Emerging Infectious Diseases (May 2015)

Delayed-Onset Hemolytic Anemia in Patients with Travel-Associated Severe Malaria Treated with Artesunate, France, 2011–2013

  • Stéphane Jauréguiberry,
  • Marc Thellier,
  • Papa Alioune Ndour,
  • Flavie Ader,
  • Camille Roussel,
  • Romain Sonneville,
  • Julien Mayaux,
  • Sophie Matheron,
  • Adela Angoulvant,
  • Benjamin Wyplosz,
  • Christophe Rapp,
  • Thierry Pistone,
  • Bénédicte Lebrun-Vignes,
  • Eric Kendjo,
  • Martin Danis,
  • Sandrine Houzé,
  • François Bricaire,
  • Dominique Mazier,
  • Pierre Buffet,
  • Eric Caumes

DOI
https://doi.org/10.3201/eid2105.141171
Journal volume & issue
Vol. 21, no. 5
pp. 804 – 812

Abstract

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Artesunate is the most effective treatment for severe malaria. However, delayed-onset hemolytic anemia has been observed in ≈20% of travelers who receive artesunate, ≈60% of whom require transfusion. This finding could discourage physicians from using artesunate. We prospectively evaluated a cohort of 123 patients in France who had severe imported malaria that was treated with artesunate; our evaluation focused on outcome, adverse events, and postartesunate delayed-onset hemolysis (PADH). Of the 123 patients, 6 (5%) died. Overall, 97 adverse events occurred. Among the 78 patients who received follow-up for >8 days after treatment initiation, 76 (97%) had anemia, and 21 (27%) of the 78 cases were recorded as PADH. The median drop in hemoglobin levels was 1.3 g/dL; 15% of patients with PADH had hemoglobin levels of <7 g/dL, and 1 required transfusion. Despite the high incidence of PADH, the resulting anemia remained mild in 85% of cases. This reassuring result confirms the safety and therapeutic benefit of artesunate.

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