Bioterrorism preparedness
Viral Hemorrhagic Fevers: Information Health Advisories & Resources
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Report all suspected cases of Viral Hemorrhagic Fevers immediately to Public Health - Seattle & King County by calling 206-296-4774.
Epidemiology and microbiology
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Virus family
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Virus/syndrome
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Geographic occurrence of natural disease
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Reservoir or vector
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Incubation period
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Mortality
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Arena-viruses
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Machupo (Bolivian hemorrhagic fever)
Junin (Argentine hemorrhagic fever)
Guanarito (Venezuelan hemorrhagic fever)
Sabia (Brazilian hemorrhagic fever)
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South America
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Rodents
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7-16 days
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15-30%
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Lassa Fever
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West Africa
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5-16 days
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Bunya-viruses
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Crimean-Congo HF
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Crimea, parts of Africa, Europe, and Asia
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Ticks
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3-12 days
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2-50%
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Rift Valley Fever
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Africa
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Mosquitoes
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2-6 days
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<1%
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Hantaviruses
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Diverse areas
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Rodents
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Usually 2-4 weeks
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5-50%
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Filo-viruses
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Ebola Hemorrhagic Fever
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Africa
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Unknown
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2-21 days
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23-90%
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Marburg Hemorrhagic Fever
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2-14 days
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Flavi-viruses
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Yellow Fever
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Tropical Africa, Latin America
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Mosquitoes
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3-6 days
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20%
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Dengue Fever
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Tropical areas
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3-14 days
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1-50%
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Kyansur Forest Disease
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India
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Ticks
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2-9 days
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3-10%
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Omsk Hemorrhagic Fever
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Siberia
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0.5-10%
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- Viral hemorrhagic fevers (VHF) are caused by a group of single-stranded RNA viruses from four families: Arenaviruses, bunyaviruses, filoviruses, and flaviviruses.
- Humans are infected via the bite of an infected arthropod, inhalation of rodent excreta, or contact with infected animal carcasses.
- Person-to-person transmission is possible with several agents, primarily through blood or body fluid exposure, and rarely, via airborne transmission.
Viral Hemorrhagic Fevers and Bioterrorism
- Agents of concern for potential use as a biological weapon include the arenaviruses, filoviruses, hantaviruses, tick-borne hemorrhagic fever viruses and yellow fever.
- All agents have an initial febrile prodrome with non-specific symptoms: headache, malaise,
- fatigue/exhaustion, arthralgia, myalgia, nausea, dizziness, non-bloody diarrhea.
- Clinical signs reflect vascular involvement with increased capillary permeability.
- Ebola, Marburg, Rift Valley fever, and Crimean-Congo hemorrhagic fever viruses can cause disseminated intravascular coagulation (DIC); other viruses generally do not.
- Illness onset is typically abrupt with filoviruses, flaviviruses, and Rift Valley fever, and more insidious with arenaviruses.
- A maculopapular rash appears about five days after onset of illness caused by filoviruses.
- Jaundice may be prominent in filovirus infections, Lassa fever, Rift Valley fever, and yellow fever.
- Meningoencephalitis can occur in Rift Valley fever, Kyasunar Forest disease, and Omsk hemorrhagic fever.
- Severe exudative pharyngitis is a characteristic early feature of Lassa fever.
- Contact Public Health for patients with suspected VHF and the following clinical criteria:
- Fever (101ºF) for less than three weeks,
- Severe illness and no predisposing factors for hemorrhagic manifestations,
- And at least two of the following hemorrhagic symptoms: hemorrhagic or purple rash, epistaxis, hematemesis, hemoptysis, blood in stools, other, and no established alternative diagnosis.
- Evaluation should include a travel history and inquiry about exposure to ticks, mosquitoes, animals, and ill persons.
- Laboratory diagnostic tests (blood/serum and other body fluids) are performed at public health labs.
- Antigen detection by antigen-capture ELISA
- Serology
- RT-PCR
- Immunohistochemistry
- Electron microscopy
- Viral isolation (performed at CDC)
- Airborne and contact precautions should be followed by all health care, environmental, and laboratory workers when VHF is suspected.
- Patients should be placed in a negative pressure room and dedicated medical equipment used, if available.
- Patients recovering from an arenavirus or filovirus infection should refrain from sexual activity for three months post-recovery.
- Treatment is primarily supportive.
- Correct coagulopathies as needed.
- Avoid anticoagulant therapies, anti-platelet drugs, and intramuscular injections.
- Maintain fluid and electrolyte balance.
- Ribavirin may be available under an investigational new drug protocol for patients with arenavirus or bunyavirus infection.
- Refer to www.bt.cdc.gov for current treatment and prophylaxis guidelines.
- Persons exposed to VHF should be monitored for fever or hemorrhagic symptoms for 21 days post-exposure.
- Ribavirin may have a role in the prophylaxis of symptomatic persons exposed to arenaviruses or bunyaviruses.
- The only vaccine currently commercially available for VHF is a live-virus vaccine for yellow fever vaccine.
- Recommended for travelers to endemic areas of South America and Africa and laboratory personnel.
- Not useful for post-exposure prophylaxis because the time-to-immunity post-vaccination (10 days) is longer than the disease incubation period (three to six days).
- Vaccines against Argentine hemorrhagic fever and Rift Valley fever are available as investigational new drugs, and research is underway to develop vaccines against other VHF viruses.
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