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Influence of temperature, filter wettability, and timing of filtration on the removal of WBCs from RBC concentrates

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BACKGROUND: The efficacy of the removal of WBCs from buffy coat‐reduced RBC concentrates by filtration is determined by many variables. The aim of this study was to investigate the influence of the filtration temperature, the wettability of the filter material, and the timing of the filtration after collection.STUDY DESIGN AND METHODS: The investigation used commercially available filters: 3 dry “online” filters (Cellselect FR, Fresenius Hemocare; BioR‐01‐max, Fresenius; Leucoflex LCG1, MacoPharma) and one wet “inline” filter (Leucoflex LCR4, MacoPharma) that contained saline‐adenine‐glucose‐mannitol additive solution for RBCs and differed from the online version only in wettability. After buffy coat removal and suspension in saline‐adenine‐glucose‐mannitol, filtrations were performed immediately at room temperature (RT) and after 2 hours' storage of the RBC concentrates at 4°C, while the Leucoflex LCR4 was also tested after 24 hours' storage of the RBC concentrates at 4°C. Sets of 12 pooled experiments were performed to prevent donor‐dependent differences.RESULTS: The Cellselect FR gave significantly better WBC removal from RBC concentrates at 4°C than at RT, with residual WBCs of 1.44 ± 0.58 × 106 and 2.78 ± 1.23 × 106, respectively (p<0.001). The BioR‐01‐max gave no significant difference: 0.62 ± 0.27 × 106 WBCs (at 4°C) versus 0.61 ± 0.25 × 106 WBCs (at RT). Filtration with the Leucoflex LCG1 resulted in 0.06 ± 0.03 × 106 and 0.07 ± 0.07 × 106 WBCs at 4°C and RT, respectively, which is not a significant difference. The Leucoflex LCR4, however, gave 2.08 ± 0.84 × 106 WBCs at RT, 0.52 ± 0.44 × 106 WBCs at 4°C after 2 hours' cooling, and 0.05 ± 0.10 × 106 WBCs at 4°C after 24 hours' cooling (all p<0.001).CONCLUSION: Temperature, filter wettability, and timing of filtration after collection influence the efficacy of a filter for RBC concentrates. These variables need to be established, validated, and controlled before a filter can be selected for routine use.
Title: Influence of temperature, filter wettability, and timing of filtration on the removal of WBCs from RBC concentrates
Description:
BACKGROUND: The efficacy of the removal of WBCs from buffy coat‐reduced RBC concentrates by filtration is determined by many variables.
The aim of this study was to investigate the influence of the filtration temperature, the wettability of the filter material, and the timing of the filtration after collection.
STUDY DESIGN AND METHODS: The investigation used commercially available filters: 3 dry “online” filters (Cellselect FR, Fresenius Hemocare; BioR‐01‐max, Fresenius; Leucoflex LCG1, MacoPharma) and one wet “inline” filter (Leucoflex LCR4, MacoPharma) that contained saline‐adenine‐glucose‐mannitol additive solution for RBCs and differed from the online version only in wettability.
After buffy coat removal and suspension in saline‐adenine‐glucose‐mannitol, filtrations were performed immediately at room temperature (RT) and after 2 hours' storage of the RBC concentrates at 4°C, while the Leucoflex LCR4 was also tested after 24 hours' storage of the RBC concentrates at 4°C.
Sets of 12 pooled experiments were performed to prevent donor‐dependent differences.
RESULTS: The Cellselect FR gave significantly better WBC removal from RBC concentrates at 4°C than at RT, with residual WBCs of 1.
44 ± 0.
58 × 106 and 2.
78 ± 1.
23 × 106, respectively (p<0.
001).
The BioR‐01‐max gave no significant difference: 0.
62 ± 0.
27 × 106 WBCs (at 4°C) versus 0.
61 ± 0.
25 × 106 WBCs (at RT).
Filtration with the Leucoflex LCG1 resulted in 0.
06 ± 0.
03 × 106 and 0.
07 ± 0.
07 × 106 WBCs at 4°C and RT, respectively, which is not a significant difference.
The Leucoflex LCR4, however, gave 2.
08 ± 0.
84 × 106 WBCs at RT, 0.
52 ± 0.
44 × 106 WBCs at 4°C after 2 hours' cooling, and 0.
05 ± 0.
10 × 106 WBCs at 4°C after 24 hours' cooling (all p<0.
001).
CONCLUSION: Temperature, filter wettability, and timing of filtration after collection influence the efficacy of a filter for RBC concentrates.
These variables need to be established, validated, and controlled before a filter can be selected for routine use.

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