Implementation of national blood conservation recommendations at an adult sickle cell center. Issue 9 (15th July 2022)

• Record Type: Journal Article
• Authors: Jones, Jennifer M.; Swett, Ariel D.; Crowe, Elizabeth P.; Lawrence, Courtney; Bloch, Evan M.; Lanzkron, Sophie M.
• Is Part Of: Transfusion. Volume 62:Issue 9(2022)
• Page Start: 1763
• Page End: 1771
• Publication Date: 2022-07-15
• Subjects: blood conservation -- chronic exchange transfusions -- sickle cell disease; Hematology -- Periodicals; Blood -- Transfusion -- Periodicals; Blood Group Antigens -- Periodicals; Blood Preservation -- Periodicals; Blood Transfusion -- Periodicals; 615
• DOI: 10.1111/trf.17007
• Languages: English
• ISSNs: 0041-1132

Abstract

Abstract: Background: Due to the national blood supply crisis caused by the COVID‐19 pandemic, the American Society of Hematology proposed guidance to decrease blood utilization for sickle cell patients on chronic transfusion therapy (CTT). Little evidence exists to support the efficacy and safety of these blood conservation strategies. Study Design and Methods: Through retrospective analysis, we sought to describe outcomes following implementation of these recommendations in 58 adult sickle cell patients on chronic exchange transfusions. The strategies employed included: relaxing the goal fraction of cells remaining (FCR) to 30%–50%, utilizing depletion exchanges in select patients, and transitioning select patients to monthly simple transfusions. We compared hemoglobin S%, hemoglobin values, and other laboratory parameters, acute care visits, and red blood cell usage during the first year of the COVID‐19 pandemic to the year prior using Wilcoxon signed rank test. Results: Of 53 patients who remained on chronic exchanges during the pandemic, use of depletion exchange increased (15%–23%) and FCR increased (34.9 [SD 4.7] vs. 37.6 [SD 4.5], p < .05). These changes resulted in 854 units conserved without clinically significant changes to pre‐exchange laboratory parameters, including hemoglobin S%, or number of acute care presentations. In contrast, five patients who transitioned to predominantly simple transfusions, experienced difficulty maintaining hemoglobin S% less than 30 and worsening anemia. Discussion: Our data suggest that in a blood shortage crisis, optimizing the exchange procedure itself may be the safest means of conserving blood in a population of adult patients with sickle cell disease. Abstract : See editorial on page 1688–1692, in this issue