Aubf Week 1 Flashcards

1
Q

describe The safety policies

A

Centers for Disease Control and Prevention (CDC) and the Occupational Safety and Health Administration (OSHA)

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2
Q

provides the guidelines for writing these procedures and policies.

A

Clinical and Laboratory Standards Institute (CLSI)

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3
Q

It states that all patients are considered to be possible carriers of bloodborne pathogens. (CDC, 1987)

A

Universal precautions

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4
Q

are not limited to blood-borne pathogens
– they consider all body fluids and moist body substances to be potentially infectious.

A

Body substance isolation

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5
Q

In 1996 the CDC and the Healthcare Infection Control Practices Advisory Committee (HICPAC) combined the major features of UP and BSI guidelines and called the new guidelines

A

Standard Precautions

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6
Q

includes both hand washing and using alcohol based antiseptic cleansers.

A

Hand hygiene

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7
Q

has developed hand washing guidelines to be followed for correct hand washing.

A

Center for disease control
And prevention

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8
Q

When skin contact occurs, the best first aid is to flush the area with large
amounts of water for at least _________ minutes, then seek medical attention.

A

Chemical spill and exposure; 15 minutes

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9
Q

It refers to the of guaranteeing quality patient care and is regulated throughout the total testing system.

A

Quality assessment

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10
Q

refers to all of the laboratory’s policies, processes, procedures, and resources needed to achieve quality testing.

A

Quality system

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11
Q

Quality assessment program includes not only testing controls, referred to as quality control (QC), but also encompasses:

A

– Preexamination variables
– Examination variables
– Postexamination variables

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12
Q

occur before the actual testing of the specimen

A

Pre examination variables

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13
Q

are the processes that directly affect the testing of specimens

A

Examination variable

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14
Q

Calibration of centrifuges
every ____ months, and the appropriate relative centrifugal force for each setting is recorded.

A

every 3 months

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15
Q

refers to the materials, procedures, and techniques that monitor the accuracy, precision, and reliability of a laboratory test.

A

Quality control

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16
Q

are performed to ensure that acceptable standards are met during the process of patient testing.

A

Quality control procedures

17
Q

are used to verify the accuracy and precision of a test and are exposed to the same conditions as the patient samples.

A

External quality control

18
Q

is the ability to maintain both precision and accuracy.

A

Reliability

19
Q

consists of internal monitoring systems built in to the test system and are called internal or procedural controls.

A

Internal quality control

20
Q

uses a mechanical or electrical device in place of a liquid QC specimen.

A

Electronic controls

21
Q

can be internal or an external component inserted into a point of care (POC) instrument.

A

Electronic controls

22
Q

verifies the functional ability of a testing device,

A

Electronic controls

23
Q

is the testing of unknown samples received from an outside agency, and provides unbiased validation of the quality of patient test results.

A

Proficiency Testing (External Quality Assessment)

24
Q

mandates comparison testing for laboratory accreditation.

A

Clinical Laboratory Improvement Amendments

25
are processes that affect the reporting of results and correct interpretation of data.
Post examination variable
26
requires that all employees have a right to know about all chemical hazards present in their workplace.
OSHA Federal Hazard Communication Standard
27
Criteria for specimen rejection for both physical characteristics and labeling errors must be present
Specimen Collection and Handling
28
Reagent strips should be checked against known negative and positive control solutions on each ________ or at a minimum ___________, and whenever a new bottle is _______.
- each shift - at a minimum once a day - whenever a new bottle is opened.