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Routine Examination Urine
Investigation Result Units Biological Reference Interval

PHYSICAL EXAMINATION
Quantity 20 5 - 30
Colour Pale Yellow Pale Yellow
Appearance Slightly Hazy ml Clear
CHEMICAL EXAMINATION
pH 5.0 . 4.6 - 8
Specific gravity 1.015 . 1.003 - 1.035
Glucose Absent . Absent
Urine Protein (Albumin) Absent . Absent
Urine Ketones (Acetone) Absent . Absent
Blood Absent . Absent
Nitrite Absent . Absent
Urobilinogen Absent . Normal
Bilirubin Absent . Absent
Leukocytes Present(++) . Absent
MICROSCOPIC EXAMINATION
Pus Cells 35-40 /HPF 0 - 5
Epithelial Cells 18-20 /HPF 2 - 10
Red Blood Cells Occasionally /HPF
Crystals Absent Absent
casts Absent /HPF Absent
Dysmorphic RBCs Absent /HPF Absent
Yeast Absent Absent
Bacteria Absent Absent
Amorphous Material Absent Absent
Others Absent
Advice Please correlate clinically -

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Thyroid Function Test (TFT)
Investigation Result Units Biological Reference Interval

T3 (Triiodothyronine) 1.83 ng/mL 0.8 - 2.0
• Sample Type : Serum.
• Method : ECLIA.
T4 (Thyroxine) 10.39 ug/dl 5.1 - 14.1
• Sample Type : Serum.
• Method : ECLIA.
ULTRA Thyroid Stimulating Hormone (TSH) 3.81 uIU/mL 0.27 - 4.2
Frist trimester: 0.3- 4.5
Second trimester : 0.5 -4.6
Third trimester : 0.8 -5.2
• Sample Type : Serum.
• Method : ECLIA.

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) Recommended test for T3 and T4 is unbound fraction or free levels as it is metabolically active. --3) Physiological rise in Total T3 / T4 levels is seen in pregnancy and in patients on steroid therapy. --Clinical Use : --• Primary Hypothyroidism --• Hyperthyroidism --• Hypothalamic – Pituitary hypothyroidism --• Inappropriate TSH secretion --• Nonthyroidal illness --• Autoimmune thyroid disease --• Pregnancy associated thyroid disorders. --• References : --- Henry’s Clinical Diagnosis and Management, 23rd edition. ---Tietz Fundamentals of Clinical Chemistry and Molecular Diagnosis, 7th edition. --•Disclaimer: --1) The above result relate only to the specimens received and tested in laboratory and should be always correlate with clinical findings and other laboratory markers. --2) Improper specimen collection, handling,storage and transportation may result in false negative/Positive results.

--End Of Report--
P011B000403104
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Glucose (Blood Sugar), Random
Investigation Result Units Biological Reference Interval

Glucose (Blood Sugar), Random 71.5 mg/dl 70 - 140
• Sample Type : Fluoride plasma.
• Method : Hexokinase.


Interpretation -

The American Diabetes Association’s (ADA’s) Standards of Medical Care in Diabetes 2022
Criteria for the Screening and Diagnosis of Prediabetes and Diabetes
Test Prediabetes Diabetes
HbA1c 5.7–6.4% (39–47 mmol/mol)* 6.5% (48 mmol/mol)†
Fasting plasma glucose 100–125 mg/dL (5.6–6.9 mmol/L)* 126 mg/dL (7.0 mmol/L)†
2-hour plasma glucose during 75-g OGTT 140–199 mg/dL (7.8–11.0 mmol/L)* 200 mg/dL (11.1 mmol/L)†
Random plasma glucose — 200 mg/dL (11.1 mmol/L)‡

Adapted from Tables 2.2 and 2.5 in the complete 2022 Standards of Care.*
For all three tests, risk is continuous, extending below the lower limit of the range and becoming disproportionately greater at the higher end of the range.†
In the absence of unequivocal hyperglycemia, diagnosis requires two abnormal test results from the same sample or in two separate samples‡
Only diagnostic in a patient with classic symptoms of hyperglycemia or hyperglycemic crisis.