Selected article for: "blood component and donor laboratory screening"

Author: Kleinman, Steve; Stassinopoulos, Adonis
Title: Risks associated with red blood cell transfusions: potential benefits from application of pathogen inactivation
  • Document date: 2015_8_25
  • ID: qlddzgbg_2
    Snippet: RESULTS: Minimum and maximum per-unit risk were calculated as 0.0003% (1 in 323,000) and 0.12% (1 in 831), respectively. The minimum estimate is for known lower-risk pathogens while the maximal estimate also includes an emerging infectious agent (EIA) and endemic area Babesia risk. Minimum and maximum per-patient lifetime risks by diagnosis grouping were estimated as 1.5 and 3.3%, respectively, for stem cell transplantation (which includes additi.....
    Document: RESULTS: Minimum and maximum per-unit risk were calculated as 0.0003% (1 in 323,000) and 0.12% (1 in 831), respectively. The minimum estimate is for known lower-risk pathogens while the maximal estimate also includes an emerging infectious agent (EIA) and endemic area Babesia risk. Minimum and maximum per-patient lifetime risks by diagnosis grouping were estimated as 1.5 and 3.3%, respectively, for stem cell transplantation (which includes additional risk for cytomegalovirus transmission); 1.2 and 3.7%, respectively, for myelodysplastic syndrome; and 0.2 and 44%, respectively, for hemoglobinopathy. DISCUSSION: There is potential for PI technologies to reduce infectious RBC risk and to provide additional benefits (e.g., prevention of transfusion-associated graftversus-host disease and possible reduction of alloimmunization) due to white blood cell inactivation. PI-RBCs should be viewed in the context of having a fully PI-treated blood supply, enabling a blood safety paradigm shift from reactive to proactive. Providing insurance against new EIAs. Further, when approved, the use of PI for all components may catalyze operational changes in blood donor screening, laboratory testing, and component manufacturing.

    Search related documents:
    Co phrase search for related documents
    • additional risk and Babesia risk: 1
    • additional risk and blood cell inactivation: 1
    • additional risk and blood donor: 1, 2, 3
    • additional risk and blood donor screening: 1
    • additional risk and blood safety: 1, 2, 3
    • additional risk and blood safety paradigm: 1
    • additional risk and blood safety paradigm shift: 1
    • additional risk and blood supply: 1, 2, 3
    • additional risk and cell inactivation: 1, 2
    • additional risk and component manufacturing: 1
    • additional risk and component manufacturing laboratory testing: 1
    • additional risk and cytomegalovirus transmission: 1
    • additional risk and cytomegalovirus transmission additional risk: 1
    • alloimmunization possible reduction and blood supply: 1
    • alloimmunization possible reduction and cell inactivation: 1
    • alloimmunization possible reduction and component manufacturing: 1
    • alloimmunization possible reduction and component manufacturing laboratory testing: 1
    • alloimmunization possible reduction and cytomegalovirus transmission: 1
    • alloimmunization possible reduction and cytomegalovirus transmission additional risk: 1