Malaria: Difference between revisions
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*'''CDC Malaria Hotline''': 770-488-7788 | *'''CDC Malaria Hotline''': 770-488-7788 | ||
*Malaria is a US nationally notifiable disease and all cases should be reported | *Malaria is a US nationally notifiable disease and all cases should be reported | ||
*Malaria vaccine with ~30% efficacy will be piloted in African countries in 2018, study to assess pediatric mortality<ref>WHO. Ghana, Kenya and Malawi to take part in WHO malaria vaccine pilot programme. 24 April 2017. http://www.afro.who.int/en/media-centre/pressreleases/item/9533-ghana-kenya-and-malawi-to-take-part-in-who-malaria-vaccine-pilot-programme.html</ref> | |||
===Traveler Precautions=== | ===Traveler Precautions=== | ||
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'''Severe''' | '''Severe''' | ||
*Any one of the following: | *Any one of the following: | ||
**[[ | **[[Altered mental status]]/coma | ||
**Severe normocytic anemia [hemoglobin < 7] | **Severe normocytic anemia [hemoglobin < 7] | ||
**Renal failure | **Renal failure | ||
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**Hemoglobinuria | **Hemoglobinuria | ||
**[[Jaundice]] | **[[Jaundice]] | ||
**Hepatomegaly | |||
**Splenomegaly | |||
**Repeated generalized [[seizures]] | **Repeated generalized [[seizures]] | ||
**Parasitemia >5% | **Parasitemia >5% | ||
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{{Fever in Traveler DDX}} | {{Fever in Traveler DDX}} | ||
== | ==Evaluation== | ||
*First smear positive in >90% of cases (thick and thin Giemsa stain) | *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 | **If initial negative, must be repeated BID x 2-3 days for proper exclusion of malaria | ||
**Determines degree of parasitemia and type ( | **Determines degree of parasitemia and type (e.g. ''P. falciparum'') | ||
*Additional lab findings | *Additional lab findings | ||
**Normocytic [[anemia]] | **Normocytic [[anemia]] | ||
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**False positive VDRL | **False positive VDRL | ||
==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> | ==Management== | ||
*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'')<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> | |||
*[[Hyponatremia]] in the setting of hypovolemia does not require treatment beyond rehydration | *[[Hyponatremia]] in the setting of hypovolemia does not require treatment beyond rehydration | ||
*Treat [[hypoglycemia]] | *Treat [[hypoglycemia]] | ||
*Check HIV status (coinfection can lead to worse clinical outcomes) | *Check [[HIV]] status (coinfection can lead to worse clinical outcomes) | ||
*Exchange transfusion for patients with: | *[[Exchange transfusion]] for patients with: | ||
**''P falciparum'' malaria with a parasitemia greater than 10% | **''P falciparum'' malaria with a parasitemia greater than 10% | ||
**Life-threatening complications (ie, coma, respiratory failure, coagulopathy, fulminant kidney failure) | **Life-threatening complications (ie, coma, respiratory failure, coagulopathy, fulminant kidney failure) | ||
{{Malaria antibiotics}} | |||
===Cerebral Malaria=== | ===Cerebral Malaria=== | ||
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==Disposition== | ==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. [[altered mental status]], repeated [[seizures]], coma) | |||
*Parasitemia | |||
**>2% in non-immune (i.e. travelers) | |||
**>5% in semi-immune (i.e. locals) | |||
==See Also== | ==See Also== | ||
*[[Travel Medicine]] | *[[Travel Medicine]] | ||
*[[Parasitic Diseases]] | *[[Parasitic Diseases]] | ||
==External Links== | |||
*[https://www.iamat.org/risks/malaria?gclid=CIDPmoaO7csCFZSGfgod24UAfQ IAMAT world map and country details ] | |||
==References== | ==References== |
Revision as of 22:51, 18 January 2019
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
- Malaria vaccine with ~30% efficacy will be piloted in African countries in 2018, study to assess pediatric mortality[1]
Traveler Precautions
The CDC recommends travelers to malaria-endemic regions take the following precautions:[2]
- 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:
- Altered mental status/coma
- Severe normocytic anemia [hemoglobin < 7]
- Renal failure
- ARDS
- Hypotension
- DIC
- Spontaneous bleeding
- Acidosis
- Hemoglobinuria
- Jaundice
- Hepatomegaly
- Splenomegaly
- Repeated generalized seizures
- Parasitemia >5%
Uncomplicated
- None of the above
Differential Diagnosis
Fever in traveler
- Normal causes of acute fever!
- Malaria
- Dengue
- Leptospirosis
- Typhoid fever
- Typhus
- Viral hemorrhagic fevers
- Chikungunya
- Yellow fever
- Rift valley fever
- Q fever
- Amebiasis
- Zika virus
Evaluation
- 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 (e.g. P. falciparum)
- Additional lab findings
- Normocytic anemia
- Thrombocytopenia
- ↑ ESR
- ↑ LDH
- LFT abnormalities
- ↑ Cr
- Hyponatremia
- Hypoglycemia
- False positive VDRL
Management
- 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)[3]
- 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 evidence of 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
- P. vivax and P. ovale have dormant hypnozoites in the liver which require treatment with primaquine phosphate for complete eradication
Severe Malaria
- Do not delay treatment in the unstable patient if strong suspicion for malaria as initial smear may be falsely negative
- Treatment (IV for ≥24 hours then 3 days PO course)
- Artesunate (IV)
- Clears malaria faster than quinine
- Distributed only through CDC
- Quinidine (IV) also appropriate choice; more available in US
- Artesunate (IV)
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. altered mental status, repeated seizures, coma)
- Parasitemia
- >2% in non-immune (i.e. travelers)
- >5% in semi-immune (i.e. locals)
See Also
External Links
References
- ↑ WHO. Ghana, Kenya and Malawi to take part in WHO malaria vaccine pilot programme. 24 April 2017. http://www.afro.who.int/en/media-centre/pressreleases/item/9533-ghana-kenya-and-malawi-to-take-part-in-who-malaria-vaccine-pilot-programme.html
- ↑ 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
- ↑ World Health Organization. Guidelines for the treatment of malaria, 3rd ed, WHO, Geneva 2015. http://www.who.int/malaria/publications/atoz/9789241549127/en/