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198 Cards in this Set

  • Front
  • Back

Diagram of a kidney

Flow of urine through the nephron

Glomerulus>proximal tube> descending/ascending Loop of Henle> distal and collecting tubules

Nephron physiology

1. Major functional unit of the kidney


2. Approximately 1 million nephrons per kidney


3. Each nephron is composed of glomerulus and renal tubules

Glomerulus physiology

1. Coil of capillary vessels


2. Glomerulus is a NON-SPECIFIC filter of plasma substances less than 70,000 MW


3. Glomerular filtrate is composed of water, glucose, electrolytes, amino acids, urea, uric acid, creatinine, and ammonia


4. Filters 120 ml/minute, or 1/5 of renal plasma

Function of the proximal tubule

1. Reabsorbs water, sodium chloride (salt), bicarbonate, potassium, calcium, amino acids, phosphates, protein and glucose


2. Glucose: threshold substance, reabsorbs at 160-180 mg/dl or less


3. Secretes sulfates, glucuronides, hydrogen ions and drugs



Reminder: there should be no glucose in urine!

Fuction of descending loop of henle

Reabsorbs water


No solutes reabsorbed



As the filtrate travels down the loop of henle, the filtrate becomes more concentrated.

Function of ascending loop of henle

1. Reabsorbs solutes (sodium, chloride, calcium, magnesium)


2. NO WATER REABSORBED



As filtrate travels back up the ascending loop of henle, it becomes less concentrated. The ascending loop is the only point in the whole process where water cannot go in our out of the tubules!!!

Distal convoluted tubule

PH regulation


Reabsorption and secretion of H+ ions

Collecting tubules functions

Final point of water regulation!!


The body utilizes hormones to regulate the amount of water in our body (ADH- anti-dieurtic hormone)


Diurese: the act of urinating

Functions of distal and collecting tubules

1. Reabsorbs sodium


2. Secretes potassium, ammonia, and hydrogen ions


3. Potassium ions exchanged for sodium ions

Reabaorption and secretion photo

Hormones that influence urine output

1. Aldosterone: electrolyte concentrations


2. Angiotensin: blood pressure


3. Anti-dieurtic hormone: water



The process of regulating the amount of urine secreted by the body is controlled by hormones that respond in fluctuations in electrolyte concentrations, blood pressure, and water concentrations

Normal urine output

0.5 liters- 1.5 liters per day OR


1200-1500 ml per day

Polyuria

Increased urine output


>2500 ml per day



Diseases/causes: diabetes insipidus and mellitus, dieuretics, caffine, alcohol, excessive water intake

Oliguria

Decreased urine output


<500 ml per day



Diseases/causes: dehydration, vomiting, diarrhea, burns, perspiration

Anuria

Complete cessation (no urine output, or just DROPS)



Diseases/causes: kidney damage, decreased blood flow to kidneys

Nocturia

Increased volume at NIGHT

Urine composition

1. Urea (non-protein nitrogen): metabolic waste product produced in liver from breakdown of protein, 1/2 total urinary dissolved organic solids


2. Other organic solids (non-protein nitrogens): uric acid, creatinine


3. Inorganic solids: chloride (primary constitute), sodium, potassium


4. Water

Hormones: aldosterone

Source: adrenal cortex


Action: increases rate of sodium reabsorption

Hormones: Arginine Vasopressin (AVP)

**previously called ADH**


Source: posterior pituitary gland


Action: reabsorption of water from distal tubules



Deficiency of AVP: diabetes insipidus



Diabetes insipidus- disorder of salt and water metabolism marked by intense thirst and polyuria

Hormones: erythropoietin

Source: kidney


Action: stimulates production of erythrocytes

Urine Collection methods

1. Random (clean catch): most common, easiest to collect


2. First morning: ideal screening specimen (most concentrated)


3. Midstream clean catch: clean external genetalia, specimen of choice for bacterial cultures


4. Cath: insertion of cath directly into bladder via urethra, avoids external contamination, but my introduce infection


5. Pediatric: sterile, plastic bag, bag checked every 15 minutes, many sources of contamination


6. Suprapubic aspiration: needle through abdomen directly into bladder, BEST specimen for bacterial culture, invasive procedure

24 hour urine

1. Collected over 24 hours


2. First specimen discarded while all others collected


3. Used for quantitative urine studies


4. Completeness of collection method monitored by creatinine levels (should be >1.0 mg/dl)

Analysis of urines

Analyze within 1 HOUR of collection

Effects of prolonged sitting of specimens at room temperature

Increased: nitrates (bacterial growth), pH ( urea converted to ammonia), turbidity



Decreased: glucose (glycolysis due to bacteria and yeast), ketones (exposure to air), bilirubin (exposure to light), urobilinogen, cells and casts (lysis)



Changes in color occur due to oxidation or reduction of metabolites

Specimen preservation

The best urine sample is freshly voided, midstream clean catch.



Freeze: okay for chemical analysis, NOT UA


Refrigerate: okay for UA, may have crystal formation, slows down bacterial growth


Chemically preserve: BEST, boric acid powder

Refrigeration of urine

Preservation method of choice! (Up to 24 hours)


May result in precipitation of amorphous crystals


After removal from fridge, let sample return to room temperature before testing (about 15 minutes)

Physical examination: odor

Not evaluated, but may provide clues



1. Fruity- ketones


2. Ammonia- old urine


3. "Mousy"- PKU (phenylketonuria)


4. Maple syrup- maple syrup disease

Physical examination: clarity

Normal urine is clear



Any of the urinary elements (cells, casts, crystals) or bacteria may make the urine cloudy

Physical examination: color

Normal urine is a pale yellow (straw) to yellow color


Urochrome gives urine its normal color



Urochromes or urobilin are products of RBC metabolism

Physical examination: pH

Normal urine is slightly acidic (6.0)


Random samples: 4.5-8.0


Post prandial sample (2 hours post eating) may be alkaline


When urine stands at room temperature for some time, ot becomes alkaline



1. Acidic: metabolic or respiratory acidosis, high protein diet, cranberry juice


2. Alkaline: vegetarian


Color: Red

Hemoglobin


Red blood cells


Myoglobin


Porphrin


Uroerythrin

Color: Red-brown

Hemoglobin


Red blood cells


Myoglobin

Color: yellow-brown or yellow-green

Bilirubin


Biliverdin

Color: yellow-orange

Bilirubin


Urobilin


Pyridium (drug)

Color: bright yellow

Vitamin C

Color: dark yellow

Concentrated specimen


Bilirubin


Urobilin

Color: brown-black

Methemoglobin (oxidized RBC)


Homogentistic acid (Alkaptonuria)


Melanin

Color: blue

Indican (Tryptophane Metabolic Disorder)


Methylene blue

Color: green-blue

Old urine


Pseudomonas

Color: port wine

Porphyrin

Specific gravity

1. Offers the simplest way to check concentration and dilutiom function of kidney tubules


2. Normal: 1.002-1.035


3. Specific gravity is directly proportional to color, the higher the specific gravity, to darker the urine



Exception: a pale color urine with high specific gravity is most likely due to glucose! Urine is diluted due to loss of concentrating ability by diabetics

Highest specific gravity the kidneys can concentrate

1.040



Higher values are due to either large amounts of glucose or radiographic dyes from renal x-ray procedures.



Reagent strips for specific gravity are NOT affected by radiographic dyes

Diabetes insipidus vs. Mellitus

Polyuria- excess urine output (>2500)


Polydipsia- excess thirst



Specific gravity:


DM- increased, remember the kidneys have a hard time reabsorbing glucose, and excess glucose causes increase specific gravity


DI- decreased (excess water, less concentrated solutes)

Refractometer- TS

Measure: refractive index


No temperature corrections


Correct for large amounts of protein and glucose



Corrections:


Glucose- subtract 0.004 per gram


Protein- subtract 0.003 per gram

Specific gravity reagent strip

Measures: indirect- colorimetric



pKa change of polyelectrolytes (relative to ionic concentration)

Chemical analysis of UA

Specific gravity, pH, blood, leukocytes, nitrite, protein, glucose, bilirubin, urobilinogen

Protein

Proteins are produced by tubules in the kidneys (uromodulin)



Smaller proteins (microalbumins) can pass through the glomerulus, but mostbprotein that passes through the glomerulus is reabsorbed.

Protein on reagent strips

Principle: "protein error of indicators"


Albumin in urine binds to dye, changing color from yellow to green


The reagent strip is more sensitive tl albumin than globulin



False positive: highly alkaline urine

Proteinuria

1. First indicator of RENAL DISEASE or dysfunction (not detected on reagent strips)


2. Multiple myeloma


3. Orthostatic proteinuria (benign condition resulting in proteinuria after standing)


4. Filtration problem (in glomerulus) or reabsorption problem


5. Strenous exercise

Microalbuminuria

Detected by sensitive albumin tests (level too low to be detected by routine reagent strip)


Periodic monitoring benefits patients with diabetes, hypertension, and peripheral vascular disease


Enables patients with low levels of albuminuria to begin treatment


Several commercial methods for screening

Protein confirmation

Confirmed by SSA (sulfosalicyclic acid)


The acidic pH of SSA denatures yhe structure of proteins, causing them to precipitate


A urine sample positive for protein goes from clear to cloudy with the addition of SSA

Glucose

Should NEVER be in urine!!


Essentially all glucose that enters the kidney is reabsorbed by the tubules


The kidneys have a glucose reabsorption threshold of about 175 mg/dl


Normal blood glucose is 110 mg/dl

Glucose on reagent strips

Specific for glucose ONLY


Principle: glucose oxidase (double sequential enzyme reaction)- glucose oxidase turns glucose into gluconic acid and hydrogen peroxide



False positive: inteference by oxidizing agents (bleach or peroxide)


False negative: reducing substances (ascorbic acid or bacteria- it eats glucose!)

Two causes for glucosuria

1. Diabetes mellitus


2. Reabsorption problems

Diabetes mellitus v. Insipidus

Mellitus: HIGH blood sugar, caused by decreases insulin, increased specific gravity, sugar and ketones present



Insipidus: NORMAL blood sugar, caused by decreased ADH levels, decreased specific gravity, excessive thirst

Clinitest tablet

For glucose and other reducing sugars


Positive: galactose, lactose, fructose, maltose, and pentose



Screening test for galactosemia (rare congenital carbohydrate metabolic condition in pediatrics)



Principle: Benedict's copper reduction test


Copper reduction test vs. reagent strip

RS -/CRT + = non-glucose sugar or other reducing substance



RS +/CRT - = strip more sensitive to glucose than copper reduction

Benedict's copper reduction test results

Positive copper reduction test: sugar (or other reducing substance) other than glucose



Negative copper reduction test with positive strip: glucose, because strip is more sensitive than copper reduction method



False negative: ascorbic acid (vitamin C) in extremely high doses

Ketones

In the absence of sugar, your body uses its fat storage for energy


The metabolism of fat as a primary energy source reaults in the formation of ketone bodies



Ketone bodies seen in urine:


1. Beta-hydroxy-butyric acid: 78%


2. Acetoacetic acid (aka diacetic acid): 20%


3. Acetone: 2%

Ketones on reagent strip

Principle: sodium nitroprusside + ketones = PURPLE color



**acetoacetic (diacetic) acid is the only ketone body detected on reagent strips**



False positives: highly pigmented urine and levadopa metabolites, high specific gravity


False negative: left at room temperature (acetoacetic acid is concerted to acetone, which evaporates upon standing)

Confirmation of ketones

Acetest tablets



Specific for acetoacetic acid (diacetic acid) and acetone

Increased ketones in urine seen in

1. Uncontrolled diabetes mellitus


2. High protein diets


3. GI disturbances

Blood in urine come in a few forms:

1. Hematuria: intact red blood cells, cloudy, red


2. Hemoglobinuria: lysed red blood cells, clear, red


3. Myoglobinuria: muscle hemoglobin, more brown than hemoglobin

Hematuria causes

Intact red blood cells in urine



Pathogenic causes: trauma to bladder, systemic bleeding disorders, renal diseases, kidney stones (calculi), strenous excerise



Non-pathogenic causes: menstration

Hemoglobinuria causes

RBCs readily lyse in alkaline or dilute urine


In most cases, the lysing of RBCs happen AFTER the kidney! (Like in the bladder)



Causes for cell lysis before the kidney: sickle cell/hemolytic anemias, incompatible transfusions, maleria

Myoglobinuria causes

Myoglobin is heme-containing protein involved in the transport of oxygen in muscles


Anything that causes strain on the muscles can release myoglobin into the blood



Causes: muscle destruction, exercise, muscle trama, seizures, electric shock

Blood on reagent strips

2-step enzymatic process:


1. Peroxide on strip +blood= O2


2. O2 + chromagen = color change



False positive: bleach and other oxidizing substances


False negative: ascorbic acid (vitamin C), protein, high specific gravity, increased nitrates



Hemoglobin and myoglobin have peroxidase activity

Lifespan and breakdown of bilirubin

Bilirubin is a normal breakdown product of RBCs.


1. Bilirubin from RBCs floating in the blood. Albumin binds it up so it cannot get into cells (toxic to cells)


2. Uncongugated bilirubin: this albumin-bilirubin complex is too large to pass through glomerulus


3. The complex stays in circulation until it reaches the LIVER


4. Conjugated bilirubin: The liver removes the albumin and conjugates the bilirubin


5. Conjugated bilirubin can pass through the glomerulus. Almost all bilirubin is sent from liver to the intestines


6. The intestines break down bilirubin to urobilinogen


7. Most urobilinogen is broken down further and passed in feces


8. Some goes back into circulation where it ends up in kidneys

Photo of breakdown of bilirubin

Pathology of bilirubin

Jaundice



3 causes for disrupted bilirubin:


1. Pre-hepatic (before liver)


2. Hepatic (in the liver)


3. Post hepatic (after the liver)

Post hepatic bilirubin causes

Obstruction!!


Conjugated bilirubin never makes it to the intestines, not bilirubin is NEVER converted to urobilinogen


Increased urine bilirubin


**white/grey feces

Bilirubin on reagent strip

Diazo reaction: diazonium salts+ bilirubin= blue/purple color



Confirmed by Ictotest



False negative: ascorbic acid (vit C), strips exposed to light

Bilirubinuria

Associates with bile duct obstruction and liver damage (hepatitis or cirrhosis)

Urobilinogen on reagent strips

Principle:


Ehrlich's reaction: para-dimethylaminobenzaldehyde in acid buffer + urobilinogen = pink/ cherry red color



False negatives: formalin (preservative)


False positive: some medication, highly pigmented urine

Increased urobilinogen

Liver damage


Hemolytic disease

Negative urobilinogen

Indicates bile duct obstruction!

Normal bilirubin/urobilinogen in urine

Bilirubin: <0.02 mg/dL


Urobilinogen: <1 mg/dL

Nitrites

Nitrate is a common food byproduct passed in the urine


The bacteria that most often causes UTIs (E. Coli and Klebsiella) contain the enzyme nitrate reductase.


This enzyme breaks down the normally found nitrAte into nitrite

Nitrites on reagent strips

The nitrate pad contains an amine and aromatic compound. The nitrite changes the amine into a diazo salt



The diazo salt + aromatic compound = pink color change



Any shade of pink is considered to represent a clinically significant bacteria



Normal: negative

False negatives on the nitrite reagent strip

1. Lack of dietary nitrites


2. Urine not in bladder long enough (4 hours minimum) for bacteria to reduce nitrate to nitrite


3. Bacteria are present, but not nitrate reducers


4. Ascorbic acid (vit C)

Leukocyte Esterase (enzymes)

Enzyme produced by granulocytic white blood cells


Lymphs DO NOT produce


Leukocytes on reagent strip

Principle: leukocyte esterase splits an ester to form pyrrole compound which reacts with a diazo reagent = PURPLE



Positive indicates presence of leukocytes (pyuria)



False positive: vaginal discharge

Positive strip correlations

pH- nitrite, leukocyte, microscopic


Protein- blood, nitrite, leukocyte, micro


Glucose- ketone


Ketones- glucose


Blood- protein, microscopic


Bilirubin- urobilinogen


Urobilinogen- bilirubin


Nitrite- protein, leukocyte, microscopic


Leukocyte- protein, nitrite, microscopic


Specific gravity- none

Reagent strip reactions: pH

Reaction principle: 2 indicators provide wide spectrum of color changes



False positives/negatives: none



Significance: alkaline may indicate "old"

Reagent strip reactions: protein

Reaction principle: protein error of indicators- pH of strip = 3.0, dye changes color of strip



False positive: alkaline urine



False negative: high salt



Significance: proteinuria: best single indicator of early disease (glomerular involvement), can be elevated after strenous exercise

Reagent strip reactions: glucose

Reaction principle: glucose oxidase method (double sequential enzyme)



False positive: bleach



False negative: ascorbic acid, ketones, high SG, low pH



Significance: diabetes mellitus

Reagent strip reactions: ketones

Reaction principle: Na notroprusside + ketone = purple



False positive: highly pigmented urine, Levapoda metabolites



False negative: ascorbic acid, high specific gravity



Significance: uncontrolled diebetes mellitus, high protein diet, dehydration

Reagent strip reactions: blood

Reaction principle: peroxide +blood = O2 + color indicator = color change



False positive: bleach



False negative: ascorbic acid, ketones, high SG, low pH



Significance:


1. Hematuria (systemic bleeding, renal disease, cystitis, calculi, strenous exercise, menstruation),


2. Hemoglobinuria (incompatible blood transfusion, malaria, hemolytic anemia)


3. Myoglobin (muscle destruction)

Reagent strip reactions: bilirubin

Reaction principle: diazo salt + bilirubin = blue/purplish color



False positive: medication color



False negative: ascorbic acid, increased SG, nitrite



Significance: bile duct obstruction, liver damage (hepatitis and cirrhosis)

Reagent strip reactions: urobilinogen

Reaction principle: para-dimethylaminobinzaldehyde + urobilinogen = peach/pink/cherry red color (Ehrlich's reaction)



False positive: highly pigmented urine, some medication



False negative: nitrite



Significance: liver damage (hepatitis and cirrhosis), hemolytic anemias

Reagent strip reactions: nitrite

Reaction principle: nitrite+amine reagent =diazo compound (diazo compound+3-hydroxy-1.2.3.4 tetrahydrobenz)-quinolin =PINK color



False positive: medication color



False negative: ascorbic acid



Significance: bacteria (UTI)

Reagent strip reactions: leukocytes

Reaction principle: leukocyte esterase splits ester to form pyrrole compound. Pyrrole + diazo reagent = purple



False positive: bleach



False negative: glucose, protein, high SG, some antibiotics



Significance: WBC in urine most likely indicates presence of bacteria, reacts with granulocytes, NOT lymphocytes

Reagent strip reactions: specific gravity

Reaction principle: pKa change of polyelectrolyte



False positive: protein



False negative: alkaline urine



Significance: decreased in diabetes insipidus, radiopaque dye

4 Urine Stains

1. Supravital stain: most common is Sternheimer-Malbin, stains everything


2. Gram stain: stains bacteria


3. Hansel stain: stains eosinophils (ex. Patient may be allergic to catheter)


4. Fat stains: Sudan III or Oil Red O (only fat cells pick up stain, confirms presence of fat or triglyceride)

Normal urine sediment constituents

0-2 RBC


0-5 WBC


0-2 hyaline cast


Slight mucus

Abnormal urine constitutes: red cells

Normal 0-2


May indicate glomerular damage or menstrual contamination


May be altered by pH and osmltic pressure to form "ghost", crenated or swollen cells


May be confised with yeast cells and oil droplets; add 2% acetic acid to lyse RBC

Abnormal urine constitutes: white cells

May indicate inflammation or infection (pyuria)

Casts

Cylindrical form Having parallel sides


Formed in the lumen of the distal convoluted tubule and collecting duct


Major constitute of casts is uromodulin, a glycoprotein secreted by renal tubular epithelial cells

Factors that influence cast formation:

Decreased pH


Decreased output


Increased specific gravity


Increased protein

7 types of casts

1. Hyaline


2. Red cell cast


3. White cells cast


4. Granular cast


5. Waxy cast


6. Fatty cast


7. Broad cast

Hyaline cast

Most frequently seen


Primarily uromodulin protein


Seen in dehydration

Red cell cast

**Glomerular nephritis** (also known as intrinsic renal disease)


Extensive damage to the glomerulus, bleeding from nephron, glomerular dysfunction


Solid mass of tightly packed RBC with characteristic orange-red color (unstained sediment)

Granular casts

Severe dehydration


Disintegration of cellular casts

Waxy cast

End stage renal disease cast


Advanced stage of hyaline, granular, or cellular casts


Indicates prolonged urinsry stasis (chronic renal disease)


Square edges

Fatty cast

Breakdown of epithelial cell casts that contain oval fat bodies.


Rare


Significance: Nephrotic syndrome


Must do a confirmatory stain (sudan or oil red)


If cholesterol is present, the fat droplets will show a maltese cross pattern under polarized light

Squamous epithelial cells

Largest, abudant irregular cytoplasm, central nucelus (RBC size)



Notes: least significant, most frequently seen, normal in vaginal lining and lower uretha

Transitional epithelial cell

Round or pear shaped, central nucleus, absorbs water (swell to 3x normal size)



Notes: renal carcinoma, renal pelvis, bladder, upper urethra

Renal tubular epithelial cells

Most significant, round, eccentric nucleus, larger than WBC



Notes: tubular necrosis, renal tubules

Crystals

Most crystals are clinically insignificant, because they can be formed in relation to changes in pH, and temperature.


Significant Crystals are found in fresh urine!



Presence of crystals may indicate renal calculi (kidney stones), metabolic disorders or drug overdose

Crystals in alkaline urine (pH >7.0)

1. Amorphous phosphates: white precipitate in urine, microscopically identical to amorphous urates


2. Triple phosphate: "coffin lid"


3. Ammonium biurate: "thorny apple"


4. Calcium carbonate: dumbell


5. Calcium phosphate: needles in a flower shape


6. Calcium oxalate

Abnormal crystals

Indicate metabolic disorders or drug metabollites


1. Bilirubin: small yellow-brown cluster of fine needles


2. Cystine: colorless hexagonal plates


3. Cholesterol: tectangular plates with corner notches


4. Leucine: yellow-brown spheres with concentric circles


5. Tyrosine: fine, delicate needles (**when seen with leucine, liver disease indicated**)


6. Sulfonamide: needles or brown spheres, or fans


7. Radiographic dye: empty plates


8. Ampicillin: needles

Review: crystals seen in normal acidic urine

Calcium oxalate


Uric acid

Review: crystals seen in normal alkaline urine

Triple phosphate


Ammonium biurate


Calcium carbonate


Calcium oxalate

Review: abnormal crystals

Bilirubin


Cystine (memory: sweet 16- six sides!)


Leucine


Tyrosine


Cholesterol

Other constitutes found in urine

1. Bacteria- correlate with presence/absence of leukocyte esterase


2. Yeast- most often represents vaginal infection


3. Parasites- trich, enterobius vermicularis


4. Mucus- no significance


5. Clue cells- squamous epis with bacterial vaginosis

Artifacts

1. Powder (starch)


2. Fat/oil droplets


3. Fibers- fibers polarize, casts don't


4. Hair

Inclusion bodies

1. In viral infections, such as rubella and herpes, cells may contain inclusion bodies


2. CMV produces large intranuclear inclusions


3. Lead poisoning produces cytoplasmic inclusions


4. Hemosiderin (form of iron) contained in urine sediment indicates severe intravascular hemolysis, delayed transfusion reaction, PCH, or as a result of hemochromatosis


Microscopic correlations: Red blood cell

Physical appearance: turbidity, red color


Chemical: blood

Microscopic correlations: white blood cells

Physical appearance: turbidity


Chemical: protein, nitrites, leukocyte esterase

Microscopic correlations: epithelial cells

Physical appearance: turbidity


Chemical: protein

Microscopic correlations: casts

Physical appearance: none


Chemical: protein

Microscopic correlations: bacteria

Physical appearance: turbidity


Chemical: pH, nitrites, leukocyte esterase

Microscopic correlations: crystals

Physical appearance: turbidity


Chemical: pH

Diseases of the urinary tract: glomerulonephritis

RBC cast, increased blood, renal epis, WBCs


Symptoms: fever, edema, nausea, oliguria (low urine output)


Glomerulus involved,

Diseases of the urinary tract: Nephrotic Syndrome

Change in glomerular permeability, increased fat production



Symptoms: edema (due to sodium retention), increased lipids in blood, blood pressure changes



Clinical findings: increased protein**, blood, fatty cast, oval fat bodies, renal cells


Diseases of the urinary tract: acute tubular necrosis (ATN)

Tubular disease, causes the destruction of renal tubular cells. Possible afer trauma or post-surgical


Toxic buildup of hemoglobin and myoglobin



Symptoms: azotremia (BUN/creatinine), oliguria



Clinical findings: decresed specific gravity, renal epi cast***, renal epithelial cells***

Diseases of the urinary tract: cystinuria

Inherited disease where the proximal tubules cannot reabsorb cystine. Cystine readily precipitates in acidic urine and can cause kidney stones. People with cystinuria must always stay hydrated to prevent calculi formation

Inherited metabolic disorders: Tyrosinuria

Seen most often in newborns because the liver is immature.


May see tyrosine and leucine crystals in acid urine



Catecholamines (metabolic product of tyrosine) test is ordered, results will be decreased due to the body not breaking down tyrosine!

Inherited metabolic disorders: Phenylketonuria (PKU)

Increased urinary excretion of phenylpyruvate (keton) and its metabolites.


Can result in severe brain damage or other developmental disorders



This is why PKUs are done on ALL newborns!

Inherited metabolic disorders: Maple Syrup Urine Disease

Rare and most often seen in newborns. Its the accumulation of branched chain amino acids



**Distinct maple syrup or caramalized sugar odor**

Inherited metabolic disorders: Galactosuria

Galactosuria is a lack of the enzyme or a deficient enzyme needed to break galactose into glucose



Can result in liver damage, cataracts, ovarian failure, and brain damage

Inherited metabolic disorders: Pyelonephritis (kidney disease)

Acute: infection of renal tubules. Symptoms include flank pain, fever, nausea, increased frequency to urinate


Clinical: leukocyte esterase, nitrites**, increased WBC, bacteria



Chronic: long lasting inflammation of tubules. Urine is allowed to flush backwards from the bladder up into the renal pelvis and back into the kidney


Clinical: maybe leukocyte?, NO NITRITE, WBC cast, NO BACTERIA

Pregnancy testing

Human chorionic gondatropin (HCG), a glycoprotein composed of alpha and beta subunits is secreted by the placenta.


Can be detected as early as 8-10 days after ovulation


HCG peaks at 8-10 weeks


First morning specimen is preferred

Renal function tests

Used to test glomerular filtration and tubular function



Tests for glomerular filtration:


1. Clearance tests


2. B2-macroglobulin


3. Cystatin C

Creatnine clearance

Most commonlu used clearance test to access GFR (glomerular filtration rate)


This measures the amount of blood filtered to a particular substance in a given time



Production and excecretion of CREATININE is fairly constant day to day



24 hour urine


Creatinine >1 mg measures adequacy of collection



(Urine creatinine × volume) ÷ serum creatinine = creatinine clearance

Creatinine clearance formula with correction for kidney mass

Mililiters of plasma cleared of creatinine by the kidney per minute



(urine creatinine ÷ serum creatinine) × (urine volume ÷ 1440 minutes) ×


(1.73 ÷ body surface area)

Normal creatinine clearance

90-120 ml/minute for adults


Decreases with age

Estimated GFR

Assists in detecting chronic kidney disease


More sensitive than creatinine clearance


Calculation based on serum creatinine, patient's age, gender, and ethnicity

B2-Microglobulin

Useful marker of renal tubular function



Increased plasma concentration indicate a reduced GFR (not specific)

Cystatin C

May provide an equal or better detection of adverse changes in GFR



Disadvantages:


1. Higher cost than creatinine clearance


2. Possible variable results among individuals

Lab findings of acute glomerulonephritis

Gross hematuria


Smoky turbidity


RBC casts


Waxy casts

Lab findings of chronic glomerulonephritis

Hematuria


All types of casts, but only occasional to few RBC casts

Lab findings of acute Pyelonephritis

Turbidity


Positive nitrite


Positive leukocyte esterase


WBC casts


Bacteria

Lab findings of chronic Pyelonephritis

Positive nitrite


Positive leukocyte esterase


All types of casts, but only occasional WBC cast

Lab findings of nephrotic Syndrome

May see "free" fat droplets


Fatty casts


Oval fat bodies

Lab findings of cystitis/ lower urinary tract infection

Bacteria


WBCs

Reasons for analysis of Cerebrospinal fluid (CSF)

Meningitis


Encephalitis


Syphilis


Brain abcess/tumor


Intracranial hemorrhage


Leukemia/lymphoma with CNS involvement

CSF characteristics

1. Normally clear, colorless


2. Xanthochromia: pink, orange, or yellow CSF supernatant (usually due to hemoglobin)



Important to differentiate between intracranial hemorrhage and tramatic tap!!

Differentiate between intracranial hemorrhage and tramatic tap

Hemorrhage


Appears: all tubes equally bloody


Supernate: xanthochromic


Clots: none



Tramatic tap


Appears: clearing of blood in each tube


Supernate: clear


Clots: yes, due to fibrinogen

Distribution of CSF tubes

1. Chemistry/serology: protein, glucose, lactate, VDRL, latex agglutination tests


2. Microbiology: gram stain, culture, india ink


3. Hematology: cell count and diff

Normal CSF lab values

Protein: 15-45


Glucose: 60-70% plasma glucose


Cells: 0-5 WBC


Differential: 70% lymph, 30% mono

CSF electrophoresis

OLIGOCLONAL BANDING = Multiple sclerosis


Decreased glucose, increased protein

Manual cell count calculation for body fluids

(# cells × dilution)÷ (# squares x depth- 0.1)



**For CSF, pleural, pericardial and pertioneal fluids

Differentiate causes of meningitis- CSF studies

Bacterial


Protein: very increased


Glucose: decreased


WBC: neutrophils


Lactate: increased



Viral


Protein: increased


Glucose: normal


WBC: lymphocytes


Lactate: normal



Fungal


Protein: increased


Glucose: normal to decreased


WBC: lymphocytes and monocytes


Lactate: increased

Reasons for semen analysis

1. Infertility (most common)


2. Post vasectomy


3. Forensic medicine (presence of acid phosphatase confirms presence of semen in alleged rape cases; flavin in semen fluoresces on clothing under UV light)

Male reproductive system

Under the influence of testosterone, sperm are produced in the testicles and are stored in the epididymis



In the epididymis, the sprem mature and become motile



The sperm remain in the epididymis until ejaculation (sperm move to the vas deferens where they are carried to the ejaculatory duct)



In the ejaculatory duct, fluid from seminal vesicles are added



Semen is the joining of sperm and fluids!!

Normal sperm morphology

Counted as % of normal forms, normal range is greater than 50%

Abnormal morphology

Range: <30% abnormal forms

Reference ranges of sperm analysis

Volume: 2-5 ml


Count: 20-250 million/ml


Motility: >50%


Morphology: <30% abnormal forms


Viability: >75% live forms

Viability

Normal: >75% live forms



Azoospermia- no sperm


Oligospermia- <20 million/ml



(Normal count is 20-250 million/ml)

Serous fluids and reasons for analysis

Sepsis


Malignancy


Systemic disease



Pleural, pericardial, peritoneal (ascites)

Pleural fluid source

Thoracic cavity (around lungs)

Pleural fluid appearance

Normal: clear to pale yellow


Turbid: WBC cells, bacteria


Bloody: trauma, malignancy


Milky: chylous fluid

Pleural fluid lab tests:

Cell count


Glucose


PH


Amalyse


CEA (carcinoembryonic antigen)

Pleural fluid: cell count significance

Increased RBC: trauma, malignancy


Increaced neutrophils: bacteria


Increased lymphs: tuberculosis, malignancy

Pleural fluid lab value clinical significance: glucose, pH, amalyse, CEA

Decreased glucose: TB, rheumatoid inflammation, malignancy



Decreased pH: TB, malignancy, esophageal rupture



Increased amalyse: pancreatitis



Increased CEA: malignancy

Pericardical fluid source

Pericardial cavity (around heart)

Pericardial fluid appearance

Normal: clear to pale yellow


Turbid: infection, malignancy


Bloody: TB, tumor, cardiac puncture


Milky: lymphatic drainage

Pericardial lab tests

Cell counts


Glucose


CEA

Pericardial fluid lab tests clinical significance

Cell count:


Increased RBC: TB, tumor, cardiac puncture


Increased neutrophils: bacterial endocarditis



Decreased glucose: bacterial infection



Increased CEA: malignancy

Peritoneal (ascites) fluid source

Peritoneal cavity (around abdomen)

Peritoneal fluid appearance

Normal: clear to pale yellow


Turbid: pertionitis, cirrhosis


Bloody: trauma


Milky: chylous fluid (rich in fats)


Green: bile

Peritoneal fluid lab tests

Cell counts


Glucose


Amalyse


Alkaline phosphatase


Urea/creatinine

Peritoneal lab tests significance

Cell count


Increased RBC: trauma


Inceeased neutrophils: peritonitis



Decreased glucose: tubercular peritonitis, malignancy



Increased amalyse: pancreatitis, GI perforation



Increased ALKP: Intestinal periforation



Increased urea/creatinine: ruptured bladder

Effusion

Build up of a body fluid in a body cavity due to a pathologic process



Pleural, pericardial, and peritoneal

Reasons for analysis for synovial fluid

Sepsis


Hemorrhage


Crystal induced inflammation

Synovial fluid source

Synovial membrane (around joints)

Synovial fluid appearance

Normal: clear, pale yellow and viscous


Bloody: hemorrhagic arthritis


Milky: crystals, cells


Green tinge: bacteria


Deep yellow: inflammation

Synovial fluid cell counts

Normal:


<200 WBC


<2000 RBC



Increased RBC: hemorrhage


Increased neutrophils: sepsis (>25%)


Increased lymphs: non-septic infection

Sweat

Source: sweat glands (of skin)


Appearance: clear and colorless



Increased sweat electrolytes (sodium and chloride) confirms diagnosis of cystic fibrosis

Gastric fluid source

HCL and pepsin (secreted in stomach)

Gastric fluid appearance

Depends on diet

Gastric fluid lab test and significance

Titratable acidity



Increased: duodenal ulcer, Zollinger-Ellison syndrome



Decreased: pernicious anemia (no intrinsic factor)

Reasons for amniotic fluid analysis

Fetal well being


Fetal lung maturity- 3 tests


1. Lecithin/Sphingomyelin ratio (L/S)


2. Phosphatidylglycerol (PG)


3. Lamellar body counts

Lectin/Sphingomyelin (L/S) ratio

Measures the phospholipids lecithin and sphingomyelin to assess fetal lung maturity


If >2.0, fetal lungs are MATURE


**(for diabetic mothers-PG must be present for fetal lung maturity)

Phosphatidylglycerol (PG)

Lipid component of pulmonary surfactants


Not detected until about 35 weeks


Absence does not rule out mature fetal lungs

Lamellar body counts

Secreted into aveolar lumen at 20-24 weeks


Amniotic fluid is analyzed on automated instruments by using platelet count value



Advantages:


1. Small sample volume


2. Short turnaround time


3. Low cost


4. Easily interpreted

Other amniotic fluid testing

1. Alpha-fetoprotein (AFP): if INCREASED, associated with neural tube disorders such as Spina Bifida


2. Bilirubin: reliable estimate of fetal red cell destruction due to maternal antibody, increased in HDFN


3. Creatinine: fetal age


4. Foam stability index


5. Fluorescence Polarization Assay

Amniotic fluid appearance

Normal: clear and colorless


Yellow-green: bilirubin


Red: red cell destruction (HDFN)

Transudate vs. Exudate: color

Transudate: colorless



Exudate:


Yellow-white: inflammation


Red-brown: hemorrhage


Yellow-brown: bilirubin


Milky-green: chylous fluid (fatty)

Transudate vs. Exudate: turbidity

Transudate: clear, watery



Exudate: cloudy, viscous

Transudate vs. Exudate: specific gravity

Transudate: <1.015



Exudate: >1.015

Transudate vs. Exudate: protein

Transudate: <3 g/dl



Exudate: >3 g/dl

Transudate vs. Exudate: LD (lactic dehydrogenase)

Transudate: <200 IU



Exudate: >200 IU

Transudate vs. Exudate: cell count

Transudate: <1000/microliter



Exudate: >1000/microliter

Transudate vs. Exudate: increases associated with...

Transudate: congestive heart failure, changes in hydrostatic pressure



Exudate: infections and malignancies

Differentiating benign and malignant cells in fluids chart picture