Can volume‐reduced plasma products prevent transfusion‐associated circulatory overload in a two‐hit animal model?

Author:

Bulle Esther B.12ORCID,Klanderman Robert B.123ORCID,de Wissel Marit B.2,Roelofs Joris J. T. H.45,Veelo Denise P.3,van den Brom Charissa E.126,Kapur Rick7,Vlaar Alexander P. J.12

Affiliation:

1. Department of Intensive Care Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands

2. Laboratory of Experimental Intensive Care and Anesthesiology Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands

3. Department of Anesthesiology Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands

4. Department of Pathology Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands

5. Amsterdam Cardiovascular Sciences, Microcirculation University of Amsterdam Amsterdam The Netherlands

6. Department of Anesthesiology Amsterdam UMC, VU University Amsterdam The Netherlands

7. Sanquin Research, Department of Experimental Immunohematology Landsteiner Laboratory, Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands

Abstract

AbstractBackground and ObjectivesTransfusion‐associated circulatory overload (TACO) is a pulmonary transfusion complication and a leading cause of transfusion‐related morbidity and mortality. Volume overload and rising hydrostatic pressure as a consequence of transfusion are seen as the central pathway leading to TACO. A possible preventative measure for TACO could be the use of low‐volume blood products like volume‐reduced lyophilized plasma. We hypothesize that volume‐reduced lyophilized plasma decreases circulatory overload leading to a reduced pulmonary capillary pressure and can therefore be an effective strategy to prevent TACO.Materials and MethodsA validated two‐hit animal model in rats with heart failure was used. Animals were randomized to receive 4 units of either solvent‐detergent pooled plasma (SDP) as control, standard volume lyophilized plasma (LP‐S) or hyperoncotic volume‐reduced lyophilized plasma (LP‐VR). The primary outcome was the difference between pre‐transfusion and post‐transfusion left ventricular end‐diastolic pressure (ΔLVEDP). Secondary outcomes included markers for acute lung injury.ResultsLVEDP increased in all randomization groups following transfusion. The greatest elevation was seen in the group receiving LP‐VR (+11.9 mmHg [5.9–15.6]), but there were no significant differences when compared to groups receiving either LP‐S (+6.3 mmHg [2.9–13.4], p = 0.29) or SDP (+7.7 mmHg [4.5–10.5], p = 0.55). There were no significant differences in markers for acute lung injury, such as pulmonary wet/dry weight ratios, lung histopathology scores or PaO2/FiO2 ratio between the three groups.ConclusionTransfusion with hyperoncotic volume‐reduced plasma did not attenuate circulatory overload compared to standard volume plasma and was therefore not an effective preventative strategy for TACO in this rat model.

Funder

Landsteiner Foundation for Blood Transfusion Research

Publisher

Wiley

Subject

Hematology,General Medicine

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