Lab Orientation & Quality Assessment Flashcards

1
Q

Must be readily available in the laboratory

A

Safety procedure manuals

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2
Q

It states that all patients are considered to he possible carriers of bloodborne pathogens

A

Universal precautions

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3
Q

Consider all body fluid and moist body substances to be potentially infectious

A

Body substance isolation guidelines

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4
Q

Who combined the major features of UP and BSI Guidelines?

A

CDC (Centers for Disease Control and Prevention) and HICPAC (Healthcare Infectious Control Practices Advisory Committee

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5
Q

What are the Standard Precautions

A
  1. Hand hygiene
  2. Gloves
  3. Mouth, nose, and eye protection
  4. Gown
  5. Patient care equipment
  6. Environmental control
  7. Linen
  8. Patient placement
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6
Q

Includes both handwashing and using alcohol based antiseptic cleansers

A

Hand hygiene

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7
Q

All buologic waste, except _____, must be placed in appropriate containers labeled with the biohazard symbol

A

Urine

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8
Q

Empty urine confainers can be discarded as

A

Non-biologically hazardous waste

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9
Q

Urine may be discarded by pouring it into laboratory sink under a

A

Plexiglas countertop shield

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10
Q

All sharp objects must be disposed in

A

Puncture-resistant, leak-proof container with biohazard symbol

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11
Q

Information contained in an MSDS

A
  • physical and chemical characteristics
  • fire and explosion potential
  • reactivity potential
  • health hazards and emergency first aid procedures
  • methods for safe handling and disposal
  • primary routes of entry
  • exposure limits and carcinogenic potential
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12
Q

Refers to the overall process of guaranteeing quality patient care and is regulated throughout the total testing system

A

Quality assessment

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13
Q

Refers to all laboratories policies, professes, procedures, and resources needed to achieve quality testing

A

Quality system

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14
Q

Quality assessment program referred to as

A

Quality control

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15
Q

What is PPPR

A

Policies
Processess
Procedures
Resources

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16
Q

Referring to three phases of examination

A

Quality assessment program

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17
Q

What are the QAP

A
  • procedure manuals
  • internal quality control
  • external quality control
  • electronic quality control
  • standardization
  • record keeping
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18
Q

Contains all the procedures performed in the urinalysis section and must be available for reference in the working area and must comply wity the CLSI guidelines

A

Procedure manual

19
Q

Occur beforr the actual testing of the specimen

A

Preexamination

20
Q

What are examples of preexamination?

A

Test requests, patient preparation, timing, specimen collection, handling and storage

21
Q

We reject tye sample if the specimen is:

A
  • contaminated
  • insufficient sanple of urine
  • improper transport or improper behavior reservatives
  • delay
22
Q

Policy for handling mislabled specimen

A
  • do not assume any information about the specimen or patient
  • do not relabel an incorrectly labeled specimen
  • do not discard the specimen until investigation is complete
23
Q

Process that directly affect the testing of specimens

A

Examination variables

24
Q

Example of examination variables

A
  • reagents
  • instrumentation or equipment
  • quality control
  • testing procedure
  • preventive maintenance
25
Q

It should be checked against known negatige and positive control solutions on each shift or at a minimum once a day

A

Reagent strip

26
Q

Frequently encountered instruments

A

Refractometers , osmometers

27
Q

Common equipment

A

Refrigerator, centrifuge, microscope

28
Q

Used to calibrate centrifuge

A

Tachometer

29
Q

When do you perform QC?

A

At the beginning of each shift or before testing the patient samples

30
Q

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

A

External Quality Control

31
Q

Consists of internal monitoring systems built in to the test system and are called internal and procedural controls

A

Internal quality control

32
Q

Uses a mechanical or electrical device in place of a liquid QC specimen

A

Electronic control

33
Q

Can be internal or external component inserted into a point of care instrument

A

Electronic controls

34
Q

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

A

Proficiency testing or external quality assessment

35
Q

Proficiency testing also known as

A

External quality assessment

36
Q

RA4688

A

Clinical Laboratory Law

37
Q

NRL for clinical chemistry

A

Lung Center of the Philippines

38
Q

NRL for hematology

A

National Kidney and Transplant Institute

39
Q

NRL for toxicology, water testing analysis and drug testing

A

East Avenue Medical Center

40
Q

NRL for microbiology and parasitology

A

Research Institute for Tropical Medicine

41
Q

Process that affect the reporting of results and correct interpretation of data

A

Postexamination variables

42
Q

Quality assessment error in preexamination

A
  • patient misidentification
  • wrong test ordered
  • insufficient urine volume
  • delayed transport of urine to the laboratory
  • incorrect storage or preservatives of urine
43
Q

Quality assessment errors in examination

A
  • sample misidentification
  • poor testing technique
  • instrument malfunction
44
Q

Quality assessment errors of postexamination

A
  • patient misidentification
  • poor handwriting
  • transcription error
  • failure to send report
  • poor quality of instrument printer