Unmasking delayed hemolytic transfusion reactions in patients with sickle‐cell disease: Challenges and opportunities for improvement-Reference-Cited by-同舟云学术

Unmasking delayed hemolytic transfusion reactions in patients with sickle‐cell disease: Challenges and opportunities for improvement

Published:2022-07-02 Issue:8 Volume:62 Page:1662-1670
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Covington Mischa L.¹^ORCID,Cone‐Sullivan Jensyn K.²^ORCID,Andrzejewski Chester³,Lu Wen¹^ORCID,Thomasson Reggie R.⁴,O'Brien Kerry⁵^ORCID,Brunker Patricia A. R.⁶,Stowell Sean R.¹^ORCID

Affiliation:

1. Department of Pathology, Brigham and Women's Hospital Harvard Medical School Boston Massachusetts USA

2. Department of Pathology and Laboratory Medicine Tufts Medical Center Boston Massachusetts USA

3. Transfusion Medicine Service Baystate Medical Center, Baystate Health Springfield Massachusetts USA

4. Department of Pathology and Laboratory Medicine Boston Medical Center and Boston University School of Medicine Boston Massachusetts USA

5. Department of Pathology, Beth Israel Deaconess Harvard Medical School Boston Massachusetts USA

6. Department of Pathology Massachusetts General Hospital, Harvard Medical School Boston Massachusetts USA

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.16967

Reference46 articles.

1. Fatalities Reported to FDA Following Blood Collection and Transfusion Annual Summary for Fiscal Year [monograph on the internet].https://www.fda.gov/media/147628/download;2019.

2. Red cell transfusion and alloimmunization in sickle cell disease

3. Hemolytic transfusion reactions in sickle cell disease: underappreciated and potentially fatal

4. Risk factors for red blood cell alloimmunization in the Recipient Epidemiology and Donor Evaluation Study (REDS-III) database

5. Red blood cell alloimmunization is influenced by recipient inflammatory state at time of transfusion in patients with sickle cell disease

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