Biosafety At the University of Ottawa
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Transcript Biosafety At the University of Ottawa
BIOSAFETY
TRAINING
Tina Preseau*
& Rita ToussaintArchambault
*Office of Risk Management
Human Resources - Occupational Health
Disability & Leave
COURSE OUTLINE
Introduction
Laboratory Associated Infections
Blood-borne Pathogens
Classification of Biohazards
Infection/Biohazard Control
BIOSAFETY
Spill Response
Biomedical Waste
Regulations
INTRODUCTION
WHAT IS A BIOHAZARD?
A potential hazard to humans, animals or the
environment caused by a biological organism, or by
material produced by such an organism
Examples:
Viruses, bacteria, fungi, and parasites and their product.
Blood and body fluids, as well as tissues from humans and
animals.
Transformed cell lines and certain types of nucleic acids .
WHAT IS BIOSAFETY?
Measures employed when handling biohazardous
materials to avoid infecting oneself, others or the
environment.
Achieved through;
Administrative Controls
Engineering Controls
Personal Protective Equipment
Practices and Procedures
WHAT IS BIOSECURITY?
Measures employed to protect biohazardous
materials, or critical relevant information, against
theft or diversion by those who intend to pursue
intentional misuse.
Achieved through;
Physical barriers
Psychological barriers
Monitoring Activities
Personnel Clearance
WHO ARE THE STAKEHOLDERS?
INTERNALLY
EXTERNALLY
Vice-President (Research)
Committees
University Services (ORM, HR,
PRS, PS)
Deans, Chairs, Principal
Investigators, Employees,
Students
Manager of Biological
Containment Suite
Public Health Agency of
Canada
Canadian Food Inspection
Agency
Environment Canada
Transport Canada
Ontario Ministry of Labour
Emergency Response
Personnel
Suppliers & Contractors
Community
KEY SERVICES
Office of Risk Management
Training
Interface with Regulatory Bodies
Biosafety Program
certifications
training
procedures
inspections
contingency planning
accident/incident follow-up
KEY SERVICES
HR (Occupational Health, Disability and Leave)
Medical surveillance
Immunizations
Medical Follow-up
Interface with Workplace Safety and Insurance Board
WHY ARE WE CONCERNED?
Potential for acquiring a laboratory-associated
infection (LAI)
Contamination of the environment
Contamination of research
Public perception
LABORATORY ASSOCIATED
INFECTIONS
LABORATORY ASSOCIATED INFECTIONS
Infection Source
Susceptible Host
Immune system
Vaccination status
Age
Cultures and stocks
Research animals
Specimens
Items contaminated with
above
Route of Transmission
Percutaneous inoculation
Inhalation of aerosols
Contact of mucous membranes
Ingestion
LAIS
Only 20% causative or defined event
80% of which are caused by human factors
20% are caused by equipment failure
Top 4 accidents resulting in infection
Spillages & splashes
Needle and syringe
Sharp object, broken glass
Bite or scratch from animals or ectoparasites
http://www.weizmann.ac.il/safety/bio2.html
LAIS
WHO
WHAT
WHERE
WHEN
HOW
Researcher
SARS
Taiwan
December 2003
Microbiologist
West Nile Virus
United States
August 2002
Laceration
Laboratory
Worker
Meningococcal
Disease
United States
2000
Aerosol?
Laboratory
worker
Vaccinia virus
United States
2004
Many ways
BLOOD-BORNE PATHOGENS
BLOODBORNE PATHOGENS (BBP)
Sources
Blood
Semen
Vaginal Secretions
Other Bodily Fluids
Cerebrospinal
Amniotic
Synovial
Tissue Cultures
Organ Cultures
Infected Experimental Animals
RISK OF EXPOSURE
Pathogen involved
Type of body fluid
Route of exposure
Duration of exposure
Volume of blood involved in exposure
Concentration of virus at time of exposure
PPE worn
SPECIFIC EXAMPLES OF BBPS
Hepatitis B
Hepatitis C
HIV
ISSUES TO CONSIDER
Symptoms
Mode of transmission
Incubation period
Survival outside host
Communicability
Immunization
Prophylaxis / Treatment
IF AN EXPOSURE OCCURS
Initiate first aid
Notify your supervisor / designated person
Report to hospital emergency department or
University’s Health Services
Report incident to OHDL
Occupational Health, Disability and Leave Office telephone ext. 1472
http://www.rh.uottawa.ca/00_main/index_f.asp
UNIVERSAL PRECAUTIONS
Minimum standard of practice for preventing the
transmission of BBP includes:
Education
Hand washing
Wearing protective barriers
Use safe work practices
If samples cannot be guaranteed noninfective …… treat as infectious!
BIOHAZARD
CLASSIFICATION
BIOHAZARD CLASSIFICATION
Conventional Agents
Recombinant DNA
Tissue Culture
Animal Work
Anatomical Specimens
Unconventional Agents
Class D, division 3 of WHMIS
(Poisonous and Infectious Material - Biohazardous
Infectious Material)
BIOHAZARD CLASSIFICATION
Organisms are categorized into a group base on the
particular characteristics of each organism, such as
Pathogenicity
Infectious dose
Mode of transmission
Host Range
Availability of effective preventive measures
Availability of effective treatment
BIOHAZARD CLASSIFICATION
Organisms are categorized base on the measures
required for handling each organism safely in a
laboratory setting, such as
Engineering Requirements
Operational Requirements
Technical Requirements
Physical Requirements
CONVENTIONAL AGENTS
Risk
Group
Individual
Risk
Community
Risk
Containment
Level
1
Low
Low
Level 1
E.coli, B. subtilis, S. aureus,
Trichoderma reesei
Level 2
Streptococcus & Salmonella
spp, Measles, Adenoviruses,
Hepatitis A, B & C, Influenza
Level 3
Bacillus anthracis,
Mycobacterium tuberculosis,
HIV, Yellow fever virus
Level 4
Lassa virus, Ebola virus,
Marburg virus
Unlikely to cause disease
in healthy workers or
animals
2
Moderate
Limited
Rarely cause serious
human or animal disease
3
High
Low
May cause serious disease
4
High
High
Likely to cause very
serious disease
Examples
RECOMBINANT DNA
Genetic Engineering = in vitro incorporation of genetic
material from one cell into another
In Canada the level of risk depends on source of
DNA, vector and host.
The Office of Risk Management will assist the
investigator in this determination.
TISSUE CULTURE
Have the potential to contain pathogenic organisms
In general;
Human & non-human primate, and mycoplasma-containing cell
lines
Level 2
Others
Level 1
A detailed risk assessment should be
undertaken when using a new cell line.
ANIMAL WORK
Animals can harbour infectious organisms (naturally
or introduced)
Level dependent on type of work being conducted.
Special Animal Care training is required for all
personnel working with animals.
All work involving animal use must receive prior
approval from the Animal Care Committee
ANATOMICAL SPECIMENS
All specimens should be considered infectious due to
potential presence of infectious agents
Important to consider the type of specimen
blood, organs, tissues
Spinal sample, brain tissue
From infectious patient
In general Level 2 but it depends on the nature of the
work.
UNCONVENTIONAL PATHOGENS
TSE
prion
diseases;
lethal
neurodegenerative conditions
transmissible
Creutzfeld-Jakob disease, Variant C-J Disease, Mad Cow
Disease, Scrapie, Chronic Wasting Disease
Resistant to destruction by procedures that normally
inactivate viruses.
Contact ORM to assess requirements (containment,
procedures, waste disposal, etc.)
WHERE CAN WE FIND THESE?
Biology
Earth
Sciences
Bio-Engineering
University
Engineering
Human
Kinetics
Civil
Chemical
Chemistry
Medicine/
Nursing
INFECTION/BIOHAZARD
CONTROL
INFECTION/BIOHAZARD CONTROL
Administrative Controls
Engineering Controls
Personal Protective Equipment
Practices and Procedures
ADMINISTRATIVE CONTROLS
Program based, information and methods to
minimize risk of exposure:
Risk assessment
Medical Surveillance
Training/Education
Resources
Inspections
Signs & Labeling
ADMINISTRATIVE CONTROLS
Risk Assessment
Will determine type of containment, procedures, and safety
equipment required
Responsibility of users, additional assistance is available from
the ORM
Consider areas such as; experimental design, procedures to be
employed and personal experience/knowledge, etc.
Know and understand the various characteristics of the agent(s)
you are working with. (Material Safety Data Sheets and
suppliers or manufacturers)
ADMINISTRATIVE CONTROLS
Medical Surveillance
Training & Education
WHMIS
Lab specific policies and procedures
Biosafety training
Resources
ORM web site, Biosafety page
Faculty web sites
Biosafety Manual
Training Videos
ADMINISTRATIVE CONTROLS
Inspections
Routine self-inspections
Biosafety Inspection Checklist available on-line
In addition, ORM, EHSOs and OH&S will inspect labs to ensure
compliance with regulations/ guidelines and provide feedback.
ADMINISTRATIVE CONTROLS
Signs & Labeling
Biohazard warning signs must be posted on doors to rooms
where biohazardous materials are used.
Biohazard labels should be placed on containers, equipment
and storage units used with biological agents.
ENGINEERING CONTROLS
Technology based, reduce or eliminate exposure to
hazards by changes at the source of the hazard.
Containment:
Types: Primary and Secondary
Containment levels
PRIMARY CONTAINMENT
First line of defence.
Ensures protection of personnel and immediate
environment from exposure to the infectious agent.
‘Protective envelope’ that encapsulates the infectious
agent or animal.
Petrie dish, vial, stoppered bottle….
Biological safety cabinets, glove boxes and animal caging
equipment, etc.
Effectiveness of control is based on the
integrity of the containment.
SECONDARY CONTAINMENT
Protects the environment external to the laboratory
from exposure
Includes facility design and operational practices
CONTAINMENT LEVEL 1
Basic laboratory
Requires no special design features
Biosafety cabinets are not required and work may be
performed on the open bench.
CONTAINMENT LEVEL 2
Clinical, diagnostic, research and teaching facilities
with level 2 agents.
Requires a class I or class II biological safety cabinet if
any potential for aerosol or splash exists.
An emergency plan for handling spills must be
developed.
Access should be controlled.
CONTAINMENT LEVEL 3
Specialized design and construction
primary barriers to protect the individual
secondary barriers to protect the environment
All staff must undergo special training on the agents
being used, PPE, equipment, waste management as
well as practices and procedures above and beyond
the scope of this course.
CONTAINMENT LEVEL 4
Only one level 4 facility in Canada (Canadian Centre
for Human and Animal Health in Winnipeg, Man.)
Design specifications are extremely stringent, worker
is completely isolated from infectious material.
BIOLOGICAL SAFETY CABINETS
Effective means of primary physical containment for
biological agents, especially when aerosols are
generated.
HEPA filters remove particles (min 0.3 microns) with
99.97% efficiency.
There are 3 main classes of cabinets (I, II, III) which
provide various levels of protection.
BIOLOGICAL SAFETY CABINETS
Biological Safety Cabinet
Laminar flow hoods
HEPA filtered laminar air flow
Exhaust
Personnel,
environment
&
product protection
Vertical or horizontal laminar
flow
HEPA filtered air (intake only)
Product protection only
VS
WORKING SAFELY IN A BSC
Before using the cabinet:
Ensure BSC is certified
Turn off UV lamp; turn on fluorescent lamp
Disinfect work surfaces with appropriate disinfectant
Place essential items inside cabinet
Allow the blower to run for 5-10 min before work
WORKING SAFELY IN A BSC
While using the cabinet:
Ensure material and equipment is placed near the back of
the hood, especially aerosol-generating equipment. Do not
block any vents
Use techniques that reduce splatter and aerosols.
General work flow should be from clean to contaminated
areas
Minimize movement so as not to impede air flow
Open flame in BSC’s is controversial
WORKING SAFELY IN A BSC
WORKING SAFELY IN A BSC
After using the cabinet:
Leave blower on at least 5 minutes to purge cabinet
Remove and decontaminate equipment and materials
Disinfect cabinet surfaces
Turn off blower and fluorescent lamp, turn on UV lamp
WORKING SAFELY IN A BSC
Maintenance:
Before and after each use - Work surfaces wiped down
Weekly - UV lamp should be wiped clean
Monthly - All vertical surfaces wiped down
Annually- UV lamp intensity verified
- Decontamination with formaldehyde gas (ORM)
- Certification (ORM)
PERSONAL PROTECTIVE EQUIPMENT
(PPE)
PPE can become an important line of defence (last
line of defense)
Responsibility of both the user and the supervisor to
ensure that PPE is worn
PPE
Criteria for consideration
Routes of exposure that need to be blocked
Degree of protection offered
Ease of use
Only effective if correctly selected, fitted, used and
cared for, and the individual is trained
Ensure PPE is removed before leaving the lab
PPE
Footwear
Closed toed shoes should always be worn. Booties are worn in
some higher containment labs and animal facilities.
Lab Coats/Gowns
Long-sleeved, knee length with snaps
Elastic cuffs
Back-closing gowns
Periodic cleaning required
PPE
Gloves
Latex, nitrile & vinyl for work with biological agents.
Exam gloves should not be reused, change frequently. Utility
gloves can be disinfected and reused if they show no sign of
degradation.
Consider tensile characteristics, length of cuff.
Double gloving.
ORM can provide assistance finding an alternative for people
with allergies.
PPE
Eye & Face Protection
Goggles, safety glasses to protect the eyes
Full face shield to protect facial skin.
Respirators
Only personnel who have been fit-tested and trained should
wear respirators.
PRACTICES AND PROCEDURES
General Safety Guidelines
Good Microbiological Practice
Handwashing
Suspicious Packages
Specific Procedures
Centrifuges
Needles & Syringes and other sharps
Pipettes
Blenders, Grinders, Sonicators & Lyophilizers
Inoculation Loops
Cryostats
GENERAL LABORATORY SAFETY
GUIDELINES
Mostly common sense, but you must understand the
hazards you face in the laboratory and be adequately
trained to deal with them.
Basic must be known for all labs.
b i o s a f e t y
GOOD MICROBIOLOGICAL PRACTICE
(GMP)
Basic code of practice that should be applied to all
types of work involving microorganisms.
Objectives:
prevent contamination of laboratory workers and the
environment
prevent contamination of the experiment/samples
Application of aseptic technique, minimization of
aerosols, contamination control, personal
protection, emergency response
HANDWASHING
One of the single effective means of preventing
infections if done properly and frequently
When to wash?
Before starting any manipulations
Before leaving the lab
When hands are obviously soiled
Before and after completing any task in a BSC
Every time gloves are removed
Before contact with one’s face or mouth
At the end of the day
SUSPICIOUS PACKAGES
Unopened
Do not open and do not shake
Place in secondary container or cover
Inform others of the situation
Clear the room and section off the area
All individuals who may have come into contact with the
material must wash their hands
Call Protection Services and wait for their arrival
List all the individuals present in the room or area when the
package arrived. Give this list to Protection Services for followup
SUSPICIOUS PACKAGES
Opened
Contents Intact
Do not manipulate contents further
Cover the package
Inform others of the situation
Clear the room and section off the area
All individuals who may have come into contact with the
material must wash their hands
Call Protection Services and wait for their arrival
List all the individuals present in the room or area when the
package arrived. Give this list to Protection Services for followup
SUSPICIOUS PACKAGES
Contents not intact (spilled)
Do not try to clean up the spill
Gently cover the spill
Inform others of the situation
All individuals who may have come into contact with the
material must wash their hands
Call Protection Services
Remove heavily contaminated clothing (place in bag) and
shower using soap and water
List all the individuals present in the room or area when the
package arrived. Give this list to Protection Services for followup
SAFE USE OF CENTRIFUGES
Before use
Stress lines? Overfilled? Balanced?
Caps or stoppers properly in place?
Run conditions achieved?
Use sealable buckets (safety cups) or sealed rotors
After run
Centrifuge completely stopped?
Spills or leaks?
Allow aerosols to settle (30 min) or open in a BSC.
NEEDLES AND SYRINGES
Avoid use whenever possible
Use a BSC for all operations with infectious material
Fill syringes carefully
Shield needles when withdrawing from stoppers
Do not bend, shear or recap needles.
Dispose of all used needles/syringes in yellow sharps
containers
PIPETTES
Mouth pipetting is prohibited.
Never force fluids out.
To avoid splashes, allow discharge to run down
dispense the receiving container wall.
Never mix material by suction and expulsion.
Reusable pipettes should be placed horizontally in a
disinfectant filled pan.
BLENDERS, GRINDERS, SONICATORS,
AND LYOPHILIZERS
• Operate in a BSC whenever possible. Allow aerosols
to settle for 5 minutes before opening.
• Safety Blender
Do not use glass blender jars
Decontaminate immediately after use
• Lyophilizers
Use glassware designed for vacuum work, ensure there is no
damage before using
All surfaces should be disinfected after use
Use vapour traps whenever possible
INOCULATION LOOPS
Sterilization in an open flame may create aerosols
which may contain viable microorganisms.
Use a shielded electric incinerator
Shorter handles minimize vibrations
Disposable plastic loops are good alternatives
CRYOSTATS
Wear gloves during preparation of frozen sections
and heavy gloves when accessing the cryostat.
Decontaminate frequently (100 or 70% Ethanol)
SPILL RESPONSE
SPILLS
Spill response will vary depending on:
What was spilled?
How much was spilled?
Where was the spill?
What is the potential for release to the environment?
Spills should be cleaned up immediately (unless an
aerosol was generated), to ensure proper
decontamination.
Ensure appropriate PPE is worn and clean-up
equipment is readily available.
SPILLS-GENERAL CLEAN-UP
Cover spill area with absorbent material
Soak the spill area with an appropriate disinfectant (i.e. 10%
bleach)
Pour disinfectant from the outside of the absorbent material
towards the inside
Ensure any broken glass is picked up (with forceps!) and placed
in a sharps container
Leave on for 20 to 30 minutes
Wipe up with absorbent material
Waste should be disposed in appropriate biohazard bags and
where possible autoclaved
SPILLS-SPECIAL CASES
Within a Centrifuge
Within a BSC
Open Areas (lab, during transport)
The spill response plan template is available at
(http://www.uottawa.ca/services/ehss/SPILLRESPONSEPLAN.p
df)
SPILLS
All users of biological materials should be familiar
with the spill clean-up procedures.
All spills are to be reported ASAP to the lab
supervisor and ORM.
Additional assistance is available from:
ORM x 5892
Your departmental safety officer
ERT x 5411 (through Protection Services)
BIOMEDICAL WASTE
DECONTAMINATION, DISINFECTION,
AND STERILIZATION
Decontamination: Free of contamination, the
destruction of microorganisms to a lower level such
that it removes danger of infection to individuals.
Sterilization: The complete destruction of all viable
microorganisms.
Disinfection: Use of agents (physical or chemical) to
destroy harmful organisms on inanimate objects (not
necessarily all organisms)
DECONTAMINATION: PHYSICAL
Heat:
Autoclaving (most practical and recommended)
Incineration (for disposal of sharps and tissues)
Irradiation:
UV light (wavelength of 253 nm is germicidal)
Gamma (disrupts DNA and RNA)
Filtration
HEPA (biological safety cabinets, ventilation)
AUTOCLAVES
Items that CAN be autoclaved:
Cultures and stocks of infectious material
Culture dishes and related devices
Discarded live and attenuated vaccines
Contaminated solid items (petrie dishes, eppendorf tips,
pipettes, gloves, paper towels)
AUTOCLAVES
Items that CAN NOT be autoclaved:
chemicals (flammables, oxidizers, phenols, acids, alkalides)
chemotherapeutic or radioactive waste
Bleach (or other chlorinated products)
certain kinds of plastics
sharps (not at the University of Ottawa)
AUTOCLAVES
Preparation of waste:
Use only approved autoclave bags
Do not overfill autoclave bags
Separate material for re-use from that which will be disposed
and dry from liquid material
If outside of bag is contaminated, double bag
All flasks containing biological material should be capped with
aluminum foil
Ensure items are labeled with contact information
SAFE USE OF AUTOCLAVES
Many autoclaves are now run by dedicated staff,
however, if you are operating an autoclave;
Learn how to use it!
Ensure PPE is worn
Recognize acceptable material and packaging
Proper loading and unloading
All users/operators must take the autoclave training
DECONTAMINATION: CHEMICAL
Generally for disinfection rather than sterilization
Choice depends on;
Type of material to be disinfected
Organic load
Chemical characteristics
Most common are chlorine compounds and alcohols
(broad range)
WHAT TO USE FOR MY AGENT?
Vegetative bacteria (E.coli,
Viruses
Enveloped (HIV, Herpes)
Staph)
2% domestic bleach
75% Ethanol
Quaternary ammonia
6% formulated Hydrogen peroxide
Mycobacteria and fungi
10% domestic bleach
75% Ethanol
Phenolic compounds
6% formulated Hydrogen peroxide
Spore forming bacteria
(Bacillus)
10% domestic bleach
Gluteraldehyde
Formaldehyde
6% formulated Hydrogen peroxide
2% domestic bleach
75% Ethanol
Quaternary ammonia
6% formulated Hydrogen peroxide*
Non enveloped (Hepatitis,
Adenovirus)
10% domestic bleach
6% formulated Hydrogen peroxide*
Gluteraldehyde
Formaldehyde
WASTE MANAGEMENT
Discarded biological material from teaching, clinical
and research laboratories and operations is
biomedical waste. Biomedical waste includes but is
not limited to;
Animal waste
Biological laboratory waste
Human anatomical waste
Human blood and body fluid waste
Sharps
WASTE MANAGEMENT
All biological waste should be decontaminated prior
to disposal (including level 1 agents).
Treated waste is no longer considered ‘biomedical’
(i.e. microbiological waste, blood and bodily fluid
waste) and can be disposed in the regular waste
stream.
Any waste that cannot be treated (i.e. sharps,
carcasses, tissues and body parts) remains biomedical
waste and must be incinerated off site.
WASTE DISPOSAL
Biomedical Waste (untreated)
WASTE DISPOSAL
Biomedical Waste (treated)
compliance with
* InSewer
use by-laws
With H2O 1:10
SPECIAL WASTE
EtBr
Toxins
Recombinant DNA
Contact ORM
REGULATIONS
KEY REGULATED ACTIVITIES
Purchasing & Receiving of Biological Agents
PHAC, CFIA, Environment Canada
Inventory Records
Transportation/Transfer
Transport Canada- TDG
All Agencies (provincial and federal) emphasize and
expect Biosecurity
PURCHASING
Importation permits required by Public Health
Agency Canada or CFIA for certain agents
US restrictions
Ensure you meet all criteria and have all pertinent
documentation
INVENTORY
What material is presently being used and/or stored
Location
Expiry date
Use log book for remaining amount
MSDS’s
Mandatory
SHIPPING AND RECEIVING
Transportation of Dangerous Goods Act: Class 6.2 of
(Infectious Substances)
PHAC/CFIA restrictions
Ensure;
Proper classification
Proper packaging
Proper labeling
Proper documentation
Import/Export Permits
TRANSPORTATION OF DANGEROUS
GOODS
Pre-approved
Authorized Individuals
Lead time (International Regulations….)
Appropriate Scheduling (Holidays, Weekends)
Transportation within the building
Between lab to lab
Colleague to Colleague
Between Institutions
TRANSPORTATION
Important Considerations:
does material need to be transported at all
packaging requirements
means and route of transportation
regulatory requirements
Between lab transfers - 4 sided cart, sealed primary
container, secondary container, low traffic route.
Off Campus transfers – consult ORM
THE BOTTOM LINE
If you are not careful and diligent with biological
agents you risk:
Infecting yourself, others or the environment
Contaminating your research
Having Public Health Agency of Canada, Canadian Food
Inspection Agency, Ministry of the Environment or
Transport Canada after you
CONCLUSIONS
Biohazards - microorganisms, blood and body
fluids, tissues and tissue culture
Biosafety - ensuring that individuals and the
environment are not infected
Biosecurity - used in the context of protecting
dangerous pathogens and toxins against intentional
removal
Everyone within the University community is
responsible
With proper knowledge, planning and care, a
biological exposure is avoidable.
BIOSAFETY WEBSITE
http://www.uottawa.ca/services/ehss/biosafety.htm