Patient Name : JYOTI Registered On : 25/May/2024 10:57:16
Age/Gender : 36 Y 0 M 0 D/F Collected : 25/May/2024 10:59:28
UHID/MR NO : UKNH.0001956430 Received : 25/May/2024 19:10:34
Visit ID : UK125-2425-000162 Reported : 25/May/2024 20:41:35
Ref Doctor : AKHILESH BAHUGUNA Status : Final Report
Contract By : PHC PASHCHIMI
DEPARTMENT OF HAEMATOLOGY
Test Name Result Unit Bio. Ref. Interval Method
Blood Group (ABO & Rh typing) ** , Blood
Blood Group A ERYTHROCYTE
MAGNETIZED
TECHNOLOGY / TUBE
AGGLUTINA
Rh ( Anti-D) POSITIVE ERYTHROCYTE
MAGNETIZED
TECHNOLOGY / TUBE
AGGLUTINA
RAPID PLASMA REAGIN ** NON REACTIVE FLOCCULATION TEST
Sample:Serum
Interpretation:
Note: Titers of 1:8 and above are significant
Comments:
This is a screening test for syphillis which is useful for following the progression of disease and resonse to therapy. Rising titers are
of immense value in confirming the diagnosis. Biological false positive reactions exhiit low titers and are seen in conditions like Viral
fevers, Mycoplasma infection, Chlamydia infection, Malaria, Immunizations, Pregnancy, Autoimmune disorders & past history of
treponemal infection, It is advisable to confirm the diagnosis by tests such as TPHA & FTA-ABS.
Complete Blood Count (CBC) **
TLC (WBC) 8,780.00 /Cu mm 4000-10000 ELECTRONIC IMPEDANCE
RBC Count
RBC Count 3.60 Mill./cu mm 3.7-5.0 ELECTRONIC IMPEDANCE
Haemoglobin 10.60 g/dl 1 Day- 14.5-22.5 g/dl
1 Wk- 13.5-19.5 g/dl
1 Mo- 10.0-18.0 g/dl
3-6 Mo- 9.5-13.5 g/dl
0.5-2 Yr- 10.5-13.5
g/dl
2-6 Yr- 11.5-15.5 g/dl
6-12 Yr- 11.5-15.5 g/dl
12-18 Yr 13.0-16.0
g/dl
Male- 13.5-17.5 g/dl
Female- 12.0-15.5 g/dl
Page 1 of 6
Patient Name : JYOTI Registered On : 25/May/2024 10:57:16
Age/Gender : 36 Y 0 M 0 D/F Collected : 25/May/2024 10:59:28
UHID/MR NO : UKNH.0001956430 Received : 25/May/2024 19:10:34
Visit ID : UK125-2425-000162 Reported : 25/May/2024 20:41:35
Ref Doctor : AKHILESH BAHUGUNA Status : Final Report
Contract By : PHC PASHCHIMI
DEPARTMENT OF HAEMATOLOGY
Test Name Result Unit Bio. Ref. Interval Method
Blood Indices (MCV, MCH, MCHC)
MCV 97.00 fl 80-100 CALCULATED PARAMETER
MCH 29.60 pg 27-32 CALCULATED PARAMETER
MCHC 30.50 % 30-38 CALCULATED PARAMETER
RDW-CV 14.20 % 11-16 ELECTRONIC IMPEDANCE
RDW-SD 52.60 fL 35-60 ELECTRONIC IMPEDANCE
Platelet count
Platelet Count 1.10 LACS/cu mm 1.5-4.0 ELECTRONIC
IMPEDANCE/MICROSCOPIC
PDW (Platelet Distribution width) 21.40 fL 9-17 ELECTRONIC IMPEDANCE
P-LCR (Platelet Large Cell Ratio) 51.90 % 35-60 ELECTRONIC IMPEDANCE
PCT (Platelet Hematocrit) 0.20 % 0.108-0.282 ELECTRONIC IMPEDANCE
MPV (Mean Platelet Volume) 13.20 fL 6.5-12.0 ELECTRONIC IMPEDANCE
DLC
Lymphocytes 17.00 % 20-40 ELECTRONIC IMPEDANCE
MXD % 9.00
Polymorphs (Neutrophils ) 74.00 % 40-80 ELECTRONIC IMPEDANCE
ESR
Observed 20.00 MM/1H 10-19 Yr 8.0
20-29 Yr 10.8
30-39 Yr 10.4
40-49 Yr 13.6
50-59 Yr 14.2
60-69 Yr 16.0
70-79 Yr 16.5
80-91 Yr 15.8
Pregnancy
Early gestation - 48 (62
if anaemic)
Leter gestation - 70 (95
if anaemic)
Corrected -- Mm for 1st hr. < 20
PCV (HCT) 34.70 % 40-54
CHANDAN DIAGNOSTIC CENTRE
Add:Armelia,1St Floor,56New Road, M.K.P Chowk,Dehradun
CIN : U85110DL2003PLC308206 SIN No:64580163
Page 2 of 6
Patient Name : JYOTI Registered On : 25/May/2024 10:57:16
Age/Gender : 36 Y 0 M 0 D/F Collected : 25/May/2024 10:59:28
UHID/MR NO : UKNH.0001956430 Received : 25/May/2024 19:10:34
Visit ID : UK125-2425-000162 Reported : 25/May/2024 21:09:36
Ref Doctor : AKHILESH BAHUGUNA Status : Final Report
Contract By : PHC PASHCHIMI
DEPARTMENT OF BIOCHEMISTRY
Test Name Result Unit Bio. Ref. Interval Method
LIVER FUNCTION TEST(LFT) ** , Serum
Bilirubin (Total) 0.47 mg/dl 0.3-1.2 JENDRASSIK & GROF
Bilirubin (Direct) 0.14 mg/dl < 0.30 JENDRASSIK & GROF
Bilirubin (Indirect) 0.33 mg/dl < 0.8 JENDRASSIK & GROF
SGOT / Aspartate Aminotransferase (AST) 27.19 U/L < 35 IFCC WITHOUT P5P
SGPT / Alanine Aminotransferase (ALT) 29.35 U/L < 40 IFCC WITHOUT P5P
Alkaline Phosphatase (Total) 81.61 U/L 42.0-165.0 IFCC METHOD
Protein 5.56 gm/dl 6.2-8.0 BIURET
Albumin 3.60 gm/dl 3.4-5.4 B.C.G.
Globulin 1.96 gm/dl 1.8-3.6 CALCULATED
A:G Ratio 1.84 1.1-2.0 CALCULATED
RENAL FUNCTION TEST ( DEHRADUN ) ** , Serum
Potassium 4.35 m Mol /L 3.5-5.3 ISE
Sodium 141.00 m Mol /L 135-148 ISE
Uric Acid 3.35 mg/dl 2.5-6.0 URICASE
Urea 25.14 mg/dL 15-45 UV-GLDH KINETIC
Calcium 8.83 mg/dl 8.5-10.2 mgdl ARSENAZO III
spot urine- 0.50- 35.70
mg/dl
Creatinine 0.85 mg/dl 0.5-1.20 MODIFIED JAFFES
CHANDAN DIAGNOSTIC CENTRE
Add:Armelia,1St Floor,56New Road, M.K.P Chowk,Dehradun
CIN : U85110DL2003PLC308206 SIN No:64580163
Page 3 of 6
Patient Name : JYOTI Registered On : 25/May/2024 10:57:16
Age/Gender : 36 Y 0 M 0 D/F Collected : 25/May/2024 10:59:28
UHID/MR NO : UKNH.0001956430 Received : 25/May/2024 19:10:34
Visit ID : UK125-2425-000162 Reported : 25/May/2024 20:01:13
Ref Doctor : AKHILESH BAHUGUNA Status : Final Report
Contract By : PHC PASHCHIMI
DEPARTMENT OF IMMUNOLOGY
Test Name Result Unit Bio. Ref. Interval Method
HBsAg Australia Antigen ELISA) ** 0.23 AU/ml <1.0 Non Reactive CLIA
Sample:Serum >1.0 Reactive
Interpretation:
This is the initial detectable marker found in serum in the incubation period of HBV infection. The titer of HbsAg peaks at or
shortly after the on set of elevated serum enzymes. The clinical improvement and decrease in enzyme concentration is paralleled by
fall in HbsAg titers and subsequently disappearance. The duration of HbsAg Reactive is variable depending upon the clinical
course of disease. HbsAg is detected in serum a month after the exposure, peaking in the preicteric phase and disappearing 1 - 13
weeks after the onset of enzyme abnormalities. Persistence of HbsAg after the complete clinical recovery indicates a carrier state.
Vaccination against HBV does not cause HbsAg Reactive. Causes of HbsAg Reactive are acute HBV infection and reactivation of
chronic HBV infection. Results with value <0.178 will be given as Non Reactive.
HCV-Total antibodies to Hepatitis C Virus 0.300 AU/ml <1.0 Non-reactive CLIA
(Anti HCV) ** >1.0 Reactive
Sample:Serum
Interpretation:
The hepatitis C virus HCV is now the cause of 90% post transfusion hepatitis it is also found in drug addicts and also contributes
to sporadic acute viral hepatitis –HCV is a RNA flavi virus and the incubation period may be short (1-4 weeks ) or long ( 6-12
weeks . chronicity of infection is reported in > 10 % . The frequency of post transfusion hepatitis can be definitely reduced with
help of serological assays available for HCV. Results with value <0.333 will be given as Non Reactive.
Note: - HCV RNA test by using PCR Assay is helpful as an additional or confirmatory test.
HIV 1+2 (AIDS) ** 0.510 AU/ml <1.0 Non-Reactive CLIA
Sample:Serum >1.0 Reactive
Interpretation:
1)A Non Reactive result implies that no Anti HIV – II antibodies have been detected in the sample by this method. This means that
either the patient has not been exposed to HIV-I or HIV-II infection or the sample has been tested during the “WINDOW
PHASE” (before the development of detectable levels of antibodies)
2)A Reactive result suggests the possibilities of HIV-I and / or HIV-II infection. However these results must be verified by a
confirmatory test (IFA / WESTERN BLOT I-II) before pronouncing the patient REACTIVEfor HIV-I and / r HIV-II infection.
Results with value <0.293 will be given as NON REACTIVE.
Page 4 of 6
Patient Name : JYOTI Registered On : 25/May/2024 10:57:16
Age/Gender : 36 Y 0 M 0 D/F Collected : 25/May/2024 10:59:28
UHID/MR NO : UKNH.0001956430 Received : 25/May/2024 19:10:34
Visit ID : UK125-2425-000162 Reported : 25/May/2024 20:01:13
Ref Doctor : AKHILESH BAHUGUNA Status : Final Report
Contract By : PHC PASHCHIMI
DEPARTMENT OF IMMUNOLOGY
Test Name Result Unit Bio. Ref. Interval Method
CHANDAN DIAGNOSTIC CENTRE
Add:Armelia,1St Floor,56New Road, M.K.P Chowk,Dehradun
CIN : U85110DL2003PLC308206 SIN No:64580163
Page 5 of 6
Patient Name : JYOTI Registered On : 25/May/2024 10:57:16
Age/Gender : 36 Y 0 M 0 D/F Collected : 25/May/2024 10:59:28
UHID/MR NO : UKNH.0001956430 Received : 25/May/2024 19:10:34
Visit ID : UK125-2425-000162 Reported : 26/May/2024 17:58:21
Ref Doctor : AKHILESH BAHUGUNA Status : Final Report
Contract By : PHC PASHCHIMI
DEPARTMENT OF IMMUNOLOGY
Test Name Result Unit Bio. Ref. Interval Method
T3, T4, TSH **
T3, Total (tri-iodothyronine) 175.32 ng/dl 84.61–201.7 CLIA
T4, Total (Thyroxine) 12.30 ug/dl 3.2-12.6 CLIA
TSH (Thyroid Stimulating Hormone) 3.310 µIU/mL 0.27 - 5.5 CLIA
Interpretation:
0.3-4.5 µIU/mL First Trimester
0.5-4.6 µIU/mL Second Trimester
0.8-5.2 µIU/mL Third Trimester
0.5-8.9 µIU/mL Adults 55-87 Years
0.7-27 µIU/mL Premature 28-36 Week
2.3-13.2 µIU/mL Cord Blood > 37Week
0.7-6.4 µIU/mL Child(21 wk - 20 Yrs.)
1.0-3.9 µIU/mL Child 0-4 Days
1.7-9.1 µIU/mL Child 2-20 Week
1) Patients having low T3 and T4 levels but high TSH levels suffer from primary hypothyroidism, cretinism, juvenile myxedema or
autoimmune disorders.
2) Patients having high T3 and T4 levels but low TSH levels suffer from Grave's disease, toxic adenoma or sub-acute thyroiditis.
3) Patients having either low or normal T3 and T4 levels but low TSH values suffer from iodine deficiency or secondary
hypothyroidism.
4) Patients having high T3 and T4 levels but normal TSH levels may suffer from toxic multinodular goiter. This condition is mostly a
symptomatic and may cause transient hyperthyroidism but no persistent symptoms.
5) Patients with high or normal T3 and T4 levels and low or normal TSH levels suffer either from T3 toxicosis or T4 toxicosis
respectively.
6) In patients with non thyroidal illness abnormal test results are not necessarily indicative of thyroidism but may be due to adaptation
to the catabolic state and may revert to normal when the patient recovers.
7) There are many drugs for eg. Glucocorticoids, Dopamine, Lithium, Iodides, Oral radiographic dyes, etc. which may affect the
thyroid function tests.
8) Generally when total T3 and total T4 results are indecisive then Free T3 and Free T4 tests are recommended for further confirmation
along with TSH levels.
*** End Of Report ***
(**) Test Performed at CHANDAN DIAGNOSTIC CENTRE,Armelia,1st Floor,56New Road, M.K.P Chowk,Dehradun
Result/s to Follow:
Glucose Random
CHANDAN DIAGNOSTIC CENTRE
Add:Armelia,1St Floor,56New Road, M.K.P Chowk,Dehradun
CIN : U85110DL2003PLC308206 SIN No:64580163
Page 6 of 6
