Rift valley fever: Difference between revisions
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==Clinical Features== | ==Clinical Features== | ||
*Incubation period of 2-6 days | *Incubation period of 2-6 days | ||
===Mild=== | |||
*No symptoms or flu-like illness (fever, myalgias, joint pain, headache) | |||
*Early disease can be mistaken for meningitis with occasional neck stiffness and sensitivity to light | |||
*Resolves within 1 week | |||
===Severe=== | |||
*Occular form- 0.5-2% of patients | |||
**Mild disease form + retinal lesions, blurred and decreased vision | |||
**Retinal lesions occur 1-3 weeks after disease onset and last 10-12 weeks | |||
**50% of patients with macular lesions will develop permanent vision loss | |||
*Meningoencephalitis form- <1% of patients | |||
**Severe headache, memory loss, hallucinations, confusion, vertigo, seizures, coma, and late neurological complications | |||
**Onset is 1-4 weeks after mild symptoms | |||
**Residual severe neurological deficits are common | |||
*Hemorrhagic fever form- <1% of patients | |||
**Jaundice is first sign due to liver dysfunction | |||
**Hemorrhage (vomit, stool, gums, menorrhagia), purpuric rash, echymosis | |||
**Onset is 2-4 days after illness, death in 3-6 days | |||
**Most fatalities from RVF, 50% fatality rate | |||
==Differential Diagnosis== | ==Differential Diagnosis== | ||
{{Fever in Traveler DDX}} | {{Fever in Traveler DDX}} | ||
== | ==Evaluation== | ||
*Pursue other possible causes of fever | *Pursue other possible causes of fever | ||
*IgM ELISA, viral detection, and RT-PCR can be used to diagnose acute infection. IgG ELISA for previous infection. | *IgM ELISA, viral detection, and RT-PCR can be used to diagnose acute infection. IgG ELISA for previous infection. | ||
==Management== | ==Management== | ||
*Mild | *Mild: requires no intervention (self limited_ | ||
* | *Severe | ||
**Supportive Care | **Supportive Care | ||
***Pain control | ***Pain control | ||
****DO NOT use ASA in hemorrhagic form | ****DO NOT use [[ASA]] in hemorrhagic form | ||
**[[IVFs]] | **[[IVFs]] | ||
**Blood Component [[Transfusion]] - consider in hemorrhagic shock | **Blood Component [[Transfusion]] - consider in hemorrhagic shock | ||
===Vaccines=== | |||
*Inactivated vaccine has been developed for humans | *Inactivated vaccine has been developed for humans | ||
**Not licensed and not commercially available | **Not licensed and not commercially available | ||
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*[[Travel Medicine]] | *[[Travel Medicine]] | ||
== | ==External Links== | ||
*http://www.who.int/mediacentre/factsheets/fs207/en/ | *[http://www.who.int/mediacentre/factsheets/fs207/en/ WHO - Rift Valley Fever] | ||
*http://www.cdc.gov/vhf/rvf/index.html | *[http://www.cdc.gov/vhf/rvf/index.html CDC - Rift Valley Fever] | ||
==References== | |||
<references/> | <references/> | ||
[[Category:ID]] | |||
Latest revision as of 21:08, 12 January 2021
Background
- Viral illness caused by RVF virus, a bunyaviridae
- Primarily infects domesticated animals; cattle, sheep, buffalo, etc.
- Outbreaks related to unusually heavy rainfall and flooding
- Found mostly in eastern and southern Africa where domesticated animals are raised
- Can be found in most of Africa
- Recent outbreaks in Saudi Arabia and Yemen (first outside African continent)
- Outbreaks cause major economic impact with livestock death
Transmission
- Mosquitos, most commonly Aedes, are a reservoir and vector for RVF virus
- Able to live with the virus and pass on to offspring, virus remains viable in eggs
- Bite livestock and humans to cause infection
- Increased rainfall increases mosquito numbers and is associated with outbreaks
- Humans are most commonly infected through direct contact of blood or other bodily fluids of infected livestock
- Slaughter, veterinary procedures, obstetrical procedures
- No documented human to human transmission
- Aerosolized transfer has occurred in laboratory settings
Clinical Features
- Incubation period of 2-6 days
Mild
- No symptoms or flu-like illness (fever, myalgias, joint pain, headache)
- Early disease can be mistaken for meningitis with occasional neck stiffness and sensitivity to light
- Resolves within 1 week
Severe
- Occular form- 0.5-2% of patients
- Mild disease form + retinal lesions, blurred and decreased vision
- Retinal lesions occur 1-3 weeks after disease onset and last 10-12 weeks
- 50% of patients with macular lesions will develop permanent vision loss
- Meningoencephalitis form- <1% of patients
- Severe headache, memory loss, hallucinations, confusion, vertigo, seizures, coma, and late neurological complications
- Onset is 1-4 weeks after mild symptoms
- Residual severe neurological deficits are common
- Hemorrhagic fever form- <1% of patients
- Jaundice is first sign due to liver dysfunction
- Hemorrhage (vomit, stool, gums, menorrhagia), purpuric rash, echymosis
- Onset is 2-4 days after illness, death in 3-6 days
- Most fatalities from RVF, 50% fatality rate
Differential Diagnosis
Fever in traveler
- Normal causes of acute fever!
- Malaria
- Dengue
- Leptospirosis
- Typhoid fever
- Typhus
- Viral hemorrhagic fevers
- Chikungunya
- Yellow fever
- Rift valley fever
- Q fever
- Amebiasis
- Zika virus
Evaluation
- Pursue other possible causes of fever
- IgM ELISA, viral detection, and RT-PCR can be used to diagnose acute infection. IgG ELISA for previous infection.
Management
- Mild: requires no intervention (self limited_
- Severe
- Supportive Care
- Pain control
- DO NOT use ASA in hemorrhagic form
- Pain control
- IVFs
- Blood Component Transfusion - consider in hemorrhagic shock
- Supportive Care
Vaccines
- Inactivated vaccine has been developed for humans
- Not licensed and not commercially available
- Experimental use on veterinary and lab workers
- Approved vaccines for livestock
Disposition
- Isolation precautions: standard, contact, and consider droplet
- Admit if severe form suspected, likely ICU
- Consult ID
- Consult ophthalmology for ocular form
