Unit 3.6 PRINCIPLES OF AUTOMATION IN HEMATOLOGY Flashcards

1
Q

refers to the use of laboratory instruments and processing equipment to perform clinical laboratory assays with only minimal involvement of the medical technologist

A

Automation

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2
Q

2 Classic automated methods for counting cells

A
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3
Q

Coulter Counter

A

Electronic Impedance/Resistance

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4
Q

Technicon Autoanalyzer; Ortho Diagnostic; Fisher Autocytometer

A

Optical Detection/Light Scattering

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5
Q

The Basic Components Common to Most Hematology Analyzers

A
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6
Q

includes the aspirating unit, dispensers, dilutors, mixing chambers, aperture baths, and/or flow cells, and hemoglobinometer

A

Hydraulics

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7
Q

Vacuum and pressures for operating values and moving the sample through the system

A

Pneumatics

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8
Q

Electronic analyzers and computing circuitry for processing data

A

Electrical systems

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9
Q

Blood is diluted in an isotonic solution and drawn through an aperture.

A

ELECTRIC IMPEDANCE

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10
Q

Since cells are nonconductive, the passage of cell through the aperture increases the resistance (impedance) of the electrical path between 2 electrodes that are located on each side of the aperture.

A

ELECTRIC IMPEDANCE

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11
Q

Changes in electrical resistance are counted as

A

voltage pulses.

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12
Q

Number of Voltage pulses is directly proportional to the

A

number of cells/cell cou nt.

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13
Q

Amplitude/height/size of the pulse is directly proportional to the

A

volume of the cell

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14
Q

a diluted blood specimen passes through a steady stream through which a beam of LASER light is focused.

A

LIGHT SCATTERING

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15
Q

As each cell passes through the s ensing zone, it scatters light. Scattered light is converted into an electrical pulse.

A

LIGHT SCATTERING

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16
Q

LIGHT SCATTERING

Number of pulses is directly proportional to

A

cell count

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17
Q

LIGHT SCATTERING

Patterns of scatter are measured at various angles to obtain information on the

A

cell structure.

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18
Q

Dilutions :
WBC= (?) (usual dilution, but may vary among manufacturers)
RBC=

A

1:500
1:50,000

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19
Q

graphic representation of cell size versus cell frequency

A

HISTOGRAMS:

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20
Q

produced in RBC, WBC & platelet measurements

A

HISTOGRAMS:

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21
Q

Derived from the histogram are

A

blood Indices as well as WBC differential

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22
Q

RBC histogram:

A

36 360 fL

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23
Q

It IS where MCV & RDW are derived

A

RBC Histogram

24
Q

Histogram appears (?) when cell population is (?) if there is more variation in the size of the cell

A

SYMMETRICAL/Gaussian shape

homogenous WIDER or FLATTENED shape

25
Platelet histogram:
2 - 20 fL
26
Where MPV & PDW are derived
PLATELET Histogram
27
(used in the 3-parameter Differential count)
WBC Histogram
28
WBC Populations on the histogram 35 - 90 fL: 90 - 160 fL: 160 - 450 fL:
Lymphocytes Mononuclears (Mid cells) - (Monocytes, Promyelocytes, Myelocytes, Blasts) Granulocytes - (Mature WBC, Blasts, Metamyelocyte, Bands)
29
a visual display of 2-cell characteristics such as internal cell complexity and relative size
SCATTERGRAM / CYTOGRAM / DOT PLOTS
30
It is used in the 5-part automated differential.
SCATTERGRAM / CYTOGRAM / DOT PLOTS
31
SCATTERGRAM / CYTOGRAM / DOT PLOTS Cytochemical stains Peroxidase: Alcian blue/Toluidine blue: Lipase/Esterase:
PMN & other cells basophil monocytes
32
What are the indications of histograms with left elevation? with right elevation?
33
What are the bases of separation of cells in a scattergram? _________________________ _________________________
34
WBCs are differentiated into 5 traditional categories
35
Cyanmethemoglobin principle
HEMOGLOBIN
36
HEMOGLOBIN At what wavelength? ________
37
Indirect method (calculated)
HEMATOCRIT
38
HEMATOCRIT What is the formula? ________
39
MCH & MCHC are calculated from measure & derived values RDW
INDICES
40
From where is RDW derived? ________
INDICES
41
Aperture plugs
Causes of POSITIVE errors
42
Extraneous electrical pulses (improperly grounded or shielded equipment)
Causes of POSITIVE errors
43
Bubbles in the sample (vigorous mixing)
Causes of POSITIVE errors
44
Improper setting of aperture current or threshold
Causes of POSITIVE errors
45
Agglutinated red cells or platelets
Causes of POSITIVE errors
46
Excessive lysing of RBCs
Causes of NEGATIVE errors
47
Improper setting of aperture current or threshold
Causes of NEGATIVE errors
48
Agglutination of RBCs, WBCs or platelets
Causes of NEGATIVE errors
49
a quality control check in which the averages of the MCV, MCH, MCHC are tracked for batches of 20 patients
XB
50
Patients test results are compared to his previous results
Delta Checks
51
: suggest cells types/abnormalities
Flags
52
indicate investigation before final reporting.
Flags
53
What are the causes of falsely increases and falsely decreased automated cell counts? – RBC, WBC & Platelets (Henry's Clinical Diagnosis and Management by Laboratory Methods)
54
What conditions may affect automated hemoglobin measurement? Explain each
55
(What are the indications for)/When should we perform a manual peripheral blood smear review?