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WorksheetsLAB MGT MODULE 3 ASSESSMENT
Total questions: 66
Worksheet time: 53mins
It is the process of preventing unwanted risks and hazards from entering the laboratory space.
Security
Containment
Safety
Ergonomics
It is the process that seeks to minimize risks and prevent hazards from leaving the laboratory space and causing harm to the community.
Security
Containment
Safety
Ergonomics
This addresses facility and equipment adaptation to allow safe and healthy working conditions at the laboratory site.
Security
Containment
Safety
Ergonomics
Pre-examination phase includes:
Sample testing
Sample validation
Reporting of test result
Test Selection
It is considered the most important laboratory resource.
Competent and motivated staff
Advance Machineries
Specialized Computers
Health Information System
This is essential in order to protect the lives of employees and patients, to protect laboratory equipment and facilities, and protect the laboratory environment as well.
Laboratory safety program
Laboratory quality control program
Laboratory assessment program
Laboratory process improvement program
Neglecting laboratory safety is very costly. Secondary effects of a laboratory accident includes all of the following except?
loss of reputation
loss of customers
negative effect on staff retention
increased income
increased costs—litigation, insurance.
All of the following are duties of a laboratory director in maintaining safety in the laboratory except?
actively participate in the design and planning stages of new laboratory facilities
assess all potential risks and apply basic concepts of organization in the laboratory
consider the organization of the laboratory when developing new activities or new diagnostic techniques in the laboratory
conduct laboratory safety audits
All of the following are duties of a quality manager/safety officer except?
develop a complete and thorough description of basic safety rules and organization
ensure that personnel are trained in their specific duties when new activities or techniques are introduced into the laboratory
conduct laboratory safety audits
All of the above
None of the above
All are true about work benches in the laboratory except?
Laboratory work benches should be constructed of materials that are durable and easy to disinfect.
If the laboratory’s budget allows, ceramic tiles are good materials to use for benchtops.
Wood should not be used, as it is not easy to clean or disinfect, and will deteriorate over time when repeatedly exposed to disinfectants and detergents.
It is advisable to organize work benches according to the type of analysis that is performed.
Disinfection on work benchtops should be done by utility personnel and not by lab personnel as they have more important things to do.
Policies should be put in place that outline the safety practices to be followed in the laboratory. Standard laboratory safety practices includes all of the following except?
limiting or restricting access to the laboratory
prohibiting mouth pipetting
using techniques that minimize aerosol or splash production when performing procedures
prohibiting eating, drinking, smoking, handling contact lenses, and applying cosmetics in work areas;
use of open-toed shoes and disposable lab gowns while working in the lab
Laboratory glassware and plasticwares should be disposed on puncture-resistant, leak-proof sharps container since they can pose threats to laboratory personnel.
TRUE
FALSE
It serves as a technical bulletin for chemicals that provide detailed hazard and precautionary information of every chemicals in the laboratory.
Chemical Inserts
MSDS
Chemical Hygiene Plan
Chemical Safety program document
Chemicals can enter the human body via the following except?
Inhalation
Absorption
Ingestion
Sexual contact
It serves as the main sources of contamination within diagnostic laboratories due to activities that concern several identification of pathogens.
Aerosol
Blood
Sputum
Body fluids
To prevent exposure to droplets, a lab personnel should wear?
Disposable lab gown
Face mask
Gloves
Goggles
Contact lenses
This is compulsory in physical containment level 3 laboratories or in specific instances such as sample collection when highly dangerous pathogens is
involved, such as suspected cases of H5N1 avian influenza or SARS.
Disposable lab gown
Face mask
Gloves
Goggles
Contact lenses
When cleaning laboratory spills caused by caustic fluids, it is recommended to use ____________ as absorbent pads.
baking soda or polypropylene pads
polypropylene pads or diatomaceous earth
diatomaceous earth only
baking soda only
For spills containing large amounts of organic material,______ should be used to clean and decontaminate the surface.
1:10 household bleach or 10% hypochlorite
70% alcohol
Fire extinguishers in the laboratory shall be inspected?
Monthly
Quarterly
Annually
Daily
The design of laboratory work areas should ensure proper ventilation and surfaces that can be cleaned and disinfected.
TRUE
FALSE
This document establishes policy and describes standard procedures for handling safety and emergency issues.
Safety Manual
Chain of infection manual
Laboratory procedure manual
Disinfection manual
Benefits of a good equipment management program includes all of the following except?
helps to maintain a high level of laboratory performance;
reduces variation in test results, and improves the technologist’s confidence in the accuracy of testing results;
lengthens instrument life
reduces interruption of services due to breakdowns and failures
increases replacement and purchase of equipment to promote greater customer satisfaction.
Things to consider when collecting and acquiring equipment.
how the equipment will be used
cost of the equipment
facility requirements, including the requirements for physical
space
safety issues to consider
All of the above
Things to consider when installing new equipment.
ventilation and water supply
electrical supply
space
All of the above
This is a very important process that can help calculate how much is required of any particular item for a given period of time, and it is an essential part of a successful inventory management program.
Forecasting
Quantification
Advantages of a computerized inventory management system except?
generate statistics that will help when planning and making purchases
ease the burden of inventory management
allow for good management of expiration dates
on-site computer is needed and it could be expensive to purchase
Sample management is a part of ?
Information management
Customer service
Equipment
Assessment
Process control
Defined by ISO as one or more parts taken from a system and intended to provide information on the system.
Specimen
Sample
It is a sample taken from the human body.
Specimen
Sample
The laboratory should keep an inventory log of all equipment in the laboratory. The log should be updated with information on new equipment. Documentation for old retired equipment is not necessary unless required by standards.
TRUE
FALSE
Equipment logbook shall contain the following information except?
preventive maintenance activities and schedule
recording of function checks and calibration
full information on any problem that the instrument develops, the subsequent troubleshooting activity and follow-up information regarding resolution of the problem. In recording problems, be sure to record
any changes to procedure for maintenance or function checks as a result of the problem
None of the above
Establishing a purchasing and inventory management program will ensure that:
supplies and reagents are always available when needed;
high-quality reagents are obtained at an appropriate cost;
reagents and supplies are not lost due to improper storage, or kept and used beyond expiration.
All of the above
None of the above
This quantification technique allows the laboratory to study and take into account the actual number of episodes, illnesses and health problems that require laboratory testing. This helps them accurately estimate the needed reagents and supplies for laboratory testing.
Morbidity based quantification
Consumption based quantification
Death rate based quantification
Monthly based quantification
On this process, patients are instructed on the timing (e.g fasting issues) that pertains to blood glucose, hormones , drug analysis etc.
Patient preparation
Patient identification
Type of container
Sample labelling
Special handling
This process includes immediate refrigeration, protection from light or prompt delivery to the laboratory.
Patient preparation
Patient identification
Type of container
Sample labelling
Special handling of specimens
Handle all samples as if they are infectious.
TRUE
FALSE
All potentially hazardous material requires triple packaging.
TRUE
FALSE
The goal of Quality Control is to detect, evaluate, nd correct errors due to test system failure, environmental conditions or operator performance, before patient
results are reported.
TRUE
FALSE
These substances contain an established amount of the substance being tested and are tested at the same time and in the same way as patient samples to validate the reliability of the test system and evaluate the operator’s performance and environmental conditions that might impact results.
Patient samples
Control Samples
Calibration Samples
All of the above
These are solutions with a specified defined concentration that are used to set or calibrate an instrument, kit, or system before testing is begun.
Patient samples
Control Samples
Calibration Samples
All of the above
Controls are usually available in "high", "normal" and "low" ranges.
TRUE
FALSE
All are measures of central tendency except?
Mean
Median
Mode
Standard Deviation
It is defined as the closeness of a measurement to its true value.
Acurracy
Precision
Reliability
Reproducibility
Bias
It is defined as the amount of variation in the measurements.
Acurracy
Precision
Reliability
Reproducibility
Bias
It is the difference between the expectation of a test result and an accepted reference method.
Acurracy
Precision
Reliability
Reproducibility
Bias
It occurs when an abrupt change is followed by six or more
consecutive QC results that fall on one side of the mean.
Shift
Trend
It occurs when values gradually, but continually, move in one direction over six or more analytical runs.
Shift
Trend
This type of examination measure the presence or absence of a substance, or evaluate cellular characteristics such as morphology.
Quantitative examination
Qualitative Examination
Semi-qualitative Examination
Semi-quantitative Examination
Built-in controls are those that are integrated into the
design of a test system such as a test kit device. Usually, the device is marked with designated areas where coloured lines, bars or dots should appear to indicate success or failure of positive and negative controls, and these controls are performed automatically with each test.
TRUE
FALSE
QC in microbiology requires use of dead/inactivated control organisms with predictable reactions to verify that stains, reagents and media are working correctly.
TRUE
FALSE
Assessments conducted by groups or agencies from outside the laboratories are called?
external audits
internal audits
Licensing
Accreditation
Type of assessment that laboratories can utilize
where staff working in one area of the laboratory conduct assessments on another area of the same laboratory.
external audits
internal audits
Licensing
Accreditation
It is the most commonly employed type of External Quality Assessment program that allows external provider sends unknown samples for testing to a set of laboratories, and the results of all laboratories are analyzed, compared and reported to the laboratories.
On site evaluation
Rechecking or retesting
Proficiency testing
None of the above
It is a document that provides rules, guidelines or characteristics for activities or their results. It covers such documents as standards, technical specifications, codes of practice and regulations.
Normative Document
Standard Document
Regulatory Documents.
Procedure Manuals
It is any standard that is mandated by a governmental agency or authoritative body.
Normative Document
Standard Document
Regulation
Procedure Manuals
It is the procedure by which an independent body gives written assurance that a product, process or service conforms to specific requirements
External qualification
Certification
Licensing
Accreditation
It is the procedure by which an authoritative body gives formal recognition that a body or person is competent to carry out specific tasks.
External qualification
Certification
Licensing
Accreditation
It is the granting of ability to practice, usually provided by a local governmental agency. Licensure is usually based on demonstrated knowledge, training and skills
External qualification
Certification
Licensing
Accreditation
Management must establish appropriate personnel qualifications for all positions in the laboratory.
TRUE
FALSE
It is defined as the application of knowledge, skills and behaviors used in performing specific job tasks.
Competency
Skills
Talents
Capability
It is required when competency assessment reveals the need for improving an employee’s knowledge and skills.
Retraining
Cross training
Continuing education
None of the above
It provides an opportunity for staff to acquire skills outside their own discipline. This allows for flexibility in shifting or reassigning personnel whenever needed; this may occur in crisis situations or with absences of staff due to illness or vacation.
Retraining
Cross training
Continuing education
None of the above
This enables employees to be up to-date in a particular area of knowledge or skills.
Retraining
Cross training
Continuing education
None of the above
Good customer service is capable to provide: valuable information for best patient car, valuable information to improve surveillance and other public health actions and gives professional image for the laboratory.
TRUE
FALSE
This are documents that contain written step-by-step instructions that laboratory staff should meticulously follow when performing a procedure.
Safety Manual
Chain of infection manual
Standard operating procedure manual
Disinfection manual
