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Abstract

Sickle cell anemia patients present challenges and complexities in resolving immunohematology testing which can lead to severe transfusion complications. Solve it!

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Reference

  1. Centers for Disease Control and Prevention. National healthcare safety network biovigilance component, hemovigilance module surveillance protocol v2.6, Atlanta, GA. March 2021. Available from: https://www.cdc.gov/nhsn/PDFs/Biovigilance/BV-HV-protocol-current.pdf Accessed 4 Jan 2022.

Further Reading

  • Klein HG, Anstee DJ. Haemolytic transfusion reactions. In: Klein HG, Anstee DJ, editors. Mollison’s blood transfusion in clinical medicine. 12th ed. West Sussex: Wiley; 2014. p. 472.

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  • Win N, Doughty H, Telfer P, Wild BJ, Pearson TC. Hyperhemolytic transfusion reaction in sickle cell disease. Transfusion. 2001;41(3):323–8.

    Article  CAS  PubMed  Google Scholar 

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Correspondence to Mark T. Friedman .

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Friedman, M.T., West, K.A., Bizargity, P., Annen, K., Gur, H.D., Hilbert, T. (2023). The Perils of Transfusing the Sickle Cell Patient. In: Immunohematology, Transfusion Medicine, Hemostasis, and Cellular Therapy. Springer, Cham. https://doi.org/10.1007/978-3-031-14638-1_63

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  • DOI: https://doi.org/10.1007/978-3-031-14638-1_63

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  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-031-14637-4

  • Online ISBN: 978-3-031-14638-1

  • eBook Packages: MedicineMedicine (R0)

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