Fanello C1,2, Onyamboko M3, Lee SJ4,5, Woodrow C4,5, Setaphan S4, Chotivanich K4,6, Buffet P7,8,9, Jauréguiberry S9, Rockett K10, Stepniewska K5,11, Day NPJ4,5, White NJ4,5, Dondorp AM4,5.
Abstract
BACKGROUND:
Parenteral artesunate is the treatment of choice for severe malaria. Recently, haemolytic anaemia occurring 1 to 3 weeks after artesunate treatment of falciparum malaria has been reported in returning travellers in temperate countries.
METHODS:
To assess these potential safety concerns in African children, in whom most deaths from malaria occur, an open-labelled, randomized controlled trial was conducted in Kinshasa, Democratic Republic of Congo. 217 children aged between 6 months and 14 years with acute uncomplicated falciparum malaria and parasite densities over 100,000/μL were randomly allocated to intravenous artesunate or quinine, hospitalized for 3 days and then followed for 42 days.
RESULTS:
The immediate reduction in haemoglobin was less with artesunate than with quinine: median (IQR) fall at 72 h 1.4 g/dL (0.90-1.95) vs. 1.7 g/dL (1.10-2.40) (p = 0.009). This was explained by greater pitting then recirculation of once infected erythrocytes. Only 5% of patients (in both groups) had a ≥ 10% reduction in haemoglobin after day 7 (p = 0.1). One artesunate treated patient with suspected concomitant sepsis had a protracted clinical course and required a blood transfusion on day 14.
CONCLUSIONS:
Clinically significant delayed haemolysis following parenteral artesunate is uncommon in African children hospitalised with acute falciparum malaria and high parasitaemias.
TRIAL REGISTRATION:
ClinicalTrials.gov ; Identifier: NCT02092766 (18/03/2014).
Lien pour Full-text https://www.ncbi.nlm.nih.gov/pubmed/28818049