Malaria: Difference between revisions

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(Uncomplicated Malaria management update 2015)
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**False positive VDRL
**False positive VDRL


==Management<ref>World Health Organization. Guidelines for the treatment of malaria. Second edition. Geneva: World Health Organization; 2009:1-194</ref>==
==Management<ref>World Health Organization. Guidelines for the treatment of malaria, 3rd ed, WHO, Geneva 2015. http://www.who.int/malaria/publications/atoz/9789241549127/en/</ref>==
*Mixed infections involving more than one species of Plasmodium may occur in areas of high endemicity (have a low threshold for including treatment for ''P falciparum'')
*Mixed infections involving more than one species of Plasmodium may occur in areas of high endemicity (have a low threshold for including treatment for ''P falciparum'')
*[[Hyponatremia]] in the setting of hypovolemia does not require treatment beyond rehydration
*[[Hyponatremia]] in the setting of hypovolemia does not require treatment beyond rehydration
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===Uncomplicated Malaria===
===Uncomplicated Malaria===
*Chloroquine-sensitive areas: Central America, Caribbean
*Uncomplicated:
*Chloroquine-resistant areas: S. America, S. Asia, Africa
**No e/o organ dysfunction
*[[Atovaquone-proguanil]] '''OR'''
**Parasitemia <5%
*Arthemeter-lumefantrine '''OR'''
**Able to tolerate PO
*[[Quinine]] '''plus''' [[Tetracycline]], [[doxycycline]], or [[clindamycin]]
*Hospitalize:
**Severe clinical manifestations in non-immune host for P. falciparum or P. knowlesi
*Report to state health department
*For non-pregnant patients (3 day course)
**Artemether + lumefantrine
**Artesunate + amodiaquine
**Artesunate + mefloquine
**Dihydroartemisinin + piperaquine
**Artesunate + sulfadoxine–pyrimethamine (SP)
*For pregnant (1st trimester)
**Quinine + clindamycin x 7 days
*Additional considerations
**Avoid artesunate + SP in HIV/AIDS patients taking co-trimoxazole
**Avoid artesunate + amodiaquine in HIV/AIDS patients taking efavirenz or zidovudine


===Severe Malaria===
===Severe Malaria===

Revision as of 17:08, 20 January 2016

Background

  • Caused by parasitic protozoa species of the genus Plasmodium (P ovale, P vivax, P malariae, P knowlesi, and P falciparum) carried by the Anopheles mosquito
    • P falciparum most severe
  • Failure to consider for febrile illness following travel, even if seemingly temporally remote, can result in significant morbidity or mortality, especially in children and pregnant or immunocompromised patients
  • Chemoprophylaxsis does not guarantee protection
  • CDC Malaria Hotline: 770-488-7788
  • Malaria is a US nationally notifiable disease and all cases should be reported

Traveler Precautions

The CDC recommends travelers to malaria-endemic regions take the following precautions:[1]

  • Chemoprophylaxis
  • Use of insecticide-treated bed nets
  • Use of DEET-containing insect repellents
  • Wear long-sleeve shirts and pants

Clinical Features

  • Fever + exposure to endemic country
    • Cyclic fever only after chronic infection
  • Headache, cough, GI symptoms

Classification

Severe

  • Any one of the following:
    • AMS/coma
    • Severe normocytic anemia [hemoglobin < 7]
    • Renal failure
    • ARDS
    • Hypotension
    • DIC
    • Spontaneous bleeding
    • Acidosis
    • Hemoglobinuria
    • Jaundice
    • Repeated generalized seizures
    • Parasitemia >5%

Uncomplicated

  • None of the above

Differential Diagnosis

Fever in traveler

Diagnosis

  • First smear positive in >90% of cases (thick and thin Giemsa stain)
    • If initial negative, must be repeated BID x 2-3 days for proper exclusion of malaria
    • Determines degree of parasitemia and type (i.e. P. falciparum)
  • Additional lab findings

Management[2]

  • Mixed infections involving more than one species of Plasmodium may occur in areas of high endemicity (have a low threshold for including treatment for P falciparum)
  • Hyponatremia in the setting of hypovolemia does not require treatment beyond rehydration
  • Treat hypoglycemia
  • Check HIV status (coinfection can lead to worse clinical outcomes)
  • Exchange transfusion for patients with:
    • P falciparum malaria with a parasitemia greater than 10%
    • Life-threatening complications (ie, coma, respiratory failure, coagulopathy, fulminant kidney failure)
For specific dosing see the CDC Recommendations or call the Malaria CDC Hotline(855) 856-4713

Uncomplicated Malaria

  • Uncomplicated:
    • No e/o organ dysfunction
    • Parasitemia <5%
    • Able to tolerate PO
  • Hospitalize:
    • Severe clinical manifestations in non-immune host for P. falciparum or P. knowlesi
  • Report to state health department
  • For non-pregnant patients (3 day course)
    • Artemether + lumefantrine
    • Artesunate + amodiaquine
    • Artesunate + mefloquine
    • Dihydroartemisinin + piperaquine
    • Artesunate + sulfadoxine–pyrimethamine (SP)
  • For pregnant (1st trimester)
    • Quinine + clindamycin x 7 days
  • Additional considerations
    • Avoid artesunate + SP in HIV/AIDS patients taking co-trimoxazole
    • Avoid artesunate + amodiaquine in HIV/AIDS patients taking efavirenz or zidovudine

Severe Malaria

  • Intravenous quinidine plus tetracycline, or doxycycline or clindamycin

Cerebral Malaria

  • Insufficient evidence for or against giving antiepileptics
  • For severe cerebral edema, mannitol and steroids have not shown a demonstrable benefit

Disposition

  • Admit for:
    • Patients with suspected or confirmed P falciparum or P knowlesi infection
    • Young children
    • Pregnant women
    • Immunocompromised patients
  • Admit to ICU for:
    • Severe complications (e.g.coagulopathy or end-organ failure)
    • Cerebral malaria (e.g. AMS, repeated seizures, coma)
    • Parasitemia
      • >2% in non-immune (i.e. travelers)
      • >5% in semi-immune (i.e. locals)

See Also

References

  1. WHO Malaria Policy Advisory Committee and Secretariat. Malaria Policy Advisory Committee to the WHO: conlusionsions and recommendations of September 2013 meeting. Malar J. 2013;12(1):456
  2. World Health Organization. Guidelines for the treatment of malaria, 3rd ed, WHO, Geneva 2015. http://www.who.int/malaria/publications/atoz/9789241549127/en/