350 REAL QUESTIONS WITH VERIFIED
ANSWERS & RATIONALES | MEDICAL
LABORATORY SCIENTIST CERTIFICATION
PREP | GRADED A+ (MOST RECENT!!)
Section 1: General Laboratory & Quality Control
1. A laboratory receives a serum specimen for potassium testing that is visibly
hemolyzed. What is the most likely effect on the potassium result, and why?
A) Falsely decreased due to potassium movement into cells
B) Falsely increased due to potassium released from RBCs
C) No significant effect because serum is used
D) Falsely decreased due to binding of potassium to hemoglobin
Rationale: Hemolysis releases intracellular potassium from red blood cells into the
serum, causing a falsely elevated potassium result. The intracellular concentration of
potassium is approximately 20 times higher than in serum, so even slight hemolysis
can significantly increase the measured potassium level.
2. According to CLIA '88, which of the following is a requirement for laboratory
quality control?
A) Running controls only when a new lot of reagents is opened
B) Running at least two levels of controls each day of patient testing
C) Running controls only after instrument maintenance
D) Running controls only when patient results are abnormal
Rationale: CLIA '88 requires that laboratories run at least two levels of controls (e.g.,
normal and abnormal) each day of patient testing to ensure the accuracy and precision
of test results. Controls must be run at regular intervals, not just when new reagents
are opened or after maintenance.
,3. A technologist is reviewing a Levey-Jennings chart and observes that 6
consecutive control values have fallen on the same side of the mean. This
pattern is best described as:
A) Shift
B) Trend
C) Random error
D) Outlier
Rationale: A shift occurs when a series of control observations remains on one side of
the established mean, suggesting a persistent systematic change. A trend is a gradual
movement in one direction. Random error produces unpredictable variation, while
carryover occurs when material from one specimen influences a subsequent specimen.
4. Which calculation expresses standard deviation as a percentage of the mean?
A) Coefficient of variation
B) Reference interval
C) Mean deviation
D) Analytical sensitivity
Rationale: The coefficient of variation is calculated by dividing the standard deviation
by the mean and multiplying by 100. It allows comparison of imprecision between
methods with different means. Standard deviation alone describes absolute dispersion,
whereas coefficient of variation expresses dispersion relative to the magnitude of the
measured values.
5. A laboratory method has a mean control value of 100 mg/dL and a standard
deviation of 5 mg/dL. What is the coefficient of variation?
A) 0.05%
B) 5%
C) 20%
D) 500%
Rationale: Coefficient of variation equals standard deviation divided by the mean,
multiplied by 100. Here, 5 ÷ 100 × 100 equals 5%. The value therefore indicates that
the method's standard deviation represents 5% of its mean measurement, providing a
useful measure of relative imprecision.
,6. Which organization establishes and enforces the Clinical Laboratory
Improvement Amendments requirements for laboratory testing in the United
States?
A) OSHA
B) HIPAA
C) FDA
D) CMS
Rationale: The Centers for Medicare & Medicaid Services administers CLIA
requirements for laboratory testing performed on human specimens. OSHA primarily
addresses workplace safety, HIPAA addresses protected health information, and the
FDA regulates many medical products and devices. CLIA establishes quality standards
intended to ensure reliable laboratory results.
7. Which information is most directly protected by HIPAA?
A) A patient's protected health information
B) The laboratory's reagent inventory
C) An analyzer's maintenance schedule
D) A centrifuge's operating speed
Rationale: HIPAA establishes requirements concerning protected health information
and its privacy and security. Patient-identifying laboratory results can constitute
protected health information. Reagent inventories, maintenance schedules, and
equipment settings are operational information and are not themselves the central
subject of HIPAA's privacy protections.
8. A chemical reagent bottle has an unfamiliar hazard symbol. What is the most
appropriate resource for determining its hazards and recommended
precautions?
A) The laboratory's monthly workload report
B) The specimen accession log
C) The Safety Data Sheet
D) The patient chart
Rationale: A Safety Data Sheet provides standardized information about chemical
hazards, handling, storage, exposure controls, and emergency procedures. It is an
essential laboratory safety resource when working with hazardous chemicals. Patient
, records, workload reports, and accession logs do not provide the required chemical-
safety information.
9. Which microscope component primarily controls the amount of light
reaching the specimen?
A) Condenser iris diaphragm
B) Ocular lens
C) Mechanical stage
D) Revolving nosepiece
Rationale: The iris diaphragm regulates the diameter of the light beam passing through
the condenser, thereby controlling the amount of light that reaches the specimen. The
ocular lens magnifies the image, the mechanical stage holds and moves the slide, and
the revolving nosepiece allows selection of different objective lenses.
10. A technologist is performing a manual differential and observes that the
peripheral blood smear has uneven staining with pink edges and blue centers.
The most likely cause is:
A) Prolonged fixation
B) Inadequate drying of the smear
C) Buffers with incorrect pH
D) Excessive staining time
Rationale: Uneven staining with pink edges and blue centers (pH artifact) is caused by
buffers with incorrect pH. Wright's stain is pH-sensitive; acidic buffers produce pink/red
cells while alkaline buffers produce blue cells. Prolonged fixation causes pale staining;
inadequate drying causes poor morphology; excessive staining causes overly dark cells.
11. What are Class A fire extinguishers used for?
A) Electric equipment
B) Flammable liquids
C) Ordinary combustibles
D) Powdered metal (combustible) material
Rationale: Class A fire extinguishers are classified as ordinary combustible. Additionally,
Class A fire extinguishers have a numerical rating based on UL-conducted tests and