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General Urine Examination(GUE)

The urine should be tested as part of every general
medical examination and not just in patients with
known renal or urinary tract disease. The urine
specimen should be passed into a clean container
without additives. Testing should normally be
conducted as soon as possible, and if delayed more
than 2 hours the urine should be refrigerated (not
frozen) and returned to room temperature before
testing. A midstream specimen is essential for
microbiological assessment and desirable for
microscopic examination.
QUANTITY

Normal adults in temperate climates usually pass
between 750 and 2500mL of urine every 24 hours. The
minimum daily urine output compatible with normal
renal excretory function varies from person to person,
and also with other factors such as diet. Abnormally
low urine output (oliguria or anuria) implies that the
flow rate is below the minimum required to allow
excretion of the daily solute load.
COLOUR 
Urochrome and uroerythrin are pigments that contribute
to the natural yellow tinge of urine. Darkening occurs on
staining as a result of oxidation of urobilinogen to coloured
urobilin. The colour of urine is also heavily influenced by
the urinary flow rate: high flow leads to dilute urine and
hence a pale colour. Bile pigments in excess colour the
urine brown, with a characteristic yellow froth on shaking.
Small to moderate quantities of blood impart a smoky
appearance, with larger amounts leading to progressive
brown or, in the case of brisk bleeding, bright red
discoloration. Free haemoglobin from intravascular
haemolysis (e.g. in severe malaria - blackwater fever)
produces a darker red colour, verging on black in severe
cases. Myoglobin may appear in the urine after acute
muscle necrosis (rhabdomyolysis), causing a brown-red
discoloration.

Certain drugs discolour the urine - examples include
rifampicin (red), anthraquinone purgatives such as
senna (orange), nitrofurantoin (brown) and
methyldopa (grey). Urine is normally transparent
when freshly passed and still warm, but may be cloudy
if there are large numbers of red blood cells or
leukocytes, or if phosphates have precipitated in
significant amounts.
SPECIFIC GRAVITY AND
OSMOLALITY

These measurements yield similar information, and in the
absence of significant glycosuria are functions of the
urinary concentrations of sodium, chloride and urea. The
range of specific gravity is 1.001-1.035, which is equivalent to
50-1350mOsmol/kg water. The presence of renal
insufficiency leads to a reduction in the range of osmolality
that the kidneys can generate, and in advanced renal
disease the osmolality becomes relatively fixed at about
300mOsmol/kg water - close to that of the glomerular
filtrate . This is termed isosthenuria, and predisposes the
patient to sodium and water overload if intake is high, and
to salt and water depletion if intake is low.
pH

This varies from 4 to 8 and can be measured crudely
using paper strips impregnated with an indicator. If
more accurate measurements are needed, as in
suspected renal tubular acidosis, a pH electrode is
used. Most people pass acid urine most of the time,
exceptions being some 1)vegetarians, 2)certain types of
renal tubular acidosis, 3)rapid water diuresis,
4)metabolic alkalosis, and 5)urine infection with urea-
splitting organisms.
GLUCOSE 
Glucose oxidase-impregnated dipsticks provide a quick and
semiquantitative test for glucose in urine. By far the
commonest causes of abnormal glycosuria are 1)elevation
of the plasma glucose to a point where the tubular
reabsorptive capacity for glucose is exceeded (usually seen
in people with diabetes), and 2)during pregnancy, in which
glycosuria occurs with normal plasma glucose
concentrations. Very rarely,3) tubular transport defects may
be associated with glycosuria at normal plasma glucose
concentrations, and more frequently - but less predictably -
patients with 4)acquired chronic renal diseases may exhibit
glycosuria at normal plasma glucose concentrations.
Collectively these disorders are termed renal glycosuria.
PROTEIN

The normal daily urine protein output is <150mg. Dipsticks
reactive to urine albumin provide a simple semiquantitative
test. They are sensitive to 200-300mg protein/L . The urinary
protein excretion rate generally rises in the upright posture
and with activity, and in some normal individuals this may
lead to apparently abnormal proteinuria on spot urine
specimens in ambulant patients, and even in 24-hour urine
collections (orthostatic proteinuria). Measurement of protein
in an early-morning urine, however, reveals no protein, and
this serves to distinguish abnormal proteinuria from
orthostatic proteinuria. A further refinement is the specific
measurement of urine albumin, which is increasingly used
and should be <20mg/day. Albumin excretion in the range 20-
200mg/day is termed microalbuminuria. Although this range
is frequently too low to be detectable by stick testing, it is an
important finding, particularly in diabetics, in whom it
predicts the later onset of overt diabetic nephropathy.

The albumin:creatinine ratio is a useful surrogate
marker for proteinuria and is used instead of the 24
hour urine collection for quantification of protein
excretion. The diagnostic implications of proteinuria
depend greatly on its magnitude . Heavy proteinuria
(>1.5g/24h) is nearly always glomerular in origin and
albumin predominates over larger proteins such as
globulins. Other proteins, rarely measured, arise from
the renal tubules and include Tamm-Horsfall protein,
retinol-binding protein and nephrocalcin, the latter
helping to prevent the formation of urinary stones.
MICROBIOLOGICAL EXAMINATION
OF THE URINE

Midstream urine specimens are normally satisfactory,
but are always contaminated to a certain extent during
passage to the exterior. Extensive studies have shown
that the finding of more than 105 bacteria per mL in a
midstream specimen is usually associated with active
urinary infection, especially when accompanied by
leukocytes. Occasionally urine is taken directly from
the bladder for diagnostic purposes. It should be
sterile.

THANK YOU
FOR LISTENING

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GUE.pptx

  • 1.
  • 2. General Urine Examination(GUE)  The urine should be tested as part of every general medical examination and not just in patients with known renal or urinary tract disease. The urine specimen should be passed into a clean container without additives. Testing should normally be conducted as soon as possible, and if delayed more than 2 hours the urine should be refrigerated (not frozen) and returned to room temperature before testing. A midstream specimen is essential for microbiological assessment and desirable for microscopic examination.
  • 3. QUANTITY  Normal adults in temperate climates usually pass between 750 and 2500mL of urine every 24 hours. The minimum daily urine output compatible with normal renal excretory function varies from person to person, and also with other factors such as diet. Abnormally low urine output (oliguria or anuria) implies that the flow rate is below the minimum required to allow excretion of the daily solute load.
  • 4. COLOUR  Urochrome and uroerythrin are pigments that contribute to the natural yellow tinge of urine. Darkening occurs on staining as a result of oxidation of urobilinogen to coloured urobilin. The colour of urine is also heavily influenced by the urinary flow rate: high flow leads to dilute urine and hence a pale colour. Bile pigments in excess colour the urine brown, with a characteristic yellow froth on shaking. Small to moderate quantities of blood impart a smoky appearance, with larger amounts leading to progressive brown or, in the case of brisk bleeding, bright red discoloration. Free haemoglobin from intravascular haemolysis (e.g. in severe malaria - blackwater fever) produces a darker red colour, verging on black in severe cases. Myoglobin may appear in the urine after acute muscle necrosis (rhabdomyolysis), causing a brown-red discoloration.
  • 5.  Certain drugs discolour the urine - examples include rifampicin (red), anthraquinone purgatives such as senna (orange), nitrofurantoin (brown) and methyldopa (grey). Urine is normally transparent when freshly passed and still warm, but may be cloudy if there are large numbers of red blood cells or leukocytes, or if phosphates have precipitated in significant amounts.
  • 6. SPECIFIC GRAVITY AND OSMOLALITY  These measurements yield similar information, and in the absence of significant glycosuria are functions of the urinary concentrations of sodium, chloride and urea. The range of specific gravity is 1.001-1.035, which is equivalent to 50-1350mOsmol/kg water. The presence of renal insufficiency leads to a reduction in the range of osmolality that the kidneys can generate, and in advanced renal disease the osmolality becomes relatively fixed at about 300mOsmol/kg water - close to that of the glomerular filtrate . This is termed isosthenuria, and predisposes the patient to sodium and water overload if intake is high, and to salt and water depletion if intake is low.
  • 7. pH  This varies from 4 to 8 and can be measured crudely using paper strips impregnated with an indicator. If more accurate measurements are needed, as in suspected renal tubular acidosis, a pH electrode is used. Most people pass acid urine most of the time, exceptions being some 1)vegetarians, 2)certain types of renal tubular acidosis, 3)rapid water diuresis, 4)metabolic alkalosis, and 5)urine infection with urea- splitting organisms.
  • 8. GLUCOSE  Glucose oxidase-impregnated dipsticks provide a quick and semiquantitative test for glucose in urine. By far the commonest causes of abnormal glycosuria are 1)elevation of the plasma glucose to a point where the tubular reabsorptive capacity for glucose is exceeded (usually seen in people with diabetes), and 2)during pregnancy, in which glycosuria occurs with normal plasma glucose concentrations. Very rarely,3) tubular transport defects may be associated with glycosuria at normal plasma glucose concentrations, and more frequently - but less predictably - patients with 4)acquired chronic renal diseases may exhibit glycosuria at normal plasma glucose concentrations. Collectively these disorders are termed renal glycosuria.
  • 9. PROTEIN  The normal daily urine protein output is <150mg. Dipsticks reactive to urine albumin provide a simple semiquantitative test. They are sensitive to 200-300mg protein/L . The urinary protein excretion rate generally rises in the upright posture and with activity, and in some normal individuals this may lead to apparently abnormal proteinuria on spot urine specimens in ambulant patients, and even in 24-hour urine collections (orthostatic proteinuria). Measurement of protein in an early-morning urine, however, reveals no protein, and this serves to distinguish abnormal proteinuria from orthostatic proteinuria. A further refinement is the specific measurement of urine albumin, which is increasingly used and should be <20mg/day. Albumin excretion in the range 20- 200mg/day is termed microalbuminuria. Although this range is frequently too low to be detectable by stick testing, it is an important finding, particularly in diabetics, in whom it predicts the later onset of overt diabetic nephropathy.
  • 10.  The albumin:creatinine ratio is a useful surrogate marker for proteinuria and is used instead of the 24 hour urine collection for quantification of protein excretion. The diagnostic implications of proteinuria depend greatly on its magnitude . Heavy proteinuria (>1.5g/24h) is nearly always glomerular in origin and albumin predominates over larger proteins such as globulins. Other proteins, rarely measured, arise from the renal tubules and include Tamm-Horsfall protein, retinol-binding protein and nephrocalcin, the latter helping to prevent the formation of urinary stones.
  • 11.
  • 12. MICROBIOLOGICAL EXAMINATION OF THE URINE  Midstream urine specimens are normally satisfactory, but are always contaminated to a certain extent during passage to the exterior. Extensive studies have shown that the finding of more than 105 bacteria per mL in a midstream specimen is usually associated with active urinary infection, especially when accompanied by leukocytes. Occasionally urine is taken directly from the bladder for diagnostic purposes. It should be sterile.