The in vitro quality of washed, prestorage leucocyte-depleted red blood cell concentrates

V Weisbach1, W Riego, E Strasser

  • 1Department of Transfusion Medicine and Haemostaseology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany. Volker.Weisbach@trans.imed.uni-erlangen.de

Vox Sanguinis
|July 21, 2004
PubMed

Insights

Washing red blood cell concentrates (RCCs) significantly reduces 2,3-diphosphoglycerate (2,3-DPG), impacting erythrocyte quality. This loss is more pronounced in older RCCs and during post-wash storage, potentially affecting neonatal transfusions.

Area of Science:

  • Transfusion Medicine
  • Blood Banking
  • Red Blood Cell Physiology

Background:

  • Limited data exists on the quality of washed prestorage leucocyte-depleted red blood cell concentrates (RCCs).
  • Washing is a procedure used to remove plasma components from red blood cells.

Purpose of the Study:

  • To evaluate the quality of washed red blood cell concentrates (RCCs) stored in additive solution (SAG-M).
  • To assess the impact of washing on key erythrocyte metabolites and parameters.

Main Methods:

  • Five groups of RCCs (2-5 days or 11-15 days old) were washed using saline, SAG-M, or 5% albumin.
  • Measurements included ATP, 2,3-DPG, hemolysis, cell count, electrolytes, pH, gases, and lactate before and after washing, and during 6-hour post-wash storage at 4°C or room temperature.

Main Results:

  • Erythrocyte ATP content slightly increased post-washing.
  • A significant decrease in 2,3-diphosphoglycerate (2,3-DPG) was observed, ranging from 15-40% depending on RCC age and washing conditions.
  • Further 2,3-DPG loss occurred during post-wash storage, especially at room temperature and in older RCCs.

Conclusions:

  • Washing RCCs stored in SAG-M leads to substantial loss of erythrocyte 2,3-DPG, particularly in older units.
  • This loss is exacerbated during post-wash storage, even at 4°C.
  • The decline in erythrocyte quality may negate the benefits of washed SAG-M RCCs in massive neonatal transfusions.
Abstract

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