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MR Gorank: Colorimetric

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0% found this document useful (0 votes)
24 views8 pages

MR Gorank: Colorimetric

Uploaded by

Kein Hew
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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Patient NAME : Mr Gorank

DOB/Age/Gender : 23 Y/Male Report STATUS : Final Report


Patient ID / UHID : 9996587/OF9996587 Barcode NO : HQ548402
Referred BY : Dr. M S Rathore Sample Type : Whole blood EDTA
....

Sample Collected : Oct 05, 2024, 07:03 PM Report Date : Oct 05, 2024, 08:10 PM.
Test Description Value(s) Unit(s) Reference Range

Complete Blood Count (CBC)

RBC Parameters
Hemoglobin 15.8 g/dL 13.0 - 17.0
colorimetric
RBC Count 5.5 10^6/µl 4.5 - 5.5
Electrical impedance
PCV 47.3 % 40 - 50
Calculated
MCV 85.8 fl 83 - 101
Calculated
MCH 28.7 pg 27 - 32
Calculated
MCHC 33.5 g/dL 31.5 - 34.5
Calculated
RDW (CV) * 12 % 11.6 - 14.0
Calculated
RDW-SD * 39.9 fl 35.1 - 43.9
Calculated
WBC Parameters
TLC 5.8 10^3/µl 4 - 10
Electrical impedance and microscopy
Differential Leucocyte Count
Neutrophils 75 % 40-80
Lymphocytes 20 % 20-40
Monocytes 4 % 2-10
Eosinophils 1 % 1-6
Basophils 0 % <2
Absolute Leukocyte Counts
Calculated
Neutrophils. 4.35 10^3/µl 2-7
Lymphocytes. 1.16 10^3/µl 1-3
Monocytes. 0.23 10^3/µl 0.2 - 1.0
Eosinophils. 0.06 10^3/µl 0.02 - 0.5
Basophils. 0 10^3/µl 0.02 - 0.5
Platelet Parameters
Platelet Count 202 10^3/µl 150 - 410
Electrical impedance and microscopy
Mean Platelet Volume (MPV) * 11.1 fL 9.3 - 12.1
Calculated
PCT * 0.2 % 0.17 - 0.32
Calculated
PDW * 19.2 fL 8.3 - 25.0

(*) Parameter(s) are outside the scope of tests recognized under the NABL M(EL)T Scheme.

Booking Centre :- ACHARYA TULSI DIAGNOSTIC, Udaipur


Processing Lab :- Redcliffe Lifetech Pvt. Ltd., 2nd Floor 47, Panchwati, Saheli Marg, Udaipur-313001

Page 1 of 7
Patient NAME : Mr Gorank
DOB/Age/Gender : 23 Y/Male Report STATUS : Final Report
Patient ID / UHID : 9996587/OF9996587 Barcode NO : HQ548402
Referred BY : Dr. M S Rathore Sample Type : Whole blood EDTA
Sample Collected : Oct 05, 2024, 07:03 PM Report Date : Oct 05, 2024, 08:10 PM.
Test Description Value(s) Unit(s) Reference Range
Calculated
P-LCR * 43.4 % 18 - 50
Calculated
P-LCC * 87 10^9/L 44 - 140
Calculated
Mentzer Index * 15.6 % > 13
Calculated

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 :- ACHARYA TULSI DIAGNOSTIC, Udaipur


Processing Lab :- Redcliffe Lifetech Pvt. Ltd., 2nd Floor 47, Panchwati, Saheli Marg, Udaipur-313001

Page 2 of 7
Patient NAME : Mr Gorank
DOB/Age/Gender : 23 Y/Male Report STATUS : Final Report
Patient ID / UHID : 9996587/OF9996587 Barcode NO : HQ548402
Referred BY : Dr. M S Rathore Sample Type : Whole blood EDTA
....

Sample Collected : Oct 05, 2024, 07:03 PM Report Date : Oct 05, 2024, 08:28 PM.
Test Description Value(s) Unit(s) Reference Range

Malarial Parasite (MP) Smear

MP(PBF FOR MP) Not seen - Not seen


Microscopy

Interpretation:
1. Malaria is a serious parasitic diseases characterized by fever, chills, and anemia and is caused by a parasite that is transmitted human to
human by the bite of infected female Anopheles mosquitoes.
2. Malarial Parasite test is performed on the blood sample to find out the level of Malaria Parasite in the blood.
3. It is conducted to conclude on Malaria and also during the treatment and after the treatment of Malaria.
4. Most people will have symptoms within 14 days of being bitten by an infected mosquito. But symptoms can show up as soon as seven days
afterward or can take as long as a year to appear.
5. Clinical decision should not be based on the results of this test, but should be made by the physician after all clinical and laboratory findings
have been evaluated.

(*) Parameter(s) are outside the scope of tests recognized under the NABL M(EL)T Scheme.

Booking Centre :- ACHARYA TULSI DIAGNOSTIC, Udaipur


Processing Lab :- Redcliffe Lifetech Pvt. Ltd., 2nd Floor 47, Panchwati, Saheli Marg, Udaipur-313001

Page 3 of 7
Patient NAME : Mr Gorank
DOB/Age/Gender : 23 Y/Male Report STATUS : Final Report
Patient ID / UHID : 9996587/OF9996587 Barcode NO : SI670242
Referred BY : Dr. M S Rathore Sample Type : Serum
....

Sample Collected : Oct 05, 2024, 07:03 PM Report Date : Oct 05, 2024, 08:23 PM.
Test Description Value(s) Unit(s) Reference Range

Chikungunya IgM, Rapid Card

Chikungunya IgM, Rapid Card Negative Negative


Immunochromatographic Assay

Interpretation:
The Onsite Chikungunya IgM Rapid test is limited to the qualitative detection of IgM in human sera . A negative result indicates absence of
detectable IgM antibodies. However a negative result does not preclude the possibility of exposure or infection with CHIK. It is a screening test .
Any reactive or non reactive report is recommended to be confirmed with additional test like PCR.

Dengue NS1, Rapid Card

DENGUE NS1 ANTIGEN (Rapid)* Negative - Negative


Rapid

Interpretation:
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.

Interpretation: 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.

(*) Parameter(s) are outside the scope of tests recognized under the NABL M(EL)T Scheme.

Booking Centre :- ACHARYA TULSI DIAGNOSTIC, Udaipur


Processing Lab :- Redcliffe Lifetech Pvt. Ltd., 2nd Floor 47, Panchwati, Saheli Marg, Udaipur-313001

Page 4 of 7
Patient NAME : Mr Gorank
DOB/Age/Gender : 23 Y/Male Report STATUS : Final Report
Patient ID / UHID : 9996587/OF9996587 Barcode NO : SI670242
Referred BY : Dr. M S Rathore Sample Type : Serum
Sample Collected : Oct 05, 2024, 07:03 PM Report Date : Oct 05, 2024, 08:23 PM.
Test Description Value(s) Unit(s) Reference Range

(*) Parameter(s) are outside the scope of tests recognized under the NABL M(EL)T Scheme.

Booking Centre :- ACHARYA TULSI DIAGNOSTIC, Udaipur


Processing Lab :- Redcliffe Lifetech Pvt. Ltd., 2nd Floor 47, Panchwati, Saheli Marg, Udaipur-313001

Page 5 of 7
Patient NAME : Mr Gorank
DOB/Age/Gender : 23 Y/Male Report STATUS : Final Report
Patient ID / UHID : 9996587/OF9996587 Barcode NO : YB258165
Referred BY : Dr. M S Rathore Sample Type : Spot Urine
....

Sample Collected : Oct 05, 2024, 07:03 PM Report Date : Oct 05, 2024, 09:00 PM.
Test Description Value(s) Unit(s) Reference Range

Urine Routine and Microscopic Examination

Physical Examination
Volume * 15 ml -
visual
Colour * Pale Yellow - Pale yellow
visual
Transparency * Clear - Clear
visual
Deposit * Absent - Absent
visual
Chemical Examination
Reaction (pH) 6 - 4.5 - 8.0
Double Indicator
Specific Gravity 1.015 - 1.010 - 1.030
Ion Exchange
Urine Glucose (sugar) Negative - Negative
Oxidase / Peroxidase
Urine Protein (Albumin) Negative - Negative
Acid / Base Colour Excahnge
Urine Ketones (Acetone) Negative - Negative
Legals Test
Blood Negative - Negative
Peroxidase Hemoglobin
Leucocyte esterase Negative - Negative
Enzymatic Reaction
Bilirubin Urine Negative - Negative
Coupling Reaction
Nitrite Negative - Negative
Griless Test
Urobilinogen Normal - Normal
Ehrlichs Test
Microscopic Examination
Pus Cells (WBCs) * 1-2 /hpf 0-5
Epithelial Cells * 0-2 /hpf 0-4
Red blood Cells * Absent /hpf Absent
Crystals * Absent - Absent
Cast * Absent - Absent
Yeast Cells * Absent - Absent
Amorphous deposits * Absent - Absent
Bacteria * Absent - Absent
Protozoa * Absent - Absent
Interpretation:

(*) Parameter(s) are outside the scope of tests recognized under the NABL M(EL)T Scheme.

Booking Centre :- ACHARYA TULSI DIAGNOSTIC, Udaipur


Processing Lab :- Redcliffe Lifetech Pvt. Ltd., 2nd Floor 47, Panchwati, Saheli Marg, Udaipur-313001

Page 6 of 7
Patient NAME : Mr Gorank
DOB/Age/Gender : 23 Y/Male Report STATUS : Final Report
Patient ID / UHID : 9996587/OF9996587 Barcode NO : YB258165
Referred BY : Dr. M S Rathore Sample Type : Spot Urine
Sample Collected : Oct 05, 2024, 07:03 PM Report Date : Oct 05, 2024, 09:00 PM.
Test Description Value(s) Unit(s) Reference Range
URINALYSIS- Routine urine analysis assists in screening and diagnosis of various metabolic, urological, kidney and liver disorders.

Protein: Elevated proteins can be an early sign of kidney disease. Urinary protein excretion can also be temporarily elevated by strenuous
exercise, orthostatic proteinuria, dehydration, urinary tract infections and acute illness with fever

Glucose: Uncontrolled diabetes mellitus can lead to presence of glucose in urine. Other causes include pregnancy, hormonal disturbances,
liver disease and certain medications.

Ketones: Uncontrolled diabetes mellitus can lead to presence of ketones in urine. Ketones can also be seen in starvation, frequent vomiting,
pregnancy and strenuous exercise.

Blood: Occult blood can occur in urine as intact erythrocytes or haemoglobin, which can occur in various urological, nephrological and bleeding
disorders.

Leukocytes: An increase in leukocytes is an indication of inflammation in urinary tract or kidneys. Most common cause is bacterial urinary tract
infection.

Nitrite: Many bacteria give positive results when their number is high. Nitrite concentration during infection increases with length of time the
urine specimen is retained in bladder prior to collection.

pH: The kidneys play an important role in maintaining acid base balance of the body. Conditions of the body producing acidosis/ alkalosis or
ingestion of certain type of food can affect the pH of urine.

Specific gravity: Specific gravity gives an indication of how concentrated the urine is. Increased specific gravity is seen in conditions like
dehydration, glycosuria and proteinuria while decreased specific gravity is seen in excessive fluid intake, renal failure and diabetes insipidus.

Bilirubin: In certain liver diseases such as biliary obstruction or hepatitis, bilirubin gets excreted in urine.

Urobilinogen: Positive results are seen in liver diseases like hepatitis and cirrhosis and in cases of haemolytic anaemia.

*** End Of Report ***

(*) Parameter(s) are outside the scope of tests recognized under the NABL M(EL)T Scheme.

Booking Centre :- ACHARYA TULSI DIAGNOSTIC, Udaipur


Processing Lab :- Redcliffe Lifetech Pvt. Ltd., 2nd Floor 47, Panchwati, Saheli Marg, Udaipur-313001

Page 7 of 7
Terms and Conditions of Reporting

1. The presented findings in the Reports are intended solely for informational and interpretational purposes by the
referring physician or other qualified medical professionals possessing a comprehensive understanding of
reporting units, reference ranges, and technological limitations. The laboratory shall not be held liable for any
interpretation or misinterpretation of the results, nor for any consequential or incidental damages arising from
such interpretation.

2. It is to be presumed that the tests performed pertain to the specimen/sample attributed to the Customer's name
or identification. It is presumed that the verification particulars have been cleared out by the customer or his/her
representation at the point of generation of said specimen / sample. It is hereby clarified that the reports
furnished are restricted solely to the given specimen only.

3. It is to be noted that variations in results may occur between different laboratories and over time, even for the
same parameter for the same Customer. The assays are performed and conducted in accordance with standard
procedures, and the reported outcomes are contingent on the specific individual assay methods and equipment(s)
used, as well as the quality of the received specimen.

4. This report shall not be deemed valid or admissible for any medico-legal purposes.

5. The Customers assume full responsibility for apprising the Company of any factors that may impact the test
finding. These factors, among others, includes dietary intake, alcohol, or medication / drug(s) consumption, or
fasting. This list of factors is only representative and not exhaustive.

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