3 4 2
Laboratory Report
Name : SHANDHIYA Sr. Number :3
Age : 4 Gender : FEMALE Invoice Date : 21-10-2024 04:26 PM
Address : AJMER Invoice Number : 342
Ref. By Dr : SELF Registration No.: 342
Report On : 21-10-2024 06:47 PM
HAEMATOLOGY
Complete Blood Cell Count
Test Name Observed Values Reference Intervals Units
WBC 6.12 4--11 10*3/UL
LYM% 35.2 20--40 %
MID% /MXD% 13.1 1--15 %
GRANS% / NEUT% 51.7 50--70 %
LYM# 2.15 0.6--4.1 10*3/UL
MID# /MXD# 0.80 0.1--1.8 10*3/UL
GRANS# / NEUT# 3.17 2--7.8 10*3/UL
RBC 4.72 3.5--5.5 10*12/L
HGB 11.7 11--18 g/dL
HCT L 34.8 36--48 %
MCV L 73.8 80--99 fL
MCH L 24.8 26--32 pg
MCHC 33.6 32--36 g/dL
RDW-SD 39.6 37--54 fL
RDW-CV 14.4 11.5--14.5 %
PLT 374 100--450 10*3/UL
MPV 8.8 7.4--10.4 fL
PDW-CV 14.5 10--17 %
PDW-SD 10.5 fL
PCT H 0.330 0.1--0.28 %
P-LCR 19.1 13--43 %
P-LCC 71 30--90 10*9/L
MALARIA ANTIGEN CARD TEST
TECHNOLOGIST PATHOLOGIST
T&C : * This Reports is Not Valid For Medico Legal Purposes. * Identification and name of person is not our resposnibility.
* No part of this report should be reproduced for any purpose. * Interpret result after considering Age,sex effect of drug and other relevant factor.
Create and Print By: Narendra Khatana Page 1/3
3 4 2
Laboratory Report
Name : SHANDHIYA Sr. Number :3
Age : 4 Gender : FEMALE Invoice Date : 21-10-2024 04:26 PM
Address : AJMER Invoice Number : 342
Ref. By Dr : SELF Registration No.: 342
Report On : 21-10-2024 06:47 PM
Test Name Observed Values Reference Intervals Units
Pf Negative
Pv Negative
ADVANTAGE MALARIA CARD is an immunoassay based on the "Sandwich principle". Colloidal gold is conjugated to P.f.
specific monoclonal anti-HRP-2 antibody and monoclonal anti-pan specific pLDH (plasmodium lactate dehydrogenase)
antibody. The test uses monoclonal anti-Pf HRP-2 antibody (test line F) & monoclonal anti-P.v specific pLDH antibody
(test line V) immobilized on a nitrocellulose strip. The test sample is added to the device. On addition of assay buffer, the
red blood cells get lysed. If the sample contains P.falciparum or P.vivax or both, the colloidal gold conjugate complexes
the HRP-2 / P.vivax specific pLDH in the lysed sample. This complex migrates through the nitrocellulose strip by capillary
action. When the complex meets the line of the corresponding immobilized antibody, the complex is trapped forming a
purplish pink band which confirms a reactive test result. Absence of a coloured band in the test region indicates a negative
test result. To serve as a procedural control an additional line of anti-mouse antibody has been immobilized on the strip as
control.
TECHNOLOGIST PATHOLOGIST
T&C : * This Reports is Not Valid For Medico Legal Purposes. * Identification and name of person is not our resposnibility.
* No part of this report should be reproduced for any purpose. * Interpret result after considering Age,sex effect of drug and other relevant factor.
Create and Print By: Narendra Khatana Page 2/3
3 4 2
Laboratory Report
Name : SHANDHIYA Sr. Number :3
Age : 4 Gender : FEMALE Invoice Date : 21-10-2024 04:26 PM
Address : AJMER Invoice Number : 342
Ref. By Dr : SELF Registration No.: 342
Report On : 21-10-2024 06:47 PM
IMMUNOLOGY
DENGUE IgG, IgM
Test Name Observed Values Reference Intervals Units
IgG Negative
IgM Negative
NS1 Negative
Detected samples should be conformed by a supplemental assay enzyme-linked immunosorbent assay (elisa) test
INSTRODUCTION
Dengue virus is a flavivirus found largely in areas of the tropic and sub-tropics. There are four distinct but antigenically
related serotypes of dengue viruses, and transmission is by mosquito, principally Aedes aegypti Aedes albopictus.
The mosquito-borne dengue viruses (serotype 1-4) cause dengue fever, a severe flu-like illness.
IgM antibodies are not detectable until 5 -10 days in case of primary dengue infection and untile 4-5 days of secondary
infection after the onset of illness.
IgG appears after 14 days and persist for the life in case of primary infection and rise within 1-2 days after the onset of
symtoms in sectonday infection
Primary dengue virus infection is characterized by elevations in specific NS1 antigen levels 0 to 9 days after the onset of
symptoms; this generally persist upto 15 days.
INTENDED USE
Dengue Day 1 Test is a rapid solid phase immuno-chromatographic test for the qualitative detection of Dengus NS1
antigen and differential detection of IgM and IgG antibodies to dengue virus in human serum/ plasma.
LIMITATION OF TEST
This rapid test device will indicate the presence of Dengue antibodies only &should not used as the sole criteria for the
diagnosis of Dengue .Serological cross reactivity acrossthe flavivirus group[Dengue,1,2 3 4 ,StLouisencephelitis West
nelievirus,japanese encephalitis &yellow fevere virus]is common.
Positive result should be confirmed By Other methods[Elisa,P C R ,cell Culture].
If result is negative &clinical sysmptoms persist ,additional testing using other clinical methodsis essential .A negative
result dose not at any time preculdesthe possibility of Dengue infection .
Advise :- Close follow up &if suspicion persist repeat after 2days.,&confirm by Elisa
<<< END OF REPORT >>>
TECHNOLOGIST PATHOLOGIST
T&C : * This Reports is Not Valid For Medico Legal Purposes. * Identification and name of person is not our resposnibility.
* No part of this report should be reproduced for any purpose. * Interpret result after considering Age,sex effect of drug and other relevant factor.
Create and Print By: Narendra Khatana Page 3/3
Powered by TCPDF (www.tcpdf.org)
