260 - 261, Tribhuvan Complex, Ishwar Nagar, New Delhi - 110 065
260 - 261, Tribhuvan Complex, Ishwar Nagar, New Delhi - 110 065
260 - 261, Tribhuvan Complex, Ishwar Nagar, New Delhi - 110 065
Thyrocare
260 - 261, Tribhuvan Complex,
Ishwar Nagar,
New Delhi - 110 065
PATIENTID : PK21436206
MOBILE NO : 8587052757 PAN ID : HN1-22057
DOB : 09/13/1991
Reference Range :-
Note :
The assay could be affected mildly and may result in anomalous values if serum samples have heterophilic antibodies, hemolyzed ,
icteric or lipemic. The concentration of Glucose in a given specimen may vary due to differences in assay methods, calibration and
reagent specificity. For diagnostic purposes results should always be assessed in conjunction with patients medical history, clinical
findings and other findings.
Please correlate with clinical conditions.
Method:- GOD-PAP METHOD
PATIENTID : PK21436206
MOBILE NO : 8587052757 PAN ID : HN1-22057
DOB : 09/13/1991
TEST NAME TECHNOLOGY VALUE UNITS NORMAL RANGE
TOTAL CHOLESTEROL PHOTOMETRY 254 mg/dL < 200
HDL CHOLESTEROL - DIRECT PHOTOMETRY 45 mg/dL 40-60
LDL CHOLESTEROL - DIRECT PHOTOMETRY 186 mg/dL < 100
TRIGLYCERIDES PHOTOMETRY 152 mg/dL < 150
TC/ HDL CHOLESTEROL RATIO CALCULATED 5.7 Ratio 3-5
TRIG / HDL RATIO CALCULATED 3.41 Ratio < 3.12
LDL / HDL RATIO CALCULATED 4.2 Ratio 1.5-3.5
HDL / LDL RATIO CALCULATED 0.24 Ratio > 0.40
VLDL CHOLESTEROL CALCULATED 30.48 mg/dL 5 - 40
Please correlate with clinical conditions.
Method :
CHOL - CHOLESTEROL OXIDASE, ESTERASE, PEROXIDASE
HCHO - DIRECT ENZYMATIC COLORIMETRIC
LDL - DIRECT MEASURE
TRIG - ENZYMATIC, END POINT
TC/H - DERIVED FROM SERUM CHOLESTEROL AND HDL VALUES
TRI/H - DERIVED FROM TRIG AND HDL VALUES
LDL/ - DERIVED FROM SERUM HDL AND LDL VALUES
HD/LD - DERIVED FROM HDL AND LDL VALUES.
VLDL - DERIVED FROM SERUM TRIGLYCERIDE VALUES
*REFERENCE RANGES AS PER NCEP ATP III GUIDELINES:
TOTAL CHOLESTEROL (mg/dl) HDL (mg/dl) LDL (mg/dl) TRIGLYCERIDES (mg/dl)
Alert !!! 10-12 hours fasting is mandatory for lipid parameters. If not, values might fluctuate.
PATIENTID : PK21436206
MOBILE NO : 8587052757 PAN ID : HN1-22057
DOB : 09/13/1991
TEST NAME TECHNOLOGY VALUE UNITS NORMAL RANGE
BLOOD UREA NITROGEN (BUN) PHOTOMETRY 8.01 mg/dL 7.04-20.07
CREATININE - SERUM PHOTOMETRY 0.53 mg/dL 0.55-1.02
BUN / SR.CREATININE RATIO CALCULATED 15.11 Ratio 9:1-23:1
UREA (CALCULATED) CALCULATED 17.14 mg/dL Adult : 17-43
UREA / SR.CREATININE RATIO CALCULATED 32.34 Ratio < 52
URIC ACID PHOTOMETRY 4.71 mg/dL 3.2 - 6.1
Please correlate with clinical conditions.
Method :
BUN - KINETIC UV ASSAY.
SCRE - CREATININE ENZYMATIC METHOD
B/CR - DERIVED FROM SERUM BUN AND CREATININE VALUES
UREAC - DERIVED FROM BUN VALUE.
UR/CR - DERIVED FROM UREA AND SR.CREATININE VALUES.
URIC - URICASE / PEROXIDASE METHOD
PATIENTID : PK21436206
MOBILE NO : 8587052757 PAN ID : HN1-22057
DOB : 09/13/1991
TEST NAME TECHNOLOGY VALUE UNITS NORMAL RANGE
BILIRUBIN - TOTAL PHOTOMETRY 0.8 mg/dL 0.3-1.2
ASPARTATE AMINOTRANSFERASE (SGOT ) PHOTOMETRY 28.94 U/L < 31
ALANINE TRANSAMINASE (SGPT) PHOTOMETRY 34.75 U/L < 34
SGOT / SGPT RATIO CALCULATED 0.83 Ratio <2
Please correlate with clinical conditions.
Method :
BILT - VANADATE OXIDATION
SGOT - IFCC* WITHOUT PYRIDOXAL PHOSPHATE ACTIVATION
SGPT - IFCC* WITHOUT PYRIDOXAL PHOSPHATE ACTIVATION
OT/PT - DERIVED FROM SGOT AND SGPT VALUES.
PATIENTID : PK21436206
MOBILE NO : 8587052757 PAN ID : HN1-22057
DOB : 09/13/1991
TEST NAME TECHNOLOGY VALUE UNITS REFERENCE RANGE
Comments : ***
Method :
References :
1. Carol Devilia, C I Parhon. First Trimester Pregnancy ranges for Serum TSH and Thyroid Tumor reclassified as Benign. Acta Endocrinol.
2016; 12(2) : 242 - 243
2. Kulhari K, Negi R, Kalra DK et al. Establishing Trimester specific Reference ranges for thyroid hormones in Indian women with normal
pregnancy : New light through old window. Indian Journal of Contemporary medical research. 2019; 6(4)
Disclaimer :
Results should always be interpreted using the reference range provided by the laboratory that performed the test.
Different laboratories do tests using different technologies, methods and using different reagents which may cause difference
In reference ranges and hence it is recommended to interpret result with assay specific reference ranges provided in the reports.
To diagnose and monitor therapy doses, it is recommended to get tested every time at the same Laboratory.
PATIENTID : PK21436206
MOBILE NO : 8587052757 PAN ID : HN1-22057
DOB : 09/13/1991
> = 90 : Normal
60 - 89 : Mild Decrease
45 - 59 : Mild to Moderate Decrease
30 - 44 : Moderate to Severe Decrease
15 - 29 : Severe Decrease
Clinical Significance
The normal serum creatinine reference interval does not necessarily reflect a normal GFR for a patient. Because mild and moderate
kidney injury is poorly inferred from serum creatinine alone. Thus, it is recommended for clinical laboratories to routinely estimate
glomerular filtration rate (eGFR), a “gold standard” measurement for assessment of renal function, and report the value when serum
creatinine is measured for patients 18 and older, when appropriate and feasible. It cannot be measured easily in clinical practice,
instead, GFR is estimated from equations using serum creatinine, age, race and sex. This provides easy to interpret information for the
doctor and patient on the degree of renal impairment since it approximately equates to the percentage of kidney function remaining.
Application of CKD-EPI equation together with the other diagnostic tools in renal medicine will further improve the detection and
management of patients with CKD.
Reference
Levey AS, Stevens LA, Schmid CH, Zhang YL, Castro AF, 3rd, Feldman HI, et al. A new equation to estimate glomerular filtration rate.
Ann Intern Med. 2009;150(9):604-12.
PATIENTID : PK21436206
MOBILE NO : 8587052757 PAN ID : HN1-22057
DOB : 09/13/1991
TEST NAME OBSERVATION UNITS REFERENCE RANGE
Complete Urinogram
Physical Examination
VOLUME 3 mL -
COLOUR PALE YELLOW - Pale Yellow
APPEARANCE CLEAR - Clear
SPECIFIC GRAVITY 1.02 - 1.003-1.030
PH 6 - 5-8
Chemical Examination
URINARY PROTEIN ABSENT mg/dL Absent
URINARY GLUCOSE ABSENT mg/dL Absent
URINE KETONE ABSENT mg/dL Absent
URINARY BILIRUBIN ABSENT mg/dL Absent
UROBILINOGEN Normal mg/dL <=0.2
BILE SALT ABSENT - Absent
BILE PIGMENT ABSENT - Absent
URINE BLOOD ABSENT - Absent
NITRITE ABSENT - Absent
MICROALBUMIN 10 mg/L < 30
Microscopic Examination
MUCUS ABSENT - Absent
RED BLOOD CELLS 3 cells/HPF 0-5
URINARY LEUCOCYTES (PUS CELLS) 6 cells/HPF 0-5
EPITHELIAL CELLS 4 cells/HPF 0-5
CASTS ABSENT - Absent
CRYSTALS ABSENT - Absent
BACTERIA PRESENT - Absent
YEAST ABSENT - Absent
PARASITE ABSENT - Absent
PATIENTID : PK21436206
MOBILE NO : 8587052757 PAN ID : HN1-22057
DOB : 09/13/1991
~~ End of report ~~
v The reported results are for information and interpretation of the referring doctor only.
v It is presumed that the tests performed on the specimen belong to the patient; named or identified.
v Results of tests may vary from laboratory to laboratory and also in some parameters from time to time for the
same patient.
v Should the results indicate an unexpected abnormality, the same should be reconfirmed.
v Only such medical professionals who understand reporting units, reference ranges and limitations of
technologies should interpret results.
v This report is not valid for medico-legal purpose.
v Neither Thyrocare, nor its employees/representatives assume any liability, responsibility for any loss or
damage that may be incurred by any person as a result of presuming the meaning or contents of the report.
EXPLANATIONS
v Majority of the specimen processed in the laboratory are collected by Pathologists and Hospitals we call them
as "Clients".
v Name - The name is as declared by the client and recored by the personnel who collected the specimen.
v Ref.Dr - The name of the doctor who has recommended testing as declared by the client.
v Labcode - This is the accession number in our laboratory and it helps us in archiving and retrieving the data.
v Barcode - This is the specimen identity number and it states that the results are for the specimen bearing
the barcode (irrespective of the name).
v SCP - Specimen Collection Point - This is the location where the blood or specimen was collected as declared by
the client.
v SCT - Specimen Collection Time - The time when specimen was collected as declared by the client.
v SRT - Specimen Receiving Time - This time when the specimen reached our laboratory.
v RRT - Report Releasing Time - The time when our pathologist has released the values for Reporting.
v Reference Range - Means the range of values in which 95% of the normal population would fall.
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