Patient Name : Saroj Gupta Lab No : GGN24043584
Age / Sex : 65 Y / F Registration On : 23-Apr-24 11:58
Referred By : SELF Patient ID : UHOM.0000105168
Centre : GURUGRAM
Glucose Random Sodium Fluoride Sample
Accession No: CL01867968 Collected On: 23-Apr-24 11:58 Received On: 23-Apr-24 15:51 Approved On: 23-Apr-24 17:36
Observation Result Unit Biological Ref. Interval Method
Blood Sugar Random 111 mg/dL 70 - 140 GOD/POD, colorimetric
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Sample Type: Sodium Fluoride
Technology: Dry Chemistry (VITROS MicroSlide, MicroSensor & Intellicheck Technology)
Analyzer: Fully Automated Integrated Biochemistry & ImmunoAssay Analyzer: VITROS 5600
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Remarks: Please correlate clinically.
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Liver Function Test Serum Sample
Accession No: CL01867969 Collected On: 23-Apr-24 11:58 Received On: 23-Apr-24 14:58 Approved On: 23-Apr-24 17:15
Observation Result Unit Biological Ref. Interval Method
Total Protein 7.0 g/dL 6.5-7.8 Biuret, No Serum Blank
Albumin 4.1 g/dL 4.2 - 5.0 Bromocresol Green
Globulin 2.9 gm/dL 2.0-3.5 Calculated
A/G Ratio 1.41 Ratio 1.5-2.5 Calculated
Total Bilirubin 0.43 mg/dL 0.2-1.3 Azobilirubin/dyphylline
Conjugated Bilirubin 0.23 mg/dL <0.3 Calculated
Unconjugated Bilirubin 0.20 mg/dL <1.1 Spectrophotometry
SGOT (AST) 28 U/L 18-39 Enzymatic Colorimetric
SGPT (ALT) 34 U/L 4-35 UV with P5P
SGOT/SGPT Ratio 0.82 Ratio Calculated
Alkaline Phosphatase 87 U/L 46 - 122 PNPP, AMP buffer
Gamma Glutamyl Transferase 36 U/L 10 - 54 G-glutamyl-p-nitroanilide
Scan to Validate
Page 1 of 4
SCO-304, Sector 29, Gurugram, Haryana- 122002
Patient Name : Saroj Gupta Lab No : GGN24043584
Age / Sex : 65 Y / F Registration On : 23-Apr-24 11:58
Referred By : SELF Patient ID : UHOM.0000105168
Centre : GURUGRAM
-----------------------------------------------------------------------------------------------------------------
Technology: Dry Chemistry (VITROS MicroSlide, MicroSensor and Intellicheck Technology)
Analyzer: Fully Automated Biochemistry and ImmunoAssay Analyzer: VITROS 5600
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Clinical Significance of LFT: The clinical suspicion of liver disease usually leads to the measurement of the liver function tests (LFT) which include measurement of several
enzymes, serum bilirubin and albumin. These parameters may point to an underlying pathological process and direct further investigation. The aim of investigation in patients with
suspected liver disease are:
· To detect hepatic abnormality · Measurement of severity of liver damage · Identify the specific cause
· Investigate possible complications
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Remarks: Please correlate clinically.
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In case of any unexpected or alarming results, please contact us immediately for re-confirmation, clarifications, and rectifications, if needed.
Scan to Validate
Page 2 of 4
SCO-304, Sector 29, Gurugram, Haryana- 122002
Patient Name : Saroj Gupta Lab No : GGN24043584
Age / Sex : 65 Y / F Registration On : 23-Apr-24 11:58
Referred By : SELF Patient ID : UHOM.0000105168
Centre : GURUGRAM
CBC EDTA Whole Blood Sample
Accession No: ED00925385 Collected On: 23-Apr-24 11:58 Received On: 23-Apr-24 14:45 Approved On: 23-Apr-24 15:57
Observation Result Unit Biological Ref. Interval Method
Hemoglobin 11.9 gm/dL 12.0 - 15.0 Photometric Measurement
Total RBC 4.19 million/µL 3.8 - 4.8 Coulter Principle
Platelet Count 240 X 10³ / µL 150 - 410 x 10³/µL Impedance
Total Leucocyte Count (WBC) 13.1 X 10³ / µL 4.0 - 10.0 Coulter Principle
Differential Leucocyte Count (DLC)
Neutrophils 68.5 % 40 - 80 Flow Cytometry
Lymphocytes 24.5 % 20 - 40 Flow Cytometry
Monocytes 5.4 % 2 - 10 Flow Cytometry
Eosinophils 1.4 % 1-6 Flow Cytometry
Basophils 0.2 % 0-1 Flow Cytometry
Absolute Neutrophil Count 8.97 X 10³ / µL 2.0 - 7.5 Flow Cytometry
Absolute Lymphocyte Count 3.21 X 10³ / µL 1.0 - 4.0 Flow Cytometry
Absolute Monocyte Count 0.71 X 10³ / µL 0.2 - 1.0 Flow Cytometry
Absolute Eosinophil Count 0.18 X 10³ / µL 0.04 - 0.44 Flow Cytometry
Absolute Basophil Count 0.04 X 10³ / µL 0.00 - 0.30 Flow Cytometry
Indices
Hematocrit 35.6 % 36 - 46 Calculated
Mean Corpuscular Volume (MCV) 85.0 fL 83 - 101 Calculated
Mean Corp. Hemoglobin (MCH) 28.4 pg 27 - 32 Calculated
MCH Concentration (MCHC) 33.4 g/dl 31.5 - 34.5 Calculated
Red Cell Dist. Width (RDW-CV) 14.2 % 11.5 - 14.5 Calculated
Red Cell Dist. Width (RDW-SD) 42.4 fL 39 - 46 Calculated
Mean Platelet Volume (MPV) 10.1 fL 7-5 - 12.0 Calculated
Neutrophil-Lymphocyte Ratio (NLR) 2.8 Ratio Calculated
Mentzer Index 20.29 Index Calculated
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Remarks: Please correlate with clinical conditions.
-----------------------------------------------------------------------------------------------------------------
In case of any unexpected or alarming results, please contact us immediately for re-confirmation, clarifications, and rectifications, if needed.
Scan to Validate
Page 3 of 4
SCO-304, Sector 29, Gurugram, Haryana- 122002
Patient Name : Saroj Gupta Lab No : GGN24043584
Age / Sex : 65 Y / F Registration On : 23-Apr-24 11:58
Referred By : SELF Patient ID : UHOM.0000105168
Centre : GURUGRAM
Anti CCP Serum Sample
Accession No: SE00246852 Collected On: 23-Apr-24 11:58 Received On: 23-Apr-24 14:58 Approved On: 23-Apr-24 17:17
Observation Result Unit Biological Ref. Interval Method
Anti CCP < 0.40 U/mL <5.0 CLIA
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Biological Reference Range:
Negative < 5.00 U/mL
Positive >/= 5.00 U/mL
Reference values apply to all ages.
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Clinical Significance of Anti CCP:
Anti-cyclic citrullinated peptide (Anti-CCP) levels are useful in evaluating patients suspected of having rheumatoid arthritis (RA) and differentiating RA from other connective tissue
diseases that may present with arthritis. Rheumatoid arthritis (RA) is a systemic autoimmune disease characterized by chronic joint inflammation that ultimately leads to joint
destruction. RA affects approximately 1% of the world's population. The diagnosis of RA is established primarily on clinical criteria and serologic findings.
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Clinical Notes for Anti CCP:
- A positive result for CCP antibodies indicates a high likelihood of rheumatoid arthritis. CCP antibodies have also been reported in approximately 40% of seronegative RA patients,
and, like rheumatoid factor (RF), a positive CCP antibody result indicates an increased likelihood of erosive disease in patients with RA. High levels of CCP antibodies may be useful
to identify patients with aggressive disease, but further studies are needed to document this association.
- Positive results for CCP antibodies may occur in some patients with systemic lupus erythematosus (SLE) or other autoimmune, connective tissue diseases. Anti-rheumatic therapy
should not be initiated based solely on a positive test for CCP antibodies, and changes in treatment should not be based upon the levels of CCP antibodies.
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Please correlate results with clinical conditions
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In case of any unexpected or alarming results, please contact us immediately for re-confirmation, clarifications, and rectifications, if needed.
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Page 4 of 4
SCO-304, Sector 29, Gurugram, Haryana- 122002
Experience Care
Conditions Of Reporting
The report results are for information and interpretation for your referring doctor. Reports are to be
correlated with the patient’s clinical history.
Biological Reference Range/Interval is suggested for your Gender and Age on the basis of available
literature. All reference ranges are to be reconsidered by physician’s advice for your specific care.
This Medical Report is a professional opinion, not a diagnosis.
The report will carry the name and age provided at the time of registration. To maintain confidentiality,
certain reports may not be e-mailed at the discretion of the management.
All the notes and interpretation beneath the pathology result in the report provided are for educational
purpose only. It is not intended to be a substitute for physician's consultation.
Results of tests may vary from laboratory to laboratory and in some parameters from time to time for the
same patients. Test results and reference range may also vary depending on the technology and
methodology used. Laboratory test results may also vary depending on the age, sex, time of the day
sample has been taken, diet, medication and limitation of modern technology.
In case of any unexpected or alarming test results, please contact us immediately for re-confirmation,
further discussion, clarifications and rectifications, if needed.
In case of any discrepancy due to typing error, kindly get it rectified immediately.
Neither HOD or its employees/representatives assume any liability or responsibility for any loss or
damage that may be incurred by any person as a result of interpreting the meaning of this report.
Test results are not valid for medico legal purposes.
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and the results of the tests. Our liability is limited to the amount of investigations booked with us.
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