Malaria Treatment With Injectable ArteSunate

Inclusion Criteria

• •Patients (= 2 months old) admitted to one of the study sites and treated for severe malaria with IV quinine in the first part of the study and patients treated with IV/IM artesunate in the second part of the study will be included. Patients need to fulfill the WHO criteria for severe malaria and must be unable to take oral treatment (WHO, 2010, WHO, 2011). In addition all participants need to give their informed consent
• •Conditions: Positive rapid diagnostic test (RDT) for Plasmodium falciparum HRP2 or lactate dehydrogenase and/or a positive blood slide (thick smear). Patient will be considered to be positive if one of the two tests is positive. In case of negative result of both tests, the patient will not be enrolled in the study and will receive care according to the usual routine practice in the hospital/health center in question.
• •Definition of severe malaria according to WHO (WHO, 2010): In a patient with P. falciparum asexual parasitaemia and no other obvious cause for the symptoms, the presence of one or more of the following clinical or laboratory features classifies the patient as suffering from severe malaria:
• •Clinical features (hospitals and health centers):
• •impaired consciousness or unrousable coma
• •prostration, i.e. generalized weakness so that the patient is unable walk or sit up without assistance
• •failure to feed
• •multiple convulsions - more than two episodes in 24 h
• •deep breathing, respiratory distress (acidotic breathing)
• •circulatory collapse or shock, systolic blood pressure \< 70 mm Hg in adults and \< 50 mm Hg in children
• •clinical jaundice plus evidence of other vital organ dysfunction
• •Complementary Laboratory findings (hospitals only)
• •severe anaemia (Hb \< 5g/dl, packed cell volume \< 15%)
• •hypoglycemia (blood glucose \< 2.2 mmol/l or \< 40 mg/dl)
• •metabolic acidosis (plasma bicarbonate \< 15 mmol/l)
• •serum creatinine \> 265 ìmol/l suggesting renal impairment