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Aerosol Information and Courses from MediaLab, Inc.

These are the MediaLab courses that cover Aerosol and links to relevant pages within the course.

Learn more about laboratory continuing education for medical technologists to earn CE credit for AMT, ASCP, NCA, and state license renewal and recertification. Or get information about laboratory safety and compliance courses that deliver cost-effective OSHA safety training and continuing education to your laboratory's employees.



General Laboratory Question Bank - Review Mode (no CE)
Which of the following sources is most likely to result in an infection from the AIDS virus:View Page

Introduction to Bioterrorism
Biological Agents

Biological agents are organisms or toxins that can kill or incapacitate people, live stock, and crops. The three basic groups of biological agents that would likely be used as weapons are bacteria, viruses, and toxins. Biological agents can be dispersed as aerosols or airborne particles.

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Agent: Botulism (bacterium)

Most likely means of dissemination: Aerosol (eating contaminated food)Primary route of entry: Inhalation (oral)General signs and symptoms: Difficulty with speaking, swallowing, or blurred or double vision, drooping eyelids (ptosis), dilated pupils, dry mouth, decreased gag reflex, weakening of the reflexes (hyporeflexia), abnormal sensations such as numbness, prickling, tingling, and arm or leg weakness.Botulism is caused by a neurotoxin and technically could be classified as a chemical WMD. For our discussion it is placed under biological agents because the toxin is derived from a bacterium. Botulism is potentially life-threatening, producing a characteristic clinical picture of muscular paralysis leading to respiratory failure.                Photo courtesy of the CDC archives.    

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Chemical Agents

Chemical warfare agents are poisonous vapors, aerosols, liquids, or solids that have toxic effects on people, animals or plants. They can be released in a number of ways such as by bombs or sprayed from aircraft. Some chemical agents are odorless and tasteless. They can have an immediate effect (such as a few seconds to a few minutes), or a delayed effect (from several hours to several days). Even though chemical agents have the potential to be lethal, they are difficult to deliver in lethal concentrations, particularly in outdoor situations where they tend to dissipate rapidly.

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Responding to an Alarm

If you receive an alert that an aerosol device was triggered or that a biological agent was released in the area: Make sure any fans are turned off. Leave the area immediately. Close the door to the area to keep others out. Notify your supervisor or emergency personnel immediately. Shut down the air handling system in the building. Make a list of all persons that were in the area to give to authorities if requested.

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What if: Chemical Attack

A chemical attack involves poisonous vapors, aerosols, liquids, or compounds. A terrorist might spread harmful chemicals with a bomb; spray from aircraft, boats, or vehicles; pour the chemicals into water or onto food; or leave a container of poisonous chemical in a confined public space.

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Microbiology / Serology Question Bank - Review Mode (no CE)
Which one of the following statements about Coxiella burnetii is not true:View Page

Molecular Methods in Clinical Microbiology
Challenges for Implementation: Separation of Key Activities

Prevention of contamination is a very key consideration when introducing molecular methods into the routine diagnostic laboratory setting. Because amplification methods are so sensitive, the incidental introduction of even a few copies of exogenous nucleic acid can lead to false positive results. Both physical design and process controls are key aspects of preventing erroneous results.Significant potential sources of contamination are the large quantities of target molecules from previously amplified materials. Amplicons may contaminate work surfaces, air space, pipettes, and reagents. Scrupulous technique is one aspect of preventing contamination; another is the physical separation of specific steps of the process. Ideally, all molecular work will take place in distinct areas designated for key aspects of the workflow, with each area having its own dedicated equipment (especially pipetting equipment). The three designated areas are:Clean area: Where master mixes and other reagents are prepared in the absence of any specimen material. In this area, protection from aerosol contamination is a key consideration. Use of a dead air box with ultraviolet (UV) lighting for decontamination, or a separated area with controlled airflow, are two ways to address this need.Specimen preparation and extraction area: Separated from the area where amplification and detection of amplified product occurs, in order to prevent contamination of samples with amplicons of previously processed specimens.Amplification, detection, and identification of the amplified product: Ideally, this area would be both separated and enclosed.To some extent, the introduction of platforms that utilize automated specimen processing equipment and/or closed amplification and detection systems mitigates stringent separation and space requirements. Good practice, however, would always include designated spaces for each activity, as well as a defined workflow.

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Challenges for Implementation: Required Work Skills

In addition to instilling a consciousness about movement from one area to the next, other work skills are critical and key to obtaining accurate results:Aseptic techniquePipetting skillsAseptic technique Due to the sensitivity of molecular assays, there is little margin for error. Cross contamination from specimens with large numbers of organism/target nucleic acid can result from the slightest deviation in aseptic technique. The use of aerosol barrier pipette tips and positive displacement pipette devices go a long way in preventing aerosol contamination, but do not replace the attentiveness of the technologist during each transfer of specimen material. When working with specimens, only one specimen container should be opened at a time.Pipetting skills Although more and more assays are being introduced with pre-prepared master mixes, invariably some reagent preparation is required. This often entails the transfer of very small volumes, which leaves no margin of error during pipetting. Attentiveness to accuracy of pipetting is a must.

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Why is it important to consider work space and workflow design for molecular methods? (Select all that apply.):View Page

Parasitology Question Bank - Review Mode (no CE)
Which of the following safety measures must be in place when handling initial samples for parasite study?View Page

Preliminary Identification of the Primary Select Agents of Bioterrorism
Brucella species

Brucella is a dangerous, highly virulent organism and the aerosols are highly infectious. It is the MOST common cause of laboratory-associated bacterial infections. Laboratory acquired cases have occurred by aerosol generating procedures, direct skin contact with cultures, and by sniffing cultures. It should NOT be manipulated on an open bench.Catalase: Brucella is catalase positive. Catalase testing MUST be performed with extreme caution in a biosafety cabinet (BSC) due to the creation of aerosols. Oxidase: PositiveBeta-lactamase: PositiveUrease: PositiveXV factors: Not required for growth (satellite phenomenon with S. aureus is negative)Serological testing: Often used because so difficult to grow. An acute and convalescent phase specimen should be collected 21 days apart.

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Toxins

Toxin Comment Most Likely Means of Dissemination Primary Route of Entry General Signs and Symptoms Laboratory Testing Botulism toxin: Gram stained image of C. botulinum courtesy of CDC Produced by Clostridium botulinum Could be purified and used in a bioterrorist event to contaminate food or aerosolized to cause disease Aerosol Food contamination Inhalation Ingestion Difficulty speaking or swallowing Blurred or double vision Drooping eyelids (ptosis) Dilated pupils Dry mouth, decreased gag reflex Weakening of the reflexes (hyporeflexia) Abnormal sensations such as numbness, tingling, and progressive arm or leg weakness Flaccid paralysis Culture, anaerobic Digoxigen-labeled IgG ELISA to detect A, B, E, and F toxins Mouse Bioassay for all toxin types and to confirm DIG ELISA Ricin toxin: Extracted from Castor beans Inhibits protein synthesis Causes death approximately 72 hours after initial exposure As an aerosol Inhalation Fever Cough Chest tightness Dyspnea Cyanosis Gastroenteritis Necrosis Antibody detection in clinical specimens Clinical testing not performed unless known exposure has occurred

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Viruses

VirusMost Likely Means of Dissemination Primary Route of EntryGeneral Signs and SymptomsLaboratory TestingSmallpox: Image courtesy of CDCAs an aerosol Inhalation High fever with extreme lethargySevere headache, backache, and abdominal painRash that starts as red bumps but quickly develops into small, itchy blisters Consult local APHL prior to sample collectionShell vial and DFA Monoclonal IFAMolecular tests Viral Hemorrhagic Fevers (Ebola, Marburg, Lassa, and Argentine): SolidLiquidAerosol AbsorptionInhalationIngestion Vary by type of viral hemorrhagic fever (VHF), but initial signs and symptoms often include: Marked feverFatigueDizzinessMuscle aches, loss of strength, and exhaustionSevere cases of VHF often show signs of bleeding under the skin, within internal organs, or from body orifices like the mouth, eyes, or ears Enzyme-linked immunosorbent assay (ELISA)Polymerase chain reaction (PCR)Viral culture

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Location Where Organisms Naturally Occur, Disease Produced, and Mode of Transmission, continued:

Brucella species: Brucella is distributed in nature worldwide and found in domesticated and wild animals, such as cattle, sheep, and pigs. Infection with Brucella species, known as brucellosis, is caused in humans by exposure to infected animal fluids or food products. This includes ingesting non-pasteurized dairy products, such as milk or cheese, inhaling aerosols, and skin contact with the fluids of infected animals. Brucellosis poses an increased risk of occupational exposure to laboratory, veterinary, and slaughterhouse workers. Brucella is the most commonly reported laboratory-associated bacterial infection.Burkholderia mallei and B. pseudomallei: Most Burkholderia are found in soil, but B. mallei is only found in mammals. B.mallei is the causative agent for Glanders which primarily affects animals such as donkeys, mules, and horses. Horses, the organism's natural host, are highly susceptible to infection. Human infection is rare and usually occurs in people working with infected animals or laboratory workers handling the organism. The organism is endemic in Africa, Asia, the Middle East, and Central and South America, and usually enters via the eyes, nose, mouth, abrasions or cuts in the skin, or through inhalation. B. pseudomallei is found in soil and water and can accidentally infect animals, plants, and rarely humans. It is the causative agent of melioidosis, which is endemic in areas of southeast Asia, Taiwan, and northern Australia. The organism generally enters through cuts in the skin, ingestion of contaminated water, or by inhalation of an aerosol.

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Category A Agents: Reasons Why They May be Used to Create Public Health Emergencies

Anthrax (B. anthracis): Inhalation of anthrax spores is virtually 100% fatal Spores can remain infectious for decadesBotulism: Most lethal toxic agent known Toxin could be used to contaminate food supplies Can be aerosolized in enclosed areasPneumonic Plague (Y. pestis): Aerosolized in large amounts Short incubation period, usually in less than three days, and invariably fatal without early and effective antimicrobial therapy Untreated, fatality rate exceeds 90% Disease is spread from direct exposure to respiratory droplets of infected humansSmallpox: Highly contagious and deliberate spread by aerosol is extremely infectious Mass panic would be createdTularemia (F. tularensis): Highly contagious and easily spread An aerosol containing as few as 25 organisms can cause infection Easily penetrates the smallest breaks in the skinViral Hemorrhagic Fever: Causes internal and external bleeding and would likely cause great panic and easily spread by direct contact with body fluids or respiratory droplets Outbreak due to bioterrorist attack could lead to mass illness and death

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The Influenza A Virus: 2009 H1N1 Subtype
Epidemiology of the Virus

The Influenza A 2009 H1N1 virus spreads from person to person in a similar way to the seasonal flu in previous years.The primary route of influenza virus transmission and infection are by respiratory droplets and aerosols. Transmission may also occur via contaminated hands (person-to-person) and surfaces. Infected individuals can shed the virus and spread Influenza A 2009 H1N1 to others anywhere from 1 day prior to getting sick up until 5-7 days after symptoms arise. This range of viral shedding can be even longer in children and in some individuals who are immunocompromised.

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Tuberculosis Awareness for Health Care Workers
Procedures with Increased TB Risk

Some procedures increase the potential for TB risk because they create aerosols. They include:Sputum induction and aerosol treatments Bronchoscopy Endotracheal intubation and suctioning Autopsy Microbiology processing TB specimens Surgical drainage of TB abscesses

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TB Infection Control in the Laboratory

The laboratory director is responsible for the development of a risk-based infection control plan for the laboratory.The personnel are trained in methods that minimize the production of aerosols.The personal protective equipment that is specified in the infection control plan is used consistently. A respirator is used when performing procedures that can result in aerosolization outside a biological safety cabinet.Disposable gloves are worn for all laboratory procedures.

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Which of the following barriers are recommended in microbiology laboratories where manipulation of biosafety level 3 agents (e.g., Mycobacterium tuberculosis) is performed?View Page
Biosafety Level Criteria and Requirements for Handling Specimens Suspected of Containing Mycobacterium tuberculosis

All specimens suspected of containing M. tuberculosis (including specimens processed for other microorganisms) should be handled in a Class I or II biological safety cabinet (BSC). Appropriate personal protective equipment (PPE) must be used. At a minimum, this includes gloves and fluid-resistant laboratory coat or gown. Non-aerosol-producing manipulations (eg, preparing direct smears for acid-fast staining when done in conjunction with training and periodic checking of competency) can be performed using biosafety level-2 (BSL-2) practices and procedures, containment equipment, and facilities. BSL-3 practices, safety equipment, and facility design and construction are applicable to microbiology laboratories that work with indigenous or exotic agents with a potential for respiratory transmission, and which may cause serious and potentially lethal infection. If the laboratory is propagating and manipulating cultures for M. tuberculosis, BSL-3 practices, containment equipment, and facilities are required. Barriers include controlled access to the laboratory and ventilation requirements that minimize the release of infectious aerosols from the laboratory. Secondary barriers should include self-closing double-door access and negative airflow into the laboratory. Exhausted air must not be recirculated. Work surfaces must be decontaminated, using the laboratory-approved disinfectant, upon completion of procedures, immediately following a spill, and at the end of the work shift, if the surface was recontaminated since the last cleaning. Laboratory equipment should be routinely decontaminated.Hands must be washed upon completion of work with potentially infectious materials and before leaving the laboratory.

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