Lab Management 10% Flashcards

1
Q

TRUE about the preanalytical phase?
A. Refers to all the complex steps that must take place before a sample
can be analyzed
B. Phase where 32 to 75 % of all testing errors occur
C. Most frequent errors include improperly filling the tube, placing
specimen in wrong containers and selecting incorrect test
D. A and C
E. All of the above

A
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2
Q

Clinical laboratories are regulated through the

A

Clinical Laboratory Improvement Act of 1988

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3
Q

Leader Vs. Manager. Implementer.

A

Manager

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4
Q

Leader Vs. Manager. Organizer and developer

A

Leader

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5
Q

Risk taker

A

Leader

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6
Q

Ask how and when

A

manager

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6
Q

watches bottom line

A

manager

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7
Q

accepts status quo

A

manager

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8
Q

good soldier

A

manager

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9
Q

does the right thing

A

leader

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10
Q

does things right

A

manager

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11
Q

SWOT analysis. Increased test volume will decrease cost per test

A

strength

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12
Q

swot analysis. Competition from other local hospital laboratories

A

threats

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12
Q

morale issues

A

weaknesses

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13
Q

having access to hospital marketing department

A

opportunities

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14
Q

Traditional Thinking VS. TQM Thinking. Error-free quality

A

TQM

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15
Q

Traditional Thinking VS. TQM Thinking. Department focused.

A

Traditional Thinking

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15
Q

Traditional Thinking VS. TQM Thinking. Quality as means to lower cost.

A

TQM Thinking

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16
Q

Traditional Thinking VS. TQM Thinking. Defects by workers.

A

Traditional thinking

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17
Q

Traditional Thinking VS. TQM Thinking. Empowered worker

A

TQM Thinking

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18
Q

Traditional Thinking VS. TQM Thinking. Status Quo

A

Traditional Thinking

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19
Q

Traditional Thinking VS. TQM Thinking. Manage by fact.

A

TQM Thinking

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20
Q

Traditional Thinking VS. TQM Thinking. Intangible Quality.

A

Traditional Thinking

21
Q

Traditional Thinking VS. TQM Thinking. US relationship.

A

TQM Thinking

22
Traditional Thinking VS. TQM Thinking. End process focus.
Traditional Thinking
23
Traditional Thinking VS. TQM Thinking. Proactive Systems.
TQM Thinking
23
Within the Six Sigma process, defects are generally measured by defects per million opportunities (DPMO), The goal of six sigma is to reach how many DPMOs?
3.4 DPMO
24
This is a system for reducing waste (non valued activities) in production of manufacturing process
Lean Six Sigma
25
Give the suggested guideline for retention of the following. Requisitions
2 years
26
Give the suggested guideline for retention of the following. Quality Control Records
2 years
27
Give the suggested guideline for retention of the following. Blood bank QC records
5 years
28
Give the suggested guideline for retention of the following. Blood bank deferred donor records.
Indefinite
29
Give the suggested guideline for retention of the following. Urine
24 hours
30
Give the suggested guideline for retention of the following. Serum/CSF/Body fluids
48 hours
31
Give the suggested guideline for retention of the following. Cytology slides
5 years
32
Give the suggested guideline for retention of the following. FNA slides
10 years
33
Give the suggested guideline for retention of the following. Paraffin blocks.
10 years
34
Give the suggested guideline for retention of the following. Flo cytometry plots/histograms
10 years
35
Give the suggested guideline for retention of the following. cytogenetic reports/images
20 years
36
Order of draw For MULTIPLE BLOOD EXTRACTIONS
1 Yellow Top 2 Blue Top 3 Red Top 4 Green Top 5 Lavander Top (hematology cell counts and cell morphology) 6 Gray Top (best used for measurements of GLUCOSE)
37
At what time should the specimen be drawn for plasma cortisol determination?
8AM, 8PM
38
The presence of visible hemolysis will significantly increase serum level of which electrolyte?
Potassium
39
What is the anticoagulant of choice for hematology cell counts and cell morphology?
EDTA
40
Gray to tubes are best used for measurements of
GLUCOSE.
41
What is the content of GRAY TOP?
potassium citrate
42
43
Types of Water Based on American Society of Testing and Materials
Type I Reagent Water: The Purest Form Type II Reagent Water: General Laboratory Use Type III Reagent Water: Less Critical Applications Type IV Reagent Water: Non-Critical Applications
44
Typically used for sensitive analytical procedures like atomic absorption, gas chromatography, and trace analysis.
Type I Reagent Water: The Purest Form
45
Type I Reagent Water Purity Requirements
Purity Requirements: Requires a resistivity of at least 18 MΩ-cm at 25°C and a total organic carbon (TOC) level of less than 50 ppb.
46
Type II Reagent Water: General Laboratory Use Purity Requirements
Purity Requirements: Should have a resistivity of at least 1 MΩ-cm at 25°C, with total organic carbon (TOC) levels typically less than 50 ppb.
47
Type III Reagent Water: Less Critical Applications Purity Requirements
Purity Requirements: Requires a resistivity of at least 4 MΩ-cm at 25°C, with TOC levels expected to be less than 200 ppb.
48
Type IV Reagent Water: Non-Critical Applications Purity Requirements
Purity Requirements: Requires a minimum resistivity of 0.2 MΩ-cm at 25°C, with no specific TOC limit.
49
50
Microbiological Quality Sub-Classifications: A, B, and C The ASTM D1193-06 standard also includes sub-classifications (A, B, and C) that define acceptable microbiological quality levels, particularly regarding Heterotrophic Bacteria Count (CFU/ml) and Endotoxin (EU/ml) standards.
Option A: Specifies the highest level of purity, with stringent limits on contaminants. Suitable for high-precision analytical methodologies like mass spectrometry. Option B: Slightly less stringent but still suitable for most analytical applications requiring high sensitivity. Option C: The least stringent, used for general laboratory applications that require high purity but not ultra-low levels of contaminants.
51