2009
DOI: 10.1186/1475-2875-8-277
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Cardiac complication after experimental human malaria infection: a case report

Abstract: A 20 year-old healthy female volunteer participated in a clinical Phase I and IIa safety and efficacy trial with candidate malaria vaccine PfLSA-3-rec adjuvanted with aluminium hydroxide. Eleven weeks after the third and last immunization she was experimentally infected by bites of Plasmodium falciparum-infected mosquitoes. When the thick blood smear became positive, at day 11, she was treated with artemether/lumefantrine according to protocol. On day 16 post-infection i.e. two days after completion of treatme… Show more

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Cited by 47 publications
(41 citation statements)
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“…One serious cardiac adverse event was reported; the true nature and patho-physiological explanation of that event remains unclear [21]. Severe adverse events (grade 3) related to clinical malaria occur in up to half of the volunteers and persist for several days.…”
Section: Discussionmentioning
confidence: 99%
“…One serious cardiac adverse event was reported; the true nature and patho-physiological explanation of that event remains unclear [21]. Severe adverse events (grade 3) related to clinical malaria occur in up to half of the volunteers and persist for several days.…”
Section: Discussionmentioning
confidence: 99%
“…However, the epidemiology and clinical course of vivax malaria appears to be changing with cases of vivax malaria being complicated with ARDS, acute kidney injury, anaemia and cerebral malaria 3. Considering the high incidence of malaria in sub-Saharan Africa, India and South-East Asia, very few cardiac complications have been reported 4 5. Malaria may be a risk factor for acute myocardial infarction (MI).…”
Section: Discussionmentioning
confidence: 99%
“…Hematological and biochemical parameters were monitored daily. Because of a previous cardiac-related serious adverse event (SAE) following CHMI with Pf infection,39 markers of cardiac damage and coagulation were assessed. Troponin, lactate dehydrogenase (LDH), platelets, and D-dimer were assessed daily during the period when blood stage parasitemia was expected, and for 3 days after initiating curative treatment with atovaquone/proguanil.…”
Section: Methodsmentioning
confidence: 99%