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3.
Biosecur Bioterror ; 2(4): 281-93, 2004.
Article in English | MEDLINE | ID: mdl-15650438

ABSTRACT

Many vaccines for bioterrorism agents are investigational and therefore not available (outside of research protocol use) to all at-risk laboratory workers who have begun working with these agents as a result of increased interest in biodefense research. Illness surveillance data archived from the U.S. offensive biological warfare program (from 1943 to 1969) were reviewed to assess the impact of safety measures on disease prevention (including biosafety cabinets [BSCs]) before and after vaccine availability. Most laboratory-acquired infections from agents with higher infective doses (e.g., anthrax, glanders, and plague) were prevented with personal protective measures and safety training alone. Safety measures (including BSCs) without vaccination failed to sufficiently prevent illness from agents with lower infective doses in this high-risk research setting. Infections continued with tularemia (average 15/year), Venezuelan equine encephalitis (1.9/year), and Q fever (3.4/year) but decreased dramatically once vaccinations became available (average of 1, 0.6, and 0 infections per year, respectively). While laboratory-acquired infections are not expected to occur frequently in the current lower-risk biodefense research setting because of further improvements in biosafety equipment and changes in biosafety policies, the data help to define the inherent risks of working with the specific agents of bioterrorism. The data support the idea that research with these agents should be restricted to laboratories with experience in handling highly hazardous agents and where appropriate safety training and precautions can be implemented.


Subject(s)
Biological Warfare , Communicable Diseases/epidemiology , Hazardous Substances , Laboratory Infection/epidemiology , Medical Laboratory Personnel , Brucellosis/epidemiology , Encephalomyelitis, Venezuelan Equine/epidemiology , Glanders/epidemiology , Humans , Laboratory Infection/prevention & control , Maryland/epidemiology , Military Medicine , Occupational Exposure/prevention & control , Occupational Health , Plague/epidemiology , Q Fever/epidemiology , Risk Assessment , Tularemia/epidemiology , United States/epidemiology , Vaccines
5.
Emerg Med Clin North Am ; 20(2): 501-24, 2002 May.
Article in English | MEDLINE | ID: mdl-12120489

ABSTRACT

The future success of our preparations for bioterrorism depends on many issues as presented in this article. If these issues are properly addressed, the resulting improvements in bioterrorism preparations will allow us to better deter and mitigate a bioterrorism incident and will also provide us with the added benefit of improvements in early detection, diagnosis, and treatment of natural disease outbreaks. Emergency physicians must take an active leading role in working with the various disciplines to produce a better-prepared community.


Subject(s)
Bioterrorism , Disaster Planning , Bioterrorism/prevention & control , Communicable Disease Control/methods , Communicable Disease Control/organization & administration , Decontamination/methods , Disaster Planning/methods , Disaster Planning/organization & administration , Environmental Monitoring/methods , Health Education , Health Personnel/education , Humans , Population Surveillance/methods , Research , United States
6.
JAMA ; 287(17): 2236-52, 2002 May 01.
Article in English | MEDLINE | ID: mdl-11980524

ABSTRACT

OBJECTIVE: To review and update consensus-based recommendations for medical and public health professionals following a Bacillus anthracis attack against a civilian population. PARTICIPANTS: The working group included 23 experts from academic medical centers, research organizations, and governmental, military, public health, and emergency management institutions and agencies. EVIDENCE: MEDLINE databases were searched from January 1966 to January 2002, using the Medical Subject Headings anthrax, Bacillus anthracis, biological weapon, biological terrorism, biological warfare, and biowarfare. Reference review identified work published before 1966. Participants identified unpublished sources. CONSENSUS PROCESS: The first draft synthesized the gathered information. Written comments were incorporated into subsequent drafts. The final statement incorporated all relevant evidence from the search along with consensus recommendations. CONCLUSIONS: Specific recommendations include diagnosis of anthrax infection, indications for vaccination, therapy, postexposure prophylaxis, decontamination of the environment, and suggested research. This revised consensus statement presents new information based on the analysis of the anthrax attacks of 2001, including developments in the investigation of the anthrax attacks of 2001; important symptoms, signs, and laboratory studies; new diagnostic clues that may help future recognition of this disease; current anthrax vaccine information; updated antibiotic therapeutic considerations; and judgments about environmental surveillance and decontamination.


Subject(s)
Anthrax , Bioterrorism , Gastrointestinal Diseases/microbiology , Respiratory Tract Infections/microbiology , Skin Diseases, Bacterial/microbiology , Adolescent , Adult , Aged , Anthrax/diagnosis , Anthrax/epidemiology , Anthrax/history , Anthrax/prevention & control , Anthrax/therapy , Anthrax Vaccines , Anti-Bacterial Agents/therapeutic use , Antibiotic Prophylaxis , Bacillus anthracis , Child , Child, Preschool , Decontamination , Environmental Exposure , Female , Gastrointestinal Diseases/diagnosis , Gastrointestinal Diseases/therapy , History, 20th Century , History, 21st Century , Humans , Immunocompromised Host , Infant , Infection Control , Male , Middle Aged , Pregnancy , Respiratory Tract Infections/diagnosis , Respiratory Tract Infections/therapy , Skin Diseases, Bacterial/diagnosis , Skin Diseases, Bacterial/therapy , Spores, Bacterial , United States , Vaccination
7.
JAMA ; 287(18): 2391-405, 2002 May 08.
Article in English | MEDLINE | ID: mdl-11988060

ABSTRACT

OBJECTIVE: To develop consensus-based recommendations for measures to be taken by medical and public health professionals if hemorrhagic fever viruses (HFVs) are used as biological weapons against a civilian population. PARTICIPANTS: The Working Group on Civilian Biodefense included 26 representatives from academic medical centers, public health, military services, governmental agencies, and other emergency management institutions. EVIDENCE: MEDLINE was searched from January 1966 to January 2002. Retrieved references, relevant material published prior to 1966, and additional sources identified by participants were reviewed. CONSENSUS PROCESS: Three formal drafts of the statement that synthesized information obtained in the evidence-gathering process were reviewed by the working group. Each draft incorporated comments and judgments of the members. All members approved the final draft. CONCLUSIONS: Weapons disseminating a number of HFVs could cause an outbreak of an undifferentiated febrile illness 2 to 21 days later, associated with clinical manifestations that could include rash, hemorrhagic diathesis, and shock. The mode of transmission and clinical course would vary depending on the specific pathogen. Diagnosis may be delayed given clinicians' unfamiliarity with these diseases, heterogeneous clinical presentation within an infected cohort, and lack of widely available diagnostic tests. Initiation of ribavirin therapy in the early phases of illness may be useful in treatment of some of these viruses, although extensive experience is lacking. There are no licensed vaccines to treat the diseases caused by HFVs.


Subject(s)
Arenaviridae Infections/prevention & control , Biological Warfare , Bioterrorism , Bunyaviridae Infections/prevention & control , Civil Defense/standards , Filoviridae Infections/prevention & control , Flavivirus Infections/prevention & control , Hemorrhagic Fevers, Viral/prevention & control , Public Health Administration/standards , Public Health Practice/standards , Aerosols , Antiviral Agents/therapeutic use , Arenaviridae/pathogenicity , Arenaviridae Infections/diagnosis , Arenaviridae Infections/drug therapy , Arenaviridae Infections/epidemiology , Arenaviridae Infections/transmission , Bunyaviridae/pathogenicity , Bunyaviridae Infections/diagnosis , Bunyaviridae Infections/drug therapy , Bunyaviridae Infections/epidemiology , Bunyaviridae Infections/transmission , Cadaver , Clinical Laboratory Techniques , Disaster Planning/standards , Disease Outbreaks/prevention & control , Filoviridae/pathogenicity , Filoviridae Infections/diagnosis , Filoviridae Infections/drug therapy , Filoviridae Infections/epidemiology , Filoviridae Infections/transmission , Flaviviridae/pathogenicity , Flavivirus Infections/diagnosis , Flavivirus Infections/drug therapy , Flavivirus Infections/epidemiology , Flavivirus Infections/transmission , Hemorrhagic Fevers, Viral/diagnosis , Hemorrhagic Fevers, Viral/drug therapy , Hemorrhagic Fevers, Viral/epidemiology , Hemorrhagic Fevers, Viral/transmission , Infection Control , Research , Ribavirin/therapeutic use , United States , Viral Vaccines
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