Posted September 30, 2019. Past health advisories and alerts are archived for historical purposes and are not maintained or updated.
No human nor equine cases of West Nile Virus (WNV) have been reported in Washington residents in 2019 to date. Positive mosquito samples have been detected this summer in Benton, Grant and Yakima Counties, but none so far in Spokane. Due to limited resources, ongoing WNV monitoring is limited both for Spokane Regional Health District (SRHD) and Panhandle Health District in North Idaho, thus we are unable to definitively determine actual local prevalence of disease.
Continued mild weather will contribute to ongoing mosquito activity, prolonging the risk for acquiring WNV. SRHD would like to remind healthcare providers of this possible risk to advise their patients to take appropriate precautions.
Symptoms & Clinical Management
The incubation period is usually two to 14 days. While most (80%) of WNV infections are asymptomatic, symptomatic persons can experience an acute systemic febrile illness that often includes headache, weakness, myalgia, and/or arthralgia. Gastrointestinal symptoms and a transient maculopapular rash are less common symptoms. Less than 1% of infected persons develop neuroinvasive disease, which typically manifests as meningitis, encephalitis, or acute flaccid paralysis. Neuroinvasive disease is more likely to occur in immunocompromised individuals and/or those over age 60.
Rarely, cardiac dysrhythmias, myocarditis, rhabdomyolysis, optic neuritis, uveitis, chorioretinitis, pancreatitis, and hepatitis have been described in patients with WNV disease. The case fatality rate for neuroinvasive disease is around 10%
Routine clinical laboratory studies are generally nonspecific. In patients with neuroinvasive disease, CSF examination generally shows lymphocytic pleocytosis, but neutrophils may predominate early in the course of illness. Brain MRI is frequently normal, but signal abnormalities in the basal ganglia, thalamus, and brainstem may be seen in patients with encephalitis, and in the anterior spinal cord in patients with poliomyelitis.
There is no specific treatment for WNV; clinical management is supportive. Patients with severe meningeal symptoms often require pain control for headaches and antiemetic therapy and rehydration for associated nausea and vomiting. Treatment for neuroinvasive disease often involves hospitalization, intravenous fluids, respiratory support, and prevention of secondary infection.
The most efficient diagnostic method for WNV infection is detection of virus using the IgM antibody-capture enzyme immunoassay (MAC-EIA) or microsphere immunoassay (MIA) of IgM antibody to WNV in serum collected eight to 14 days after onset or CSF collected within eight days of illness onset. More than 90% of those infected have detectible serum IgM eight days after onset; serum collected within eight days of illness onset may not have detectable IgM and testing should be repeated on a convalescent-phase sample. The EIA can exhibit serologic cross-reactivity in patients who have been recently vaccinated against or recently infected with related flaviviruses (such as St. Louis encephalitis virus). In addition, since most WNV infections are asymptomatic and IgM can persist in the serum for up to 500 days, the presence of IgM in residents from an endemic area may indicate a previous rather than current infection.
The diagnosis can also be confirmed by a four-fold rise in antibody titer between acute and convalescent (14 to 21 days after acute) sera. Since serum IgM does not cross the blood-brain barrier, IgM in the CSF strongly suggests central nervous system infection.
Reverse transcription polymerase chain reaction (RT-PCR) assay to detect WNV nucleic acid in serum or CSF is useful for patients with immune dysfunction but is not recommended for routine diagnosis of WNV disease.
Testing should be done at commercial laboratories.
The primary route of transmission is through the bite of an infected mosquito. WNV is not transmitted through casual contact. In very rare cases, it has been transmitted through blood transfusions, organ transplants, percutaneous injuries in the laboratory, and from mother to baby via the placenta and possibly breastmilk.
There is no vaccine for humans. WNV prevention depends on mosquito bite prevention. Personal protective measures include use of mosquito repellants, wearing long-sleeved shirts and long pants, and limiting outdoor exposure from dusk to dawn. Using air conditioning, installing window and door screens, and reducing mosquito breeding sites can further reduce the risk for WNV exposure. To reduce mosquito breeding sites around the home, advise patients to twice weekly drain and routinely empty anything that holds water, such as gutters, pet bowls, tires, bird baths, etc. Keep water moving in ornamental ponds by recirculating water or by installing a fountain.
Further information on WNV Surveillance in Washington can be found here: doh.wa.gov/DataandStatisticalReports/DiseasesandChronicConditions/WestNileVirus.
Further information on mosquito prevention can be found at srhd.org/bringit.