Résumé
L’artésunate (AS), dérivé semi-synthétique de l’artémisinine, est un antipaludique très puissant. Dans le traitement du paludisme grave en zones d’endémie palustre, l’AS intraveineux (IV) est supérieur à la quinine (Q), tant chez l’adulte que chez l’enfant. En France, l’AS n’est disponible que depuis mai 2011, soumis à une autorisation temporaire d’utilisation (ATU). Cette mise au point retrace l’histoire de l’AS dans le monde, rapporte les principales études cliniques démontrant sa supériorité sur la Q, puis détaille l’utilisation de l’AS en France et en Europe, ainsi que les modalités pratiques de sa prescription et de sa surveillance. Abstract Artesunate, a semi-synthetic derivative of artemisinin, has proven to be an efficient therapy for severe malaria. In endemic areas, the findings clearly support the superiority of intravenous artesunate over quinine for the treatment of severe malaria in both adults and children. In France, artesunate is available since May 2011. This review describes the history of artesunate, reports the major studies supporting the superiority of artesunate over quinine, details the use of artesunate in France and Europe, and describes the prescription practices and monitoring of artesunate.
Références
World Health Organization (2010) World malaria report 2010. WHO, Geneva, http://www.who.int/malaria/world_malaria_report_2010/worldmalariareport2010.pdf
O’Meara WP, Mangeni JN, Steketee R, Greenwood B (2010) Changes in the burden of malaria in sub-Saharan Africa. Lancet Infect Dis 10:545–555
Institut national de veille sanitaire, Centre national de référence du paludisme (2009) Rapport d’activités
World Health Organization (2000) Severe falciparum malaria. Trans R Soc Trop Med Hyg 94(Suppl 1):1–90
Société de pathologie infectieuse de langue française, Collège des universitaires de maladies infectieuses et tropicales, Société de réanimation de langue française, et al (2008) Recommandations for clinical practice. Management and prevention of imported Plasmodium falciparum malaria (Revision 2007 of the 1999 consensus conference). Med Mal Infect 38:39–117
Bruneel F, Tubach F, Corne P, et al (2010) Severe imported falciparum malaria: a cohort study in 400 critically ill adults. PLoS One 5(10):e13236
Klayman DL (1985) Qinghaosu (artemisinin): an antimalarial drug from China. Science 228:1049–1055
1994) Artemisinin. Trans R Soc Trop Med Hyg 88(Suppl 1):1–65
Brewer TG, Peggins JO, Grate SJ, et al (1994) Neurotoxicity in animals due to arteether and artemether. Trans R Soc Trop Med Hyg 88(Suppl 1):33–36
Wesche DL, DeCoster MA, Tortella FC, et al (1994) Neurotoxicity of artemisinin analogs in vitro. Antimicrob Agents Chemother 38:1813–1819
Brewer TG, Grate SJ, Peggins JO, et al (1994) Fatal neurotoxicity of arteether and artemether. Am J Trop Med Hyg 51:251–259
Tran TH, Day NP, Nguyen HP, et al (1996) A controlled trial of artemether or quinine in Vietnamese adults with severe falciparum malaria. N Engl J Med 335:76–83
van Hensbroek MB, Onyiorah E, Jaffar S, et al (1996) A trial of artemether or quinine in children with cerebral malaria. N Engl J Med 335:69–75
Artemether-Quinine Meta-analysis Study Group (2001) Trans R Soc Trop Med Hyg 95:637–650
Eastman RT, Fidock DA (2009) Artemisinin-based combination therapies: a vital tool in efforts to eliminate malaria. Nat Rev Microbiol 7:864–874
Buffet PA, Safeukui I, Deplaine G, et al (2011) The pathogenesis of Plasmodium falciparum malaria in humans: insights from splenic physiology. Blood 117:381–392
Dondorp A, Nosten F, Stepniewska K, et al (2005) Artesunate versus quinine for treatment of severe Falciparum malaria: a randomised trial. Lancet 366:717–725
World Health Organization (2006) Guidelines for the treatment of malaria. WHO, Geneva, http://www.who.int/malaria/docs/TreatmentGuidelines2006.pdf
Lalloo DG, Shingadia D, Pasvol G, et al (2007) UK malaria treatment guidelines. J Infect 54:111–121
Dondorp AM, Fanello CI, Hendriksen IC, et al (2010) Artesunate versus quinine in the treatment of severe falciparum malaria in African children (AQUAMAT): an open-label, randomised trial. Lancet 376:1647–1657
Sinclair D, Donegan S, Lalloo DG (2011) Artesunate versus quinine for treating severe malaria. Cochrane Database Syst Rev (3): CD005967
Zoller T, Junghanss T, Kapaun A, et al (2011) Intravenous artesunate for severe malaria in travelers, Europe. Emerg Infect Dis 17:771–777
Teuscher F, Gatton ML, Chen N, et al (2010) Artemisinininduced dormancy in Plasmodium falciparum: duration, recovery rates, and implications in treatment failure. J Infect Dis 202:1362–1368
Morch K, Strand O, Dunlop O, et al (2008) Severe malaria and artesunate treatment, Norway. Emerg Infect Dis 14:1816–1818
Bartoloni A, Tomasoni L, Bartalesi F, et al (2010) Combined intravenous treatment with artesunate and quinine for severe malaria in Italy. Am J Trop Med Hyg 83:274–276
Mali S, Steele S, Slutsker L, et al (2010) Malaria surveillance-United States, 2008. MMWR Surveill Summ 59:1–15
Watts G (2011) Use artesunate not quinine to treat severe malaria, say experts. BMJ 342:d2590. doi: 10.1136/bmj.d2590
Dondorp AM, Nosten F, Yi P, et al (2009) Artemisinin resistance in Plasmodium falciparum malaria. N Engl J Med 361:455–467
Dondorp AM (2011) Interscience conference on antimicrobial agents and chemotherapy, communication orale, Chicago
Author information
Authors and Affiliations
Corresponding author
Additional information
Cet article correspond à la conférence faite par l’auteur au congrès de la SRLF 2012 dans la session: Actualités en infectiologie.
Rights and permissions
About this article
Cite this article
Bruneel, F. Traitement du paludisme grave par artésunate intraveineux. Réanimation 21 (Suppl 2), 399–405 (2012). https://doi.org/10.1007/s13546-011-0339-7
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s13546-011-0339-7