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All samples should be midstream and collected in a clean sterile
container. Suprapubic aspiration or fresh catheter samples are
ideal, but not always practical.
Physical examination
Color The color of
the urine can vary greatly. Normal urine varies from colorless
to dark yellow. Various factors can affect urine color.
|
Common
Causes of Urine Discoloration |
|
Color |
Pathologic causes |
Food and drug causes |
| Brown |
Bile pigments,myoglobin,
fava beans |
Levodopa, metronidazole,
nitrofurantoin, some antimalarial agents |
| Brownish-black |
Bile pigments, melanin,
methemoglobin |
Cascara, levodopa,
methyldopa, senna |
| Green or blue |
Pseudomonal UTI,
biliverdin |
Amitriptyline, indigo
carmine, IV cimetidine,
IV promethazine, methylene blue, triamterene |
| Orange |
Bile pigments |
Phenothiazines,
phenazopyridine |
| Red |
Hematuria,
hemoglobinuria, myoglobinuria, porphyria |
Beets, blackberries,
rhubarb
Phenolphthalein, rifampicin |
| Yellow |
Concentrated urine
(orange to gold in dehydration) |
Carrots
Cascara |
Turbidity Cloudy urine may be
due to excess phosphate crystals precipitating in alkaline
urine, which is of no significance. It can however also be seen
in pyuria secondary to infection, chyluria (usually secondary to
filariasis), hyperuricosuria secondary to a diet high in purine-rich
foods, lipiduria and hyperoxaluria.
Odor The normal odor is
described as urinoid. In concentrated specimens this can be
strong but does not imply infection which has a more pungent
smell. Alkaline fermentation causes an ammoniacal smell, and
patients with diabetic ketoacidosis produce a urine that may
have a sweet or fruity odor. Other causes of abnormal odors are
cystine decomposition (a sulphuric smell),
gastrointestinal-bladder fistulae (a fecal smell), medications (e.g.vitamin
B6), and diet (e.g. asparagus).
Dipstick Analysis Immerse the dipstick
completely in fresh urine and withdraw immediately, drawing the
edge along rim of container to remove excess. Hold the dipstick
horizontally before reading.
Specific Gravity SG <1.008 is
dilute and >1.020 is concentrated.
Increased specific gravity is seen in conditions causing
dehydration, glycosuria, renal artery stenosis, heart failure
(secondary to decreased blood flow to the kidneys),
inappropriate antidiuretic hormone secretion and proteinuria.
Some dipsticks give falsely high readings in the presence of
dextran solutions and IV radiopaque dyes, but this varies, so
check the manufacturer's leaflet9
Decreased specific gravity is seen in excessive fluid intake,
renal failure, pyelonephritis, and central and nephrogenic
diabetes insipidus. False low readings are associated with
alkaline urine (e.g. high-citrate diet).
pH The range is
4.5 to 8, but urine is commonly acidic (i.e. 5.5-6.5) due to
metabolic activity.
Acidic urine (low pH) may be caused by diet (e.g. acidic
fruits such as cranberries). Urine pH generally reflects the
blood pH but in renal tubular acidosis (RTA) this is not the
case. In type 1 RTA (distal) the urine is acidic but the blood
alkaline. in type 2 (proximal) the urine is initially alkaline
but becomes more acidic as the disease progresses. Acidic urine
may be associated with uric acid calculi.
Alkaline urine (high pH) is seen in the initial stages of
type 2 RTA and also with infection with urease-splitting
organisms. Alkaline urine may be associated with the formation
of stag-horn calculi.
Hematuria Dipstick
testing for hematuria is based on the peroxidase activity of
erythrocytes. However, hemoglobin and myoglobin will also
catalyze this reaction. False positives are also seen in
dehydration and menstruation.
False negatives are seen in patients taking captopril and
vitamin C, proteinuria, elevated specific gravity, pH less than
5.1, and baceturia.
Dipstick testing for hematuria is therefore at best a
screening tool which needs the support of microscopy to make a
definitive diagnosis.
The causes of hematuria can be divided into those occurring
at the glomerular level, renal (i.e. non-glomerular) and
urological causes. Glomerular hematuria is typically associated
with erythrocyte cases, dysmorphic red blood cells and
significant proteinuria, although 20% of patients present with
hematuria alone. Renal hematuria is also associated with
significant proteinuria, but there are no associated dysmorphic
RBCs or erythrocyte casts. Urologic hematuria is distinguished
from other etiologies by the absence of proteinuria, dysmorphic
RBCs, and erythrocyte casts. Exercise-induced hematuria is a
benign, relatively common condition often is associated with
long-distance running. Results of repeat urinalysis after 48 to
72 hours should be negative.
|
Causes of
Hematuria |
|
Glomerular Causes |
| Familial causes |
Fabry's disease |
Hereditary nephritis
(Alport's syndrome) |
| Primary
glomerulonephritis |
Focal segmental
glomerulonephritis |
IgA nephropathy (Berger's
disease) |
| Nail-patella syndrome |
Thin basement-membrane
disease |
Goodpasture's disease |
| Henoch-Schönlein purpura |
Mesangioproliferative
glomerulonephritis |
Postinfectious
glomerulonephritis |
| Rapidly progressive
glomerulonephritis |
Secondary
glomerulonephritis |
Hemolytic-uremic syndrome |
| Systemic lupus nephritis |
Thrombotic
thrombocytopenic purpura |
Vasculitis |
|
Renal
Causes |
| Arteriovenous
malformation |
Hypercalciuria |
Hyperuricosuria |
| Loin pain-hematuria
syndrome |
Malignant hypertension |
Medullary sponge kidney |
| Metabolic Causes |
Papillary necrosis |
Polycystic kidney disease |
| Renal artery embolism |
Renal vein thrombosis |
Sickle cell disease or
trait |
| Tubulointerstitial causes |
Vascular
causes |
|
Urologic
Causes |
| Benign prostatic
hyperplasia |
Cancer (kidney, ureteral,
bladder, prostate, and urethral |
Cystitis/pyelonephritis |
| Nephrolithiasis |
Prostatitis |
Tuberculosis |
| Schistosoma hematobium
infection |
Drugs (e.g., heparin,
warfarin, NSAIDs,cyclophosphamide) |
Trauma (e.g. running,
catheters,
contact sports) |
Proteinuria Normal
urinary proteins include serum globulins, albumin, and proteins
secreted by the nephron. Proteinuria is defined as
albumin:creatinine ratio >30mg/mmol or albumin concentration
>200mg/l. The loss of up to 150 mg of protein per day is normal.
This may be expressed as less than 4 mg per hour per square
meter of body surface area. Clinical proteinuria is indicated at
greater that 0.5g or protein per day (greater or equal to 0.3g/L
on a test strip)
Most dipstick tests will pick up albumin but may not detect
low concentrations of Bence-Jones protein or gamma-globulins.
Bence-Jones protein can be detected by a specific antibody test
on a mid-stream sample, whilst urine gamma-globulins can be
detected by urine electrophoresis.
Proteinuria may be transient or persistent. Transient
proteinuria is usually due to temporary changes in glomerular
hemodynamics, and follows a benign course. Orthostatic
proteinuria is a subset of this category, in which the
phenomenon is seen after prolonged standing. It is confirmed by
obtaining a negative result after eight hours of lying flat.
The causes of persistent proteinuria may be divided into
glomerular, tubular and overflow. The commonest is glomerular
proteinuria, in which albumin is the primary urine protein.
Tubular protein is caused by malfunctioning tubule cells which
are unable to reabsorb normally filtered protein. Low-molecular
weight proteins predominate in this condition. Overflow
proteinuria is caused by low-molecular weight proteins
overwhelming the ability of the tubules to reabsorb filtered
proteins.
Persistent significant proteinuria detected by dipstick
requires further assessment with 24-hour urinary protein
excretion, urinary protein-creatinine ratio, microscopic
examination of the urinary sediment, urinary protein
electrophoresis, and assessment of renal function.
|
Causes of
Proteinuria |
|
Transient proteinuria |
| Congestive heart failure |
Dehydration |
Emotional stress |
| Exercise |
Fever |
Orthostatic (postural)
proteinuria |
| Seizures |
Persistent proteinuria |
Primary glomerular causes |
| Focal segmental
glomerulonephritis |
IgA nephropathy (i.e.,
Berger's disease) |
IgM nephropathy |
| Membranoproliferative
glomerulonephritis |
Membranous nephropathy |
Minimal change disease |
|
Secondary glomerular causes |
| Alport's syndrome |
Amyloidosis |
Collagen vascular
diseases
(e.g., systemic lupus erythematosus) |
| Diabetes mellitus |
Drugs (e.g., NSAIDs,
penicillamine [Cuprimine],
gold, ACE inhibitors) |
Fabry's disease |
| Sickle cell disease |
Malignancies (e.g.,
lymphoma, solid tumors) |
Sarcoidosis |
|
Infections
(e.g., HIV, syphilis, hepatitis, post-streptococcal
infection) |
|
Tubular
causes |
| Aminoaciduria |
Drugs (e.g., NSAIDs,
antibiotics) |
Fanconi syndrome |
| Heavy metal ingestion |
Hypertensive
nephrosclerosis |
Interstitial nephritis |
|
Overflow
causes |
| Hemoglobinuria |
Multiple myeloma |
Myoglobinuria |
Glycosuria Glucose is
normally filtered by the glomerulus, but small amounts
(1.67mmol/L or 30mg/dL) do reach the urine. These amounts are
usually below the sensitivity level of dipsticks but may
occasionally produce a positive result. Causes of glycosuria
include diabetes mellitus, Cushing's syndrome, liver and
pancreatic disease, and Fanconi's syndrome.
The test is specific for glucose but false positive results
may be seen when high levels of ketones are present, and in
patients taking levodopa.
False negatives are seen where specific gravity is elevated,
in uricosuria and in patients taking ascorbic acid.
Ketones Ketones
are not normally found in urine. The reagent on a dipstick
detects acetic acid, but does not react to acetone or beta-hydroxybutyric
acid. A positive test is associated with uncontrolled diabetes,
pregnancy without diabetes, carbohydrate-free diets and
starvation.
False trace results may be seen in highly-pigmented urine and
in patients taking levodopa.
Delay in testing a sample may result in a false negative
result.
Nitrites This test
relies on the breakdown of urinary nitrates to nitrites, which
are not found in normal urine. Many gram-negative and some gram
positive bacteria are capable of producing this reaction, and a
positive test suggests their presence in significant numbers
(i.e. more than 10,000 per ml). A negative result does not rule
out a urinary tract infection.
The reagent is highly sensitive to air exposure, which may
cause a false positive response.
False negative results may be seen where bladder incubation
time is shortened (less than 4 hours), in the absence of dietary
nitrate, in the presence of nitrate-reductase negative organisms
(e.g. some Mycobateria strains), when urine specific gravity is
elevated, where pH is less than 6.0, and in the presence of
urobilinogen and urinary vitamin C.
Leucocytes This
relies on the reaction of leukocyte esterase produced by
neutrophils and a positive result suggests pyuria associated
with urinary tract infection. Isolated trace results may be of
questionable significance, but repeated ones should not be
ignored.
False positive results may be caused by contamination with
vaginal discharge.
Elevated urine glucose or oxalic acid concentrations may
reduce sensitivity, and this may also be seen in patients taking
tetracycline or cefalexin.
Bilirubin and Urobilinogen
Unconjugated bilirubin is water insoluble and not normally
present in the urine. The presence of conjugated bilirubin
indicates further evaluation for liver dysfunction and biliary
obstruction. A small amount of urobilinogen is normally found in
urine, but significant amounts suggest that further assessment
for hemolytic and hepatocellular disease is indicated.
Urobilinogen levels can be increased in conditions associated
with elevated nitrite levels (e.g. UTIs).
Microscopy is best
performed on a centrifuged specimen. 10-15mls of freshly-voided
urine should be spun at 1,500-3,000 rpm for five minutes, the
supernatant decanted, and the sediment re-suspended in the
remaining liquid. A single drop is transferred to a clean glass
slide and a cover slip applied. The sample is then examined for
the following:
-
Cells - an excess of leucocytes suggests pyuria, but
there is a gender difference. Men normally have fewer than
two white blood cells (WBCs) per high power field (HPF),
whilst women normally have fewer than five WBCs per HPF. The
presence of transitional cells, which are small round cells
with large nuclei, is normal. The presence of squamous
epithelial cells, which are large irregular cells with small
nuclei, suggests contamination. The presence of renal tubule
cells indicates renal pathology. Dysmorphic erythrocytes may
be indicative of glomerular disease.
-
Casts - protein coagulum forms casts in the renal
tubule, trapping any contents within them.
RBC casts occur in glomerular bleeding, commonly in
glomerulonephritis. The predominant cellular elements
determine the type of cast: hyaline, erythrocyte, leukocyte,
epithelial, granular, waxy, fatty, or broad.
-
Crystals - these may be seen in healthy patients, but
may also be helpful in assessing patients with urinary
stones. Uric acid crystals are yellow to orange brown and
may be diamond or barrel-shaped. Calcium oxalate crystals
can vary in size, and have a refractile square 'envelope'
shape. Triple phosphate crystals are colorless, have a
'coffin lid' shape, and may be associated with UTI
(particularly Proteus). Cysteine crystals have a hexagonal
shape and are colorless. Crystals may be seen in the urinary
sediment of healthy patients. Calcium oxalate
crystals have a refractile square
-
Bacteria - Gram staining may be helpful in specimens
suspected of being contaminated, and in diagnosing the type
of infection. Gram-negative streptococci and staphylococci
can be distinguished by their characteristic appearance
under high-powered magnification.
In women, 5 bacteria per high power field represents a count
of approximately 100,000 per ml and is the standard
concentration for the diagnosis of UTI in a possibly
contaminated sample. Some authorities maintain that lower
colony counts of 1,000 would be more accurate, particularly
in a clean specimen.In men, any bacteria in a properly
collected specimen is significant.
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