Propensity Score Analysis of Artesunate Versus Quinine for Severe Imported Plasmodium falciparum Malaria in France

Author:

El Ket Nermine1,Kendjo Eric12,Thellier Marc123,Assoumou Lambert1,Potard Valérie1,Taieb Aida24,Tantaoui Ilhame24,Caumes Eric15,Piarroux Renaud123,Roussel Camille46,Buffet Pierre246,Costagliola Dominique1,Jauréguiberry Stéphane125ORCID

Affiliation:

1. Sorbonne Université, Institut National de la Santé et de la Recherche Médicale (INSERM), Institut Pierre-Louis d’Epidémiologie et de Santé Publique, France

2. Assistance Publique–Hôpitaux de Paris (AP-HP), Centre de Référence du Paludisme, Hôpital Pitié-Salpêtrière, France

3. Service de Parasitologie Mycologie, AP-HP, Hôpital Pitié-Salpêtrière, France

4. Paris Diderot Université, INSERM, Biologie Intégrée du Globule Rouge, Institut National de la Transfusion Sanguine, France

5. Service de Maladies Infectieuses et Médecine Tropicale, AP-HP, Hôpital Pitié-Salpêtrière, France

6. Paris Descartes Université, France

Abstract

Abstract Background Little is known on the use of artesunate compared with quinine for the treatment of imported malaria cases in nonendemic countries with a high level of care. Therefore, we compared the 2 treatments in terms of mortality and hospital and intensive care unit (ICU) discharge rates. Methods We analyzed the cohort of all severe imported malaria patients reported to the French National Reference Center from 2011 to 2017. After controlling for differences between quinine- and artesunate-treated individuals using the inverse probability of treatment weighting method, 28-day mortality rate was compared between the groups as well as hospital and ICU discharge rates using Kaplan–Meier estimation and weighted Cox proportional hazard models. Results Overall, 1544 patients were enrolled. Fifty patients died, 18 in the quinine group (n = 460) and 32 in the artesunate group (n = 1084), corresponding to death rates of 3.9% and 2.9%, respectively. No difference was evident between quinine and artesunate either in mortality or in hospital discharge rate, with hazard ratios (HRs) of 1.03 (95% confidence interval [CI], 0.47–2.25) and 1.12 (95% CI, 0.94–1.34), respectively. Artesunate was associated with a faster ICU discharge rate (HR, 1.18. 95% CI, 1.02–1.36). Conclusions In a country with a high level of care, artesunate was associated with a shorter length of stay in the ICU, which supports the actual therapeutic transition; however, no difference was found in terms of mortality or in hospital discharge rates between artesunate- and quinine-treated patients.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

Reference26 articles.

1. Artesunate versus quinine for treatment of severe falciparum malaria: a randomised trial;Dondorp;Lancet,2005

2. Artesunate versus quinine in the treatment of severe falciparum malaria in African children (AQUAMAT): an open-label, randomised trial;Dondorp;Lancet,2010

3. ATU nominative, protocole d’utilisation thérapeutique et de recueil d’informations, Malacef® (artésunate) 60 mg, poudre et solvant pour solution injectable. Available at: http://ansm.sante.fr/Activites/Autorisations-temporaires-d-utilisation-ATU/PUT-Specialites-soumises-a-un-protocole-d-utilisation-therapeutique/Liste-des-specialites-soumises-a-un-protocole-d-utilisation-therapeutique/MALACEF-60-mg-poudre-et-solvant-pour-solution-injectable. Accessed 26 March 2019.

4. Société de Pathologie Infectieuse de Langue Française. Prise en charge et prévention du paludisme d’importation. Mise à jour 2017 des RPC 2007. Available at: http://www.infectiologie.com/UserFiles/File/spilf/recos/2017-palu-texte-final-flash.pdf. Accessed 26 March 2019.

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