Blood components utilization in hematopoietic stem cell transplantation: Thirteen-year analysis from an apex oncology center of India.

Asian J Transfus Sci

Department of Medical Oncology, Tata Memorial Center-Advanced Center for Treatment Research and Education in Cancer, Homi Bhabha National Institute, Navi Mumbai, Maharashtra, India.

Published: September 2022

AI Article Synopsis

  • HSCT is an effective treatment for hematological disorders, but it significantly impacts blood transfusion services due to varying needs based on disease type and transplant specifics.
  • A study of 617 adult patients from 2007 to 2019 found that allogenic HSCT required more packed red blood cells (PRBC) and platelets (PLT) than autologous HSCT, particularly during the peri-transplant phase for certain donor types.
  • Key factors influencing blood product requirements include the type of HSCT, donor compatibility, and primary diagnosis, which can affect treatment costs and help manage blood inventory effectively.

Article Abstract

Background: Hematopoietic stem cell transplantation (HSCT) is a potentially curative treatment modality for a range of hematological disorders including malignancies. The increasing volumes of HSCTs impact transfusion services and the requirement of blood products vary depending on the primary disease, type and phase of transplant, and the HSCT donor type.

Materials And Methods: This study analyzed the factors affecting blood component requirements in patients undergoing HSCT. The authors studied the transfusion requirement of packed red blood cells (PRBC) and platelets (PLT) up to 100 days post-transplant among 617 adult patients undergoing HSCT during the study period (2007-2019).

Results: Requirement of PRBC and PLT was significantly higher ( < 0.05) in allogenic HSCT cases across all three phases of transplant compared to autologous HSCT. Unlike PRBC requirement, the PLT requirement was significantly higher during peri-transplant period for haploidentical HSCT and major ABO-incompatible HSCT group compared to matched related donor HSCT and ABO identical HSCT, respectively. In subset analysis based on diagnosis with leukemia as reference, the multiple myeloma group required less while the anemia group required more PRBC and PLT transfusions. The leukemia group required more PRBC than lymphoma group, while the PLT requirement was vice-versa.

Conclusion: Factors such as allogeneic HSCT, haploidentical donor type, major ABO-incompatible HSCT, and primary diagnosis as leukemia or anemia were the predictors for increased need of blood products. As higher transfusion requirements may translate into increased costs of treatment, a study like this can help in managing blood component inventory and planning treatment costs of a HSCT program.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10807528PMC
http://dx.doi.org/10.4103/ajts.ajts_12_22DOI Listing

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