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Published Reports of Delayed Hemolytic Anemia After Treatment with Artesunate for Severe Malaria — Worldwide, 2010–2012

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Published Reports of Delayed Hemolytic Anemia After Treatment with Artesunate for Severe Malaria — Worldwide, 2010–2012

HHS, CDC and MMWR Logos
MMWR Weekly
Volume 62, No. 1
January 11, 2013

Published Reports of Delayed Hemolytic Anemia After Treatment with Artesunate for Severe Malaria — Worldwide, 2010–2012

Weekly

January 11, 2013 / 62(01);5-8

Artesunate has been recommended by the World Health Organization (WHO) as the first-line treatment for severe malaria since 2010. It is not licensed in the United States but is available from CDC under an investigational new drug (IND) protocol. During 2010–2012, a total of 19 cases of delayed hemolytic anemia after treatment of severe malaria with artesunate were published in the peer-reviewed medical literature, but no such cases have been reported in the United States. CDC Malaria Branch staff reviewed each published report of delayed hemolysis after artesunate use. Based on the pathogenesis of malaria, the hemolysis likely is a result of severe malaria and not the treatment itself. However, artesunate used in the United States is produced by the U.S. Army Medical Materiel Development Activity, and artesunate used outside of the United States is not. An unrecognized difference might exist between the U.S. artesunate and the artesunate used elsewhere. Alternatively, cases of artesunate-associated hemolysis might have occurred in the United States but were not reported. To better assess these possibilities, CDC has amended the artesunate IND protocol and now recommends that persons treated for severe malaria with artesunate be followed for 4 weeks after treatment and evaluated for hemolytic anemia.
A literature search was performed using the terms "artesunate" and either "hemolytic anemia" or "delayed anemia." All reports were reviewed, and additional case reports referenced in these reports also were obtained and reviewed. Case reports were considered relevant if the patient had received artesunate therapy for the treatment of severe malaria and then experienced worsening hemolytic anemia after initial clinical improvement and resolution of parasitemia. In total, six articles (describing 19 cases) fit these requirements. One incident of hemolytic anemia was reported in two different articles, one published in 2002 and the other in 2010. Only the 2010 report is included in this summary.
All cases except one were in adults (median age: 50 years; age range: 5–71 years) (Table). Eighteen patients had traveled to sub-Saharan Africa, and one to India. All 12 patients with documentation of parasitemia were hyperparasitemic (>5% of red blood cells [RBCs] infected), with a mean highest parasitemia reported of 22% (range: 7%–45%). Seven of the patients also received artemether-lumefantrine, an oral drug similar to artesunate, for either initial treatment or to complete the treatment regimen. Ten patients received nonartemisinin antimalarials before or after artesunate therapy. All 14 patients for whom multiple hemoglobin measurements were available had a reduction in hemoglobin within the first week of treatment, from a mean of 12.3 g/dL on admission to 8.8 g/dL on follow-up. Seven patients received transfusions with either packed RBCs or platelets during their initial presentation, including three who received exchange transfusions. All patients responded well to artesunate therapy, and complete parasite clearance was documented on average by day 5.
For all patients, hemolysis and worsening anemia were described after parasite clearance, 8–32 days after completion of artesunate therapy. The mean hemoglobin nadir was 6.2 g/dL (range: 4.4–8.6 g/dL) (n = 18). Other reported laboratory measurements supported the diagnosis of hemolysis including elevated lactate dehydrogenase, low or absent haptoglobin, elevated bilirubin, and/or elevated reticulocyte count (n = 12). Twelve patients required transfusions, ranging from 2–24 units, after artesunate treatment. The hemolysis resolved, and hemoglobin improved in all patients within 4–8 weeks after artesunate therapy. Two patients had documented moderate anemia more than 30 days after treatment.
Two studies included information on patients with severe malaria both with and without delayed hemolysis. One reported that the six patients with hemolysis had received a higher mean cumulative dose of artesunate than the 19 patients without hemolysis (12.8 mg/kg versus 7.6 mg/kg) (1). However, the mean cumulative dose in patients with hemolysis in the other article was 7.2 mg/kg, and no correlation between dose and hemolysis was observed (2). Although not specifically discussed, the reported parasitemia in the patients with delayed hemolysis was higher in both studies (mean parasitemia of 16% versus 11%, and median parasitemia of 27% versus 5%, respectively).

Reported by

Melissa Briggs, MD, Paul M. Arguin, MD, Div of Parasitic Diseases and Malaria, Center for Global Health, CDC. Corresponding contributor: Melissa Briggs, vka5@cdc.gov, 404-718-4805.

Editorial Note

This review of published cases found reports of 19 cases of delayed hemolysis after artesunate therapy for severe malaria in nonendemic countries outside of the United States. Thus far, no published studies have assessed whether artesunate actually causes or increases the risk for delayed hemolysis; therefore, it remains unknown whether the hemolysis described is a direct effect of the treatment or simply a consequence of severe malaria itself.
In 2010, a total of 176 cases of severe malaria in the United States were reported to CDC, 39 (22%) of which were in patients who received artesunate through the CDC IND protocol (3). Thus far, delayed hemolytic anemia has not been reported in patients treated with artesunate in the United States. Artesunate has been recommended by WHO as first-line treatment for severe malaria since 2010. It has been shown to be superior to quinine, with increased survival and decreased adverse events (4). Recently, many nonendemic countries have begun to use artesunate in patients with travel-associated severe malaria. The United States is the only country where the artesunate used has been certified as meeting good manufacturing practice (GMP) standards. In all other countries, the only form of artesunate available has not been certified as having been produced according to GMP standards, but has been prequalified by WHO as an essential drug (1,5). WHO prequalification involves a review of safety data and a manufacturing site assessment but is not thought to be as stringent as GMP certification. Various authors have expressed concern that these delayed hemolytic events might be a direct toxicity of the non-GMP artesunate that is currently used outside of the United States (1,2). However, based on this review on malaria and hemolysis, there appear to be more compelling mechanisms that might explain these delayed hemolytic events related to the pathogenesis of severe malaria itself.
There have been multiple published reports of hemolytic anemia in malaria not associated with artesunate. These include reports of "blackwater fever" (dark red or black urine associated with acute malaria) and prolonged hemolytic anemia in severe malaria patients treated with older antimalarial medications. In 1979, one study showed that circulating RBCs in patients with acute malaria continued to have a decreased life-span for up to 4–5 weeks after parasite clearance. Patients in this study treated with chloroquine experienced a mean 9% decline in their hemoglobin, occurring 3–22 days after completion of their treatment. Researchers also detected mild suppression of RBC production and complement-containing immune complexes on RBC surfaces after infection, likely promoting increased splenic removal of RBCs (6). A study conducted in The Gambia showed that patients with severe malaria, but without severe anemia, experienced an initial drop in hemoglobin when started on treatment. In addition, in a subset of children without hemoglobinopathies or glucose-6-phosphate dehydrogenase deficiency (n = 17), 16 were direct antiglobulin test (DAT)–positive, and nine were positive for immunoglobulin G autoantibodies, with higher parasitemia being associated with increased DAT positivity (7). In 1993, researchers in Germany detected immunoglobulin M antiglycolytic antibodies in patients with severe malaria and prolonged hemolysis after parasite clearance. These antibodies were only present in patients with severe malaria from Plasmodium falciparum, persisted up to >40 days after treatment, and resolved as hemolysis resolved. The typical hemoglobin nadir in this study occurred 6–12 days postdiagnosis (8).
In 1997, a study using antibodies against ring-infected erythrocyte surface antigens (RESA) to label P. falciparum–infected cells found that RBCs with the RESA antigen, but without parasites, could be detected if labeled in vivo. This led to the hypothesis that the spleen or another organ removed or killed the parasites without destroying the RBCs (9). A follow-up study found that, in patients with severe malaria, artesunate treatment generated a much higher number of unparasitized RESA-positive RBCs than quinine. It also noted that artesunate-treated RBCs were more deformable then quinine-treated or parasitized RBCs, likely further extending their lifespan (10). This increase in RBCs surviving after parasitemia, albeit with a shorter lifespan than healthy RBCs, might explain the delayed postartesunate treatment decrease in hemoglobin observed in the cases reported.
Further comparative data would be required to determine how artesunate influences the risks for this complication, both in travelers and in the increasing proportion of patients receiving artesunate for severe malaria in highly endemic countries. There is insufficient evidence at present to attribute these few reported hemolytic events directly to artesunate treatment itself, and these events should not reduce confidence in artesunate, which has many other benefits for patients with severe malaria. In addition, all patients with reported delayed hemolysis have recovered without long-term complications. However, to further understand the relationship between delayed hemolysis and artesunate use, CDC is requesting that patients treated with artesunate in the United States be evaluated and have their hemoglobin assessed 4 weeks after treatment. Significant declines in hemoglobin should be reported to CDC's Malaria Branch and should prompt an evaluation for hemolysis and closer monitoring.

References

  1. Zoller T, Junghanss T, Kapaun A, et al. Intravenous artesunate for severe malaria in travelers, Europe. Emerg Infect Dis 2011;17:771–7.
  2. Kreeftmeijer-Vegter AR, van Genderen PJ, Visser LG, et al. Treatment outcome of intravenous artesunate in patients with severe malaria in the Netherlands and Belgium. Malar J 2012;11:102.
  3. CDC. Malaria surveillance—United States, 2010. MMWR 2012;61(No. SS-2).
  4. Dondorp AM, Fanello CI, Hendriksen IC, et al. Artesunate versus quinine in the treatment of severe falciparum malaria in African children (AQUAMAT): an open-label, randomised trial. Lancet 2010;376:1647–57.
  5. World Health Organization. Prequalification programme: a United Nations programme managed by WHO. Geneva, Switzerland: World Health Organization; 2010. Available at http://apps.who.int/prequalExternal Web Site Icon.
  6. Woodruff AW, Ansdell VE, Pettitt LE. Cause of anaemia in malaria. Lancet 1979;1:1055–7.
  7. Abdalla S, Weatherall DJ, Wickramasinghe SN, Hughes M. The anaemia of P. falciparum malaria. Br J Haematol 1980;46:171–83.
  8. Ritter K, Kuhlencord A, Thomssen R, Bommer W. Prolonged haemolytic anaemia in malaria and autoantibodies against triosephosphate isomerase. Lancet 1993;342:1333–4.
  9. Angus BJ, Chotivanich K, Udomsangpetch R, White NJ. In vivo removal of malaria parasites from red blood cells without their destruction in acute falciparum malaria. Blood 1997;90:2037–40.
  10. Chotivanich K, Udomsangpetch R, Dondorp A, et al. The mechanisms of parasite clearance after antimalarial treatment of Plasmodium falciparum malaria. J Infect Dis 2000;182:629–33.

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