Assessment CM Flashcards

1
Q

What is the LAST STEP in the handwashing procedure?

Dry hands with a paper towel.
Turn off faucet with a clean paper towel to prevent recontamination.
Rub to form lather, create friction, and loosen debris.
Rinse hands in a downward position.

A

Turn off faucet with a clean paper towel to prevent recontamination.

CORRECT HANDWASHING TECHNIQUE
1. Wet hands with warm water.
2. Apply antimicrobial soap.
3. Rub to form lather, create friction, and loosen debris.
4. Thoroughly clean between fingers, including thumbs, under fingernails and rings, and up
to the wrist, for at least 15 SECONDS. (6th 20 seconds)
5. Rinse hands in a DOWNWARD POSITION.
6. Dry with a paper towel.
7. Turn off faucets with a clean paper towel to prevent recontamination.

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2
Q

The required amount of urine for drug testing (COC):

5 to 10 mL
10 to 15 mL
20 to 30 mL
30 to 45 mL

A

30 to 45 mL

Urine specimen collections may be “witnessed” or “unwitnessed.” The decision to obtain a witnessed collection is indicated when it is suspected that the donor may alter or
substitute the specimen or it is the policy of the client ordering the test. If a witnessed specimen collection is ordered, a same-gender collector will observe the collection of 30
to 45 mL of urine. Witnessed and unwitnessed collections should be immediately handed to the collector.

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3
Q

Acceptable urine temperature for drug testing (COC):

20 to 24C
30 to 35C
32.5 to 37.7C
37.7 to 42C

A

32.5 to 37.7C

The urine temperature must be taken within 4 minutes from the time of collection to confirm the specimen has not been adulterated. The temperature should read within the
range of 32.5°C to 37.7°C. If the specimen temperature is not within range, the temperature should be recorded and the supervisor or employer contacted immediately.
Urine temperatures outside of the recommended range may indicate specimen contamination. Recollection of a second specimen as soon as possible will be necessary.

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4
Q

Primary inorganic component of urine:

Urea
Creatinine
Chloride
Potassium

A

Chloride

UREA: primary ORGANIC component; product of protein and amino acid
metabolism
CHLORIDE: primary INORGANIC component; found in combination with sodium (table salt)
and many other inorganic substances

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5
Q

Polyuria, an increase in daily urine volume:

Greater than 400 mL/day in adults
Greater than 1200 mL/day in adults
Greater than 2L/day in adults
Greater than 2.5 L/day in adults

A

Greater than 2.5 L/day in adults

Normal daily urine output is usually 1200 to 1500 mL, a range of 600 to 2000 mL is considered normal.
Polyuria, an increase in daily urine volume (greater than 2.5 L/day in adults and 2.5 to 3 mL/kg/day in children), is often associated with diabetes mellitus and diabetes insipidus;
however, it may be artificially induced by diuretics, caffeine, or alcohol, all of which suppress the secretion of antidiuretic hormone.
Oliguria, a decrease in urine output (which is less than 1 mL/kg/hr in infants, less than 0.5 mL/kg/hr in children, and less than 400 mL/day in adults), is commonly seen when the
body enters a state of dehydration as a result of excessive water loss from vomiting, diarrhea, perspiration, or severe burns.

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6
Q

The most routinely used method of urine preservation is:

Boric acid
Formalin
Refrigeration
Sodium fluoride

A

Refrigeration

The most routinely used method of preservation is refrigeration at 2°C to 8°C, which decreases bacterial growth and metabolism.
If the urine is to be cultured, it should be refrigerated during transit and kept refrigerated until cultured up to 24 hours.2 The specimen must return to room temperature before
chemical testing by reagent strips.

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7
Q

A 24-hour urine for CATECHOLAMINE determination may be preserved
with:

Formalin
Boric acid
Hydrochloric acid, 6N
Sodium fluoride

A

Hydrochloric acid, 6N

FROM HENRY: 24-HOUR URINE COLLECTION PRESERVATIVES
None (refrigerate): amino acids, amylase, calcium, citrate, chloride, copper, creatinine, delta ALA, glucose, 5-HIAA, heavy metals (arsenic, lead, mercury), histamine, immunoelectrophoresis, lysozyme, magnesium, methylmalonic acid, microalbumin, mucopolysaccharides, phosphorus, porphobilinogen, porphyrins, potassium, protein,
protein electrophoresis, sodium, urea, uric acid, xylose tolerance

10 g boric acid: aldosterone, cortisol
10 mL 6N HCl: catecholamines, cystine, homovanillic acid, hydroxyproline, metanephrines, oxalate, VMA

If processing delayed longer than 24 hours: equal amounts of 50% alcohol, Saccomanno’s fixative, and SurePath or Preserve CT Cytologic examination

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8
Q

In the three-glass collection technique for diagnosis of prostatic infection,
which tube is used as a control for bladder and kidney infection?

First specimen
Second specimen
Third specimen
None of these

A

Second specimen

THREE-GLASS COLLECTION
In prostatic infection, the third specimen will have a white blood cell/ high-power field count and a bacterial count 10 times that of the first specimen. Macrophages containing lipids may also be present.
The second specimen is used as a control for bladder and kidney infection. If it is positive, the results from the third specimen are invalid because infected urine has contaminated
the specimen.

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9
Q

The human kidneys receive approximately ___ % of the blood pumped through the heart at all times.

Approximately 5%
Approximately 15%
Approximately 25%
Approximately 50%

A

Approximately 25%

The renal artery supplies blood to the kidney.
The human kidneys receive approximately 25% of the blood pumped through the heart at
all times.

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10
Q

The part of the nephron that functions as a SIEVE:

Glomerulus
Loop of Henle
Proximal convoluted tubules
Distal convoluted tubules

A

Glomerulus

The glomerulus functions as a sieve or filter.
The glomerulus serves as a nonselective filter of plasma substances with molecular weights less than 70,000, several factors influence the actual filtration process.
These include the cellular structure of the capillary walls and Bowman’s capsule, hydrostatic pressure and oncotic pressure, and the feedback mechanisms of the reninangiotensin-aldosterone system (RAAS).

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11
Q

It corrects renal blood flow in the following ways: causing VASODILATION OF THE AFFERENT ARTERIOLES and CONSTRICTION OF THE EFFERENT ARTERIOLES, stimulating reabsorption of sodium and water in the proximal convoluted tubules, and triggering the release of the sodium-retaining hormone aldosterone by the adrenal cortex and antidiuretic hormone by the hypothalamus:

Renin
Angiotensin I
Angiotensin II
Aldosterone

A

Angiotensin II

Angiotensin II corrects renal blood flow in the following ways: causing vasodilation of the afferent arterioles and constriction of the efferent arterioles, stimulating reabsorption of
sodium and water in the proximal convoluted tubules, and triggering the release of the sodium-retaining hormone aldosterone by the adrenal cortex and antidiuretic hormone by the hypothalamus.

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12
Q

The original reference method for clearance tests:

Creatinine clearance
Inulin clearance
Urea clearance
Beta2- microglobulin

A

Inulin clearance

Although inulin was the original reference method for clearance tests, current methods are available that are endogenous and can provide accurate GFR results.
The earliest glomerular filtration tests measured urea because of its presence in all urine specimens and the existence of routinely used methods of chemical analysis.

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13
Q

Calculate the creatinine clearance using these date obtained from a person with 1.73 m2 body surface area: serum creatinine: 1.8 mg/dL;
urine creatinine: 54 mg/dL; and urine volume 640 mL in 24 hours.

3 mL/min
13 mL/min
21 mL/min
68 mL/min

A

13 mL/min

Urine volume (mL/min)
640 mL/24 hours x 1 hour/60 minutes = 0.44 mL/min.
Creatinine clearance (mL/min)
Formula: UV/P (patient is of the average body surface area)
[(54 mg/dL) x (0.44 mL/min)]/1.8 mg/dL = 13.2 mL/min

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14
Q

Calculate the creatinine clearance using these data: Serum creatinine: 1.8 mg/dL; urine volume: 640 mL in 24 hours; urine creatinine: 54 mg/dL; and body surface area: 1.25 m2.

1.1 mL/min
5 mL/min
13 mL/min
18 mL/min

A

18 mL/min

Urine volume (mL/min)
640 mL/24 hours x 1 hour/60 minutes = 0.44 mL/min

Creatinine clearance (mL/min)
Formula: (UV/P) x (1.73 m2/A)
[(54 mg/dL) (0.44 mL/min) / 1.8 mg/dL] x 1.73 m2/1.25 m2 = 18.3 mL/min

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15
Q

The test most commonly associated with tubular secretion and renal blood flow

Creatinine clearance
Fishberg test
Mosenthal test
p-aminohippuric acid (PAH) test

A

p-aminohippuric acid (PAH) test

The test most commonly associated with tubular secretion
and renal blood flow is the p-aminohippuric acid (PAH) test

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16
Q

Patients with DIABETES INSIPIDUS tend to produce urine in _____ volume with _____ specific gravity.

Increased; decreased
Increased; increased
Decreased; decreased
Decreased; increased

A

Increased; decreased

DIABETES INSIPIDUS: high urine volume, low specific gravity
DIABETES MELLITUS: high urine volume, high specific gravity

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17
Q

A catheterized urine specimen is collected:

After stimulating urine production with intravenous histamine
By aspirating it with a sterile syringe inserted into the bladder
Following midstream, clean-catch urine collection procedures
From a sterile tube passed through the urethra into the bladder

A

From a sterile tube passed through the urethra into the bladder

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18
Q

All of the following should be discarded in biohazardous waste containers EXCEPT:

Urine specimen containers, urine
Towels used for decontamination
Disposable lab coats
Blood collection tubes

A

Urine specimen containers, urine

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19
Q

The correct method for labeling urine specimen containers is to:

Attach the label to the lid
Attach the label to the bottom
Attach the label to the container
Use only a wax pencil for labeling

A

Attach the label to the container

Labels must be ATTACHED TO THE CONTAINER, NOT TO THE LID, and should not become detached if the container is refrigerated or frozen.

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20
Q

Storage of urine specimens for BILIRUBIN and UROBILINOGEN testing:

Clear container
Amber container
Preserved with formalin
None of these

A

Amber container

Because of the instability of bilirubin and urobilinogen in urine when exposed to room temperature and light, testing should be performed as soon as possible. Specimens should be stored in darkness or collected in amber tubes or amber 24-hour containers.

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21
Q

First-morning urine, EXCEPT:

Routine screening
Pregnancy testing
Urobilinogen determination
Evaluation of orthostatic proteinuria

A

Urobilinogen determination

AFTERNOON SPECIMEN (2 PM to 4 PM)
UROBILINOGEN DETERMINATION
GREATEST UROBILINOGEN EXCRETION

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22
Q

Phenol derivatives found in certain intravenous medications produce ______ urine on oxidation.

Yellow
Orange
Green
Purple

A

Green

STRASINGER PAGE 62: Green
STRASINGER PAGE 62: Brown/black

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23
Q

The clarity of a urine sample should be determined:

Using glass tubes only, never plastic
Following thorough mixing of the specimen
After addition of salicylic acid
After the specimen cools to room temperature

A

Following thorough mixing of the specimen

n routine urinalysis, clarity is determined in the same manner that ancient physicians used: by visually examining the MIXED SPECIMEN while holding it IN FRONT OF A LIGHT
SOURCE. The specimen should, of course, be in a clear container.

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24
Q

Many particulates, print blurred through urine:

Hazy
Cloudy
Turbid
Milky

A

Cloudy

URINE CLARITY
Clear: no visible particulates, transparent
Hazy: few particulates, print easily seen through urine
Cloudy: many particulates, print blurred through urine
Turbid: print cannot be seen through urine
Milky: may precipitate or be clotted

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25
Q

Sensitivity of the urine specific gravity reagent pad:

1.010 to 1.035
1.015 to 1.035
1.000 to 1.002
1.000 to 1.030

A

1.000 to 1.030

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26
Q

A routine urinalysis on a urine specimen collected from a hospitalized patient revealed a specific gravity greater than 1.050 with the use of
REFRACTOMETRY. The best explanation for this specific gravity result is that the urine:

Old and has deteriorated
Contains radiographic contrast media
Concentrated because the patient is ill and dehydrated
Contains abnormally high levels of sodium and other electrolytes because the
patient is taking diuretics

A

Contains radiographic contrast media

Abnormally high results—above 1.040—are seen in patients who have recently undergone an intravenous pyelogram. This is caused by the excretion of the injected radiographic
contrast media.
The reagent strip specific gravity measures only ionic solutes, thereby eliminating the interference by the large organic molecules, such as urea and glucose, and by radiographic contrast media and plasma expanders that are included in physical measurements of
specific gravity.

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27
Q

Cabbage urine odor:

Isovaleric acidemia
Methionine malabsorption
Phenylketonuria
Urinary tract infection

A

Methionine malabsorption

Aromatic: normal
Foul, ammonia-like: bacterial decomposition, urinary tract infection
Fruity, sweet: ketones (diabetes mellitus, starvation, vomiting)
Maple syrup: maple syrup urine disease
Mousy: phenylketonuria
Rancid: tyrosinemia
Sweaty feet: isovaleric acidemia
Cabbage: methionine malabsorption
Bleach: contamination

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28
Q

A lack of any urine odor may indicate:

Acute tubular necrosis
Isovaleric acidemia
Methionine malabsorption
Phenylketonuria

A

Acute tubular necrosis

Lack of odor in urine from patients with acute renal failure suggests acute tubular necrosis rather than prerenal failure.

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29
Q

All of the following are important to protect the integrity of reagent strips EXCEPT:

Removing the desiccant from the bottle
Storing in an opaque bottle
Storing at room temperature
Resealing the bottle after removing a strip

A

Removing the desiccant from the bottle

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30
Q

Which of the following tests is affected LEAST by standing or improperly stored urine?

Glucose
Protein
pH
Bilirubin

A

Protein

CHANGES IN UNPRESERVED URINE
1. Color - modified or darkened
2. Clarity - decreased
3. Odor - increased
4. pH - increased
5. Glucose - decreased
6. Ketones - decreased
7. Bilirubin - decreased
8. Urobilinogen - decreased
9. Nitrite - increased
10. RBCs, WBCs - decreased
11. Bacteria - increased

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31
Q

A sensitive, although not specific indicator of damage to the kidneys:

Urea
Creatinine
Proteinuria
Ketonuria

A

Proteinuria

Demonstration of proteinuria in a routine analysis does not always signify renal disease; however, its presence does require additional testing to determine whether the protein
represents a normal or a pathologic condition.

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32
Q

An indicator of PREECLAMPSIA:

Cylindruria
Hematuria
Ketonuria
Proteinuria

A

Proteinuria

Preeclampsia is a pregnancy condition characterized by hypertension, proteinuria, and often edema, usually occurring late in the second trimester or early in the third trimester,
and affecting 5 to 10% of pregnancies. It is a major cause of maternal and perinatal mortality.
If the mother develops convulsions, the condition is called eclampsia.
The only cure for preeclampsia is delivery of the placenta.

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33
Q

Concentration of SSA in the cold precipitation method:

1% sulfosalicylic acid
3% sulfosalicylic acid
5% sulfosalicylic acid
10% sulfosalicylic acid

A

3% sulfosalicylic acid

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34
Q

REPORTING OF SSA TURBIDITY: Turbidity, granulation, no flocculation:

Trace
1+
2+
3+
4+

A

2+

SULFOSALICYLIC ACID (3% SSA) PRECIPITATION TEST
Negative No increase in turbidity <6 mg/dL
Trace Noticeable turbidity 6-30 mg/dL
1+ Distinct turbidity with no granulation 30-100 mg/dL
2+ Turbidity with granulation, no flocculation 100-200 mg/dL
3+ Turbidity with granulation and flocculation 200-400 mg/dL
4+ Clumps of protein >400 mg/dL

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35
Q

Significant albumin excretion rate (AER):

0.02 to 1 ug/min
1 to 2 ug/min
5 to 15 ug/min
2 to 20 ug/min
20 to 200 ug/min

A

20 to 200 ug/min

Microalbumin was considered significant when 30 to 300 mg of albumin is excreted in 24 hours or the AER is 20 to 200 μg/min.

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36
Q

Sensitivity of the Multistix protein pad:

1 to 5 mg/dL albumin
5 to 10 mg/dL albumin
10 to 15 mg/dL albumin
15 to 30 mg/dL albumin

A

15 to 30 mg/dL albumin

PROTEIN REAGENT PAD
Multistix: 15 to 30 mg/dL albumin
Chemstrip: 6 mg/dL albumin

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37
Q

Bence Jones protein precipitates at temperatures between ___, and redissolves at near ___C.

Precipitates at 100-120C, and redissolves at 60C
Precipitates at 10 to 20C, and redissolves at 100C
Precipitates at 80-100C, and redissolves at 60C
Precipitates at 40 to 60C, and redissolves at 100C

A

Precipitates at 40 to 60C, and redissolves at 100C

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38
Q

The principle of “protein error of indicators” is based on:

Protein changing the pH of the specimen
Protein changing the pKa of the specimen
Protein accepting hydrogen from the indicator
Protein giving up hydrogen to the indicator

A

Protein accepting hydrogen from the indicator

Protein (primarily albumin) accepts hydrogen ions from the indicator.

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39
Q

A patient’s random urine consistently contains a trace of protein but no casts, cells, or other biochemical abnormality. The first voided morning
sample is consistently negative for protein. These findings can be explained by:

Normal diurnal variation in protein loss
Early glomerulonephritis
Orthostatic or postural albuminuria
Microalbuminuria

A

Orthostatic or postural albuminuria

ORTHOSTATIC (POSTURAL) PROTEINURIA
Patients suspected of orthostatic proteinuria are requested to empty the bladder before going to bed, collect a specimen immediately upon arising in the morning, and collect a second specimen after remaining in a vertical position for several hours.
Both specimens are tested for protein, and if orthostatic proteinuria is present, a negative reading will be seen on the first morning specimen, and a positive result will be found on
the second specimen.

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40
Q

A urine specimen is tested by a reagent strip test and the sulfosalicylic acid test to determine whether protein is present. The former yields a negative protein, whereas the latter results in a reading of 2+ protein. Which of the following statements best explains this difference?

-Urine contained excessive amount of amorphous urates or phosphates that caused the turbidity seen with SSA
-Urine pH was greater than 8, exceeding the buffering capacity of the strip, thus causing false-negative reaction
-Protein other than albumin must be present in the urine
-Reading time of the reagent strip test was exceeded, causing a false negative reaction to be detected

A

Protein other than albumin must be present in the urine

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41
Q

Most frequently performed chemical analysis on urine:

Bilirubin
Glucose
Ketone
Protein

A

Glucose

Because of its value in the detection and monitoring of diabetes mellitus, the glucose test is the most frequently performed chemical analysis on urine.

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42
Q

A patient sends the following question to an online consumer health Web site: “I am a 22-year-old female who experienced increasing headaches,
thirst, and decreasing energy. I was studying in the library when I felt lightheaded and passed out. I was taken to a hospital emergency department and they told me that my serum Acetest® was 40 mg/dL and urine glucose was 500 mg/dL. What does this mean?” How would you reply?

Your lab results pattern suggests diabetes mellitus.
You probably have been crash dieting recently.
The two results do not fit any disease pattern.
The tests need to be repeated because they could not possibly occur together.

A

Your lab results pattern suggests diabetes mellitus.

A positive urine glucose plus a positive serum ketone strongly suggest uncontrolled diabetes mellitus. There is an increased rate of fatty acid oxidation occurring in light of the
inaccessibility of the glucose, especially to skeletal muscle. If the patient had only been dieting, the glucose would be negative.

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43
Q

Glucosuria not accompanied by hyperglycemia can be seen in which of the following?

Hormonal disorders
Gestational diabetes
Diabetes mellitus
Renal disease

A

Renal disease

RENAL GLYCOSURIA
Glycosuria occurs in the absence of hyperglycemia when the reabsorption of glucose by the renal tubules is compromised.
This is frequently referred to as “renal glycosuria” and is seen in end-stage renal disease, cystinosis, and Fanconi syndrome.

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44
Q

The primary reason for performing a Clinitest is to:

Check for high ascorbic acid levels
Confirm a positive reagent strip glucose
Check for newborn galactosuria
Confirm a negative glucose reading

A

Check for newborn galactosuria

Depending on the laboratory population Clinitest is often performed on pediatric specimens from patients up to at least the age of 2 years.
Galactose in the urine of a newborn represents an “inborn error of metabolism” in which lack of the enzyme galactose-1-phosphate uridyl transferase prevents breakdown of
ingested galactose and results in failure to thrive and other complications, including death.
All states have incorporated screening for galactosemia into their required newborn screening programs because early detection followed by dietary restriction can control the
condition.

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45
Q

Negative Clinitest:

Glucose
Galactose
Lactose
Sucrose

A

Sucrose

Keep in mind that table sugar is sucrose, a nonreducing sugar, and does not react with Clinitest or glucose oxidase strips.

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46
Q

A urine sample that tests positive for ketones but negative for glucose is most likely from a patient suffering from:

Diabetes mellitus
Diabetes insipidus
Polydipsia
Starvation

A

Starvation

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47
Q

Ketonuria may be caused by all of the following except:

Bacterial infections
Diabetic acidosis
Starvation
Vomiting

A

Bacterial infections

CLINICAL SIGNIFICANCE OF KETONES
Clinical reasons for increased fat metabolism include the inability to metabolize carbohydrate, as occurs in diabetes mellitus; increased loss of carbohydrate from vomiting; and inadequate intake of carbohydrate associated with starvation and malabsorption.

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48
Q

The primary reagent in the reagent strip test for ketones is:

Glycine
Lactose
Sodium hydroxide
Sodium nitroprusside

A

Sodium nitroprusside

Reagent strip tests use the sodium nitroprusside (nitroferricyanide) reaction to measure ketones.
In this reaction, acetoacetic acid in an alkaline medium reacts with sodium nitroprusside to produce a purple color.
The test does not measure B-hydroxybutyrate and is only slightly sensitive to acetone when glycine is also present.

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49
Q

Positive result in the ketone reagent pad:

Brown
Blue
Pink
Purple

A

Purple

Acetoacetate (and acetone) + sodium nitroprusside + (glycine)
= PURPLE COLOR

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50
Q

Reagent pad positive result in the presence of hemoglobin or myoglobin:

Brown
Red
Pink-purple
Green-blue

A

Green-blue

In the presence of free hemoglobin/myoglobin, uniform color ranging from a negative yellow through green to a strongly positive green-blue appears on the pad.

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51
Q

A speckled pattern on the blood pad of the reagent strip indicates:

Hematuria
Hemoglobinuria
Myoglobinuria
All of the above

A

Hematuria

Intact red blood cells are lysed when they come in contact with the pad, and the liberated hemoglobin produces an isolated reaction that results in a speckled pattern on the pad.

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52
Q

Significant albumin excretion rate (AER):

0.02 to 1 ug/min
1 to 5 ug/min
5 to 15 ug/min
2 to 20 ug/min
20 to 200 ug/min

A

20 to 200 ug/min

Microalbumin was considered significant when 30 to 300 mg of albumin is excreted in 24 hours or the AER is 20 to 200 μg/min.

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53
Q

Bilirubin combines with 2,6-dichlorobenzene-diazonium-tetrafluoroborate in an acid medium to produce an azodye, with colors ranging from:

Green to blue
Green to brown
Pink to purple
Yellow to orange

A

Pink to purple

BILIRUBIN REAGENT PAD
2, 4-dichloroaniline diazonium salt: TAN
2,6-dichlorobenzene-diazonium-tetrafluoroborate: PINK TO VIOLET

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54
Q

Which of the following are characteristic urine findings from a patient with hemolytic jaundice?

A positive test for bilirubin and an increased amount of urobilinogen
A positive test for bilirubin and a decreased amount of urobilinogen
A negative test for bilirubin and an increased amount of urobilinogen
A negative test for bilirubin and a decreased amount of urobilinogen

A

A negative test for bilirubin and an increased amount of urobilinogen

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55
Q

Which of the following results show characteristic urine findings from a patient with an obstruction of the bile duct?

A positive test for bilirubin and an increased amount of urobilinogen
A positive test for bilirubin and a decreased amount of urobilinogen
A negative test for bilirubin and an increased amount of urobilinogen
A negative test for bilirubin and a decreased amount of urobilinogen

A

A positive test for bilirubin and a decreased amount of urobilinogen

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56
Q

False positive Ehrlich’s reaction for urobilinogen, EXCEPT:

Porphobilinogen
Formalin
Indican
Sulfonamides

A

Formalin

UROBILINOGEN REAGENT PAD (MULTISTIX)
False-positive:
Porphobilinogen
Indican
p-aminosalicylic acid
Sulfonamides
Methyldopa
Procaine
Chlorpromazine
Highly pigmented urine

False-negative:
Old specimens
Preservation in formalin

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57
Q

The positive reagent strip test for nitrite in this patient is probably caused by which of the following?

An infection from gram-negative bacteria
An infection from gram-positive bacteria
A yeast infection
An old urine specimen, unsuitable for examination

A

An infection from gram-negative bacteria

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58
Q

A positive nitrite test and a negative leukocyte esterase test is an indication of a:

Dilute random specimen
Specimen with lysed leukocytes
Vaginal yeast infection
Specimen older than 2 hours

A

Specimen older than 2 hours

False-positive results are obtained if nitrite testing is not performed on fresh samples, because multiplication of contaminant bacteria soon produces measurable amounts of nitrite. A true positive nitrite test should be accompanied by a positive leukocyte esterase test.

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59
Q

Reagent pad contains para-arsanilic acid or sulfanilamide:

pH
Protein
Leukocyte
Nitrite

A

Nitrite

Nitrite is detected by the Greiss reaction, in which 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.

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60
Q

Positive reagent pad for nitrite:

Blue
Brown
Pink
Purple

A

Pink

Nitrite is detected by the Greiss reaction, in which 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.

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61
Q

Nitrite tests should be performed on first morning specimens or specimens collected after urine has remained in the bladder for at least ___ hours.

At least 1 hour
At least 2 hours
At least 3 hours
At least 4 hours

A

At least 4 hours

Nitrite tests should be performed on first morning specimens or specimens collected after urine has remained in the bladder for at least 4 hours.

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62
Q

Chemical testing in urine that requires patients to include diet that contains green vegetables:

Bilirubin
Glucose
Ketone
Nitrite

A

Nitrite

The reliability of the test depends on the presence of adequate amounts of nitrate in the urine.
This is seldom a problem in patients on a normal diet that contains green vegetables; however, because diet usually is not controlled prior to testing, the possibility of a falsenegative result owing to lack of dietary nitrate does exist.

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63
Q

High urine specific gravity:

False positive nitrite
False negative nitrite
False positive blood
False positive glucose

A

False negative nitrite

HIGH URINE SPECIFIC GRAVITY
FALSE POSITIVE: Protein
FALSE NEGATIVE: Glucose, blood, nitrite

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64
Q

The reagent strip reaction that requires the longest reaction time is the:

Bilirubin
pH
Leukocyte esterase
Glucose

A

Leukocyte esterase

READING TIMES
30 seconds: glucose, bilirubin
40 seconds: ketone
45 seconds: specific gravity
60 seconds (1 minute): pH, protein, blood, urobilinogen and nitrite
120 seconds (2 minutes): leukocyte esterase

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65
Q

All of the following can be detected by the leukocyte esterase reaction except:

Neutrophils
Eosinophils
Lymphocytes
Basophils

A

Lymphocytes

The LE test detects the presence of esterase in the granulocytic white blood cells (neutrophils, eosinophils, and basophils) and monocytes, but not lymphocytes

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66
Q

Urine volume frequently used because multiparameter reagent strips are
easily immersed in this volume:

5 mL volume
12 mL volume
30 mL volume
45 mL volume

A

12 mL volume

A standard amount of urine, usually between 10 and 15 mL, is centrifuged in a conical tube. This provides an adequate volume from which to obtain a representative sample of the elements present in the specimen.
A 12-mL volume is frequently used because multiparameter reagent strips are easily immersed in this volume, and capped centrifuge tubes are often calibrated to this volume.

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67
Q

Centrifugation speed that produces an optimum amount of urine sediment with the least chance of damaging the elements:

5 minutes at a relative centrifugal force (RCF) of 400
5 minutes at a relative centrifugal force (RCF) of 500
5 minutes at a relative centrifugal force (RCF) of 600
5 minutes at a relative centrifugal force (RCF) of 1,000

A

5 minutes at a relative centrifugal force (RCF) of 400

The speed of the centrifuge and the length of time the specimen is centrifuged should be consistent. Centrifugation for 5 minutes at a relative centrifugal force (RCF) of 400 produces an optimum amount of sediment with the least chance of damaging the elements.

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68
Q

Initial magnification:

Objective
Ocular

A

Objective

SLIDE > OBJECTIVE > OCULAR
Objective: FIRST LENS SYSTEM, INITIAL MAGNIFICATION
Ocular: SECOND LENS SYSTEM, FURTHER MAGNIFICATION

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69
Q

Further magnification:

Objective
Ocular

A

Ocular

SLIDE > OBJECTIVE > OCULAR
Objective: FIRST LENS SYSTEM, INITIAL MAGNIFICATION
Ocular: SECOND LENS SYSTEM, FURTHER MAGNIFICATION

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70
Q

Microscope component that GATHERS AND FOCUSES THE ILLUMINATION LIGHT onto the specimen for viewing.

Aperture diaphragm
Rheostat
Condenser
Ocular

A

Condenser

CONDENSER
Focuses the light on the specimen and controls the light for uniform illumination

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71
Q

Which of the following should be used to REDUCE LIGHT INTENSITY in bright-field microscopy?

Aperture diaphragm
Rheostat
Condenser
Objective

A

Rheostat

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72
Q

Type of microscope that ENHANCES VISUALIZATION OF ELEMENTS WITH LOW REFRACTIVE INDICES, such as hyaline casts, mixed cellular casts, mucous threads, and Trichomonas.

Fluorescence microscope
Interference-contrast microscope
Phase-contrast microscope
Polarizing microscope

A

Phase-contrast microscope

Bright-field microscopy: used for routine urinalysis

Phase-contrast microscopy: enhances visualization of elements with low refractive indices, such as hyaline casts, mixed cellular casts, mucous threads and Trichomonas

Polarizing microscopy: aids in identification of cholesterol in oval fat bodies, fatty casts, and crystals

Dark-field microscopy: aids in identification of Treponema pallidum

Fluorescence microscopy: allows visualization of naturally fluorescent microorganisms or those stained by a fluorescent dye

Interference-contrast: produces a three-dimensional microscopy-image and layer-by-layer imaging of a specimen

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73
Q

A type of microscope that produces a three-dimensional microscopy image and layer-by-layer imaging of a specimen

Fluorescence microscope
Interference-contrast microscope
Phase-contrast microscope
Polarizing microscope

A

Interference-contrast microscope

Two types of interference-contrast microscope
1. Hoffman - modulation contrast
2. Nomarski - differential interference contrast
Bright-field microscopes can be adapted for both methods

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74
Q

Of all the urine sediment elements, _____ are the most difficult to recognize.

RBCs
WBCs
RTE cells
Sperms

A

RBCs

The reasons for this include RBCs’ lack of characteristic structures, variations in size, and close resemblance to other urine sediment constituents. RBCs are frequently confused
with yeast cells, oil droplets, and air bubbles.

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75
Q

Significant number of eosinophils in urine:

More than 1% eosinophils
More than 5% eosinophils
More than 10% eosinophils
More than 15% eosinophils

A

More than 1% eosinophils

The percentage of eosinophils in 100 to 500 cells is determined. Eosinophils are not normally seen in the urine; therefore, the finding of more than 1% eosinophils is considered significant.

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76
Q

FECAL CONTAMINATION of a urine specimen can also result in the presence of ova from intestinal parasites in the urine sediment. The most
common contaminant is:

Enterobius vermicularis
Schistosoma haematobium
Trichomonas vaginalis
Entamoeba histolytica

A

Enterobius vermicularis

Fecal contamination of a urine specimen can also result in the presence of ova from intestinal parasites in the urine sediment. The most common contaminant is ova from the
pinworm Enterobius vermicularis.

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77
Q

MOST FREQUENT PARASITE ENCOUNTERED IN THE URINE:

Enterobius vermicularis
Schistosoma haematobium
Trichomonas vaginalis
Entamoeba histolytica

A

Trichomonas vaginalis

The most frequent parasite encountered in the urine is Trichomonas vaginalis. The Trichomonas trophozoite is a pear-shaped flagellate with an undulating membrane. It is
easily identified in wet preparations of the urine sediment by its rapid darting movement in the microscopic field. Trichomonas is usually reported as rare, few, moderate, or many per hpf.

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78
Q

Reporting of Trichomonas vaginalis:

With WBCs
With motility

A

With motility

Because their characteristic motility provides the best means of positively identifying them, a fresh urine specimen is needed.

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79
Q

When not moving, Trichomonas is more difficult to identify and may resemble a:

WBC
Transitional epithelial cell
Renal tubular epithelial cell
All of these

A

All of these

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.

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79
Q

Reporting of spermatozoa:

Do not report
Rare, few, moderate or many per LPF
Rare, few, moderate or many per HPF
Present, based on laboratory protocol

A

Present, based on laboratory protocol

STRASINGER:
Reporting of spermatozoa:
Present, based on laboratory protocol

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80
Q

Only elements found in the urinary sediment that are unique to the kidney:

Red blood cells
Epithelial cells
Casts
Crystals

A

Casts

Casts are the only elements found in the urinary sediment that are unique to the kidney. They are formed within the lumens of the distal convoluted tubules and collecting ducts, providing a microscopic view of conditions within the nephron.

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81
Q

During microscopy casts are usually seen:

Center of coverslip
Near the edge of coverslip
Outside the coverslip
All of these

A

Near the edge of coverslip

Examination of the sediment for the detection of casts is performed using lower power magnification. When the glass cover-slip method is used, low-power scanning should be
performed along the edges of the cover slip.

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82
Q

Casts increased in CONGESTIVE HEART FAILURE:

Granular casts
Hyaline casts
WBC casts
Epithelial casts

A

Hyaline casts

The most frequently seen cast is the hyaline type, which consists almost entirely of uromodulin.
The presence of zero to two hyaline casts per lpf is considered normal, as is the finding of increased numbers following strenuous exercise, dehydration, heat exposure, and
emotional stress.
Pathologically, hyaline casts are increased in acute glomerulonephritis, pyelonephritis, chronic renal disease, and congestive heart failure.

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83
Q

Pyelonephritis can be differentiated from cystitis by the presence of
________.

Eosinophils
Hyaline casts
WBC casts
Bacteriuria

A

WBC casts

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).

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84
Q

Which of the following could be a broad cast?

Hyaline cast
Granular cast
Waxy cast
All of these

A

All of these

All types of casts may occur in the broad form. However, considering the accompanying urinary stasis, the most commonly seen broad casts are granular and waxy casts.

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85
Q

Most commonly seen broad casts:

RBC and WBC casts
WBC and epithelial casts
Hyaline and granular casts
Granular and waxy casts

A

Granular and waxy casts

All types of casts may occur in the broad form. However, considering the accompanying urinary stasis, the most commonly seen broad casts are granular and waxy casts.

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86
Q

A 62-year-old patient with hyperlipoproteinemia has a large amount of protein in his urine. Microscopic analysis yields moderate to many fatty, waxy, granular and cellular casts. Many oval fat bodies are also noted.This is most consistent with:

Nephrotic syndrome
Acute pyelonephritis
Viral infection
Acute glomerulonephritis

A

Nephrotic syndrome

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87
Q

Reporting of normal crystals:

Averaged and reported per LPF
Averaged and reported per HPF
Rare, few, moderate or many per LPF
Rare, few, moderate or many per HPF

A

Rare, few, moderate or many per HPF

Crystals are usually reported as rare, few, moderate, or many per hpf. Abnormal crystals may be averaged and reported per lpf.

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88
Q

Lemon-shaped crystals:

Ammonium biurate
Calcium phosphate
Uric acid
Triple phosphate

A

Uric acid

HENRY
Uric acid crystals occur at low pH (5–5.5) and are seen in a variety of shapes, including rhombic or four-sided flat plates, prisms, oval forms with pointed ends (lemon-shaped),
wedges, rosettes, and irregular plates.

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89
Q

Increased amounts of these crystals in fresh urine is seen in patients with leukemia who are receiving chemotherapy:

Calcium phosphate
Calcium oxalate
Triple phosphate
Uric acid

A

Uric acid

Increased amounts of uric acid crystals, particularly in fresh urine, are associated with:
1. Increased levels of purines and nucleic acids and are seen in patients with leukemia
who are receiving chemotherapy
2. Patients with Lesch-Nyhan syndrome
3. Patients with gout

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90
Q

MT notices calcium oxalate crystals in urine, but the atypical form. To confirm identity of these crystals:

Soluble with acetic acid
Soluble with dilute HCl
Soluble with acetic acid and dilute HCl
None of these

A

Soluble with dilute HCl

Weddelite (dihydrate CaOx, most common): envelope, pyramidal
Whewellite (monohydrate CaOx, less frequent): dumbbell, oval

Calcium oxalate crystals:
Soluble in dilute HCl
Insoluble in acetic acid

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91
Q

Crystals associated with ethylene glycol poisoning:

Envelope or pyramidal crystals
Oval or dumbbell crystals

A

Oval or dumbbell crystals

Ethylene glycol (antifreeze) poisoning (monohydrate forms) - dumbbell, oval
The MONOHYDRATE FORM is most frequently seen in children and pets because antifreeze tastes sweet and uncovered containers left in the garage can be very tempting.

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92
Q

Apatite crystals:

Calcium phosphate
Monohydrate calcium oxalate
Dihydrate calcium oxalate
Triple phosphate

A

Calcium phosphate

Calcium phosphate: APATITE
Monohydrate calcium oxalate: WHEWELLITE
Dihydrate calcium oxalate: WEDDELITE
Triple phosphate: STRUVITE

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93
Q

Calculi formation at pH > 7:

Uric acid, cystine, xanthine
Triple phosphate, calcium phosphate
Calcium oxalate, apatite
All of these

A

Triple phosphate, calcium phosphate

pH < 5.5: Uric acid, cystine, or xanthine calculi
pH 5 to 6: Calcium oxalate and apatite calculi
pH >7: Magnesium ammonium phosphate or calcium phosphate

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94
Q

Calculi associated with RAPID PROTEIN CATABOLISM:

Calcium oxalate
Cystine
Uric acid
None of these

A

Uric acid

URIC ACID AND URATE CALCULI
1. Gout
2. Polycythemia
3. Leukemia
4. Lymphoma
5. Liver disease
6. Acid isohydria
7. Theophylline and thiazide therapy
8. Conditions associated with rapid protein catabolism

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95
Q

Calculi associated with EXCESSIVE GLYCOGEN BREAKDOWN:

Calcium oxalate
Cystine
Uric acid
None of these

A

Calcium oxalate

CALCIUM OXALATE CALCULI
1. Oxaluria
2. Incomplete catabolism of carbohydrates
3. Isohydria at pH 5.5 to 6.0
4. Excessive glycogen breakdown

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96
Q

The most common composition of renal calculi is:

Calcium oxalate
Magnesium ammonium phosphate
Cystine
Uric acid

A

Calcium oxalate

Approximately 75% of the renal calculi are composed of calcium oxalate or calcium phosphate.
Magnesium ammonium phosphate (struvite), uric acid, and cystine are the other primary calculi constituents.

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97
Q

Urinalysis on a patient with severe back pain being evaluated for renal calculi would be most beneficial if it showed:

Heavy proteinuria
Low specific gravity
Uric acid crystals
Microscopic hematuria

A

Microscopic hematuria

Urine specimens from patients suspected of passing or being in the process of passing renal calculi are frequently received in the laboratory.
The presence of microscopic hematuria resulting from irritation to the tissues by the moving calculus is the primary urinalysis finding.

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98
Q

Positive result for the acid-albumin and CTAB test for mucopolysaccharides:

White turbidity
Yellow turbidity
Yellow spot
Blue spot

A

White turbidity

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99
Q

Positive result for the METACHROMATIC STAINING SPOT TEST for mucopolysaccahrides:

White turbidity
Yellow turbidity
Yellow spot
Blue spot

A

Blue spot

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100
Q

Key to the diagnosis is the demonstration of antineutrophilic cytoplasmic antibody (ANCA) in the patient’s serum:

Berger disease
Goodpasture’s syndrome
Henoch-Schonlein purpura
Wegener granulomatosis

A

Wegener granulomatosis

Wegener granulomatosis causes a granuloma-producing inflammation of the small blood vessels primarily of the kidney and respiratory system.
Key to the diagnosis of Wegener granulomatosis is the demonstration of antineutrophilic cytoplasmic antibody (ANCA) in the patient’s serum.

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101
Q

The presence of renal tubular epithelial cells and casts is an indication of:

Acute interstitial nephritis
Chronic glomerulopnephritis
Minimal change disease
Acute tubular necrosis

A

Acute tubular necrosis

Urinalysis findings include mild proteinuria, microscopic hematuria, and, most noticeably, the presence of RTE cells and RTE cell casts containing tubular fragments consisting of
three or more cells.

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102
Q

Increased eosinophils, WBC casts without bacteria:

Acute glomerulophritis
Acute interstitial nephritis
Acute pyelonephritis
Acute tubular necrosis

A

Acute interstitial nephritis

ACUTE INTERSTITIAL NEPHRITIS
AIN is primarily associated with an allergic reaction to medications that occurs within the renal interstitium, possibly caused by the medication binding to the interstitial protein.
Urinalysis results include hematuria, possibly macroscopic, mild to moderate proteinuria, numerous WBCs, and WBC casts without bacteria. Differential leukocyte staining for the presence of increased eosinophils may be useful to confirm the diagnosis.

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103
Q

The only protein produced by the kidney is:

Albumin
Uromodulin
Uroprotein
Globulin

A

Uromodulin

Uromodulin is a more recent name for Tamm-Horsfall protein
Uromodulin is a glycoprotein and is the only protein produced by the kidney. It is produced by the proximal and distal convoluted tubules.

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104
Q

In automated microscopy, the DNA within the cells is stained by an orange dye:

Phenathridine
Carbocyanine

A

Phenathridine

PHENATHRIDINE: ORANGE, DNA
CARBOCYANINE: GREEN
Nuclear membranes, mitochondria, and negatively charged cell membranes

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105
Q

In automated microscopy, the nuclear membranes, mitochondria and negatively charged cell membranes are stained by the green dye:

Phenathridine
Carbocyanine

A

Carbocyanine

PHENATHRIDINE: ORANGE, DNA
CARBOCYANINE: GREEN
Nuclear membranes, mitochondria, and negatively charged cell membranes

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106
Q

The concentration of hCG is generally at a particular level in serum about 2 to 3days after implantation. This is the concentration at which most sensitive laboratory assays can give a positive serum hCG result. What is
the lowest level of hormone for which most current serum hCG tests can give a positive result?

25 mIU/mL
50 mIU/mL
100 mIU/mL
100, 000 mIU/mL

A

25 mIU/mL

In a normal pregnancy, detectable amounts of about 25 mIU/mL β- hCG are secreted 2 to 3 days (48 to 72 hours) after implantation, or approximately 8 to 10 days after conception or fertilization.

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107
Q

The most specific assays for human chorionic gonadotropin (hCG) use antibody reagents against which subunit of hCG?

Alpha
Beta
Gamma
Chorionic

A

Beta

Alpha subunit of HCG - similar to LH, FSH and TSH
Beta subunit is unique for HCG

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108
Q

In the card pregnancy test: no band appears at T and a black or gray band is visible at the C position

Positive
Negative
Invalid

A

Negative

CARD PREGNANCY TEST
1. POSITIVE: Two separate black or gray bands, one at T and the other at C, are visible in the results window, indicating that the specimen contains detectable levels of hCG.
Although the intensity of the test band may vary with different specimens, the appearance of two distinct bands should be interpreted as a positive result.
2. NEGATIVE: If no band appears at T and a black or gray band is visible at the C position, the test can be considered negative, indicating that a detectable level of hCG is not present.
3. INVALID: If no band appears at C or incomplete or beaded bands appear at the T or C position, the test is invalid. The test should be repeated using another Card Pregnancy Test device.

If the test band appears very faint, it is recommended that a new sample be collected 48 hours later and tested again using another Card Pregnancy Test device

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109
Q

What department is the CSF tube labeled 3 routinely sent to?

Hematology
Chemistry
Microbiology
Serology

A

Hematology

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110
Q

Fourth CSF tube may be drawn for:

Cell counts
Chemical tests
Chemistry and cell counts
Microbiology or additional serologic tests

A

Microbiology or additional serologic tests

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111
Q

If only a small amount of CSF is obtained, which is the most important procedure to perform first?

Cell count
Chemistry
Immunology
Microbiology

A

Microbiology

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112
Q

A web-like pellicle in a refrigerated CSF specimen indicates:

Tubercular meningitis
Multiple sclerosis
Primary CNS malignancy
Viral meningitis

A

Tubercular meningitis

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113
Q

A CSF total cell count is diluted with:

Distilled water
Normal saline
Acetic acid
Hypotonic saline

A

Normal saline

Dilutions for total cell counts are made with normal saline, mixed by inversion, and loaded into the hemocytometer with a Pasteur pipette.

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114
Q

A CSF WBC count is diluted with:

Distilled water
Normal saline
Acetic acid
Hypotonic saline

A

Acetic acid

Lysis of RBCs must be obtained before performing the WBC count on either diluted or undiluted specimens. Specimens requiring dilution can be diluted in the manner described
previously, substituting 3% glacial acetic acid to lyse the RBCs.
Adding methylene blue to the diluting fluid stains the WBCs, providing better differentiation between neutrophils and mononuclear cells.

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115
Q

As little as 0.1 mL of CSF combined with one drop of ________ produces an adequate CELL YIELD when processed with the cytocentrifuge.

10% albumin
30% albumin
1% HCl
3% acetic acid

A

30% albumin

Adding albumin increases the cell yield and decreases the cellular distortion frequently seen on cytocentrifuged specimens.

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116
Q

The purpose of adding albumin to CSF before cytocentrifugation is to:

Increase the cell yield
Decrease the cellular distortion
Improve the cellular staining
Increase cell yield and decrease cellular distortion

A

Increase cell yield and decrease cellular distortion

Adding albumin increases the cell yield and decreases the cellular distortion frequently seen on cytocentrifuged specimens.

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117
Q

The presence of which of the following cells is increased in a parasitic infection?

Neutrophils
Macrophages
Eosinophils
Lymphocytes

A

Eosinophils

Increased eosinophils are seen in the CSF in association with parasitic infections, fungal infections (primarily Coccidioides immitis), and introduction of foreign material, including
medications and shunts, into the CNS.

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118
Q

Fungal infection associated with increased eosinophils in CSF:

Blastomyces dermatitidis
Coccidioides immitis
Cryptococcus neoformans
Histoplasma capsulatum

A

Coccidioides immitis

Increased eosinophils are seen in the CSF in association with parasitic infections, fungal infections (primarily Coccidioides immitis), and introduction of foreign material, including
medications and shunts, into the CNS.

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119
Q

Which of the following may resemble a LYMPHOCYTE in CSF?

Blastoyces
Coccidioides
Cryptococcus
Histoplasma

A

Cryptococcus

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120
Q

Nonpathologically significant cells are most frequently seen after DIAGNOSTIC PROCEDURES such as PNEUMOENCEPHALOGRAPHY and
in fluid obtained from VENTRICULAR TAPS or during NEUROSURGERY:

Choroidal cells
Ependymal cells
Spindle-shaped cells
All of these

A

All of these

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121
Q

Myeloblasts are seen in the CSF:

In bacterial infections
In conjunction with CNS malignancy
After cerebral hemorrhage
As a complication of acute leukemia

A

As a complication of acute leukemia

Lymphoblasts, myeloblasts, and monoblasts in the CSF are frequently seen as a serious complication of acute leukemias.
Nucleoli are often more prominent than in blood smears.

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122
Q

The most frequently performed chemical test on CSF:

Glucose determination
Lactate determination
Protein determination
India ink staining

A

Protein determination

The most frequently performed chemical test on CSF is the protein determination.

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123
Q

The reference range for CSF protein is:

6 to 8 g/dL
15 to 45 g/dL
6 to 8 mg/dL
15 to 45 mg/dL

A

15 to 45 mg/dL

Reference values for total CSF protein are usually listed as 15 to 45 mg/dL, but are somewhat method dependent, and higher values are found in infants and people over age 40.
This value is reported in milligrams per deciliter and not grams per deciliter, as are plasma protein concentrations.

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124
Q

CSF can be differentiated from serum by the presence of:

Albumin
Globulin
Prealbumin
Tau transferrin

A

Tau transferrin

Transferrin is the major beta globulin present; also, a separate carbohydrate-deficient transferrin fraction, referred to as “tau,” is seen in CSF and not in serum.

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125
Q

In serum, the second most prevalent protein is IgG; in CSF, the second most prevalent protein is:

Transferrin
Prealbumin
IgA
Ceruloplasmin

A

Prealbumin

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126
Q

Elevated CSF protein values can be caused by all of the following except:

Meningitis
Multiple sclerosis
Fluid leakage
CNS malignancy

A

Fluid leakage

Abnormally low values are present when fluid is leaking from the CNS.
The causes of elevated CSF protein include damage to the blood–brain barrier, immunoglobulin production within the CNS, decreased normal protein clearance from the
fluid, and neural tissue degeneration. Meningitis and hemorrhage conditions that damage the blood–brain barrier are the most common causes of elevated CSF protein.

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127
Q

The integrity of the blood–brain barrier is measured using the:

CSF/serum albumin index
CSF/serum globulin ratio
CSF albumin index
CSF IgG index

A

CSF/serum albumin index

CSF/SERUM ALBUMIN INDEX
An index value less than 9 represents an intact blood– brain barrier. The index increases relative to the amount of damage to the barrier.

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128
Q

The finding of oligoclonal bands in the CSF and not in the serum is seen with:

Multiple myeloma
CNS malignancy
Multiple sclerosis
Viral infections

A

Multiple sclerosis

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129
Q

Oligoclonal banding in cerebrospinal fluid but not in serum, EXCEPT:

Encephalitis
Multiple myeloma
Neurosyphilis
Guillain-Barre disease

A

Multiple myeloma

The presence of two or more oligoclonal bands in the CSF that are not present in the serum can be a valuable tool in diagnosing multiple sclerosis, particularly when accompanied by an increased IgG index.
Other neurologic disorders including encephalitis, neurosyphilis, Guillain-Barré syndrome, and neoplastic disorders also produce oligoclonal banding that may not be present in the serum.

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130
Q

Measurement of which of the following can be replaced by CSF GLUTAMINE analysis in children with Reye syndrome?

Ammonia
Lactate
Glucose
Alpha-ketoglutarate

A

Ammonia

Glutamine is produced from ammonia and alpha ketoglutarate by the brain cells. This process serves to remove the toxic metabolic waste product ammonia from the CNS.
The normal concentration of glutamine in the CSF is 8 to 18 mg/dL. Elevated levels are associated with liver disorders that result in increased blood and CSF ammonia.

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131
Q

Before performing a Gram stain on CSF, the specimen must be:

Filtered
Warmed to 37C
Centrifuged
Mixed

A

Centrifuged

All smears and cultures should be performed on concentrated specimens because often only a few organisms are present at the onset of the disease. The CSF should be centrifuged at 1500 g for 15 minutes, and slides and cultures should be prepared from the sediment.

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132
Q

The procedure recommended by the CDC to diagnose neurosyphilis:

RPR
VDRL
MHA-TP
FTA-ABS

A

VDRL

Although many different serologic tests for syphilis are available when testing blood, the procedure recommended by the CDC to diagnose neurosyphilis is the Venereal Disease
Research Laboratories (VDRL), even though it is not as sensitive as the fluorescent treponemal antibody-absorption (FTA-ABS) test for syphilis.
The rapid plasma regain (RPR) test is not recommended because it is less sensitive than the VDRL.

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133
Q

An elevated maternal serum AFP, may indicate an amniocentesis at:

15 to 18 weeks
20 to 42 weeks

A

15 to 18 weeks

INDICATIONS FOR PERFORMING AMNIOCENTESIS
INDICATED AT 15 TO 18 WEEKS’ GESTATION
 Mother’s age of 35 or older at delivery
 Family history of chromosome abnormalities, such as trisomy 21 (Down syndrome)
 Parents carry an abnormal chromosome rearrangement
 Earlier pregnancy or child with birth defect
 Parent is a carrier of a metabolic disorder
 Family history of genetic diseases such a sickle cell disease, Tay-Sachs disease,
hemophilia, muscular dystrophy, sickle cell anemia, Huntington chorea, and cystic fibrosis
 Elevated maternal serum alpha-fetoprotein
 Abnormal triple marker screening test
 Previous child with a neural tube disorder such as spina bifida, or ventral wall defects
(gastroschisis)
 Three or more miscarriages
INDICATED LATER IN THE PREGNANCY (20 TO 42 WEEKS)
 Fetal lung maturity
 Fetal distress
 HDN caused by Rh blood type incompatibility
 Infection

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134
Q

The amount of amniotic fluid increases in quantity throughout pregnancy, reaching a peak of approximately ____ mL during the third trimester, and then gradually decreases prior to delivery.

100 to 200 mL
200 to 400 mL
400 to 800 mL
800 to 1, 200 mL

A

800 to 1, 200 mL

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135
Q

A maximum of ___ mL of amniotic fluid is collected in sterile syringes.

5 mL
10 mL
20 mL
30 mL

A

30 mL

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136
Q

Presence of meconium in amniotic fluid:

Colorless
Blood-streaked
Yellow
Dark green
Dark red-brown

A

Dark green

Meconium, which is usually defined as a newborn’s first bowel movement, is formed in the intestine from fetal intestinal secretions and swallowed amniotic fluid. It is a dark green,
mucus-like material. It may be present in the amniotic fluid as a result of fetal distress.

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137
Q

Dark red-brown amniotic fluid:

Traumatic tap, abdominal trauma, intra-amniotic hemorrhage
Hemolytic disease of the newborn
Meconium
Fetal death

A

Fetal death

A very dark red-brown fluid is associated with fetal death

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138
Q

Amniotic fluid specimens are placed in amber-colored tubes prior to sending them to the laboratory to prevent the destruction of:

Alpha-fetoprotein
Bilirubin
Cytogenetics
Lecithin

A

Bilirubin

139
Q

Why are amniotic specimens for cytogenetic analysis incubated at 37°C prior to analysis?

To detect the presence of meconium
To differentiate amniotic fluid from urine
To prevent photo-oxidation of bilirubin to biliverdin
To prolong fetal cell viability and integrity

A

To prolong fetal cell viability and integrity

140
Q

How are specimens for FLM testing delivered to and stored in the laboratory?

Delivered on ice and refrigerated
Immediately centrifuged
Kept at room temperature
Delivered in a vacuum tube

A

Delivered on ice and refrigerated

141
Q

Amniotic fluid bilirubin is measured by:

Turbidimetric method
Dye-binding method
Spectrophotometric analysis
Fluorometric analysis

A

Spectrophotometric analysis

Amniotic fluid bilirubin is measured by spectrophotometric analysis using serial dilutions.
When bilirubin is present, a rise in OD is seen at 450 nm because this is the wavelength of maximum bilirubin absorption.

142
Q

A significant rise in the OD of amniotic fluid at 450 nm indicates the presence of which analyte?

Bilirubin
Lecithin
Oxyhemoglobin
Sphingomyelin

A

Bilirubin

143
Q

For OD 450, specimens that are contaminated with blood are generally unacceptable because maximum absorbance of oxyhemoglobin occurs
at ___ nm and can interfere with the bilirubin absorption peak

Oxyhemoglobin and bilirubin 410 nm
Oxyhemoglobin and bilirubin 450 nm
Oxyhemoglobin 410 nm, bilirubin 450 nm
Oxyhemoglobin 450 nm, bilirubin 410 nm

A

Oxyhemoglobin 410 nm, bilirubin 450 nm

Specimens that are contaminated with blood are generally unacceptable because maximum absorbance of oxyhemoglobin occurs at 410 nm and can interfere with the
bilirubin absorption peak.
This interference can be removed by extraction with chloroform if necessary

144
Q

A ΔA450 value that falls into Zone I indicates:

Normal finding without significant hemolysis
Moderate hemolysis
Severe hemolysis
High fetal risk

A

Normal finding without significant hemolysis

Zone I: no more than a mildly affected fetus
Zone II: moderate hemolysis and require careful monitoring anticipating an early delivery
or exchange transfusion upon delivery
Zone III: severe hemolysis and suggests a severely affected fetus; intervention through
induction of labor or intrauterine exchange transfusion must be considered

145
Q

Plotting the amniotic fluid OD on a Liley graph represents the severity of hemolytic disease of the newborn. A value that is plotted in ZONE II
indicates what condition of the fetus?

No hemolysis
Mildly affected fetus
Moderately affected fetus requiring close monitoring
Severely affected fetus that requires intervention

A

Moderately affected fetus requiring close monitoring

Zone I: no more than a mildly affected fetus
Zone II: moderate hemolysis and require careful monitoring anticipating an early delivery
or exchange transfusion upon delivery
Zone III: severe hemolysis and suggests a severely affected fetus; intervention through
induction of labor or intrauterine exchange transfusion must be considered

146
Q

In the FOAM OR SHAKE TEST, amniotic fluid is mixed with:

1% NaOH
10% NaOH
70% ethanol
95% ethanol

A

95% ethanol

Amniotic fluid is mixed with 95% ethanol, shaken for 15 seconds, and allowed to sit undisturbed for 15 minutes. At the end of this time, the surface of the fluid is observed for
the presence of a continuous line of bubbles around the outside edge.
The presence of bubbles indicates that a sufficient amount of phospholipid is available to reduce the surface tension of the fluid even in the presence of alcohol, an antifoaming agent.

147
Q

Increases the OD of the amniotic fluid at 650 nm:

AFP
Bilirubin
Lamellar bodies
Oxyhemoglobin

A

Lamellar bodies

OD 650 nm: LAMELLAR BODIES (FETAL LUNG MATURITY)
An OD of 0.150 has been shown to correlate well with an L/S ratio of greater than or equal to 2.0 and the presence of phosphatidyl glycerol.

148
Q

When severe HDN is present, which of the following tests on the amniotic
fluid would the physician NOT ORDER to determine whether the fetal
lungs are mature enough to withstand a premature delivery?

AFP levels
Foam stability index
Lecithin/sphingomyelin ratio
Phosphatidylglycerol detection

A

AFP levels

Neural tube defects (NTD) are one of the most common birth defects. It can be detected by maternal serum alpha-fetoprotein (MSAFP) blood test, high-resolution ultrasound, and amniocentesis. Increased levels of alpha-fetoprotein (AFP) in both the maternal circulation and the amniotic fluid can be indicative of fetal neural tube defects, such as anencephaly
and spina bifida.

149
Q

True for SPUTUM:

Green in color
Secreted by the tracheobronchial tree
Healthy individual normally produce sputum
All of these

A

Secreted by the tracheobronchial tree

SPUTUM is the material secreted by the tracheobronchial tree and brought up by coughing. The healthy individual does not normally produce sputum.

150
Q

Formed elements in sputum are best studied by which CYTOLOGICAL techniques?

AFB stain
Gram’s stain
Pap’s stain
Wright’s stain

A

Pap’s stain

Pap’s stain: SPUTUM CYTOLOGY
Wright’s stain: DIFFERENTIATES NEUTROPHILS FROM EOSINOPHILS

151
Q

Which of the following may resemble MYELIN GLOBULE in sputum?

Blastomyces
Coccidioides
Cryptococcus
Histoplasma

A

Blastomyces

Myelin globules: little or no significance but may be mistaken for Blastomyces (yeastlike fungi). They are colorless, round, oval or pea-shaped of various sizes.

152
Q

Dense, crystalline concretions (may be large enough to be grossly visible) may be seen in sputum in:

Bronchial asthma
Broncholithiasis
Pneumonia
Tuberculosis

A

Broncholithiasis

153
Q

Which of the following stimulate the parietal cells to produce hydrochloric acid?

Gastrin
Intrinsic factor
Pepsin
Trypsin

A

Gastrin

154
Q

Gastric tube inserted through the mouth:

Levin tube
Rehfuss tube

A

Rehfuss tube

The gastric juice is obtained by insertion of a gastric tube into the stomach
1. REHFUSS tube (introduced through the mouth)
2. LEVIN tube (inserted through the nose)
3. Disposable plastic tubes are usually employed

155
Q

Gastric tube inserted through the nose:

Levin tube
Rehfuss tube

A

Levin tube

The gastric juice is obtained by insertion of a gastric tube into the stomach
1. REHFUSS tube (introduced through the mouth)
2. LEVIN tube (inserted through the nose)
3. Disposable plastic tubes are usually employed

156
Q

Normal fasting gastric fluid appears:

Dark red-brown
Clear and pale yellow
Pale yellow with food particles
Pale gray and slightly mucoid

A

Pale gray and slightly mucoid

157
Q

What is the preferred gastric stimulant?

Histamine
Histalog
Insulin
Pentagastrin

A

Pentagastrin

Pentagastrin is the preferred stimulant because it resembles true gastrin

158
Q

Hypoglycemia is induced with which of the following to test for the completeness of VAGOTOMY?

Histamine
Histalog
Insulin
Pentagastrin

A

Insulin

159
Q

The cell most frequently seen in bronchoalveolar lavage (BAL):

Macrophages
Lymphocytes
Neutrophils
Eosinophils

A

Macrophages

160
Q

In bronchoalveolar lavage (BAL), which cell type is elevated in CIGARETTE SMOKERS, and in cases of bronchopneumonia, toxin exposure, and diffuse alveolar damage:

Macrophages
Lymphocytes
Neutrophils
Eosinophils

A

Neutrophils

161
Q

Normal lymphocyte count in bronchoalveolar lavage (BAL):

Less than 1%
Less than 3%
1 to 15%
56 to 80%

A

1 to 15%

162
Q

The entire process of spermatogenesis takes approximately ___ days

50 days
70 days
90 days
120 days

A

90 days

When spermatogenesis is complete, the immature sperm (nonmotile) enter the epididymis. In the epididymis, the sperm mature and develop flagella. The entire process takes approximately 90 days.
The sperm remain stored in the epididymis until ejaculation, at which time they are propelled through the ductus deferens (vas deferens) to the ejaculatory ducts

163
Q

Produce most of the fluid present in semen (60%to 70%):

Testes and epididymis
Seminal vesicles
Prostate gland
Bulbourethral gland

A

Seminal vesicles

Semen is composed of four fractions that are contributed by the testes, epididymis,
seminal vesicles, prostate gland, and bulbourethral glands.
The seminal vesicles produce most of the fluid present in semen (60% to 70%), and this fluid is the transport medium for the sperm.

164
Q

Produces milky acidic fluid containing high concentrations of acid phosphatase, citric acid, zinc, and proteolytic enzymes responsible for
both the coagulation and liquefaction of the semen following ejaculation:

Testes and epididymis
Seminal vesciles
Prostate gland
Bulbourethral gland

A

Prostate gland

Approximately 20% to 30% of the semen volume is acidic fluid produced by the prostate
gland. The milky acidic fluid contains high concentrations of acid phosphatase, citric acid,
zinc, and proteolytic enzymes responsible for both the coagulation and liquefaction of the
semen following ejaculation.

165
Q

Semen is collected following a period of sexual abstinence of at least___ days to not more than ___ days.

At least 1 day to not more than 3 days
At least 2 days to not more than 7 days
At least 5 days to not more than 7 days
At least 7 days to not more than 10 days

A

At least 2 days to not more than 7 days

Specimens are collected following a period of sexual abstinence of at least 2 days to not more than 7 days.
Specimens collected following prolonged abstinence tend to have higher volumes and decreased motility.

166
Q

Liquefaction of a semen specimen should take place within:

1 hour
2 hours
3 hours
4 hours

A

1 hour

A fresh semen specimen is clotted and should liquefy within 30 to 60 minutes after collection; therefore, recording the time of collection is essential for evaluating semen
liquefaction.
Failure of liquefaction to occur within 60 minutes may be caused by a deficiency in prostatic enzymes and should be reported

167
Q

If after 2 hours, the seminal fluid has not liquefied, which of the following may be added to induce liquefaction?

Dulbecco’s phosphate-buffered saline
Dulbecco’s phosphate-buffered saline and hyaluronidase
Dulbecco’s phosphate-buffered saline, alpha-chymotrypsin and bromelain
Alpha-chymotrypsin and bromelain

A

Dulbecco’s phosphate-buffered saline, alpha-chymotrypsin and bromelain

If after 2 hours the specimen has not liquified, an equal volume of physiologic Dulbecco’s phosphate-buffered saline or proteolytic enzymes such as alpha-chymotrypsin or bromelain may be added to induce liquefaction and allow the rest of the analysis to be performed.

168
Q

Normal seminal fluid volume

2 to 5 mL
3 to 10 mL
10 to 15 mL
15 mL to 20 mL

A

2 to 5 mL

Normal semen volume ranges between 2 and 5 mL. It can be measured by pouring the specimen into a clean graduated cylinder calibrated in 0.1-mL increments.

169
Q

Watery seminal fluid:

Viscosity grade of 0
Viscosity grade of 4

A

Viscosity grade of 0

Ratings of 0 (watery) to 4 (gel-like) can be assigned to the viscosity report.

170
Q

Gel-like seminal fluid:

Viscosity grade of 0
Viscosity grade of 4

A

Viscosity grade of 4

Ratings of 0 (watery) to 4 (gel-like) can be assigned to the viscosity report.

171
Q

Normal pH of semen:

pH of 2.0 to 4.0
pH of 4.5 to 8.0
pH of 7.4 to 7.5
pH of 7.2 to 8.0

A

pH of 7.2 to 8.0

The normal pH of semen is alkaline with a range of 7.2 to 8.0.
Increased pH indicates infection within the reproductive tract.
A decreased pH may be associated with increased prostatic fluid, ejaculatory duct obstruction, or poorly developed seminal vesicles.

172
Q

Increased pH of semen:

Increased prostatic fluid
Ejaculatory duct obstruction
Poorly developed seminal vesicles
Infection within the reproductive tract

A

Infection within the reproductive tract

The normal pH of semen is alkaline with a range of 7.2 to 8.0.
Increased pH indicates infection within the reproductive tract.
A decreased pH may be associated with increased prostatic fluid, ejaculatory duct obstruction, or poorly developed seminal vesicles.

173
Q

SPERM MOTILITY: slower speed, some lateral movement.

0
1.0
2.0
3.0
4.0

A

3.0

4.0 (a) Rapid, straight-line motility
3.0 (b) Slower speed, some lateral movement
2.0 (b) Slow forward progression, noticeable lateral movement
1.0 (c) No forward progression
0 (d) No movement

174
Q

SPERM MOTILITY: no forward progression.

0
1.0
2.0
3.0
4.0

A

1.0

4.0 (a) Rapid, straight-line motility
3.0 (b) Slower speed, some lateral movement
2.0 (b) Slow forward progression, noticeable lateral movement
1.0 (c) No forward progression
0 (d) No movement

175
Q

SPERM MOTILITY: slow forward progression, noticeable lateral
movement

a
b
c
d

A

b

4.0 (a) Rapid, straight-line motility
3.0 (b) Slower speed, some lateral movement
2.0 (b) Slow forward progression, noticeable lateral movement
1.0 (c) No forward progression
0 (d) No movement

176
Q

Included in computer-assisted semen analysis (CASA):

Sperm velocity
Sperm velocity and trajectory
Sperm velocity, trajectory and morphology
Sperm velocity, trajectory, sperm concentration and morphology

A

Sperm velocity, trajectory, sperm concentration and morphology

CASA provides objective determination of both sperm velocity and trajectory (direction of motion). Sperm concentration and morphology are also included in the analysis.
Currently, CASA instrumentation is found primarily in laboratories that specialize in andrology and perform a high volume of semen analysis.

177
Q

Location of the nucleus of sperm:

No nucleus
Head
Neckpiece
Midpiece
Tail

A

Head

178
Q

Critical to ovum penetration:

Acrosomal cap
Cell membrane
Mitochondria
Tail

A

Acrosomal cap

179
Q

The acrosomal cap should encompass approximately ___ of the head and
cover approximately___ of the sperm nucleus.

Half of the head and covers half of the sperm nucleus
Half of the head and covers 2/3 of the sperm nucleus
Two-thirds of the head and covers half of the sperm nucleus
Two-thirds of the head and covers 2/3 of the sperm nucleus

A

Half of the head and covers 2/3 of the sperm nucleus

The acrosomal cap should encompass approximately half of the head and cover approximately two thirds of the sperm nucleus.

180
Q

It is surrounded by a mitochondrial sheath that produces the energy required by the tail for motility:

Head
Neckpiece
Midpiece
Flagellum

A

Midpiece

The midpiece is approximately 7.0 μm long and 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.

181
Q

Round cells that are of concern and may be included in sperm counts and morphology analysis are:

Leukocytes
Spermatids
RBCs
Leukocytes and spermatids

A

Leukocytes and spermatids

Immature sperm and WBCs, often referred to as “round” cells.

Only fully developed sperm should be counted. Immature sperm and WBCs, often referred to as “round” cells, must not be included. However, their presence can be significant, and
they may need to be identified and counted separately. Stain included in the diluting fluid aids in differentiating between immature sperm cells (spermatids) and leukocytes, and
they can be counted in the same manner as mature sperm.

A count greater than 1 million leukocytes per milliliter is associated with inflammation or infection of the reproductive organs that can lead to infertility.

The presence of more than 1 million spermatids per milliliter indicates disruption of spermatogenesis. This may be caused by viral infections, exposure to toxic chemicals, and
genetic disorders.

182
Q

Living sperm cells in the eosin-nigrosin stain:

Green against a yellow background
Purple against a red background
Red against a purple background
Not infiltrated by the dye and remain bluish white

A

Not infiltrated by the dye and remain bluish white

Living cells are not infiltrated by the dye and remain bluish white, whereas dead cells stain red against the purple background.
Normal vitality requires 50% or more living cells and should correspond to the previously evaluated motility.

183
Q

Dead sperm cells in the eosin-nigrosin stain:

Green against a yellow background
Purple against a red background
Red against a purple background
Not infiltrated by the dye and remain bluish white

A

Red against a purple background

Living cells are not infiltrated by the dye and remain bluish white, whereas dead cells stain red against the purple background.
Normal vitality requires 50% or more living cells and should correspond to the previously evaluated motility.

184
Q

Seminal fluid specimens can be screened for the presence of fructose using the resorcinol test that produces an _____ color when fructose is
present.

Black
Blue
Green
Orange

A

Orange

Specimens can be screened for the presence of fructose using the resorcinol test that produces an orange color when fructose is present.

185
Q

Specimens for fructose levels should be tested within 2 hours of collection or _____ to prevent fructolysis.

Frozen
Incubated at 37C
Preserved with formalin
Refrigerated

A

Frozen

Specimens for fructose levels should be tested within 2 hours of collection or frozen to prevent fructolysis.

186
Q

Decreased sperm motility with clumping:

Decreased sperm vitality
Lack of seminal vesicle support medium
Female anti-sperm antibodies
Male anti-sperm antibodies

A

Male anti-sperm antibodies

The presence of antibodies in a male subject can be suspected when clumps of sperm are observed during a routine semen analysis. Sperm-agglutinating antibodies cause sperm to
stick to each other in a head-to-head, head-to-tail, or tail to- tail pattern.1 The agglutination is graded as “few,” “moderate,” or “many” on microscopic examination.
Two frequently used tests to detect the presence of antibody-coated sperm are the mixed agglutination reaction (MAR) test and the immunobead test.

187
Q

A decreased neutral alpha-glucosidase suggests a disorder of the:

Epididymis
Seminal vesicles
Prostate gland
Bulbourethral gland

A

Epididymis

Just as decreased fructose levels are associated with a lack of seminal fluid, decreased neutral alpha-glucosidase, glycerophosphocholine, and L-carnitine suggest a disorder of
the epididymis.
Decreased zinc, citric acid, glutamyl transpeptidase, and acid phosphatase indicate a lack of prostatic fluid. Spectrophotometric methods are used to quantitate citric acid and zinc.

188
Q

For post-vasectomy semen analysis, specimens are tested:

-Beginning 1 month post-vasectomy and continuing until two consecutive monthly
specimens show no sperm
-Beginning 2 months post-vasectomy and continuing until two consecutive
monthly specimens show no sperm
-Beginning 3 months post-vasectomy and continuing until two consecutive monthly
specimens show no sperm
-Beginning 3 months post-vasectomy and continuing until three consecutive
monthly specimens show no sperm

A

Beginning 2 months post-vasectomy and continuing until two consecutive
monthly specimens show no sperm

FOR POSTVASECTOMY SEMEN ANALYSIS:
Specimens are routinely tested at monthly intervals, beginning at 2 months postvasectomy and continuing until two consecutive monthly specimens show no spermatozoa.
A negative wet preparation is followed by specimen centrifugation for 10 minutes and examination of the sediment

189
Q

Before testing, very viscous synovial fluid should be treated with:

Normal saline
Hyaluronidase
Distilled water
Hypotonic saline

A

Hyaluronidase

Very viscous fluid may need to be pretreated by adding one drop of 0.05% hyaluronidase in phosphate buffer per milliliter of fluid and incubating at 37°C for 5 minutes.

190
Q

Normal volume of synovial fluid:

Less than 1.5 mL
Less than 3.5 mL
Less than 7.5 mL
Less than 10.5 mL

A

Less than 3.5 mL

The normal amount of fluid in the adult knee cavity is less than 3.5 mL, but can increase to greater than 25 mL with inflammation.

191
Q

A synovial fluid string measuring _____ is considered normal.

0.5 to 1 cm string
1 to 2 cm string
2 to 4 cm string
4 to 6 cm string

A

4 to 6 cm string

A string measuring 4 to 6 cm is considered normal.

192
Q

ROPE’S (MUCIN CLOT) TEST: when added to a solution of 2% to5% acetic acid, normal synovial fluid forms:

No clot
Friable clot
Soft clot
Solid clot

A

Solid clot

When added to a solution of 2% to 5% acetic acid, normal synovial fluid forms a solid clot
surrounded by clear fluid.

Good (solid clot)
Fair (soft clot)
Low (friable clot)
Poor (no clot)

193
Q

Normal synovial fluid WBC count:

Less than 200 cells/uL
Less than 400 cells/uL
Less than 1,000 cells/uL
Less than 2,000 cells/uL

A

Less than 200 cells/uL

RBC COUNT: LESS THAN 2,000 cells/uL
WBC COUNT: LESS THAN 200 cells/uL

SYNOVIAL FLUID WBC COUNT:
WBC counts less than 200 cells/uL are considered normal and may reach 100,000 cells/uL
or higher in severe infections

194
Q

Joint disorder with WBC count of 800/uL:

Group I, non-inflammatory
Group II, inflammatory
Group III, septic
Group IV, hemorrhagic
Normal synovial fluid WBC count

A

Group I, non-inflammatory

SYNOVIAL FLUID WBC COUNT
Normal: less than 200 cells/uL
Noninflammatory: less than 1, 000 cells/uL
Immunologic: 2,000 to 75,000 cells/uL
Crystal-induced: up to 100,000 cells/uL
Septic: 50,000 to 100,000 cells/uL
Hemorrhagic: WBCs equal to blood

195
Q

When diluting a synovial fluid WBC count, all of the following are acceptable except:

Acetic acid
Isotonic saline
Hypotonic saline
Saline with saponin

A

Acetic acid

SYNOVIAL FLUID + ACETIC ACID = CLOT FORMATION
Traditional WBC diluting fluid cannot be used because it contains acetic acid that causes the formation of mucin clots.

If it is necessary to lyse the RBCs, hypotonic saline (0.3%) or saline that contains saponin is a suitable diluent. Methylene blue added to the normal saline stains the WBC nuclei,
permitting separation of the RBCs and WBCs during counts performed on mixed specimens.

196
Q

Vacuolated macrophage with ingested neutrophils:

LE cell
Ragocyte
Reiter cell
Rice bodies

A

Reiter cell

197
Q

Neutrophil with dark cytoplasmic granules containing immune
complexes:

LE cell
Ragocyte
Reiter cell
Rice bodies

A

Ragocyte

198
Q

Synovial fluid crystals found in cases of gout:

Calcium phosphate (apatite)
Calcium pyrophosphate
Calcium oxalate
Monosodium urate

A

Monosodium urate

Increased serum uric acid resulting from impaired metabolism of purines; increased consumption of high-purine-content foods, alcohol, and fructose; chemotherapy treatment
of leukemias; and decreased renal excretion of uric acid are the most frequent causes of gout.

199
Q

Synovial fluid crystals found in cases of pseudogout:

Calcium phosphate (apatite)
Calcium pyrophosphate
Calcium oxalate
Monosodium urate

A

Calcium pyrophosphate

Pseudogout is most often associated with degenerative arthritis, producing cartilage calcification and endocrine disorders that produce elevated serum calcium levels.

200
Q

Synovial fluid crystals found in cases of osteoarthritis:

Calcium phosphate (apatite)
Calcium pyrophosphate
Calcium oxalate
Monosodium urate

A

Calcium phosphate (apatite)

201
Q

Shape of calcium pyrophosphate crystals in synovial fluid:

Envelopes
Flat, variable-shaped plates
Needles
Rhomboid square, rods

A

Rhomboid square, rods

202
Q

Most frequently requested test in synovial fluid:

Gram stain and culture
Glucose
Protein
Uric acid

A

Glucose

The most frequently requested test is the glucose determination, because markedly decreased glucose values indicate inflammatory (group II) or septic (group III) disorders.

203
Q

Required tube for synovial fluid glucose analysis:

Sterile heparinized
Nonanticoagulated
Tube with liquid EDTA
Tube with sodium fluoride

A

Tube with sodium fluoride

To prevent falsely decreased values caused by glycolysis, specimens should be analyzed within 1 hour or preserved with sodium fluoride.

Sterile heparinized or SPS: Gram stain and culture
Liquid EDTA or heparin: cell counts
Sodium fluoride: glucose analysis
Non-anticoagulated: all other tests

204
Q

Serous fluid for pH determination must be:

Maintained aerobically and incubated at 37C
Maintained anaerobically and incubated at 37C
Maintained aerobically in ice
Maintained anaerobically in ice

A

Maintained anaerobically in ice

Specimens for pH must be maintained anaerobically in ice.

205
Q

Fluid: serum protein and lactic dehydrogenase ratios are performed on serous fluids:

When malignancy is suspected
To classify transudates and exudates
To determine the type of serous fluid
When a traumatic tap has occurred

A

To classify transudates and exudates

Traditionally, a variety of laboratory tests have been used to differentiate between transudates and exudates, including appearance, total protein, lactic dehydrogenase, cell
counts, and spontaneous clotting.
However, the most reliable differentiation is usually obtained by determining the fluid: blood ratios for protein and lactic dehydrogenase.

206
Q

If the blood is from a HEMOTHORAX, the fluid hematocrit is ______ of the whole blood hematocrit.

Less than 20% of the whole blood hematocrit
More than 20% of the whole blood hematocrit
Less than 50% of the whole blood hematcrit
More than 50% of the whole blood hematocrit

A

More than 50% of the whole blood hematocrit

To differentiate between a hemothorax and hemorrhagic exudate, a hematocrit can be run on the fluid.
If the blood is from a hemothorax, the fluid hematocrit is more than 50% of the whole blood hematocrit, because the effusion comes from the inpouring of blood from the injury.

207
Q

These cells are increased in pleural effusions resulting from pancreatitis and pulmonary infarction:

Mesothelial cells
Neutrophils
Lymphocytes
Plasma cells

A

Neutrophils

Similar to other body fluids, an increase in pleural fluid neutrophils indicates a bacterial infection, such as pneumonia.
Neutrophils are also increased in effusions resulting from pancreatitis and pulmonary infarction.

208
Q

Adenosine deaminase (ADA) levels higher than 40 U/L are highly indicative of:

Chylous effusion
Pancreatitis
Tuberculosis
Rheumatoid inflammation

A

Tuberculosis

ADENOSINE DEAMINASE (ADA)
ADA levels higher than 40 U/L are highly indicative of tuberculosis. They are also frequently elevated with malignancy.

209
Q

The recommended test for determining whether peritoneal fluid is a transudate or an exudate is the:

Fluid:serum albumin ratio
Serum ascites albumin gradient
Fluid:serum lactic dehydrogenase ratio
Absolute neutrophil count

A

Serum ascites albumin gradient

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 to detect transudates of hepatic origin.
Fluid and serum albumin levels are measured concurrently, and the fluid albumin level is then subtracted from the serum albumin level. A difference (gradient) of 1.1 or greater
suggests a transudate effusion of hepatic origin, and lower gradients are associated with exudative effusions.

210
Q

Elements containing concentric striations of collagen-like material and can be seen in benign conditions and are also associated with ovarian
and thyroid malignancies:

Lipophages
Macrophages
Mesothelial cells
Psammoma bodies

A

Psammoma bodies

211
Q

Detection of the CA 125 tumor marker in peritoneal fluid indicates:

Colon cancer
Ovarian cancer
Gastric malignancy
Prostate cancer

A

Ovarian cancer

The presence of CA 125 antigen with a negative CEA suggests the source is from the ovaries, fallopian tubes, or endometrium.

212
Q

The brown color of feces is due to:

Urochrome
Uroeythrin
Urobilinogen
Urobilin

A

Urobilin

The brown color of the feces results from intestinal oxidation of stercobilinogen to urobilin.

213
Q

Blood that originates from the esophagus, stomach, or duodenum takes approximately ___ day(s) to appear in the stool.

Approximately 1 day to appear in stool
Approximately 3 days to appear in stool
Approximately 7 days to appear in stool
Approximately 10 days to appear in stool

A

Approximately 3 days to appear in stool

Blood that originates from the esophagus, stomach, or duodenum takes approximately 3 days to appear in the stool; during this time, degradation of hemoglobin produces the
characteristic black, tarry stool

214
Q

Bulky and frothy stool:

Upper GI bleeding
Lower GI bleeding
Barium sulfate
Pancreatic disorders

A

Pancreatic disorders

215
Q

Black stool:

Barium sulfate
Bile duct obstruction
Beets and food coloring
Bismuth (antacid), iron therapy

A

Bismuth (antacid), iron therapy

216
Q

Microscopic examination reveals presence of fecal WBCs EXCEPT in diarrhea caused by:

Enteroinvasive E. coli (EIEC)
Salmonella, Shigella
Staphylococcos aureus, Vibrio spp.
Yersinia, Campylobacter

A

Staphylococcos aureus, Vibrio spp.

Microscopic screening is performed as a preliminary test to determine whether diarrhea is being caused by invasive bacterial pathogens including Salmonella, Shigella,
Campylobacter, Yersinia, and enteroinvasive E. coli.

Bacteria that cause diarrhea by toxin production, such as Staphylococcus aureus and Vibrio spp., viruses, and parasites usually do not cause the appearance of fecal leukocytes.

217
Q

By far the most frequently performed fecal analysis is the detection of:

Carbohydrates
Fats
Occult blood
pH

A

Occult blood

By far the most frequently performed fecal analysis is the detection of occult blood (hidden blood).

218
Q

Reagent for the APT test:

1% NaOH
10% NaOH
70% ethanol
95% ethanol

A

1% NaOH

APT Test (Fetal Hemoglobin)
The material to be tested is emulsified in water to release hemoglobin (Hb) and, after centrifugation, 1% sodium hydroxide is added to the pink hemoglobin-containing
supernatant.

In the presence of alkali-resistant fetal hemoglobin, the solution remains pink (HbF), whereas denaturation of the maternal hemoglobin (HbA) produces a yellow-brown
supernatant after standing for 2 minutes.

219
Q

Normal stool pH:

Between pH 4 and 5
Between pH 5 and 6
Between pH 7 and 8
Between pH 8 and 9

A

Between pH 7 and 8

Normal stool pH is between 7 and 8; however, increased use of carbohydrates by intestinal bacterial fermentation increases the lactic acid level and lowers the pH to below 5.5 in
cases of carbohydrate disorders.

220
Q

CHECK 4 BOXES: Variables in the Cockroft and Gault formula.

Urine ceatinine
Serum creatinine
Age
Race
Gender
Body weight in kilograms
BUN
Albumin

A

Serum creatinine
Age
Gender
Body weight in kilograms

221
Q

CHECK 6 BOXES: Variables in the MODIFICATION OF DIET IN RENAL DISEASE (MDRD) formula.

Urine ceatinine
Serum creatinine
Age
Race
Gender
Body weight in kilograms
BUN
Albumin

A

Serum creatinine
Age
Race
Gender
BUN
Albumin

222
Q

In the urinalysis laboratory the primary source in the chain of infection would be:

Patients
Needlesticks
Specimens
Biohardous wastes

A

Specimens

In the clinical laboratory, the most direct contact with a source of infection is through contact with patient specimens, although contact with patients and infected objects also
occurs.

223
Q

All of the following should be discarded in biohazardous waste containers except:

Urine specimen containers
Towels used for decontamination
Disposable lab coats
Blood collection tubes

A

Urine specimen containers

224
Q

An acceptable disinfectant for blood and body fluid decontamination is:

Sodium hydroxide
Antimicrobial soap
Hydrogen peroxide
Sodium hypochlorite

A

Sodium hypochlorite

225
Q

Centrifuging an uncapped specimen may produce a biologic hazard in the form of:

Vectors
Sharps contamination
Aerosols
Specimen contamination

A

Aerosols

226
Q

The first thing to do when a fire is discovered is to:

Rescue person in danger
Activate the alarm system
Close doors to other areas
Extinguish the fire if possible

A

Rescue person in danger

227
Q

If a red rash is observed after removing gloves, the employee:

May be washing her hands too often
May have developed a latex allergy
Should apply cortisone cream
Should not rub the hands so vigorously

A

May have developed a latex allergy

228
Q

The classification of a fire that can be extinguished with water is:

Class A
Class B
Class C
Class D

A

Class A

229
Q

Employers are required to provide free immunization for:

HIV
HTLV-1
HBV
HCV

A

HBV

230
Q

The current routine infection control policy developed by CDC and followed in all health-care settings is:

Universal precautions
Isolation precautions
Blood and body fluid precautions
Standard precations

A

Standard precations

In 1987 the CDC instituted Universal Precautions (UP). Under
UP all patients are considered to be possible carriers of bloodborne pathogens.
In 1996 the CDC and the Healthcare Infection Control Practices Advisory Committee (HICPAC) combined the major features of UP and blood safety isolation (BSI) guidelines
and called the new guidelines Standard Precautions.

231
Q

Which of the following would be least affected in a specimen that has remained unpreserved at room temperature for more than 2 hours?

Urobilinogen
Ketones
Protein
Nitrite

A

Protein

232
Q

Which of the tubules is impermeable to water?

Proximal convoluted tubule
Descending loop of Henle
Ascending loop of Henle
Distal convoluted tubule

A

Ascending loop of Henle

233
Q

Decreased production of ADH: (two possible answers)

Produces a large volume of urine
Produces high urine volume
Increases ammonia excretion
Affects active transport of sodium

A

Produces high urine volume

Two possible answers:
In diabetes insipidus: deficiency of ADH
High or large urine volume
Decreased urine specific gravity

234
Q

The largest source of error in creatinine clearance tests is:

Secretion of creatinine
Improperly timed urine specimens
Refrigeration of the urine
Time of collecting blood sample

A

Improperly timed urine specimens

235
Q

Variables that are included in the MDRD-IDSM estimated creatinine clearance calculations include all of the following except:

Serum creatinine
Weight
Age
Gender

A

Weight

236
Q

A patient with a viscous orange specimen may have been:

Treated for urinary tract infection
Taking vitamin B
Eating fresh carrots
Taking antidepressants

A

Treated for urinary tract infection

Phenazopyridine (Pyridium)
Drug commonly administered for urinary tract infections

237
Q

Orange in alkaline urine, colorless in acid urine.

Phenazopyridine (Pyridium)
Phenindione
Methyldopa
Metronidazole (Flagyl)

A

Phenindione

PHENINDIONE
Anticoagulant, orange in alkaline urine, colorless in acid urine

238
Q

The principle of refractive index is to compare:

Light velocity in solutions with light velocity in solids
Light velocity in air with light velocity in solutions
Light scattering by air with light scattering by solutions
Light scattering by particles in solution

A

Light velocity in air with light velocity in solutions

239
Q

A specimen with a specific gravity of 1.001 would be considered:

Hyposthenuric
Not urine
Hypersthenuric
Isosthenuric

A

Not urine

Specimens measuring lower than 1.002 probably are not urine.
Most random specimens fall between 1.015 and 1.030.

240
Q

Leaving excess urine on the reagent strip after removing it from the specimen will:

Cause run-over between reagent pads
Alter the color of the specimen
Cause reagents to leach from the pads
Not affect the chemical reactions

A

Cause run-over between reagent pads

241
Q

Testing a refrigerated specimen that has not warmed to room temperature will adversely affect:

Enzymatic reactions
Dye-binding reactions
Sodium nitroprusside reaction
Diazo reactions

A

Enzymatic reactions

242
Q

Quality control of reagent strips is performed:

Using positive and negative controls
When results are questionable
At least once every 24 hours
All of the above

A

All of the above

Quality Control: REAGENT STRIP TESTING
1. Test open bottles of reagent strips with known positive and negative controls every 24 hours.
2. Resolve control results that are out of range by further testing.
3. Test reagents used in backup tests with positive and negative controls.
4. Perform positive and negative controls on new reagents and newly opened bottles of reagent strips.
5. Record all control results and reagent lot numbers.

243
Q

All of the following are important to protect the integrity of reagent strips except:

Removing the desiccant from the bottle
Storing in an opaque bottle
Storing at room temperature
Resealing the bottle after removing a strip

A

Removing the desiccant from the bottle

244
Q

A urine specimen with a pH of 9.0:

Indicates metabolic acidosis
Should be recollected
May contain calcium oxalate crystals
Is seen after drinking cranberry juice

A

Should be recollected

A pH above 8.5 is associated with an improperly preserved specimen and indicates that a fresh specimen should be obtained to ensure the validity of the analysis.

245
Q

The principle of the protein error of indicators reaction is that:

Protein keeps the pH of the urine constant
Albumin accepts hydrogen ions from the indicator
Indicator accepts hydrogen ions from albumin
Albumin changes the pH of the urine

A

Albumin accepts hydrogen ions from the indicator

246
Q

Testing for microalbuminuria is valuable for early detection of kidney disease and monitoring patients with:

Hypertension
Diabetes mellitus
Cardiovascular disease risk
All of the above

A

All of the above

Microalbuminuria
The development of diabetic nephropathy leading to reduced glomerular filtration and eventual renal failure is a common occurrence in persons with both type 1 and type 2
diabetes mellitus. Onset of renal complications can first be predicted by detection of microalbuminuria, and the progression of renal disease can be prevented through better
stabilization of blood glucose levels and control of hypertension. The presence of microalbuminuria is also associated with an increased risk of cardiovascular disease.

247
Q

The primary reason for performing a Clinitest is to:

Check for high ascorbic acid levels
Confirm a positive reagent strip glucose
Check for newborn galactosuria
Confirm a negative glucose reading

A

Check for newborn galactosuria

248
Q

A speckled pattern on the blood pad of the reagent strip indicates:

Hematuria
Hemoglobinuria
Myoglobinuria
All of the above

A

Hematuria

249
Q

An elevated urine bilirubin with a normal urobilinogen is indicative of:

Cirrhosis
Hemolytic disease
Hepatitis
Biliary obstruction

A

Biliary obstruction

250
Q

A positive nitrite test and a negative leukocyte esterase test is an indication of a:

Dilute random specimen
Specimen with lysed leukocytes
Vaginal yeast infection
Specimen older than 2 hours

A

Specimen older than 2 hours

Possible bacterial contamination

251
Q

Initial screening of the urine sediment is performed using an objective power of:

4x
10x
40x
100x

A

10x

252
Q

Crenated RBCs are seen in urine that is:

Hyposthenuric
Hypersthenuric
Highly acidic
Highly alkaline

A

Hypersthenuric

253
Q

Differentiation among RBCs, yeast, and oil droplets maybe accomplished by all of the following except:

Observation of budding in yeast cells
Increased refractility of oil droplets
Lysis of yeast cells by acetic acid
Lysis of RBCs by acetic acid

A

Lysis of yeast cells by acetic acid

254
Q

When pyuria is detected in a urine sediment, the slide should be carefully checked for the presence of:

RBCs
Bacteria
Hyaline casts
Mucus

A

Bacteria

An increase in urinary WBCs is called pyuria and indicates the presence of an infection or inflammation in the genitourinary system.

255
Q

The largest cells in the urine sediment are:

Squamous epithelial cells
Urothelial epithelial cells
Cuboidal epithelial cells
Columnar epithelial cells

A

Squamous epithelial cells

256
Q

Following an episode of hemoglobinuria, RTE cells may contain:

Bilirubin
Hemosiderin granules
Porphobilinogen
Myoglobin

A

Hemosiderin granules

Following episodes of hemoglobinuria (transfusion reactions, paroxysmal nocturnal hemoglobinuria, etc.), the RTE cells may contain the characteristic yellow-brown hemosiderin granules. The granules may also be seen free-floating in the urine sediment.

Confirmation of the presence of hemosiderin is performed by staining the urine sediment with Prussian blue.

257
Q

A structure believed to be an oval fat body produced a Maltese cross formation under polarized light but does not stain with Sudan III. The structure:

Contains cholesterol
Is not an oval fat body
Contains neutral fats
Is contaminated with immersion oil

A

Contains cholesterol

258
Q

The finding of yeast cells in the urine is commonly associated with:

Cystitis
Diabetes mellitus
Pyelonephritis
Liver disorders

A

Diabetes mellitus

Yeast cells, primarily Candida albicans, are seen in the urine of diabetic patients, immunocompromised patients, and women with vaginal moniliasis. The acidic, glucosecontaining urine of patients with diabetes provides an ideal medium for the growth of yeast.

259
Q

All of the following contribute to urinary crystals formation except:

Protein concentration
pH
Solute concentration
Temperature

A

Protein concentration

Crystals are formed by the precipitation of urine solutes, including inorganic salts, organic
compounds, and medications (iatrogenic compounds). Precipitation is subject to changes
in temperature, solute concentration, and pH, which affect solubility.

260
Q

Casts and fibers can usually be differentiated using:

Solubility characteristics
Patient history
Polarized light
Fluorescent light

A

Polarized light

Examination under polarized light can frequently differentiate between fibers and casts.
Fibers often polarize, whereas casts, other than fatty casts, do not polarize.

261
Q

Three-dimensional images:

Bright-field microscope
Phase contrast microcope
Interference contrast microscope
Fluorescent microscope

A

Interference contrast microscope

Interference-contrast microscopy provides a three-dimensional image showing very fine
structural detail by splitting the light ray so that the beams pass through different areas of
the specimen.

262
Q

Anti-neutrophilic cytoplasmic antibody is diagnostic for:

IgA nephropathy
Wegener granulomatosis
Henoch-Schönlein purpura
Goodpasture syndrome

A

Wegener granulomatosis

263
Q

The only protein produced by the kidney is:

Albumin
Uromodulin
Uroprotein
Globulin

A

Uromodulin

264
Q

The presence of renal tubular epithelial cells and casts is an indication of:

Acute interstitial nephritis
Chronic glomerulonephritis
Minimal change disease
Acute tubular necrosis

A

Acute tubular necrosis

265
Q

Urinalysis on a patient with severe back pain being evaluated for renal
calculi would be most beneficial if it showed:

Heavy proteinuria
Low specific gravity
Uric acid crystals
Microscopic hematuria

A

Microscopic hematuria

Urine specimens from patients suspected of passing or being in the process of passing
renal calculi are frequently received in the laboratory. The presence of microscopic
hematuria resulting from irritation to the tissues by the moving calculus is the primary
urinalysis finding.

266
Q

False-positive levels of 5-HIAA can be caused by a diet high in:

Meat
Carbohydrates
Starch
Bananas

A

Bananas

Patients must be given explicit dietary instructions before collecting any sample to be
tested for 5-HIAA, because serotonin is a major constituent of foods such as bananas,
pineapples, and tomatoes.
Medications, including phenothiazines and acetanilids, also interfere with results. Patients
should be directed to withhold medications for 72 hours before specimen collection.

267
Q

Which type of urine sample is needed for a D-xylose absorption test on an
adult patient?

24-hour urine sample collected with 20 mL of 6N HCl
2-hour timed postprandial urine preserved with boric acid
5-hour timed urine kept under refrigeration
Random urine preserved with formalin

A

5-hour timed urine kept under refrigeration

The D-xylose absorption test is used to distinguish pancreatic insufficiency from intestinal
malabsorption.
The test requires a blood sample taken 2 hours after oral administration of 25 g of Dxylose, and a 5-hour timed urine sample.
D-xylose is absorbed without the aid of pancreatic enzymes, and is not metabolized by the
liver. Therefore, deficient absorption (denoted by a plasma level < 25 mg/dL and urine
excretion of < 4g/5hours) points to malabsorption syndrome.

268
Q

In automated microscopy, Sysmex UF series, the DNA within the cells is
stained by the orange dye:

Carbocyanine
Phenathridine
Eosin
Bromcresol green

A

Phenathridine

The DNA within the cells is stained by the orange dye, phenathridine; the nuclear
membranes, mitochondria, and negatively charged cell membranes are stained with a
green dye, carbocyanine.

269
Q

In automated microscopy, Sysmex UF series, the nuclear membranes,
mitochondria, and negatively charged cell membranes are stained with a
green dye:

Carbocyanine
Phenathridine
Eosin
Bromcresol green

A

Carbocyanine

The DNA within the cells is stained by the orange dye, phenathridine; the nuclear
membranes, mitochondria, and negatively charged cell membranes are stained with a
green dye, carbocyanine.

270
Q

The UF-100 and UF-50 use laser-based flow cytometry along with:

Impedance detection
Imedance detection and forward light scatter
Impedance detection and fluorescence
Impedance detection and forward light scatter
Impedance detection, forward light scatter and fluorescence

A

Impedance detection, forward light scatter and fluorescence

The UF-100 and UF-50 use laser-based flow cytometry along with impedance detection,
forward light scatter, and fluorescence to identify the individual characteristics and stained
urine sediment particles in a flowing stream.

271
Q

Graphic display of size distribution of any small sediment particles
(ranging from 1 to 6 um2) found during the microscopic examination;
helps to decide whether bacteria are present in these small ranges or if
the detected particles are small crystals or amorphous.

Near-infrared reflectance spectroscopy
Reflectance photomtery
Small-particle histogram
Mass gravity meter

A

Small-particle histogram

IRIS SLIDELESS MICROSCOPE
Small particle histograms are graphic display of size distribution of f any small sediment
particles (ranging from 1 to 6 um2) found during the microscopic examination. The
histograms help to decide whether bacteria are present in these small ranges or if the
detected particles are small crystals or amorphous.

272
Q

The functions of the CSF include all of the following except:

Removing metabolic wastes
Producing an ultrafiltrate of plasma
Supplying nutrients to the CNS
Protecting the brain and spinal cord

A

Producing an ultrafiltrate of plasma

273
Q

What department is the CSF tube labeled 3 routinely sent to?

Hematology
Chemistry
Microbiology
Serology

A

Hematology

274
Q

The presence of xanthochromia can be caused by all of the following except:

Immature liver function
RBC degradation
A recent hemorrhage
Elevated CSF protein

A

A recent hemorrhage

275
Q

A web-like pellicle in a refrigerated CSF specimen indicates:

Tubercular meningitis
Multiple sclerosis
Primary CNS malignancy
Viral meningitis

A

Tubercular meningitis

276
Q

CSF total cell count is diluted with:

Distilled water
Normal saline
Acetic acid
Hypotonic saline

A

Normal saline

Dilutions for total cell counts are made with normal saline, mixed by inversion, and loaded into the hemocytometer with a Pasteur pipette.

277
Q

A CSF WBC count is diluted with:

Distilled water
Normal saline
Acetic acid
Hypotonic saline

A

Acetic acid

Lysis of RBCs must be obtained before performing the WBC count on either diluted or
undiluted specimens. Specimens requiring dilution can be diluted in the manner described
previously, substituting 3% glacial acetic acid to lyse the RBCs. Adding methylene blue to
the diluting fluid stains the WBCs, providing better differentiation between neutrophils and
mononuclear cells.

278
Q

A total CSF cell count on a clear fluid should be:

Reported as normal
Not reported
Diluted with normal saline
Counted undiluted

A

Counted undiluted

Clear specimens may be counted undiluted, provided no overlapping of cells is seen during the microscopic examination. When dilutions are required, calibrated automatic pipettes, not mouth pipetting, are used.

279
Q

The purpose of adding 30% albumin to CSF before cytocentrifugation is to:

Increase the cell yield
Decrease the cellular distortion
Improve cellular staining
Increase cell yield and decrease cellular distortion

A

Decrease the cellular distortion
Increase cell yield and decrease cellular distortion

As little as 0.1 mL of CSF combined with one drop of 30% albumin produces an adequate
cell yield when processed with the cytocentrifuge. Adding albumin increases the cell yield
and decreases the cellular distortion frequently seen on cytocentrifuged specimens.

280
Q

Neutrophils with pyknotic nuclei may be mistaken for:

Lymphocytes
Nucleated RBCs
Malignant cells
Spindle-shaped cells

A

Nucleated RBCs

Neutrophils with pyknotic nuclei indicate degenerating cells. They may resemble nucleated
red blood cells (NRBCs) but usually have multiple nuclei.

281
Q

Macrophages appear in the CSF after:

Hemorrhage
Repeated spinal taps
Diagnostic procedures
All of the above

A

All of the above

The purpose of macrophages in the CSF is to remove cellular debris and foreign objects
such as RBCs. Macrophages appear within 2 to 4 hours after RBCs enter the CSF and are
frequently seen following repeated taps. They tend to have more cytoplasm than
monocytes in the peripheral blood (PB). The finding of increased macrophages indicates a
previous hemorrhage.

282
Q

Nucleated RBCs are seen in the CSF as a result of:

Elevated blood RBCs
Treatment of anemia
Severe hemorrhage
Bone marrow contamination

A

Bone marrow contamination

NRBCs are seen as a result of bone marrow contamination during the spinal tap. This is
found in approximately 1% of specimens. Capillary structures and endothelial cells may be
seen following a traumatic tap.

283
Q

Myeloblasts are seen in the CSF:

In bacterial infections
In conjunction with CNS malignancy
After cerebral hemorrhage
As a complication of acute leukemia

A

As a complication of acute leukemia

284
Q

The reference range for CSF protein is:

6 to 8 g/dL
15 to 45 g/dL
6 to 8 mg/dL
15 to 45 mg/dL

A

15 to 45 mg/dL

Reference values for total CSF protein are usually listed as 15 to 45 mg/dL, but are somewhat method dependent, and higher values are found in infants and people over age
40.
This value is reported in milligrams per deciliter and not grams per deciliter, as are plasma
protein concentrations.

285
Q

Elevated CSF protein values can be caused by all of the following except:

Meningitis
Multiple sclerosis
Fluid leakage
CNS malignancy

A

Fluid leakage

286
Q

The integrity of the blood–brain barrier is measured using the:

CSF/serum albumin index
CSF/serum globulin ratio
CSF albumin index
CSF IgG index

A

CSF/serum albumin index

ALBUMIN INDEX
An index value less than 9 represents an intact blood– brain barrier. The index increases
relative to the amount of damage to the barrier.

287
Q

Measurement of which of the following can be replaced by CSF glutamine analysis in children with Reye syndrome?

Ammonia
Lactate
Glucose
Alpha-ketoglutarate

A

Ammonia

Reye syndrome
Acute encephalopathy and liver infiltration seen in children following viral infections

288
Q

Determining CSF ________ provides an indirect test for the presence of excess ammonia in the CSF.

Alpha-ketoglutarate
Glucose
Glutamine
Lactate

A

Glutamine

Determining CSF glutamine provides an indirect test for the presence of excess ammonia
in the CSF.
The normal concentration of glutamine in the CSF is 8 to 18 mg/dL

289
Q

Before performing a Gram stain on CSF, the specimen must be:

Filtered
Warmed to 37C
Centrifuged
Mixed

A

Centrifuged

The Gram stain is routinely performed on CSF from all suspected cases of meningitis,
although its value lies in detecting bacterial and fungal organisms. All smears and cultures
should be performed on concentrated specimens because often only a few organisms are
present at the onset of the disease. The CSF should be centrifuged at 1500 g for 15
minutes, and slides and cultures should be prepared from the sediment. Use of the
cytocentrifuge provides a highly concentrated specimen for Gram stains.

290
Q

Particular attention should be paid to the Gram stain for the CLASSIC STARBURST PATTERN produced by:

Hemophilus influenzae
Neisseria meninigitidis
Cryptococcus neoformans
Coccidioides immitis

A

Cryptococcus neoformans

291
Q

Maturation of spermatozoa takes place in the:

Sertoli cells
Seminiferous tubules
Epidiymis
Seminal vesicles

A

Epidiymis

292
Q

Enzymes for the coagulation and liquefaction of semen are produced by the:

Seminal vesicles
Bulbourethral glands
Ductus deferens
Prostate gland

A

Prostate gland

293
Q

If the first portion of a semen specimen is not collected, the semen analysis will have which of the following?

Decreased pH
Increased viscosity
Decreased sperm count
Decreased sperm motility

A

Decreased sperm count

When a part of the first portion of the ejaculate is missing, the sperm count will be
decreased, the pH falsely increased, and the specimen will not liquefy.
When part of the last portion of ejaculate is missing, the semen volume is decreased, the
sperm count is falsely increased, the pH is falsely decreased, and the specimen will not
clot.

294
Q

A semen specimen delivered to the laboratory in a condom has a normal sperm count and markedly decreased sperm motility. This indicates:

Decreased fructose
Antispermicide in the condom
Increased semen viscosity
Increased semen alkalinity

A

Antispermicide in the condom

Specimens should be collected by masturbation. If this is not possible, only nonlubricantcontaining rubber or polyurethane condoms should be used.
Ordinary condoms are not acceptable because they contain spermicides.

295
Q

Liquefaction of a semen specimen should take place within:

1 hour
2 hours
3 hours
4 hours

A

1 hour

A fresh semen specimen is clotted and should liquefy within 30 to 60 minutes after
collection; therefore, recording the time of collection is essential for evaluating semen
liquefaction.
Failure of liquefaction to occur within 60 minutes may be caused by a deficiency in
prostatic enzymes and should be reported.

296
Q

Proteolytic enzymes may be added to semen specimens to:

Increase the viscosity
Dilute the specimen
Decrease the viscosity
Neutralize the specimen

A

Decrease the viscosity

Analysis of the specimen cannot begin until liquefaction (normal is within 30 to 60
minutes) has occurred.
If after 2 hours the specimen has not liquified, an equal volume of physiologic Dulbecco’s
phosphate-buffered saline or proteolytic enzymes such as alpha-chymotrypsin or
bromelain may be added to induce liquefaction and allow the rest of the analysis to be
performed.

297
Q

The primary reason to dilute a semen specimen before performing a sperm concentration is to:

Immobilize the sperm
Facilitate chamber count
Decrease the viscosity
Stain the sperm

A

Immobilize the sperm

The most commonly used dilution is 1:20 prepared using a mechanical (positivedisplacement) pipette.
Dilution of the semen is essential because it immobilizes the sperm before counting.
The traditional diluting fluid contains sodium bicarbonate and formalin, which immobilize
and preserve the cells; however, good results can also be achieved using saline and
distilled water.

298
Q

For determination of sperm concentration, both sides of the Neubauer
hemocytometer are loaded and allowed to settle for 3 to 5 minutes; then
they are counted, and the counts should agree within ___%.

Agree within 5%
Agree within 10%
Agree within 20%
Agree within 30%

A

Agree within 10%

Using the Neubauer hemocytometer, sperm are usually counted in the four corner and
center squares of the large center square, similar to a manual RBC count.
Both sides of the hemocytometer are loaded and allowed to settle for 3 to 5 minutes; then
they are counted, and the counts should agree within 10%. An average of the two counts is
used in the calculation. If the counts do not agree, both the dilution and the counts are
repeated.

299
Q

The purpose of the acrosomal cap is to:

Penetrate the ovum
Protect the the nucleus
Create energy for tail movement
Protect the neckpiece

A

Penetrate the ovum

300
Q

The sperm part containing a mitochondrial sheath is the:

Head
Neckpiece
Midpiece
Tail

A

Head

The midpiece 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.

301
Q

All of the following are associated with sperm motility except the:

Head
Neckpiece
Midpiece
Tail

A

Head

Abnormalities in head morphology are associated with poor ovum penetration, whereas
neckpiece, midpiece, and tail abnormalities affect motility.

302
Q

Additional parameters measured by Kruger’s strict morphology include all
of the following except:

Vitality
Presence of vacuoles
Acrosome size
Tail length

A

Vitality

Additional parameters in evaluating sperm morphology include measuring head, neck, and
tail size; measuring acrosome size; and evaluating for the presence of vacuoles. Inclusion
of these parameters is referred to as Kruger’s strict criteria.
Strict criteria evaluation requires the use of a stage micrometer or morphometry. At
present, evaluation of sperm morphology using strict criteria is not routinely performed in
the clinical laboratory but is recommended by the WHO. Strict criteria evaluation is an
integral part of assisted reproduction evaluations.

303
Q

Round cells that are of concern and may be included in sperm counts and
morphology analysis are:

Leukocytes
Spermatids
RBCs
Leukocytes and spermatids

A

Leukocytes and spermatids

Differentiation and enumeration of round cells (immature sperm and leukocytes) can also
be made during the morphology examination.
Peroxidase-positive granulocytes are the predominant form of leukocyte in semen and can
be further differentiated from spermatogenic cells and lymphocytes using a peroxidase
stain.

304
Q

Following an abnormal sperm motility test with a normal sperm count,
what additional test might be ordered?

Fructose level
Zinc level
Mixed agglutination reaction
Eosin-nigrosin stain

A

Eosin-nigrosin stain

Decreased sperm vitality may be suspected when a specimen has a normal sperm
concentration with markedly decreased motility. Sperm vitality should be assessed within
1 hour of ejaculation. Vitality is evaluated by mixing the specimen with an eosin-nigrosin
stain, preparing a smear, and counting the number of dead cells in 100 sperm using a
brightfield or phase-contrast microscope.
Living cells are not infiltrated by the dye and remain bluish white, whereas dead cells stain
red against the purple background. Normal vitality requires 50% or more living cells and
should correspond to the previously evaluated motility.

305
Q

Follow-up testing for a low sperm concentration would include testing for:

Antisperm antibodies
Seminal fluid fructose
Sperm vitality
Prostatic acid phosphatase

A

Seminal fluid fructose

Low sperm concentration may be caused by lack of the support medium produced in the
seminal vesicles, which can be indicated by a low to absent fructose level in the semen.

306
Q

Measurement of alpha-glucosidase is performed to detect a disorder of the:

Seminiferous tubules
Epididymis
Prostate gland
Bulbourethral glands

A

Epididymis

decreased neutral alpha-glucosidase, glycerophosphocholine, and L-carnitine suggest a disorder of the epididymis.

307
Q

A specimen delivered to the laboratory with a request for prostatic acid
phosphatase and glycoprotein p30 was collected to determine:

Prostatic infection
Presence of antisperm antibodies
A possible rape
Successful vasectomy

A

A possible rape

On certain occasions, the laboratory may be called on to determine whether semen is
actually present in a specimen. A primary example is in cases of alleged rape.
Microscopically examining the specimen for the presence of sperm
may be possible, with the best results being obtained by enhancing the specimen with
xylene and examining under phase microscopy.
Seminal fluid contains a high concentration of prostatic acid phosphatase, so detecting
this enzyme can aid in determining the presence of semen in a specimen.
A more specific method is the detection of seminal glycoprotein p30
(prostatic specific antigen [PSA]), which is present even in the absence of sperm.
Further information can often be obtained by performing ABO blood grouping and DNA
analysis on the specimen.

308
Q

Following a negative postvasectomy wet preparation, the specimen
should be:

Centrifuged and reexamined
Stained and reexamined
Reported as no sperm seen
Detect presence of male antibodies

A

Centrifuged and reexamined

A negative wet preparation is followed by specimen centrifugation for 10 minutes and
examination of the sediment.

309
Q

Normal synovial fluid resembles:

Egg white
Normal serum
Dilute urine
Lipemic serum

A

Egg white

The word “synovial” comes from the Latin word for egg, ovum.
Normal viscous synovial fluid resembles egg white.

310
Q

When diluting a synovial fluid WBC count, all of the following are acceptable except:

Acetic acid
Isotonic saline
Hypotonic saline
Saline with saponin

A

Acetic acid

Traditional WBC diluting fluid cannot be used because it contains acetic acid that causes
the formation of mucin clots.
Normal saline can be used as a diluent. If it is necessary to lyse the RBCs, hypotonic saline
(0.3%) or saline that contains saponin is a suitable diluent.
Methylene blue added to the normal saline stains the WBC nuclei, permitting separation of
the RBCs and WBCs during counts performed on mixed specimens.

311
Q

Synovial fluid crystals associated with inflammation in dialysis patients
are:

Calcium pyrophosphate dihydrate
Calcium oxalate
Corticosteroid
Monosodium urate

A

Calcium oxalate

Calcium oxalate crystals in renal dialysis patients.

312
Q

Synovial fluid for crystal examination should be examined as a/an:

Wet preparation
Wright’s stain
Gram stain
Acid-fast stain

A

Wet preparation

Fluid is examined as an unstained wet preparation. One drop of fluid is placed on a precleaned glass slide and cover slipped. The slide can be initially examined under low
and high power using a regular light microscope.
Crystals may be observed in Wright’s-stained smears; however, this should not replace the
wet prep examination and the use of polarized and red-compensated polarized light for identification.

313
Q

The most frequently performed chemical test on synovial fluid is:

Total protein
Uric acid
Calcium
Glucose

A

Glucose

The most frequently requested test is the glucose determination, because markedly
decreased glucose values indicate inflammatory (group II) or septic (group III) disorders.

314
Q

An increase in the amount of serous fluid is called a/an:

Exudate
Transudate
Effusion
Malignancy

A

Effusion

315
Q

Fluid:serum protein and lactic dehydrogenase ratios are performed on serous fluids:

When malignancy is suspected
To classify transudates and exudates
To determine the type of serous fluid
When a traumatic tap has occurred

A

To classify transudates and exudates

Traditionally, a variety of laboratory tests have been used to differentiate between
transudates and exudates, including appearance, total protein, lactic dehydrogenase, cell
counts, and spontaneous clotting.
However, the most reliable differentiation is usually obtained by determining the fluid:
blood ratios for protein and lactic dehydrogenase

316
Q

A differential observation of pleural fluid associated with tuberculosis is:

Increased neutrophils
Decreased lymphocytes
Decreased mesothelial cells
Increased mesothelial cells

A

Decreased mesothelial cells

317
Q

A pleural fluid pH of 6.0 indicates:

Esophageal rupture
Mesothelioma
Malignancy
Rheumatoid effusion

A

Esophageal rupture

A pH value as low as 6.0 indicates an esophageal rupture that is allowing the influx of
gastric fluid.
Pleural fluid pH lower than 7.2 may indicate the need for chest-tube drainage, in addition
to administration of antibiotics in cases of pneumonia.
In cases of acidosis, the pleural fluid pH should be compared with the blood pH. Pleural
fluid pH at least 0.30 degrees lower than the blood pH is considered significant.

318
Q

Plasma cells seen in pleural fluid indicate:

Bacterial endocarditis
Primary malignancy
Metastatic lung malignancy
Tuberculosis infection

A

Tuberculosis infection

319
Q

The recommended test for determining whether peritoneal fluid is a
transudate or an exudate is the:

Fluid:serum albumin ratio
Serum ascites albumin gradient
Fluid:serum lactic dehydrogenase ratio
Absolute neutrophil count

A

Serum ascites albumin gradient

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 to detect transudates of
hepatic origin.

320
Q

Differentiation between bacterial peritonitis and cirrhosis is done by
performing a/an:

WBC count
Differential
Absolute neutrophil count
Absolute lymphocyte count

A

Absolute neutrophil count

Normal PERITONEAL FLUID WBC counts are less than 350 cells/μL, and the count
increases with bacterial peritonitis and cirrhosis.
To distinguish between those two conditions, an absolute neutrophil count should be
performed. An absolute neutrophil count >250 cells/μL or >50% of the total WBC count
indicates infection.

321
Q

Ascitic fluid TRANSUDATE:

Bacterial peritonitis
Cirrhosis
Intestinal perforation, ruptured appendix
Malignancy

A

Cirrhosis

322
Q

Detection of the CA 125 tumor marker in peritoneal fluid indicates:

Colon cancer
Ovarian cancer
Gastric malignancy
Prostate cancer

A

Ovarian cancer

323
Q

What is the primary cause of the normal increase in amniotic fluid as a
pregnancy progresses?

Fetal cell metabolism
Fetal swallowing
Fetal urine
Transfer of water across the placenta

A

Fetal urine

324
Q

How are specimens for FLM testing delivered to and stored in the laboratory?

Delivered on ice and refrigerated
Immediately centrifuged
Kept at room temperature
Delivered in a vacuum tube

A

Delivered on ice and refrigerated

Fluid for fetal lung maturity (FLM) tests should be placed in ice for delivery o the
laboratory and kept refrigerated.
Specimens for bilirubin testing must be immediately 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.
Specimens for cytogenetic studies or microbial studies must be processed aseptically and
maintained at room temperature or body temperature (37°C incubation) prior to analysis to
prolong the life of the cells needed for analysis.

325
Q

Why are amniotic specimens for cytogenetic analysis incubated at 37°C
prior to analysis?

To detect the presence of meconium
To differentiate amniotic fluid from urine
To prevent photo-oxidation of bilirubin to biliverdin
To prolong fetal cell viability and integrity

A

To prolong fetal cell viability and integrity

Specimens for cytogenetic studies or microbial studies must be processed aseptically and
maintained at room temperature or body temperature (37°C incubation) prior to analysis to
prolong the life of the cells needed for analysis.

326
Q

Plotting the amniotic fluid OD on a Liley graph represents the severity of
hemolytic disease of the newborn. A value that is plotted in zone II
indicates what condition of the fetus?

No hemolysis
Mildly affected fetus
Moderately affected fetus that requires close monitoring
Severely affected fetus that requires intervention

A

Moderately affected fetus that requires close monitoring

Notice that the Liley graph plots the A450 against gestational age and is divided into three zones that represent the extent of hemolytic severity.

Values falling in zone I indicate no more than a mildly affected fetus; those in zone II indicate moderate hemolysis and require careful monitoring anticipating an early delivery
or exchange transfusion upon delivery, whereas a value in zone III indicates severe
hemolysis and suggests a severely affected fetus.

Intervention through induction of labor or intrauterine exchange transfusion must be
considered when a D A450 is plotted in zone III.

327
Q

When severe HDN is present, which of the following tests on the amniotic
fluid would the physician NOT ORDER to determine whether the fetal
lungs are mature enough to withstand a premature delivery?

AFP levels
Foam stability index
Lecithin/sphingomyelin ratio
Phosphatidyl glycerol detection

A

AFP levels

Increased levels of alpha-fetoprotein (AFP) in both the maternal circulation and the
amniotic fluid can be indicative of fetal neural tube defects, such as anencephaly and
spina bifida.

328
Q

Amniocentesis may be indicated at 15 to 18 weeks’ gestation for the
following conditions to determine early treatment or intervention: CHECK
FOUR (4) BOXES

-Family history of chromosome abnormalities, such as trisomy 21 (Down
syndrome)
-Earlier pregnancy or child with birth defect
-Fetal lung maturity
-HDN caused by Rh blood type incompatibility
-Elevated maternal serum alpha-fetoprotein
-Abnormal triple marker screening test

A

-Family history of chromosome abnormalities, such as trisomy 21 (Down
syndrome)
-Earlier pregnancy or child with birth defect
-Elevated maternal serum alpha-fetoprotein
-Abnormal triple marker screening test

329
Q

Amniocentesis is indicated later in the pregnancy (20 to 42 weeks) to
evaluate: CHECK TWO (2) BOXES

-Family history of chromosome abnormalities, such as trisomy 21 (Down syndrome)
-Earlier pregnancy or child with birth defect
-Fetal lung maturity
-HDN caused by Rh blood type incompatibility
-Elevated maternal serum alpha-fetoprotein
-Abnormal triple marker screening test

A

-Fetal lung maturity
-HDN caused by Rh blood type incompatibility

330
Q

When performing an L/S ratio by thin-layer chromatography, a mature
fetal lung will show:

Sphingomyelin twice as concentrated as lecithin
No sphingomyelin
Lecithin twice as concentrated as sphingomyelin
Equal concentrations of lecithin and sphingomyelin

A

Lecithin twice as concentrated as sphingomyelin

The L/S ratio will rise to 2.0 or higher as the lecithin production increases to prevent alveolar collapse.

331
Q

A rapid immunologic test for FLM that does not require performance of
thin-layer chromatography is:

AFP levels
Amniotic acetylcholinesterase
Aminostat-FLM
Bilirubin scan

A

Aminostat-FLM

AMNIOSTAT FLM: IMMUNOLOGIC AGGLUTINATION TEST FOR PHOSPHATIDYLGLYCEROL

332
Q

The presence of phosphatidyl glycerol in amniotic fluid fetal lung maturity
tests must be confirmed when:

Hemolytic disease of the newborn is present
The mother has maternal diabetes
Amniotic fluid is contaminated by hemoglobin
Neural tube disorder is suspected

A

The mother has maternal diabetes

The presence of another lung surface lipid, phosphatidyl glycerol (PG), is also essential for
adequate lung maturity and can be detected after 35 weeks’ gestation.

The production of PG normally parallels that of lecithin, but its production is delayed in
cases of maternal diabetes.

In this circumstance, respiratory distress occurs in the presence of an L/S ratio of 2.0.
Therefore, a thin-layer chromatography lung profile must include lecithin, sphingomyelin,
and PG to provide an accurate measurement of FLM.

333
Q

OD 650 nm:

Bilirubin
Lamellar bodies
Lecithin
Oxyhemoglobin

A

Lamellar bodies

The presence of lamellar bodies increases the OD of the amniotic fluid. Specimens are
centrifuged at 2000 g for 10 minutes and examined using a wavelength of 650 nm.

334
Q

A lamellar body count of 50,000 correlates with:

Absent phosphatidyl glycerol and L/S ratio of 1.0
L/S ratio of 1.5 and absent phosphatidyl glycerol
OD at 650 nm of 1.010 and an L/S ratio of 1.1
OD at 650 nm of 0.150 and an L/S ratio of 2.0

A

OD at 650 nm of 0.150 and an L/S ratio of 2.0

The number of lamellar bodies present in the amniotic fluid correlates with the amount of
phospholipid present in the fetal lungs.

The presence of lamellar bodies increases the OD of the amniotic fluid. Specimens are
centrifuged at 2000 g for 10 minutes and examined using a wavelength of 650 nm, which
rules out interference from hemoglobin but not other contaminants, such as meconium.

An OD of 0.150 has been shown to correlate well with an L/S ratio of greater than or equal
to 2.0 and the presence of phosphatidyl glycerol.

A consensus protocol for noncentrifuged samples considers LBCs greater than 50,000/uL
an indication of FLM and values below 15,000/uL as immature.

335
Q

The normal composition of feces includes all of the following except:

Bacteria
Blood
Electrolytes
Water

A

Blood

The normal fecal specimen contains bacteria, cellulose, undigested foodstuffs, GI
secretions, bile pigments, cells from the intestinal walls, electrolytes, and water.

336
Q

The normal brown color of the feces is produced by:

Cellulose
Pancreatic enzymes
Undigested foodstuffs
Urobilin

A

Urobilin

337
Q

Stool specimens that appear ribbon-like are indicative of which condition?

Bile duct obstruction
Colitis
Intestinal constriction
Malignancy

A

Intestinal constriction

338
Q

What is the fecal test that requires a 3-day specimen?

Fecal occult blood
APT test
Elastase 1
Quantitative fecal fat testing

A

Quantitative fecal fat testing

Quantitative fecal analysis requires the collection of at least a 3-day specimen. The patient
must maintain a regulated intake of fat (100 g/d) before and during the collection period.

339
Q

What is the significance of an APT test that remains pink after addition of
sodium hydroxide?

Fecal fat is present
Fetal hemoglobin is present
Fecal trypsin is present
Vitamin C is present

A

Fetal hemoglobin is present

In the presence of alkali-resistant fetal hemoglobin, the solution remains pink (HbF),
whereas denaturation of the maternal hemoglobin (HbA) produces a yellow-brown
supernatant after standing for 2 minutes.

340
Q

A patient whose stool exhibits increased fats, undigested muscle fibers,
and the inability to digest gelatin may have:

Bacterial dysentery
A duodenal ulcer
Cystic fibrosis
Lactose intolerance

A

Cystic fibrosis

341
Q

A stool specimen collected from an infant with diarrhea has a pH of 5.0.
This result correlates with a:

Positive APT test
Negative trypsin test
Positive Clinitest
Negative occult blood test

A

Positive Clinitest

Normal stool pH is between 7 and 8; however, increased use of carbohydrates by intestinal
bacterial fermentation increases the lactic acid level and lowers the pH to below 5.5 in
cases of carbohydrate disorders.

342
Q

What is the recommended number of samples that should be tested to
confirm a negative occult blood result?

One random specimen
Two samples taken from different parts of three stools
Three samples taken from the outermost portion of the stool
Three samples taken from different parts of two stools

A

Two samples taken from different parts of three stools

Two samples from three different stools should be tested before a negative result is
confirmed.

343
Q

A positive amine (Whiff) test is observed in which of the following syndromes?

Bacterial vaginosis
Vulvovaginal candidiasis
Atrophic vaginitis
Desquamative inflammatory vaginitis

A

Bacterial vaginosis

Amine (Whiff) Test
1. Apply one drop of the saline vaginal fluid suspension to the surface of a clean glass
slide.
2. Add one drop of 10% KOH directly to the vaginal sample.
3. Holding the slide in one hand, gently fan above the surface of the slide with the other
hand and assess for the presence of a fishy amine odor.
4. Report as positive or negative.
Positive: The presence of a fishy odor after adding KOH.
Negative: The absence of a fishy odor after adding KOH.

344
Q

The presence of fetal fibronectin in vaginal secretions between 24 and 34
weeks’ gestation is associated with:

Bacterial vaginosis
Candidiasis
Desquamative inflmmatory vaginitis
Preterm delivery

A

Preterm delivery

The presence of fetal fibronectin in vaginal secretions between 24 and 34 weeks’ gestation is associated with preterm delivery.