Professional Documents
Culture Documents
CM Lecture 2022 Batch
CM Lecture 2022 Batch
Terminologies:
1. CDC- Centers for Disease Control and Prevention
2. OSHA- Occupational Safety and Health Administration
3. CLSI-Clinical and Laboratory Standards Institute
4. PPE- Personal Protective Equipment
5. UP- Universal Precautions
6. BSI-Body Substance Isolation
7. NFPA- National Fire Protection Association
“BIOLOGIC HAZARD”
A. SOURCE – Infectious agents
B. Possible Injury – bacterial, fungal, viral, prions, or parasitic infections
MODES OF TRANSMISSION
0
A 0.5% bleach solution, prepared by adding 1 part household bleach to 9 parts water (1/10 dilution), is stable for 1 week
“SHARP HAZARDS”
A. SOURCE- Needles/Syringe, lancet, broken glass wares
B. Possible Injury- cuts, punctures, or blood-borne pathogen exposure
⊖
-
❖ The biohazard sharp containers should not over-filled and must always be replaced when the
safe capacity mark is reached
I.K AYTONA 1
“CHEMICAL/POISON HAZARDS”
A. SOURCE- Preservatives and reagents
B. Possible Injury- Exposure to toxic, carcinogenic, or caustic agents
❖ Hazardous chemicals should be labeled with a description of their particular hazard, such as poisonous,
corrosive, flammable, explosive, teratogenic, or carcinogenic.
❖ In case of chemical spills, when skin contact occurs, the best aid is to flush the area with large amount of water for at
15 mins
least _________, then seek medical attention
❖ Material Safety Data Sheets (MSDS)=Contains the information about the chemical
hazards
1. Physical and chemical characteristics
2. Fire and explosion potential
3. Reactivity potential
4. Health hazards and emergency first aid procedures
5. Methods for safe handling and disposal
6. Primary route of entry
7. Exposure limits and carcinogenic potential
“RADIOACTIVE HAZARDS”
A. SOURCE- Equipment and radioisotopes
B. Possible Injury- Radiation exposure
❖ The amount of radiation exposure is related to a combination of time, distance, and shielding.
❖ Exposure to radiation during pregnancy presents a danger to the fetus; personnel who are
pregnant or think they may be should avoid areas with this symbol
“ELECTRICAL HAZARDS”
A. SOURCE- Ungrounded or wet equipment; frayed cords
B. Possible Injury- Burns or shock
❖ Laboratory personnel should continually observe for any dangerous conditions, such as frayed
cords and overloaded circuits, and report them to the supervisor.
❖ All electrical equipment must be grounded with _______________________.
3 pronged plug
-
“FIRE/EXPLOSIVE HAZARDS”
A. Source: Open flames, organic chemicals
B. Possible Injury: Burns or dismemberment
=
(Hg, Mg, Na, and Li)
Dry chemicals for A, B, C
Class E Detonation or Arsenal fire Allowed to burn out and nearby materials are protected
-
Class K Grease, oils, fats Liquid designed to prevent splashing and cool the fire.
I.K AYTONA 2
“PHYSICAL HAZARDS”
A. SOURCE- Wet floors, heavy boxes, patients
B. Possible Injury- Falls, sprains, or strains
❖ General Precautions
1. Avoid running in rooms and hallways
2. Watch for wet floors
3. Bend knees when lifting heavy objects
4. Keep long hair pulled back
5. Avoid dangling jewelry
6. Maintain a clean organized work area
7. Use a Closed-toed shoes
HAND HYGIENE- includes both hand washing and using alcohol based antiseptic cleansers.
❖ Hand contact is the primary method of infection transmission Hand Washing Songs:
A. Happy Birth day
❖ Father of handwashing: Dr. Ignaz Semmelweis B. Twinkle-Twinkle little star
C. Alphabet song
❖ Laboratory personnel must always sanitize hands
1. Before patient contact
2. After gloves are removed
3. Before leaving the work area
4. Anytime when hands have been knowingly contaminated
5. Before going to designated break areas
6. Before and after using bathroom facilities
❖ soiled
HAND WASHING – Used when hands are _______________________________
E-
1. Wet hands with warm water
2. Apply anti-microbial soap
3. Rub from a lather, create friction, and loosen debris.
seconds.
-
0
4. Thoroughly clean between fingers, including thumbs, under fingernails and rings, and up to the wrist, for at least 15/20
Degree of Hazard
O No hazard
1+ Slight Hazard
2+ Moderate Hazard
3+ Serious Hazard
4+ Extreme Hazard
I.K AYTONA 3
ADDENDUM
€
The last step in handwashing Turn off faucets with a clean paper towel to prevent recontamination
The most important step in handwashing
-
Rubbing /Applying friction
Susceptible host Complete the chain of infection:
The source/causative agent – transmission --_____________
RENAL FUNCTION
RENAL PHYSIOLOGY
A. The kidneys are bean shaped and are located on the posterior abdominal wall in the area known as the retroperitoneum. An
-
depth
B. Each kidney contains approximately _______________ functional units called nephrons
C. Cortical nephron- makes up approximately 85% of the total nephron. Found mainly in the cortex of the kidney and are
responsible primarily for removal of waste products and reabsorption of nutrients.
-
D. Juxtamedullary nephrons- have loops of Henle that extend deep into the medulla of the kidney. Their primary function is
the concentration of urine
E-
and is the driving force behind glomerular filtration. The plasma ultrafiltrate already in Bowman’s space exerts a hydrostatic
pressure of 15 mm Hg that opposes filtration
The outcome of these three pressure differences is a net filtration pressure of 10 mm Hg, which favors the formation
of a plasma ultrafiltrate in Bowman’s space
GLOMERULAR FILTRATION
CHARACTERISTIC:
0
The glomerulus consists of a coil of approximately eight capillary lobes referred to collectively as the capillary tuft. It
resembles as sieve
The glomerulus is located - within the Bowman’s
- capsule.
70K daltons
A non-selective filter for plasma substances with molecular weights of less than _____________
- 0
Normally, the fluid leaving the glomerulus has a specific gravity of 1.010
Analysis of the fluid as it leaves the glomerulus shows the filtrate to have a specific gravity of 1.010 and•
confirms that it is
chemically an ultrafiltrate of plasma.
#
Approximately 120 mL/min, or one -
fifth, of the renal plasma is filtered through the glomeruli forming what is
known as the ultrafiltrate, which is further processed as it travels through the nephron. The ultrafiltrate has the same
composition as blood plasma but it is normally free of protein except for about- 10 mg/dL of low molecular-weight protein
-
270Th
I.K AYTONA 4
Cellular Structure of Glomerulus:
Plasma filtrate must pass through three cellular layers:
1. Capillary wall membrane
2. Basement membrane
3. Visceral epithelium of Bowman’s capsule
GLOMERULAR PRESSURE
a. ______________________
juxta glomerular cells ÷
➢ Juxtaglomerular apparatus- maintains the glomerular blood pressure
-
b. ______________________
Macula densa cells - found in the①DCT, sensor of ÷ change in blood pressure
Decrease Blood Pressure = Dilation of afferent arteriole, Constriction of efferent arteriole D- DAE
Increase Blood pressure = Constriction of afferent arteriole, Dilation of efferent arteriole 1- CADE
Functions:
1. Dilation of the afferent arteriole and constriction of the efferent arteriole
2. Stimulation of sodium reabsorption in the proximal convoluted tubule
a- o
-
3. Triggers the adrenal cortex to release the sodium-retaining hormone, aldosterone, to cause reabsorption of sodium and
-0--0
-
tubules. It is -
not a normal body constituent, however, and must be infused by IV at a constant rate throughout
-
"
F : 87 -107
4. Beta-2 Microglobulin
5. Radioisotopes plasma 0.5 -1.5mg 1dL
:
Formula for the computation of GFR using the creatinine clearance test
1. -
By far the greatest source of error in any clearance procedure utilizing urine is the use of improperly timed urine
specimens
-
2.
3.
Plasma/serum
-
=
creatinine can be collected anytime within 24 hours of urine collection
Specimen collection, therefore, must include both a 24-hour urine specimen and a serum creatinine value, ideally
collected at the midpoint of the 24-hour urine collection. The urine container must be kept refrigerated
-
T O
throughout the duration of both the collection procedure and the subsequent storage period until laboratory analysis can
be performed.
4. 0
A blood sample of 1 mL (minimum 0.5 mL) in a labeled tube, preferably stored in refrigerated or frozen temperature
-
O
-
5. The patient is required to drink at least 8 cups of liquid on the day of urine collection.
-
I.K AYTONA 5
Disadvantage of using Creatinine
1. Some creatinine is secreted by the tubules, and secretion increases as blood levels rise
2. Medications, including gentamicin, cephalosporins, and cimetidine (Tagamet), inhibit tubular secretion of creatinine, thus
causing falsely low serum levels
3. Bacteria will break down urinary creatinine if specimens are kept at room temperature for extended periods, thus leads
to false low result
4. A diet heavy in meat consumed during collection of a 24-hour urine specimen will influence the results if the plasma
specimen is drawn before the collection period = false increase results
5. Not reliable indicator in athletes, persons involved in heavy exercise, and patients with muscle diseases
6. Drugs such as trimethoprim-sulfamethoxazole can increase serum creatinine level by approximately 0.4 to 0.5 mg/d
7. Creatinine clearance is affected by sex and race. Women have less muscle mass and a lower rate of creatinine
production in comparison to me
CYSTATIN C
0--0 -1€
A small protein (molecular weight 13,359) produced at a constant rate by all nucleated cells. It is readily filtered by the
glomerulus and reabsorbed and broken down by the renal tubular cells. It has potential as a marker for long-term monitoring of
renal function
_
BETA-2-MICROGLOBULIN
-"=
It dissociates from human leukocyte antigens (MHC class I) at a constant rate and is rapidly removed from the plasma by
glomerular filtration. It is a better marker of reduced renal tubular function than of glomerular function
Original MDRD GFR = 173 × serum creatinine–1.154 × age–0.203 × 0.742 (if patient is female) × 1.212 (if patient is black)
Formula
MDRD-IDMS GFR = 175 × serum creatinine–1154 × age–0.203 × 0.742 (if patient is female) × 1.202 (if patient is
Traceable formula black/African-american)
Other MDRD
formula
¥
included in MDRD 6 PARAMETERS (BASES) = BUN, Age, Serum creatinine, Ethnicity, Serum albumin
CKD-EPI (Chronic Kidney eGFR (mL /min/1.73 m2) = 141 x min(SCr/k,1)a x max(SCr/k,1)−.209 x 0.993Age x (1.018 if
Disease Epidemiology female) x (1.159 if Black)
Collaboration) formula
TUBULAR REABSORPTION
The body must not lose 120mL of water-containing essential substances every minute.
The loss of tubular function capability is often the first function affected in renal disease.
URINE COMPOSITION
a. 95 % water
b. 5= O_0
% solutes - Total solute in 24’hours = 60 grams (35 grams organic substances, -0
25 grams inorganic substances)
e
Active transport – the substance to be reabsorbed must combine with a carrier protein contained in the membranes of
-
Passive transport- the movement of molecules across a membrane as a result of differences in their concentration or
-
electrical potential on opposite sides of the membrane. It is Characterized by movement of a substance from an area of
=
higher
-
concentration to one of lower concentration
Passive Transport
SAPAUW -Urea (40% are reabsorbed) Proximal convoluted tubule and
ascending loop of Henle
I.K AYTONA 6
NOTE
A#
Passive reabsorption of water takes place in all parts of the nephron except the ________.
Sodium is actively transport in all part of the nephron except in the Ascending loop of henle
0
Maximal Tubular reabsorptive capacity - Denoted Tm, the maximal rate of reabsorption of a solute by the tubular
epithelium per minute (milligrams per minute). Reabsorptive capacity varies with each solute and depends on the
glomerular filtration rate
€
The plasma concentration at which active transport stops is termed the renal threshold
Ex: Glucose renal threshold is _____________ mg/dl or equivalent to 350mg/min
Sodium renal threshold is 110 to 130 mmol/L
RENAL CONCENTRATION
Renal concentration begins in the descending and ascending loop of henle and the final concentration of urine
continues to the -Collecting Duct.
Water is -
removed by osmosis
#
0in the descending loop of Henle, and sodium and chloride are reabsorbed in the ascending loop.
Osmolality - The movement of water--_--_
across a semipermeable membrane in an attempt to achieve an osmotic equilibrium
between two compartments or solutions of differing osmolality (i.e., an osmotic gradient). This mechanism is passive, that is, it
requires no energy
Excessive reabsorption of water as the filtrate passes through the highly concentrated medulla is prevented by the 0 water-
←
-
impermeable walls of the ascending loop. This selective reabsorption process is called the countercurrent mechanism and serves
to maintain the osmotic gradient of the medulla
€-0
TEST FOR TUBULAR REABSORPTION
Results
Urine osmolality >800mOm Neurogenic DI
Urine: Serum ratio is⊖3:1 HADA
Urine osmolality <400mOsm Nephrogenic DI
Urine: Serum ratio is ①
1:1 kidney tubules
Fullday ←h⑧¥nma
•
• ,
________________ =#
________________– patients deprived of fluids for 24 hours before measuring Specific Gravity
– compared the volume and S.G of day and night urine samples
↳ sundamom
D. Free water clearance test
F-
• The free water clearance is determined by first calculating the osmolar clearance using the standard clearance
formula
•
= =
The calculation of the free water clearance is used to determine the ability of the kidney to respond to the state of
body hydration.
• Calculating osmolar clearance indicates how much water must be cleared each minute to produce a urine with the
same osmolality as the plasma.
I.K AYTONA 7
cap tabular filtrate
blood to Peri
→
➢
➢
➢
←= RENAL SECRETION
Involves the passage of substances from the blood in the peritubular capillaries to the tubular filtrate
In contrast to tubular reabsorption, in which substances are removed from the glomerular filtrate and returned to the blood,
tubular secretion involves the passage of substances from the blood in the peritubular capillaries to the tubular filtrate
Two major functions of tubular secretion:
a. Elimination of waste products not filtered by the glomerulus
hydrogen
b. Regulation of acid-base balance in the body through the secretion of ____________________
hydrogen forms : "
Regulation of pH Ungs → kidneys ammonium INAH hydrogen phosphate HM w%u%"^
, ,
Along with the lungs, the kidneys are the major regulators of the acid–base content in the body. They do this through the secretion
of hydrogen in the form of ammonium ions, hydrogen phosphate, and weak organic acids, and by the reabsorption of -2
- - -
bicarbonate
from the filtrate in the convoluted tubules.
-
-
Note ☺ - A disruption of secretory function of the renal can result in metabolic acidosis or-
renal tubular acidosis, wherein the
-
kidney is unable to produce an acid Urine (In short: Urine is alkaline and blood Ph is acidic)
- -
-
TEST FOR RENAL SECRETION AND BLOOD FLOW
C. Titratable acidity
D. Urinary ammonia patient must take ORAL Ammonium attitude
8-
Measurement of urine pH, titratable acidity, and urinary ammonia can be used to determine the defective function. The
tests can be run simultaneously on either fresh or toluene-preserved urine specimens collected at 2-hour intervals from
patients who have been primed with an acid load consisting of oral ammonium chloride. By titrating the amount of free H+
(titratable acidity) and then the total acidity of the specimen, the ammonium concentration can be calculated as the
-
INTRODUCTION TO URINALYSIS
HISTORY AND IMPORTANCE
References of the study of urine can be found in the drawings of 0 0
cavemen and in Egyptian hieroglyphics, such as the Edwin
=
smith surgical papyrus.
-
URINE COMPOSITION
Urine consists of urea and other organic and inorganic chemicals dissolved in water.
Urine is normally 95% water and 5% solutes, although considerable variations in the concentrations of these solutes can
occur owing to the influence of factors such as dietary intake, physical activity, body metabolism, and endocrine
-
-
functions.
The single most useful substance that identifies a fluid as urine is its uniquely - high creatinine concentration
(approximately= 50 times that of plasma).
Urea Primary organic component. Product ofIn protein and amino acid metabolism
Creatinine Product of creatine metabolism by muscles
Uric acid Product of nucleic acid breakdown in food and cells
Chloride Primary inorganic component. Found in combination with sodium and many other inorganic substances
Sodium Primarily from0salt, varies by intake
-
I.K AYTONA 8
NOTE ☺
Urea is the major organic component of urine
•
Chloride is the major inorganic component of urine followed by Sodium then Potassium
- -
Ao
high urea and ocreatinine content can identify fluid as•
_
urine.
URINE VOLUME
Urine volume depends on the amount of water that the kidneys excrete.
=
Factors that influence urine volume include –fluid intake, fluid loss from non-renal sources, variations in the secretion of ADH,
and need to excrete increased amounts of dissolved solids, such as glucose or salts.
_
-
O
-
Normal daily urine output is usually 1200 to 1500 mL, a range of 600 to 2000 mL is considered normal
The kidney excretes two
=
to three times more urine during theO
-
day than during the night
-
Diabetes Insipidus
-77
✓ Due to decrease production or function of ADH
✓ ___________Urine Specific gravity
-
SPECIMEN COLLECTION
2 hrs
Urine specimens should be delivered to the laboratory promptly and tested within _____________
Never discard a specimen before checking with a supervisor
I. CHARACTERISTICS OF CONTAINER
❖ Clean, Dry, Leak-proof
❖ With Screw top lids – they are less likely to leak than snap-on lids
-
- Containers should stand upright, have an opening of at least 4 to 5 cm, and have a capacity of 50 to 100 ml
÷
&
II. LABELS
❖ Patient’s name
❖ Patient identification number
❖ Date and time of collection
❖ Additional information such as age, sex, etc.
*Labels must be attached to the BODY OF CONTAINER, not to the lid and should not become detached if the
=
container is refrigerated/frozen.
I.K AYTONA 9
V. WHEN TO REJECT SPECIMEN? ☺
1. Specimen in unlabeled containers
2. Non matching labels and requisition forms
3. Specimens contaminated with feces or toilet papers
4. Containers with contaminated exteriors
5. Specimens of insufficient quantity
6. Specimens that have improperly transported
÷
CHANGES IN UNPRESERVED URINE (Strasinger)
Analyte Change Cause
Color Modified / Darkened Oxidation or reduction of metabolites
Ph Increased Breakdown of urea to ammonia by urease-producing bacteria / loss of CO2
Bacteria Increased Multiplication
Odor Increased Bacterial multiplication or breakdown of urea to ammonia
=
Nitrite Increased Multiplication of nitrate reducing bacteria
Clarity Decreased Bacterial growth, and precipitation of amorphous material
Glucose Decreased Glycolysis and bacterial use
Ketones Decreased Volatilization and bacterial metabolism
Bilirubin Decreased Photo oxidation to biliverdin / light exposure
Urobilinogen Decreased Oxidation to urobilin
RBC, WBC, and casts Decreased Disintegration in dilute alkaline urine
Trichomonads Decreased Loss of characteristic, motility and death
NOTE ☺ Protein/Albumin is least or not affected.
URINE PRESERVATIVES
Preservatives Advantages Disadvantages Additional Information
Refrigeration (2-8’C) Does not interfere with
-
PRECIPITATES AMORPHOUS Prevents bacterial growth
←
*the easiest and most-
chemical tests CRYSTALS for 24 hours.
-
common
= Raises specific gravity by
hydrometer
Thymol Preserves glucose and Interfere with acid precipitation test
t
I.K AYTONA 10
r
Note: If a routine urinalysis is also requested, the culture should be performed first to
prevent contamination of the specimen.
Midstream Clean catch Safer, less traumatic method for obtaining urine for bacterial culture and routine
urinalysis
The specimen is less contaminated by epithelial cells, and bacteria.
Before collection of a midstream clean catch specimen, the glans penis of the male or
the urethral meatus of the female is thoroughly cleansed and rinsed
Supra-pubic aspiration - $0m ADDER For bacterial culture (especially for anaerobic microbes)
anaerobic microbes
cytology
_________________
Pediatric specimen We –we bag
Soft, clear plastic bags with hypoallergenic skin adhesive to attach to the genital area of
both boys and girls
If the third specimen will have a white cell / hpf count and bacterial count 10x that of the first
specimen – positive for Prostatic infection
The second specimen serves as control for bladder and kidney infections and should not be positive for
bacteria.
The second specimen can be used for routine UA if additional testing is required
Quantitative cultures are performed on all specimens
Macrophages containing lipids may also be present
Pre and Post In the pre- and post-massage test (PPMT), a clean-catch midstream urine specimen is collected.
Massage Test A second urine sample is collected after the prostate is massaged positive result is significant
Post = > 10
bacteria than pre bacteriuria in the post-massage specimen of greater than 10 times the pre-massage count
massage massage
Stamey-Mears Types of four Glass specimens
(Four glass) VB1 Initial voided urine, For bacterial cultures, Urethral infection or inflammation testing
VB2 Midstream urine and is used to tests for urinary bladder infection.
Pos : > 10-20 WBC / thpf EPS Expressed prostatic secretion
VB3 Post prostatic massage urine
The prostatic secretions are cultured and examined for white blood cells. More than 10 to 20 white
blood cells per high-power field is considered abnormal.
I.K AYTONA 11
Drug Testing Specimen Collection
Chain of custody / Evidence
___________________________- process that provides documentation of proper sample identification from the time of
collection to the receipt of laboratory results
The COC is a standardized form that must document and accompany every step of drug testing, from collector to courier to
laboratory to medical review officer to employer
For urine specimens to withstand legal scrutiny, it is necessary to prove that no tampering of the specimen occurred,
such as substitution, adulteration, or dilution. UAD : substitution ,adulteration , dilution
The collector adds bluing agent (dye) to the toilet water reservoir to prevent an adulterated specimen
Most common adulterant is 0 water.
60mL
*Container capacity: ________
30 -45mL
*Urine volume collected: _____________
32.5 37.7°C
*Urine Temperature: read within 4 minutes, range of ________________.
-
NOTE- If the specimen temperature is not within range, the temperature should be recorded and the supervisor or employer
contacted immediately.
Orange- yellow -Phenazopyridine (Pyridium) - drug commonly administered for urinary tract infection, produces
↳ can be mistaken for BILIRUBIN also a yellow foam when shaken
I.K AYTONA 12
Red -RBCs -cloudy urine with positive chemical results for blood and visible RBCs
-Hemoglobin
-Myoglobin
⇐
when viewed on the microscope
-For hemoglobin, clear urine with positive chemical test for blood; due
to intravascular hemolysis
-clear urine with positive chemical test for blood; muscle damage
-Beets -alkaline urine of genetically susceptible person
-Rifampin -medication for Tuberculosis
-Menstrual contamination -
-cloudy specimen with RBCs, mucus, and clots
Red- brown -RBCs oxidized to methemoglobin -seen in acidic urine after standing; positive chemical test for blood
-Fuchsin, aniline dye -Foods, Candy
-myoglobin (25 mg/dl)
Port Wine -porphyrins/ Porphyria -negative test for blood, may require additional testing
/Burgundy red -maybe colorless in Lead poisoning
Brown 0
Homogentisic acid (Alkaptonuria) -seen in 0alkaline urine after standing
Black Melanin or Melanogen, Malignant -urine darkens on standing and reacts with nitroprusside and ferric
melanoma chloride
-Argyrol (anti-septic) - color disappears with ferric chloride
-Methyldopa or Levodopa -antihypertensive drug
-Metronidazole (Flagyl) -darkens on standing, for parasitic infection
-Phenol derivates -Interfere with copper reduction tests
Note!☺
A purple staining may occur in catheter bags and is caused by indicant in the urine or a bacterial infection, frequently caused by
Klebsiella or Providencia species.
I.K AYTONA 13
URINE ODOR
➢ Seldom of clinical significance and is not a part of the routine urinalysis
ODOR CAUSE
Aromatic Normal
Foul, ammonia-like, fetid Bacterial decomposition, urinary tract infection, old urine
Fruity, sweet Ketones, DM, Starvation, vomiting, strenuous exercise, diarrhea
Maple syrup Maple syrup urine disease, caramel sugar
Mousy odor, Barny or musty odor Phenylketonuria
Rancid Tyrosinemia
Sweaty feet Isovaleric academia
Cabbage, Hops Methionine malabsoprtion
Bleach Contamination
Odorless Acute tubular necrosis
Rotting fish Trimetylaminuria
Pungent or distinctive odor Asparagus, Garlic, Onion ingestion, UTI(Brunzel), bacteruria, increase urinary amines
Swimming pool Hawkinsinuria
Sulfur odor cystinuria
Menthol-like Phenol-containing medications
Mercaptan odor Asparagus, garlic, and egg
I.K AYTONA 14
URINE SPECIFIC GRAVITY
➢ Specific gravity is defined as the density of a solution compared with the density of a similar volume of distilled water (S.G
1.000) at a similar temperature
➢ Specific gravity is influenced by the number of particles present, and the size of the particles.
➢ The evaluation of urine concentration is included in the routine urinalysis by measuring the specific gravity
➢ The specific gravity of the plasma filtrate entering the glomerulus is 1.010
a. Isosthenuric- term to describe urine with S.G 1.010
b. Hyposthenuric/Diluted urine – term to describe urine with S.G below 1.010
c. Hypersthenuric/Concentrated urine- term to describe urine with S.G above 1.010
1-002-1-035
-S.G of Normal random urine: _____________, where most of the random specimen falls between 1.015 -1.030.
-Abnormally high S.G results- above 1.040 – are seen in patients who have recently undergone an intravenous pyelogram
(Ex. Radiographic contrast dye /X-ray film, Dextran, and other Plasma expanders)
Harmonic Oscillation Based on the principle that the frequency of a sound wave entering a solution changes in
Densitometry proportion to the density of the solution
It is rarely used today despite its ability to accurately and precisely determine urine specific gravity with
linearity up to 1.080 This method was initially used on a semiautomated urinalysis workstation known as
the Yellow IRIS
During testing, a portion of the urine sample is held in a U-shaped glass tube that has an
electromagnetic coil on one end and a motion detector on the other end. An electrical current applied to
the coil generates a sound wave of fixed frequency. This sonic oscillation is transmitted through the
specimen, and the frequency attenuation is measured. The frequency (the oscillating cycle period)
observed is directly proportionate to the sample density, and a microprocessor converts the
frequency to a corresponding specific gravity value.
Reagent strip The reagent strip reaction is based on the change in the pKa(dissociation constant) of a
PRIN change in pKa of poly electrolyte
:
polyelectrolyte in an alkaline medium
in alkaline medium • S.G reading is not affected by radiographic contrast dye, protein, and
glucose.
Hydrometer (Urinometer) The urinometer consists of a weighted float attach to a scale that has been calibrated in terms
of urine specific gravity
• When using urinometer, an adequate amount of urine is poured into a proper-size
container and the urinometer is added with a spinning motion. The scale reading is
then taken at the bottom of the urine meniscus.
• A major disadvantage of using a urinometer to measure specific gravity is that it
10 15mL
requires a __________________
-
of specimen
• It is less accurate that other methods and is not recommended by the CLSI
• The urinometer reading needs to be corrected for temperature, glucose and protein.
• The calibrated temperature printed on the instrument is usually about 20 oC.
• To Correct for the S.G:
a. Add 0.001 for every 30C above the calibration temp.
b. Subtract 0.001 for every 3oC below the calibration temp.
c. Subtract 0.004 for every 1 gram of glucose
d. Subtract 0.003 for every 1 gram of protein
Example:
A specimen that has been left at 29 oC has been reported to contain 2g/dl of glucose and 1g/dl
of protein. The initial S.G was 1.035.Calculate the corrected S.G
CALIBRATION
Potassium sulfate = S.G should be read at 1.015
Water = S.G should be read at 1.000
I.K AYTONA 15
Refractometer (TS meter) It determines the concentration of dissolved particles in a specimen. It does this by measuring
refractive index.
• Refractive index is a comparison of the velocity of light in air with the
velocity of light in a solution(urine).
• The refractometer provides the distinct advantage of determining specific gravity
using a small volume of specimen (one or two drops).
• Temperature corrections are not necessary.
• Temperature is compensated between 15 oC and 38 oC.
• Corrections for glucose and protein are calculated.
Glucose = subtract 0.004 for each gram
Protein = subtract 0.003 for each gram
Example:
A specimen containing 1 g/dL protein and 1 g/dL glucose has a S.G reading of 1.030. calculate
the corrected reading
Method Correction for temperature Correction for glucose Correction for protein
Urinometer Yes Yes Yes
Refractometer No Yes Yes
Reagent strip No No No
S.G DILUTION
FORMULA: S.G x DILUTION = ACTUAL S.G
EXAMPLE: A specimen diluted 1:5 with a reading of 1.010 would have an actual S.G of
A. 1.050 B. 5.050 C.1.015 D. Prayers
Reagent strips – provide, simple, rapid means for performing medically significant analysis of urine
Reagent strips consist of chemical-impregnated absorbent pads attached to a plastic strip. A color producing
chemical reaction takes place when the absorbent pad comes in contact with urine.
A fresh, well-mixed, uncentrifuged specimen is used for testing
10 parameters: pH, protein, glucose, ketones, blood, bilirubin, urobilinogen, nitrite, leukocytes, and S.G
bit C
11th parameter: __________________
-
I.K AYTONA 16
Specimens must be returned to room temperature before chemical testing by reagent strips because the enzyme reactions on the
strips perform best at room temperature
CONFIRMATORY TESTS
Confirmatory tests are defined as test using different reagents or methodologies to detect the same substances as detected by the
reagent strips with the same or greater sensitivity or specificity
Non-reagent strip testing procedures using tablets and liquid chemicals may be available when questionable results are obtained or
highly pigmented specimens are encountered.
I.pH
Important in the identification of urinary crystals and determination of unsatisfactory specimens.
Important in aid of existence of systemic acid-base balance disorders. Urinary pH is controlled primarily by dietary
regulation, although medications also may be used.
Urinary pH can be used for Determination of unsatisfactory specimens
Other clinical significance of measuring Urinary pH is for Treatment of urinary tract infections and Renal calculi formation and
prevention
Normal Urine pH 4. 5 -
8.0
First morning urine pH 5.0 -6.0
II.SPECIFIC GRAVITY
Density of a solution compared with density of similar volume of distilled water at a similar temperature
Influenced by number and size of particles on a solution.
The reagent strip specific gravity test does not measure the total solute content but only those solutes that are ionic.
Normal random SG ___________
1- 002 1.035
-
I.K AYTONA 17
Reagents Multistix= poly (methyl vinyl ether/ maleic anhydride) bromthymol blue
Chemstrip= Ethylene glycol diaminoethyl ether tetra acetic acid, bromthymol blue
Sensitivity 1.000(Blue) to 1.030(Yellow)
Interference False positive: High concentration of protein (100-500mg/dl), ketoacidosis
False negative: Highly alkaline urines (greater than pH 6.5 –add 0.005 SG reading)
III.PROTEIN
Most Indicative of renal disease
Normal urine contains very little protein: usually, less than 10 mg/dL or 100 mg per 24 hours is excreted. (Strasinger)
Normal urine contains <150mg/24hrs of protein (Henry’s)
Albumin is the major protein found in normal urine due to its low molecular weight
Other Proteins Normally found:
Serum and tubular microglobulins, Tamm-Horsfall protein (Uromodulin), protein derived from prostatic and vaginal
secretion
Produces a white foam in urine
Clinical proteinuria = ≥30mg/dl or ≥300mg/L
Pre –Renal or Caused by conditions that affect the plasma prior to its reaching the kidney
Overflow
A. Hemoglobin =intravascular hemolysis
Proteinuria
B. Myoglobin = Muscle injury
C. Acute phase reactants = inflammation and infections
D. Bence Jones protein = multiple myeloma
BENCE JONES PROTEIN
An immunoglobulin light chains (kappa and lambda) found in cases of Multiple myeloma
Confirmatory Test: Serum electrophoresis
40 600
Heat reactivity test in Urine: Coagulates/Precipitates at _____________
-
and dissolves
100
at____________ oC
Benign Proteinuria
The discovery of protein, particularly in a random sample, is not always of pathologic significance, because several benign causes of
renal proteinuria exist. Benign proteinuria is usually transient and can be produced by conditions such as strenuous
exercise, high fever, dehydration, and exposure to cold.
I.K AYTONA 18
TESTS FOR MICROALBUMINURIA ( First morning)
Albumin Excretion Normal: 0-20 ug/min
Rate (AER) Microalbuminuria: ao Ho us / min y Bo Wo
-
-
/ 24 hrs
my
Immunologic Micral-Test ImmunoDip
• Principle: Enzyme immunoassay • Principle: Immunochromographics
• Sensitivity: 0 to 10 mg/dL • Sensitivity: 1.2 to 8.0 mg/dL
• Reagents: Gold-labeled antibody, • Reagents: Antibody-coated blue latex particles
B-galactosidase, Chlorophenol red Interference: False-negative: Dilute urine
galactoside
NOTE NOTE
*Strips are dipped into the urine up to a Strips are individually packaged in specially designed
level marked on the strip and held for 5 containers. The container is placed in the urine
seconds specimen for 3 minutes
*reading time is 1minute Appearance Amount(mg/dl) Interpretation
*negative result is white color Darker bottom <1.2 Negative
*positive result is red band
Equal band colors 1.2 to 1.8 Borderline
Interferences: Darker top band 2 to 8 Positive
False-positive: Strong oxidizing agent(soap)
False-negative: Dilute urine
Albumin:Creatinine The Clinitek Microalbumin reagent strips and the Multistix Pro reagent strips (Siemens Healthcare
ratio Diagnostics, Deerfield, IN) provide simultaneous measurement of albumin/protein and creatinine that
permits an estimation of the 24-hour microalbumin excretion. The strips can be read manually or on
automated Clinitek instruments. Results from the Clinitek are automatically calculated. Results are
reported as normal or abnormal.
Interferences:
• Highly buffered alkaline urine can be controlled by using paper treated with
bis- (heptapropylene glycol) carbonate
• Falsely elevated results can be caused by visibly bloody urine, and
abnormally colored urines
Results: Reported as 10, 50, 100, 200, 300 mg/dL, or 0.9, 4.4, 8.8, 17.7, or 26.5
mmol/L of creatinine
Interferences:
False increased: visibly bloody urine, presence of the gastric acid–reducing medication
cimetidine (Tagamet), and abnormally colored urines
I.K AYTONA 19
NOTE
a. Proteins mainly albumin accepts Hydrogen ions from the indicator
b. The test is more sensitive to albumin because albumin contains more amino groups to accept the
hydrogen ions than other proteins
a. The pH of the medium remains constant (pH of 3 buffered with citrate)
b. Reagent strip is sensitive to Albumin only
c. The S.G of urine sample should be check because a trace protein in diluted sample is more
significant than in concentrated sample
d. Indicators appear yellow in the absence of protein; however, as the protein concentration
increases, the color progresses through various shades of green and finally to blue
Reagents Multistix = Tetrabromphenol blue
Chemstrip = Tetrachlorophenoltetrabromosulfonphthalein
Grading Grading Quantity of Albumin
Trace <30 mg/dl
1+ 30mg/dl
2+ 100mg/dl
3+ 300mg/dl
4+ 2000mg/dl
Interference False positive False negative
• Highly buffered interference alkaline urine • Proteins other than albumin
• Pigmented specimens, phenazopyridine • Microalbuminuria
•
•
Quaternary ammonium compounds (detergents)
Antiseptics, chlorhexidine Ltfimmelstiel Wilson
• Loss of buffer from prolonged exposure of the
strip to the specimen reagent
• High specific gravity
The specific gravity of the urine specimen should be considered in evaluating urine protein because a trace protein in a dilute
specimen is more significant than in a concentrated specimen.
PROCEDURE – 3mL of 3% SSA (Exton’s reagent) or 7%SSA + 3ml centrifuged urine = (+) cloudiness
SSA GRADING
GRADE TURBIDITY PROTEIN RANGE (mg/dl)
Negative No increase turbidity <6
Trace Noticeable turbidity 6-30
1+ Distinct turbidity with no granulation 30-100
2+ Turbidity with granulation, no flocculation 100-200
3+ Turbidity with granulation, and flocculation 200-400
4+ Clumps of protein >400
SSA INTERFERENCES
False increase/positive • Radiographic contrast dye/x-ray film
• Drugs (Tulbotamide, Penicillin, Sulfonamide, Cephalosporin)
• para-amino-salicylic acid/Salicylates
False decrease/negative • Highly alkaline urine
• Quaternary ammonium compounds (e.g Detergents, and soap)
MICROSCOPICALLY, WHAT IS THE SSA PATTERN IF PROTEINS CAUSE A POSITIVE REACTION? Amorphous
MICROSCOPICALLY, WHAT IS THE SSA PATTERN IF DRUGS AND RADIOGRAPHIC CONTRAST DYE Crystalline
CAUSE A POSITIVE REACTION?
IV.GLUCOSE
Most frequently performed chemical analysis on urine (due to monitoring of DM).
Renal threshold- plasma concentration of a substance at which tubular reabsorption stops
Renal threshold for glucose = 160-180 mg/dl
Specimens used: Fasting/8-Hours urine sample/ First morning urine / Second Morning urine/2hr post prandial
A first morning specimen does not always represent a fasting specimen because glucose from an evening meal may remain in
the bladder overnight, and patients should be advised to empty the bladder and collect the second specimen
I.K AYTONA 20
REAGENT STRIP REACTION FOR GLUCOSE (30 seconds)
Principle double sequentialenzyme
Glucose oxidase
Glucose + O2 --------------------------→gluconic acid + Hydrogen Peroxide
Peroxidase
Hydrogen Peroxide + Chromogen-----------------→ Oxidized chromogen + Water
STEP: In the first step, glucose oxidase catalyzes a reaction between glucose and room air (oxygen) to produce
gluconic acid and peroxide. In the second step, peroxidase catalyzes the reaction between peroxide and
chromogen to form an oxidized colored compound that is directly proportional to the concentration of glucose.
Color charts provide quantitative measurements ranging from 100 mg/dL to 2 g/dL, or 0.1% to 2%.
Reagents Multistix = glucose oxidase, peroxidase, Potassium iodide (blue to green to brown)
Chemstrip = glucose oxidase, peroxidase, tetramethylbenzidine (yellow to green)
Other chromogens:
Aminopropylcarbazole (yellow to orange brown) and O-toluidine (pink to purple)
Grading
Grading Trace 1+ 2+ 3+ 4+
Amount of 1/10 g/dl (%) ¼ g/dl (%) 1/2 g/dl (%) 1 g/dl (%) 2g/dl (%)
glucose or or or or or
100 mg/dl 250 mg/dl 500 mg/dl 1000 mg/dl 2000 mg/dl
Interference False positive:
a. Contamination of oxidizing agents and detergents
False negative:
stairs
a. High levels of ascorbic acid
b. High levels of ketones
c. High SG
d. Low temp
e. Improperly preserved specimens
Iodate It is added by the manufacturers in the glucose reagent strip to minimize interference by ascorbic
acid. This chemical oxidizes ascorbic acid so that it cannot interfere with the oxidation of the
chromogen
The tablet, when placed in a mixture of water and urine, the tablet is rapidly dissolved by the action
of sodium carbonate and citric acid which act as an effervescent. The sodium hydroxide provides the
alkaline medium necessary for the reaction, and the heat required is provided by the reaction of
sodium hydroxide with water and citric acid
Procedure 5 gtts urine + 10gtts distilled H2O + Clinitest tablet ---→ observe the reaction
Note: Wait 15 seconds after boiling (there is effervescent formation) has stopped and
gently shake the contents of the tube
* Upon addition of the tablet to water and urine, heat is produced by the hydrolysis of sodium
hydroxide and its reaction with sodium citrate, and carbon dioxide is released from the sodium
carbonate to prevent room air from interfering with the reduction reaction.
* Clinitest tablets are very hygroscopic and should be stored in their tightly closed packages. A
strong blue color in the unused tablets suggests deterioration due to moisture accumulation,
as does vigorous tablet fizzing.
CuSO4(cupric sulfide) + reducing substance --- > Cu2O (cuprous oxide) + oxidized substance -→color
* The sensitivity of Clinitest to glucose is reduced to a minimum of 200 mg/dL so the Clinitest
cannot be used as a confirmatory test for glucose.
Interference False Positive:
Reducing agents such as vitamin C, formalin, uric acid, and some drugs (cephalosporin)
False Negative:
Oxidizing agents such as detergent
I.K AYTONA 21
Grading
B 610¥
Grading Color Sugar level Negative clear blue color, blue precipitate may form
negative Blue ¼% Trace-bluish-green color
1+ Green ½% 1 + green color, green or yellow precipitate
2+ Yellow ¾% 2+yellow to green color, yellow precipitate
3+ Orange 1% 3+yellow-orange color, yellow-orange precipitate
a
V.KETONES
Result from increased fat metabolism. They are formed from beta oxidation of fats.
a. Inability to metabolize or utilize available carbohydrate – ex. DM type1
b. Increased loss of carbohydrates – ex. Vomiting
c. Inadequate intake of carbohydrate – ex. Starvation and malabsorption/pancreatic disorder
d. Overuse of available carbohydrates – frequent strenuous exercise
Ketone Bodies:
a. 78% Beta Hydroxybutyric acid – major ketone but not detected in reagent strip
b. 20% Acetoacetic acid (AAA) / Diacetic acid – parent ketone
c. 2 % Acetone – detected only when glycine is present
When the blood ketone concentration exceeds 70 mg/dL (the renal threshold level), ketones are excreted in the urine
ACETEST TABLET -
confirmatory
Composition:
a. Sodium nitroprusside
b. Disodium phosphate
c. Lactose –gives better color differentiation
The Acetest tablet test has been used as a confirmatory test for
questionable reagent strip results; however, it was primarily used for
testing serum and other bodily fluids and dilutions of these fluids for severe
ketosis
Read for 30 seconds
Report as negative, small (5 to10mg/dl), moderate (30 to
40mg/dl, or large (80 to 100mg/dl).
Acetest tablets are hygroscopic; if the specimen is not completely absorbed
within 30 seconds, a new tablet should be used.
Acetest can be used to test urine, serum, plasma, or whole blood
10 times more sensitive to diacetic acid than to acetone
I.K AYTONA 22
VI.BLOOD
The finding of a positive reagent strip test result for blood indicates the presence of red blood cells, hemoglobin, or
myoglobin.
Any amount of blood greater than five cells per microliter of urine is considered clinically significant Stocks / UL
Reabsorption of filtered hemoglobin also results in the appearance of large yellow-brown granules of denatured ferritin called
hemosiderin in the renal tubular epithelial cells and in the urine sediment.
The heme portion of myoglobin is toxic to the renal tubules, and high concentrations can cause acute renal failure
Hemoglobin
Hydrogen peroxide + chromogen -----------------------------→ oxidized chromogen + H20
Pseudoperoxidase
Through pseudoperoxidase activity of the heme moiety, peroxide is reduced and the chromogen becomes
oxidized, producing a color change on the reaction pad from yellow to green
Reagents Multistix = diisopropylbenzenedehydroperoxidetetramethylbenzidine
Chemstrip = dimethyldihydroperoxyhexanetetramethylbenzidine
Interference False positive:
a. Strong oxidizing agents
b. Vegetable and Bacterial peroxidases (e.g Escherichia coli)
c. Menstrual contamination
False negative:
a. High SG / Crenated cells
b. Formalin
c. Captopril
d. Ascorbic acid (>25mg/dl)
e. Unmixed specimen / failure to mix the specimen prior to testing
f. High concentration of nitrite (>10mg/dl)
I.K AYTONA 23
VII.BILIRUBIN
The appearance of bilirubin in the urine can provide an early indication of liver disease. It is associated with:
a. Hepatic jaundice = Hepatitis and Cirrhosis
b. Post hepatic jaundice = Biliary obstruction (gallstones, carcinoma)
Only the B2 or conjugated bilirubin is water soluble thus can be seen in urine and can be detected.
It produces an amber urine with yellow foam
Conjugated bilirubin is normally excreted in the bile into the duodenum, and normal adult urine contains only 0.02 mg of
bilirubin per deciliter. This small amount is not detected by the usual testing methods.
Excretion of bilirubin is enhanced by alkalosis
Reagent strip color reactions for bilirubin are more difficult to interpret than other reagent strip reactions and are
easily influenced by other pigments present in the urine
Contimatrons
ICTOTEST (Tablet) FOR BILIRUBIN
A confirmatory test for bilirubin is the Ictotest
Ictotest is much more sensitive than the dipsticks, being able to detect as
-
VIII.UROBILINOGEN
✓ A bile pigment that results from hemoglobin degradation
✓ Conjugated bilirubin is reduced by intestinal bacteria into urobilinogen
✓ A small amount of urobilinogen – less than 1mg/dl or Ehrlich unit – is normally found in the urine.
✓ Clinical significance: urine urobilinogen greater than 1 mg/dl is seen in liver disease and hemolytic disorders.
I.K AYTONA 24
REAGENT STRIP REACTION FOR UROBILINOGEN (60 seconds)
Principle Ehrlich ‘s reaction
-
Multistix: Uses Ehrlich reagent
f- dimethylbenzal
amino dehyde Urobilinogen + p-dimethlyaminobenzaldehyde ----------→ red color
What would be the result of urobilinogen measurements if the reagent strip is performed at a higher temperature?
ANS: Falsely increased
RATIO: The sensitivity of the Ehrlich reaction increases with temperature, and testing should be performed at room temperature
WATSON-SCHWARTZ TEST
• Used to differentiate urobilinogen, porphobilinogen, and other Ehrlich reactive compounds
• Uses extraction with organic solvents chloroform and Butanol
Interpretation:
1. When the tube is shaken, the red color is seen throughout the solution. The test detects approximately 2 mg/dL of
porphobilinogen,
2. Urobilinogen is inhibited by the highly acidic pH.
3. High concentrations of methyldopa and indican, and highly pigmented urines, may produce false positive results.
I.K AYTONA 25
1st morning / 4h our fasting
r
IX.NITRITE
✓ Provides a rapid screening test for the presence of UTI and bacteriuria.
✓ The nitrite test also can be used to evaluate the success of antibiotic therapy and to periodically screen persons with recurrent
infections, patients with diabetes, and pregnant women, all of whom are considered to be at high risk for UTI
✓ It is not intended to replace the urine culture as the primary test for diagnosing and monitoring bacterial infection.
✓ Specimen used: 1st morning or 4 hours urine
✓ The chemical basis of the nitrite test is the ability of certain bacteria to reduce nitrate, a normal constituents of
urine, to nitrite, which does not normally appear in the urine.
*Nitrite at an acidic pH reacts with an aromatic amine (para-arsanilic acid or sulfanilamide) to form a
diazonium compound that then reacts with tetrahydrobenzoquinolin compounds to produce a pink-
colored azodye
Reagents Multistix = p-arsanilic acid, tehtrahydrobenzoquinolin-3-ol
Chemstrip = sulfanilamide, hydroxytetrahydrobenzoquinoline
Interference False positive:
a. Improperly preserved specimens
b. Highly pigmented urine
False Negative
a. Non reductase containing bacteria
b. Insufficient contact time between bacteria and urinary nitrate
c. Large quantities of bacteria converting nitrite to nitrogen
d. Presence of antibiotics
e. Ascorbic acid
f. High specific gravity
Note Positive result should uniform/Homogenous pink
Pink spots/edge is considered as NEGATIVE
Results are reported only as negative or positive.
Positive nitrite corresponds to 3100
___________
, on organisms/ml
-It is for gram negative bacteria/bacilli which are mostly nitrite positive
-Enterobacteriaceae/coliform gives nitrite positive result
X.LEUKOCYTES
Significance: UTI/inflammation, Screening of urine culture specimen, bacterial and non-bacterial infection
It detects the presence of leukocyte that have been lysed, particularly in dilute alkaline urine
It offers a more standardized means for detection of leukocytes
The test is not designed to measure the concentration of leukocytes, and it is recommended that quantitation should be done
by microscopic examination.
LE test detects esterase found in
a. Neutrophil
b. Basophil
c. Eosinophil
] Granulocytes
d. Monocytes
-
e. Trichomonas
f. Chlamydia
g. Yeast
h. Histiocytes
Screening urine specimens using LE test should be correlated with nitrite chemical reactions
NEGATIVE FOR LYMPHOCYTES
Lymphocytes, erythrocytes, bacteria, and renal tissue cells do not contain esterases
Infections involving trichomonads, mycoses (e.g., yeast), chlamydia, mycoplasmas, viruses, or tuberculosis cause leukocyturia
or pyuria without bacteriuria
LE
Indoxylcarbonic acid ester---------→indoxyl + acid indoxyl + Diazonium salt -→ (+) Purple azodye
* The reagent strip reaction uses the action of LE to catalyze the hydrolysis of an acid ester embedded on
the reagent pad to produce an aromatic compound and acid. The aromatic compound then combines with
a diazonium salt present on the pad to produce a purple azodye.
Reagent Multistix = Diazonium salt, derivatized pyrrole amino acid ester
Chemstrip =Diazonium salt, Indoxylcarbonic acid ester
Sensitivity Multistix = 5 to 15 WBC/hpf
Chemstrip = 10 to 25 WBC/hpf
I.K AYTONA 26
Interference False positive:
a. Strong oxidizing agents
b. Formalin
c. Highly pigmented urine, nitrofurantoin, beets, phenazopyridine
d. False-positive results for leukocyte esterase are most often obtained on urine specimens
contaminated with vaginal secretions
False negative:
a. High concentration of protein (Greater than 500 mg/dl), high glucose (≥3g/dl), oxalic acid
(in acidified urine that has 4.4pH or below) and ascorbic acid
b. Antibiotics such as gentamicin, cephalosporins, tetracyclines,
c. Inaccurate timing
The LE reaction requires the longest time of all the reagent strip reactions (2 minutes). Trace readings may not be significant and
should be repeated on a fresh specimen.
ASCORBIC ACID
It is the 11th parameter
Causes False Negative result to BBLNG (Blood, Bilirubin, Leukocyte, Nitrite, Glucose)
Causes False Positive result to Clinitest
Ascorbic acid level that causes a negative reaction to Bilirubin and Nitrite ≥25mg/dl
Ascorbic acid level that causes a negative reaction to glucose ≥50mg/dl
tabw SUMMARY
make
Test Principle (+) result Reading time
Bilirubin Be Diazo reaction Violet, tan, or pink 30 secs
Glucose ] Good 130s ) Double sequential enzymatic reaction Potassium iodide 30secs
= blue-green to brown
Ketones Sod. Nitroprusside (Legal’s reaction) Purple 40secs
S.G pKa change of polyelectrolyte Diluted = blue 45secs
_ÉÉ
Concentrated =yellow
pH Double indicator system Acidic = red to yellow 60secs
PPBUN
]
Alkaline = green to blue
Protein 60s Protein (Sorensen’s) error of indicator Blue-green 60secs
Blood Pseudoperoxidase activity of hemoglobin Green to blue 60secs
urobilinogen Ehrlich’s reaction Red 60secs
Nitrite Greiss reaction Pink 60secs
Leukocyte Leukocyte esterase Purple 120secs
Specimen Preparation
Urine 10 -15 ml
↓
Centrifuge at 400 RCF for 5 minutes
↓
Decant
↓
Get the sediment (0.5-1.0mL)
↓
Place the sediment on the microscopic slide (20 ul or 0.02ml)
↓
Covered by glass cover slip (22x22mm)
↓
Observe under the microscope (Bright field –reduced lightning)
To correct for differences in the diameter of centrifuge heads, RCF rather than revolutions per minute (RPM) is used.
Formula: RCF(g) = 1.118 x 10-5 x radius (cm) x RPM2
I.K AYTONA 27
SEDIMENT STAINS
STAIN ACTION FUNCTION
Sternheimer-Malbin(a supravital -Delineates structure and contrasting -Identifies WBCs, epithelial cells, and
stain consisting of Crystal violet and colors of the nucleus and cytoplasm casts
safranin)
WEC
0.5%Toluidine blue -Enhances nuclear detail Differentiates WBCs and renal
(a metachromatic supravital stain) tubular epithelial (RTE) cells
2% acetic acid Lyses RBCs and enhances nuclei of Distinguishes RBCs from WBCs, yeast, oil
WBCs droplets, and crystals
Lipid Stains: Oil Red Stain triglycerides and neutral fats Identifies free fat droplets and lipid
O and Sudan III orange-red containing cells and casts
Gram stain Differentiates gram-positive and Identifies bacterial casts
gram negative bacteria
Hansel stain Methylene blue + EosinY Identifies urinary eosinophils
Stains eosinophilic granules
Prussian blue stain Stains structures containing iron Identifies yellow-brown granules of
hemosiderin in cells and casts
Sedi and KOVA stain Modified Sternheimer Malbin Hyaline cast appears as pink
The dye is absorbed well by WBCs, WEC Motile bacteria are unstained
epithelial cells, and casts, providing Non-motile bacteria stains purple
clearer delineation of structure and T.vaginalis stains Light blue-green
contrasting colors of the nucleus and
cytoplasm
ADDITIONAL INFORMATION
1. One disadvantage of its use is that in strongly alkaline urines, this stain can precipitate, which obstructs the visualization of
sediment components.
2. In Oil Red O and Sudan III, cholesterol and cholesterol esters do not stain and must be confirmed by polarizing
Microscopy
3. Wright’s stain or Giemsa stain also distinguishes urinary eosinophils, but Hansel stain is preferred.
CYTODIAGNOSTIC URINALYSIS
Play an important role in the early detection of renal allograft rejection and in the differential diagnosis of renal disease.
Involves making a 10:1 concentration of a first morning urine specimen, followed by cytocentrifugation of the urine
sediment and Papanicolaou’s staining
MICROSCOPY
Phase contrast Enhances visualization of elements with low refractive indices, such as hyaline casts,
microscopy mixed cellular casts, mucous threads, and Trichomonas
-
Type of microscopy in which variations in the specimen’s refractive index are converted into
low refractive index variations in light intensity or contrast
Adaptation of a bright-field microscope with a phase-contrast objective lens and a matching
condenser. Two phase rings that appear as “targets” are placed in the condenser and the
objective.
Light passes to the specimen through the clear circle in the phase ring in the condenser, forming
a halo of light around the specimen
Polarizing Aids in identification of cholesterol in oval fat bodies, fatty casts, and crystals.
microscopy It uses halogen quartz lamp that produces light rays of many different waves
A substance that rotates the plane of polarized light 90 degrees in a clockwise direction is said
to have positive birefringence.
Substance that rotates the plane in a counterclockwise direction has negative
birefringence
Bright-field microscopes can be adapted for polarizing microscopy. Two polarizing filters
must be installed in a crossed configuration
I.K AYTONA 28
Dark field Aids in identification of spirochetes such as Treponema pallidum
microscopy bright-field microscope is easily adapted for dark-field microscopy by replacing the condenser
with a dark-field condenser that contains an opaque disk
The specimen appears light against the black background or dark-field
Fluorescence Allows visualization of naturally fluorescent microorganisms or those stained by a fluorescent dye
microscopy Fluorescence microscopy uses two filters: one to select a specific wavelength of illumination light
(excitation filter) that is absorbed by the specimen, and another (barrier filter) to transmit the
different, longer-wavelength light emitted from the specimen to the eyepiece for viewing
PARTS OF MICROSCOPE
Lens system Illumination system BODY
1. Oculars 0 1. Light source 1. Base
2. Objectives 2. Condenser UCS 2. Body tube
BBN
3. Adjustment knobs 3. Stage field 3. Nose piece
4. Iris diaphragms
CARE OF MICROSCOPE
1. Carry microscope with two hands, supporting the base with one hand.
2. Always hold the microscope in a vertical position.
3. Clean optical surfaces only with a good quality lens tissue and commercial lens cleaner.
4. Do not use the 10× and 40× objectives with oil.
5. Clean the oil immersion lens after use.
6. Always remove slides with the low-power objective raised.
7. Store the microscope with the low-power objective in position and the stage centered.
TERMINOLOGIES
Aperture diaphragm Microscope component that regulates the angle of light presented to the specimen.
Birefringent/ doubly The ability of a substance to refract light in two directions.
refractile
Chromatic aberration Unequal refraction of light rays by a lens that occurs because the different wavelengths of light
refract or bend at different angles
condenser Microscope component that gathers and focuses the illumination light onto the specimen for
viewing.
Eyepiece The microscope lens or system of lenses located closest to the viewer’s eye. It produces the
secondary image secondary image magnification of the specimen
Field diaphragm Microscope component that controls/regulates the diameter of light beams that strike the specimen
and hence reduces stray light.
Field of view The circular field observed through a microscope
Köhler illumination Type of microscopic illumination in which a lamp condenser (located above the light source) focuses
the image of the light source (lamp filament) onto the front focal plane of the substage condenser
(where the aperture diaphragm is located)
Mechanical stage Microscope component that holds the microscope slide with the specimen for viewing.
Objectives The lens or system of lenses located closest to the specimen. The objective produces the primary
primary image image magnification of the specimen.
Parcenter Term describing objective lenses that retain the same field of view when the user switches from
one objective to another of a differing magnification
Parfocal Term describing objective lenses that remain in focus when the user switches from one objective to
another of a differing magnification.
Resolution Ability of a lens to distinguish two points or objects as separate.
Cytocentrifugation A technique used to produce permanent microscope slides of urine sediment and body fluids. The
end result is a monolayer of the urine sediment components with their structural details greatly
enhanced by staining
Magnification Process of enlarging or magnifying an object’s size without affecting its actual or physical size
I.K AYTONA 29
LENS Individual magnification Total magnification (Eyepiece x Objective)
Eyepiece 10x --
Scanner 5x or 4x 50x or 40x
LPO 10x 100x
HPO 40x 400x
OIO 100x 1000x
I.K AYTONA 30
II.White Blood Cells Renal transplant rejection lymphocytes
-
WBCs are larger than RBCs, measuring average of about 12-um in diameter
Pyuria or leukocytoruia- Term used to denote increase urinary WBCs and is associated with bacterial infection
(UTI), Interstitial nephritis, and SLE
Neutrophil is the predominant WBC found in urine
Neutrophils lyse rapidly in dilute alkaline urine and begin to lose nuclear detail.
In Hypotonic urine, white blood cell swells and become spherical balls that lyse as rapidly as 50% in 2 to 3 hours at
room temperature
Hypotonic Urine: Glitter Cells – WBC with sparkling appearance due to Brownian movement of the
granules. When stained with Sternheimer-Malbin stain, these large cells stain light blue as opposed to the violet
color usually seen with neutrophils
In hypertonic urine, leukocytes become smaller as water is lost osmotically from the cells, but they do not crenate.
Another degenerative change in WBC is the development of numerous finger-like or wormlike projections protruding
from their surfaces. These long filaments, termed myelin forms, result from the breakdown of the cell membrane
Eosinophil - The presence of urinary eosinophils is primarily associated with drug-induced interstitial
nephritis; however, small numbers of eosinophils may be seen with urinary tract infection (UTI) and renal transplant
rejection. Eosinophils are not normally seen in the urine; therefore, the finding of more than 1% eosinophils is
considered significant
Lymphocytes predominate in urine from patients experiencing renal transplant rejection.
Normal WBC in urine = 0-5 WBC/hpf for male, and 0-8 WBC/hpf for female
eccentrically located
III.Epithelial Cells
Originates from the linings of the vagina and female urethra and the lower portion of the male urethra.
Squamous cells are the largest cells found in the urine sediment. They contain abundant, irregular cytoplasm and
a prominent nucleus about the size of an RBC. They may appear as flagstone-shaped with distinct cell borders
The point of reference in microscopic analysis
They may occasionally appear folded, possibly resembling a cast, and will begin to disintegrate in urine that
is not fresh.
Increased amounts are more frequently seen in females.
Clue cells: pathologic squamous epithelial cell covered with the Gardnerella vaginalis coccobacillus
To be considered a clue cell, the bacteria should cover most of the cell surface and extend beyond the
edges of the cell. This gives the cell a granular, irregular appearance.
B.
percentrally located
Transitional Epithelial (Urothelial) cells/ Bladder epithelial cells
Transitional epithelial cells originate from the lining of the renal pelvis, calyces, ureters, and bladder,
and from the upper portion of the male urethra.
nor
Transitional epithelial cells are smaller than squamous cells and appear in several forms, including spherical,
polyhedral, and caudate. The differences are caused by the ability to absorb large amounts of water.
They are two to four times as large as white cells. They may be round, pear-shaped, or may have taillike
¥6k
projections. Occasionally, these cells may contain two nuclei.
Spherical forms of transitional epithelial cells are sometimes difficult to distinguish from RTE cells.
The presence of a centrally located rather than eccentrically placed nucleus, and supravital staining,
can aid in the differentiation.
Increased numbers of transitional cells seen singly, in pairs, or in clumps (syncytia)are present following invasive
urologic procedures such as catheterization and are of no clinical significance. An increase in
transitional cells exhibiting abnormal morphology such as vacuoles and irregular nuclei may be
indicative of malignancy or viral infection.
collecting :
Cells from the distal convoluted tubule (DCT) are smaller than those from the PCT and are round or oval.
Collecting duct RTE cells are cuboidal and are never round. Along with the eccentrically placed nucleus, the
presence of at least one straight edge differentiates them from spherical and polyhedral transitional cells. Cells
from the collecting duct that appear in groups of three or more are called renal fragments. They are
frequently seen as large sheets of cells. Renal fragments are an indication of severe tubular injury with
basement membrane disruption.
a-
RTE cells often resemble casts and they should be closely examined for the presence of a nucleus, as a
nucleus would not be present in a cast.
-
I.K AYTONA 31
Tubular Injury: presence of more than 2 RTE/HPF
RTE cells are the most clinically significant of the epithelial cells and the presence of increased amounts
is indicative of necrosis of the renal tubules
They are the precursor of oval fat bodies
Conditions producing tubular necrosis include exposure to heavy metals, drug-induced toxicity, hemoglobin and myoglobin
toxicity, viral infections (hepatitis B), pyelonephritis, allergic reactions, malignant infiltrations, salicylate poisoning, and acute
allogenic transplant rejection
Bubble cells – RTE cells containing large, nonlipid-filled vacuoles that is mainly associated with Acute tubular
necrosis. They appear to represent injured cells in which the endoplasmic reticulum has dilated prior to cell death
V.Bacteria
UM = bacteria + WBCS
They appear as small spherical and rod-shaped structures
Bacteria are not normally present in urine
To be considered significant for UTI, bacteria should be accompanied by WBCs.
They are motile and is useful to differentiate from similar appearance, amorphous urates and
phosphates
The actual bacteria producing an UTI cannot be identified with the microscopic examination.
VI.Yeast
Yeast cells appear in the urine as small, refractile oval structures that may or may not contain a bud.
In severe infections, they may appear as branched, mycelial forms
Yeast cells, primarily Candida albicans, are seen in the urine of diabetic, immunocompromised
patients and women with vaginal moniliasis.
A true yeast infection should be accompanied by the presence of WBCs.
FAVORABLE URINE CONDITION: ACIDIC urine and with glucose
VII.Parasites
Trichomonas vaginalis – most frequent parasite encountered in urine
Schistosoma haematobium – bladder parasite, associated with bladder tumors
Enterobius vermicularis- most common contaminant ova
Cyst of Giardia lamblia- observed in urine sediment as the result of fecal contamination of infected individuals
When not moving, Trichomonas is more difficult to identify and may resemble a WBC, transitional, or RTE cell. Use of phase
microscopy may enhance visualization of the flagella or undulating membrane.
I.K AYTONA 32
VIII. Spermatozoa
Spermatozoa are easily identified in the urine sediment by their oval, slightly tapered heads and long, flagellalike
tails
Urine is toxic to spermatozoa; therefore they rarely exhibit the motility observed when examining a semen
specimen.
They are rarely of clinical significance except in cases of male infertility or retrograde ejaculation in
which sperm is expelled into the bladder instead of the urethra.
Laboratory protocols vary with regard to reporting or not reporting the presence of spermatozoa in a urine
specimen
IX.Mucus
Mucus is a protein material produced by the glands and epithelial cells of the lower genitourinary tract and the
RTE cells.
Mucus appears microscopically as thread-like structures with a low refractive index
Uromodulin / Tamm-Horsfall protein is the major constituent or matrix of the mucus
Mucus is more frequently present in female urine specimens. It has no clinical significance when present in either
female or male urine.
Increase in numbers are found in cases of UTI.
Hemosiderin granules are found in the urine sediment 2 to 3 days after a severe hemolytic episode (e.g.,
transfusion reaction, paroxysmal nocturnal hemoglobinuria).
Hemosiderin granules may be found free floating or within macrophages, casts, or tubular epithelial cells.
The Prussian blue reaction, also known as the Rous test, is used to identify hemosiderin in the urine sediment
and in tissues.
The urine sediment is suspended in a freshly prepared solution of potassium ferricyanide–HCl and is allowed to
stand at room temperature for 10 minutes. After centrifugation and discarding of the supernatant, the
sediment is reexamined for the presence of coarse blue granules
URINARY CAST
CYLINDRURIA– presence of urinary cast
Casts are the only elements found in the urinary sediment that are unique to the kidney.
The major constituent/mould /template/ matrix of cast is UROMODULIN which is secreted by the RTE Cells.
The protein (uromodulin) gels more readily under conditions of urine-flow stasis, acidity, and the presence of sodium and
calcium.
Uromodulin protein is found in both normal and abnormal urine
Casts are Formed in DCT, and Collecting duct
Examination of casts should be performed along the edges of the cover slip.
Cylindroids – formed at the ALH and DCT with tapered end or have a tail at the other tail. They have the same
significance as casts (hyaline cast).
Cylindroids are product of incomplete cast formation, or cast disintegration.
↳ incomplete cast formation
CAST FORMATION
From least significant to the most significant
Hyaline Cast→ Cellular cast→ Coarse granular cast → Fine granular cast → Waxy cast → Broad Cast
NOTE
Hypotonic and alkaline urine promotes the disintegration of casts in the urine sediment.
Acid pH, increased solute concentration, urine stasis, and increased plasma proteins (particularly albumin) enhance cast
formation
If the conventional glass-slide method is being used, casts have a tendency to locate near the edges of the cover slip;
therefore, low-power scanning of the cover-slip perimeter is recommended
I.K AYTONA 33
HYALINE CAST
Most frequently seen cast which consists almost entirely of uromodulin
Pro – cast
Hyaline casts appear colorless in unstained sediments and have a low refractive index similar to that of urine; thus, they
can easily be overlooked if specimens are not examined under subdued light
The morphology of hyaline casts is varied, consisting of normal parallel sides and rounded ends, cylindroid forms, and
wrinkled or convoluted shapes that indicate aging of the cast matrix
The accompanying dehydration of the protein fibrils and internal tension may account for the wrinkled and convoluted
appearance of older hyaline casts Physiologic increase HER
Physiologic increase: 1. Strenuous exercise 2. Dehydration 3. Heat exposure 4. Emotional stress
Pathologic increase: 1. Acute glomerulonephritis 2. Pyelonephritis 3. Chronic renal disease 4. Congestive
heart failure
WBC CAST
primary marker differentiating
-
The appearance of WBC casts in the urine signifies infection or inflammation within the nephron.
They are most frequently associated with pyelonephritis and are a primary marker for distinguishing pyelonephritis (upper
UTI) from Cystitis (lower UTI)
They are also present in non-bacterial inflammations such as acute interstitial nephritis and may accompany RBC casts in
glomerulonephritis
WBC casts are visible under low-power magnification but must be positively identified using high power
Staining and the use of phase microscopy can be helpful to enhance the nuclear detail needed for differentiating WBC cast
from Epithelial cast
FATTY CAST
Fatty casts are seen in conjunction with oval fat bodies and free fat droplets in disorders causing lipiduria.
They are most frequently associated with the nephrotic syndrome, but are also seen in toxic tubular necrosis, diabetes
mellitus, and crush injuries
Confirmation of fatty casts is performed using polarized microscopy and Sudan III or Oil Red O fat stains.
I.K AYTONA 34
BROAD CAST Renal failure casts
-
Granular, dirty, brown casts representing hemoglobin degradation products such as methemoglobin may also be present
They are associated with the acute tubular necrosis often caused by the toxic effects of massive hemoglobinuria
that can lead to renal failure.
These dirty, brown casts must be present in conjunction with other pathologic findings such as RTE cells and a positive
reagent strip test for blood
OTHER CAST
Mixed cellular cast
-The presence of mixed elements in a cast may make identification more difficult. Staining or phase microscopy aids in the
identification. When mixed casts are present, there should also be homogenous casts of at least one of the cell types, and
they will be the primary diagnostic marker
Bilirubin cast
Epithelial cast / RTE cast
LOOK-A-LIKES
1. Mucus threads = can be misidentified as hyaline cast
2. Cotton threads or diaper fibers = resembles waxy cast
3. Folded squamous epithelial cells
4. Aggregates of amorphous crystals
SOURCES OF ERROR
Cast Sources of error
Hyaline Cast Mucus, fibers, hair, increased lighting
RBC Cast RBC clumps
WBC Cast WBC clumps
Bacterial Cast Granular casts
Epithelial / RTE Cast WBC cast
Granular Cast Artifacts such as Clumps of small crystals, Fecal debris
Columnar RTE cells
Waxy Cast Fibers and fecal material
Fatty Cast Fecal debris
Broad Cast Fecal material, fibers
URINARY CYRSTALS
➢ Crystals are formed by the precipitation of urine solutes, including inorganic salts, organic compounds, and medications
(iatrogenic).
➢ Crystal formation is affected by changes in: pH, Temperature, solute concentration frystal Iara tempura 8-hake
➢ Solutes precipitate more readily at low temperatures.
➢ Usually reported as rare, few, moderate, or many per hpf
➢ Abnormal crystals may be averaged and reported per lpf
Crystals formed in acidic urine Amorphous urates, Calcium oxalate, uric acid, and all abnormal crystals
Crystals formed in alkaline urine Amorphous phosphates, ammonium biurate, calcium carbonate, calcium phosphate, and
Triple phosphate
I.K AYTONA 35
NORMAL URINARY CRYSTALS
Crystal Information Significance Solubility
Amorphous urates Brick dust / yellow brown granules None Alkali and heat
Pink sediment (uroerythrin) *
Note! It will convert to uric acid crystals orange sand
with acidification with acetic acid diaper
↑
Uric acid Rhombic, wedge, hexagonal, four-sided flat Lesch Nyhan syndrome Alkali
Lesch Nyman LGC
plate(whetsone), lemon shaped, nipple Gout
-
Gout
chemotherapy shaped. SEEN IN VARIETY OF SHAPE Chemotherapy leukemia
Calcium oxalate Forms: ↑food high in ascorbic acid and Dilute HCL
•
dihydrate envelope /pyramidal
-
0
a.dihydrate (weddelite) oxalic acid
fwedellite
)
dumbbell /oval • envelope or pyramidal.
monohydrate
-
wnewellitegf
[
b. monohydrate (whewellite)
• oval/dumbbell/hour glass shape Ethylene glycol poisoning
Amorphous Granular in appearance None Dilute acetic acid
phosphates White precipitate
Ammonium biurate Thorny apples Presence of urea- splitting Acetic acid with heat
SINE
Seen in old specimens bacteria
Triple phosphate / Colorless, prism-shape or “coffin lid” Presence of urea-splitting Dilute acetic acid
magnesium Feathery appearance when they bacteria
P.HU/garisapatiH-
ammonium disintegrate, Fern-leaf shape, sheets or
phosphate/ struvite flakes Associated with P. vulgaris
Calcium phosphate/ Colorless, flat plates, thin prisms often in None Dilute acetic acid
apatite rosette form
Cystinuriaicystinosis Mistaken as _@
uric acid crystals cystinosis
Cholesterol Rectangle w/
notched sides
-
#
Mistaken as Crystal of radiographic dye
Tyrosine Colorless to yellow needles in clumps or rosettes Liver disease Alkali or heat
Leucine Yellow brown spheres with concentric circles and Liver disease Hot alkali or alcohol
radial striations
0Sulfonamide
color
-
€
Colorless to yellow brown needles, sheaves of 0
Possible tubular
chloroform, and alkali
Acetone
⑧heaves of wheat
@ wheat, rosette, rhombics, whetstone damage
1- lignin test
:25Hutun 're @
May be mistaken with calcium phosphate crystals
yellow in rosette form.
_
calcium
A-sulfonamide Calcium phosphate: soluble to dilute acetic acid
-
phosphate
Sulfonamide:
(+) lignin test (urine+25%HCL=Yellow)
Ampicillin Colorless needles that tend to form bundles Massive dose of Refrigeration forms bundles
following refrigeration penicillin
I.K AYTONA 36
=
ADDITIONAL INFORMATION
The most common crystals seen in acidic urine are urates, consisting of amorphous urates, uric acid, acid
urates, and sodium urates. Microscopically, most urate crystals appear yellow to reddish brown and are the
only normal crystals found in acidic urine that appear colored.
Acid urates appear as larger granules and may have spicules similar to the ammonium biurate crystals seen in alkaline
urine
Sodium urate crystals are needle-shaped and are seen in synovial fluid during episodes of gout, but may also appear in the
urine.
I.K AYTONA 37
The most common form of calcium oxalate crystals is the dihydrate that is easily recognized as a colorless,
octahedral envelope or as two pyramids joined at their bases
Calcium oxalate crystals are sometimes seen in clumps attached to mucous strands and may resemble casts.
Calcium oxalate crystals are also associated with foods high in oxalic acid, such as tomatoes and asparagus, and
ascorbic acid, because oxalic acid is an end product of ascorbic acid metabolism
Phosphates represent the majority of the crystals seen in alkaline urine
Ammonium biurate crystals resemble other urates in that they dissolve at 60°C and convert to uric acid crystals when
glacial acetic acid is added
Cholesterol crystals are rarely seen unless specimens have been refrigerated, because the lipids remain in droplet form
Manner of Reporting
RBC, WBC Average number per 10 HPF
Casts Average number per LPF
Squamous epithelial cells Rare, few, moderate, or many per LPF
Transitional epithelial cells Rare, few, moderate, or many per HPF
RTE cells Average number per 10 HPF
Oval fat bodies Average number per HPF
Bacteria, yeast Rare, few, moderate, or many per HPF
Trichomonas Rare, few, moderate, or many per HPF
Spermatozoa Present, based on laboratory protocol
Mucus Rare, few, moderate, or many per LPF
Normal crystals Rare, few, moderate or many per HPF
Abnormal crystals Average number per LPF
RENAL DISORDERS
GLOMERULAR DISORDERS
DISORDER ETIOLOGY CLINICAL COURSE PRIMARY OTHER SIGNIFICANT
URINALYSIS TESTS
RESULT
Acute Deposition of immune Rapid onset of Macroscopic Antistreptolysin O titer
Glomerulonephritis complexes formed in hematuria and edema. hematuria,
conjunction with group A Proteinuria, Anti- group A
Streptococcus infection, Permanent renal Red Blood Cell Streptococcal enzymes
on the glomerular damage seldom occurs casts, oliguria
membranes Granular casts
Rapidly Ere: creatinine Deposition of immune Rapid onset with Macroscopic Blood Urea Nitrogen
clearance
progressive(crescentic) complexes from system glomerular damage and hematuria, Creatinine
glomerulonephritis immune disorders on the possible progression to Proteinuria, Creatinine clearance
glomerular membrane end-stage renal failure Red Blood Cell casts
I.K AYTONA 38
Wegener’s Antineutrophilic cytoplasmic Pulmonary symptoms Macroscopic Antineutrophilic
Granulomatosis autoantibody binds to including hemoptysis hematuria Cytoplasmic antibody
anti neutrophil ic
-
decrease platelets
platelets disrupts vascular stools and eventual Red Blood Cell casts
test integrity renal involvemen.
-
Minimal change disease Disruption of podocytes Frequent complete Heavy proteinuria Serum albumin
(Lipid nephrosis) occurring primarily in remission following Transient hematuria Cholesterol
children following allergic corticosteroid treatment Fat droplets Triglycerides
reactions and
immunizations
Focal segmental Disruption of podocytes in May resemble nephrotic Proteinuria Drug of Abuse
glomerulosclerosis certain areas of glomeruli syndrome or minimal Microscopic HIV tests
Heroin 4 analgesic abuse associated with heroin change disease. hematuria
and analgesic abuse and
acquired immunodeficiency
syndrome
Alport syndrome Genetic disorder showing Slow progression to to See Nephrotic
lamellated and thinning nephritic syndrome and syndrome
of glomerular basement end stage renal disease
membrane
Diabetic Nephropathy Most common cause of (+)Microalbuminuria
(Kimmelstiel- Wilson ESRD (+)Micral test
disease) Deposition of glycosylated
proteins on the glomerular
basement membranes
caused by poorly controlled
blood glucose levels
I.K AYTONA 39
NEPHROTIC SYNDROME LAB FINDINGS
URINE FINDINGS PLASMA OR BLOOD FINDINGS
1. Proteinuria 1. Increase A2-Macroglobulin in electrophoresis
2. Lipiduria 2. Hypoproteinemia and hypoalbuminemia
3. Hematuria 3. Hyperlipidemia
4. Cylindruria (fatty cast) 4. INCREASE PLASMA SODIUM AND WATER LEVEL DUE TO INCREASE SODIUM
AND WATER REABSORPTION IN THE KIDNEY that will eventually lead to EDEMA
b. Nephrogenic DI
-inability of the renal tubules to respond to
ADH
-Normal to increase ADH
I.K AYTONA 40
ADDENDUM
Rapidly progressive Some forms may demonstrate increased fibrin degradation products, cryoglobulins, and the
(Crescentic) glomerulonephritis deposition of IgA immune complexes in the glomerulus
Good pasture’s syndrome A cytotoxic autoantibody can appear against the glomerular and alveolar basement membranes
after viral respiratory infections Initial pulmonary complaints are hemoptysis and dyspnea,
followed by the development of hematuria
Henoch Schonlein purpura Disease occurs primarily in children after upper respiratory infections. As its name implies,
initial symptoms include the appearance of raised, red patches on the skin. Respiratory and
gastrointestinal symptoms, including blood in the sputum and stools, may be present
Membranous glomerulonephritis Disorders associated with membranous glomerulonephritis development include systemic lupus
erythematosus, Sjögren syndrome, secondary syphilis, hepatitis B, gold and mercury treatments,
and malignancy.
Membranoproliferative Marked by two different alterations in the cellularity of the glomerulus and peripheral capillaries.
Glomerulonephritis A. Type 1 displays increased cellularity in the subendothelial cells of the mesangium
(interstitial area of Bowman’s capsule), causing thickening of the capillary walls
B. Type 2 displays extremely dense deposits in the glomerular basement membrane. Many of
the patients are children, and the disease has a poor prognosis
Focal Affects only certain numbers and areas of glomeruli, and the others remain normal.
Symptoms may be similar to the nephrotic syndrome and minimal change disease owing to
damaged podocytes
IgA Nephropathy Patients usually present with an episode of macroscopic hematuria following an infection or
strenuous exercise.
Disorder may remain essentially asymptomatic for 20 years or more
Chronic renal Progressive loss of renal function caused by an irreversible and intrinsic renal disease characterizes
failure (CRF). chronic renal failure (CRF).
Associated with azotemia, acid-base imbalance, water and electrolyte imbalance, and abnormal calcium
and phosphorus metabolism
CRF progresses to an advanced renal disease often termed end stage renal disease or end-stage
kidneys
Urinalysis findings associated with end-stage renal disease include a fixed specific gravity
(isosthenuria, at 1.010), significant proteinuria, minimal to moderate hematuria, and the presence
of all types of casts, particularly waxy and broad casts.
The progression to end-stage renal disease is characterized by a marked decrease in the
glomerular filtration rate (less than 25 mL/min) steadily rising serum BUN and creatinine values
(azotemia); electrolyte imbalance; lack of renal concentrating ability producing an isothenuric urine;
proteinuria; renal glycosuria; and an abundance of granular, waxy, and broad casts, often referred to
as a telescoped urine sediment
f. Infections (ex. -
UTI)
g. Nucleation (initial crystal deposition and formation)
I.K AYTONA 41
RENAL CALCULI CHARACTERISTICS
Caox Major constituent of renal calculi nucleic acid metabolism
Very hard, dark brown color with rough surface
uric acid
Associated with increase intake of foods with high purine content, and uromodulin-associated kidney disease
Yellowish to brownish red and moderately hard
Seen in hereditary disorders of cystine metabolism
cystine calculi
Yellow brown, greasy and resembles an old soap
Least common calculi (1-2%) stag horn
Ca
phosphate /Apatite Pale and friable
ADDITIONAL INFORMATION
1. Calcium oxalate or a mixture of oxalate and calcium phosphate is often found in stones (≈80%). Mixed calcium
phosphate, magnesium ammonium phosphate, and uric acid are the next most common constituents (3% to 10% each), and
these are followed by cystine stones (1% to 2%).
2. Males are more often affected with calcium stones than females, and children are not often affected with calcium stones.
3. Struvite (Triple phosphate) stones may become large, forming casts of the kidney pelvis and showing staghorns
4. staghorn calculi resembling the shape of the renal pelvis and smooth, round bladder stones with diameters of 2 or more inches
TELESCOPED SEDIMENTS
Simultaneous appearance of the elements of acute/chronic glomerulonephritis, ESRD and nephrotic syndrome
A telescoped sediment might therefore include red blood cells, red blood cell casts, cellular casts, broad waxy casts, lipid droplets,
oval fat bodies, and fatty casts
Such sediment may be found in collagen vascular disease (notably lupus nephritis) and subacute bacterial endocarditis.
ATHLETIC PSEUDONEPHRITIS
Associated with strenuous exercise such as marathon running
Normal /physiologic condition characterized by appearance of CELLS AND CASTS (shower of cast) in urine
Positive in RBC, WBC, Granular cast, Hyaline cast
AMINOACIDURIA
PHENYLALANINE-TYROSINE DISORDERS
DISORDER Enzyme deficient Information Tests
Phenylketonuria ____________________
phenylalanine hydroxylase Mousy or musty odor FeCl3 tube test = (+) BLUE GREEN
- Inherited as an autosomal Urine ibarny Phenistix strip = (+) gray to gray green
recessive disease, it is Guthrie bacterial inhibition test
characterized by increased urinary
excretion of phenylpyruvic acid (a
-associated with mental ▪ Bacillus subtilis is cultured with
ketone) and its metabolites retardation beta2 –thienylalanine
▪ Beta2-thienylalanine inhibits
growth of B.subtilis
▪ Phenylalanine counteracts the
action of Beta2-thienylalanine
▪ (+) result: _____________
growth
Tyrosyluria/Tyrosinemia Type1: “Rancid Butter odor FeCl3 tube test = (+) TRANSIENT GREEN
Fumarylacetoacetate urine”
hydrolase Nitroso-naphtol = (+) Orange Red
Type 2:
Tyrosine aminotransferase
Type 3:
p-hydroxyphenylpyruvic
acid dioxygenase
Alkaptonuria Homogentisic acid oxidase Urine darkens after FeCl3 tube test = (+) TRANSIENT BLUE
becoming alkaline from Clinitest = (+) Yellow ppt
standing at room
temperature
I.K AYTONA 42
Melanuria -- Due to overproliferation FeCl3 tube test = (+) BLACK /GRAY PPT
-Melanin is produced from of melanocytes Sodium nitroprusside test = (+) Purple
tyrosine by melanocytes and is Urine darkens upon air Ehrlich test (+) = Red
the pigment responsible for the exposure
color of hair, skin, and eyes.
Deficient production of melanin
results in albinism.
5,6-dihydroxyindole A colorless precursor of melanin, which can be oxidized to melanogen and then to melanin, producing the
characteristic of dark urine.
NOTE! In MSUD, the metabolic pathway begins normally, with the transamination of the three amino acids in the liver to the keto
acids (a -ketoisovaleric, a -ketoisocaproic, and a -keto-b -methylvaleric). Failure to inherit the gene for the enzyme necessary to
produce oxidative decarboxylation of these keto acids results in their accumulation in the blood and urine.
I.K AYTONA 43
Second metabolic pathway of tyrosine is responsible for the production of melanin, thyroxine, epinephrine, protein,
and tyrosine sulfate
TRYPTOPHAN DISORDERS
Disorder Information Test
Indicanuria Indigo blue color urine Obermayer’s test
(upon air exposure or oxidized) - FeCl3 + Urine + Chloroform → (+) purple
Tryptophan→ indole → indican
Seen in: Intestinal disorders, and
Hartnup’s disease
Argentaffinoma Carcinoid tumor involving argentaffin FeCl3 tube test = (+) blue – green
cells Nitroso-naphthol w/ nitrous acid = (+) Violet
✓ Produce 5-HIAA, a metabolite of to black
serotonin
banana , pineapple avocado tomato
✓ Avoid ____________________, ,
NOTE! A second metabolic pathway of tryptophan is for the production of serotonin used in the stimulation of smooth muscles.
Serotonin is produced from tryptophan by the argentaffin cells in the intestine and is carried through the body primarily by the platelets
Normally, the body uses most of the serotonin, and only small amounts of its degradation product, 5-HIAA, are available for excretion
in the urine
CYSTINE DISORDERS
Disorder Information Test
Cystinuria Renal type aminoaciduria Brand’s modification of Legal’s nitroprusside
↑ cystine ornithine leucine arginine ( COLA)
, , , Rgt: Cyanide nitroprusside = (+) Red-purple
Defective tubular reabsorption of:
- renal disease
__________________________
Cystinosis Inborn Error of metabolism Brand’s modification of Legal’s nitroprusside
(-) gene that codes for an enzyme responsible for Rgt: Cyanide nitroprusside = (+) Red-purple
cysteine metabolism
Homocystinuria Defects in the metabolism of methionine that leads to Silver-nitroprusside test = (+) Red-Purple
increase homocysteine. Associated with methionine -Fresh urine should be used
malabsorption
MUCOPOLYSACCHARIDE DISRODERS
Disorder Information Test
Hurler syndrome Mucopolysaccharides accumulate in the
cornea of the eye cornea of the eye
PURINE DISORDER -
uric acid
Lesch-Hyhan disease
Lack Hypoxanthine-guanine phosphoribosyl transferase
Increase uric acid in blood and urine
Patients suffer from severe motor defects, mental retardation, a tendency toward self-destruction, gout, and renal calculi
Development is usually normal for the first 6 to 8 months, and the first sign is often uric acid crystals resembling orange
sand in diapers
I.K AYTONA 44
PORPHYRIN DISORDER (PORPHYRIAS/VAMPIRE’S DISEASE)
Disorder of porphyrin metabolism
Urine color = Red/purple/Burgundy red/ Port wine/ Purplish red
Normal or Colorless in = Lead poisoning
Screening test Specimen = urine, stool, blood, bile
a. Ehrlich’s reaction – detects D-ALA porphobilinogen
b. Fluorescence at 550-600nm – test for uroporphyrin, coproporphyrin and protoporphyrin
(+) result: Violet/pink/red Fluoresence
c. Free Erythrocyte Protoporpyrin (FEP) – CDC recommended test for lead poisoning
CARBOHYDRATES DISORDER
Melituria = general term for the presence of urinary sugar
Galactosuria, pentosuria, lactosuria, fructosuria, and glucosuria
Galactosuria = indicates inability to properly metabolize galactose to glucose such as in case of newborn errors
SYNOVIAL FLUID
Formed as a non-selective ultrafiltrate of plasma across synovial membrane except
for the exclusion of high molecular weight protein.
A.K. A= joint fluid
“Synovial” = Latin word for synovia means “egg or ovum”
Viscous fluid circulating in °
diarthroses (movable joints)
-
FUNCTIONS
1. Lubricates joints
2. Reduce friction between bones
3. Provides nutrients to the articular cartilage
4. Lessen shock of joint compression occurring during activities such as walking and jogging
SPECIMEN COLLECTION
drthrocentesis
Method: ___________________
If possible, patients should be fasting a minimum of 4 to 6 hours to allow for the equilibration of chemical constituents
between plasma and synovial fluid (Brunzel, 3rd ed.)
Volume: Normal = 0.1 to 3.5 ml, Inflammation = >25 ml
REQUIRED TUBE TYPES FOR SYNOVIAL FLUID TESTS AND ORDER OF DISTRIBUTION
1. Chemistry and Serology = non-anticoagulated
2. Hematology and cytology = sodium heparin or liquid EDTA
3. Microbiology= Sterilized heparin or SPS
I.K AYTONA 45
COLOR AND CLARITY
Colorless to pale yellow Normal
Turbid WBC, Synovial cell debris, and fibrin
Deeper yellow Inflammation
Greenish tinge Bacterial infection
Red Traumatic tap, hemorrhagic arthritis
Milky
VISCOSITY
4- 6cm long
Normal: able to form a string ___________ GRADING Interpretation
Test: Ropes/ Mucin clot test (Hyaluronate polymerization Test) Good Solid clot
▪ Reagent: uses 2-5 % acetic acid Fair Soft clot
▪ When added to a solution of 2% to 5% acetic acid, Low Friable clot
normal synovial fluid forms a solid clot surrounded by clear fluid Poor No clot
CELL COUNT
The total leukocyte count is the most frequently performed cell count on synovial fluid. Red blood cell (RBC) counts are
seldom requested. To prevent cellular disintegration, counts should be performed as soon as possible or the
specimen should be refrigerated.
WBC COUNT
Most frequently performed count
Diluting fluid: NSS with methylene blue, Hypotonic saline 0.3%), Saline with saponin
Automated cell counters can be used for synovial fluid counts; however, highly viscous fluid may block the apertures, and the
presence of debris and tissue cells may falsely elevate counts. As described previously, incubating the fluid with hyaluronidase
decreases specimen viscosity. Analyzing scattergrams can aid in detecting tissue cells and debris
Methylene blue added to the normal saline stains the WBC nuclei, permitting separation of the RBCs and WBCs during
counts performed on mixed specimens
For very viscous fluid may need to be pretreated by adding a pinch of hyaluronidase to 0.5ml fluid or add 1 drop of 0.05%
hyaluronidase in phosphate buffer per ml of fluid and incubate at 37’C for 5 minutes
Neutrophils 2t%
Monocyte and macrophages 65 %
15h
Lymphocytes Neutrophils <25 %
-
Lymphocytes <15 %
Note An eosinophil of greater than 2 %is associated with allergic disease with arthritis,
hemorrhagic joint effusion, Lyme disease, parasitic arthritis, RA, and tubercular arthritis
I.K AYTONA 46
Rice bodies Macroscopically resembles polished rice Tuberculosis, septic and
TB , rheumatic arthritis / septic arthritis Microscopically shows collagen and fibrin rheumatoid arthritis
They are fragments of degenerating proliferative synovial
cells or microinfarcted synovium
Fat droplets - Traumatic
injury a
Refractile intracellular and extracellular globules stain with Sudan Traumatic injury
chronic inflammation dyes Chronic inflammation
Hemosiderin Inclusions within clusters of synovial cells Pigmented villonodular synovitis
Ochronotic shards Ground pepper appearance Joint prosthesis, ochronosis
CRYSTAL IDENTIFICATION
Causes of crystal formation:
a. Metabolic disorders
b. Decreased renal excretion that produce increased blood levels of crystallizing chemicals
c. Degeneration of cartilage and bones
d. Injection of medications (corticosteroid)
Ideally, crystal examination should be performed soon after fluid collection to ensure that crystals are not affected by
changes in temperature and pH
Both MSU and CPPD crystals are reported as being located extracellularly and intracellularly (within neutrophils); therefore,
fluid must be examined before WBC disintegration.
CPPD crystals are usually located within vacuoles of the neutrophils while MSU crystals lyse phagosome membranes and
therefore do not appear in vacuoles
Crystals may be observed in Wright’s-stained smears
Polarizing microscope = detects for the presence or absence of birefringence
Compensated polarizing microscope = confirms the type of birefringence (positive or negative)
✓ A red compensator is placed between crystal and analyzer
✓ Yellow= parallel = (negative) Birefringence
✓ Blue = perpendicular = (positive) Birefringence
Control slide for the polarization properties of MSU (monosodium urates) can be prepared using
betamethasone acetate corticosteroid.
NOTE!
Specimens for crystal analysis should not be refrigerated because they can produce additional crystals that can interfere with the
identification of significant crystals. Avoid using powderized anticoagulant because it can cause artifacts and may interfere in
crystal identification
Pseudogout Most often associated with degenerative arthritis, producing cartilage calcification and endocrine
disorders that produce elevated serum calcium levels.
CHEMISTRY TEST
Glucose Most frequently test in chemistry. Done in conjunction with blood glucose. Simultaneous blood and synovial fluid
samples should be obtained, preferably after the patient has fasted for 8 hours to allow equilibration between
the two fluids
❖ Normal Value = the difference between the Blood glucose and Synovial fluid glucose should be less than
10mg/dl
❖ BLOOD GLUCOSE – S.F GLUCOSE = <10mg/dl (normal)
❖ Decreased in Type II and III arthritis or inflammatory disorder
To prevent falsely decreased values caused by glycolysis, specimens should be analyzed within
1 hour or preserved with sodium fluoride
Lactate Normal value = <250 mg/dl
<
250mg 1dL Increase in infection
I.K AYTONA 47
Lactate or ACP Maybe requested to monitor the severity and prognosis of Rheumatoid arthritis
Protein Normal value = <3 g/dl Blood :< 10mg /dl
Increased in inflammatory
- and hemorrhagic disorders
Uric acid Normal value = same as blood
Increase in gout
Joint Disorders
Group I. Non inflammatory IIa. Inflammatory – IIb. Inflammatory- III. Septic IV. Hemorrhagic
Immunologic origin Crystal induced
Significance Degenerative joint Immunologic Gout Microbial infection Traumatic injury
disorder disorders Pseudogout Coagulation
deficiency
Color and Clear, yellow fluid Cloudy, yellow Cloudy or milky Cloudy, yellow- Cloudy, red fluid
Clarity fluid fluid green fluid
Viscosity Good solid aot Poor No dot Low Friable Variable Low Friable
WBC count <1,000 / ul 2000-75000/ul Up to 100,000 /ul 50K-100K / ul Equal to blood
Neutrophils <30 % >50% <70% >75% Equal to blood
Glucose Similar to blood glucose Decreased Decreased Decreased Normal 136-56=510 mgldl
Others +Auto antibodies + Crystals + Culture and GS + RBC
Associated Osteoarthritis Rheumatoid Crystal synovitis -Bacterial infection, -Trauma
diseases Osteochondritis arthritis, SLE, (gout, pseudogout) -Fungal infection, -Tumor
Osteochondromatosis ankylosing -Mycobacterial -Joint prosthesis
Traumatic arthritis Spondylitis, Lyme infection -Blood disease such
Neuroarthropathy arthritis as sickle cell disease
000 . .
TN -
and hemophilia
MICROBIOLOGY
Common organisms that infect the synovial fluid:
1. Staphylococcus aureus
2. Streptococcus SSHN
3. Haemophilus
4. Neisseria gonorrheae
SEROLOGIC TEST
Auto antibody detection for RA, SLE
Detection of antibodies to Lyme disease
wall)
paternitySEROUS FLUID
A Fluid between parietal membrane (lines the cavity wall) and
visceral membranes (covers the organ)
Serous fluids are formed from ultra-filtrate of plasma
Production and reabsorption are subject to hydrostatic
pressure and colloidal pressure (oncotic pressure) from the
capillaries that serve the cavities and the capillary permeability.
FUNCTION
To provide lubrication between the 2 membranes as the surfaces move
against each other.
EFFUSION
Accumulation of fluid between the membranes
Classified as exudate or transudate
TRANSUDATE EXUDATE
Effusion caused by a systemic disorder that disrupts the fluid Effusion caused by direct damage to the membrane
production and regulation between membranes
Causes: pa-H-yc-ONIM-arkI.IM Causes: / MIL
1. Hypoproteinemia = decrease oncotic pressure 1. Infection
2. Congestive heart failure- increase hydrostatic 2. Malignancy
3. Nephrotic syndrome= decrease oncotic pressure 3. Inflammation
4. Malnutrition= decrease oncotic pressure 4. Lymphatic duct obstruction
5. Hepatic cirrhosis = decrease oncotic pressure
I.K AYTONA 48
TRANSUDATE VS EXUDATE
Transudate Exudate
Appearance Clear Cloudy
Fluid: serum protein ratio <0.5 >0.5
Fluid: serum LD ratio <0.6 >0.6
WBC count <1,000 cell/ul >1,000 cell/ul
Spontaneous clotting No Possible
Pleural fluid cholesterol (mg/dl) <45-60 >45-60
Pleural fluid: serum cholesterol ratio <0.3 >0.3
Pleural fluid: bilirubin ratio <0.6 >0.6
Serum ascites albumin gradient (SAAG) >1.1 <1.1
Glucose Decrease Increase
Rivalta’s test Negative Positive
Acetic acid + water + Unknown fluid
(+) heavy precipitation
Differentiation between ascitic fluid transudates and exudates is more difficult than for pleural and pericardial effusions.
The serum-ascites albumin gradient (SAAG) is recommended over the fluid:serum total protein and LD ratios for the detection of
transudates of hepatic origin
Specimen Distribution
1. EDTA = Cell count and differential count
2. Sterile heparin or SPS = Microbiology and cytology
3. Plain tubes or heparin tubes= Chemistry
PLEURAL FLUID
Appearance Significance
Clear, pale yellow Normal
Turbid, white Microbial infection (TB)
Brown Rupture of amoebic liver abscess
Viscous Malignant mesothelioma (increase hyaluronic acid/)
Black Aspergillous
Milky Chylous material
Pseudochylous material
Bloody Hemothorax= due to traumatic aspiration PF HOT 250% WB Hit
▪ Uneven distribution of blood, pleural fluid Hct is>50% WB blood Hct
wᵈTᵈw / cholesterol
Hemorrhagic
▪ Pleural fluid Hct is <50% Whole blood Hct
0 →
CHYLOUS EFFUSION PSEUDOCHYLOUS EFFUSION
Cause Thoracic duct leakage Chronic inflammation
Appearance Milky / white Milky / green tinge / gold paint
Leukocytes Increase lymphocyte Mixed cells
Cholesterol crystals Absent Present
Triglycerides >110 mg/dl C-realer than <50 mg/dl
Sudan III staining +++ Negative or weakly + gamay ang the
-
I.K AYTONA 49
SIGNIFICANCE OF CELLS SEEN IN PLEURAL FLUID
Cell Significance
Neutrophil (normal is 1-2%) Pneumonia, pancreatitis, pulmonary infarction
Lymphocyte (Normal is 18-30%) TB, viral infection, autoimmune disorders, malignancy
Mesothelial cell Fried-eg.GS Normal and reactive forms have no significance
(Characterized by fried egg appearance) Decrease in TB
Plasma cells TB
Malignant cells Primary adenocarcinoma, small cell carcinoma
Eosinophil Allergic reaction, parasitic infection, pneumothorax, and hemothorax
Normally, only a small amount (10 to 50 mL) of fluid is found between the pericardial serous membranes
SUMAS
Metabolic disorders such as uremia, hypothyroidism, and autoimmune disorders are the primary causes of transudates.
TRAN
An effusion is suspected when cardiac compression (tamponade) is noted during the physician’s examination
I.K AYTONA 50
PSAMMOMA BODIES
Contain concentric striations of collagen-like material
Seen in benign conditions and associated with ovarian and thyroid carcinomas
LIPOPHAGES
Macrophage containing fat droplets
AMNIOTIC FLUID
Amniotic fluid is present in the amnion, a membranous sac that surrounds the fetus
FUNCTIONS
The primary functions of the fluid are:
1. to provide a protective cushion for the fetus,
2. allow fetal movement,
3. stabilize the temperature
4. to protect the fetus from extreme temperature changes, and to permit proper lung development.
VOLUME
Amniotic fluid volume is regulated by a balance between the production of fetal urine and lung fluid and the absorption from
fetal swallowing and intramembranous flow.
The amount of amniotic fluid increases throughout pregnancy, reaching a peak of approximately 1 L during the third
trimester, and then gradually decreases prior to delivery.
During the first trimester, the approximately 35 mL of amniotic fluid is derived primarily from the maternal
circulation.
After the first trimester, fetal urine is the major contributor to the amniotic fluid volume.
POLYHYDRAMNIOS OLIGOHYDRAMNIOS
Increase amniotic fluid volume Decrease amniotic fluid volume
a. Decrease fetal swallowing a. Increase fetal swallowing
b. Neural tube defects (Ex. Spina bifida and anencephaly) b. Membrane leakage
c. Urinary tract deformities
SPECIMEN COLLECTION
AMNIOCENTESIS- term for the collection of amniotic fluid
A maximum of 30 mL of amniotic fluid is collected in sterile syringes. The first 2 or 3 mL collected can be contaminated
by maternal blood, tissue fluid, and cells and are discarded.
2ND trimester amniocentesis: Assess genetic defects (e.g., Down syndrome)
3rdtrimester amniocentesis: Assess Fetal lung maturity and Hemolytic disease of newborn
I.K AYTONA 51
SPECIMEN HANDLING
Test for fetal lung maturity Should be placed in ice for delivery to the laboratory and kept refrigerated.
Filtration prevents loss of lung surfactants such as phospholipids.
Test for cell culture and cytogenetic studies Maintained at room temp or body temp
Test for HDN Specimen must be protected from light. This can be accomplished by placing the
specimens in amber-colored tubes, wrapping the collection tube in foil, or by use of a
black plastic cover for the specimen container
FERN TEST
➢ A vaginal fluid is spread on glass and allowed to completely air dry at RT
CREATININE LEVEL
Creatinine level
= provides a mean of determining fetal age
= creatinine level that is greater than 2mg/dl indicates fetal age greater than 36 weeks
Meconium = defined as a newborn’s first bowel. It is formed in the intestine from fetal intestinal secretions and swallowed amniotic
fluid. Biliverdin is responsible for its dark green color. It may be present in the amniotic fluid as a result of fetal distress.
I.K AYTONA 52
TEST FOR NEURAL TUBE DEFECT
Neural tube defects, also known as spinal dysraphisms, are a category of neurological disorders related to malformations of
the spinal cord, such as spina bifida, anencephaly, meningocele, myelomeningocele and tethered spinal cord syndrome of
the developing fetus
(
AFP Alpha few protein)
Screening test = ___________________
-
TEST INFORMATION
Lecithin / Sphingomyelin ▪ Reference method
ratio ▪ Lecithin for alveolar stability
reference method ▪ Sphingomyelin serves as a control
measured using TLC ▪ Prior to 35 weeks’ gestation, the L/S ratio is usually less than 1.6 because large amounts of
lecithin are not being produced at this time. After 35 weeks’ gestation, the lecithin
concentration increases while the sphingomyelin concentration remains constant
> 2.0 = mature
▪ Measured using Thin Layer chromatography (TLC)
lungs ▪ Ratio of > 2.0 = mature lungs
▪ Cannot be done on specimen contaminated with blood (false increase) or meconium
(false increase value) -Strasinger 6th edition
Foam stability / Shake ▪ Amniotic fluid + 95 % Ethanol ---→ shake for 15 seconds ---→ stand for 15 minutes
test ▪ (+) Result = foam/bubbles/effervescence = mature lungs
Lamellar body count ▪ Lamellar bodies are densely packed layers of phospholipids that represent a storage form
of pulmonary surfactant.
▪ They are secreted by the type II pneumocytes of the fetal lung
▪ Specimens may be stored at 2°C to 8°C but never frozen
▪ Uses hematology analyzer for counting
▪ They have similar size with platelets when counted
▪ ≥32,000 / ml lamellar body count = adequate FLM
▪ The advantages of lamellar body counting include: (1) rapid turnaround time, (2) low reagent
cost, (3) wide availability, (4) low degree of technical difficulty, (5) low volume of amniotic
fluid required, and (6) excellent clinical performance.
OD 650nm ▪ Specimens are centrifuged at 2000 g for 10 minutes and examined using a
(Lamellar bodies) wavelength of 650 nm
A- ↑
Increase lamellar bodies = Increase O.D absorbance
.
▪
▪ An O.D of ≥0.150 is equivalent to L/S ratio of ≥2.0
I.K AYTONA 53
SUMARRY OF TESTS FOR WELL BEING AND MATURITY
Test Reference values Significance
Bilirubin scan OD 450 >.025 Hemolytic disease of the newborn
Alpha feto protein <2.0 MoM (Multiples of median) Neural tube disorders
Lecithin sphingomyelin ratio ≥2.0 Fetal lung maturity
Amniostat fetal lung maturity Positive Fetal lung maturity/phosphatidyl glycerol
Foam Stability Index ≥47 Fetal lung maturity
Optical density 650 nm ≥0.150 Fetal lung maturity
Lamellar body count ≥32,000/mL Fetal lung maturity
ADDENDUM
Fetal epithelial cells A cell that indicate the genetic material and biochemical substances from the fetus that is
found in amniotic fluid. These cells can be separated, cultured and can be analyzed and
examined for chromosomal abnormalities thru karyotyping, FISH, fluorescent mapping
spectral karyotyping (SKY), and DNA testing.
Spectrophotometer Amniotic fluid bilirubin (O.D 450) is measured by ___using serial dilutions
Centrifugation at 2000rpm for 10minutes What is the Specimen preparation prior to measuring Lamellar bodies?
CEREBROSPINAL FLUID
The 3rd Major body fluid
FUNCTION
1. Supply nutrients to the CNS
2. Remove metabolic waste
3. Produce a mechanical barrier to cushion the brain and
spinal cord against trauma
MENINGES
Lines the brain and spinal cord and composed of three layers
1. Dura mater = outer layer, lines the skull and vertebral canal
2. Arachnoid mater = spider like, filamentous inner membrane
3. Pia mater = innermost layer, lines the surface of the brain
and spinal cord
Note: Subarachnoid space = where CSF flows
CHOROID PLEXUS
- Specific part of the brain that produces CSF
- The choroid plexuses are capillary networks that form the
CSF from plasma by mechanisms of selective filtration under hydrostatic pressure and active transport secretion. Therefore,
the chemical composition of the CSF does not resemble an ultrafiltrate of plasma
_
- 20 ml/hr = rate of CSF production
Before CSF is collected, the pressure should be between 90 and 180 mmHg; this is measured by allowing fluid
to rise in a sterile, graduated manometer
Volume collected Up to 20ml collected under normal pressure (approximately 15% of the estimated total CSF volume).
-When pressure is normal, 20 mL of specimen may be removed. On closing, the pressure should be between 10 and 30 mm
Hg. A marked decrease in pressure following this procedure suggests cerebellar herniation or spinal cord compression; thus,
no additional CSF should be collected
If the CSF pressure is less than or greater than normal, only 1 to 2 mL should be removed.
Not more than 2 ml can be removed when the pressure is greater than 200 mm Hg
I.K AYTONA 54
1
/ CC CCHS
21min
Synovial 21km9 altena
Distribution EST
TUBE # LAB SECTION STORAGE TEMPERATURE
1 Chemistry, Immunology, Serology Frozen
2 Microbiology RT
3 Hematology (Cell count), and Cytology studies Ref temp
4 Microbiology (Better exclude skin contamination)
or Serology (for additional serologic test)
NOTE: Excess CSF should not be discarded and should be frozen until there is no further use of it.
OTHER CAUSES:
Increase dietary carotene
Increase rifampin intake
Increase melanin
Normal neonate
Protein concentration exceeding 150mg/dl
Previous traumatic tap
Supernatant XANTHOCROMLA
Erythrophages
D-dimer test
cleat +
+
I.K AYTONA 55
CSF CELL COUNTING
CSF CELL COUNT
✓ Performed immediately because WBCS and RBCs will begin to lyse within 1 hour.
✓ 40% of WBC disintegrates within 2 hours. If the specimen is refrigerated, WBC lysis can be reduced significantly to
approximately 15%, but not completely prevented. Similarly, RBCs do not demonstrate significant lysis at 4° C; therefore the
CSF collection tube for cell counts should be refrigerated if the count must be delayed for any reason
CSF DILUTION
Appearance Dilution
Clear Undiluted
Hazy 1:20
Bloody/Turbid 1:10,000
WBC COUNT
Routinely performed on CSF
WBC diluting fluid
-3% glacial acetic acid (HAc) with Methylene Blue (Provides better differentiation between PMNs and Mononuclear cells)
Normal values:
Adults = 0-5 WBCs/ ul
Neonates = 0-30 WBCs/ul
To prepare a clear specimen that does not require dilution for counting, place four drops of mixed specimen in a clean tube.
Rinse a Pasteur pipette with 3% glacial acetic acid, draining thoroughly, and draw the four drops of CSF into the rinsed
pipette. Allow the pipette to sit for 1 minute, mix the solution in the pipette, discard the first drop, and load the
hemocytometer. -Strasinger
To enhance the visualization of white blood cell nuclei and to eliminate any RBCs present, the CSF is treated with glacial acetic
acid before the hemacytometer chambers are filled, and 3 to 5 minutes is allowed for RBC lysis. - Brunzel
CSF CYTOCENTRIFUGATION
Procedure Spinal Fluid is added to the conical chamber, and as the specimen is centrifuged, cells present in the fluid are
forced into a monolayer within a 6-mm diameter circle on the slide. Fluid is absorbed by the filter paper blotter,
producing a more concentrated area of cells.
30% Albumin Addition of ___ to as little as 0.1mL of CSF can produce and adequate cell yield when processed with the
Cytocentrifuge. Adding albumin increases the cell yield and decreases the cellular distortion frequently seen
on cytocentrifuged specimens.
Control slide A daily control slide for bacteria should also be prepared using 0.2 mL saline and two drops of the
30% albumin currently being used. The slide is stained and examined if bacteria are seen on a patient’s slide.
Recovery Chart NUMBER OF WBCs Counted in Number of Cells on Cytocentrifuge
Chamber Slide
0 0-40
1-5 20-100
6-10 60-150
11-20 150-250
20 250
I.K AYTONA 56
NORMAL WBC IN CSF
ADULT: 70% lymphocytes, 30% monocytes
Neonate: up to 80% monocytes
Currently, with the increased cell recovery obtained using cytospin preparations, neutrophil counts of less than 10% are
considered normal – Brunzel
PLEOCYTOSIS
Abnormal condition
Term for the increase in number of normal cells in CSF
OTHERS
Uremia, Diabetes, Cushing disease, CNS tumor, Myxedema, Polyneuritis, Connective tissue
disease, Neurosyphilis, Guillain Barre syndrome
Decreased in CSF leakage/trauma, water intoxication, Rapid CSF production, Recent puncture
Major CSF Protein albumin
2nd most prevalent Pre albumin
Alpha globulin Haptoglobin, ceruloplasmin
Beta-globulins tan
______________________________
✓ Carbohydrate deficient transferrin
✓ Found on CSF not in serum
Gamma globulins IgG and some IgA
Not found in normal CSF IgM, Fibrinogen, Lipids
I.K AYTONA 57
CSF PROTEIN DETERMINATION
Turbidimetric Trick bro acetic acid
______________________
Preferred method, it precipitates both albumin and globulin
SSA
______________________
It Precipitates albumin only
To precipitate globulins, add sodium sulfate
Dye binding Cooma sie brilliant blue
Uses __________________________
CSF /Serum Albumin Assess the integrity of the blood brain barrier
Index
CSF ELECTROPHORESIS
Done in conjunction with serum electrophoresis.
For the detection of oligoclonal bands.
0
The presence of 2 or more oligoclonal bands in CSF but not in serum is valuable for the diagnosis of:
Multiple sclerosis
Neoplastic disorders ↳ MENO
Encephalitis
Guillain-Barre’ syndrome
CSF GLUCOSE
Determination Done in conjunction with blood glucose.
Specimen for blood glucose should be drawn 2 hours prior to spinal tap
Normal values 60-70%150 -80mg 1dL
Increased Due to increase plasma glucose (not significant)
Decreased in Bacterial, Fungal, and Tubercular Meningitis
Normal in Viral Meningitis
CSF LACTATE
-
10 -22
My 1dL ( I I
-
-
2.4 lnnrl / l )
➢ CSF lactate levels can be a valuable aid in diagnosing and managing meningitis cases
➢ Normal value: 10-22 mg/dl (1.1 to 2.4 mmol/L)
➢ Tissue destruction within the CNS owing to oxygen deprivation (hypoxia) increases CSF lactic acid levels. Therefore, elevated
CSF lactate is not limited to meningitis and can result from any condition that decreases oxygen flow to the tissues
➢ Inversely proportional to glucose
➢ CSF lactate levels remain elevated during initial treatment of meningitis but fall rapidly when treatment is successful, thus
offering a sensitive method for evaluating the effectiveness of antibiotic therapy.
➢ Frequently CSF lactate levels are used to monitor patients with severe head injuries
➢ RBCs contain high concentrations of lactate, and results that are falsely elevated may be obtained on xanthochromic or
hemolyzed fluid
Value
Bacterial meningitis Increased (>35mg/dl)
Fungal and tubercular meningitis Increased (>25mg/dl)
Viral meningitis Normal (remains lower than 25mg/dl)
I.K AYTONA 58
878mg 1dL
r
CSF GLUTAMINE
➢ Product of ammonia and alpha ketoglutarate
➢ Indirect test for the presence of excess ammonia in CSF
➢ This is preferred over the direct measurement of CSF ammonia because the glutamine concentration remains more stable
than the volatile ammonia concentration in the collected specimen.
➢ Normal value: 8 to 18 mg/dl
➢ Increase in: Reye’s syndrome, Disturbance of consciousness/coma (more than 35 mg/dl)
CSF ENZYMES
Lactate dehydrogenase
LD1 and 2 = Brain tissue
LD2 and 3 = Lymphocytes
LD4 and 5= Neutrophils
Serum LDH
Normal = LD2>1>3>4>5
Flipped pattern = LD1>2>3>4>5 -
AM , HA Renal infarction
,
CSF LDH
Normal = I > 2332455
Neurological abnormalities= 25 1 33 >
475
Bacterial meningitis= 5747 3 3 23 1
TYPES OF MENINGITIS
Bacterial Viral Tubercular Fungal
Predominant WBC Neutrophil Lymphocyte Lymphocyte and Monocyte Lymphocyte and Monocyte
Protein Increase Increase Increase Increase
Glucose decrease normal decrease decrease
Lactate Increase normal Increase Increase
Other information + gram stain Caused by Agent: mycobacterium Agent: Cryptococcus
+ culture smallest RNA virus tuberculosis neoformans
+limulus lysate test such as
Ex. Picornavirus +AFB stain + gram stain= classic
-Group B streptococcus , coxsackievirus, +pellicle/weblike clot starburst pattern
-H.Influenzae echovirus and formation after 12-24 hr + India ink
-N.Meningitidis poliovirus refrigeration +immunologic test for
-S.pneumoniae C.neoformans
-enterovirus
SEROLOGIC TESTING
➢ Latex agglutination test and ELISA- for detection of bacterial antigens
neuro syphilis
➢ VDRL= recommended by CDC for detection of ______________________
ADDENDUM
4 to 8 weeks Erythrophages can persist for ___ following a hemorrhage; they stain positive for hemosiderin and may
include hematoidin crystals.
2 hours RBCs must usually remain in the CSF for approximately______ before noticeable hemolysis begins
To differentiated PMNs What is the purpose of adding Methylene blue on the diluting fluid for CSF count?
and Mononuclear cell
Nucleated RBCs A Neutrophil found in CSF with PYKNOTIC nuclei may indicate a degenerating cell and can be mistaken as
Turbidimetry (SSA and TCA method) AND The two most routinely/commonly used manual
Dye Binding method (uses Coomassie brilliant blue) techniques for measuring total CSF protein
Gamma region Presence of oligoclonal band in CSF electrophoresis can be located at what region?
Silver staining In CSF electrophoresis by either IFE (Immunofixation electrophoresis) or IEF (Isoelectric focusing), what
staining technique is usually employed?
CSF Lactate It can be frequently tested on CSF sample to monitor severe head injuries.
Falsely elevated Xantochromic or Hemolyzed CSF can lead to ___________ CSF lactate values
I.K AYTONA 59
SEMINAL FLUID
spermatogonium
4
◦
1 spermatocyte
↓
2° spermatocyte
↓
spermatid / epididymis
↓
spermatium / sperm
Composition of semen
5% Spermatozoa Seminiferous tubules
site of spermatogenesis
_____________________
Sertoli cells nurse cells that support
_____________________
-
Epididymis development
SPECIMEN COLLECTION
2- 3 days 4 not more than 7-days
1. Abstinence of _________________________
2. In fertility testing WHO recommends two or three samples be collected not less than 7 days or more than 3 weeks apart, with
two abnormal samples considered significant.
3. Collect the entire ejaculate
Methods: masturbation, coitus interruptus, condom method – use a non-spermicidal, non-lubricant containing rubber or
silastic condom
4. Specimen should be delivered to the laboratory within ____1h of collection at room temp
5. Take note of the time of specimen collection, specimen receipt and liquefaction
30-60 minutes)
6. Analysis should be done after liquefaction (usually _______
7. If after 2 hours if the specimen has not liquefied, add Dulbecco’s phosphate-buffered saline, alpha chymotrypsin, or bromelain
to induce liquefaction
37%
8. Specimen awaiting analysis should be kept at ____
9. Semen specimen are potential reservoir of HIV and Hepatitis
10. Jelly-like granules (gelatinous bodies) may be present in liquefied semen specimens and have no clinical significance.
First portion of ejaculate missing Decrease sperm count, Increase PH, Specimen will not liquify
Last portion of ejaculate missing Increase sperm count, Decrease PH , Specimen will not clot, Decrease semen volume
MACROSCOPIC EXAMINATION
Appearance Gray- white, translucent, with musty or bleach odor normal
=______________________
Increased white turbidity infection ( WBC / pug / Gonorrhea
=______________________
Red or Brown coloration RBCs
=______________________
Yellow coloration prolong abstinence
=______________________
Volume Normal = 2- 5mL
) toxic urine{ medication
Increased = prolonged (viscous
-
I.K AYTONA 60
Viscosity Normal = pour in droplets
Reporting: NOTE Droplets that form threads longer than 2 cm are
watery
0 = ____________ considered highly viscous and are recorded as abnormal
like : impede mobility
gel
4 = ____________
-
Ph Normal = __________
7. 2- 8.0
infection in RT
Increase = ___________
Decrease = increased prostatic fluid, ejaculatory duct obstruction, or poorly developed seminal vesicles
SPERM CONCENTRATION
➢ Normal value = 20-250 million/ ml
➢ Borderline = between 10-20 million/ml
➢ Methods:
joiner
"
moron
1. Improved Neubauer counting chamber
Dilution: 1:20 using a mechanical (positive displacement) pipette
is 1:20
Diluents: Formalin, Sodium bicarbonate, saline, distilled water shortcut if dilution ×/M
Purpose of diluents: To immobilize the sperm 5 RBCs
•
✗ low
200 total sperm cells counted using a 1:20 dilution in the 5 RBC squares. What is the sperm concentration?
c%eY¥%•¥¥i↑- =
SPERM COUNT
➢ Normal value = > 40 million sperm / ejaculate
➢ Formula: Sperm concentration x Specimen volume
( %EFFaepdih.MY?-xmo)spxwe 2- 5 Ml
normal
SPERM MOTILITY
➢ Specimen should be liquefied first
sperm per slide
➢ Normal value = >50% motile within 1 hour 20 AM or too
➢ Quality = ≥2.0
To provide continuity in reporting, laboratories should place a consistent amount of semen on a slide under the same size cover slip,
such as 10 μL under a 22 × 22 mm cover slip using a calibrated positive-displacement pipette, and allow it to settle for
1 minute. This procedure should be done in duplicate for accuracy. the percentage of sperm showing actual forward movement can
then be estimated after evaluating approximately 20 high-power fields. An alternate procedure is to examine 200
sperm per slide
I.K AYTONA 61
SPERM MORPHOLOGY
➢ Sperm morphology is evaluated from a thinly smeared, stained slide under oil immersion. Smears are made by placing
approximately 10 μL of semen near the frosted end of a clean microscope slide
➢ Air-dried slides are stable for 24 hours
➢ At least 200 sperm should be evaluated and the percentage of abnormal sperm reported.
Acrosomal cap
Normal values:
-part of the sperm that contains enzyme
A. Routine criteria = 3- 30% normal
for ovum penetration
B. Kruger’s strict criteria = ≥ 14 % normal
This criteria measures the head, neck and tail using a 42 of head / 7s of nucleus
-Size: _______________________
Micrometer or morphometry
a. Wright’s stain
b. Giemsa stain Normal head appearance = oval
c. Shorr stain Tail = 45 um long
d. Papanicolau’s stain = best stain Midpiece: 7um
An abnormally long neckpiece may cause the sperm head to bend backward and interfere with motility.
Abnormalities in head morphology are associated with poor ovum penetration, whereas neckpiece, midpiece, and tail
abnormalities affect motility
✓ Count the number of dead cells in a 100 sperm using brightfield or phase contrast microscope
✓ Living sperm = unstained, bluish white (at least 50%)
✓ Dead sperm = red with a purple background
Low fructose levels are caused by abnormalities of the seminal vesicles, bilateral congenital absence of the vas deferens, obstruction of
the ejaculatory duct, partial retrograde ejaculation, and androgen deficiency
ANTISPERM ANTIBODIES
Detected in semen, cervical mucosa, or serum
1. 0
Mixed agglutination reaction
• Detects the presence of IgG
0antibodies
• Semen sample + AHG reagent + latex particle or treated RBCs coated with IgG
• Normal = <10% motile sperm attached to the particles
2. Immunobead test
• Detects the presence of IgG, IgM, IgA
• Demonstrate what area of the sperm the autoantibodies are affecting
• Sperm are mixed with polyacrylamide beads known to be coated with either anti-IgG, anti-IgM, or anti- IgA.
• Microscopic examination of the sperm shows the beads attached to sperm at particular areas.
• Normal = beads on less than 50 % of sperm
Head-directed antibodies can interfere with penetration into the cervical mucosa or ovum, whereas tail-directed antibodies
affect movement through the cervical mucosa
I.K AYTONA 62
CHEMICAL TESTING
Analyte Normal value Decreased Values Indicate
Fructose ≥13 umol/ ejaculate Decrease seminal fluid
Neutral alpha glucosidase ≥20 mU/ ejaculate Epididymis problem
Zinc ≥2.4 umol / ejaculate Decrease/lack prostatic fluid
Citric acid ≥52 umol/ ejaculate Decrease/lack prostatic fluid
]
"
FYI
Acid phosphatase ≥200 units/ ejaculate Decrease/lack prostatic fluid
MICROBIAL TESTING
ROUND CELLS
These are WBCs and spermatids
Normal value = si MIM
If greater than 1 million WBC/ ml =
infection
of spermatids
If greater than 1 million spermatids/ml = disruption
This is a test for chlamydia trachomatis, Mycoplasma hominis and Ureaplasma urealyticum
MIMI
100
VARICOCELE
Hardening of veins that drains the testes
Most common cause of male infertility
Sperm head = tapered head
I.K AYTONA 63
SPERM FUNCTION TEST
Test Description
Hamster egg penetration Sperms are incubated with species non-specific hamster eggs and penetration is observed
microscopically
Cervical mucus penetration Observation of sperm penetration ability of partners midcycle cervical mucus
Hypo-osmotic swelling Sperms exposed to low sodium concentrations are evaluated for membrane integrity and sperm
viability
In vitro acrosome reaction Evaluation of the acrosome to produce enzymes essential for ovum penetration
ADDENDUM
Ejaculatory duct Part of the male reproductive system that receive both the sperm from ductus deferens and fluid from
seminal vesicles
Flavin Responsible for the gray appearance of semen.
First Most of the sperm are contained in the ____ portion of the ejaculate, making complete collection
essential for accurate testing of both fertility and post-vasectomy specimens.
Sperm motility Presence of urine in semen sample may affect primarily sperm ____
Liquefying agent Purpose of Dulbecco’s phosphate-buffered Saline, and proteolytic enzymes such as alpha-chymotrypsin or
bromelain
Tests affected with an Increased semen viscosity Sperm motility, sperm concentration, anti-sperm antibody detection, and
and incomplete liquefaction measurement of biochemical markers
Midpiece It is the thickest part of the tail because it is surrounded by a mitochondrial sheath that produces the
energy required by the tail for motility.
Oil immersion objective Sperm morphology is evaluated from a thinly smeared, stained slide under what objective
24 hours Slides for Seminal smear that are air-dried are stable for how many hours?
Retrograde ejaculation / Dry An uncommon but treatable condition in which semen is directed into the urinary bladder which
orgasm eventually can be found in urine instead of being ejaculated.
lack of prostatic fluid Decreased zinc, citric acid, glutamyl transpeptidase, and acid phosphatase indicates:
Disorder of the epididymis A decreased neutral a -glucosidase, glycerol-phosphocholine, and L-carnitine suggest
Spectrophotometry Methods that can be used to quantitate citric acid and zinc on seminal fluid?
Xylene A reagent that can be added to enhance the sperm under microscopic analysis using phase contrast
microscope
Motile sperm can be detected for up to 24 hours after intercourse, whereas nonmotile sperm can persist for 3 days. As the
sperm die off, only the heads remain and may be present for 7 days after intercourse
90 days The entire process of spermatogenesis takes approximately how many days?
FECALYSIS
NORMAL STOOL
Contains bacteria, cellulose, and other undigested foodstuffs, gastrointestinal secretions, bile pigments, cells from intestinal
walls, electrolytes and water.
No BLOOD!
Human passed stool around 100-200g per day
Intestinal gas (flatus) and Odor = due to metabolism of bacterial GI normal flora
Small intestine: primary site for final breakdown and reabsorption of fats, protein and carbohydrates
Large intestine: absorbs water (maximum of 3L of Water)
Digestive enzymes secreted into the small intestine by the pancreas include trypsin, chymotrypsin, amino peptidase, and
lipase
Water and electrolytes are readily absorbed in both the small and large intestines, resulting in a fecal electrolyte content that
is similar to that of plasma
I.K AYTONA 64
RIBBON LIKE INTESTINAL CONSTRICTION
RICE WATERY CHOLERA
PEA SOUP TYPHOID
SYCBALOUS / GOAT DROPPING CONSTIPATION
BUTTER-LIKE CYSTIC FIBROSIS
MUCOID DYSENTERY, MALIGNANCY
I.K AYTONA 65
LABORATORY TESTS
D-XYLOSE TEST
I.K AYTONA 66
II.FECAL LEUKOCYTES
➢ Presenceiof ≥3 neutrophils/hpf Indicates invasive condition
➢ Presence of at least 1 Neutrophil per OIF is significant
TEST
Wet preparation Stool + Methylene blue
✓ Methylene blue staining is the faster procedure but may be more difficult to interpret
✓ Methylene blue is used to differentiate Mononuclear cells and PMNs
Lactoferrin Latex
agglutination
A test for fecal WBC that gives a positive result in invasive bacterial pathogen
✓ It remains sensitive in refrigerated and frozen specimens
Enterobacteriaceae
-
✓ Positive in diarrhea with WBC: Salmonella, Shigella, Campylobacter, Yersinia, & enteroinvasive E. coli.
✓ Negative in diarrhea without WBC: Staphylococcus aureus and Vibrio spp., viruses, and parasites
Dried preparation Stool stained with either Wright's or Gram stains provide permanent
-
- slides for evaluation.
I
Nonoeoitrobaltert
III. FECAL OCCULT BLOOD TEST
Parasites
tuimsexupt
➢ Occult means ___Hidden Vibrio
colorectal cancer
➢ Screening test for __________
➢ Significant value = >2.5ml blood / 150g stool
➢ Sample must be obtained from the center portion of the stool to avoid false positive from external contamination
➢ CHROMOGEN USED: Benzidine, Guaiac, O-toluidine
Bob
REACTION Based on pseudoperoxidase activity of Hemoglobin
MF
-_
BGC
IV. MUSCLE FIBERS 10
-
>
creatorrhea
➢ ___________________ = Increase excretion of muscle fibers in feces
➢ Presence of more than 10 undigested muscle fibers are associated with biliary obstruction, cystic fibrosis, and gastrocolic
fistulas
TEST
*Patient will undergo in a meat diet
*Procedure: Emulsified stool + 10% eosin in alcohol --→ coverslip and stand for 3 mins then observed under HPF for 5 minutes
*Count the number of undigested fibers
VI.FECAL ENZYMES
Enzymes supplied to the gastrointestinal tract by the pancreas are essential for digesting dietary proteins, carbohydrates, and fats.
Decreased production of these enzymes (pancreatic insufficiency) is associated with disorders such as chronic pancreatitis and cystic
fibrosis. Steatorrhea occurs, and undigested food appears in the feces.
I.K AYTONA 67
X-ray film test Detects trypsin enzyme (absent of trypsin is associated with cystic fibrosis)
Trypsin Absence of trypsin has been screened for by exposing x-ray paper to stool emulsified in water. When
(f) X-ray film w/ trypsin is present in the stool, it digests the gelatin on the paper, leaving a clear area.
clear omen Inability to digest the gelatin indicates a deficiency in trypsin production
Chymotrypsin more resistant to intestinal degradation and is a more sensitive indicator of less severe cases of
pancreatic insufficiency
Stable in fecal specimen up to 10 days at room temperature
Measured by spectrophotometry
0
Elastase 1 An enzyme form produced by the pancreas and accounts about 6% of all secreted pancreatic enzyme
Sensitive and specific test for exocrine pancreatic insufficiency
EUSA The test is specific in differentiating pancreatic from nonpancreatic causes inpatients with steatorrhea.
It is not affected by motility disorders or mucosal defects
It is measured by ELISA,
0
The ELISA test uses monoclonal antibodies against human pancreatic elastase-1; therefore, the result is specific for
human enzyme and not affected by pancreatic enzyme replacement therapy
VII.FECAL CARBOHYDRATES
➢ Significant for assessing lactose intolerance
➢ Normal stool pH: 7-8,
➢ Stool pH with Carbohydrate Disorders = pH <5.5
➢ Clinitest: a test for reducing sugar
A result of ≥0.5 g/dl indicates carbohydrate intolerance
DIARRHEA
➢ Stool that weight more than 200g/day with increase liquid and frequency of more than 3x a day
➢ Classified according to severity, mechanism, duration, and stool characteristic
➢ Diarrhea lasting less than 4 weeks is defined as acute, and diarrhea persisting for more than 4 weeks is termed chronic
diarrhea
➢ The major mechanisms of diarrhea are secretory, osmotic, and intestinal hypermotility
CAUSES:
Viruses (e.g rotavirus), protozoa or bacteria, Colitis, Collagen vascular disease, hormones,
endocrine disorder (Hyperthyroidism, Zollinger Ellison Syndrome, VIPoma), inflammatory bowel
disease, and neoplasm
OSMOTIC DIARRHEA Stool- with osmol gap of >50mosm/kg.
Caused by poor absorption that exerts osmotic pressure across the intestinal mucosa. Incomplete
breakdown or reabsorption of food presents increased fecal material to the large intestine, resulting in
water and electrolyte retention in the large intestine (osmotic diarrhea), which in turn results in excessive
watery stool
I.K AYTONA 68
CAUSES:
Maldigestion, Malabsorption, Lactose intolerance, Ameobiasis , Antibiotics, Magnesium
containing antacids, Poorly absorbed sugars (lactose, sorbitol, mannitol), laxatives
CAUSES:
Gastric surgery (gastrectomy), Gastric bypass, Post vagotomy, Duodenal ulcer, DM Zollinger Ellison
Rapid gastric emptying (RGE) dumping syndrome describes hypermotility of the stomach and the shortened gastric emptying half-time,
which causes the small intestine to fill too quickly with undigested food from the stomach. It is the hallmark of earl dumping syndrome
(EDS). Healthy people have a gastric emptying half-time range of 35 to 100 minutes, which varies with age and gender.
A gastric emptying time of less than 35 minutes is considered RGE.
SPUTUM COLLECTION
First morning- Most preferred (routine)
24 hour – for volume measurement
Throat swab – for pediatric patients
Sputum induction- for non-cooperative patients
Tracheal aspiration- for debilitated patient
I.K AYTONA 69
MACROSCOPIC EXAMINATION
Volume Increase in: Broncheictasis, lung abscess, edema, gangrene, tuberculosis, pulmonary hemorrhage
BAE Decrease in: Bronchial asthma, acute bronchitis, early pneumonia
Odor
Odorless Normal
Foul or Putrid Lung gangrene, Advance necrotizing tumors
Sweetish Broncheictasis, tuberculosis
Cheesy Necrosis, tumors, emphysema
Fecal Liver abscess, Enteric gram-negative bacterial infection
Color
Colorless or translucent Made up of mucus only
White or yellow Pus is present
Gray Pus and epithelial cells are present
Bright green and greenish Presence of bile, Pseudomonas aeruginosa infection
Red or bright red Fresh blood, hemorrhage, TB , bronchiectasis
Anchovy sauce or rusty brown Old blood, pneumonia, gangrene
Prune juice Pneumonia, Chronic lung cancer
Olive green/grass green Cancer
Black Inhalation of dust or dirt, carbon, charcoal, anthracosis, heavy smokers
Consistency A. Mucoid MMM = asthma, and bronchitis
B. Serous or frothy = lung edema
C. Mucopurulent = broncheictasis, TB with cavities
Structures
Dittrich’ s plugs *Yellowish or gray caseous matter, the size of the pinhead or navy bean
*Foul odor when crushed
*Occur in bronchial asthma, chronic bronchitis, healthy persons and in TB
Lung stones/ Pneumoliths Small, white or gray fragments of calcified TB tissue or calcified foreign
/ Broncholits matter
Bronchial cast Branching tree like casts of the bronchi
Curschmann’s spirals *Whitish or yellow wavy coiled threads
*Associated with bronchial asthma
Layer formation Top layer : frothy mucus
Second layer : opaque, water material
Bottom layer : pus, bacteria, and tissues
MICROSCOPIC EXAMINATION
Elastic fibers - Slender fibrils with double contour and curled ends
- Found in abscess, gangrene of the lung, and TB
Charcot-Leyden crystals - Colorless, hexagonal, double pyramid, pointed at both ends, and needle like
asthma -
-
Formed as a result of eosinophil degeneration
Most significant
- Associated with bronchial asthma
Pigmented cells - Heart failure cells: hemosiderin laden macrophages
- Carbon laden cells: angular black granules
Curshmann’s spirals - Coiled mucus strands
bronchial asthma - Can be found microscopically and macroscopically.
- Associated with bronchial asthma
Creola bodies patriot asthma - Cluster of columnar cells that is associated with Bronchial asthma
Myelin globules - Colorless, round, oval or pea shaped of various sizes
- Little or no significance and mistaken for Blastomyces
Yeast - During antibiotic treatment, they maybe-seen in large numbers
- Examples are Candida albicans, Cryptococcus neoformans, and Systemic fungi
Parasites - Ascaris, Hookwork, Threadworm, E.histolytica, Paragonimus westermani, Toxocara canis,
Entamoeba gingivalis, Trichomonas tenax, Echinococcus granulosus
Others that are stained - Neoplastic cells, Bacteria, Leukocyte
I.K AYTONA 70
BRONCHOALVEOLAR LAVAGE
✓ Provides a method of obtaining cellular and microbiological information from the lower respiratory tract
✓ Useful in evaluating immunocompromised patients, interstitial lung disease and airway diseases
✓ Important diagnostic test for Pnuemocystis carinii in immunocompromised patients
✓ A suitable respiratory specimen for culture and sensitivity
CELLS SEEN IN BRONCHOALVEOLAR LAVAGE Elements and Viral inclusions seen in respiratory
Macrophage 56-80% specimens:
Lymphocyte 1-15% • Toxoplasma gondii
Neutrophils <3% • Legionella pneumophila
Eosinophil <1 – 2% • Histoplasma capsulatum
Ciliated columnar bronchial epithelial 4-17% • Mycoplasma pneumonia
cells • Influenza A, B, and Respiratory syncytial virus
SWEAT
GASTRIC FLUID
SIGNIFICANCE
✓ Determines whether or not a patient can secrete gastric fluid
✓ Measures amount of gastric acid that can be secreted by one with ulcer symptoms
✓ Help determine the disturbed function of the GI system
2. Chief cells- produces pepsinogen that will be converted to pepsin whenever HCL is present
3. Specialized G cells – produces Gastrin that stimulates parietal cell to produce HCL.
SPECIMEN COLLECTION
I.K AYTONA 71
• Specimen: Fasting specimen, few ml to 50ml average of 30 ml
• Normal appearance of gastric specimen: Pale gray with mucus and no food particles
Types Of Specimen
Basal acid output (BAO) ✓ 1 hour collection (four 15minute specimens)
✓ Requires 12 hour fasting
✓ No gastric stimulant needed
Maximum acid output (MAO) ✓ 1 hour collection (four 15minute specimens)
✓ With gastric stimulant
GASTRIC STIMULANTS
Test meals Ewald’s meal: bread and water or weak tea
Boas meal: oatmeal, meal for detection of lactic acid
Riegel’s meal: mashed potatoes, broiled beefsteak, bouillon
pint
Chemicals ✓ Pentagastrin – most preferred, it resembles true gastrin
✓ Histamine
✓ Histalog
✓ Insulin - assess successful vagotomy procedure
Sham Feeding ✓ Fictitious feeding
✓ Sandwich is chew and then spit out
NOTE!
A. Zollinger Ellison syndrome
- Elevated gastrin levels
- Elevated BAO/MAO results (highest elevation)
B. Pernicious anemia
- Shows a zero BAO/MAO results
- Achlorydia (absence of free HCL)
-
Euchlorhydria Normal free HCL ----
Hyperchlorhydria Increased free HCL Peptic ulcer
Hypochlorhydria Gastric fluid pH >3.5 but falls after gastric stimulation Carcinoma of stomach
Decrease free HCL
Achlorhydria Gastric fluid pH >3.5 and does not fall even after gastric stimulation Pernicious anemia
Absence of free HCL
I.K AYTONA 72
Combined HCL (Bound to Titrate with NaOH
proteins) pH indicator: sodium alizarin
Endpoint: Violet
Normal value: 10 – 15 degrees
Weekly
-Disinfection of centrifuges
-Check pH and purity meter resistance of deionized water used for reagent preparation
Biweekly
-All diluents should be checked for contamination
Monthly
-Speed of centrifuge should be checked with a tachometer, and timing should be
checked with a stop watch
-Check the bacterial count of deionized water used for reagent preparation
I.K AYTONA 73
QUALITY ASSURANCE ERRORS IN CM (Strasinger, 5th edition)
PRE ANALYTICAL ERROR ANALYTICAL ERROR POST ANALYTICAL ERROR
✓ Patient misidentification ✓ Sample misidentification ✓ Patient misidentification
✓ Wrong test ordered ✓ Erroneous instrument calibration ✓ Poor handwriting
✓ Incorrect urine specimen type ✓ Reagent deterioration ✓ Transcription error
collected ✓ Poor testing technique ✓ Poor quality of instrument printer
✓ Insufficient urine volume ✓ Instrument malfunction ✓ Failure to send report
✓ Delayed transport of urine to the ✓ Interfering substances present ✓ Failure to call critical values
laboratory ✓ Misinterpretation of quality control ✓ Inability to identify interfering
✓ Incorrect storage or preservation data substances
of urine
In a clinical laboratory, a quality assessment program includes not only testing controls, referred to as quality control (QC), but also
encompasses preexamination variables (e.g., specimen collection, timing, handling, and storage), examination variables (e.g.,
reagent and test performance, instrument calibration and maintenance, personnel requirements, and technical competence),post-
examination variables (e.g., reporting of results and interpretation), and documentation that the program is being meticulously
followed
Electronic transmission is now the most common method for reporting results
The telephone is frequently used to transmit results of stat tests and critical values. Calls requesting additional results may be received
from personnel on hospital units and from healthcare providers. When telephoning results, confirm that the results are being reported
to the appropriate person. The time of the call and the name of the person receiving the results must be documented according to the
facility’s policy.
ADDENDUM
Home based 1. Principle of current PT test kit: IMMUNOLOGIC
pregnancy test (Enzyme immunoassay/immunochromatographic assay)
kit 2. Detects the Beta hCG subunit of glycoprotein/amino acid
3. It is an indirect test for the detection of fetus
4. Sensitivity: a positive result if a minimum of approximately 25mIU/ml hCG is present
5. Presence of two-color bands suggest a positive result
6. Presence of one-color band (control region) suggest a negative result
7. Absence of two-color bands suggest an invalid result
8. A VERY FAINT LINE IN THE TEST AREA SUGGEST TO REPEAT TEST AFTER 48hours
Test for renal 1. Wipe off the stone(s) and describe in terms of size(mm), shape, color and hardness/texture
calculi 2. Powderized stone and dissolve in a small amount of concentrated HCL
Foaming upon contact with HCL Carbonate
Magenta color Cysteine
Blue color Phosphate
Blue precipitate Magnesium
Pale yellow color Calcium
Orange brown color Ammonium
Yellow orange color Uric acid
Black sediment which settles and bubbles and appear from the oxalate
bottom of the tube
Biologic test for
PT
TEST/METHOD ANIMAL USED POSITIVE RESULT
(Henry’s 19th ed.)
0
Ascheim-Zondek Immature female mice Formation of
hemorrhagic follicles
Immature and corpora lutea
0
Friedman Mature virgin female rabbit Hyperemic uterus and
Mature corpora hemorrhagica
Hogben Female toad (Xenopus laevis) south African clawed oogenesis
frog-carries eggs throughout the year
Galili- manini Male frog (Rana pipiens or Rana clamitans, leopard or spermatogenesis
grass frag) male toad (Bufo bufo or Bufo americanus)
Frank Berman Immature female rats Ovarian hyperemia
Kupperman Female rat Ovarian hyperemia
I.K AYTONA 74
Chemical test in Detected Name of test
urine
Calcium Sulkowitch
Chloride Fantus, Schales Schales
Bile pigments Smith, Harrison’s spot, ictotest, Gmelin
Urobilin Schlesinger
urobilinogen Wallace and diamond
Ketones Rothera’s, Lange, acetest, Gerhardt’s
fructose Resorcinol, Seliwanoff, and Borchardt’s
Qualitative test for Heat and acetic acid, SSA, Purdy’s, picric acid, Potassium ferricyanide, Biuret,
protein Heller’s, Spiegler’s test
Quantitative test for Biuret, Kingsburry-clark, Esbach’s, Kwilecki’s
protein
Sugars 1. Biacol orcinol
2. Benedicts
3. Rubner’s (glucose = red with red yellow, Lactose = red with red ppt)
4. Moore Heller
5. Nylander’s
Urine chemistry These semi-automated instruments require the user to properly dip the reagent strip and place it onto a
Semiautomated platform.
analyzer
REFLECTANCE PHOTOMETRY
1. When light strikes a matte or unpolished surface (e.g., a reagent strip), some light is absorbed, and the
remaining light is scattered or reflected in all directions. The scattered light is known as diffuse
reflectance.
2. The relationship between reflectance and concentration is not linear
Automated ✓ Decrease labor costs and increasing productivity in the urinalysis laboratory
Microscopy ✓ Uncentrifuged urine is used, the time spent in handling and preparing concentrated urine sediment
analyzers for manual microscopy is eliminated
✓ Increased standardization of the microscopic examination, which enhances the accuracy and
reproducibility (precision) of results
Iris iQ 200 It is an automated system that performs the microscopic examination of urine, as well
as cell counts on body fluids
Uses patented technologies to capture and automatically classify digital images of urine
particles.
- APR Pre-classifies urine particles in the photographs based on size, shape, texture, and
contrast in to 1 to 12 categories. Using the computer monitor, the user can review results,
visually assess the particles present, and subclassify them into the 26 additional categories
-The field of view of the microscope is coupled to a digital video camera, and stroboscopic
illumination freezes the particles in motion as they stream past, which ensures blur-free imaging
the field of view of the microscope is coupled to a digital video camera, and stroboscopic
illumination freezes the particles in motion as they stream past, which ensures blur-free imaging.
With each sample, the camera captures 500 frames, digitizes them, and sends them to a
computer for processing
I.K AYTONA 75
Note that the 12 auto-classified sediments are the primary parameters measured.
Light source
Sysmex UF-100 model Argon laser
Sysmex UF-1000i model Red semi-conductor laser
For automated particle analysis, the UF-1000i analyzer requires a 4 mL sample volume;
however, if the instrument is used in the manual mode, only 1 mL of urine is required
Changes in the UF-1000i analyzer include a separate channel for bacterial analysis and
the monitoring of lateral or side scatter, which improves detection of bacteria
Full automated Performing fully automated urinalyses requires combining a urine chemistry analyzer with a microscopy
Urinalysis analyzer.
system
iRICELL Urinalysis
iChem Velocity urine chemistry + iQ200
Systems To perform a complete urinalysis, a minimum of 3 mL urine is poured into a barcode-
labeled tube. Specific tubes are not required; rather a variety of
tubes can be used, including commercial urinalysis tubes (e.g., KOVA, Vacuette, BD) or
disposable glass test tubes
CLINITEK AUWi ATLAS urine chemistry + Sysmex UF1000i
System For a complete urinalysis, 5 mL of uncentrifuged urine is poured into a barcode labeled
tube, which is placed into a 10-place sample rack. Tubes upto 16 mm wide can be used,
but they must be “lipless” for 10 samples to fit in a rack. The sample racks are placed
onto the system, and as each rack is moved to the sampling position of the ATLAS
analyzer, the barcoded sample tube is automatically identified
“THE SECRET RECIPE ON PASSING THE BOARD EXAM IS JUST A MIXTURE OF HARDWORK, DETERMINATION, FAITH,
AND A POSITIVE ATTITUDE
--END--
I.K AYTONA 76