Post-treatment haemolysis in African children with hyperparasitaemic falciparum malaria; a randomized comparison of artesunate and quinine

<strong>Background</strong> Parenteral artesunate is the treatment of choice for severe malaria. Recently, haemolytic anaemia occurring 1 to 3 weeks after artesunate treatment of falciparum malaria has been reported in returning travellers in temperate countries. <strong>Methods&l...

Full description

Bibliographic Details
Main Authors: Fanello, C, Onyamboko, M, Lee, S, Woodrow, C, Setaphan, S, Chotivanich, K, Buffet, P, Jauréguiberry, S, Rockett, K, Stepniewska, K, Day, N, White, N, Dondorp, A
Format: Journal article
Language:English
Published: BioMed Central 2017
_version_ 1826259965710434304
author Fanello, C
Onyamboko, M
Lee, S
Woodrow, C
Setaphan, S
Chotivanich, K
Buffet, P
Jauréguiberry, S
Rockett, K
Stepniewska, K
Day, N
White, N
Dondorp, A
author_facet Fanello, C
Onyamboko, M
Lee, S
Woodrow, C
Setaphan, S
Chotivanich, K
Buffet, P
Jauréguiberry, S
Rockett, K
Stepniewska, K
Day, N
White, N
Dondorp, A
author_sort Fanello, C
collection OXFORD
description <strong>Background</strong> Parenteral artesunate is the treatment of choice for severe malaria. Recently, haemolytic anaemia occurring 1 to 3 weeks after artesunate treatment of falciparum malaria has been reported in returning travellers in temperate countries. <strong>Methods</strong> To assess these potential safety concerns in African children, in whom most deaths from malaria occur, an open-labelled, randomized controlled trial was conducted in Kinshasa, Democratic Republic of Congo. 217 children aged between 6 months and 14 years with acute uncomplicated falciparum malaria and parasite densities over 100,000/μL were randomly allocated to intravenous artesunate or quinine, hospitalized for 3 days and then followed for 42 days. <strong>Results</strong> The immediate reduction in haemoglobin was less with artesunate than with quinine: median (IQR) fall at 72 h 1.4 g/dL (0.90–1.95) vs. 1.7 g/dL (1.10–2.40) (p = 0.009). This was explained by greater pitting then recirculation of once infected erythrocytes. Only 5% of patients (in both groups) had a ≥ 10% reduction in haemoglobin after day 7 (p = 0.1). One artesunate treated patient with suspected concomitant sepsis had a protracted clinical course and required a blood transfusion on day 14. <strong>Conclusions</strong> Clinically significant delayed haemolysis following parenteral artesunate is uncommon in African children hospitalised with acute falciparum malaria and high parasitaemias.
first_indexed 2024-03-06T18:58:10Z
format Journal article
id oxford-uuid:1293d668-89c7-4710-b64b-abb05235c100
institution University of Oxford
language English
last_indexed 2024-03-06T18:58:10Z
publishDate 2017
publisher BioMed Central
record_format dspace
spelling oxford-uuid:1293d668-89c7-4710-b64b-abb05235c1002022-03-26T10:08:45ZPost-treatment haemolysis in African children with hyperparasitaemic falciparum malaria; a randomized comparison of artesunate and quinineJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:1293d668-89c7-4710-b64b-abb05235c100EnglishSymplectic Elements at OxfordBioMed Central2017Fanello, COnyamboko, MLee, SWoodrow, CSetaphan, SChotivanich, KBuffet, PJauréguiberry, SRockett, KStepniewska, KDay, NWhite, NDondorp, A<strong>Background</strong> Parenteral artesunate is the treatment of choice for severe malaria. Recently, haemolytic anaemia occurring 1 to 3 weeks after artesunate treatment of falciparum malaria has been reported in returning travellers in temperate countries. <strong>Methods</strong> To assess these potential safety concerns in African children, in whom most deaths from malaria occur, an open-labelled, randomized controlled trial was conducted in Kinshasa, Democratic Republic of Congo. 217 children aged between 6 months and 14 years with acute uncomplicated falciparum malaria and parasite densities over 100,000/μL were randomly allocated to intravenous artesunate or quinine, hospitalized for 3 days and then followed for 42 days. <strong>Results</strong> The immediate reduction in haemoglobin was less with artesunate than with quinine: median (IQR) fall at 72 h 1.4 g/dL (0.90–1.95) vs. 1.7 g/dL (1.10–2.40) (p = 0.009). This was explained by greater pitting then recirculation of once infected erythrocytes. Only 5% of patients (in both groups) had a ≥ 10% reduction in haemoglobin after day 7 (p = 0.1). One artesunate treated patient with suspected concomitant sepsis had a protracted clinical course and required a blood transfusion on day 14. <strong>Conclusions</strong> Clinically significant delayed haemolysis following parenteral artesunate is uncommon in African children hospitalised with acute falciparum malaria and high parasitaemias.
spellingShingle Fanello, C
Onyamboko, M
Lee, S
Woodrow, C
Setaphan, S
Chotivanich, K
Buffet, P
Jauréguiberry, S
Rockett, K
Stepniewska, K
Day, N
White, N
Dondorp, A
Post-treatment haemolysis in African children with hyperparasitaemic falciparum malaria; a randomized comparison of artesunate and quinine
title Post-treatment haemolysis in African children with hyperparasitaemic falciparum malaria; a randomized comparison of artesunate and quinine
title_full Post-treatment haemolysis in African children with hyperparasitaemic falciparum malaria; a randomized comparison of artesunate and quinine
title_fullStr Post-treatment haemolysis in African children with hyperparasitaemic falciparum malaria; a randomized comparison of artesunate and quinine
title_full_unstemmed Post-treatment haemolysis in African children with hyperparasitaemic falciparum malaria; a randomized comparison of artesunate and quinine
title_short Post-treatment haemolysis in African children with hyperparasitaemic falciparum malaria; a randomized comparison of artesunate and quinine
title_sort post treatment haemolysis in african children with hyperparasitaemic falciparum malaria a randomized comparison of artesunate and quinine
work_keys_str_mv AT fanelloc posttreatmenthaemolysisinafricanchildrenwithhyperparasitaemicfalciparummalariaarandomizedcomparisonofartesunateandquinine
AT onyambokom posttreatmenthaemolysisinafricanchildrenwithhyperparasitaemicfalciparummalariaarandomizedcomparisonofartesunateandquinine
AT lees posttreatmenthaemolysisinafricanchildrenwithhyperparasitaemicfalciparummalariaarandomizedcomparisonofartesunateandquinine
AT woodrowc posttreatmenthaemolysisinafricanchildrenwithhyperparasitaemicfalciparummalariaarandomizedcomparisonofartesunateandquinine
AT setaphans posttreatmenthaemolysisinafricanchildrenwithhyperparasitaemicfalciparummalariaarandomizedcomparisonofartesunateandquinine
AT chotivanichk posttreatmenthaemolysisinafricanchildrenwithhyperparasitaemicfalciparummalariaarandomizedcomparisonofartesunateandquinine
AT buffetp posttreatmenthaemolysisinafricanchildrenwithhyperparasitaemicfalciparummalariaarandomizedcomparisonofartesunateandquinine
AT jaureguiberrys posttreatmenthaemolysisinafricanchildrenwithhyperparasitaemicfalciparummalariaarandomizedcomparisonofartesunateandquinine
AT rockettk posttreatmenthaemolysisinafricanchildrenwithhyperparasitaemicfalciparummalariaarandomizedcomparisonofartesunateandquinine
AT stepniewskak posttreatmenthaemolysisinafricanchildrenwithhyperparasitaemicfalciparummalariaarandomizedcomparisonofartesunateandquinine
AT dayn posttreatmenthaemolysisinafricanchildrenwithhyperparasitaemicfalciparummalariaarandomizedcomparisonofartesunateandquinine
AT whiten posttreatmenthaemolysisinafricanchildrenwithhyperparasitaemicfalciparummalariaarandomizedcomparisonofartesunateandquinine
AT dondorpa posttreatmenthaemolysisinafricanchildrenwithhyperparasitaemicfalciparummalariaarandomizedcomparisonofartesunateandquinine