Hyperhaemolytic transfusion reaction in two β-thalassaemia major patients: The role of eculizumab

J Clin Pharm Ther. 2022 Mar;47(3):411-414. doi: 10.1111/jcpt.13510. Epub 2021 Aug 16.

Abstract

What is known and objective: Hyperhaemolytic transfusion reactions are rare life-threatening events predominantly affecting patients with haemoglobinopathies. We report two cases in β-thalassaemia major patients on chronic transfusion therapy and highlight the role of eculizumab in its management.

Case summary: Patient 1 presented with intravascular haemolysis on day 7 (D7) post-transfusion and responded to treatment with corticosteroids and intravenous immunoglobulin. However, patient 2 presented with severe symptomatic anaemia (D4 post-transfusion) unresponsive to the aforementioned measures. Eculizumab administration led to resolution of the hyperhaemolysis.

What is new and conclusion: We report the successful management of hyperhaemolysis with eculizumab in a β-thalassemia major patient.

Keywords: delayed haemolytic transfusion reaction; eculizumab; haemoglobinopathies; hyperhaemolysis; thalassaemia.

Publication types

  • Case Reports

MeSH terms

  • Antibodies, Monoclonal, Humanized / therapeutic use
  • Hemolysis
  • Humans
  • Transfusion Reaction*
  • beta-Thalassemia* / drug therapy

Substances

  • Antibodies, Monoclonal, Humanized
  • eculizumab