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PSC Noida Sector - 78 Lpl-Noida Lab N-27, SECTOR-18, NOIDA - 201301

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0% found this document useful (0 votes)
20 views6 pages

PSC Noida Sector - 78 Lpl-Noida Lab N-27, SECTOR-18, NOIDA - 201301

Uploaded by

atharvbiswas
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
You are on page 1/ 6

.

Name : Ms. ARCHISHA


Lab No. : 179921875 Age : 24 Years
Ref By : RINKU RANI BISWAS Gender : Female
Collected : 2/6/2024 8:37:00AM Reported : 2/6/2024 2:51:42PM
A/c Status : P Report Status : Interim
Collected at : PSC NOIDA SECTOR - 78 Processed at : LPL-NOIDA LAB
N-27, SECTOR-18, NOIDA - 201301

Test Report

Test Name Results Units Bio. Ref. Interval

SWASTHFIT SUPER-4

LIPID SCREEN, SERUM


(CHO-POD)

Cholesterol, Total 134.00 mg/dL <200.00

Triglycerides 77.00 mg/dL <150.00

HDL Cholesterol 39.50 mg/dL >50.00

LDL Cholesterol, Calculated 79.10 mg/dL <100.00

VLDL Cholesterol,Calculated 15.40 mg/dL <30.00

Non-HDL Cholesterol 95 mg/dL <130

Note
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.

Treatment Goals as per Lipid Association of India 2020


--------------------------------------------------------------------------------------------
| RISK | TREATMENT GOAL | CONSIDER THERAPY |
| CATEGORY |-----------------------------------------|-------------------------------------|
| | LDL CHOLESTEROL | NON HDL CHLOESTEROL| LDL CHOLESTEROL| NON HDL CHLOESTEROL|
| | (LDL-C)(mg/dL) | (NON HDL-C) (mg/dL)| (LDL-C)(mg/dL) | (NON HDL-C) (mg/dL)|
|------------|--------------------|--------------------|----------------|--------------------|
| Extreme | <50 | <80 | | |
| Risk Group |(Optional goal ≤30) |(Optional goal ≤60) | ≥50 | ≥80 |
| Category A | | | | |
|------------|--------------------|--------------------|----------------|--------------------|
| Extreme | | | | |
| Risk Group | ≤30 | ≤60 | >30 | >60 |
| Category B | | | | |
|------------|--------------------|--------------------|----------------|--------------------|
| Very | <50 | <80 | ≥50 | ≥80 |
| High | | | | |
|------------|--------------------|--------------------|----------------|--------------------|
| High | <70 | <100 | ≥70 | ≥100 |
|------------|--------------------|--------------------|----------------|--------------------|
| Moderate | <100 | <130 | ≥100 | ≥130 |
|------------|--------------------|--------------------|----------------|--------------------|
| Low | <100 | <130 | ≥130* | ≥160* |
--------------------------------------------------------------------------------------------
*In low risk patient, consider therapy after an initial non-pharmacological intervention for at least 3 months

*179921875* Page 1 of 6
.

Name : Ms. ARCHISHA


Lab No. : 179921875 Age : 24 Years
Ref By : RINKU RANI BISWAS Gender : Female
Collected : 2/6/2024 8:37:00AM Reported : 2/6/2024 2:51:42PM
A/c Status : P Report Status : Interim
Collected at : PSC NOIDA SECTOR - 78 Processed at : LPL-NOIDA LAB
N-27, SECTOR-18, NOIDA - 201301

Test Report

Test Name Results Units Bio. Ref. Interval

GLUCOSE, FASTING (F)


(Hexokinase)

Glucose Fasting 81.00 mg/dL 70.00 - 100.00

VITAMIN B12; CYANOCOBALAMIN


(CLIA)

Vitamin B12; Cyanocobalamin 285.00 pg/mL 211.00 - 911.00

Notes
1. Interpretation of the result should be considered in relation to clinical circumstances.
2. It is recommended to consider supplementary testing with plasma Methylmalonic acid (MMA) or
plasma homocysteine levels to determine biochemical cobalamin deficiency in presence of clinical
suspicion of deficiency but indeterminate levels. Homocysteine levels are more sensitive but MMA is
more specific

3. False increase in Vitamin B12 levels may be observed in patients with intrinsic factor blocking
antibodies, MMA measurement should be considered in such patients

4. The concentration of Vitamin B12 obtained with different assay methods cannot be used
interchangeably due to differences in assay methods and reagent specificity

VITAMIN D, 25 - HYDROXY, SERUM


(Chemiluminescence)

Vitamin D, 25 Hydroxy 60.56 nmol/L 75.00 - 250.00

Interpretation
--------------------------------------------------------------------------------------------
| LEVEL | REFERENCE RANGE IN nmol/L| COMMENTS |
|---------------|--------------------------|-------------------------------------------------|
| Deficient | < 50 | High risk for developing bone disease |
|---------------|--------------------------|-------------------------------------------------|
| Insufficient | 50-74 | Vitamin D concentration which normalizes |
| | | Parathyroid hormone concentration |
|---------------|--------------------------|-------------------------------------------------|
| Sufficient | 75-250 | Optimal concentration for maximal health benefit|
|---------------|--------------------------|-------------------------------------------------|
| Potential | >250 | High risk for toxic effects |
| intoxication | | |

*179921875* Page 2 of 6
.

Name : Ms. ARCHISHA


Lab No. : 179921875 Age : 24 Years
Ref By : RINKU RANI BISWAS Gender : Female
Collected : 2/6/2024 8:37:00AM Reported : 2/6/2024 2:51:42PM
A/c Status : P Report Status : Interim
Collected at : PSC NOIDA SECTOR - 78 Processed at : LPL-NOIDA LAB
N-27, SECTOR-18, NOIDA - 201301

Test Report

Test Name Results Units Bio. Ref. Interval


--------------------------------------------------------------------------------------------
Note
· The assay measures both D2 (Ergocalciferol) and D3 (Cholecalciferol) metabolites of vitamin D.
· 25 (OH)D is influenced by sunlight, latitude, skin pigmentation, sunscreen use and hepatic function.
· Optimal calcium absorption requires vitamin D 25 (OH) levels exceeding 75 nmol/L.
· It shows seasonal variation, with values being 40-50% lower in winter than in summer.
· Levels vary with age and are increased in pregnancy.
· A new test Vitamin D, Ultrasensitive by LC-MS/MS is also available

THYROID PROFILE,TOTAL, SERUM


(Chemiluminescent Immunoassay)

T3, Total 1.22 ng/mL 0.60 - 1.81

T4, Total 4.90 µg/dL 4.50 - 11.60

TSH 6.11 µIU/mL 0.550 - 4.780

Note
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.
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
some individuals

*179921875* Page 3 of 6
.

Name : Ms. ARCHISHA


Lab No. : 179921875 Age : 24 Years
Ref By : RINKU RANI BISWAS Gender : Female
Collected : 2/6/2024 8:37:00AM Reported : 2/6/2024 2:51:48PM
A/c Status : P Report Status : Interim
Collected at : PSC NOIDA SECTOR - 78 Processed at : LPL-NOIDA LAB
N-27, SECTOR-18, NOIDA - 201301

Test Report

Test Name Results Units Bio. Ref. Interval


HbA1c (GLYCOSYLATED HEMOGLOBIN), BLOOD
(HPLC, NGSP certified)

HbA1c 4.9 % 4.00 - 5.60

Estimated average glucose (eAG) 94 mg/dL

Interpretation
HbA1c result is suggestive of non diabetic adults (>=18 years)/ well controlled Diabetes in a known Diabetic
Interpretation as per American Diabetes Association (ADA) Guidelines

------------------------------------------------------------------------------------------
| Reference Group | Non diabetic | At risk | Diagnosing | Therapeutic goals |
| | adults >=18 years | (Prediabetes) | Diabetes | for glycemic control |
| ----------------|-------------------|---------------|-------------|----------------------|
| HbA1c in % | 4.0-5.6 | 5.7-6.4 | >= 6.5 | <7.0 |
------------------------------------------------------------------------------------------

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.

---------------------------------------------------------------------------------
| FACTORS THAT INTERFERE WITH HbA1C | FACTORS THAT AFFECT INTERPRETATION |
| MEASUREMENT | OF HBA1C RESULTS |
|--------------------------------------|------------------------------------------|
| Hemoglobin variants,elevated fetal | Any condition that shortens erythrocyte |
| hemoglobin (HbF) and chemically | survival or decreases mean erythrocyte |
| modified derivatives of hemoglobin | age (e.g.,recovery from acute blood loss,|
| (e.g. carbamylated Hb in patients | hemolytic anemia, HbSS, HbCC, and HbSC) |
| with renal failure) can affect the | will falsely lower HbA1c test results |
| accuracy of HbA1c measurements | regardless of the assay method used.Iron |
| | deficiency anemia is associated with |
| | higher HbA1c |
---------------------------------------------------------------------------------

*179921875* Page 4 of 6
.

Name : Ms. ARCHISHA


Lab No. : 179921875 Age : 24 Years
Ref By : RINKU RANI BISWAS Gender : Female
Collected : 2/6/2024 8:37:00AM Reported : 2/6/2024 2:51:54PM
A/c Status : P Report Status : Interim
Collected at : PSC NOIDA SECTOR - 78 Processed at : LPL-NOIDA LAB
N-27, SECTOR-18, NOIDA - 201301

Test Report
Test Name Results Units Bio. Ref. Interval

COMPLETE BLOOD COUNT; CBC


(Photometry, Electrical Impedance, VCS Technology & Calculated)

Hemoglobin 11.70 g/dL 12.00 - 15.00

Packed Cell Volume (PCV) 35.40 % 36.00 - 46.00

RBC Count 3.77 mill/mm3 3.80 - 4.80

MCV 93.90 fL 83.00 - 101.00

MCH 30.90 pg 27.00 - 32.00

MCHC 32.90 g/dL 31.50 - 34.50

Red Cell Distribution Width (RDW) 13.00 % 11.60 - 14.00

Total Leukocyte Count (TLC) 6.40 thou/mm3 4.00 - 10.00

Differential Leucocyte Count (DLC)


Segmented Neutrophils 46.80 % 40.00 - 80.00
Lymphocytes 45.30 % 20.00 - 40.00
Monocytes 5.90 % 2.00 - 10.00
Eosinophils 1.50 % 1.00 - 6.00
Basophils 0.50 % <2.00
Absolute Leucocyte Count
Neutrophils 3.00 thou/mm3 2.00 - 7.00
Lymphocytes 2.90 thou/mm3 1.00 - 3.00
Monocytes 0.38 thou/mm3 0.20 - 1.00
Eosinophils 0.10 thou/mm3 0.02 - 0.50
Basophils 0.03 thou/mm3 0.02 - 0.10
Platelet Count 228 thou/mm3 150.00 - 410.00

Mean Platelet Volume 8.9 fL 6.5 - 12.0

Note
1. As per the recommendation of International council for Standardization in Hematology, the differential
leucocyte counts are additionally being reported as absolute numbers of each cell in per unit volume of

*179921875* Page 5 of 6
.

Name : Ms. ARCHISHA


Lab No. : 179921875 Age : 24 Years
Ref By : RINKU RANI BISWAS Gender : Female
Collected : 2/6/2024 8:37:00AM Reported : 2/6/2024 2:51:54PM
A/c Status : P Report Status : Interim
Collected at : PSC NOIDA SECTOR - 78 Processed at : LPL-NOIDA LAB
N-27, SECTOR-18, NOIDA - 201301

Test Report
Test Name Results Units Bio. Ref. Interval
blood
2. Test conducted on EDTA whole blood

Dr Parul Joshi Dr Swati Singh


MD, Pathology MD, Pathology
Chief of Laboratory Chief of Laboratory
Dr Lal PathLabs Ltd Dr Lal PathLabs Ltd

AHEEEHAPMKHIFIENLGPICNPCBILLJCECCIICIKPJNKEDFEFAPPAHEEEHA
BNFFFNBPAPBPFOJGFGEGIOIPAOAHFHALBKJOBCJKFLELNOJGMPBNFFFNB
GMDAEHFJLNPGJLGNHFIAAJHFJGFEHEDBPKPHENFLMKLMOEFLBKHDEHANP
DJNMIOFNBOOIELEBDLPELEPFANPLALBFJIFEPAOAKKNJPDNLIBPBKEMEL
LAJIJLFIOJJFDIAIJNHGMHBBJENBIDIHKKMDAKMIPLKGKPNGKFFFOIONH
IJCBBEFDPECAMLGKIAFCGIPBADHFOFAINDFCBKDLALIKOMNALNEIPGMCL
PFIMIJFJELOMPNDIEOIDFGHHIHAFJBALPHOPBLMCOJCHKNFMIJNJMDILD
BNFNAMFNALMMKAGMAANHDFGILKBMFMBHMFCCAMNNIJKDKPNGBNFNBHILL
NKLKINFJNGEGFEIPHMOIHJJKHOEFEKFBJFFKBLPFOEBIOCNKDJPHNEKLJ
OMHPHNFCEDMJJDCLAODOIDJBJDFKPNJHKEPDCLFLNKCKIGEOCIGKHKCIL
BPIKNMFLGKKKNPDMPAIEAJEEINMFHJJBJNFEBFOEONDMKPFKEPCIGCIMG
MCICGJFMMLDHHMJMHPCOJMCEIEOPPFOEBKNPBLNOOLJAIANIPKONHDICL
MNNNNNEHCHDNOOEAGCFLHPHHJBAHFHADNKPFCMNLMKJIPFNLAHFHAHIKL
APBBBPAPBJCAEBFADNCKCAMFAHECHHCAONFFOKOGOLMHNLNFEDFDGBKHH
HHHHHHHPHHHPHPPPHPHPPHPPPHPPPPPPPPPHHHHPPHHHPHPHHHHHPHPHP

Result/s to follow:
LIVER & KIDNEY PANEL, SERUM

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: [email protected]

*179921875* Page 6 of 6

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