Reg. No.
K2961356 Date 01/07/2024 12:57
K ANV A Name
Age
MISS. KASHVI PATEL
16 Year(s) Sex Female
DIAGNOSTIC SERVICES PVT. LTD.
Corporate NON CORPORATE
Centre for Hi-tech Diagnostic Services and Multi-Speciality
Polyclinic Integrated with Physiotherapy & Research
Ref. By. DR.Chandrakanth J.S.
#2/10, Dr.Rajkumar Rd, 4th N Blk, Rajajinagar, Bangalore - 10
PH: 080 69094001 (30 Lines)
E-Mail : [email protected] MC-2457
WebSite : www.kanvadiagnostic.com
HAEMATOLOGY
Test Parameter Result(s) Biological Reference Interval
Complete Blood Count (Automated Cell Counter - 5 Part)
Haemoglobin (SLS) 12.5 gm/dL Female : 12.0 - 15.0 gm/dL
Pregnancy : 10.6 – 13.5 gm/dL
Total & Differential Count (Flourescent Flowcytometry)
WBC Count (Flourescent Flowcytometry) 2400 Cells/cumm 4500 - 13000 Cells/cumm
Differential Count (Flourescent flowcytometry/EI)
Neutrophils 52 % 51 - 57 %
Lymphocytes 44 % 35 - 42 %
Monocytes 4 % 4 -5 %
Complete Blood Count (Automated Cell Counter - 5 Part)
Red Blood Corpulses (Dc Detection Method 4.85 millions/cumm 4.0 - 5.2 millions/cumm
by Hydrodynamic Focusing)
PCV (Haematocrit) (Calculated) 38.6 % 35 - 45 %
MCV (Calculated) 79.6 fl 77 - 95 fl
MCH (Calculated) 25.8 pg 25 - 33 pg
MCHC (Calculated) 32.4 % 31 - 37 %
RDW (Electrical Impedance Variation 14.3 % 11.5 - 14.0 %
/Flourescent Flowcytometry)
Platelet Count (Dc Detection Method by 1.47 Lakhs/cumm 1.7 - 4.5 lakhs/cumm
Hydrodynamic Focusing)
Sample Received At
EDTA 01/07/2024 13:00
Verified By : PRABHA
------ End of Report ------
Dr Syeda Sara Farheen
MD (Pathology)
Consultant Pathologist
KMC-104293
Reported On : 01/07/2024 13:25
Page 1 of 4
Reg. No. K2961356 Date 01/07/2024 12:57
K ANV A Name
Age
MISS. KASHVI PATEL
16 Year(s) Sex Female
DIAGNOSTIC SERVICES PVT. LTD.
Corporate NON CORPORATE
Centre for Hi-tech Diagnostic Services and Multi-Speciality
Polyclinic Integrated with Physiotherapy & Research
Ref. By. DR.Chandrakanth J.S.
#2/10, Dr.Rajkumar Rd, 4th N Blk, Rajajinagar, Bangalore - 10
PH: 080 69094001 (30 Lines)
E-Mail : [email protected]
WebSite : www.kanvadiagnostic.com
SPECIAL BIOCHEMISTRY
Test Parameter Result(s) Biological Reference Interval
Dengue IgG 0.13 < 1.00 Negative
(ELFA) > 1.00 Positive
Interpretation
Anti-DENGUE Anti-DENGUE
DENGUE NS1 Ag
Dengue infection stage IgM IgG
(DEAG)
(DENM) (DENG)
Negative NEG NEG NEG
Acute infection( 5-7 days of
POS POS/NEG POS/NEG
fever)
Post-acute infection(>7 days of
NEG POS POS
fever - up to 2-3 months)
Recovery/Secondary dengue
NEG NEG POS
infection
NOTE:
1) The assay principle combines a two-step sandwich enzyme immunoassay method with a final fluorescence detection(ELFA)
2) The timing of the appearance and duration of these biomarkers depend on whether the patient is experiencing a primary or secondary
Dengue virus infection.
3) In primary infection, the antibody response to Dengue virus infection with IgM is usually detectable early after the onset of the symptoms
and persists for 2-3 months; dengue IgG appear few days after IgM and persist for years.
4) In secondary infection, dengue IgG appear earlier and IgM have kinetics close to primary infection but at a lower level.
Dengue IgM 0.08 < 1.00 Negative
(ELFA) > 1.00 Positive
Interpretation
Anti-DENGUE Anti-DENGUE
DENGUE NS1 Ag
Dengue infection stage IgM IgG
(DEAG)
(DENM) (DENG)
Negative NEG NEG NEG
Acute infection( 5-7 days of
POS POS/NEG POS/NEG
fever)
Post-acute infection(>7 days of
NEG POS POS
fever - up to 2-3 months)
Recovery/Secondary dengue
NEG NEG POS
infection
NOTE:
1) The assay principle combines a two-step sandwich enzyme immunoassay method with a final fluorescence detection(ELFA)
2) The timing of the appearance and duration of these biomarkers depend on whether the patient is experiencing a primary or secondary
Dengue virus infection.
3) In primary infection, the antibody response to Dengue virus infection with IgM is usually detectable early after the onset of the symptoms
and persists for 2-3 months; dengue IgG appear few days after IgM and persist for years.
In secondary infection, dengue IgG appear earlier and IgM have kinetics close to primary infection but at a lower level.
Page 2 of 4
Reg. No. K2961356 Date 01/07/2024 12:57
K ANV A Name
Age
MISS. KASHVI PATEL
16 Year(s) Sex Female
DIAGNOSTIC SERVICES PVT. LTD.
Corporate NON CORPORATE
Centre for Hi-tech Diagnostic Services and Multi-Speciality
Polyclinic Integrated with Physiotherapy & Research
Ref. By. DR.Chandrakanth J.S.
#2/10, Dr.Rajkumar Rd, 4th N Blk, Rajajinagar, Bangalore - 10
PH: 080 69094001 (30 Lines)
E-Mail : [email protected]
WebSite : www.kanvadiagnostic.com
SPECIAL BIOCHEMISTRY
Test Parameter Result(s) Biological Reference Interval
Dengue Antigen (NS 1) 82.62 < 1.00 Negative
(ELFA) > 1.00 Positive
Interpretation
Anti-DENGUE Anti-DENGUE
DENGUE NS1 Ag
Dengue infection stage IgM IgG
(DEAG)
(DENM) (DENG)
Negative NEG NEG NEG
Acute infection( 5-7 days of
POS POS/NEG POS/NEG
fever)
Post-acute infection(>7 days of
NEG POS POS
fever - up to 2-3 months)
Recovery/Secondary dengue
NEG NEG POS
infection
NOTE:
1) The assay principle combines a two-step sandwich enzyme immunoassay method with a final fluorescence detection(ELFA)
2) The timing of the appearance and duration of these biomarkers depend on whether the patient is experiencing a primary or secondary
Dengue virus infection.
3) In primary infection, the antibody response to Dengue virus infection with IgM is usually detectable early after the onset of the symptoms
and persists for 2-3 months; dengue IgG appear few days after IgM and persist for years.
4) In secondary infection, dengue IgG appear earlier and IgM have kinetics close to primary infection but at a lower level.
Sample Received At
SERUM 01/07/2024 13:00
Verified By : LATHAV
------ End of Report ------
Dr Ranjeeta Gadde
Consultant Biochemist
Reported On : 01/07/2024 15:42
SEROLOGY1
Test Parameter Result(s) Biological Reference Interval
WIDAL (Tube Agglutination)
S.TYPHI 'O' < 1 : 60 Upto 1 : 60
S.TYPHI 'H' < 1 : 60 Upto 1 : 60
Page 3 of 4
Reg. No. K2961356 Date 01/07/2024 12:57
K ANV A Name
Age
MISS. KASHVI PATEL
16 Year(s) Sex Female
DIAGNOSTIC SERVICES PVT. LTD.
Corporate NON CORPORATE
Centre for Hi-tech Diagnostic Services and Multi-Speciality
Polyclinic Integrated with Physiotherapy & Research
Ref. By. DR.Chandrakanth J.S.
#2/10, Dr.Rajkumar Rd, 4th N Blk, Rajajinagar, Bangalore - 10
PH: 080 69094001 (30 Lines)
E-Mail : [email protected]
WebSite : www.kanvadiagnostic.com
SEROLOGY1
Test Parameter Result(s) Biological Reference Interval
S.PARATYPHI 'AH' < 1 : 60 Upto 1 : 60
S.PARATYPHI 'BH' < 1 : 60 Upto 1 : 60
Widal test is a presumptive agglutination test which detects serum antibodies to the ‘O’ and ‘H’ antigens of Salmonella.typhi and ‘H’ antigens of
Salmonella. Paratyphi ‘A’and Salmonella. Paratyphi ‘B’
INTERPRETATION
1. Sera from normal individuals may agglutinate the ‘O’ and ‘H’ antigens in dilutions upto 1 : 60.
2. Agglutination titres of 1 : 120 and above are significant for results of a single test. Four fold rise in titre between paired sera is definitive of
infection.
3. High ‘O’antibody titres generally indicate acute infections and ‘H’ antibody denotes the specific organism responsible for the infection.
4. Individuals with previous infection show moderately elevated titres of ‘H’ antibodies for that particular Salmonella species.
5. Individuals vaccinated with Typhoid vaccine show moderately elevated titres of all the three ‘H’ agglutinins simultaneously.
LIMITATIONS
• Diagnostic titres is observed 7 – 10 days after onset of fever.
• False negative results may be associated with early anti-microbial treatment, severe hypoproteinaemia and test performed in first week of
infection.
• False positives are known to occur in Typhus,Malaria,Brucellosis,Miliary tuberculosis, Dengue,chronic liver disease,rheumatoid arthritis,
nephritic syndrome, auto-immune disease, vaccination and previous infection.
• Interpretation in endemic areas to be based on the baseline titre of the local healthy population.
Sample Received At
SERUM 01/07/2024 13:00
Verified By : KEYURI
------ End of Report ------
Mrs. Leena K
MICROBIOLOGIST
Reported On : 02/07/2024 08:36
DISCLAIMER
The result obtained relate only to the sample given/received & tested. A single test result is not always indicative of a disease, it
has to be correlated with clinical data for interpretation.
Sample processed on the same day as collection/received date unless specified otherwise.
Page 4 of 4
