Reexamination of the chromium-51–labeled posttransfusion red blood cell recovery method

  • Richard O. Francis
  • , Sonia Mahajan
  • , Francesca Rapido
  • , Francesca La Carpia
  • , Mark Soffing
  • , Chaitanya Divgi
  • , Randy Yeh
  • , Akiva Mintz
  • , Lenhurst Leslie
  • , Irina Agrest
  • , Matthew S. Karafin
  • , Yelena Ginzburg
  • , Beth H. Shaz
  • , Steven L. Spitalnik
  • , Joseph Schwartz
  • , Tiffany Thomas
  • , Xiaoyun Fu
  • , Pascal Amireault
  • , Pierre Buffet
  • , James C. Zimring
  • Angelo D'Alessandro, Eldad A. Hod

Research output: Contribution to journalArticlepeer-review

29 Scopus citations

Abstract

BACKGROUND: The chromium-51–labeled posttransfusion recovery (PTR) study has been the gold-standard test for assessing red blood cell (RBC) quality. Despite guiding RBC storage development for decades, it has several potential sources for error. METHODS: Four healthy adult volunteers each donated an autologous, leukoreduced RBC unit, aliquots were radiolabeled with technetium-99m after 1 and 6 weeks of storage, and then infused. Subjects were imaged by single-photon-emission computed tomography immediately and 4 hours after infusion. Additionally, from subjects described in a previously published study, adenosine triphosphate levels in transfusates infused into 52 healthy volunteers randomized to a single autologous, leukoreduced, RBC transfusion after 1, 2, 3, 4, 5, or 6 weeks of storage were correlated with PTR and laboratory parameters of hemolysis. RESULTS: Evidence from one subject imaged after infusion of technetium-99m–labeled RBCs suggests that, in some individuals, RBCs may be temporarily sequestered in the liver and spleen immediately following transfusion and then subsequently released back into circulation; this could be one source of error leading to PTR results that may not accurately predict the true quantity of RBCs cleared by intra- and/or extravascular hemolysis. Indeed, adenosine triphosphate levels in the transfusates correlated more robustly with measures of extravascular hemolysis in vivo (e.g., serum iron, indirect bilirubin, non–transferrin-bound iron) than with PTR results or measures of intravascular hemolysis (e.g., plasma free hemoglobin). CONCLUSIONS: Sources of measurement error are inherent in the chromium-51 PTR method. Transfusion of an entire unlabeled RBC unit, followed by quantifying extravascular hemolysis markers, may more accurately measure true posttransfusion RBC recovery.

Original languageEnglish
Pages (from-to)2264-2275
Number of pages12
JournalTransfusion
Volume59
Issue number7
DOIs
StatePublished - Jul 2019

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