WK 1 Flashcards

(68 cards)

1
Q

quantitative lab result consists of

A

Actual test value
Unit

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2
Q

Systeme International d’Unites (SI)
was adapted in

A

1960

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3
Q

subclasses of si

A
  1. basic unit
  2. derived unit
  3. selected accepted si ntiq
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4
Q

Some non-SI units are so widely used that they
have become acceptable for use within the SI
system. These include units

A

hour, minute, day,
gram, liter, and plane angles expressed as
degrees.

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5
Q

describe si unit prefix

A

Uses standard prefixes for those of the same unit
or to indicate decimal fraction

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6
Q

Prefixes smaller than basic unit have a

A

negative
exponent and vice versa

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7
Q

Reporting of laboratory results is often expressed
in terms of

A

substance concentration (e.g., moles)
or the mass of a substance (e.g., mg/dL, g/dL, g/L,
mmol/L, and IU) rather than in SI units

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8
Q

he laboratory and the rest of medicine are moving
toward adopting universal standards promoted by
the

A

International Organization for
Standardization

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9
Q

Develops standards of practice, definitions, and
guidelines that can be adopted by everyone in a
given field, providing for more uniform
terminology.

A

iso

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10
Q

Most instrument manufacturers make the
reagents in

A

ready-to-use form or “kit” in which all
necessary reagents and respective storage
containers are prepackaged as a unit, requiring
only the addition of water or buffer for
reconstitution

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11
Q

reagent preparation use

A

i it is used in research and development,
biotechnology applications, specialized analyses,
or method validation.

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12
Q

grades of purity

A
  1. reagent grade or analytic grade
  2. ultrapure, chemicaly pure
  3. united states pharmacopeia
  4. national formulary
  5. tecnical or commercial grade
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13
Q

chemical that are suitable for use in
most analytic
laboratory procedures

A

reagent grade/analyic reagent

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14
Q

chemical that have additional
purification steps for
use in specific
procedures such as
chromatography,
immunoassays,
molecular diagnostics,
standardization, or
other techniques

A

ultrapure, chemically
pure (CP

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15
Q

Used in manufacturing
drugs

A

United States
Pharmacopeia
(USP) and National Formulary
(NF)

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16
Q

used primarily in
manufacturing and
should never be used
in the clinical
laboratory

A

technical or
commercial grade

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17
Q

These reagents may have
designations of HPLC
(high-performance liquid
chromatography) or
chromatographic on their labels.

A

ultrapure, chemically pure (CP)

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18
Q

impurity limitations are not stated,
and the preparation of these
chemicals is not uniform.

A

ultrapure, chemically pure (CP)

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19
Q

. It is not
recommended that clinical
laboratories use these chemicals
for reagent preparation unless
further purification or a reagent
blank is included.

A

ultrapure, chemically pure (CP)

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20
Q

limitations established for this
group of chemicals are based
only on the criterion of not being
injurious to individuals

A

United States Pharmacopeia (USP) and National Formulary (NF)

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21
Q

chemical that should never be used in the
clinical laboratory.

A

technical or commercial grade

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22
Q

established specifications for AR grade
chemicals, and chemical manufacturers must
either meet or exceed these requirements

A

American Chemical Society
(ACS)

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23
Q

organic reagent

A

the labels on reagents should clearly state the
actual impurities for each chemical lot or list the
maximum allowable impurities. The label should
also include one of the following designations: AR
or ACS or For laboratory use or ACS Standard-Grade Reference Materials.

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24
Q

grades of organic reagent

A

These grades include;
1. A practical grade
2. CP,
3. reagent grade (ACS), w

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25
require manufacturers to indicate any physical or biological health hazards and precautions needed for the safe use, storage, and disposal of any chemical.
laws related to the Occupational Safety and Health Administration (OSHA),
26
osha menas
Occupational Safety and Health Administration (OSHA),
27
organic reagent with some impurities
practical grade
28
approaches the purity level of reagent-grade chemicals; spectroscopic (spectrally pure) and chromatographic grade organic reagents; and
cp
29
reagent which is certified to contain impurities below established ACS levels.
reagent grade (ACS)
30
Manufacturers are required to provide a _______ . IT must be readily available to ensure the safety of laboratorians.
Manufacturers are required to provide a Safety Data Sheet (SDS). A copy of the SDS must be readily available to ensure the safety of laboratorians.
31
involved in the analysis of biochemical byproducts found in biological fluids, such as serum, plasma, or urine.
CLINCHEM
32
highly purified chemical that can be measured directly to have an exact known concentration and purity.
PRIMARY STANDARD
33
has certified standard reference materials (SRMs) that are used in place of ACS primary standard materials due to tolerance limitations of some biologic constituents.
the National Institute of Standards and Technology (NIST)
34
SRM means
standard reference material
35
nist meand
national institute of standards and technology
36
The chemical composition of these substances is certified; however, they may not have the purity of a primary standard.
srm reagent
37
it can be used in place of an ACS primary standard in clinical work and is often used to verify calibration or accuracy/bias assessments
srm
38
Many manufacturers use a ____________when producing calibrators and standard materials.
NIST “traceable to NIST” SRM
39
used for linearity studies to determine the relationship between the standard’s concentration and the instrument result. This test is required when a new test or new test methodology is introduced
srm
40
is a process that pairs an analytical signal with a concentration value of an analyte. -
calibration
41
calibration of an instrument can be made by
Using a kit or by diluting a known stock solution.
42
- Most used reagent in the laboratory
water
43
Water purification methods include:
distillation, ion exchange, reverse osmosis,ultrafioltration, UV light, sterilization and ozone treatment
44
Most procedures, along with reagent and control preparation requires substantially purified water known as
reagent-grade water.
45
According to _______ reagent-grade water based on its use rather than the method od purification or preparation.
CLSI or Clinical and laboratory standards institute,
46
- Categories of reagent-grade water:
1. Clinical laboratory reagent water (CLRW), 2. special reagent water (SRW), 3. instrument feed water, 4. water supplied by method manufacturer, 5. autoclave and wash water, and 6. commercially bottled purified water
47
s requires laboratories to define the specific type of water required for each of its testing procedures and requires water quality testing atleast annually
college of american pathologists
48
Water quality testing routinely includes
monitoring microbial colony-forming units/ml and may include other parameters
49
Purified to remove almost all organic materials using a technique where water is boiled and vaporised
distilled water
50
Excellent in removing particulate matter, microorganisms and any pyrogens or endotoxins (like ultrafiltration and nanofiltration
distilled water
51
Produced using either an anion- or cation-exchange resin, followed by replacement of the removed ions with hydroxyl or hydrogen ions
Deionized water
52
Purified from previously treated water such as prefiltered or distilled water
deionized water
53
excellent at removing dissolved ionized solids and dissolved gases.
deionized water
54
uses pressure to force water through a semipermeable membrane, producing a filtered product.
reverse osmosis
55
may be used for the pretreatment of water, however, it does not remove dissolved gases.
reverse osmosis
56
remove particulate matter from municipal water supplies before any additional treatments
filtration waer
57
Filtration cartridges can be composed of
glass, cotton, or activated charcoal, which removes organic materials and chlorine.
58
Some have submicron filters (≤0.2 μm), which remove any substances larger than the filter’s pores, including bacteria
filtration - The submicron filter may be better suited after distillation, deionization, or reverse osmosis treatment. - The submicron filter may be better suited after distillation, deionization, or reverse osmosis treatment.
59
removes some trace organic material or sterilization processes at specific wavelengths, can destroy bacteria when used as part of a system but may leave behind some residual products.
Ultraviolet oxidation
60
This technique is often followed by other purification processes
Ultraviolet oxidation
61
s acceptable for glassware washing but not for analysis or reagent preparation.
Autoclave wash water
62
used for specific techniques like the HPLC, molecular diagnostics, or mass spectrophotometry, which may require specific parameters for the analysis. ●
srw/special reagent water
63
All SRW should meet
CLRW standards and, depending on the applicationshould be stored in a manner that reduces any chemical or bacterial contamination and for short periods,
64
Testing procedures to determine the quality of reagent-grade water include
measurements of resistance, pH, colony counts on selective and nonselective media for the detection of bacterial contamination, chlorine, ammonia, nitrate or nitrite, iron, hardness, phosphate, sodium, silica, carbon dioxide, chemical oxygen demand, and metal detection.
65
Some accreditation agencies recommend that laboratories
document culture growth, pH, and specific resistance on water used in reagent preparation
66
measured because pure water, devoid of ions, is a poor conductor of electricity and has increased resistance
resistance
67
The relationship of water purity to resistance is
linear; generally, as purity increases, so does resistance
68