Malaria Journal (Jan 2012)

Comparing changes in haematologic parameters occurring in patients included in randomized controlled trials of artesunate-amodiaquine <it>vs </it>single and combination treatments of uncomplicated falciparum in sub-Saharan Africa

  • Zwang Julien,
  • Ndiaye Jean-Louis,
  • Djimdé Abdoulaye,
  • Dorsey Grant,
  • Mårtensson Andreas,
  • Karema Corine,
  • Olliaro Piero

DOI
https://doi.org/10.1186/1475-2875-11-25
Journal volume & issue
Vol. 11, no. 1
p. 25

Abstract

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Abstract Background Artesunate-amodiaquine (AS&AQ) is a widely used artemisinin combination therapy (ACT) for falciparum malaria. A comprehensive appreciation of its effects on haematology vs other anti-malarials is needed in view of potential safety liabilities. Methods Individual-patient data analysis conducted on a database from seven randomized controlled trials conducted in sub-Saharan African comparing AS&AQ to reference treatments in uncomplicated falciparum malaria patients of all ages. Haematologic values (white cells total and neutrophil counts, haemoglobin/haematocrit, platelets) were analysed as both continuous and categorical variables for their occurrence, (severity grade 1-4) and changes during follow-up. Risks and trends were calculated using multivariate logistic random effect models. Results 4,502 patients (72% p = 0.001). Multivariate analysis showed that the risk of anaemia, thrombocytopaenia, and leucopaenia decreased with follow-up time, while neutropaenia increased; the risk of anaemia and thrombocytopaenia increased with higher baseline parasitaemia and parasitological reappearance. White cells total count was not a good surrogate for neutropaenia. No systematic significant difference between treatments was detected. Older patients were at lower risks. Conclusion The effects of AS&AQ on haematologic parameters were not different from those of other anti-malarial treatments used in sub-Saharan Africa. This analysis provides the basis for a broader evaluation of haematology following anti-malarial treatment. Continuing monitoring of haematologic safety on larger databases is required.

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