Hantavirus Pulmonary Syndrome (cont.)
Charles Patrick Davis, MD, PhD
Dr. Charles "Pat" Davis, MD, PhD, is a board certified Emergency Medicine doctor who currently practices as a consultant and staff member for hospitals. He has a PhD in Microbiology (UT at Austin), and the MD (Univ. Texas Medical Branch, Galveston). He is a Clinical Professor (retired) in the Division of Emergency Medicine, UT Health Science Center at San Antonio, and has been the Chief of Emergency Medicine at UT Medical Branch and at UTHSCSA with over 250 publications.
Melissa Conrad Stöppler, MD
Melissa Conrad Stöppler, MD, is a U.S. board-certified Anatomic Pathologist with subspecialty training in the fields of Experimental and Molecular Pathology. Dr. Stöppler's educational background includes a BA with Highest Distinction from the University of Virginia and an MD from the University of North Carolina. She completed residency training in Anatomic Pathology at Georgetown University followed by subspecialty fellowship training in molecular diagnostics and experimental pathology.
In this Article
- Hantavirus pulmonary syndrome (HPS) facts
- What is hantavirus? What is hantavirus pulmonary syndrome (HPS)?
- What is the history of hantavirus pulmonary syndrome?
- What causes hantavirus pulmonary syndrome?
- What are risk factors for hantavirus pulmonary syndrome?
- Is hantavirus contagious?
- How long is hantavirus contagious?
- What is the incubation period for hantavirus?
- What are hantavirus pulmonary syndrome symptoms and signs?
- How is hantavirus pulmonary syndrome diagnosed?
- What is the treatment for hantavirus pulmonary syndrome?
- What specialties of doctors treat hantavirus?
- What are complications of hantavirus pulmonary syndrome?
- What is the prognosis of hantavirus pulmonary syndrome?
- Is it possible to prevent hantavirus pulmonary syndrome?
- Where can people get more information on hantavirus pulmonary syndrome?
- Find a local Doctor in your town
What causes hantavirus pulmonary syndrome?
As stated above, the cause of HPS is infection of the patient by hantavirus. Currently, about 14 subtypes of hantaviruses have been identified. Many subtypes have been named (for example, Sin Nombre, Black Creek hantavirus, and New York hantavirus); some investigators simply lump them under the term of "New World hantaviruses." The Sin Nombre subtype has caused the majority of current HPS disease. The virus apparently damages cells that compose blood vessel capillaries, causing them to leak fluids. This fluid leak, if it is profound in the lungs, causes the pulmonary syndrome that can lead to death.
Hantaviruses live their lifecycle in rodents but apparently do no harm; the viruses multiply and are shed in the rodent's urine, feces, and saliva. A recent study in California suggested about 15% of all deer mice examined tested positive for hantavirus. Although the deer mouse has been the source of most HPS infections, many other rodents may carry a different hantavirus subtype virus (for example, the white-footed mouse, the cotton rat, and the rice rat).
What are risk factors for hantavirus pulmonary syndrome?
The major risk factor for HPS is association with rodents, their saliva, urine, or feces or with dust, dirt, or surfaces contaminated with such items, either by direct contact or by aerosol. Barns, sheds, homes, or buildings easily entered by rodents are potential places for hantaviruses to come in contact with humans. Rural areas that have forests and fields that can support a large rodent population are areas that increase the risk of exposure to HPS. Camping and hiking in areas known to have a high rodent population and occupying areas where rodents may seek shelter increase one's risk. Those who work in areas that may be shelter for rodents (for example, crawl spaces, vacated buildings, construction sites) may also have increased risk of HPS. The risk is higher in people who work in areas known to have produced HPS infections.
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