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
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Translate to: East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski


NIH genetic and rare disease info[edit source]

Dengue fever is a rare disease.


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