Patient Name : Mrs.GOLDI Barcode : 10015743 Age/Gender : 19/Female Sample Collected On : 11/Aug/2019 03:48PM Order Id : Sample Centrifuged On : Referred By : ANAND HOSPITAL Sample Received On : 11/Aug/2019 04:28PM Customer Since : Report Generated On : 11/Aug/2019 05:27PM Sample Type : Serum Sample Temperature : Maintained Test Name Value Unit Bio. Ref Interval 0.43 mg/dl 0.2 - 1.2 0.18 mg/dl 0.0 - 0.50 0.25 mg/dl 0.0 - 0.8 BILIRUBIN SERUM - TOTAL/DIRECT/INDIRECT Serum Bilirubin, (Total) Method: Colorimetric Diazo Dye Serum Bilirubin, (Direct) Method: Colorimetric Diazo Dye Serum Bilirubin, (Indirect) Method: Calculated Comment: Bilirubin is a yellowish pigment found in bile and is a breakdown product of normal heme catabolism. Elevated levels results from increased bilirubin production (eg hemolysis and ineffective erythropoiesis); decreased bilirubin excretion (eg; obstruction and hepatitis); and abnormal bilirubin metabolism (eg; hereditary and neonatal jaundice). Conjugated (direct) bilirubin is elevated more than unconjugated (indirect) bilirubin in viral hepatitis; drug reactions, alcoholic liver disease conjugated (direct) bilirubin is also elevated more than unconjugated (indirect)bilirubin when there is some kind of blockage of the bile ducts like in Gallstones getting into the bile ducts tumors &Scarring of the bile ducts. Increased unconjugated (indirect) bilirubin may be a result of hemolytic or pernicious anemia, transfusion reaction & a common metabolic condition termed Gilbert syndrome. BLOOD GROUP ABO AND RH FACTOR BLOOD GROUP TYPE A Method: Slide Agglutination Method) Rh TYPE Negative Method: Slide Agglutination Method) Comment: Human red blood cell antigens can be divided into four groups A, B, AB and O depending on the prescence or absence of the corresponding antigens on the red blood cells. And Rh +ve or –ve depending upon presence or absence of D. All negative test results should be further tested for D”(Presence of weak / partial D's) by performing the D” test procedure using incomplete Anti-D(Rho) of IgG class. Complete Haemogram Haemoglobin (HB) 10.8 g/dl 12.0 - 16.0 10,940 cells/µL 4000 - 11000 32.8 % 40-54 Method: Modified Drabkins Method Total Leucocyte Count (TLC) Method: Electrical Resistance Impedance Hematocrit (PCV) Method: Calculated Page 1 of 5 SIN No:10015743 Patient Name : Mrs.GOLDI Barcode : 10015743 Age/Gender : 19/Female Sample Collected On : 11/Aug/2019 03:48PM Order Id : Sample Centrifuged On : Referred By : ANAND HOSPITAL Sample Received On : 11/Aug/2019 04:28PM Customer Since : Report Generated On : 11/Aug/2019 05:27PM Sample Type : Serum Sample Temperature : Maintained Test Name Red Blood Cell Count (RBC) Value Unit Bio. Ref Interval 3.97 millions/cumm 4.50 - 6.50 82.6 fl 83-101 27.2 pg 27-33 32.9 gm% 30.0-35.0 14.9 % 11.6 - 14.0 43.80 fl 39 - 46 20.81 Ratio 77 % 40 - 75 15 % 20 - 45 3.7 % 01 - 10 4.2 % 01 - 06 0 % 00 - 02 8.42 1.6 10^3/uL 1.4 - 3.5 0.40 10^3/uL 0.20 - 1.00 0.46 10^3/uL 0.04 - 0.44 Method: Automated Electrical Mean Corp Volume (MCV) Method: Calculated Mean Corp Hb (MCH) Method: Calculated Mean Corp Hb Conc (MCHC) Method: Calculated RDW - CV Method: Calculated RDW - SD Method: Calculated Mentzer Index Method: Calculated Differential Leucocyte Count Neutrophil Method: Light scatter/Peroxidase Lymphocytes Method: Light scatter/Peroxidase Monocyte Method: Light scatter/Peroxidase Eosinophils Method: Light scatter/Peroxidase Basophils Method: Light scatter/Basophil Absolute Leucocyte Count Absolute Neutrophil Count (ANC) Absolute Lymphocyte Count (ALC) Method: Calculated Absolute Monocyte Count Method: Calculated Absolute Eosinophil Count (AEC) Method: Microscopy Absolute BasophC il ount 0.03 Page 2 of 5 SIN No:10015743 Patient Name : Mrs.GOLDI Barcode : 10015743 Age/Gender : 19/Female Sample Collected On : 11/Aug/2019 03:48PM Order Id : Sample Centrifuged On : Referred By : ANAND HOSPITAL Sample Received On : 11/Aug/2019 04:28PM Customer Since : Report Generated On : 11/Aug/2019 05:27PM Sample Type : Serum Sample Temperature : Maintained Test Name Platelet Count(PLT) Value Unit Bio. Ref Interval 219 10^3/µl 150-410 46.90 % 19.7-42.9 18.8 % 11 - 18 13.1 fl 6.0 - 11.0 0.29 % 0.19 - 0.39 50 mm/1st hour 00-15 Method: Automated Electrical Resistance/ Light Micoscopy P-LCR Method: Derived/calculated PDW Method: Calculated MPV Method: Calculated PCT Method: Calculated ESR (Westergren) Method: Modified Westergren Method Comment: A complete blood count is a blood panel that gives information about the cells in a patient's blood, such as the cell count for each cell type and the concentrations of various proteins and minerals. It is done on automated cell counter. The cells that circulate in the bloodstream are generally divided into three types: white blood cells (leukocytes), red blood cells (erythrocytes), and platelets (thrombocytes). Abnormally high or low counts may indicate the presence of many forms of disease, and hence blood counts are among the most commonly performed blood tests in medicine, as they can provide an overview of a patient's general health status. VDRL QUALITATIVE- SERUM VDRL RPR Negative Negative Method: Rapid Chromatography Immunology Comment: This is a screening test for syphilis which is useful for following the progression of disease and response to therapy. Rising titers are of immense value in confirming the diagnosis. Biological false positive reactions exhibit low titers and are seen in conditions like Viral fervers, Mycoplasma infection, Chlamydia infection, Malaria, Immunizations, Pregnancy, Autoimmune disorders & past history of Treponemal infection. It is advisable to confirm the diagnosis by tests such as TPHA & FTA-ABS. Page 3 of 5 SIN No:10015743 Patient Name : Mrs.GOLDI Barcode : 10015743 Age/Gender : 19/Female Sample Collected On : 11/Aug/2019 03:48PM Order Id : Sample Centrifuged On : Referred By : ANAND HOSPITAL Sample Received On : 11/Aug/2019 04:28PM Customer Since : Report Generated On : 11/Aug/2019 05:27PM Sample Type : Serum Sample Temperature : Maintained Test Name Value Unit Bio. Ref Interval HIV I & II, Antibody HIV I AND II ANTIBODIES Non Reactive Non Reactive Method: Method: Immuno-chromatography Comment: Comment This is a visual, Rapid Immuno Chromatographic method for the differential detection of HIV-1 & HIV-2 antibodies (IgG) in Human Serum or Plasma using HIV-1 & HIV-2 Antigens immobilized on an immunofiltration membrane.This is only a screening test. All samples detected reactive by the above screening test must be confirmed by using HIV Western Blot or HIV RNA tests. A non-reactive result does not exclude the possibility of exposure to or infection with HIV or the window period. Hepatitis B Virus Surface Antigen (HBsAg) Hepatitis B Virus Surface Antigen Reactive Non- Reactive Method: Method: Immuno-chromatography Comment: COMMENT This is a visual, rapid immuno chromatographic,one step immunoassay based on antigen capture for the qualitative detection of Hepatitis B Surface Antigen (HBsAg) in Human Serum or Plasma. This is only a screening test and requires HBV DNA estimation for confirmation/ correlation. Samples containing mouse monoclonal antibodies or heterophile antibodies can give falsely reactive or non-reactive results. False Reactive results can be obtained due to the presence of other antigens or elevated levels of RF factor. Anti HCV antibody Total Anti HCV antibody (qualitative) Non Reactive Non-Reactive Method: Rapid Chromatography Immunoassay Comment: Page 4 of 5 SIN No:10015743 Patient Name : Mrs.GOLDI Barcode : 10015743 Age/Gender : 19/Female Sample Collected On : 11/Aug/2019 03:48PM Order Id : Sample Centrifuged On : Referred By : ANAND HOSPITAL Sample Received On : 11/Aug/2019 04:28PM Customer Since : Report Generated On : 11/Aug/2019 05:27PM Sample Type : Serum Sample Temperature : Maintained Test Name Value Unit Bio. Ref Interval Comment This is a visual, rapid immuno chromatographic method for the detection of antibodies to Hepatitis C Virus in human serum or plasma. This is only a screening test. All reactive samples must be confirmed by HCV RNA determination. Patients with auto-immune liver diseases, Renal disorders and Antenatal samples may show false reactive results. A Reactive result cannot distinguish between an acute and chronic infection and a Non-Reactive result does not exclude the possibility of exposure to or infection with HCV. Determination of HCV RNA by PCR is used to identify an active Hepatitis C infection and can be detected within 1-2 weeks of exposure to virus. *** End Of Report *** Page 5 of 5 SIN No:10015743
