Dengue fever

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(Redirected from Dengue shock syndrome)

Alternate names[edit | edit source]

Dengue hemorrhagic fever; Dengue shock syndrome; Philippine hemorrhagic fever; Thai hemorrhagic fever; Singapore hemorrhagic fever; Hemorrhagic dengue; DF; Dengue virus infection

Definition[edit | edit source]

Dengue fever (DF), caused by dengue virus, is an arboviral disease characterized by an initial non-specific febrile illness that can sometimes progress to more severe forms manifesting capillary leakage and hemorrhage (dengue hemorrhagic fever, or DHF) and shock (dengue shock syndrome, or DSS). File:Symptoms man - dengue.webm

Dengue


Epidemiology[edit | edit source]

DF is found in the tropics worldwide, especially in Southeast Asia, the Pacific region, and the Americas, with 40% of the global population at risk. An estimated 50 to 100 million cases of DF, 500,000 hospitalizations, and 20,000 deaths occur yearly worldwide.

Cause[edit | edit source]

  • Over 25 different viruses cause viral hemorrhagic fever.
  • Dengue virus belongs to the Flaviviridae family, genus Flavivirus. Four distinct serotypes, with significant strain variation, are recognized.
  • Dengue is caused by one of any of four related viruses: Dengue virus 1, 2, 3, and 4.  For this reason, a person can be infected with a dengue virus as many as four times in his or her lifetime.

Signs and symptoms[edit | edit source]

  • Mild symptoms of dengue can be confused with other illnesses that cause fever, aches and pains, or a rash.
  • Graphic of human body showing most common symptom of dengue is fever with any of the following: eye pain, headache, muscle pain, rash, bone pain, nausea/vomiting, joint pain

The most common symptom of dengue is fever with any of the following:

  • Nausea, vomiting
  • Rash
  • Aches and pains (eye pain, typically behind the eyes, muscle, joint, or bone pain)
  • Any warning sign
  • Symptoms of dengue typically last 2–7 days. Most people will recover after about a week.

Transmission[edit | edit source]

  • Dengue viruses are spread to people through the bites of infected Aedes species mosquitoes (Ae. aegypti or Ae. albopictus).
  • These mosquitoes typically lay eggs near standing water in containers that hold water, like buckets, bowls, animal dishes, flower pots, and vases.
  • These mosquitoes prefer to bite people, and live both indoors and outdoors near people.
  • Mosquitoes that spread dengue, chikungunya, and Zika bite during the day and night.
  • Mosquitoes become infected when they bite a person infected with the virus. Infected mosquitoes can then spread the virus to other people through bites.

From mother to child

  • A pregnant woman already infected with dengue can pass the virus to her fetus during pregnancy or around the time of birth.
  • To date, there has been one documented report of dengue spread through breast milk.
  • Because of the benefits of breastfeeding, mothers are encouraged to breastfeed even in areas with risk of dengue.
  • Dengue in pregnancy
  • Rarely, dengue can be spread through blood transfusion, organ transplant, or through a needle stick injury.

Diagnosis[edit | edit source]

Most state health departments and many commercial laboratories perform dengue diagnostic testing.

Nucleic acid amplification tests (NAATs)

  • For patients with suspected dengue virus disease, NAATs are the preferred method of laboratory diagnosis.
  • NAATs should be performed on serum specimens collected 7 days or less after symptom onset.
  • Laboratory confirmation can be made from a single acute-phase serum specimen obtained early (≤7 days after fever onset) in the illness by detecting viral genomic sequences with rRT-PCR or dengue nonstructural protein 1 (NS1) antigen by immunoassay.
  • Presence of virus by rRT-PCR or NS1 antigen in a single diagnostic specimen is considered laboratory confirmation of dengue in patients with a compatible clinical and travel history.

Serologic tests

  • IgM antibody testing can identify additional infections and is an important diagnostic tool. However, interpreting the results is complicated by cross-reactivity with other flaviviruses, like Zika, and determining the specific timing of infection can be difficult.
  • Later in the illness (≥4 days after fever onset), IgM against dengue virus can be detected with MAC-ELISA. For patients presenting during the first week after fever onset, diagnostic testing should include a test for dengue virus (RT-PCR or NS1) and IgM.
  • For patients presenting >1 week after fever onset, IgM detection is most useful, although NS1 has been reported positive up to 12 days after fever onset . In the United States, both MAC-ELISA and RT-PCR are approved as in vitro diagnostic tests.
  • IgM in a single serum sample strongly suggests a recent dengue virus infection and should be presumed confirmatory for dengue if the infection occurred in a place where other potentially cross-reactive flaviviruses (such as Zika, West Nile, yellow fever, and Japanese encephalitis viruses) are not a risk.
  • PRNTs can resolve false-positive IgM antibody results caused by non-specific reactivity, and, in some cases, can help identify the infecting virus. However, in areas with high prevalence of dengue and Zika virus neutralizing antibodies, PRNT may not confirm a significant proportion of IgM positive results. PRNT testing is available through several state health departments and CDC.

Cross-reactive flaviviruses

  • If infection is likely to have occurred in a place where other potentially cross-reactive flaviviruses circulate, both molecular and serologic diagnostic testing for dengue and other flaviviruses should be performed.
  • People infected with or vaccinated against other flaviviruses (such as yellow fever or Japanese encephalitis) may produce cross-reactive flavivirus antibodies, yielding false-positive serologic dengue diagnostic test results.
  • IgG antibody testing
  • IgG detection by ELISA in a single serum sample is not useful for diagnostic testing because it remains detectable for life after a dengue virus infection.

Treatment[edit | edit source]

No treatment: No specific antiviral agents exist for dengue. Supportive care is advised:

  • Patients should be advised to stay well hydrated and to avoid aspirin (acetylsalicylic acid), aspirin-containing drugs, and other nonsteroidal anti-inflammatory drugs (such as ibuprofen) because of their anticoagulant properties.
  • Fever should be controlled with acetaminophen and tepid sponge baths.
  • Febrile patients should avoid mosquito bites to reduce risk of further transmission.

Severe Dengue

  • For those who develop severe dengue, close observation and frequent monitoring in an intensive care unit may be required.
  • Prophylactic platelet transfusions in dengue patients are not beneficial and may contribute to fluid overload.
  • Administration of corticosteroids has no demonstrated benefit and is potentially harmful to patients; corticosteroids should not be used except in the case of autoimmune-related complication (e.g., hemophagocytic lymphohistiocytosis, immune thrombocytopenia purpura).

Prevention[edit | edit source]

Prevent dengue by avoiding mosquito bites.

  • All four dengue viruses are spread primarily through the bite of an infected Aedes species (Ae. aegypti and Ae. albopictus) mosquito. These mosquitoes also spread chikungunya and Zika viruses.
  • The mosquitoes that spread dengue are found in most tropical and subtropical regions of the world, including many parts of the United States.
  • Ae. aegypti and Ae. albopictus bite during the day and night.
  • A dengue vaccine is available for use in some parts of the world, including United States territories.
Dengue fever Resources
Wikipedia


NIH genetic and rare disease info[edit source]

Dengue fever is a rare disease.


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