58 Ebabeea 44 e 8

ITDOSE INFOSYSTEMS PVT. LTD.
Lab Id. 021704100028 Reg No 163189

Patient Name MS.SAMINA YASMIN 328223 Reg Date 10/Apr/2017 10:45AM
Age/Sex 54 YRS/Female Sample Coll. Date 10/Apr/2017 08:30AM
Refered By Dr. HEALTHIAN 08 Sample Rec.Date 10/Apr/2017 10:57AM
Client Code/Name AP000006 HEALTHIANS NET
Ref. Source Report Date 10/Apr/2017 09:14PM
Barcode No 10195842
Test Name With Methodology Result Unit Biological Ref.Interval

HAEMATOLOGY
HAEMOGLOBIN 9.6 gm/dl 11.5-16.0
Whole Blood EDTA, Cyanide free
TLC (Total Leucocyte Count) 5.54 th/cumm 4.0-10.0

Whole Blood EDTA, Flowcytometry
DIFFERENTIAL LEUCOCYTE COUNT

POLYMORPHS 49.8 % 40-75
LYMPHOCYTES 34 % 20-40
EOSINOPHILS 7.1 % 1-6

MONOCYTES 8.6 % 2-10

BASOPHILS* 0.5 % 0-1

ABSOLUTE NEUTROPHIL COUNT 2,759 /cumm 1600 - 8000

ABSOLUTE LYMPHOCYTE COUNT 1,884 /cumm 1392 - 3510

ABSOLUTE EOSINOPHIL COUNT 393 /cumm 40-440

ABSOLUTE MONOCYTE COUNT 476 /cumm 100-900

ABSOLUTE BASOPHILS COUNT* 28 /cumm 0-100

RBC 4.21 millions/cmm 3.8-5.8

Whole Blood EDTA, Impedance
HCT 34.4 % 35-45

Whole Blood EDTA, Calculated
MCV 81.71 fl 76-96

MCH 22.8 pg 27-33

MCHC 27.91 g/dl 30-35

PLATELET COUNT 307 thou/L 150-450

Whole Blood EDTA, Impedance
MPV 9.4 fl 7.4-10.4

RDW- CV 16.3 % 11.5-14.5

Page 1 of 8
Lab Id. 021704100028 Reg No 163189
Barcode No 10195842
RDW- SD 51.2 fl 35-56
PCT 0.29 % 0.10-0.28

PDW 17.7 fl 9.0-17.0

ESR [WESTERGREN] 22 mm/ 1 hr 0 -20

Modified Westergren
The tests marked with an * are not accredited by NABL.
*** End Of Report ***
Page 2 of 8
Lab Id. 021704100028 Reg No 163189

Barcode No 10195842

BIOCHEMISTRY
BLOOD SUGAR FASTING 86 mg/dl 74-106
Plasma Fluoride, Hexokinase
KIDNEY PANEL- 2
BLOOD UREA 23.9 mg/dL 17-43
Serum, Urease, GLDH
SERUM CREATININE 0.57 mg/dL 0.5-1.1

Serum, Jaffes
URIC ACID 4.2 mg/dl 2.6-6.0

Serum, Uricase
SODIUM* 140 mEq/L 135 - 148

Serum, Ion Selective Electrode
POTASSIUM* 4.43 mmol /L 3.5-5.1

CHLORIDE* 98.4 mmol /L 98 - 107

CALCIUM* 8.6 mg/dl 8.6-10.3

Serum, OCPC
PHOSPHOROUS SERUM* 3.43 mg/dl 2.6-4.5

Serum, Phosphomolybdate
BUN (Blood Urea Nitrogen ) 11 mg/dl 7.9-20.1

Serum, Calculated
BUN/CREATININE RATIO 19.6 Ratio 10-20

Serum, Calculated
UREA/CREATININE RATIO* 41.93 Ratio

Serum, Calculated
LIPID PROFILE
CHOLESTEROL 187.6 mg/dl <200
Serum, CHOD-PAP Enzymatic
TRIGLYCERIDE 77.5 mg/dl <150

Serum, GPO, Colorimetric
HDL-CHOLESTEROL 51.4 mg/dl 45-65

Serum, Immuno FS Method
LDL CHOLESTEROL 120.7 mg/dl 0-155

Serum, Calculated
VLDL CHOLESTEROL 15.5 mg/dl 5 - 40

Serum, Calculated
LDL / HDL RATIO 2.35 0 - 3.55

Serum, Calculated
Page 3 of 8
Lab Id. 021704100028 Reg No 163189
Barcode No 10195842
HDL / LDL RATIO 0.43 >0.3
Serum, Calculated
CHOL / HDL RATIO 4 0 - 4.97

Serum, Calculated
NON-HDL CHOLESTEROL 136.2 mg/dl <160

Serum, Calculated
Comment:
Lipids are a group of fats and fat-like substances that are important constituents of cells and sources of energy. The lipid profile is used as part of a
cardiac risk assessment to help determine an individual's risk of heart disease. It is recommended that healthy adults with no other risk factors for
heart disease be tested with a fasting lipid profile once every four to six years. If other risk factors are present or if previous testing revealed a high
cholesterol level in the past, more frequent testing is recommended.
TOTAL CHOLESTEROL (mg/dl) HDL (mg/dl) LDL (mg/dl) TRIGLYCERIDES (mg/dl)
DESIRABLE <200 LOW <40 OPTIMAL <100 NORMAL <150
BORDERLINE HIGH 200-239 HIGH >60 NEAROPTIMAL 100-129 BORDERLINE HIGH 150-199
HIGH >240 BORDERLINE 130-159 HIGH 200-499

HIGH
HIGH 160-189 VERYHIGH >500
VERYHIGH >190
*REFERENCE RANGES AS PER NCEP ATP III GUIDELINES
Liver Panel (LFT)

TOTAL BILIRUBIN 0.35 mg/dl 0.1-1.2
Serum, DCA
CONJUGATED BILIRUBIN 0.12 mg/dl 0.0-0.3

Serum, DCA
UNCONJUGATED BILIRUBIN 0.23 mg/dl 0.2-0.7

Serum, Calculated
SGOT (AST) 33.4 U/L 0-32

Serum, Optimized UV test with IFCC
SGPT (ALT) 35.2 IU/L 0-31

Serum, Optimized UV test with IFCC
ALK.PHOSPHATASE 164 IU/L 35-104

Serum, Kinetic, IFCC
T.PROTEIN 8.39 gm/dl 6.4-8.3

Serum, Biuret
ALBUMIN 3.87 gm/dl 3.5-5.3

Serum, Bromocresol Green
GLOBULIN 4.52 gm/dl 2.5-3.8

Serum, Calculated
A/G Ratio 0.86 1.30 - 1.70

Serum, Calculated
Page 4 of 8
Lab Id. 021704100028 Reg No 163189
Barcode No 10195842
GAMMA G.T. 54 IU/L <40
Serum, Kinetic with IFCC
SGOT/SGPT Ratio 0.95 Ratio

Serum, Calculated
Comment:
A liver panel (Liver function test) or one or more of its component tests may be used to help diagnose liver disease if a person has symptoms that indicate possible liver
dysfunction. If a person has a known condition or liver disease, testing may be performed at intervals to monitor liver status and to evaluate the effectiveness of any
treatments.
Test Method: Clinical Biochemistry
Thyroid Profile-V [FT3,FT4,TSH]

FREE TRIIODOTHYRONINE [FT3]* 3.25 pg/ml 2.0-4.4
Serum, Electro Chemi Luminescent Immuno Assay
FREE THYROXINE [FT4]* 1.24 ng/dl 0.85-1.86

TSH (ULTRASENSITIVE) 2.65 uIU/ml 0.13-6.33

COMMENT:
Hypersensitive TSH test is use to screen for and help diagnose thyroid disorders; to monitor treatment of hypothyroidism and hyperthyroidism. TSH levels are
usually increased in hypothyroidism and decreased in hyperthyroidism.
Ourreferencerangeappliesthecentral95thinterval(2.5th97.5thquantile)accordingtotheCLSI/IFCCguidelinesEP28-A3c.
A circadian variation in serum TSH in healthy subjects is well documented. TSH level is reaching peak levels between 2-4 am and at a minimum between 6-
10 pm. The variation is of the order of 50%, hence time of the day has influence on the value of TSH.
TSH levels between 5.5 and 15.0 may represent subclinical or compensated hypothyroidism or show considerable physiological & seasonal variation, suggest
clinical correlation or repeat testing with fresh sample.
TSH levels may be transiently altered because of non-thyroid illness, like severe infection, renal disease, liver disease, heart disease, severe burns, trauma,
surgery etc. Few drugs also altered the TSH values.
The combination of Free T3, Free T4 and third generation TSH offer a powerful tool for the efficient and differential diagnosis and management of thyroid disorders. Free T3 and Free
T4 estimation are unaffected by changes in Thyroid Binding Globulins (TBG). A decrease in serum Free T3 and Free T4 and increase in TSH confirms the diagnosis of
Hypothyroidism. Diagnosis of Hyperthyroidism can reliable be made in patients with low TSH and elevated Free T3 and Free T4 levels.
Age Free T3 (pg/ml) Free T4 ( ng/dl) TSH(lU/ml)

1 - 6 days 1.73 - 6.30 0.86 - 2.49 0.7 - 15.0
6 days -3 months 1.95 - 6.04 0.89 - 2.20 0.72 - 11.0
4 - 12 months 2.15 - 5.83 0.92 - 1.99 0.73 - 8.35
1 - 6 years 2.41 - 5.50 0.96 - 1.77 0.70 - 5.97
7 - 11 years 2.53 - 5.22 0.97 - 1.67 0.60 - 5.84
12 - 20 years 2.56 - 5.01 0.98 - 1.63 0.51 - 6.50
Page 5 of 8
Lab Id. 021704100028 Reg No 163189
Barcode No 10195842
>20 years 2.0 - 4.4 0.85 - 1.86 0.27 - 6.33
Method : Fully Automated Bidirectionally Interfaced Electro Chemi Luminescent Immuno Assay
Kindly correlate with clinical conditions.

Page 6 of 8
Lab Id. 021704100028 Reg No 163189

Barcode No 10195842

CLINICAL PATHOLOGY
Urine R/M (Urine Analysis)
PHYSICAL & CHEMICAL EXAMINATION
COLOUR PALE YELLOW PALE YELLOW
TRANSPARENCY* CLEAR CLEAR
pH 6.0 4.7-7.5
Urine, Double indicator
SP.GRAVITY 1.015 1.005-1.035

Urine, Hydrogenous ionogen reaction
URINE SUGAR NOT DETECTED NOT DETECTED

Urine, Oxidation reaction
URINE PROTEIN NOT DETECTED NOT DETECTED

Urine, Protein ionization
URINE BILIRUBIN NOT DETECTED NOT DETECTED

Urine, Azo- coupling reaction
KETONES NOT DETECTED NOT DETECTED

Urine, Acetoacetate and nitroprusside reaction
UROBILINOGEN NORMAL NORMAL

Urine, p-aminobenzoic acid and phenazopyridine reaction
NITRATE* NOT DETECTED NOT DETECTED

Urine, Diazotized reaction
MICROSCOPIC EXAMINATION
PUS CELLS. 1-2 /HPF 3-5
Urine, Microscopy
EPITHELIAL CELLS 2-3 /HPF 3-5

Urine, Microscopy
R.B.C. NOT SEEN /HPF NOT SEEN

Urine, Microscopy
CRYSTALS* NOT SEEN NOT SEEN

Urine, Microscopy
CASTS* NOT SEEN /LPF NOT SEEN

Urine, Microscopy
BACTERIA NOT SEEN NOT SEEN

Urine, Microscopy
.
Page 7 of 8
Lab Id. 021704100028 Reg No 163189

Barcode No 10195842

BIOCHEMISTRY
Vitamin D (25-hydroxycholecalciferol)
VITAMIN D, 25 HYDROXY* 27.23 ng/mL 30-70
Reference Range :
DEFICIENCY : <20 ng/ml
INSUFFICIENCY : 20-30 ng/ml
NORMAL : 30-70 ng/ml
Comments:
This test is used to determine the levels of 25-hydroxy-vitamin D and is used to determine if bone weakness, bone malformation, or abnormal metabolism of calcium is
occurring as a result of a deficiency or excess of vitamin D. Since vitamin D is a fat-soluble vitamin and is absorbed from the intestine like a fat, vitamin D is also s used
to monitor individuals with diseases that interfere with fat absorption, such as cystic fibrosis and Crohn's disease, and in patients who have had gastric bypass surgery and
may not be able to absorb enough Vitamin D. Vitamin D is also used to determine effectiveness of treatment when vitamin D, calcium, phosphorus, and/or magnesium
supplementation is prescribed. Reasons for suboptimal 25-OH-VitD levels include lack of sunshine exposure, inadequate intake; malabsorption eg, due to Celiac disease);
depressed hepatic vitamin D 25-hydroxylase activity, secondary to advanced liver disease; and enzyme-inducing drugs, in particular many antiepileptic drugs, including
phenytoin, phenobarbital, and carbamazepine, that increase 25-OH-VitD metabolism. In contrast to the high prevalence of 25-OH-VitD deficiency, hypervitaminosis D
is rare, and is only seen after prolonged exposure to extremely high doses of vitamin D. When it occurs, it can result in severe hypercalcemia and hyperphosphatemia.
Method : Fully Automated Bidirectionally Interfaced Electro Chemi Luminescent Immuno Assay
Kindly correlate with clinical conditions.

Page 8 of 8

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ITDOSE INFOSYSTEMS PVT. LTD.

Lab Id. 021704100028 Reg No 163189

Test Name With Methodology Result Unit Biological Ref.Interval

TLC (Total Leucocyte Count) 5.54 th/cumm 4.0-10.0

DIFFERENTIAL LEUCOCYTE COUNT

EOSINOPHILS 7.1 % 1-6

MONOCYTES 8.6 % 2-10

BASOPHILS* 0.5 % 0-1

ABSOLUTE NEUTROPHIL COUNT 2,759 /cumm 1600 - 8000

ABSOLUTE LYMPHOCYTE COUNT 1,884 /cumm 1392 - 3510

ABSOLUTE EOSINOPHIL COUNT 393 /cumm 40-440

ABSOLUTE MONOCYTE COUNT 476 /cumm 100-900

ABSOLUTE BASOPHILS COUNT* 28 /cumm 0-100

RBC 4.21 millions/cmm 3.8-5.8

HCT 34.4 % 35-45

MCV 81.71 fl 76-96

MCH 22.8 pg 27-33

MCHC 27.91 g/dl 30-35

PLATELET COUNT 307 thou/L 150-450

MPV 9.4 fl 7.4-10.4

RDW- CV 16.3 % 11.5-14.5

PCT 0.29 % 0.10-0.28

PDW 17.7 fl 9.0-17.0

ESR [WESTERGREN] 22 mm/ 1 hr 0 -20

*** End Of Report ***

Lab Id. 021704100028 Reg No 163189

Test Name With Methodology Result Unit Biological Ref.Interval

SERUM CREATININE 0.57 mg/dL 0.5-1.1

URIC ACID 4.2 mg/dl 2.6-6.0

SODIUM* 140 mEq/L 135 - 148

POTASSIUM* 4.43 mmol /L 3.5-5.1

CHLORIDE* 98.4 mmol /L 98 - 107

CALCIUM* 8.6 mg/dl 8.6-10.3

PHOSPHOROUS SERUM* 3.43 mg/dl 2.6-4.5

BUN (Blood Urea Nitrogen ) 11 mg/dl 7.9-20.1

BUN/CREATININE RATIO 19.6 Ratio 10-20

UREA/CREATININE RATIO* 41.93 Ratio

TRIGLYCERIDE 77.5 mg/dl <150

HDL-CHOLESTEROL 51.4 mg/dl 45-65

LDL CHOLESTEROL 120.7 mg/dl 0-155

VLDL CHOLESTEROL 15.5 mg/dl 5 - 40

LDL / HDL RATIO 2.35 0 - 3.55

CHOL / HDL RATIO 4 0 - 4.97

NON-HDL CHOLESTEROL 136.2 mg/dl <160

TOTAL CHOLESTEROL (mg/dl) HDL (mg/dl) LDL (mg/dl) TRIGLYCERIDES (mg/dl)

DESIRABLE <200 LOW <40 OPTIMAL <100 NORMAL <150

HIGH >240 BORDERLINE 130-159 HIGH 200-499

*REFERENCE RANGES AS PER NCEP ATP III GUIDELINES

Liver Panel (LFT)

CONJUGATED BILIRUBIN 0.12 mg/dl 0.0-0.3

UNCONJUGATED BILIRUBIN 0.23 mg/dl 0.2-0.7

SGOT (AST) 33.4 U/L 0-32

SGPT (ALT) 35.2 IU/L 0-31

ALK.PHOSPHATASE 164 IU/L 35-104

T.PROTEIN 8.39 gm/dl 6.4-8.3

ALBUMIN 3.87 gm/dl 3.5-5.3

GLOBULIN 4.52 gm/dl 2.5-3.8

A/G Ratio 0.86 1.30 - 1.70

SGOT/SGPT Ratio 0.95 Ratio

Test Method: Clinical Biochemistry

Thyroid Profile-V [FT3,FT4,TSH]

FREE THYROXINE [FT4]* 1.24 ng/dl 0.85-1.86

TSH (ULTRASENSITIVE) 2.65 uIU/ml 0.13-6.33

* End Of Report *

* End Of Report *

* End Of Report *

* End Of Report *