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
Q

are processes that affect the reporting of results and correct interpretation of data.

A

Post examination variable

26
Q

requires that all employees have a right to know about all chemical hazards present in their workplace.

A

OSHA Federal Hazard Communication Standard

27
Q

Criteria for specimen rejection for both physical characteristics and labeling errors must be present

A

Specimen Collection and
Handling

28
Q

Reagent strips should be checked against known negative and positive control solutions on each ________ or at a minimum ___________, and whenever a new bottle is _______.

A
  • each shift
  • at a minimum once a day
  • whenever a new bottle is opened.