Complete Urinalysis: A. Physical Characteristics of Urine
Complete Urinalysis: A. Physical Characteristics of Urine
Complete Urinalysis: A. Physical Characteristics of Urine
2.
Pipette 1-2 drops of urine into the plastic chamber located on the top of the
refractometer. Be sure that the plastic is pressed firmly down in place on the
refractometer.
3.
Determine the specific gravity of the urine by looking through the
refractometer and determining the value on the scale on the left hand side. The
specific gravity value is where the light and dark intersect on the scale.
4.
b.
Urinometer - Is a weighted, bulb shaped device that has a specific gravity
scale on the stem end.
1.
Fill the cylinder with enough urine so that the urinometer will float in the urine
and not touch the bottom.
2.
Be careful not to drop the urinometer in the cylinder! Gently release it in order
not to break or burst the cylinder. It should NOT touch the sides or bottom of
cylinder.
3.
The specific gravity can be read on the scale on the stern of the urinometer at
the meniscus.
4.
The specific gravity of water is 1.000 with respect to temperature. The
urinometer can be checked periodically against this standard to ensure quality
control at that temperature.
(* For very precise and exacting measurements of specific gravity, corrections
should be made +/- .001 for each 3 C above or below 25 C. Add .001 if above
25 C, subtract .001 if below 25C.
B. CHEMICAL ANALYSIS
For routine chemical analysis of urine there are several brands of chemical test
strips (dip sticks) that are commercially available. These urinalysis test strips have
small test patches impregnated with various chemicals in order to detect the
presence or absence of certain substances. Qualitative and/or quantitative results
can be obtained depending on the particular test.
1. Take a specimen cup from the lab to the bathroom; void into the cup and
return to the lab.
2. Briefly (one second or less) dip the test strip into the urine. Make sure that all
test
squares are immersed.
3. Draw the edge of the strip along the rim of the specimen cup to remove
excess urine.
4. After the appropriate times (as indicated on the vial of strips) read the tests
by
comparing to the color chart on the edge of the vial.
PLEASE DO NOT TOUCH THE TEST STRIP TO THE COLOR CHART. IF
YOU DO SO
ACCIDENTALLY, IMMEDIATELY WIPE THE VIAL WITH DISINFECTANT.
5. NOTE: For convenience, all values on the strip may be read between 1 and 2
minutes after immersion. The colors are stable for up to 120 seconds after
immersion. Color changes that occur after 2 minutes from immersion are not
of diagnostic value. Color changes that occur only along the edge of the test
area should be ignored.
6. Results are obtained by direct visual comparison with the color scale printed
on the vial
label. No calculations are necessary. Record your results.
7. NOTE: For such a test to be considered clinically acceptable for a valid
diagnosis, careful quality control should be maintained, i. e. expiration dates
respected, environmental conditions stabilized, etc. In a teaching lab these
conditions are not met. You can learn the procedure and see some variable
results among the class members, but do not base any clinical assumptions
on the results obtained in this lab. If you have any
reason to suspect a clinical problem, go to a licensed medical laboratory for
a urinalysis.
ABNORMAL
CONSTITUENT ASSOCIATED CAUSES:
:
Protein
(albumin)
Glucose
Ketones
Ketone bodies such as acetoacetic acid, betahydroxybutyric acid, and acetone can appear in
urine in small amounts. These intermediate byproducts are associated with the breakdown of
fat. Causes: diabetes mellitus, starvation, diarrhea
Bilirubin
C. MICROSCOPIC EXAMINATION
Examination of urine sediment may reveal the presence of different types of cells
such as epithelial cells, leukocytes, erythrocytes, or renal cells. Different types of
crystals, yeast, bacteria, or casts may also be present. Casts are cylindrical
structures created by protein precipitation in the renal tubules.
Procedure:
1. Transfer urine sample to a conical centrifuge tube.
2. Centrifuge your sample at a moderate speed for 5 minutes. BE SURE
TO
BALANCE CENTRIFUGE.
3. Discard the supernatant (fluid off the top) by quickly pouring off fluid.
4. Tap tube with index finger to mix sediment with remaining fluid.
5. Make a wet mount of sample by transferring 1 drop of material to a slide
and
covering with a coverslip.
6. Examine the sample under the microscope under low and high power.
7. Identify what you see by comparing to charts. Draw a few of your
observations.
Urine Analysis
Urinanalysis
Parameter
Normal Values
Aspect
Clear
Colour
Pale yellow-yellow
Atypical
Odour
Acid (5,5-6)
Reaction (pH)
No
Acid
1010-1030
Specific gravity
Negative
Leukocyte esterase
Negative
Nitrites
Negative
Glucose
Negative
Ketones
Negative
Hemoglobin
Negative
Bilirubin
Urobilinogen
0-4 p.v.f.
Epithelial cells
0-4 p.v.f.
Erythrocytes
0-4 p.v.f.
Pus cells
0-2 hyaline
Casts
Germs- fungi
None
No abnormal crystals present
Crystals
A few
Amorphous salts
No, some
Mucus
None
Lipid droplets
Return to Table of Contents
Normal values
pH
4,6-8,0
Specific gravity
1003-1030
Sodium
3-6 g/24h
Potassium
2-3,5 g/24h
Chlorine
6-9 g/24h
Calcium
0,01-0,30 g/24h
Phosphorus
0,8-2,0 g/24h
Urea
20-25 g/24h
Uric acid
400-800 mg/24h
Creatinine
1-1,6 g/24h
Bilirubin
70 g/kg BW
Urobilinogen
0,05-3,5 mg/24h