A feasibility evaluation of an automated blood component collection system platelets and red cells

Transfusion. 1999 May;39(5):460-4. doi: 10.1046/j.1537-2995.1999.39050460.x.

Abstract

Background: The purpose of these studies was to evaluate the functional properties of blood components collected with an automated collection system.

Study design and methods: Single-donor platelets (n = 44) and packed red cell (RBC) units (n = 10) were collected. In vitro and in vivo assays were used to assess the function of single-donor platelet components stored for 5 days and of packed RBC units after storage for 42 days at 4 degrees C.

Results: Adverse events observed in the 44 study subjects were minor. The mean 24-hour recovery value for the packed RBC units stored for 42 days was 83.6 +/- 5.4 percent, with a mean percentage of hemolysis on Day 42 at 0.46 +/- 0.19 percent. The 25 patients receiving platelet components achieved a mean corrected count increment of 15.1 +/- 10.4 x 10(3). All platelet concentrates had less than 1 x 10(6) total white cells.

Conclusion: Both in vitro and in vivo testing for the packed RBCs collected and stored for 42 days met the standards for both hemolysis and percentage of 51Cr 24-hour RBC recovery. The in vitro results and transfusion data on white cell-reduced platelet components transfused to thrombocytopenic patients were comparable to those on available platelet components.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Automation
  • Blood Specimen Collection / methods*
  • Erythrocytes*
  • Evaluation Studies as Topic
  • Feasibility Studies
  • Humans
  • Plateletpheresis*
  • Thrombocytopenia / therapy
  • Transplantation, Autologous