the Hydrodynamic Focussing (DC method), Flow
Cytometry Method (using a semiconductor laser), and SLS- hemoglobin method)
~~ End of report ~~

Sample Type : EDTA
Labcode : 2608068126/SP201 Dr.Prachi Sinkar MD(Path)
Barcode : V6898694 Page : 3 of 4
CONDITIONS OF REPORTING
v The reported results are for information and interpretation of the referring doctor only.
v It is presumed that the tests performed on the specimen belong to the patient; named or identified.
v Results of tests may vary from laboratory to laboratory and also in some parameters from time to time for the same
patient.
v Should the results indicate an unexpected abnormality, the same should be reconfirmed.
v Only such medical professionals who understand reporting units, reference ranges and limitations of technologies
should interpret results.
v This report is not valid for medico-legal purpose.
v Neither Thyrocare, nor its employees/representatives assume any liability, responsibility for any loss or damage that
may be incurred by any person as a result of presuming the meaning or contents of the report.
v Thyrocare Discovery video link :- https://youtu.be/nbdYeRgYyQc
v For clinical support please contact @8450950851,8450950852,8450950853,8450950854 between 10:00 to 18:00
EXPLANATIONS
v Majority of the specimen processed in the laboratory are collected by Pathologists and Hospitals we call them
as "Clients".
v Name - The name is as declared by the client and recored by the personnel who collected the specimen.
v Ref.Dr - The name of the doctor who has recommended testing as declared by the client.
v Labcode - This is the accession number in our laboratory and it helps us in archiving and retrieving the data.
v Barcode - This is the specimen identity number and it states that the results are for the specimen bearing
the barcode (irrespective of the name).
v SCP - Specimen Collection Point - This is the location where the blood or specimen was collected as declared by
the client.
v SCT - Specimen Collection Time - The time when specimen was collected as declared by the client.
v SRT - Specimen Receiving Time - This time when the specimen reached our laboratory.
v RRT - Report Releasing Time - The time when our pathologist has released the values for Reporting.
v Reference Range - Means the range of values in which 95% of the normal population would fall.
SUGGESTIONS
v Values out of reference range requires reconfirmation before starting any medical treatment.
v Retesting is needed if you suspect any quality shortcomings.
v Testing or retesting should be done in accredited laboratories.
v For suggestions, complaints or feedback, write to us at info@thyrocare.com or call us on
022-3090 0000 / 6712 3400
v SMS:<Labcode No.> to 9870666333
Page : 4 of 4

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PROCESSED AT :

NAME : MOHAMMED KHAJA FAIYAZUDDIN (31Y/M) HOME COLLECTION :

DENGUE-IGM E.L.I.S.A 2.8 OD Ratio

Sample Collected on (SCT) : 25 Aug 2021 14:00

Sample Received on (SRT) : 26 Aug 2021 12:19

NAME : MOHAMMED KHAJA FAIYAZUDDIN (31Y/M) HOME COLLECTION :

Sample Collected on (SCT) : 25 Aug 2021 14:00

NAME : MOHAMMED KHAJA FAIYAZUDDIN (31Y/M) HOME COLLECTION :

Sample Collected on (SCT) : 25 Aug 2021 14:00

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