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Malaria
Organisms
- Plasmodium falciparum
- Plasmodium vivax
- Plasmodium ovale
- Plasmodium malariae
Transmission
- Spread by bite of infected mosquitos
Course
- Non-specific prodromal symptoms
- Paroxysms
- Fatigue
- Aches
- Nausea
- Dizziness
- Trickling sensation
- Mild fever
- Acute febrile illness
- Rigors
- Sweating
- Periodic – 48-72 hours depending on species
- Severity and course depends on species & strain of parasite
- Relapse and recrudescence
- Relapse in P.vivax, P. ovale.
- Reactivation of hepatic hypnozoites
- Ill patient
- Anaemia
- Jaundice
- Hepatosplenomegaly
- Multiple organ dysfunction
- Recrudenscesc in P. falciparum, P.malariae
- Exacerbation of persistent undetectable parasitaemia
- No exo-erythrocytic cycle
- Incubation period
- Inversely proportional to dose of sporozoites
- Increased by immunity, chemo prophylaxis
- 65-95% western travellers develop malaria within 1 month
Natural Immunity
-
West Africans who lack Duffy antigen cannot develop Plasmodium
vivax malaria as there are none of the receptors to which the merozoites
attach
-
Haemoglobin S, glucose-6-phosphate dehydrogenase deficiency,
thalasseamia, pyruvate kinase deficiency all offer resistance to Plasmodium
falciparum.
malaria
most important species
- Responsible for nearly all deaths (2 million annually)
- Complications
- Cerebral malaria
- ARDS
- Renal failure
- Hpatic dysfunction
- Hypoglycaemia (5%)
- Fluid & electrolyte & acid-base disturbances
- Circulatory collapse
- Algid malaria
- Massive haemolysis
generally milder
- Lower parasitaemia
- Relapse or recrudescence
- P. malariae
associated with nephritic syndrome
In pregnancy
- transplacental infection leads to maternal or fetal death
Diagnosis
Treatment
- Quinine
- Mefloquine
- Artemisin derivatives
- Malarone
- Chloroquine – non-falciparum malarias
- Primaquine – liver stages
- doxycycline
- sulphadoxine + pyrimethamine (Fansidar)
- atovaquone + proguanil
Prevention of infection important
- Covering bare skin
- Mosquito nets
- Reducing standing water
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