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


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
02 01 2020
Historique:
received: 19 09 2018
accepted: 11 03 2019
pubmed: 16 3 2019
medline: 7 1 2021
entrez: 16 3 2019
Statut: ppublish

Résumé

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. 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. 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). 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.

Sections du résumé

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.

Identifiants

pubmed: 30874798
pii: 5381062
doi: 10.1093/cid/ciz206
doi:

Substances chimiques

Antimalarials 0
Artemisinins 0
Artesunate 60W3249T9M
Quinine A7V27PHC7A

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

280-287

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Auteurs

Nermine El Ket (N)

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

Eric Kendjo (E)

Sorbonne Université, Institut National de la Santé et de la Recherche Médicale (INSERM), Institut Pierre-Louis d'Epidémiologie et de Santé Publique, France.
Assistance Publique-Hôpitaux de Paris (AP-HP), Centre de Référence du Paludisme, Hôpital Pitié-Salpêtrière, France.

Marc Thellier (M)

Sorbonne Université, Institut National de la Santé et de la Recherche Médicale (INSERM), Institut Pierre-Louis d'Epidémiologie et de Santé Publique, France.
Assistance Publique-Hôpitaux de Paris (AP-HP), Centre de Référence du Paludisme, Hôpital Pitié-Salpêtrière, France.
Service de Parasitologie Mycologie, AP-HP, Hôpital Pitié-Salpêtrière, France.

Lambert Assoumou (L)

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

Valérie Potard (V)

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

Aida Taieb (A)

Assistance Publique-Hôpitaux de Paris (AP-HP), Centre de Référence du Paludisme, Hôpital Pitié-Salpêtrière, France.
Paris Diderot Université, INSERM, Biologie Intégrée du Globule Rouge, Institut National de la Transfusion Sanguine, France.

Ilhame Tantaoui (I)

Assistance Publique-Hôpitaux de Paris (AP-HP), Centre de Référence du Paludisme, Hôpital Pitié-Salpêtrière, France.
Paris Diderot Université, INSERM, Biologie Intégrée du Globule Rouge, Institut National de la Transfusion Sanguine, France.

Eric Caumes (E)

Sorbonne Université, Institut National de la Santé et de la Recherche Médicale (INSERM), Institut Pierre-Louis d'Epidémiologie et de Santé Publique, France.
Service de Maladies Infectieuses et Médecine Tropicale, AP-HP, Hôpital Pitié-Salpêtrière, France.

Renaud Piarroux (R)

Sorbonne Université, Institut National de la Santé et de la Recherche Médicale (INSERM), Institut Pierre-Louis d'Epidémiologie et de Santé Publique, France.
Assistance Publique-Hôpitaux de Paris (AP-HP), Centre de Référence du Paludisme, Hôpital Pitié-Salpêtrière, France.
Service de Parasitologie Mycologie, AP-HP, Hôpital Pitié-Salpêtrière, France.

Camille Roussel (C)

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

Pierre Buffet (P)

Assistance Publique-Hôpitaux de Paris (AP-HP), Centre de Référence du Paludisme, Hôpital Pitié-Salpêtrière, France.
Paris Diderot Université, INSERM, Biologie Intégrée du Globule Rouge, Institut National de la Transfusion Sanguine, France.
Paris Descartes Université, France.

Dominique Costagliola (D)

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

Stéphane Jauréguiberry (S)

Sorbonne Université, Institut National de la Santé et de la Recherche Médicale (INSERM), Institut Pierre-Louis d'Epidémiologie et de Santé Publique, France.
Assistance Publique-Hôpitaux de Paris (AP-HP), Centre de Référence du Paludisme, Hôpital Pitié-Salpêtrière, France.
Service de Maladies Infectieuses et Médecine Tropicale, AP-HP, Hôpital Pitié-Salpêtrière, France.

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