1 SAFETY AND QUALITY ASSESSMENT

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120 Terms

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SAFETY PROCEDURE MANUALS
Must be readily available in the laboratory that
describes the safety policies
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Centers for Disease Control and Prevention
(CDC) and the Occupational Safety and Health Administration
(OSHA)
Safety procedure manuals must be readily
available in the laboratory that describe the safety policies mandated by?
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laboratory personnel
strict adherence to these guidelines by
( ) is essential.
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annually
laboratory director
The manual must be updated and reviewed ( ) by the ( )
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Clinical
and Laboratory Standards Institute (CLSI)
provides the
guidelines for writing these procedures and policies.
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chain of infection
how microorganisms
are transmitted
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infection control
procedures to control and monitor infections occurring within
their facilities
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infectious agent
reservoir
portal of exit
means of transmission
portal of entry
susceptible host
The
chain of infection requires a continuous link between an
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bacteria
fungi
parasites
viruses
Infectious
agents consist of ( )
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reservoir
the location of potentially harmful microorganisms,
such as a contaminated clinical specimen or an infected
patient.
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Fomites
inanimate object that can be reservoir
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spores
Some microorganisms form
( ) or become inactive when conditions are not ideal and
wait until a suitable reservoir is available.
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mucous membranes of nose, mouth, and eyes, and blood or other body fluids
The infectious agent
must have a way to exit the reservoir to continue the chain
of infection. This can be through the
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Direct contact
Airborne
Droplet
Vehicle
Vector
Means of transmission include
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Direct contact
the unprotected host touches the patient,
specimen, or a contaminated object (reservoir)
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Airborne
inhalation of dried aerosol particles circulating
on air currents or attached to dust particles
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Droplet
the host inhales material from the reservoir (e.g.,
aerosol droplets from a patient or an uncapped centrifuge
tube, or when specimens are aliquoted or spilled)
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Vehicle
ingestion of a contaminated substance (e.g., food,
water, specimen)
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Vector
from an animal or insect bite
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portal of exit
breaks in the skin
open wounds
The portal
of entry can be the same as the ( ), which includes
the mucous membranes of the nose, mouth, and eyes, ( ), and ( ).
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patient specimens
In the clinical laboratory, the most direct contact with a source of infection is through contact with ( )
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biologic safety.
Preventing completion of the chain of infection is a primary objective of ( )
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hepatitis B virus (HBV)
hepatitis C virus (HCV)
human immunodeficiency virus (HIV)
Different blood borne pathogen
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Universal Precautions
Regulation in BBP draft by CDC nd OSHA
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1987
When does UP created
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all patients are considered to be possible carriers of bloodborne pathogens
Universal Precaution states that
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gloves
face shield
puncture-resistant containers
The UP guideline recommends wearing ( )
when collecting or handling blood and body fluids contaminated with blood and wearing ( ) when there is danger of blood splashing on mucous membranes and when disposing of all needles and sharp objects in ( ).
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urine and body fluids not visibly contaminated by blood
Ano ang hindi kasali sa UP?
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body substance isolation
The modification of UP
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Consider all specimen as infectious
Ano ang meron sa BSI na wala sa UP?
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Not performing handwashing after removing gloves except if it is visually contaminated
A major disadvantage of BSI
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Standard precaution
Combination of UP and BSI
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CDC
Healthcare Infection Control Practices Advisory Committee (HICPAC)
Created SP
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1996
When does SP created?
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The Occupational Exposure to Blood-Borne Pathogens Standard
These
controls are required by OSHA to be provided by or mandated
by the employer for all employees.
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PERSONAL PROTECTIVE EQUIPMENT (PPE)
Providing laboratory coats, gowns, face shields

and gloves to employees and laundry facilities for non-
disposable protective clothing.
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hepatitis B virus
Providing immunization for ( ) free of
charge.
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medical check up
Providing ( ) follow-up to employees who
have been accidentally exposed to blood-borne pathogens.
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annual training
Documenting ( ) of employees in
safety standards.
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safer needle devices
Documenting evaluations and implementation of
( )
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new devices
Involving employees in the selection and
evaluation of ( ) and maintaining a list of those
employees and the evaluations.
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sharp injury log
Maintaining a ( ) including the type
and brand of safety device, location and description of the
incident and confidential employee follow-up.
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biohazard symbol
All biologic waste, except urine, must be placed in appropriate
containers labeled with the ( )
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incineration
autoclaving
pickup by a certified hazardous waste company
The waste is then decontaminated
following institutional policy
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laboratory sink
water
Urine may be discarded by pouring it into a ( ) under a Plexiglas countertop shield and must be flushed with ( )
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sodium hypochlorite
Disinfection of the sink using a
1:5 or 1:10 dilution of sodium hypochlorite should be performed daily
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1 month
Sodium hypochlorite dilutions stored in plastic
bottles are effective for ( ) if protected from light after preparation
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puncture-resistant, leak-proof container
All sharp objects must be
disposed in ( ) with the
biohazard symbol.
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Sharp objects
Can caused the transfer of BBP
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needles
lancets
broken glassware
Sharp objects in the lab
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overfilled
safe capacity mark
The biohazard sharp containers should not be ( ) and must always be
replaced when the ( ) is reached.
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presumed hazardous
Every chemical in the workplace should be ( )
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15 minutes
When skin contact occurs, the best first aid is to flush the area with large amounts of water for at least ( ), then seek
medical attention
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Chemical spill kits
( ) containing protective apparel, nonreactive
absorbent material, and bags for disposing of contaminated
materials should be available for cleaning up spills.
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Acid
water
( ) should always be added to ( ) to avoid the
possibility of sudden splashing caused by the rapid generation of heat in some chemical reactions.
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goggles
fume hood
Wearing( ) and preparing reagents under a ( ) are recommended safety
precautions.
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chemical hygiene plan (CHP)
OSHA also requires all facilities that use hazardous chemicals to have a written ( ) available to employees
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Chemical Hygiene Officer
responsible for implementing and documenting compliance with the CHP
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emergency shower
eye wash station
Chemical safety aids
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Standard System for the Identification of the Fire Hazards of Materials
This symbol system is used to inform
firefighters of the hazards they may encounter with fires in
a particular area
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NFPA 704
The diamond-shaped, color-coded symbol
contains information relating to health, flammability, reactivity,
and personal protection/special precautions.
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National Fire Protection Association (NFPA)
Created Standard System for the Identification of the Fire Hazards of
Materials,
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Material Safety Data Sheets
Collection of information all about the chemicals in the laboratory
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radioisotopes
Radioactivity may be encountered in the clinical laboratory
when procedures using ( ) are
performed
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cumulative
effects of radiation are ( )
related to the amount of exposure
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time
distance
shielding
The amount of radiation
exposure is related to a combination of ( ), ( ), and
( )
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measuring devices
Persons working in a radioactive environment are
required to wear ( ) to determine the amount
of radiation they are accumulating.
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unplugged
dry
Equipment that has become wet should be ( ) and
allowed to ( )completely before reusing.
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cleaning
three-pronged plugs
Equipment also should be unplugged before ( ). All electrical equipment
must be grounded with ( ).
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nonconductive glass or wood object
Turning off the circuit breaker, unplugging
the equipment, or moving the equipment using a ( ) are safe procedures to follow
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Joint Commission (JC)
The ( ) requires that all health-care
institutions post evacuation routes and detailed plans
to follow in the event of a fire.
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Rescue
Alarm
Contain
Extinguish or Evacuate
acronym RACE
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safety cabinets
explosion-proof refrigerators
heat
Flammable chemicals
should be stored in ( ) and ( ),
and cylinders of compressed gas should be located
away from ( ) and securely fastened to a stationary device to
prevent accidental capsizing.
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burning material
fire extinguisher
The NFPA classifies fires with regard to the type of ( ). It also classifies the type of ( ) that is used to control them
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multipurpose ABC fire extinguishers
The ( ) are the most common, but the label should always be checked before using
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Pull pin
Aim at the base of the fire
Squeeze handles
Sweep nozzle side to side
The acronym
PASS can be used to remember the steps in the operation
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quality assessment
refers to the overall process
of guaranteeing quality patient care and is regulated throughout
the total testing system
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Quality system
refers to all of the laboratory’s
policies, processes, procedures, and resources needed to
achieve quality testing
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Quality control
Testing controls
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preexamination
examination
postexamination
The original terms preanalytical,
analytical, and post-analytical have been replaced with
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International Organization for Standardization (ISO) standard
What org replace the terms preanalytical,
analytical, and post-analytical
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specimen collection
handling
storage
preexamination variables
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reagent and test performance
instrument calibration and maintenance
personnel requirements
technical competence
examination variables
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reporting of results and interpretation
postexamination variables
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Preexamination variables
occur before the actual testing of the
specimen and include test requests, patient preparation, timing,
specimen collection, handling, and storage
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Turn around time
is defined as the amount of time required from the point
at which a test is ordered by the health-care provider until the
results are reported to the health-care provider.
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improvement
The laboratory can then monitor the TATs to
determine areas in the process that need ( )
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beginning
Specific information on specimen collection and handling
should be stated at the ( ) of each procedure listed in
the manual
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2 hours
preserving the specimen
All urine specimens should be examined within ( ).
If this is not possible, written instructions
for ( ) must be available
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EXAMINATION VARIABLES
Are the processes that directly affect the testing of
specimens
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Distilled or deionized water
clinical laboratory reagent water
The type of water used for preparing
reagents and controls must be specified.
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negative and positive control
once a day
Reagent strips should be checked against known ( ) solutions on each shift or at a minimum ( ), and whenever a new bottle is opened.
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refractometers
osmometers
automated reagent strip readers
automated microscopy instruments
The most frequently encountered instruments in the urinalysis laboratory are
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refrigerators
centrifuges
microscopes
water baths
Equipment found in the urinalysis laboratory commonly
includes
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daily
Temperatures of refrigerators and water baths should be taken ( ) and recorded.
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3 months
relative centrifugal force
weekly
Calibration of centrifuges is customarily
performed every ( ), and the appropriate ( ) for each setting is recorded. Centrifuges are
routinely disinfected on a ( ) basis.
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annual professional cleaning.
Microscopes should be kept clean at all times and have an ( )
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PM
A routine ( ) schedule for instruments and equipment should be prepared as mandated by the JC or CAP guidelines, and records kept of all routine and nonroutine maintenance
performed.
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pH
purity meter
monthly schedule
Deionized water used for reagent preparation is quality controlled by checking ( ) and ( ) resistance on a weekly basis and the bacterial count on a ( )
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quality control
the materials, procedures, and techniques
that monitor the accuracy, precision, and reliability of a laboratory test