Post-artemisinin delayed hemolysis after oral therapy for P. falciparum infection

Christian C Conlon1, Anna Stein1, Rhonda E Colombo1

  • 1Madigan Army Medical Center Department of Medicine, 9040 Jackson Ave, Fort Lewis McChord, Washington, 98413, USA.

Idcases
|March 21, 2020
PubMed

Insights

Post-artemisinin delayed hemolysis (PADH) is a rare but serious side effect, even after oral artemisinin treatment for severe malaria. Close patient monitoring is crucial for early detection and management of this condition.

Area of Science:

  • Malariology
  • Hematology
  • Pharmacovigilance

Background:

  • Post-artemisinin delayed hemolysis (PADH) is a known complication of artemisinin-based antimalarial drugs.
  • PADH typically occurs after parenteral administration for severe Plasmodium falciparum infections.
  • Severe PADH requiring hospitalization and blood transfusions after oral artemisinin therapy is exceptionally rare.

Observation:

  • A 24-year-old male with severe P. falciparum malaria initially treated with oral artemether-lumefantrine (AL).
  • Due to high parasitemia, treatment was switched to intravenous quinidine and doxycycline, then back to oral AL.
  • The patient was readmitted five days post-discharge with severe hemolytic anemia, diagnosed as PADH, necessitating blood transfusions.

Findings:

  • This case highlights a rare instance of severe PADH following oral artemisinin therapy.
  • High initial parasite loads in severe malaria may be a risk factor for developing PADH, even with oral treatment.
  • Absence of peripheral parasitemia at readmission confirmed PADH as the cause of hemolytic anemia.

Implications:

  • Clinicians should maintain a high index of suspicion for PADH in patients treated with oral artemisinin, especially those with initially severe malaria.
  • Close follow-up and reassessment are vital after completing oral artemisinin courses to detect delayed adverse events.
  • This case underscores the need for vigilance regarding rare but severe side effects of antimalarial drugs, irrespective of the route of administration.

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