Test Name Units Value Technology Fasting Blood Sugar Photometry MG/DL 176.9 Reference Range

NAME : RAJKUMAR MASAWAN (66Y/M) SAMPLE GIVEN BY :
REF. BY : DR DESHPANDE (8551177646),SAI LABORATORY,SR NO. 5/4,

PAWAR VASTI, NEAR PRATIMA MANGAL KARYALAYA,
TEST ASKED : BLOOD SUGAR (F) MUNDHWA, KESHAV NAGAR, PUNE,411036
TEST NAME TECHNOLOGY VALUE UNITS

FASTING BLOOD SUGAR PHOTOMETRY 176.9 mg/dL
Reference Range :-
70-99
Please correlate with clinical conditions.
Method:- GOD-PAP METHOD
0807072346/A1835 / Q7208588 / PUNL

Sample Collected on : 08 Jul 2021 08:00
Report Released on : 08 Jul 2021 19:59
Dr. Sachin Patil MD(Path)
Page : 1 of 15
REF. BY (8551177646),SAI LABORATORY,SR NO. 5/4,
: DR DESHPANDE
PAWAR VASTI, NEAR PRATIMA MANGAL
TEST ASKED : HbA1c,HEMOGRAM KARYALAYA, MUNDHWA, KESHAV NAGAR,
PUNE,411036

HbA1c - (HPLC)
H.P.L.C 9.6 %
Reference Range :
Reference Range: As per ADA Guidelines Guidance For Known Diabetics
Below 5.7% : Normal Below 6.5% : Good Control

5.7% - 6.4% : Prediabetic 6.5% - 7% : Fair Control
>=6.5% : Diabetic 7.0% - 8% : Unsatisfactory Control
>8% : Poor Control
Method : Fully Automated H.P.L.C. using Biorad Variant II Turbo
AVERAGE BLOOD GLUCOSE (ABG) CALCULATED 229 mg/dl
Reference Range :
90 - 120 mg/dl : Good Control
121 - 150 mg/dl : Fair Control
151 - 180 mg/dl : Unsatisfactory Control
> 180 mg/dl : Poor Control
Method : Derived from HBA1c values
0807072934/A1835 / U8589071 / PUNL

Dr Sachin Patil MD(Path)
Page : 2 of 15
TEST ASKED : HbA1c,HEMOGRAM
KARYALAYA, MUNDHWA, KESHAV NAGAR,
PUNE,411036
TEST NAME VALUE UNITS REFERENCE RANGE

TOTAL LEUCOCYTES COUNT 6.86 X 10³ / µL 4.0-10.0
NEUTROPHILS 66.3 % 40-80
LYMPHOCYTE PERCENTAGE 25.7 % 20-40
MONOCYTES 4.4 % 0-10
EOSINOPHILS 3.1 % 0.0-6.0
BASOPHILS 0.2 % <2
IMMATURE GRANULOCYTE PERCENTAGE(IG%) 0.3 % 0-0.5
NEUTROPHILS - ABSOLUTE COUNT 4.55 X 10³ / µL 2.0-7.0
LYMPHOCYTES - ABSOLUTE COUNT 1.76 X 10³ / µL 1.0-3.0
MONOCYTES - ABSOLUTE COUNT 0.3 X 10³ / µL 0.2-1
BASOPHILS - ABSOLUTE COUNT 0.01 X 10³ / µL 0-0.1
EOSINOPHILS - ABSOLUTE COUNT 0.21 X 10³ / µL 0-0.5
IMMATURE GRANULOCYTES(IG) 0.02 X 10³ / µL 0-0.3
TOTAL RBC 5.52 X 10^6/µL 4.5-5.5
NUCLEATED RED BLOOD CELLS Nil X 10³ / µL <0.01
NUCLEATED RED BLOOD CELLS % Nil % <0.01
HEMOGLOBIN 13.5 g/dL 13-17
HEMATOCRIT(PCV) 44.4 % 40-50
MEAN CORPUSCULAR VOLUME(MCV) 80.4 fL 83-101
MEAN CORPUSCULAR HEMOGLOBIN(MCH) 24.5 pq 27-32
MEAN CORP.HEMO.CONC(MCHC) 30.4 g/dL 31.5-34.5
RED CELL DISTRIBUTION WIDTH - SD(RDW-SD) 43.6 fL 39-46
RED CELL DISTRIBUTION WIDTH (RDW-CV) 15.1 % 11.6-14
PLATELET DISTRIBUTION WIDTH(PDW) 13.3 fL 9.6-15.2
MEAN PLATELET VOLUME(MPV) 10.9 fL 6.5-12
PLATELET COUNT 244 X 10³ / µL 150-400
PLATELET TO LARGE CELL RATIO(PLCR) 33 % 19.7-42.4
PLATELETCRIT(PCT) 0.27 % 0.19-0.39
Remarks : ALERT !!! Hypochromia
Please Correlate with clinical conditions.

Method : Fully automated bidirectional analyser (6 Part Differential SYSMEX XN-1000)
(This device performs hematology analyses according to the Hydrodynamic Focussing (DC method), Flow
Cytometry Method (using a semiconductor laser), and SLS- hemoglobin method)
0807072934/A1835 / U8589071 / PUNL


Page : 3 of 15
: DR DESHPANDE
TEST ASKED : ANANDHAM C KARYALAYA, MUNDHWA, KESHAV NAGAR,
PUNE,411036
25-OH VITAMIN D (TOTAL) C.L.I.A 12.67 ng/ml

Reference Range :
DEFICIENCY : <20 ng/ml
INSUFFICIENCY : 20-<30 ng/ml
SUFFICIENCY : 30-100 ng/ml
TOXICITY : >100 ng/ml
Vitamin D Total test is analyzed on Siemens ADVIA Centaur, standardized against ID-LC/MS/MS, as per Vitamin D Standardization
Program (VDSP).
Specifications: Intra assay (%CV):5.3%, Inter assay (%CV):11.9% ; Sensitivity:3.2 ng/ml

Method : FULLY AUTOMATED CHEMI LUMINESCENT IMMUNO ASSAY
VITAMIN B-12 C.L.I.A 252 pg/ml
Reference Range :
Normal : 211 - 911 pg/ml
Clinical significance :
Vitamin B12 or cyanocobalamin, is a complex corrinoid compound found exclusively from animal dietary sources, such as meat, eggs
and milk. It is critical in normal DNA synthesis, which in turn affects erythrocyte maturation and in the formation of myelin sheath.
Vitamin-B12 is used to find out neurological abnormalities and impaired DNA synthesis associated with macrocytic anemias. For
diagnostic purpose, results should always be assessed in conjunction with the patients medical history, clinical examination and
other findings.
Specifications: Intra assay (%CV):5.0%, Inter assay (%CV):9.2 %;Sensitivity:45 pg/ml
External quality control program participation:

College of American pathologists: ligand assay (general) survey; CAP number: 7193855-01
Kit validation references:

Chen IW,Sperling MI,Heminger IA.Vitamin B12.In:Pesce AJ,Kalpan LA,editors.Methods in clinical chemistry. St.Louis:CV
Mosby,1987.P.569-73.
Method : FULLY AUTOMATED BIDIRECTIONALLY INTERFACED CHEMI LUMINESCENT IMMUNO ASSAY
0807072411/A1835 / V2227443 / PUNL

Page : 4 of 15
: DR DESHPANDE
PUNE,411036
APOLIPOPROTEIN - A1 (APO-A1) IMMUNOTURBIDIMETRY 85 mg/dL

Reference Range :
MALE : 86 - 152
FEMALE : 94 - 162
Method : FULLY AUTOMATED RATE IMMUNOTURBIDIMETRY – BECKMAN COULTER
APOLIPOPROTEIN - B (APO-B) IMMUNOTURBIDIMETRY 61 mg/dL
Reference Range :
MALE : 56 - 145
FEMALE : 53 - 138
Method : FULLY AUTOMATED RATE IMMUNOTURBIDIMETRY – BECKMAN COULTER
APO B / APO A1 RATIO (APO B/A1) CALCULATED 0.7 Ratio
Reference Range :
MALE : 0.40 - 1.26
FEMALE : 0.38 - 1.14
Method : DERIVED FROM SERUM APO A1 AND APO B VALUES
0807072411/A1835 / V2227443 / PUNL

Page : 5 of 15
TEST ASKED : ANANDHAM C MUNDHWA, KESHAV NAGAR, PUNE,411036

HIGH SENSITIVITY C-REACTIVE PROTEIN (HS-CRP) IMMUNOTURBIDIMETRY 43.08 mg/L
Reference Range :-
ADULT : <=3.0 MG/L
INTERPRETATION:
HIGH SENSITIVITY C-REACTIVE PROTEIN, WHEN USED IN CONJUNCTION WITH OTHER CLINICAL LABORATORY EVALUATION OF ACUTE
CORONARY SYNDROMES, MAY BE USEFUL AS AN INDEPENDENT MARKER OF PROGNOSIS FOR RECURRENT EVENTS, IN PATIENTS
WITH STABLE CORONARY DISEASE OR ACUTE CORONARY SYNDROMES. HSCRP LEVELS SHOULD NOT BE SUBSTITUTED FOR
ASSESSMENT OF TRADITIONAL CARDIOVASCULAR RISK FACTORS. PATIENTS WITH PERSISTENTLY UNEXPLAINED, MARKED
EVALUATION OF HSCRP AFTER REPEATED TESTING SHOULD BE EVALUATED FOR NON - CARDIOVASCULAR ETIOLOGIES
CLINICAL SIGNIFICANCE:
HSCRP MEASUREMENTS MAY BE USED AS AN INDEPENDENT RISK MARKER FOR THE IDENTIFICATION OF INDIVIDUALS AT RISK FOR
FUTURE CARDIOVASCULAR DISEASE. ELEVATED CRP VALUES MAY BE INDICATIVE OF PROGNOSIS OF INDIVIDUALS WITH ACUTE
CORONARY SYNDROMES, AND MAY BE USEFUL IN THE MANAGEMENT OF SUCH INDIVIDUALS.
SPECIFICATIONS: PRECISION: WITHIN RUN %CV HAS BEEN RECORDED <=5%.
REFERENCES:
1. CHENILLOT O, HENNY J, STEINMEZ J, ET AL. HIGH SENSITIVITY C-REACTIVE PROTEIN: BIOLOGICAL VARIATIONS AND REFERENCE
LIMITS. CLIN CHEM LAB MED 2000;38:1003-11.
2. HIND CRH, PEPYS MB. THE ROLE OF SERUM C-REACTIVE PROTEIN MEASUREMENTS IN CLINICAL PRACTICE. INT MED
1984;5:112-51.
Method:- FULLY AUTOMATED LATEX AGGLUTINATION – BECKMAN COULTER
0807072411/A1835 / V2227443 / PUNL

Page : 6 of 15

LIPOPROTEIN (A) [LP(A)] IMMUNOTURBIDIMETRY 4.19 mg/dl
Reference Range :-
ADULTS : < 30.0 MG/DL
INTERPRETATION:
DETERMINATION OF LPA MAY BE USEFUL TO GUIDE MANAGEMENT OF INDIVIDUALS WITH A FAMILY HISTORY OF CHD OR WITH
EXISTING DISEASE. THE LEVELS OF LPA IN THE BLOOD DEPENDS ON GENETIC FACTORS; THE RANGE OF VARIATION IN A
POPULATION IS RELATIVELY LARGE AND HENCE FOR DIAGNOSTIC PURPOSE, RESULTS SHOULD ALWAYS BE ASSESSED IN
CONJUNCTION WITH THE PATIENT’S MEDICAL HISTORY, CLINICAL EXAMINATION AND OTHER FINDINGS.
SPECIFICATIONS:
PRECISION: INTRA ASSAY (%CV): 3.4 %, INTER ASSAY (%CV): 2.0 %; SENSITIVITY: 0.002 GM/L
EXTERNAL QUALITY CONTROL PROGRAM PARTICIPATION:
COLLEGE OF AMERICAN PATHOLOGISTS: GENERAL CHEMISTRY AND TDM; CAP NUMBER: 7193855-01
KIT VALIDATION REFERENCES:
KOSCHINSKY ML, MARCOVINA SM. LIPOPROTEIN A: STRUCTURAL IMPLICATION FOR PATHOPHYSIOLOGY. INT J CLIN LAB RES, 1997;
27: 14-23.
Method:- LATEX ENHANCED IMMUNOTURBIDIMETRY
0807072411/A1835 / V2227443 / PUNL

Page : 7 of 15

TESTOSTERONE C.L.I.A 279.1 ng/dL
Reference Range :-
Adult Male
21 - 49 Yrs : 164.94 - 753.38
50 - 89 Yrs : 86.49 - 788.22
Adult Female
Pre-Menopause : 12.09 - 59.46
Post-Menopause: < 7.00 - 48.93
Boys
2-10 Years : < 7.00 - 25.91
11 Years : < 7.00 - 341.53
12 Years : < 7.00 - 562.59
13 Years : 9.34 - 562.93
14 Years : 23.28 - 742.46
15 Years : 144.15 - 841.44
16-21 Years : 118.22 - 948.56
Girls
2-10 Years : < 7.00 - 108.30
11-15 Years : < 7.00 - 48.40
16-21 Years : 17.55 - 50.41
Clinical Significance:
Clinical evaluation of serum testosterone, along with serum LH, assists in evaluation of Hypogonadal males. Major causes of lowered
testosterone in males include Hypogonadotropic hypogonadism, testicular failure Hyperprolactinema, Hypopituitarism some types of
liver and kidney diseases and critical illness.
Specifications: Precision: Intra assay (%CV): 8.5 %, Inter assay (%CV): 12.6%; Sensitivity: 7 ng/dL.
External quality control program participation:

College of American pathologists: Ligand assay (special) survey; cap number: 7193855-01
Method:- FULLY AUTOMATED BIDIRECTIONALLY INTERFACED CHEMI LUMINESCENT IMMUNO ASSAY
0807072411/A1835 / V2227443 / PUNL

Page : 8 of 15
: DR DESHPANDE
PUNE,411036
IRON PHOTOMETRY 27.2 µg/dl

Reference Range :
Male : 65 - 175
Female : 50 - 170
Method : FERROZINE METHOD WITHOUT DEPROTEINIZATION
TOTAL IRON BINDING CAPACITY (TIBC) PHOTOMETRY 331 µg/dl
Reference Range :
Male: 225 - 535 µg/dl Female: 215 - 535 µg/dl
Method : SPECTROPHOTOMETRIC ASSAY
% TRANSFERRIN SATURATION CALCULATED 8.22 %
Reference Range :
13 - 45
Method : DERIVED FROM IRON AND TIBC VALUES
0807072411/A1835 / V2227443 / PUNL

Page : 9 of 15
REF. BY (8551177646),SAI LABORATORY,SR NO. 5/4, PAWAR
: DR DESHPANDE
VASTI, NEAR PRATIMA MANGAL KARYALAYA, MUNDHWA,
TEST ASKED : ANANDHAM C KESHAV NAGAR, PUNE,411036
TEST NAME TECHNOLOGY VALUE UNITS NORMAL RANGE

TOTAL CHOLESTEROL PHOTOMETRY 95 mg/dl < 200
HDL CHOLESTEROL - DIRECT PHOTOMETRY 25 mg/dl 40-60
LDL CHOLESTEROL - DIRECT PHOTOMETRY 52 mg/dl < 100
TRIGLYCERIDES PHOTOMETRY 98 mg/dl < 150
TC/ HDL CHOLESTEROL RATIO CALCULATED 3.8 Ratio 3-5
LDL / HDL RATIO CALCULATED 2.1 Ratio 1.5-3.5
VLDL CHOLESTEROL CALCULATED 19.6 mg/dl 5 - 40
NON-HDL CHOLESTEROL CALCULATED 69.8 mg/dl < 160
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
LDL/ - DERIVED FROM SERUM HDL AND LDL VALUES
VLDL - DERIVED FROM SERUM TRIGLYCERIDE VALUES
NHDL - DERIVED FROM SERUM CHOLESTEROL AND HDL VALUES
*REFERENCE RANGES AS PER NCEP ATP III GUIDELINES:
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 NEAR OPTIMAL 100-129 BORDERLINE HIGH 150-199
HIGH >240 BORDERLINE HIGH 130-159 HIGH 200-499
HIGH 160-189 VERY HIGH >500

VERY HIGH >190
Alert !!! 10-12 hours fasting is mandatory for lipid parameters. If not, values might fluctuate.
0807072411/A1835 / V2227443 / PUNL

Page : 10 of 15
: DR DESHPANDE

ALKALINE PHOSPHATASE PHOTOMETRY 82 U/L 45 - 129
BILIRUBIN - TOTAL PHOTOMETRY 0.38 mg/dl 0.3-1.2
BILIRUBIN -DIRECT PHOTOMETRY 0.12 mg/dl < 0.3
BILIRUBIN (INDIRECT) CALCULATED 0.26 mg/dl 0-0.9
GAMMA GLUTAMYL TRANSFERASE (GGT) PHOTOMETRY 10 U/l < 55
ASPARTATE AMINOTRANSFERASE (SGOT ) PHOTOMETRY 18 U/l < 35
ALANINE TRANSAMINASE (SGPT) PHOTOMETRY 21.05 U/l < 45
PROTEIN - TOTAL PHOTOMETRY 6.62 gm/dl 5.7-8.2
ALBUMIN - SERUM PHOTOMETRY 4.09 gm/dl 3.2-4.8
SERUM ALB/GLOBULIN RATIO CALCULATED 1.62 Ratio 0.9 - 2
SERUM GLOBULIN PHOTOMETRY 2.53 gm/dL 2.5-3.4
Method :
ALKP - MODIFIED IFCC METHOD
BILT - VANADATE OXIDATION
BILD - VANADATE OXIDATION
BILI - DERIVED FROM SERUM TOTAL AND DIRECT BILIRUBIN VALUES
GGT - MODIFIED IFCC METHOD
SGOT - IFCC* WITHOUT PYRIDOXAL PHOSPHATE ACTIVATION
SGPT - IFCC* WITHOUT PYRIDOXAL PHOSPHATE ACTIVATION
PROT - BIURET METHOD
SALB - ALBUMIN BCG¹METHOD (COLORIMETRIC ASSAY ENDPOINT)
A/GR - DERIVED FROM SERUM ALBUMIN AND PROTEIN VALUES
SEGB - DERIVED FROM SERUM ALBUMIN AND PROTEIN VALUES
0807072411/A1835 / V2227443 / PUNL

Page : 11 of 15
(8551177646),SAI LABORATORY,SR NO. 5/4, PAWAR
REF. BY : DR DESHPANDE
TEST NAME TECHNOLOGY VALUE UNITS REFERENCE RANGE
TOTAL TRIIODOTHYRONINE (T3) C.L.I.A 75 ng/dl 60-200

TOTAL THYROXINE (T4) C.L.I.A 6.5 µg/dl 4.5-12
THYROID STIMULATING HORMONE (TSH) C.L.I.A 3.35 µIU/ml 0.3-5.5
Comments : SUGGESTING THYRONORMALCY

Method :
T3 - COMPETITIVE CHEMI LUMINESCENT IMMUNO ASSAY
T4 - COMPETITIVE CHEMI LUMINESCENT IMMUNO ASSAY
TSH - SANDWICH CHEMI LUMINESCENT IMMUNO ASSAY
0807072411/A1835 / V2227443 / PUNL


Page : 12 of 15
: DR DESHPANDE

BLOOD UREA NITROGEN (BUN) PHOTOMETRY 11.5 mg/dl 7 - 25
CREATININE - SERUM PHOTOMETRY 0.9 mg/dl 0.6-1.1
BUN / SR.CREATININE RATIO CALCULATED 12.78 Ratio 9:1-23:1
CALCIUM PHOTOMETRY 9 mg/dl 8.8-10.6
URIC ACID PHOTOMETRY 5 mg/dl 4.2 - 7.3
Method :
BUN - KINETIC UV ASSAY.
SCRE - CREATININE ENZYMATIC METHOD
B/CR - DERIVED FROM SERUM BUN AND CREATININE VALUES
CALC - ARSENAZO III METHOD, END POINT.
URIC - URICASE / PEROXIDASE METHOD
0807072411/A1835 / V2227443 / PUNL

Page : 13 of 15

EST. GLOMERULAR FILTRATION RATE (eGFR) CALCULATED 89 mL/min/1.73 m2
Reference Range :-
> = 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.
Method:- CKD-EPI Creatinine Equation
~~ End of report ~~
0807072411/A1835 / V2227443 / PUNL

Page : 14 of 15
CONDITIONS OF REPORTING
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.
v Thyrocare Discovery video link :- https://youtu.be/nbdYeRgYyQc
v For clinical support please contact @8450950851,8450950852,8450950853,8450950854 between 10:00 to 18:00
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.
SUGGESTIONS
v Values out of reference range requires reconfirmation before starting any medical treatment.
v Retesting is needed if you suspect any quality shortcomings.
v Testing or retesting should be done in accredited laboratories.
v For suggestions, complaints or feedback, write to us at [email protected] or call us on
022-3090 0000 / 6712 3400
v SMS:<Labcode No.> to 9870666333
Page : 15 of 15

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NAME : RAJKUMAR MASAWAN (66Y/M) SAMPLE GIVEN BY :

REF. BY : DR DESHPANDE (8551177646),SAI LABORATORY,SR NO. 5/4,

TEST NAME TECHNOLOGY VALUE UNITS

0807072346/A1835 / Q7208588 / PUNL

Dr. Sachin Patil MD(Path)

TEST NAME TECHNOLOGY VALUE UNITS

Reference Range: As per ADA Guidelines Guidance For Known Diabetics

Below 5.7% : Normal Below 6.5% : Good Control

0807072934/A1835 / U8589071 / PUNL

Dr Sachin Patil MD(Path)

TEST NAME VALUE UNITS REFERENCE RANGE

Please Correlate with clinical conditions.

0807072934/A1835 / U8589071 / PUNL

Dr Sachin Patil MD(Path)

TEST NAME TECHNOLOGY VALUE UNITS

25-OH VITAMIN D (TOTAL) C.L.I.A 12.67 ng/ml

Specifications: Intra assay (%CV):5.3%, Inter assay (%CV):11.9% ; Sensitivity:3.2 ng/ml

Specifications: Intra assay (%CV):5.0%, Inter assay (%CV):9.2 %;Sensitivity:45 pg/ml

External quality control program participation:

Kit validation references:

0807072411/A1835 / V2227443 / PUNL

Dr Sachin Patil MD(Path)

TEST NAME TECHNOLOGY VALUE UNITS

APOLIPOPROTEIN - A1 (APO-A1) IMMUNOTURBIDIMETRY 85 mg/dL

0807072411/A1835 / V2227443 / PUNL

Dr Sachin Patil MD(Path)

TEST NAME TECHNOLOGY VALUE UNITS

ADULT : <=3.0 MG/L

SPECIFICATIONS: PRECISION: WITHIN RUN %CV HAS BEEN RECORDED <=5%.

0807072411/A1835 / V2227443 / PUNL

Dr. Sachin Patil MD(Path)

TEST NAME TECHNOLOGY VALUE UNITS

ADULTS : < 30.0 MG/DL

EXTERNAL QUALITY CONTROL PROGRAM PARTICIPATION:

KIT VALIDATION REFERENCES:

0807072411/A1835 / V2227443 / PUNL

Dr. Sachin Patil MD(Path)

TEST NAME TECHNOLOGY VALUE UNITS

External quality control program participation:

0807072411/A1835 / V2227443 / PUNL

Dr. Sachin Patil MD(Path)

TEST NAME TECHNOLOGY VALUE UNITS

IRON PHOTOMETRY 27.2 µg/dl

0807072411/A1835 / V2227443 / PUNL

Dr Sachin Patil MD(Path)

TEST NAME TECHNOLOGY VALUE UNITS NORMAL RANGE

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

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

HIGH >240 BORDERLINE HIGH 130-159 HIGH 200-499

HIGH 160-189 VERY HIGH >500

0807072411/A1835 / V2227443 / PUNL

Dr Sachin Patil MD(Path)

TEST NAME TECHNOLOGY VALUE UNITS NORMAL RANGE

0807072411/A1835 / V2227443 / PUNL

Dr Sachin Patil MD(Path)

TEST NAME TECHNOLOGY VALUE UNITS REFERENCE RANGE

TOTAL TRIIODOTHYRONINE (T3) C.L.I.A 75 ng/dl 60-200

Comments : SUGGESTING THYRONORMALCY

Please correlate with clinical conditions.