| Literature DB >> 35665876 |
Demian Knobel1, Jonas Scheuzger1, Andreas Buser2,3, Alexa Hollinger1,3, Caroline E Gebhard1, Rita Achermann1, Anna Zaiser1, Yann Bovey1, Chiara Nuciforo1, Julie Noëmie Netzer1, Aline Räber1, Jasprit Singh1, Martin Siegemund4,5.
Abstract
In vitro studies have thoroughly documented age-dependent impact of storage lesions in packed red blood cells (pRBC) on erythrocyte oxygen carrying capacity. While studies have examined the effect of pRBC age on patient outcome only few data exist on the microcirculation as their primary site of action. In this secondary analysis we examined the relationship between age of pRBC and changes of microcirculatory flow (MCF) in 54 patients based on data from the Basel Bedside assessment Microcirculation Transfusion Limit study (Ba2MiTraL) on effects of pRBC on sublingual MCF. Mean change from pre- to post-transfusion proportion of perfused vessels (∆PPV) was + 8.8% (IQR - 0.5 to 22.5), 5.5% (IQR 0.1 to 10.1), and + 4.7% (IQR - 2.1 to 6.5) after transfusion of fresh (≤ 14 days old), medium (15 to 34 days old), and old (≥ 35 days old) pRBC, respectively. Values for the microcirculatory flow index (MFI) were + 0.22 (IQR - 0.1 to 0.6), + 0.22 (IQR 0.0 to 0.3), and + 0.06 (IQR - 0.1 to 0.3) for the fresh, medium, and old pRBC age groups, respectively. Lower ∆PPV and transfusion of older blood correlated with a higher Sequential Organ Failure Assessment (SOFA) score of patients upon admission to the intensive care unit (ICU) (p = 0.01). However, regression models showed no overall significant correlation between pRBC age and ∆PPV (p = 0.2). Donor or recipient sex had no influence. We detected no significant effect of pRBC on microcirculation. Patients with a higher SOFA score upon ICU admission might experience a negative effect on the ∆PPV after transfusion of older blood.Entities:
Keywords: Capillary blood flow packed red blood cells, age; Oxygen supply; Red blood cell transfusion; Sex mismatch; Storage lesions; Sublingual microcirculation; Transfusion
Year: 2022 PMID: 35665876 DOI: 10.1007/s10877-022-00877-3
Source DB: PubMed Journal: J Clin Monit Comput ISSN: 1387-1307 Impact factor: 2.502