Urinalysis Flashcards

Objectives

1
Q

Describe a “clean catch” technique for evaluating urine and the importance of patient education

A
  • void small amount into toilet, then collect some urine in container
    • Why do you void first?
      • To get rid of the squamous cells and microbes from outer urethra aka to avoid bacteria
    • Was it midstream? Look for squamous cells
    • **Always instruct the pt on how to collect the urine **
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2
Q

Catheter-obtained specimen

A
  • Catheterization of the bladder through the urethra for urine collection is done only in special circumstances, i.e., in a comatose or confused adult patient, or in an infant or child unable to cooperate with obtaining a clean catch specimen
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3
Q

Performing a complete urinalysis

A
  • First do the visual exam, then the dipstick exam, and then spin the urine and look at the sediment under the microscope.
  • Remember not to discard the urine immediately – may need to send for culture!
  • Urine should be examined promptly (within 30-60 minutes) or otherwise refrigerated
  • Microscopic urinalysis at initial evaluation and on an ongoing basis can reveal vital information about the health of the kidney. Evaluation should be performed by centrifugation of at least 12 mL of a freshly voided specimen.
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4
Q

Visual Exam- Color

A
  • Color
    • normal fresh urine is pale to dark yellow in color due to urobilinogen and urobilin (metabolic products of hemoglobin breakdown)
  • Intensity of yellow color generally indicates the concentration of the urine- usually most concentrated in first AM void
  • A pink, red, orange, or brown color is abnormal and could be from:
    • The presence of RBCS (hematuria): pinkish / red
    • The presence of free hemoglobin (hemoglobinuria) or free myoglobin (myoglobinuria): reddish / reddish brown
    • Presence of bilirubin: brownish – classically “cola-colored”
  • Some drugs / foods can affect urine color: (i.e. pyridium and rifampin cause an orange discoloration; excessive beets cause a red discoloration)
    • Pyridium = Phenazopyridine = AZO Standard, a bladder analgesic available OTC that folks use when they have a UTI to help with the dysuria

***the pt’s history, as well has the subsequent dipstick and micro will help you make the determination of what is causing the color abnormality

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5
Q

Visual Exam- Clarity

A
  • Normal urine is clear
  • Turbidity or cloudiness may be caused by excessive cellular material (pyuria or hematuria), excessive crystals, or excessive protein in the urine (proteinuria)
  • Pyuria = too many WBCs in the urine
  • Hematuria = too many RBCs in the urine
  • Again, the dipstick and micro will help give you the answer as to what is causing the turbidity
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6
Q

Urine Smell

A
  • Normal urine smell is “Urinoid”
  • A more disagreeable, malodorous smell is sometimes noted with UTIs
  • The glucosuria of diabetes mellitus can cause a sweet, fruity odor
  • Some foods, most notably asparagus, will also cause a urine odor change
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7
Q

Urine Dipstick

A
  • A paper or plastic dipstick composed of sections with different test reagents embedded into the fibers
  • The reagents react with components of the urine; color changes on each segment of the strip are then compared with a chart (there are also some automated urine dipstick analyzers)
  • After the visual exam – noting the color, clarity, and odor of the urine - then do the urine dipstick
  • Dipstick is also known as “urine reagent strip”
  • Reagent: a substance used in a chemical reaction to detect, measure, examine, or produce other substances
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8
Q

Dipstick Testing

A
  • The proper way to use a dipstick is to fully immerse it in urine for 2-3 seconds, turn it horizontally on a paper towel to absorb runoff and keep chemicals from running onto the adjacent patch, and wait at least 30 seconds before reading.
  • Don’t hold it vertically!
  • Some reagents can be read in 30 seconds, others must wait up to two minutes to note change…
  • Don’t forget to put the lid back on the container of dipsticks as exposure to light and air can affect accuracy of dipsticks
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9
Q

Dipstick- standard items checked

A
  • Specific Gravity
  • pH
  • Blood (aka Heme)
  • Protein
  • Glucose
  • Ketones
  • Nitrate
  • Leukocyte Esterase
  • Bilirubin
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10
Q

Specific Gravity (sp gr)

A
  • Specific gravity is the relative weight of a specific volume of liquid compared with an equal volume of distilled water.
  • Sp gr of pure water is 1.00
  • Urine sp gr is directly proportional to urine solute concentration; i.e. sp gr is a reflection of how concentrated or dilute the urine is…
  • Specific gravity <1.008 is dilute and >1.020 is concentrated
  • As long as the pt’s kidneys are functioning well, think of sp gr as a clue to the pt’s hydration status
  • high sp gr = concentrated urine =dehydrated
  • low sp gr = dilute urine = well hydrated
  • Sp gr typically ranges between 1.002 and 1.035
  • Sp gr is generally > 1.020 after a 12 hour period without food or water (so in the morning after a long sleep)
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11
Q

Dipstick: pH

A
  • The glomerular filtrate of blood plasma is usually acidified by renal tubules and collecting ducts from a pH of 7.4 (normal arterial blood pH) to slightly acidic (i.e. 5.5 – 6.5) in the final urine
  • Recall that lactic acid, uric acid, other organic acids from metabolic processes are excreted into the urine to maintain the body’s acid/base balance, i.e. the kidneys are responsible for eliminating the daily nonvolatile metabolic acid load
  • Diminished renal acid excretion — A regular Western diet (lots of protein) generates a daily nonvolatile metabolic acid load of approximately 50 to 100 mEq/day that must be excreted by the kidneys. Acid-base balance is maintained by excreting these hydrogen ions in the urine
  • Due to variables,, urinary pH may range from as low as 4.5 to as high as 8.0.
  • One point to note is that an alkaline urine in a patient with a UTI suggests the presence of a urea-splitting organism, i.e. a bacteria that produces urease
  • Examples are Proteus, Klebsiella, or Pseudomonas species
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12
Q

Urease

A
  • activity tends to increase the pH of its environment. Ureases are found in numerous bacteria, fungi, and algae.
  • Urease is a high molecular weight cytoplasmic enzyme that hydrolyzes urea to ammonia and carbon dioxide. Ammonia combines with hydrogen to form ammonium; the ensuing reduction in free hydrogen ion concentration leads to alkalinization with the urine pH being well above 7.0 and sometimes as high as 9.0. Alkaline urine sometimes has an ammoniacal smell.
  • A urease producing bacteria that we will talk more about in the GI module is helicobacter pylori. (H.pylori create “an island of alkalinitiy in a sea of acidity” – lowing surrounding pH to survive in the low pH of stomach acids…)
  • Struvite stones are composed of magnesium ammonium phosphate (aka struvite) and calcium carbonate-apatite. Normal urine is undersaturated with ammonium phosphate, and struvite stone formation occurs only when ammonia production is increased and the urine pH is elevated, which decreases the solubility of phosphate. The only situation in which this occurs in humans is with an upper urinary tract infection with a urease-producing organism, such as Proteus or Klebsiella. Urease breaks down urinary urea into ammonia plus carbon dioxide:
    • Urea → 2NH3 + CO2
    • The ammonia produced by this reaction then combines with water:
    • NH3 + H2O → NH4+ + OH-
    • The net result is increased availability of ammonium in an alkaline urine
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13
Q

Dipstick: Blood

A
  • The dipstick test for blood detects the peroxidase activity of the hemoglobin in erythrocytes
  • A positive blood on dipstick usually reflects the presence of RBCs in the urine – even just a few extra RBCs in urine (not grossly visible)
  • Less common reasons to have a positive heme result on dipstick are the presence of free hemoglobin (from severe hemolytic anemia) or free myoglobin (from rhabdomyolysis) in the urine. In these cases, the microscopic evaluation would NOT show the expected RBCs generally seen with the most common cause of a positive dipstick for blood – RBCs in the urine!
  • Bottom line, confirm positive blood/heme on dipstick by looking for RBCs in micro exam!
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14
Q

Dipstick testing for hematuria

A
  • is at best a screening tool which needs the support of microscopy to make a definitive diagnosis
  • Make sure you know if a reproductive-aged woman is on her period or not before pursuing a work-up of hematuria!
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15
Q

Rhabdomyolysis

A
  • is a potentially life-threatening syndrome resulting from the breakdown of skeletal muscle fibers with leakage of muscle contents into the circulation. Rhabdomyolysis literally means striated muscle dissolution or disintegration
  • Clinical features are often nonspecific, and tea-colored urine is usually the first clue to the presence of rhabdomyolysis. Screening may be performed with a urine dipstick in combination with urine microscopy. A positive urine myoglobin test provides supportive evidence.
  • With muscle injury, large quantities of potassium, phosphate, myoglobin, creatine kinase (CK) and urate leak into the circulation. Under physiologic circumstances, the plasma concentration of myoglobin is very low (0 to 0.003 mg per dL). If more than 100 g of skeletal muscle is damaged, serum haptoglobin binding capacity becomes saturated.6 The circulating myoglobin becomes “free” and is filtered by the kidneys.
  • Myoglobin in the renal glomerular filtrate can precipitate and cause renal tubular obstruction, leading to renal damage.
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16
Q

Hemolytic anemia

A
  • is a form of anemia due to hemolysis, the abnormal breakdown of red blood cells (RBCs), either in the blood vessels (intravascular hemolysis) or elsewhere in the human body (extravascular, but usually in the spleen). Large amounts of “free” hemoglobin are then seen in the urine….
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17
Q

The dipstick test for blood

A
  • detects the peroxidase activity of the hemoglobin in erythrocytes. However, myoglobin and free hemoglobin will also catalyze this reaction, so a positive test may indicate hematuria, myoglobinuria, or hemoglobinuria.
  • False positive readings are most often due to contamination with menstrual blood. Generally, try not to get your urinalysis on female pts done during their menstrual cycles…
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18
Q

Dipstick: Protein

A
  • In general, only a small amount of filtered plasma proteins and protein secreted by the nephron tubules (“Tamm-Horsfall” protein) can be found in normal urine.
  • Abnormal amounts of protein in the urine is termed proteinuria
  • The dipstick reagent is most sensitive to the presence of albumin, which is typically the major protein “spilled”
  • The glomerular capillary wall is permeable only to substances with a molecular weight of less than 20,000 daltons..once filtered, low molectular weight proteins are mostly reabsorbed by the proximal tubule cells. A very small amount of protein (known as Tamm-Horsfall protein) is actually secreted by the tubular cells and is normally found in the urine.
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19
Q

Dipstick: protein results

A
  • Trace or 1+ corresponds to about 300-500 mg/24hrs
  • 2+ more protein in urine
  • 3+ even more protein in urine
  • 4+ even more protein in the urine…
    • The dipstick provides a rough estimate of degree of proteinuria; pts with persistent postitive urine dipsticks should do 24 hour urine collection to more precisely quantify degree of protein loss….
  • Trace to 1+ proteinuria can be defined as transient / functional (e.g. due to fever,, exercise-induced, UTI) or persistent (present on at least two out of three specimens and not in the setting of a known cause of transient proteinuria) increased.
  • The results are graded as negative (less than 10 mg per dL), trace (10 to 20 mg per dL), 1+ (30 mg per dL), 2+ (100 mg per dL), 3+ (300 mg per dL) or 4+ (1,000 mg per dL). This method preferentially detects albumin and is less sensitive to globulins or parts of globulins (heavy or light chains or Bence Jones proteins).
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20
Q

Immunoglobulins and Bence-Jones proteins

A
  • One fairly important limitation to the standard dipstick for protein is its relative selectivity for albumin
  • Dipsticks detect globulins and Bence-Jones* protein poorly
  • If suspected, this type of protein may be picked up by testing the urine with a sulfosalicylic acid protein precipitation test**
  • *Immunoglobulins and Bence-Jones proteins (monoclonal immunoglobulin light chains ) are spilled in the urine in some disease states – the most important and common being Multiple Myeloma (a hematologic malignancy of immunoglobulin-producing cells, i.e. plasma cells)
  • Detection of non-albumin proteinuria — The dipstick is insensitive to non-albumin proteins, most notably nephrotoxic immunoglobulin light chains in the setting of multiple myeloma. A screen for the presence of such proteins may be performed with the sulfosalicylic acid test.
  • Sulfosalicylic acid (SSA) detects all proteins in urine and may be useful in patients with acute kidney injury (AKI) of unclear etiology and a urine dipstick that is negative for protein. A positive SSA test in conjunction with a negative dipstick usually indicates the presence of non-albumin proteins in the urine, most often immunoglobulin light chains.
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21
Q

albumin dipstick

A
  • Persistent albumin excretion of 30-300 mg/day is termed moderately increased albuminuria (formerly termed “microalbuminuria”)
  • Persistent albumin excretion > 300 mg/day (the level at which a standard dipstick generally becomes positive) is termed severely increased albuminuria (formerly termed “macroproteinuria”)
  • Recall that Increased urinary protein excretion may be the earliest manifestation CKD….However, when assessing protein excretion, the urine dipstick is a relatively insensitive marker for initial increases in protein excretion, not becoming positive until protein excretion exceeds 300 to 500 mg/day …so, you need to order the spot urine albumin to creatinine ratio
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22
Q

Nephrotic Syndrome

A
  • Proteinuria > 3.5 gm/24 hours known as “Nephrotic range” proteinuria and represents a profound disorder of glomerular selective filtration
  • In addition to nephrotic range Proteinuria, the syndrome consists of hypoAlbuminemia, hyperLipidemia, and generalized Edema (PALE mnemonic)
  • Common causes of nephrotic syndrome:
    • minimal change disease
    • diabetic nephropathy
    • focal segmental glomerulosclerosis
  • On a dipstick 4+ protein usually represents nephrotic range proteinuria
  • Nephrotic syndrome is more common in children, where the MC cause is “Minimal change disease” also known as lipoid nephrosis
  • Also see increased risk of thrombosis and increased risk of infections in nephrotic syndrome….
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23
Q

Dipstick: Glucose

A
  • Less than 0.1% of glucose normally filtered by the glomerulus appears in urine (< 130 mg/24 hr) because it is almost completely reabsorbed by the proximal tubule
  • The serum glucose level generally is 180- 200 before the glucose “spills over” into the urine (filtered load of glucose exceeds the ability of the tubules to reabsorb it)
  • Glycosuria (excess sugar in urine) is abnormal and generally indicates diabetes mellitus
  • Glycosuria leads to excessive water loss into the urine, a process termed “osmotic diuresis” – causes the excessive urination with resultant dehydration and the excessive thirst seen in symptomatic diabetes…
24
Q

Dipstick: Ketones

A
  • Ketones (acetone, aceotacetic acid, beta-hydroxybutyric acid) are products of body fat metabolism and normally appear in the urine in very small amounts; the dipstick detects acetoacetic acid
  • Ketonuria is most associated with uncontrolled DM (“diabetic ketoacidosis”) or less commonly from some other form of calorie deprivation / starvation
25
Q

Ketonuria

A
  • is the presence of ketones in in the urine. This condition indicates that abnormal metabolic processes are occurring. Ketonuria can be caused by starvation, diets very low in carbohydrates or disease conditions that reduce the bodies ability to utilize carbohydrates for energy – e.g. lack of insulin. Coupled with glycosuria it indicates diabetes mellitus.
26
Q

Dipstick: Nitrates

A
  • Some bacteria are able to convert the nitrate in urine to nitrite
  • A positive nitrite test indicates that bacteria are present in significant numbers in urine – big clue to the presence of a UTI
  • Gram negative rods such as E. coli are most likely to give a positive test
27
Q

Dipstick: Leukocyte Esterase

A
  • Leukocyte esterase is an enzyme found in WBCs
  • Leukocyte esterase positivity is a sign of pyuria (excessive WBCs in the urine) and generally represents UTI

**Positive nitrite and positive leuk. esterase is practically always indicates bacterial urine infection…

28
Q

Dipstick: Bilirubin

A
  • The presence of bilirubin in the urine reflects direct / conjugated hyperbilirubinemia and therefore underlying liver disease
  • Pt will generally be yellow (jaundiced), so that will be a bigger clue than their darker urine….
  • Conjugated bilirubin only appears in urine in the presence of liver disease or obstruction of the bile ducts.
  • Unconjugated (aka indirect) bilirubin is water-insoluble and therefore not present in the urine.
  • The bilirubin pad on the multi-reagent dipstick detects bilirubin using a diazo reagent. This is a very nonspecific test and will produce many false positive results. Further testing will be required.
  • The color change indicating a positive reaction may be a subtle transition among shades of beige and is sometimes obscured by the colour of the urine itself (eg, in marked haemoglobinuria).
29
Q

Normal Dipstick

A
30
Q

Urinalysis: Microscopy Methodology

A
  • Centrifuge 12-15 ml of the urine sample at 3,000 rpm for 5 minutes
  • Decant all but a few drops containing the sediment
  • Use pipette to transfer a single drop of the sediment onto a glass slide, apply cover slip
  • View under low then high power magnification for…
    • Cells
    • Casts
    • Crystals
    • Bacteria
  • Can get a lot of information from the dipstick…if the dipstick has any abnormalities, move on to the microscopic exam.
  • The entire specimen is initially scanned at low-power (100x) with particular attention to the edges of the coverslip where casts tend to migrate. High-power (400x) should then be used to better characterize structures that were identified at lower power.
31
Q

UA microscopy: What are you looking for?

A
  • Cells – RBCs, WBCs, renal tubule cells, transitional epithelial cells, squamous epithelial cells
  • Casts – Tubular-shaped collections of cells admixed with Tamm-Horsefall mucoprotein; the predominate cellular element determines the type of cast
  • Crystals- some types present normally, others pathologic
32
Q

UA microscopy: 1st evaluate..

A
  • ..sediment under low power to to look for casts
  • The numbers of casts seen are usually reported as number of each type found per low power field (LPF). (Since the number of elements found in each field may vary considerably from one field to another, several fields are averaged.)
    • Example: 5-10 RBC casts/LPF
33
Q

UA microscopy: 2nd evaluate…

A
  • examine the urine at high power to look for RBCs, WBCs, crystals, and bacteria. RBCs and WBCs are described as the number of each type found per average high power field (HPF).
  • Examples: 3-5 WBC/HPF
  • TNTC = Too Numerous to Count
34
Q

RBC in UA microscopy

A
  • Theoretically, no RBCs should be found in urine, but a few generally present even in healthy individuals
  • Abnormal numbers of RBCs in urine is called hematuria - hematuria is commonly defined as the presence of 3 or more RBCs per high power field in a spun urine sediment on two out of three samples
  • A few extra RBCs in urine cannot be seen to the naked eye; urine that is visibly discolored by blood is termed “gross hematuria”
35
Q

Increased RBCs in urine may be seen such things as …

A
  • UTIs (bladder or kidney infections), malignant tumors anywhere in the urinary tract (bladder or kidney), kidney stones, renal infarcts, glomerular damage / disease, acute tubular necrosis, and sometimes physical stress or trauma, i.e. post-marathon running or falling off a bike a bruising a kidney
  • Recall that positive blood on dipstick does not necessarily represent RBCs, may represent free hemoglobinuria or myoglobinuria. Positive dipstick for blood must be followed by micro exam to visualize RBCs. (Only 3-5 RBCs / hpf necessary to turn dipstick positive for heme.)
36
Q

Determine if the RBCs look normal

A
  • The presence of dysmorphic RBC’s in urine suggests a glomerular damage such as a glomerulonephritis.
  • Dysmorphic RBC’s have odd shapes as a consequence of being distorted via passage through the damaged glomerular structure.
  • Nondysmorphic RBCs suggests a non-glomerular source – such as bleeding into the ureters or bladder
  • Passage of clots almost always indicates a lower urinary tract source of bleeding
  • Also called glomerular disease, glomerulonephritis can be acute — a sudden attack of glomerular inflammation— or chronic — coming on gradually.
  • If glomerulonephritis occurs on its own, it’s known as a primary glomerulonephritis. If another disease, such as lupus or polyarteritis nodosa or Hep C, is the cause, it’s called secondary glomerulonephritis,)
37
Q

Glomerular vs Non-glomerular

A
38
Q

WBC in UA microscopy

A
  • Pyuria defined as 5 or more WBCs per HPF
  • Abnormal numbers of leukocytes are most associated with infection in either the upper or lower urinary tract, but may also be seen with acute glomerulonephritis, interstitial nephritis or nephrolithiasis
  • The WBCs are neutrophils in infections
  • In interstitial nephritis, there are more eosinophils than expected…
39
Q

Renal Tubular cells in UA microscopy

A
  • Renal tubular epithelial cells, usually larger than granulocytes, contain a large round or oval nucleus and normally slough into the urine in small numbers.
  • However, with nephrotic syndrome and in conditions leading to tubular degeneration such as acute tubular necrosis, the number sloughed is increased
  • Renal tubular cells are larger and have a single rather than multi-lobulated nucleus
40
Q

Renal Tubular cells filled with fat in UA microscopy

A
  • When lipiduria occurs, renal tubular cells fill up with fat. When filled with numerous fat droplets, such cells are called oval fat bodies.
  • Oval fat bodies are indicative of nephrotic syndrome
  • Recall that with nephrotic syndrome (PALE mnemonic) there is hyperlipidemia…some of these excess lipids show up in the renal tubular cells and show up in the urine….
  • The origin of urinary lipid is not well understood. The initial step is the filtration of lipoprotein-bound cholesterol, particularly HDL-cholesterol. Filtration of lipoproteins is minimal in normal individuals but is markedly enhanced when glomerular permeability to macromolecules is increased in the nephrotic syndrome. Some of the filtered lipoprotein is taken up by the proximal tubular cells. The cholesterol will be seen in the urine sediment as an oval fat body when the cell is desquamated and/or as free droplets or in fatty casts if the lipid is extruded from the cells.
  • Sometimes may also see free fat droplets in the urine…they can be distinquished by their “maltese cross” appearance on polarized microscopy
41
Q

transitional epithelial cells in UA microscopy

A
  • Transitional epithelial (“urothelial”) cells line the renal pelvis, ureter, and bladder and have more regular cell borders, larger nuclei, and smaller overall size than squamous epithelium.
  • Renal tubular epithelial cells are smaller and rounder than transitional epithelium, and their nucleus occupies more of the total cell volume.
  • Transitional cells = uroepithelial cells
42
Q

squamous epithelial cell in UA microscopy

A
  • Squamous epithelial cells from the skin surface or from the outer urethra can appear in urine
  • Their significance is that they represent possible contamination of the specimen with skin flora – i.e. may not have been
43
Q

Casts in UA microscopy

A
  • Formed by precipitation of Tamm Horsefall proteins and agglutination of cells (i.e. RBCs,WBCs) “trapped” within the renal tubules
  • Cylindrical shape reflects the tubule in which they were formed and which is retained when the casts are pushed downstream
  • Urinary casts are formed only in the distal convoluted tubule (DCT) or the collecting duct (distal nephron).
  • Only urine element that is truly unique to the kidney!
  • Urine casts are cylindrical, cigar-shaped bodies that represent molds or “casts” of the lumen of the renal tubule in which they were formed.
44
Q

Hyaline Casts

A
  • Hyaline casts are composed primarily of a mucoprotein (Tamm-Horsfall protein) normally secreted by tubule cells
  • Hyaline casts are seen even in healthy pts and do not represent renal disease (green below represents the T-H protein)
  • Hyaline casts, which appear very pale and slightly refractile, are common findings in urine.
  • Consists largely of mucoprotein (Tamm-Horsfall protein) from renal epithelium
  • Do not have cellular elements
45
Q

RBC Casts in UA microscopy

A
  • Red blood cells may stick together and form red blood cell casts. Such casts are indicative of glomerulonephritis, with leakage of RBC’s from glomeruli
  • The presence of red blood cell casts in urine microscopic exam strongly suggests glomerular injury- like from SLE
46
Q

WBC cast in UA microscopy

A
  • White blood cell casts are most typical for acute pyelonephritis, but they may also be present with interstitial nephritis
  • Would you see wbc casts in a bladder infection?
    • No
  • The presence of casts indicates some infection “higher up” in the urinary tract than the bladder as casts are exclusively formed in the kidney tubules
47
Q

Granular Casts in UA microscopy

A
  • When cellular casts remain in the nephron for some time before they are flushed into the bladder urine, the cells may degenerate to become a coarsely granular cast, later a finely granular cast, and ultimately, a waxy cast. Granular and waxy casts are be believed to derive from renal tubular cell casts and are associated with advanced renal disease
  • Casts which persist may break down, so that the cells forming it are degenerated into granular debris, as has occurred in this granular cast
  • Considered a phase of breakdown of cellular casts – unclear primary cell type, but most likely renal tubular cells…
48
Q

Waxy cast in UA microscopy

A
  • Yellow, brittle, irregularly shaped, corkscrew appearance
  • Final stage of degeneration
  • Chronic renal disease
49
Q

Crystals in UA microscopy

A
  • Crystals do not necessarily indicate dz
  • Common crystals seen even in healthy patients include calcium oxalate (envelope shaped) and uric acid (rhomboid shaped)
  • Excessive uric acid crystals can be seen in acute uric acid nephropathy (“tumor lysis syndrome” ) and uric acid stone dz ; excessive calcium oxalate crystals can be seen in calcium oxalate stone dz
  • Crystals form as the urine cools to room temperature and the concentrated solutes precipitate out of the urine. The urine pH influences which crystals are formed. Most crystals are not clinically significant; and if the urines are not analyzed immediately, crystals will be present. Many laboratories do not report the presence of the normal crystals unless they are present in very large quantities
50
Q

Calcium oxalate crystals in UA microscopy

A
  • are common and do not necessarily indicate pathology
51
Q

Magnesium ammonium phosphate crystals in UA microscopy

A
  • (aka “triple phosphate” or “struvite”) crystals are the constituents of struvite stones (“staghorn” calculi) that may occur after repeated infections with urease producing organisms such as Proteus, Klebsiella, or Pseudomonas
  • Struvite stones are rectangular or “coffin-lid” shaped
  • Elevated pH decreases the solubility of phosphate
  • Both increased ammonia production and increased urine pH occur only in the setting of a urinary tract infection with a urease-producing organism, such as Proteus or Klebsiella.
52
Q

Cystine crystals in UA microscopy

A
  • Cystine crystals, with their characteristic hexagonal shape, are always abnormal
  • Presence diagnostic of cystinuria - a genetic cause of kidney stones with an average prevalence of 1 in 7000 births.
  • Cystine stones are found in 1 to 2 % of stone formers, although they represent a higher percentage of kidney stones in children (about 5 %)
53
Q

Urine Culture and Sensitivities (C + S)

A
  • Among patients with symptoms suggestive of a UTI (i.e. dysuria and frequency), dx should be confirmed by sending a clean-catch specimen for urine culture
  • One suggested exception recommended by most experts is a symptomatic young who has apparently uncomplicated cystitis* The hx is generally sufficient to prescribe an empiric course (usually three days) of antimicrobial therapy; i.e. tx can be initiated without performing a urine culture
  • uncomplicated meaning cystitis in a non-pregnant young female that is not accompanied by s/s of pyelonephritis such as significant fever, N/V, flank pain. Also, should get urine cx if the pt has recently been on antibiotics (roughly past three months) as there may be a resistant or less common organism….
54
Q

Urine Culture and Sensitivities (C + S) positive result

A
  • The standard definition of a positive urine culture is ≥105 CFU/mL
  • It has been suggested that a CFU count ≥102/mL be considered positive on a midstream urine specimen in women with acute symptoms and pyuria.
55
Q

Sterile Pyria

A
  • What if your microscopic urine exam shows too many WBCs (remember pyuria = 5 or more WBCs/HPF) but the urine culture is negative?
    • Consider the following possibilities:
      • Contamination of urine by vaginal leukocytes
      • Pt self-medicated with antibiotics taken prior to evaluation
      • Atypical organisms, such as Chlamydia, Ureaplasma urealyticum, or tuberculosis
      • Nephrolithiasis
      • The presence of pyuria with a negative culture…