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Analysis Of Urine and other Body Fluids

Week 1 & 2 / Strasinger’s Urinalysis and Body Fluids 6th Edition

INTRODUCTION TO URINALYSIS  Urine contains information, which can be


obtained by inexpensive laboratory tests.
TOPIC OUTLINE
 According to CLSI, urinalysis define as “the
1 History
testing of urine with procedures commonly
2 Urine Composition performed in an expeditious, reliable,
3 Urine Volume accurate, safe, and cost- effective manner
4 Urine Specimen and Collection
5 Specimen Collection and Handling
NOTES
Ultrafiltrate of Plasma
HISTORY  Can be used to evaluate or monitor our
Hippocrates Wrote a book on “uroscopy” bodies homeostasis in Aldosterone system
(5th century
BC)
Frederik Discover albuminuria. Urine Composition
Dekkers
Normally 95% of water and 5 % of solutes
(1694)
Thomas Examination of urinary sediment by ORGANIC INORGANIC
Addis his method of quantitating the COMPONENTS COMPONENTS
microscopic sediment.  Urea- Major organic  Sodium Chloride-
Richard Introduced concept of urinalysis as component Major inorganic
Bright part of doctor’s routine patient  Creatinine- derived component;
(1827) examination from creatine Principal salt
 Uric acid- common  Potassium
NOTE component in  Sulfate- Derived
kidney stones; from amino acids
 1140 Common Era – developed color chart
derived from  Phosphate
 Albuminuria – protein in urine; discovered
from boiling urine
catabolism of  Ammonium
 Thomas Brian – reveal the contribution of
nucleic acid in food.  Magnesium
 Hippuric acid-  Calcium
early physician ; was first medical law’s in
benzoic acid is
England
eliminated in this
form, increases
with high vegetable
WHY WE STUDY URINE? diet. Other
 The kidney is the only organ with such a substances
noninvasive means by which to directly (carbohydrates,
evaluate its status. pigments, fatty
 Urine is an ULTRAFILTRATE of plasma. acids, enzymes etc).
 Urine is a readily available and easily collected
specimen.

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IS THIS FLUID URINE?
 At times it is necessary to verify that the fluid
present in a urine container is in fact urine.
 The single most useful substance that
identifies a fluid as urine is its uniquely HIGH
CREATININE CONCENTRATION (approximately
50 times that of plasma)
 In addition, concentrations of urea, sodium
and chloride are significantly higher in urine
than in other body fluids.
URINE SPECIMEN & COLLECTION

URINE VOLUME
TYPES OF SPECIMEN
 Urine volume depends on the amount of water
that the kidney excrete. Amount excreted is  The composition of urine depends on the
usually determined by the body’s state of patient’s metabolic state and the timing and
hydration. procedure used for collection.
 Patients must be instructed when special
 Normal Daily Urine Output: 1200 to 1500 mL a collection techniques are required.
range of 600 to 2000 mL is considered normal.

1 FIRST MORNING SPECIMEN


OLIGURIA  Decrease in urine output
 Also known as the 8 hour specimen
 Result of excessive water loss
 The ideal screening specimen
from vomiting, diarrhea,
 It is a concentrated specimen thereby assuring
perspiration, or severe burn
detection of chemicals and formed elements
< 1ml/kg/hr → Infants
not seen in random specimen.
< 0.5 ml/kg/hr →Children
 Essential for preventing false- negative
< 400 ml/day → Adults
pregnancy tests and for evaluating orthostatic
ANURIA  Cessation of urine flow result
proteinuria.
from any serious damage to the
 The specimen must be collected immediately
kidney or decrease flow of blood
and deliver to the laboratory within 2 hours.
to the kidney
2 RANDOM SPECIMEN
NOCTURIA  Normally, kidneys excrete 2 or 3
times more urine during the day
 Can be collected at any time, usually during
 Increase nocturnal excretion of
daytime hours, and without prior patient
urine
preparation.
POLYURIA  Increase in daily urine volume
 The most commonly received specimen.
 Greater than 2.5 L/ day →Adults  Usually satisfactory for routine screening and
2.5- 3 mL/kg/day → Children
are capable of detecting abnormalities that
Associated with Diabetes mellitus
indicate disease process.
and Diabetes Insipidus
3 FASTING SPECIMEN (SECOND MORNING)
artificially induced by diuretics,
caffeine and alcohol

2
 The second voided specimen after a period of
fasting.
 This specimen will not contain any metabolites
from food ingested before the beginning of
the fasting period.
 Recommended for glucose monitoring.
4 2 HOUR- POSTPRANDIAL SPECIMEN

 The patient is instructed to void shortly before


consuming a routine meal and to collect a
specimen 2 hours after eating.
 Specimen is tested for glucose
 Results are used primarily for insulin therapy
monitoring for persons with diabetes mellitus
5 GLUCOSE TOLERANCE SPECIMEN 7 MIDSTREAM “CLEAN CATCH” SPECIMEN

 Collected correspond with blood samples  Less traumatic method for obtaining urine for
drawn during glucose tolerance test (GTT). bacterial culture and routine urinalysis.
 Number of specimens varies with the length of  Used to avoid contamination (ex. Vaginal
the test. discharge)
 Urine is tested for glucose and ketones  Before collection, the glans penis or urethral
6 24 HOUR (TIMED) SPECIMEN meatus are thoroughly cleansed and rinsed.
 After cleansing, midstream specimen is
 Specimen used for urine quantitative assay. obtained when the px passes some urine in
 Many solutes exhibit diurnal variation. the toilet and then stops and urinate the mid
 Catecholamines, 17- hydroxysteroids, portion to the container.
electrolytes  Care should be taken not to contaminate the
 The patient must begin and end the collection specimen container.
period with empty bladder. 8 CATHETERIZED SPECIMEN
 On its arrival in the laboratory, the specimen
must be thoroughly mixed and the volume  Obtained following catheterization of the
accurately measured and recorded. patient, that is insertion of a sterile catheter
 All specimen should be refrigerated or kept on through urethra into the bladder.
ice during the collection period.  Urine flows directly from the bladder through
 The most common error encountered are the indwelling catheter and accumulates in a
related to specimen collection or to handling plastic reservoir bag.
problems.  Most often these specimen are sent for
bacterial culture.
 Involves collecting urine directly from the
bladder by puncturing the abdominal wall and
distended bladder using needle and syringe.
 This procedure is used principally for bacterial
cultures, especially for anaerobic microbes and

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in infants, in whom specimen contamination is 12 PROSTATITIS SPECIMEN
often unavoidable Also known as “three glass collection”
• 1 st container → first passed urine
• 2 nd container → midstream portion of urine
• 3 rd container → urine with prostatic fluid
• 4 th container → post prostatic massage urine
specimen (Stamey –Mears)

IMPORTANCE:
9 SUPRAPUBIC ASPIRATION • 1 st container → Urethral infection or
inflammation
 Completely free of contamination for bacterial • 2 nd container → urinary bladder infection
culture and cytology • 3 rd and 4th container → Prostatic infection (+
 External needle aspiration from the bladder WBC and 10x bacteria compared to 1st container)
 Possible pediatric specimen
Prostatic Infection
10 PEDIATRIC COLLECTION  higher WBC/hpf count in specimen 3 than
specimen 1
 Pediatric and newborn infants pose a challenge  bacterial count in specimen 3 is 10 times higher
in collecting an appropriate urine specimen. than specimen 1
 Commercially available plastic urine collection
bags with hypoallergenic skin adhesive are Specimen 2 is a control for bladder or kidney
used. infection
 The bag is placed over the penis in the male
and around the vagina (excluding the anus) in  Positive culture in specimen 2 invalidates
the female, and the adhesive is firmly attached positive culture in specimen 3 (cannot
to the perineum. differentiate urinary tract infection from
11 DRUG SPECIMEN COLLECTION prostate infection)

 Chain of custody Prostate specimen variations


 Provides this documentation of proper sample
identification from the time of collection to Stamey-Mears: 4-glass collection
the receipt of laboratory results  Initial voided (VB1)
 withstand legal scrutiny  Midstream (VB2)
 No tampering of spx  Massaged Prostate Excretions (EPS)
 Spx must be handled securely  Post-massage urine (VB3)
 Proper ID is required
 30-45ml (60ml in PHL) Cultures on all specimens
 Urine tempt must be checked within 4 mins  VB1 and VB2 positive = urinary infection
(32.5-37.7C)  EPS examined for WBCs >10-20/ hpf:abnormal

Negative cultures on VB1 and VB2 and positive on


EPS and VB3 show prostatitis

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PLACE LABEL ON CONTAINER, NOT LID
Pre-and Post-Massage Test:
 Specimen 1 – midstream clean-catch Requisition form: Must accompany specimen
specimen  Information must match label
 Specimen 2 – post-massage specimen  Time of receipt is stamped on requisition
 Other info: Type of specimen, Interfering
Prostatitis is indicated by a quantitative culture meds
result in the second glass that is 10 times higher C URINE SPECIMEN REJECTION
than specimen 1  Unlabeled urine specimen container
Mislabeled urine specimen
 Names or identification number on container
SPECIMEN COLLECTION & HANDLING
label and request slip do not match
A SPECIMEN COLLECTION  Inappropriate urine collection technique or
 Gloves should be worn at all times specimen type for test requested
 Routine urinalysis protocols typically require  Specimen not properly preserved during a
10 to 15 ml of urine. Less than 12 ml hinder time of delay or inappropriate preservative
performance of microscopic examination. used
 Containers for urine collection must be  Visibly contaminated urine (fecal material,
clean, dry and made of clear or translucent toilet tissue)
disposable material such as plastic or glass.  Insufficient volume of urine for test/s
 The container should stand upright have an requested
opening of at least 4-5 cm and have a D SPECIMEN INTEGRITY
capacity of 50 to 100 mL.
 All specimen containers must be labelled  Test within 2 hours of collection
before or immediately after collection.  Refrigerate if testing is delayed
Patient identification label is always placed  Most problems are caused by bacterial
directly on the container holding the multiplication
specimen.  Increased: Color, Turbidity, pH, Nitrite,
 Specimens should be delivered to the Bacteria, Odor
laboratory promptly and tested within 2  Decreased: Glucose, Ketones, Bilirubin,
hours. Urobilinogen, RBCs, WBCs, Casts
NOTE
 Delivered within 2 hrs E CHANGES IN UNPRESERVED URINE
 Accurate time for reading of result
 must be 1hr
 labelled on container not on lid

B SPECIMEN LABELING
Information on label:
 Patient’s Name, ID Number, Date, Time
 Additional information: Age, Location,
Physician

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F SPECIMEN PRESERVATION

 Most routinely used method of preservation


is refrigeration at 2ºC to 8ºC

 When a specimen must be transported over


a long distance and refrigeration is
impossible, chemical preservatives may be
added.

Examples of chemical preservatives:


 Thymol
 Formalin
 Saccomanno’s Fixative
 Acids (HCl, glacial acetic acid, Boric acid)
Sodium Carbonate
 Sodium Fluoride
 Toluene
NOTE
 Phenol
 Trichomonads: parasitic infection
(tumbling, can see under urine
IDEAL PRESERVATIVE
microscopy)
 Bactericidal
 Precipitation of Protein: Sulfosalicylic
 Inhibit urease
Acid is the reagent for confirmatory of
 Able to preserve formed elements
presence of protein in urine
 Must not interfere with chemical tests  Porphyrins and Porphobilinogen:
chemicals that help to make
Ideal preservative does not exist as of the hemoglobin
moment
G URINE PRESERVATIVE

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