The role of tocilizumab in the treatment of post‐transfusion hyperhaemolysis

Author:

Desai Naeem1ORCID,Peters Jayne12,Davies Elizabeth1ORCID,Sharif Joseph1

Affiliation:

1. Haematology Manchester Royal Infirmary Manchester UK

2. Department of Haematology NHS Blood and Transplant Manchester UK

Abstract

AbstractHyperhaemolysis syndrome (HHS) is a serious complication of transfusion mostly reported in patients with sickle cell disease. HHS is characterised by the destruction of both donor and autologous red blood cells. Tocilizumab is a recombinant humanised monoclonal antibody that inhibits the binding of interleukin‐6 and has been used in the treatment of severe/critical coronavirus disease 2019 infection but also some cases of HHS. We describe two further cases of HHS successfully treated with tocilizumab and propose a decision aid for when to consider this treatment.

Publisher

Wiley

Subject

General Earth and Planetary Sciences

Reference15 articles.

1. Hyperhemolysis syndrome in sickle cell disease

2. Hyperhemolysis in Patients With Hemoglobinopathies: A Single-Center Experience and Review of the Literature

3. American Society of Hematology 2020 guidelines for sickle cell disease: transfusion support

4. NHS England Clinical Commissioning Policy.Rituximab and eculizumab for the prevention and management of delayed haemolytic transfusion reactions and hyperhaemolysis in patients with haemoglobinpathies.https://www.england.nhs.uk/publication/rituximab‐and‐eculizumab‐for‐the‐prevention‐and‐management‐of‐delayed‐haemolytic‐transfusion‐reactions‐and‐hyperhaemolysis‐in‐patients‐with‐haemoglobinopathies/Accessed 21 June 2023

5. Acute Hyperhemolysis Syndrome in a Patient with Known Sickle Cell Anemia Refractory to Steroids and IVIG Treated with Tocilizumab and Erythropoietin: A Case Report and Review of Literature

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1. Eculizumab/immune-globulin/methylprednisolone;Reactions Weekly;2024-04-06

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