TY - JOUR A1 - Kurth, Florian Michael A1 - Develoux, Michel A1 - Mechain, Matthieu A1 - Malvy, Denis A1 - Clerinx, Jan A1 - Antinori, Spinello A1 - Gjørup, Ida E. A1 - Gascon, Joaquím A1 - Mørch, Kristine A1 - Nicastri, Emanuele A1 - Ramharter, Michael A1 - Bartoloni, Alessandro A1 - Visser, Leo A1 - Rolling, Thierry A1 - Zanger, Philipp A1 - Calleri, Guido A1 - Salas‑Coronas, Joaquín A1 - Nielsen, Henrik A1 - Just‑Nübling, Gudrun A1 - Neumayr, Andreas A1 - Hachfeld, Anna A1 - Schmid, Matthias L. A1 - Antonini, Pietro A1 - Lingscheid, Tilman A1 - Kern, Peter A1 - Kapaun, Annette A1 - Cunha, José Saraiva da A1 - Pongratz, Peter A1 - Soriano‑Arandes, Antoni A1 - Schunk, Mirjam A1 - Suttorp, Norbert A1 - Hatz, Christoph A1 - Zoller, Thomas T1 - Severe malaria in Europe : an 8-year multi-centre observational study T2 - Malaria journal N2 - Background: Malaria remains one of the most serious infections for travellers to tropical countries. Due to the lack of harmonized guidelines a large variety of treatment regimens is used in Europe to treat severe malaria. Methods: The European Network for Tropical Medicine and Travel Health (TropNet) conducted an 8-year, multicentre, observational study to analyse epidemiology, treatment practices and outcomes of severe malaria in its member sites across Europe. Physicians at participating TropNet centres were asked to report pseudonymized retrospective data from all patients treated at their centre for microscopically confirmed severe Plasmodium falciparum malaria according to the 2006 WHO criteria. Results: From 2006 to 2014 a total of 185 patients with severe malaria treated in 12 European countries were included. Three patients died, resulting in a 28-day survival rate of 98.4%. The majority of infections were acquired in West Africa (109/185, 59%). The proportion of patients treated with intravenous artesunate increased from 27% in 2006 to 60% in 2013. Altogether, 56 different combinations of intravenous and oral drugs were used across 28 study centres. The risk of acute renal failure (36 vs 17% p = 0.04) or cerebral malaria (54 vs 20%, p = 0.001) was significantly higher in patients ≥60 years than in younger patients. Respiratory distress with the need for mechanical ventilation was significantly associated with the risk of death in the study population (13 vs 0%, p = 0.001). Post-artemisinin delayed haemolysis was reported in 19/70 (27%) patients treated with intravenous artesunate. Conclusion: The majority of patients with severe malaria in this study were tourists or migrants acquiring the infection in West Africa. Intravenous artesunate is increasingly used for treatment of severe malaria in many European treatment centres and can be given safely to European patients with severe malaria. Patients treated with intravenous artesunate should be followed up to detect and manage late haemolytic events. KW - Malaria KW - Falciparum KW - Severe malaria KW - Artesunate KW - Quinine KW - Plasmodium KW - Europe KW - Clinical study Y1 - 2017 UR - http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/45465 UR - https://nbn-resolving.org/urn:nbn:de:hebis:30:3-454658 SN - 1475-2875 N1 - © The Author(s) 2017. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/ publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. VL - 16 IS - 1, Art. 57 SP - 1 EP - 11 PB - BioMed Central CY - London ER -