Bloodborne Pathogen Training for Laboratory Workers

1 / 52
About This Presentation
Title:

Bloodborne Pathogen Training for Laboratory Workers

Description:

Bloodborne Pathogen Training for Laboratory Workers –

Number of Views:107
Avg rating:3.0/5.0
Slides: 53
Provided by: matthewp5
Category:

less

Transcript and Presenter's Notes

Title: Bloodborne Pathogen Training for Laboratory Workers


1
Bloodborne Pathogen Trainingfor Laboratory
Workers
Louisiana State University
  • Safety precautions to prevent laboratory-acquired
    infections among research laboratory personnel.

2
Application
  • Handling human specimens or bloodborne pathogens
    must conform to federal regulations (OSHA
    Bloodborne Pathogen Standard, 29 CFR 1910.1030).
  • The regulations cover all research with
  • live human bloodborne pathogens (HIV, HBV, HCV,
    etc.)
  • unfixed human tissues, blood, and body fluids

3
Bloodborne Pathogens
  • A bloodborne pathogen is any human pathogen that
    is transmitted to humans by perenteral contact
    with infected blood.
  • Includes, but not limited to the following
  • retroviruses HIV-1, HIV-2, HTLV-I, -II
  • hepatitis viruses HBV, HCV
  • arboviruses causing encephalitis, YF virus,
    Dengue virus, others
  • other microbial pathogens Plasmodium spp.,
    Franciscella tularensis, Treponema pallidum,
    others

4
HBV
HIV
YFV
5
HIV Infection
  • HIV viruses establish a chronic infection of
    human CD4 cells helper T-lymphocytes and
    macrophage.
  • Currently there is no vaccine available and drug
    therapies are effective at limiting progression
    of disease but not curing infection.

6
Transmission
  • HIV is mainly transmitted by sexual contact with
    an infected person.
  • sexual transmission can occur at genital or
    colonic mucosa
  • virus is present in semen or vaginal fluids
  • virus gains access to the bloodstream by passing
    through openings in the mucous membranes - the
    protective tissue layer that lines the mouth,
    vagina and rectum- and through breaks in the skin
    of the penis.

7
Transmission
  • Exposure to infected blood or blood products
  • transfusions, mainly in the developing world
    today
  • intravenous drug use, sharing of needles
  • main transmission in eastern Europe and former
    Soviet Union states
  • accidental needle-sticks or exposure of blood to
    open cuts or scrapes

8
Transmission
  • The third major route of infection is from mother
    to child
  • mainly occurs during birth, when there is mixing
    of the blood
  • can also occur before birth the virus can cross
    the placenta and invade the developing fetus
  • virus is present in milk, but there is no
    evidence for transmission by breast-feeding

9
Epidemiology of HIV in U.S.
10
Early Signs / Symptoms of HIV infection
  • Initial signs are mononucleosis-like
  • swollen, tender lymph nodes
  • fever
  • sore throat, headache
  • muscle aches
  • rash, diarrhea may be present
  • A vigorous immune response occurs
  • virus levels in blood decline
  • Sharp decline in circulating CD4 T-cells, then
    numbers recover

11
HBV Infection
  • HBV is a small DNA virus in the family
    Hepadnaviridae that causes both self-limiting and
    chronic infections of humans
  • self limiting - resolve within 6 months
  • most are sub-clinical
  • some result in acute hepatitis
  • persistent - a fraction of infections become
    persistent and may continue for many years or
    life.
  • can lead to liver damage or hepatocellular
    carcinoma

12
HBV Infection
  • Clearance of HBV in infected persons is
    associated with development of immune responses
    to the product of the S gene, the major surface
    protein, HbsAg.

13
Self-limiting Typical course of acute infections
with HBV
14
Self-limiting Sub-clinical infection in HBsAg
negative individuals
15
Typical course of persistent infections with HBV
HbsAg persists
No antibody to HbsAg
16
Vaccine
  • The vaccine for HBV is purified recombinant
    HbsAg.
  • Series of three injections 0, 1 and 6 months.
  • Duration of immunity is at least 15 years.
  • Efficacy is 95 safety is excellent
  • side effects are nearly always mild and occur at
    low incidence

17
Transmission of HBV
  • Humans are the only reservoir, and chronic
    carriers are the main source of new infections.
  • HBV is present in and can be transmitted from
    contact with
  • blood and serum
  • saliva
  • semen

18
Transmission of HBV
  • Virus is also present in
  • feces
  • cerebrospinal fluid
  • bile
  • breast milk
  • sweat
  • vaginal secretions
  • mosquitoes and bedbugs
  • Transmission is rare or not possible from the
    above fluids.

19
Transmission of HBV
  • Established routes of infection
  • percutaneous transfer of blood
  • mucous membrane contact with blood
  • homosexual and heterosexual intercourse
  • contact between mucous membranes or cuts and
    environmental surfaces contaminated with virus
  • neonatal transmission is mainly at birth
  • 5-10 of neonatal infections may be in utero

20
HBV Epidemiology
Currently there are about 8800 new cases of HBV
reported each year estimated 80,000 total. Of
these, about 10 will become chronic
carriers. About 1.25 million people in U.S. have
chronic HBV infection.
21
(No Transcript)
22
(No Transcript)
23
(No Transcript)
24
Exposure Control Plan
  • Universal precautions
  • Engineering controls
  • Work practice controls
  • Medical management

25
Universal Precautions
  • The universal precautions were developed in the
    early 1980s to protect health care workers from
    HIV infection.
  • The philosophy of universal precautions is that
    all patients, samples, and specimens should be
    treated as if infected at all times.
  • barrier and procedural protections are used when
    handling all samples or specimens.

26
Strategies for Protection
  • Strategies for protection against bloodborne
    pathogens include the following
  • appropriate protective clothing and barriers
  • minimizing the use of sharps
  • practices that minimize the risk of infection are
    used in all manipulations
  • appropriate safety equipment and supplies are
    used when handling infectious materials
  • vaccination

27
Personal Protective Equipment
Personal protective equipment (PPE) should be
used for all manipulations of blood, tissue,
infected cultures, or other potentially
infectious materials (OPIM).
28
Personal Protective Equipment
  • Gloves
  • protection from direct skin contact
  • some protective effect from needle
    -sticks
  • required for any hand contact with
    blood, cultures, infected animals,
    potentially contaminated equipment
  • use for all procedures, cleaning spills and
    handling wastes
  • should use two layers when working with cultures
    or using sharps with infectious materials
  • removed inside out for discard

29
Personal Protective Equipment
  • Protective outer clothing
  • lab coats, gowns, or aprons are required
    at all times in a BBP lab
  • solid-front, fluid-resistant gowns should be
    used for any procedure where splashes are
    possible
  • as necessary, add hoods, caps, face protection
    and disposable shoe coverings
  • all protective clothing must be removed before
    leaving the lab and either disposable, laundered
    on-site, or autoclaved before removal from site

30
Personal Protective Equipment
  • Eye protection
  • eye protection should be worn at all times in the
    lab
  • appropriate eye protection include safety glasses
    with side-splash protection, safety goggles or
    full face shield
  • prescription eyeglasses are not a substitute
    safety glasses should be worn over eyeglasses

31
Safety Engineered Materials
  • Glassware should be avoided if possible and
    replaced with plastic tubes, flasks, etc.
  • Capillary tubes, if used for micro-hematocrit
    measurements, should be made of unbreakable
    plastic or glass coated with plastic.

32
Safety Engineered Materials
  • If needles are used, safety needles should be
    substituted for standard if possible
  • If other sharps are necessary, safety-engineered
    substitutes should be employed

33
Biological Safety Cabinets
  • A properly maintained and certified BSC must be
    used for all open work with infectious materials
    in a BBP research laboratory.

some procedures may not be feasible inside a
cabinet in such cases, extra PPE may substitute.
34
Use of a BSC should not substitute for protective
clothing or eye protection.
35
Work Practices
  • BSL-2 practices apply
  • no eating, drinking, smoking, storage of food or
    drinks, application of cosmetics or handling of
    contact lenses in lab
  • procedures involving potentially infectious
    materials done in ways that minimize splashing or
    the production of droplets
  • PPE is removed and replaced when contaminated,
    and removed before exiting the lab

36
Mouth pipetting is not permitted.
Work surfaces should be kept free of potential
hazards.
37
Vacuum tubes of blood and other potentially
infectious materials should be covered with
absorbent matting during opening.
38
Handwashing is an effective way to prevent mucous
membrane exposures. It should be done 1)
whenever hands become visibly contaminated with
material 2) after completion of work with
infectious materials 3) after removal of
gloves 4) before leaving the laboratory
After leaving the lab, hands should again be
washed before 1) eating, drinking or smoking 2)
handling contact lenses
39
Absorbent lab matting reduces the risk of
splashes if infectious materials are spilled on
work surfaces. Lab matting also helps
contain spills.
40
Cleaning and disinfection of work surfaces
should be done after completion of each
procedure and at the end of each work day.
A variety of chemical agents are effective
against most bloodborne pathogens iodophors,
phenolics, alcohol, diluted bleach (10 v/v). The
presence of blood or other organic material can
limit the effectiveness of most chemical agents.
41
Infectious Spill Management
1) Alert co-workers and use PPE. 2) Flood the
spill with an appropriate disinfectant bleach to
final 10 is a good choice. 3) If glass is
present, use tongs to pick up and discard in
sharps container. 4) Absorb the
spill/disinfectant mix with paper towels, lab
matting, or granular material. 5) Carefully
scrape up the absorbent materials and discard in
biohazard waste. 6) Clean and disinfect the area.
42
Sharps Management
The use of sharps in bloodborne pathogen labs is
responsible for gt90 of researcher exposures
mainly needle-sticks.
43
Sharps Management
1) Wear two pairs of gloves when working with
sharps and infectious materials. 2) Discard used
sharps immediately without recapping into
hard-sided, leak-proof disposal containers.
44
Waste Management
1) Solid wastes should be collected into two
layers of autoclavable biohazard bags, placed
within leak-proof, labeled secondary
containers. 2) Collection bags should be removed
from secondary containers before overflowing and
only at the time of decontamination. 3) All
laboratory wastes should be autoclaved before
disposal into the waste stream (BSL-3).
45
Waste Management
Liquid wastes with low numbers of pathogens may
be decontaminated by exposure to chemical
disinfectant, and discarded by sanitary
sewer. Culture fluids and other materials
expected to have large numbers of pathogens
should be autoclaved before discard.
46
Restricted Access
1) Lab doors are closed when work is in
progress. 2) PI establishes specific entry
requirements and policies. 3) All persons enter
the lab must be made aware of the hazards present
in the lab. 4) A biohazard warning sign is posted
at the entrance to the lab, other signs as
appropriate.
47
Medical Management
  • Hepatitis B vaccine
  • Post-exposure evaluation
  • Occupational surveillance

48
Hepatitis B Vaccine
  • All BBP lab workers are offered the hepatitis B
    vaccine free of charge.
  • LSU Student Health Center administers the vaccine
    and maintains the records.
  • People who have previously been vaccinated, have
    antibody to HbsAg, or are contraindicated for
    medical reasons do not need the vaccine.
  • Those who refuse the vaccine must sign a
    declination form.
  • may reconsider vaccine at any time

49
Post-Exposure Evaluation
  • Exposure - eye, mouth, other mucous membrane,
    non-intact skin, or parenteral contact with blood
    or other potentially infectious materials
    resulting from the performance of employees
    duties.
  • All work-related exposures require immediate
    action and follow-up evaluation.

50
Immediate Action
  • Needle-sticks or other non-intact skin exposures
  • Immediately wash with soap and hot water, then
    seek medical treatment.
  • Splashes to nose, mouth, or eyes
  • flush extensively with water, saline or sterile
    irrigating solution, then seek medical treatment.
  • Notify lab director / principle investigator.
  • documentation and reports are required by LSU

51
Follow-up Evaluation
  • LSU Student Health Center will offer the exposed
    individual
  • confidential medical evaluation
  • blood collection and HIV testing
  • post-exposure prophylaxis with anti-retroviral
    drugs
  • as directed by current CDC recommendations
  • counseling
  • evaluation of subsequent reported illnesses
    resulting from the exposure

52
Thank you for your attention!
  • For additional questions or concerns
  • Contact
  • Occupational and Environmental Safety
  • 126 Public Safety Building
  • 578-5640
Write a Comment
User Comments (0)
About PowerShow.com