WM17S
WM17S
WM17S
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Test Report
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Test Name Results Units Bio. Ref. Interval
SWASTHFIT SUPER 4
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Creatinine 1.00 mg/dL 0.70 - 1.30
(Modified Jaffe,Kinetic)
GFR Estimated 107 mL/min/1.73m2 >59
(CKD EPI Equation 2021)
GFR Category G1
(KDIGO Guideline 2012)
Urea
(Urease UV)
R 40.00 mg/dL 13.00 - 43.00
(Oxidation)
Bilirubin Indirect 0.80 mg/dL <1.10
(Calculated)
Total Protein 8.00 g/dL 5.70 - 8.20
(Biuret)
Albumin 4.00 g/dL 3.20 - 4.80
(BCG)
A : G Ratio 1.00 0.90 - 2.00
(Calculated)
Globulin(Calculated) 4.00 gm/dL 2.0 - 3.5
*WM17SPF* Page 1 of 7
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Test Name Results Units Bio. Ref. Interval
Phosphorus 4.00 mg/dL 2.40 - 5.10
(Molybdate UV)
Sodium 140.00 mEq/L 136.00 - 145.00
(Indirect ISE)
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Potassium 4.00 mEq/L 3.50 - 5.10
(Indirect ISE)
Chloride 100.00 mEq/L 98.00 - 107.00
(Indirect ISE)
Cholesterol, Total
R 100.00 mg/dL <200.00
(CHO-POD)
Triglycerides 100.00 mg/dL <150.00
(GPO-POD)
HDL Cholesterol 30.00 mg/dL >40.00
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(Enz Immunoinhibition)
LDL Cholesterol, Calculated 50.00 mg/dL <100.00
(Calculated)
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Note
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1. Measurements in the same patient can show physiological & analytical variations. Three serial
samples 1 week apart are recommended for Total Cholesterol, Triglycerides, HDL& LDL Cholesterol.
2. Additional testing for Apolipoprotein B, hsCRP, Lp(a ) & LP-PLA2 should be considered
among patients with moderate risk for ASCVD for risk refinement.
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Test Name Results Units Bio. Ref. Interval
|------------|--------------------|--------------------|----------------|--------------------|
| High | <70 | <100 | ≥70 | ≥100 |
|------------|--------------------|--------------------|----------------|--------------------|
| Moderate | <100 | <130 | ≥100 | ≥130 |
|------------|--------------------|--------------------|----------------|--------------------|
| Low | <100 | <130 | ≥130* | ≥160* |
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*In low risk patient, consider therapy after an initial non-pharmacological intervention for at least 3 months
(CLIA)
Interpretation
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| LEVEL | REFERENCE RANGE IN nmol/L| COMMENTS |
|---------------|--------------------------|-------------------------------------------------|
| Deficient | < 50 | High risk for developing bone disease |
|---------------|--------------------------|-------------------------------------------------|
| Insufficient | 50-74 | Vitamin D concentration which normalizes |
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Test Name Results Units Bio. Ref. Interval
· Levels vary with age and are increased in pregnancy.
· A new test Vitamin D, Ultrasensitive by LC-MS/MS is also available
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THYROID PROFILE,TOTAL, SERUM
(CLIA)
Note
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1. TSH levels are subject to circadian variation, reaching peak levels between 2 - 4.a.m. 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 measured serum TSH concentrations.
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2. Alteration in concentration of Thyroid hormone binding protein can profoundly affect Total T3 and/or
Total T4 levels especially in pregnancy and in patients on steroid therapy.
3. Unbound fraction ( Free,T4 /Free,T3) of thyroid hormone is biologically active form and correlate
more closely with clinical status of the patient than total T4/T3 concentration
4. Values <0.03 uIU/mL need to be clinically correlated due to presence of a rare TSH variant in
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some individuals
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Test Name Results Units Bio. Ref. Interval
HbA1c (GLYCOSYLATED HEMOGLOBIN), BLOOD
(HPLC, NGSP certified)
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HbA1c 10.0 % 4.00 - 5.60
Interpretation
HbA1c result is suggestive of Diabetes/ Higher than glycemic goal in a known Diabetic patient.
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Please note, Glycemic goal should be individualized based on duration of diabetes, age/life expectancy,
comorbid conditions, known CVD or advanced microvascular complications, hypoglycaemia unawareness,
and individual patient considerations
Note: Presence of Hemoglobin variants and/or conditions that affect red cell turnover must be considered,
particularly when the HbA1C result does not correlate with the patient’s blood glucose levels.
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| FACTORS THAT INTERFERE WITH HbA1C | FACTORS THAT AFFECT INTERPRETATION |
| MEASUREMENT | OF HBA1C RESULTS |
|--------------------------------------|------------------------------------------|
| Hemoglobin variants,elevated fetal | Any condition that shortens erythrocyte |
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Test Name Results Units Bio. Ref. Interval
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(Photometry)
Packed Cell Volume (PCV) 45.00 % 40.00 - 50.00
(Calculated)
RBC Count 5.00 mill/mm3 4.50 - 5.50
(Electrical Impedence)
MCV 100.00 fL 83.00 - 101.00
(Electrical Impedence)
MCH
R 30.00 pg 27.00 - 32.00
(Calculated)
MCHC 33.00 g/dL 31.50 - 34.50
(Calculated)
Red Cell Distribution Width (RDW) 12.00 % 11.60 - 14.00
e
(Electrical Impedence)
Total Leukocyte Count (TLC) 5.00 thou/mm3 4.00 - 10.00
(Electrical Impedence)
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*WM17SPF* Page 6 of 7
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leucocyte counts are additionally being reported as absolute numbers of each cell in per unit volume of
blood
2. Test conducted on EDTA whole blood
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Dr Ajay Gupta Dr Gurleen Oberoi Dr Himangshu Mazumdar Dr Jatin Munjal
MD, Pathology DM(Hematopathology), MD, Biochemistry MD,Pathology
Technical Director - Hematology & MD,DNB,MNAMS Sr. Consultant Biochemist Consultant Pathologist
Immunology Senior Consultant and Lead- NRL - Dr Lal PathLabs Ltd Dr Lal PathLabs Ltd
NRL - Dr Lal PathLabs Ltd Hematopathology
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NRL - Dr Lal PathLabs Ltd
This is a revised report & supersedes all the previously issued reports
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BNFFFNBPAOFOFGEOACFDEDFHAHFHACEHMGIOEOJPMDAPNPBNFFFNB
GPFAACFPJNFNMACOFODKIGJOGABFDCIGKFPCBNFBOKKKMLECFGHOL
CJPHPNFBFNNAMGCGEAKLJLPGMPHELLIIKNGOFNMFOMCHFKNAFGFCG
OCPAHJFPNIBLHBDOGNKCFCIMCGHDCJKAOCNIBKOIKEDGHKFPGKPCH
HGNCLKFMEIMKBPEBALFCKKEGBGDDKECNOONFCCGJMLAAEMFEBIPKO
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ICMCAHFHAFIKOJLMNCIPCKLIAHFHAKBEMLNCAKFFOKKFAHFHAKHHK
FGKPCDFGABGGDAGDHAPAHJPCGFEBFLBJPCECBNFFOBDGCCCFBHDDL
CFAGDIFKGPJLKMLNAMKAFPPDFEFFPHCDKKNKBMMBKNCIBACDIFHOC
MJDBGAFJKBJKNKMPBALJCFLDIPLCFHKHPFHNBDGPJNDPKBOIIEHCP
FMKBNJFMBIEAOIHLOIGDJEOKPLIFFNLHKFNCBIMNNKDOLFGIKKNNL
MNNFNNEHCEIPKKEAEMGAOKIDAHFHAFKHMKFGHLNPONKIAHFHACPPL
APBBBPAPBALONHHCOOIJFIELBCHDACAJOGMIBNNBOLCBCHHCFABAJ
HHHHHHHPHPHHHPHHPPHPPHPHHHPHPHHHPPPPHPPHPHHHPHPPHPHPP
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IMPORTANT INSTRUCTIONS
ŸTest results released pertain to the specimen submitted .ŸAll test results are dependent on the quality of the sample received by the Laboratory .
ŸLaboratory investigations are only a tool to facilitate in arriving at a diagnosis and should be clinically correlated by the Referring Physician .ŸReport
delivery may be delayed due to unforeseen circumstances. Inconvenience is regretted .ŸCertain tests may require further testing at additional cost
for derivation of exact value. Kindly submit request within 72 hours post reporting.ŸTest results may show interlaboratory variations .ŸThe
Courts/Forum at Delhi shall have exclusive jurisdiction in all disputes /claims concerning the test(s) & or results of test(s).ŸTest results are not valid
for medico legal purposes.ŸThis is computer generated medical diagnostic report that has been validated by Authorized Medical
Practitioner/Doctor. ŸThe report does not need physical signature.
(#) Sample drawn from outside source.
If Test results are alarming or unexpected, client is advised to contact the Customer Care immediately for possible remedial action.
Tel: +91-11-49885050,Fax: - +91-11-2788-2134, E-mail: lalpathlabs@lalpathlabs.com
National Reference lab, Delhi, a CAP (7171001) Accredited, ISO 9001:2015 (FS60411) & ISO 27001:2013 (616691) Certified laboratory.
*WM17SPF* Page 7 of 7