Haemolytic anaemia in an HIV-infected patient with severe <it>falciparum </it>malaria after treatment with oral artemether-lumefantrine

<p>Abstract</p> <p>Intravenous (i.v.) artesunate is now the recommended first-line treatment of severe <it>falciparum </it>malaria in adults and children by WHO guidelines. Nevertheless, several cases of haemolytic anaemia due to i.v. artesunate treatment have been repo...

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Bibliographic Details
Main Authors: Corpolongo Angela, De Nardo Pasquale, Ghirga Piero, Gentilotti Elisa, Bellagamba Rita, Tommasi Chiara, Paglia Maria, Nicastri Emanuele, Narciso Pasquale
Format: Article
Language:English
Published: BMC 2012-03-01
Series:Malaria Journal
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Online Access:http://www.malariajournal.com/content/11/1/91
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Summary:<p>Abstract</p> <p>Intravenous (i.v.) artesunate is now the recommended first-line treatment of severe <it>falciparum </it>malaria in adults and children by WHO guidelines. Nevertheless, several cases of haemolytic anaemia due to i.v. artesunate treatment have been reported. This paper describes the case of an HIV-infected patient with severe <it>falciparum </it>malaria who was diagnosed with haemolytic anaemia after treatment with oral artemether-lumefantrine.</p> <p>The patient presented with fever, headache, and arthromyalgia after returning from Central African Republic where he had been working. The blood examination revealed acute renal failure, thrombocytopaenia and hypoxia. Blood for malaria parasites indicated hyperparasitaemia (6%) and <it>Plasmodium falciparum </it>infection was confirmed by nested-PCR. Severe malaria according to the laboratory WHO criteria was diagnosed. A treatment with quinine and doxycycline for the first 12 hours was initially administered, followed by arthemeter/lumefantrine (Riamet<sup>®</sup>) for a further three days. At day 10, a diagnosis of severe haemolytic anaemia was made (Hb 6.9 g/dl, LDH 2071 U/l). Hereditary and autoimmune disorders and other infections were excluded through bone marrow aspiration, total body TC scan and a wide panel of molecular and serologic assays. The patient was treated by transfusion of six units of packed blood red cell. He was discharged after complete remission at day 25. At present, the patient is in a good clinical condition and there is no evidence of haemolytic anaemia recurrence.</p> <p>This is the first report of haemolytic anaemia probably associated with oral artemether/lumefantrine. Further research is warranted to better define the adverse events occurring during combination therapy with artemisinin derivatives.</p>
ISSN:1475-2875