Patient NAME : Ms Himani Joshi
DOB/Age/Gender : 17 Y/Female Report STATUS : Final Report
Patient ID / UHID : 10065168/RCL9332856 Barcode NO : HQ588432
Referred BY : Self Sample Type : Whole blood EDTA
....
Sample Collected : Oct 12, 2024, 05:59 AM Report Date : Oct 12, 2024, 03:06 PM.
Test Description Value(s) Unit(s) Reference Range
Complete Blood Count (CBC)
RBC Parameters
Hemoglobin 12.3 g/dL 12.0 - 15.0
colorimetric
RBC Count 3.7 10^6/µl 3.8 - 4.8
Electrical impedance
PCV 37.9 % 36 - 46
Calculated
MCV 101.7 fl 83 - 101
Calculated
MCH 33.1 pg 27 - 32
Calculated
MCHC 32.5 g/dL 31.5 - 34.5
Calculated
RDW (CV) * 14.1 % 11.6 - 14.0
Calculated
RDW-SD * 51 fl 35.1 - 43.9
Calculated
WBC Parameters
TLC 5.3 10^3/µl 4 - 10
Electrical impedance and microscopy
Differential Leucocyte Count
Neutrophils 73 % 40-80
Lymphocytes 20 % 20-40
Monocytes 4 % 2-10
Eosinophils 3 % 1-6
Basophils 0 % <2
Absolute Leukocyte Counts
Neutrophils. 3.87 10^3/µl 2-7
Lymphocytes. 1.06 10^3/µl 1-3
Monocytes. 0.21 10^3/µl 0.2 - 1.0
Eosinophils. 0.16 10^3/µl 0.02 - 0.5
Basophils. 0 10^3/µl 0.02 - 0.5
Platelet Parameters
Platelet Count 65 10^3/µl 150 - 410
Electrical impedance and microscopy
Mean Platelet Volume (MPV) * 13.8 fL 9.3 - 12.1
Calculated
PCT * 0.1 % 0.17 - 0.32
Calculated
PDW * 20.3 fL 8.3 - 25.0
Calculated
(*) Parameter(s) are outside the scope of tests recognized under the NABL M(EL)T Scheme.
Booking Centre :- Home Collection
Processing Lab :- Redcliffe Lifetech Pvt. Ltd., MCD. no.48/3, Ground Floor & Basement Moolraj Building, Main Market
Yusuf Sarai, New Delhi-110016
Page 1 of 5
Patient NAME : Ms Himani Joshi
DOB/Age/Gender : 17 Y/Female Report STATUS : Final Report
Patient ID / UHID : 10065168/RCL9332856 Barcode NO : HQ588432
Referred BY : Self Sample Type : Whole blood EDTA
Sample Collected : Oct 12, 2024, 05:59 AM Report Date : Oct 12, 2024, 03:06 PM.
Test Description Value(s) Unit(s) Reference Range
P-LCR * 55.8 % 18 - 50
Calculated
P-LCC * 27 10^9/L 44 - 140
Calculated
Mentzer Index * 27.49 % > 13
Calculated
Note:- Result Rechecked With Given Sample
Kindly Correlate Clinically
Interpretation:
CBC provides information about red cells, white cells and platelets. Results are useful in the diagnosis of anemia, infections, leukemias, clotting
disorders and many other medical conditions.
(*) Parameter(s) are outside the scope of tests recognized under the NABL M(EL)T Scheme.
Booking Centre :- Home Collection
Processing Lab :- Redcliffe Lifetech Pvt. Ltd., MCD. no.48/3, Ground Floor & Basement Moolraj Building, Main Market
Yusuf Sarai, New Delhi-110016
Page 2 of 5
Patient NAME : Ms Himani Joshi
DOB/Age/Gender : 17 Y/Female Report STATUS : Final Report
Patient ID / UHID : 10065168/RCL9332856 Barcode NO : HQ588432
....
Referred BY : Self Sample Type : Whole blood EDTA
Sample Collected : Oct 12, 2024, 05:59 AM. Report Date : Oct 12, 2024, 10:22 PM.
Peripheral Smear General Blood Picture
Normocytic normochromic cells to Macrocytic Normochromic cells with mild anisopoikilocytosis and
RBCs
polychromatophills.
WBCs Normal in number and distribution.
Platelets Reduced in number on smear.
Hemoparasite No Hemoparasite seen.
Impression Macrocytic Normochromic blood picture with Thrombocytopenia.
Advise : Kindly correlate clinically.
A peripheral blood smear (also known as a general blood picture or blood film) is a laboratory test that involves examining a drop of blood under a
microscope to evaluate the cells present. This test provides detailed information about the size, shape, and appearance of blood cells, which can
help diagnose a variety of blood disorders and conditions.
Clinical Use:
1. Diagnosing Anaemias: Helps determine the type and cause of anaemia.
2. Identifying Infections: Detects the presence of abnormal or immature white blood cells.
3. Blood Disorders: Diagnoses conditions like leukaemia, lymphoma, and other blood cancers.
4. Monitoring Treatment: Evaluates the effectiveness of treatment for blood disorders and infections.
Interpretation:
1. Normal Blood Smear: Shows normal size, shape, and colour of red blood cells, normal types and appearance of white blood cells, and normal
number and appearance of platelets.
2. Abnormal Blood Smear: Can indicate a variety of conditions, depending on the specific abnormalities observed.
A peripheral blood smear is a valuable diagnostic tool that provides detailed information about the health and characteristics of blood cells,
assisting in the diagnosis and management of a wide range of medical conditions.
(*) Parameter(s) are outside the scope of tests recognized under the NABL M(EL)T Scheme.
Booking Centre :- Home Collection
Processing Lab :- Redcliffe Lifetech Pvt. Ltd., MCD. no.48/3, Ground Floor & Basement Moolraj Building, Main Market
Yusuf Sarai, New Delhi-110016
Page 3 of 5
Patient NAME : Ms Himani Joshi
DOB/Age/Gender : 17 Y/Female Report STATUS : Final Report
Patient ID / UHID : 10065168/RCL9332856 Barcode NO : SI679686
Referred BY : Self Sample Type : Serum
....
Sample Collected : Oct 12, 2024, 05:59 AM Report Date : Oct 12, 2024, 12:45 PM.
Test Description Value(s) Unit(s) Reference Range
WIDAL By Slide Agglutination
Salmonella typhi O (TO) 1:160 Titre < 1:80
Salmonella typhi H (TH) 1:80 Titre < 1:160
Salmonella paratyphi A(H) 1:40 Titre < 1:80
Salmonella Paratyphi B(H) 1:40 Titre < 1:80
Interpretation:
METHOD-(Slide Agglutination)
[Link] >1:80 of “O” antigen & >1:160 of “H” antigen for Salmonella typhi and titres >1:80 of “H” antigen for Salmonella paratyphi A & B are
reactive.
2. Rising titres in paired samples taken 7-10 days apart are more significant than a single test.
3. Reactive results indicates ongoing or recent infection by Salmonella spp. and the diagnosis should be confirmed by gold standard test such
as Blood culture.
4. The reactivity will vary with stage of the disease with appearance in 1st week to increase in titres till end of 4th week post which it starts
decreasing.
5. In TAB vaccinated patients, high titres of H antibody of ≥1:160 to each of Salmonellae is observed. They tend to persist for many months and
even years while O antibody shows lower titres and disappears within 6 months.
6. Antibiotic treatment during 1st week before the appearance of antibodies tend to supress the immune response in the form of no or
decreasing antibody levels.
7. False positive results/anamnestic response may be seen in patients with past enteric infection and during unrelated fevers like Malaria,
Influenzae etc. in the form of transient rise in H antibody in Widal test.
8. False negative results may be due to processing of sample collected early in the course of disease (1st week) and immunosuppression.
9. Test conducted on serum.
Uses
To diagnose infection due to Salmonella spp. (Enteric fever).
To monitor the progression of disease.
To assess the response to therapy (decreasing titres) in patients being treated for Enteric fever
(*) Parameter(s) are outside the scope of tests recognized under the NABL M(EL)T Scheme.
Booking Centre :- Home Collection
Processing Lab :- Redcliffe Lifetech Pvt. Ltd., MCD. no.48/3, Ground Floor & Basement Moolraj Building, Main Market
Yusuf Sarai, New Delhi-110016
Page 4 of 5
Patient NAME : Ms Himani Joshi
DOB/Age/Gender : 17 Y/Female Report STATUS : Final Report
Patient ID / UHID : 10065168/RCL9332856 Barcode NO : SI679686
Referred BY : Self Sample Type : Serum
....
Sample Collected : Oct 12, 2024, 05:59 AM Report Date : Oct 12, 2024, 06:42 PM.
Test Description Value(s) Unit(s) Reference Range
Dengue Ns1 Antigen Test, EIA
DENGUE NS1 ANTIGEN 10.97 Ag Unit NEGATIVE <0.9
(Serum,EIA)
Interpretation:
BIOLOGICAL REFERANCE INTERVAL
NEGATIVE < 0.9
BORDERLINE 0.9-1.1
POSITIVE >1.1
Note: As per regulation, specimen collecting Laboratory is responsible for reporting positive Dengue cases to Municipal corporation.
Indication: The Dengue (NS1) Antigen assay is a Enzyme linked immunoassay (EIA) for the detection of Dengue virus NS1 Antigen in human serum or
plasma(heparin).
The serological detection of the highly specific dengue virus NS1antigen in patients with a dengue virus infection is possible at the onset of clinical symptoms in
primary as well as secondary infections. Thus determination of Dengue (NS1) Antigen is an important supportive aid for diagnosis of acute dengue virus
infections.
Clinical background: Dengue virus (serotypes Den 1, Den 2, Den 3, Den 4) is a flavivirus with global distribution and is transmitted by mosquitoes ( Aedes
aegyptii, Aedes albopictus etc). It may cause Dengue fever, Dengue haemorrhagic fever or Dengue Shock syndrome.
Following the dengue infection, an incubation period of 3 to7 days, some infections maybe asymptomatic. Symptomatic patients develop fever with or without
rash, severe musculoskeletal pain, headache, retro-orbital pain, petechiae etc. In most individuals there is resolution of illness without complications. In some
individuals the Dengue fever may progress to Dengue haemorrhagic fever or Dengue Shock syndrome especially during repeat infection with a new Dengue
Virus serotype.
Dengue virus antigen usually appears in blood within 24 hours of onset of symptoms to symptoms till 9 days post onset of symptoms.
Positive: The presence of Dengue nonstructural protein 1 (NS1) antigen is consistent with acute infection with dengue virus. The NS1 antigen is typically
detectable within 1 to 2 days following infection and up to 9 days following symptom onset. NS1 antigen may also be detectable during secondary dengue virus
infection, but for a shorter duration of time (1-4 days following symptom onset).
Negative: The absence of dengue NS1 antigen is suggestive of absence of acute phase of the infection. The NS1 antigen may be negative if specimen is
collected too early such as immediately following dengue virus infection (<24-48 hours) or is collected following 9 to 10 days of symptoms. Results should always
be interpreted in conjunction with clinical presentation and exposure history.
Limitations: Uncommonly, false positive Dengue NS1 antigen results may be seen in individuals with other flaviviruses west nile virus as well as Yellow fever.
Negative NS1 antigen results may occur if the specimen was collected greater than 7 days following symptom onset. Serologic testing for the presence of IgM
and IgG antibodies to Dengue Virus is recommended in such cases.
*** End Of Report ***
(*) Parameter(s) are outside the scope of tests recognized under the NABL M(EL)T Scheme.
Booking Centre :- Home Collection
Processing Lab :- Redcliffe Lifetech Pvt. Ltd., MCD. no.48/3, Ground Floor & Basement Moolraj Building, Main Market
Yusuf Sarai, New Delhi-110016
Page 5 of 5
HEALTH REPORT
MC-5280
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