PROCESSED AT :

Thyrocare
Chouhatta, Opp Darbhanga
house,Ashok Rajpath Rd,
Patna–800 004

NAME : LUV KRISHNA (20Y/M) SAMPLE COLLECTED AT :

REF. BY : DR MEDICAL OFFICER BHARADWAJ BHAWAN, BARI BAZAR, MUNGER. -
811201
TEST ASKED : T3-T4-USTSH,URIC ACID,DENGUE RAPID TEST
(IGG/IGM),DGNS1

PATIENTID : LK22615142
TEST NAME TECHNOLOGY VALUE
DENGUE NS1 ANTIGEN RAPID TEST IMMUNOASSAY POSITIVE

Positive : Presence of Dengue Ns1 Antigen

Negative : Absence of Dengue Ns1 Antigen

Clinical Significance :
1. This is a screening and Qualitative test and a positive report does not confirm diagnosis. All positive cases should be verified by
confirmatorymethods like ELISA.
2. A false negative test can be seen in early course of the disease
3. The tests should be interpreted in conjunction with patient’s clinical history and other findings
4. All positive tests should be reconfirmed after 7-10 days of fever onset with Dengue IgG and IgM test
5. Dengue NS1 antigen can be detected in first five days of fever.

Sensitivity : 92.9% ; Specificity : 98.7%

References :
Dengue Guidelines for Diagnosis and treatment, prevention and control. WHO . New edition 2009"

Note: This is a screening test and a positive report does not confirm diagnosis. All positive cases should be verified by
confirmatory methods.

Please correlate with clinical conditions.

Method:- RAPID IMMUNOCHROMATOGRAPHIC ASSAY

Sample Collected on (SCT) : 29 Oct 2023 18:25

Sample Received on (SRT) : 30 Oct 2023 00:06
Report Released on (RRT) : 30 Oct 2023 04:26
Sample Type : SERUM
Dr T Priyanka MD(Path)
Labcode : 2910098240/BIH06
Barcode : BK379991 Page : 1 of 8
 PROCESSED AT :
Thyrocare
Chouhatta, Opp Darbhanga
house,Ashok Rajpath Rd,
Patna–800 004

NAME : LUV KRISHNA (25Y/M) SAMPLE COLLECTED AT :

BHARADWAJ BHAWAN, BARI BAZAR, MUNGER. - 811201
REF. BY : DR MEDICAL OFFICER
TEST ASKED : T3-T4-USTSH,URIC ACID,DENGUE RAPID TEST
(IGG/IGM),DGNS1

PATIENTID : LK22615142

TEST NAME TECHNOLOGY VALUE UNITS Bio. Ref. Interval.

TOTAL TRIIODOTHYRONINE (T3) C.L.I.A 81 ng/dL 60-200

TOTAL THYROXINE (T4) C.L.I.A 7.6 µg/dL 4.5-12
TSH - ULTRASENSITIVE C.L.I.A 2.961 µIU/mL 0.55-4.78

The Biological Reference Ranges is specific to the age group. Kindly correlate clinically.
Method :
T3 - COMPETITIVE CHEMI LUMINESCENT IMMUNO ASSAY
T4 - COMPETITIVE CHEMI LUMINESCENT IMMUNO ASSAY
USTSH - Third Generation Ultrasensitive Chemi Luminescent Immuno Assay

Disclaimer :Results should always be interpreted using the reference range provided by the laboratory that
performed the test. Different laboratories do tests using different technologies, methods and using different
reagents which may cause difference. In reference ranges and hence it is recommended to interpret result with
assay specific reference ranges provided in the reports. To diagnose and monitor therapy doses, it is recommended
to get tested every time at the same Laboratory.

Sample Collected on (SCT) : 29 Oct 2023 18:25

Sample Received on (SRT) : 30 Oct 2023 00:06
Report Released on (RRT) : 30 Oct 2023 04:26
Sample Type : SERUM
Labcode : 2910098240/BIH06 Dr T Priyanka MD(Path)
Barcode : BK379991 Page : 2 of 8
PROCESSED AT :
Thyrocare
Chouhatta, Opp Darbhanga
house,Ashok Rajpath Rd,
Patna–800 004

NAME : LUV KRISHNA (25Y/M) SAMPLE COLLECTED AT :

REF. BY BHARADWAJ BHAWAN, BARI BAZAR, MUNGER. - 811201
: DR MEDICAL OFFICER
TEST ASKED : T3-T4-USTSH,URIC ACID,DENGUE RAPID TEST
(IGG/IGM),DGNS1
PATIENTID : LK22615142
TEST NAME TECHNOLOGY VALUE UNITS Bio. Ref. Interval.
URIC ACID PHOTOMETRY 9.3 mg/dL 4.2 - 7.3
Please correlate with clinical conditions.

Method :
URIC - Uricase / Peroxidase Method

Sample Collected on (SCT) : 29 Oct 2023 18:25

Sample Received on (SRT) : 30 Oct 2023 00:06
Report Released on (RRT) : 30 Oct 2023 04:26
Sample Type : SERUM
Labcode : 2910098240/BIH06 Dr T Priyanka MD(Path)

Barcode : BK379991 Page : 3 of 8

PROCESSED AT :
Thyrocare
Chouhatta, Opp Darbhanga
house,Ashok Rajpath Rd,
Patna–800 004

NAME : LUV KRISHNA (25Y/M) SAMPLE COLLECTED AT :

REF. BY : DR MEDICAL OFFICER BHARADWAJ BHAWAN, BARI BAZAR, MUNGER. -
811201
TEST ASKED : T3-T4-USTSH,URIC ACID,DENGUE RAPID TEST
(IGG/IGM),DGNS1

PATIENTID : LK22615142
TEST NAME TECHNOLOGY VALUE
DENGUE - IGG RAPID TEST IMMUNOASSAY NEGATIVE
Bio. Ref. Interval. :-

Positive : Presence of Dengue IgG antibody

Negative : Absence of Dengue IgG antibody

Clinical significance :
1. This is a screening and Qualitative test and a positive report does not confirm diagnosis. All positive cases should be verified by
confirmatory methods like ELISA.
2. Presence of IGG dengue antibodies indicates patient is recently exposed to or currently infected with Dengue virus
3. Cross reactivity seen in flavivirus group between dengue virus, yellow fever etc
4. Recommended test is Dengue NS1 antigen in first 5 days of fever and Dengue IgG and IgM after 7-10 days of fever.

Sensetivity : 97.2% ; Specificity : 96.2%

References :
Dengue Guidelines for Diagnosis and treatment, prevention and control. WHO . New edition 2009"

Please correlate with clinical conditions.

Method:- LATERAL FLOW IMMUNOASSAY

Sample Collected on (SCT) : 29 Oct 2023 18:25

Sample Received on (SRT) : 30 Oct 2023 00:06
Report Released on (RRT) : 30 Oct 2023 04:26
Sample Type : SERUM
Dr T Priyanka MD(Path)
Labcode : 2910098240/BIH06
Barcode : BK379991 Page : 4 of 8
PROCESSED AT :
Thyrocare
Chouhatta, Opp Darbhanga
house,Ashok Rajpath Rd,
Patna–800 004

NAME : LUV KRISHNA (25Y/M) SAMPLE COLLECTED AT :

REF. BY : DR MEDICAL OFFICER BHARADWAJ BHAWAN, BARI BAZAR, MUNGER. -
811201
TEST ASKED : T3-T4-USTSH,URIC ACID,DENGUE RAPID TEST
(IGG/IGM),DGNS1

PATIENTID : LK22615142
TEST NAME TECHNOLOGY VALUE
DENGUE - IGM RAPID TEST IMMUNOASSAY NEGATIVE
Bio. Ref. Interval. :-

Positive : Presence of Dengue IgM antibody

Negative : Absence of Dengue IgM antibody

Clinical significance :
1. This is a screening and Qualitative test and a positive report does not confirm diagnosis. All positive cases should be verified by
confirmatory methods like ELISA.
2. Presence of IGM dengue antibodies indicates patient is recently exposed to or currently infected with Dengue virus
3. Cross reactivity seen in flavivirus group between dengue virus, yellow fever etc
4. Recommended test is Dengue NS1 antigen in first 5 days of fever and Dengue IgG and IgM after 7-10 days of fever.

Sensetivity : 97.5% ; Specificity : 96.6%

References : Dengue Guidelines for Diagnosis and treatment, prevention and control. WHO . New edition 2009"

Please correlate with clinical conditions.

Method:- LATERAL FLOW IMMUNOASSAY

Sample Collected on (SCT) : 29 Oct 2023 18:25

Sample Received on (SRT) : 30 Oct 2023 00:06
Report Released on (RRT) : 30 Oct 2023 04:26
Sample Type : SERUM
Dr T Priyanka MD(Path)
Labcode : 2910098240/BIH06
Barcode : BK379991 Page : 5 of 8
PROCESSED AT :
Thyrocare
Chouhatta, Opp Darbhanga
house,Ashok Rajpath Rd,
Patna–800 004

NAME : LUV KRISHNA (25Y/M) SAMPLE COLLECTED AT :

REF. BY BHARADWAJ BHAWAN, BARI BAZAR, MUNGER. -
: DR MEDICAL OFFICER
811201
TEST ASKED : MALARIAL ANTIGEN

PATIENTID : LK22615142
TEST NAME TECHNOLOGY RESULT

PLASMODIUM FALCIPARUM IMMUNOASSAY NEGATIVE

Method : RAPID IMMUNOASSAY

PLASMODIUM VIVAX IMMUNOASSAY NEGATIVE

Method : RAPID IMMUNOASSAY

Please correlate with clinical conditions.

METHODOLOGY : RAPID CARD BASED ON THE PRINCIPLE OF IMMUNOCHROMATOGRAPHY

CLINICAL SIGNIFICANCE : Malaria is caused by four species of Plasmodium:- P. falciparum, P. Vivax, P. ovale & P.malariae.
The disease results from the multiplication of malaria parasites within red blood cells of the host causing symptoms that typically
include fever, headache, joint pain, vomiting, anemia, hemoglobinuria, retinal damage, convulsions, in severe cases progressing
to coma and death. Rapid Test can be used as an aid in detection of specific antigen to Plasmodium vivax (Pv) PLDH and
Plasmodium falciparum (Pf) HRP-2 in human whole blood.

SPECIFICATIONS : Sensitivity: For PfHRP-II: 98.5% & For PvLDH: 100% Specificity: For PfHRP-II: 99% & For PvLDH: 99%

KIT VALIDATION REFERENCE : Makler, M. et al (1993) Parasite lactate assay for Plasmodium falciparum drug sensitivity AmJ .
Trop. Med. Hyg. 48(6), 739-741

Please correlate with clinical conditions.

Note : This is a screening test and a positive report does not confirm diagnosis. All positive cases should be verified by
confirmatory methods

~~ End of report ~~

Sample Collected on (SCT) : 29 Oct 2023 18:25

Sample Received on (SRT) : 29 Oct 2023 23:26

Report Released on (RRT) : 30 Oct 2023 01:12
Sample Type : EDTA
Labcode : 2910040860/BIH06 Dr T Priyanka MD(Path)
Barcode : BP924924
Page : 6 of 8
 CUSTOMER DETAILS

As declared in our data base

Name: LUV KRISHNA Age: 25Y Sex: M

Barcodes/Sample_Type : BP924924 (EDTA),BK379991 (SERUM)

Labcode : 2910040860,2910098240
Ref By : DR MEDICAL OFFICER
Sample_Type/Tests : EDTA:MALARIAL ANTIGEN
SERUM:DENGUE RAPID TEST (IGG/IGM) , DGNS1 , T3-T4-USTSH ,
URIC
Sample Collected At : BHARADWAJ BHAWAN, BARI BAZAR, MUNGER. - 811201

Sample Collected on (SCT) : 29 Oct 2023 18:25

Report Released on (RRT) : 30 Oct 2023 01:12
Amount Collected : Rs.1600/-(one thousand six hundred only)

Thyrocare,D-37/1,MIDC,Turbhe,Navi Mumbai - 400703. | Phone:022 - 6712 3400 |www.thyrocare.com | info@thyrocare.com

Page : 7 of 8
 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 @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

*As per a survey on doctors' perception of laboratory diagnostics (IJARIIT,2023)

Page : 8 of 8