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Bloodborne Pathogens (BBP) Training for the Researcher Update for employees with potential exposure to blood or other potentially infectious materials (OPIM) - Safety precautions to prevent infections 2008 Louisiana State University A&M Louisiana AgCenter Office of Occupational & Environmental Safety (OES) Public Safety Building, Suite 126 South Stadium Drive Phone: (225) 578-5640 Fax: (225) 578-7489 Biological Safety Manager Training Manager Gregory V. Hayes, DrPH Pat F. West (225) 578-4658 [email protected] (225) 578-0534 [email protected] 2 BBP Training Outline 3 Bloodborne Pathogens (BBP) The following training meets requirements set forth by the OSHA Bloodborne Pathogens Standard. This module and accompanied quiz is a self-study designed to provide a review of the following: Understanding bloodborne pathogens (BBP) and the modes of transmission Understanding the epidemiology of bloodborne diseases Recognizing workers and tasks that may involve exposure Learning containment practices for safe handling of BBP Awareness of the need for Exposure Control Plans Acquiring Information on the Hepatitis B vaccine Bloodborne Pathogens Standard This training was based upon Federal regulations and guidelines: OSHA (1991)- “Occupational Exposure to Bloodborne Pathogens” (29 CFR 1910.1030) NIOSH/CDC - Preventing Needle stick Injures in Health-Care Setting CDC - Exposure to Blood: What Health-Care Workers Need to Know 5 What are Bloodborne Pathogens (BBP)? Any pathogenic microorganisms or OPIM (other potentially infectious materials) present in human blood that can cause disease in humans. Primary focus in our setting is HBV, HCV, and HIV which will be detailed further in this presentation. Other examples of BBP include microorganisms that cause: malaria, syphilis, babesiosis, brucellosis, tularemia, leptospirosis, arbovirus infections ( i.e., Dengue), relapsing fever, Creutzfeldt-Jakob disease, viral hemorrhagic fever and many many more. 6 Working with human or primate cell lines? LSU developed a policy on the use of human & primate cell lines in 2006 All cell and organ cultures of human origin, including well established cell lines as well as primate cell lines, shall be handled in accordance with the OSHA Bloodborne Pathogens Standard and under Biosafety Level 2 (BSL2) containment. All University personnel working with these cultures shall maintain a written record of their annual training as required under the OSHA Bloodborne Pathogens Standard. http://appl003.lsu.edu/PubSafety/oes.nsf/$Content/Bloodborne+Pathogens+and+Uni versal+Precautions+at+LSU?OpenDocument 7 Exposure to Blood For some employees the potential for infection from occupational exposure to blood or other potentially infectious materials (OPIM) is high, especially from: o Needle sticks o Cuts from other sharp instruments contaminated with blood o And through eye, nose, mouth or skin contacts with patients 8 OPIM includes the following: 9 Synovial, pleural, pericardial, and peritoneal fluid 9 Cerebrospinal fluid 9 Semen 9 Vaginal secretions 9 Amniotic fluid 9 Any unfixed tissue or organ from a human 9 Any body fluid visibly contaminated with blood 9 All body fluid where it is difficult to distinguish between body fluids 9Cell or tissue cultures 9 Saliva (in dental procedures) 9 Risk Factors for Infection Most exposure does not result in infection. The risk of infection may vary with certain factors: Pathogenicity of organism Dose (how much blood or infectious agent) Route of entry (injection vs. contact with mucous membrane or open wound) Host susceptibility Work practices 10 Duties that might put you at risk for an occupational exposure: o Disposing of waste contaminated with blood or OPIM o Transporting blood or OPIM o Working in a laboratory where equipment or work benches can become contaminated o Handling containers of infectious wastes o Cleaning blood spills, including dried blood o Handling laundry that contains sharps or is soiled with blood or OPIM o Performing lifesaving procedures o Working in a faulty biological safety cabinet 11 Duties that might put you at risk for an occupational exposure - continued: o Performing a blood draw from human patients or animals o Processing blood for experimentation o Using human or animal blood or body fluids in experimentation o Using unfixed tissue in preparations or experimentation o Cleaning glassware contaminated with blood or OPIM o Performing flow cytometry with unfixed cells 12 Modes of transmission of BBP Percutaneous - the direct inoculation of infectious material by piercing through the skin barrier (needle stick or other accidental injury with a sharp, contaminated object) Penetration by contaminated sharps is the most common mode of transmission of bloodborne pathogens in the workplace. 13 Modes of transmission of BBP Direct inoculation - exposure of blood or OPIM to pre-existing lesions, cuts, abrasions, or rashes (dermatitis) provides a route of entry into the body. Mucous membrane contact - splashing blood or serum into an individual's unprotected eyes, nose, or mouth in clinical or laboratory settings poses a genuine risk of infection. 14 Human Immunodeficiency virus (HIV) HIV is the virus that causes AIDS (Acquired Immune Deficiency Syndrome). Once a person has been infected with HIV, it may be many years before AIDS actually develops. computer generated art quality graphics of HIV was done by Russell Kightley of Canberra, Australia. HIV kills or damages cells in the body’s immune system, gradually destroying the body’s ability to fight infection and certain cancers. 15 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 16 HIV Transmission Exposure to infected blood or blood products: ¾ transfusions, mainly in the developing world today ¾ intravenous drug use, sharing of needles (main transmission in eastern Europe and former Soviet Union states) ¾ accidental needle-sticks or exposure of blood to open cuts or scrapes 17 Early Signs / Symptoms of HIV infection Initial signs are mononucleosis-like: ¾ ¾ ¾ ¾ ¾ swollen, tender lymph nodes fever sore throat, headache muscle aches rash, diarrhea may be present A vigorous immune response occurs: ¾ virus levels in blood decline Sharp decline in circulating CD4+ T-cells, then numbers recover 18 Hepatitis B Virus (HBV) Hepatitis B is caused by a virus that attacks the liver and can cause lifelong infection, cirrhosis, liver cancer, liver failure, or death. In 2003, an estimated 73,000 people were infected with HBV. People of all ages get hepatitis B and about 5,000 die per year of sickness caused by HBV. 19 Hepatitis B Virus HBV infection is a well recognized occupational risk for healthcare personnel. The average volume of blood inoculated during a needle stick injury with a 22gauge needle is approximately 1 µl, a quantity sufficient to contain up to 100 infectious doses of HBV. HBV can survive outside the body at least 7 days and still be capable of causing infection. 20 Hepatitis B Virus About 30% of infected persons have no sign or symptoms of HBV. If symptoms occur, they usually begin to appear on the average of 12 weeks (range 921 weeks) after exposure to hepatitis B virus. If you have symptoms, they might include: • jaundice • dark urine • joint pain • fatigue • loss of appetite • abdominal discomfort • clay-colored bowel movements • nausea 21 What treatment is available for HBV? In the occupational setting, multiple doses of Hepatitis B Immune Globulin initiated within 1 week following percutaneous exposure to hepatitis B surface antigen-positive blood provides an estimated 75% protection from HBV infection. There is no cure available for acute HBV infection. There are antiviral drugs available for the treatment of chronic HBV infection. 22 HBV Infection HBV is a small DNA virus in the family Hepadnaviridae that causes both self-limiting and chronic infections of humans: ¾ self limiting - resolve within 6 months o most are sub-clinical o some result in acute hepatitis ¾ persistent - a fraction of infections become persistent and may continue for many years or life. o can lead to liver damage or hepatocellular carcinoma 23 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: o blood and serum o saliva o semen 24 Transmission of HBV Established routes of infection: o percutaneous transfer of blood o mucous membrane contact with blood o homosexual and heterosexual intercourse o contact between mucous membranes or cuts and environmental surfaces contaminated with virus o neonatal transmission is mainly at birth; 5-10% of neonatal infections may be in utero 25 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. 26 HBV IS PREVENTABLE! A safe & effective vaccine is available. Hepatitis B vaccine prevents hepatitis B infection and its serious consequences. The vaccine for HBV is purified recombinant HbsAg If the vaccine is administered before infection, it prevents the development of the disease and the carrier state in almost all individuals Hepatitis B vaccine consists of a series of three injections – initial, one a month later, and one six months from the first. Available FREE of charge from employer for at risk employees Principal Investigators should make the vaccine available to at risk employees 27 Hepatitis B Vaccine FREE to employee - paid for by your department if you are at high-risk for exposure 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 o may reconsider vaccine at any time 28 Hepatitis C Virus (HCV) Of every 100 persons infected with HCV about: • 55-85 of persons might develop long-term infection • 70 persons might develop chronic liver disease • 5-20 persons might develop cirrhosis over a period of 20 to 30 years • 1-5 of persons might die from the consequences of long term infection (liver cancer or cirrhosis) Hepatitis C is one of the leading indicators for liver transplantation. 29 Hepatitis C Virus (HCV) 80% of persons infected have no signs or symptoms for HCV. When present, symptoms may include: • jaundice • fatigue • dark urine abdominal pain loss of appetite nausea 30 Hepatitis C Virus (HCV) Currently, there is no cure for hepatitis C, and no effective vaccine is currently available. National recommendations for the control of occupational exposure to HCV rely more on the prevention of transmission. In addition, several blood tests that measure either antibodies to HCV or HCV-RNA are available for hepatitis C screening. These tests are useful in determining current immune status and monitoring ongoing infection. 31 32 Epidemiology Types of employees who have the potential for infection from occupational exposure to blood or OPIM are: o Healthcare workers o Custodial and maintenance workers who respond to spills o Public Safety workers o Laboratory workers who work with infectious agents 33 Epidemiology Bloodborne Pathogens can enter your body through: o Open cuts, nicks, and skin abrasions. o Mucous membranes of your mouth, eyes, and nose. o Indirect transmission - touching a contaminated surface and then touching your mouth, eyes or open skin. o Accidental injury by a contaminated sharp object. 34 Compliance Control Occupational Exposure Prevention The risk of occupational exposure can be minimized or eliminated using a combination of standard precautions, and personal hygiene, personal protective equipment, work practice controls, engineering controls, training, medical surveillance, vaccination, warning signs or labels, and other provisions described in this section. 35 Standard Precautions Universal Precautions • All human/primate blood, untreated tissues, cell lines and bodily fluids are treated as infectious o Treat all blood and bodily as if they are contaminated. o All body fluids must be considered as potentially infectious materials. o Proper cleanup and decontamination o Always wear appropriate PPE o Replace PPE that is torn or punctured o Remove PPE before leaving the work area 36 Employee Responsibilities Completing training as required Following an Exposure Control Plan developed by your program or Principal Investigator Using work practices, engineering controls, and personal protective equipment as outlined in the Exposure Control Plan Obtaining the HBV vaccine if advised by your supervisor 37 Employee Responsibilities Continued Reporting exposure incidents to your supervisor Pursuing follow-up care after an occupational exposure 38 Compliance Control Methods Personal Hygiene o Do not touch anything that is contaminated, such as sharps or body fluids. o Take care to minimize splashing of all infectious materials. o Eating, drinking, smoking, applying cosmetics or lip balm, and handling contact lenses are prohibited in areas where there is a potential for occupational exposure. 39 Compliance Control Methods Personal Hygiene Cont. Use CDC guidelines for hand hygiene: o If hands are not visibly soiled, use alcohol gel o When hands are visibly soiled, wash hands with soap and water o Always wash your hands before eating and after using the restroom 40 Hand washing Employees must wash their hands immediately or as soon as feasible after removal of gloves or other personal protective equipment. Wash as soon as possible if gross contamination occurs Alternate methods: Antiseptic towelettes Waterless hand washing gels 41 Compliance Control Methods Personal Protective Equipment (PPE) o PPE must be used to prevent potentially infectious materials from coming in contact with work clothes, street clothes, undergarments, skin or mucous membranes o Employees must wear gloves when there is potential contact with blood, potentially infectious materials, mucous membranes or broken skin o Remove gloves promptly after use, and before touching non-contaminated items and environmental surfaces. 42 Personal Protective Equipment Protective outer clothing o lab coats, gowns, or aprons are required at all times in a BBP lab o 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 o all protective clothing must be removed before leaving the lab and either disposable, laundered on-site, or autoclaved before removal from site 43 Personal Protective Equipment (PPE) PPE is appropriate only if it does not permit blood/OPIM to pass through and/or reach the employee’s clothing, skin, eyes, mouth, or other mucous membranes under normal use. 44 Personal Protective Equipment Gloves (latex or non-latex) o When to use them: when there is reasonable anticipation of employee hand contact with blood, OPIM, mucous membranes, or non-intact skin when performing vascular access procedures when handling or touching contaminated surfaces or items. o Remove prior to leaving the work area and discard as biohazard waste 45 Specific Practices & Techniques Personal Protective Equipment for employees (PPE) When there is occupational exposure, the employer shall provide at no cost to the employee, appropriate PPE Gloves, face shields or masks, eye protection, gowns, aprons, laboratory coats, etc. The employer is responsible for cleaning, laundering, disposal and replacement of PPE at no cost to employee Laundry: o Contaminated laundry shall be bagged o It shall not be sorted or rinsed at the location of use o Contaminated laundry shall be transported in bags labeled with proper warnings and symbols o Wear proper PPE when handling contaminated laundry 46 Latex Allergies Latex gloves have proven effective in preventing transmission of many infectious diseases to health care workers. However, for some workers, exposures to latex may result in allergic reactions. For further reading: http://www.cdc.gov/niosh/topics/latex/ 47 48 Work Practice Controls Mouth pipetting is not permitted. Work surfaces should be kept free of potential hazards. 49 Sharps Management The use of sharps in bloodborne pathogen labs is responsible for >90% of researcher exposures; mainly needle-sticks. 50 Sharps Management Keep sharps container upright readily available in the work area Never place sharps into the regular trash Use a leak-proof, puncture-resistant sharps container labeled with the biohazard symbol Do not overfill - dispose of sharps container as biohazard waste when it is 2/3 full 51 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. 52 Waste Management Solid wastes should be collected into two layers of autoclavable biohazard bags, placed within leak-proof, labeled secondary containers Collection bags should be removed from secondary containers before overflowing and only at the time of decontamination All laboratory wastes should be autoclaved before disposal into the waste stream 53 Disinfection 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. 54 Spill Specific Practices & Techniques Surface Contamination - Spill Control: Define and isolate spill area Put on proper personnel protective equipment - Includes gloves, gowns, aprons, laboratory coats, face shields or masks, eye protection, etc. Remove glass/sharps with forceps or scoop Place paper towel on spill surface and wet the paper towel with at least 10% bleach solution Allow for ADEQUATE CONTACT TIME - at least 15 minutes Remove towel and wipe clean - Repeat applying disinfectant to towel surface and allow contact time - Clean area with soapy water Properly dispose of spilled materials into biomedical waste container 55 Spill Specific Practices & Techniques Recommended Spill Kit Contents Fresh sodium hypochlorite solution (bleach) - use for general spill (at least 10% - 1:9) Personnel protective equipment o Gloves, gowns, laboratory coats, face shields or masks, eye protection, etc. o Brushes, dust pan, tongs or forceps for picking up contaminated sharps o Paper towels and biohazard bags 56 Spill Specific Practices & Techniques Bleach - Hypochlorite solution Large spill: o Use undiluted from bottle Small spill/virus inactivation: o Use at least 10% bleach solution o EPA registered tuberculocidal solution General surface disinfections: o Use at least 5% bleach solution Always have fresh solution on hand 57 Work Practice Controls Absorbent lab matting reduces the risk of splashes if infectious materials are spilled on work surfaces. Lab matting also helps contain spills. 58 Work Practice Controls Vacuum tubes of blood and other potentially infectious materials should be covered with absorbent matting during opening. 59 Restricted Access Lab doors are closed when work is in progress PI establishes specific entry requirements and policies All persons enter the lab must be made aware of the hazards present in the lab A biohazard warning sign is posted at the entrance to the lab, other signs as appropriate. 60 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. 61 Safety Engineered Materials If needles are used, safety needles should be substituted for standard if possible • If other sharps are necessary, safetyengineered substitutes should be employed 62 More Examples of Engineered Sharps Safety Devices In use Retractable needle technology After use Retractable lancets Add-ons (needle covers) Self-blunting needles 63 Biological Safety Cabinets A properly maintained and annually certified BSC must be used for all* open work with infectious materials in a BBP BSL-2 research laboratory Use of a BSC should not substitute for protective clothing or eye protection. * some procedures may not be feasible inside a cabinet; in such cases, extra PPE may substitute. 64 Training Training should be provided by the supervisor or Principal Investigator: o at the time of initial employment (or transfer) for job tasks where occupational exposure may occur o within one year of the employee's previous training and annually thereafter (if the employee remains in an at-risk position) o when changes such as modification of tasks or institution of new tasks affect the employee's potential for occupational exposures, and as new standards for safe work practices evolve 65 Warning Signs and Labels Fluorescent orange or orange-red label with word “Biohazard” and biohazard symbol in contrasting color must be provided on: o o o o Containers of regulated waste Refrigerators/freezers used to store blood/OPIM Containers used to store, transport, or ship blood/OPIM Contaminated equipment Red bags may be substituted for biohazard labels on biohazardous waste bags. 66 Exposure Control Plan (ECP) LSU exposure control plan can be found at: http://appl003.lsu.edu/PubSafety/oes.nsf/$Content/Bloodborne +Pathogens+and+Universal?OpenDocument There needs to be a plan developed specific to the work area. Each employer having an employee with potential occupational exposure shall establish a written ECP designed to eliminate or minimize employee exposure The plan should discuss, universal precautions, engineering controls, work practice controls and medical management The plan should be reviewed annually and requires record keeping of the standard 67 Exposure Control Plan Updates should include: Changes in technology that reduce/eliminate exposure (engineering controls) Annual documentation of consideration and implementation of safer medical devices Input from non-managerial employees in selecting and evaluating safer medical devices 68 Specific Practices & Techniques Personal Contamination Alert co-workers Flush and clean exposed skin surface with soap and water For eye exposure - use eye-washer or flush eye with plenty of water For mouth exposure - use saline solution or rinse with plenty of water Notify supervisor for counseling and to determine proper reporting requirements If necessary, confidential medical evaluation and follow-up will be made available 69 Post-Exposure Exposure Definition: “Any eye, mouth, other mucous membrane, non-intact skin, or parenteral contact with blood or other potentially infectious materials resulting from the performance of an employee’s duties” All work-related exposures require action! 70 Post Exposure Contact LSU Student Health Center for Post Exposure Evaluation or for Immunizations Student Health Center Infirmary Road & West Chimes Baton Rouge, LA 70803-2401 Phone: 225/578-6271 Fax: 225/578-5655 E-mail: [email protected] Immunizations:[email protected] 71 Post Exposure Complete LSU Occupational Accident Report Contact LSU Office of Risk Management Office of Risk Management Public Safety Building, Suite 124 South Stadium Road Baton Rouge, LA 70803 -7907 Email: [email protected] Phone: 225/578-3297 Forms available at: http://appl003.lsu.edu/pubsafety/riskmgt.nsf /index 72 Thank you for completing the selfstudy review session. 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