Introduction Red blood cell (RBC) transfusions are used to increase oxygen delivery; however, a restrictive transfusion strategy (predefined hemoglobin threshold of 7 g/dl) was demonstrated to be associated with lower mortality and incidence of nosocomial infections than a liberal one [1,2]. This may be related to the storage process, which could affect the ability of RBCs to transport and delivery oxygen, or to immunomodulating effects of cytokines from residual leukocytes [2]. (Figure presented) The aim of the study is to evaluate the effects, on microcirculation of septic patient, of three types of RBCs. Methods A controlled randomized prospective study on 45 patients with sepsis, severe sepsis or septic shock requiring RBC transfusion. Patients are randomized into three groups receiving: (1) fresh standard RBCs (storage <10 days); (2) leukodepleted RBCs; and (3) old standard RBCs (storage >20 days) respectively. Before and 1 hour after the transfusion, microcirculation is evaluated using sidestream dark-field imaging [3] and near-infrared spectroscopy with a vascular occlusion test. We also monitor temperature, heart rate, mean blood pressure, hemochrome, blood gases, blood lactates and SOFA score. Results Preliminary data on 18 patients, six for each group: before and after transfusion, in group 2, but not in groups 1 and 3, there is a trend to an increase in MFIs (P = 0.09), DeBacker score (Figure 1, P <0.05), PPV (P = 0.07) and PVD (P = 0.07). No relevant differences for other parameters. Conclusion After transfusion, microcirculation seems to be improved in the leukodepleted RBC group with a significant improvement of De Backer score and a trend to improve the other microcirculatory parameters, while in the other three groups there was not this trend.
CITATION STYLE
Donati, A., Damiani, E., Domizi, R., Scorcella, C., Carsetti, A., Lombrano, M., … Pelaia, P. (2012). Microcirculation and blood transfusion: effects of three different types of concentrated red blood cells - preliminary results. Critical Care, 16(S1). https://doi.org/10.1186/cc10811
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