Intravenous Artesunate for Imported Severe Malaria in Children Treated in Four Tertiary Care Centers in Germany: A Retrospective Study
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Intravenous Artesunate for Imported Severe Malaria in Children Treated in Four Tertiary Care Centers in Germany: A Retrospective Study. / Bélard, Sabine; Brand, Judith; Schulze-Sturm, Ulf; Janda, Ales; von Both, Ulrich; Tacoli, Costanza; Alberer, Martin; Kempf, Caroline; Stegemann, Miriam S; Krüger, Renate; Varnholt, Verena; Blohm, Martin; Reiter, Karl; Zoller, Thomas; Suttorp, Norbert; Mall, Marcus; von Bernuth, Horst; Gratopp, Alexander; Hübner, Johannes; Hufnagel, Markus; Kobbe, Robin; Kurth, Florian.
In: PEDIATR INFECT DIS J, Vol. 38, No. 11, 11.2019, p. e295-e300.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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TY - JOUR
T1 - Intravenous Artesunate for Imported Severe Malaria in Children Treated in Four Tertiary Care Centers in Germany: A Retrospective Study
AU - Bélard, Sabine
AU - Brand, Judith
AU - Schulze-Sturm, Ulf
AU - Janda, Ales
AU - von Both, Ulrich
AU - Tacoli, Costanza
AU - Alberer, Martin
AU - Kempf, Caroline
AU - Stegemann, Miriam S
AU - Krüger, Renate
AU - Varnholt, Verena
AU - Blohm, Martin
AU - Reiter, Karl
AU - Zoller, Thomas
AU - Suttorp, Norbert
AU - Mall, Marcus
AU - von Bernuth, Horst
AU - Gratopp, Alexander
AU - Hübner, Johannes
AU - Hufnagel, Markus
AU - Kobbe, Robin
AU - Kurth, Florian
PY - 2019/11
Y1 - 2019/11
N2 - BACKGROUND: Intravenous artesunate (ivA) is the standard treatment for severe malaria. Data systematically evaluating the use of ivA in pediatric patients outside malaria-endemic regions are limited. The aim of this case series was to summarize efficacy and safety of ivA for imported severe malaria in children in Germany.METHODS: Our retrospective case series included pediatric patients with imported severe malaria treated with at least 1 dose of ivA (Artesun, Guilin Pharmaceutical; Shanghai, China) at 4 German tertiary care centers. Severe malaria was defined according to World Health Organization criteria.RESULTS: Between 2010 and 2018, 14 children with a median [interquartile range (IQR)] age of 6 (1;9.5) years were included. All children were of African descent. All but 2 patients had Plasmodium falciparum malaria; 1 child had P. vivax malaria and 1 child had P. falciparum and P. vivax co-infection. Median (IQR) parasitemia at admission in patients with P. falciparum was 9.5% (3;16.5). Patients were treated with 1-10 [median (IQR) 3 (3;4)] doses ivA. All but one patient received a full course of oral antimalarial treatment. Parasite clearance was achieved within 2-4 days, with the exception of 1 patient with prolonged clearance of peripheral parasitemia. Three patients experienced posttreatment hemolysis but none needed blood transfusion. Otherwise ivA was safe and well tolerated.CONCLUSIONS: ivA was highly efficacious in this pediatric cohort. We observed episodes of mild to moderate posttreatment hemolysis in approximately one-third of patients. The legal status and usage of potentially lifesaving ivA should be evaluated in Europe.
AB - BACKGROUND: Intravenous artesunate (ivA) is the standard treatment for severe malaria. Data systematically evaluating the use of ivA in pediatric patients outside malaria-endemic regions are limited. The aim of this case series was to summarize efficacy and safety of ivA for imported severe malaria in children in Germany.METHODS: Our retrospective case series included pediatric patients with imported severe malaria treated with at least 1 dose of ivA (Artesun, Guilin Pharmaceutical; Shanghai, China) at 4 German tertiary care centers. Severe malaria was defined according to World Health Organization criteria.RESULTS: Between 2010 and 2018, 14 children with a median [interquartile range (IQR)] age of 6 (1;9.5) years were included. All children were of African descent. All but 2 patients had Plasmodium falciparum malaria; 1 child had P. vivax malaria and 1 child had P. falciparum and P. vivax co-infection. Median (IQR) parasitemia at admission in patients with P. falciparum was 9.5% (3;16.5). Patients were treated with 1-10 [median (IQR) 3 (3;4)] doses ivA. All but one patient received a full course of oral antimalarial treatment. Parasite clearance was achieved within 2-4 days, with the exception of 1 patient with prolonged clearance of peripheral parasitemia. Three patients experienced posttreatment hemolysis but none needed blood transfusion. Otherwise ivA was safe and well tolerated.CONCLUSIONS: ivA was highly efficacious in this pediatric cohort. We observed episodes of mild to moderate posttreatment hemolysis in approximately one-third of patients. The legal status and usage of potentially lifesaving ivA should be evaluated in Europe.
U2 - 10.1097/INF.0000000000002417
DO - 10.1097/INF.0000000000002417
M3 - SCORING: Journal article
C2 - 31626041
VL - 38
SP - e295-e300
JO - PEDIATR INFECT DIS J
JF - PEDIATR INFECT DIS J
SN - 0891-3668
IS - 11
ER -