Physical & Chemical Examination of Urine Flashcards
Why analyze urines?
fluid biopsy of kidney
noninvasive means to evaluate kidney
readily available
urine is ultrafiltrate of plasma
First morning specimen
most concentrated; often preferred specimen
most acidic- formed elements are better preserved
Random specimen
for routine screening
can be affected by excess fluid intake or exercise
Timed specimen
collections for predetermined length of time or at a specific time of day
primarily used for chemistry testing
Midstream ‘clean catch’
for bacterial cultures or to prevent vaginal contamination
begin urination into toilet, collect midstream portion in container, finish voiding in toilet
Catheterized specimen
requires collection by medical personnel
sterile catheter insterted through urethra into bladder
Suprapubic Aspiration
requires collection by medical personnel
involves puncturing of abdominal wall & distended bladder by using needle & syringe
normally sterile
used for cultures or in infants (anaerobic infections)
Pediatric collections
plastic urine collection bag attached to perineal skin
routine testing
Reasons for specimen rejection
unlabeled/ mislabeled mismatch of specimen name with order inappropriate collection technique not properly preserved time delay in receipt of specimen visibly contaminated insufficient volume
Containers
clean, dry, clear, sterile containers
preservation of samples
preserve specimen if not processed in 2 hours or more
pH change after 2 hours at RT
increased pH because of the break down of urea into ammonia by bacteria
glucose change after 2 hr at RT
decreased
glycolysis & bacterial utilization
ketone change after 2 hr at RT
decreased
volatilization of compounds
bilirubin change after 2 hr at RT
decreased
exposure to light
urobiliogen change after 2 hr at RT
decreased bc of oxidation to urobilin
nitrite change after 2 hr at RT
increased or decreased
bacterial reduction to nitrate or all the way to nitrogen gas
bacteria change after 2 hr at RT
increased
color change after 2 hr at RT
varying changes due to oxidation or reduction of metabolites
turbidity change after 2 hr at RT
increased bc bacterial growth & precipitation of amorphous material
sediment change after 2 hr at RT
disintegration bc of dilute alkaline urine
most common preservation technique for urines
REFRIGERATION!!
should not be used for routine testing if urine will be analyzed within 2 hr
other urine preservatives
10% formalin
thymol/toluol
boric acid
NaF
urine color
due to the presence of urochrome- by product of bilirubin
foam
not normally included on report forms
stable white foam indicates large amounts of albumin
yellow foam is increased bilirubin
causes of cloudiness
contamination from skin, vaginal secretions, bacterial growth or fecal material
precipitation of dissolved solutes, x-ray contrast media
RBCs, WBCs, clots, casts
normal daily volume
600-1800 ml/day
polyuria
> 3L per day of urine
oliguria
<400 mL per day
anuria
0 mL per day
nocturia
> 500 mL at night
highly suggestive of chronic progressive renal failure
odor
normally has aromatic odor
urine on standing becomes more odorous due to bacterial conversion of urea to ammonia
Specific gravity
an expression of concentration in terms of density: mass of solutes present per volume of solution
1.002-1.040
read via refractometry & reagent strip chemical method
3 factors that affect the refractive index of a solution
wavelength of light used
temperature of solution
concentration of solution
Specific Gravity strip test principle
indirect measurement
strip pad impregnated with a polyelectrolyte & a pH indicator at an alkaline pH
protons are released from polyelectrolyet in proportion to ionic concentration of the urine; released protons change pH of test pad
False decrease of Specific gravity test
high glucose & urea concentrations
pH >6.5
false increase of specific gravity test
high protein & ketoacids
X-RAY CONTRAST MEDIA - will make it so elevated that the urine will need to be diluted
pH of urine & clinical significance
4.5-8.0
precipitation of crystals, treatment of UTI, determination of poor specimen