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Peer-reviewed veterinary case report

Do leukoreduced blood transfusions reduce inflammation in critically

By Bosch Lozano, Luis et al.·Published in Journal of veterinary emergency and critical care (San Antonio, Tex. : 2001)·2019·Department of Clinical Studies, Canada·View original on PubMed

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Original publication title: A pilot study evaluating the effects of prestorage leukoreduction on markers of inflammation in critically ill dogs receiving a blood transfusion.

Species:
dog

Plain-English summary

A group of 23 critically ill dogs needing a blood transfusion were given either leukoreduced (LR) or non-leukoreduced (non-LR) red blood cells to see how it affected inflammation and survival. The study found that while the total white blood cell count was higher in the non-LR group 24 hours after the transfusion, most other inflammation markers were similar between the two groups. Both groups had high survival rates, with 8 out of 11 dogs in the LR group and 9 out of 12 in the non-LR group surviving to discharge. This suggests that using leukoreduced blood may not significantly impact inflammation in these cases.

People also search for: dog blood transfusion reactions · critically ill dog treatment · leukoreduced blood benefits for dogs

Abstract

OBJECTIVES: To compare markers of inflammation after transfusion of leukoreduced (LR) packed RBCs (pRBCs) versus non-LR pRBCs in dogs with critical illness requiring blood transfusion, and to report survival to discharge and rates of transfusion reactions in these dogs. DESIGN: Prospective randomized blinded clinical study June 2014-September 2015. SETTING: University veterinary teaching hospital. ANIMALS: Twenty-three client-owned critically ill dogs, consecutively enrolled. INTERVENTIONS: Dogs requiring a single pRBC transfusion were randomized into the LR or non-LR pRBC group. Exclusion criteria included: requirement for multiple blood products, history of previous blood transfusion, and administration of anti-inflammatory or immunosuppressive medication prior to enrollment. MEASUREMENTS: Blood samples were obtained immediately prior to transfusion, then 2 and 24 hours following transfusion. Parameters measured at each time point included: PCV, WBC count, segmented and band neutrophil counts, fibrinogen, and plasma lactate and C-reactive protein concentrations. Acute patient physiologic and laboratory evaluation fast score was calculated on admission. RESULTS: Eleven dogs were included in the LR group and 12 in the non-LR group; scores of illness severity were not significantly different between groups. Total WBC count was significantly higher in the non-LR versus LR group 24 hours following pRBC transfusion, but this difference was not evident 2 hours following transfusion. No other inflammatory parameters at any time point were significantly different between LR versus non-LR pRBC transfused dogs. Survival rates to discharge for LR and non-LR groups were 8/11 and 9/12, respectively. Acute transfusion reactions were identified in 1/11 and 2/12 dogs in the LR and non-LR group, respectively. All transfused blood was stored ≤12 days. CONCLUSIONS: Most markers of inflammation did not significantly increase following transfusion of LR versus non-LR pRBCs stored ≤12 days in ill dogs. Further prospective, randomized trials are needed in clinically ill dogs to determine the benefit of prestorage leukoreduction.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/31218809/