Prophylactic furosemide to prevent transfusion-associated circulatory overload: a randomized controlled study in rats

Transfusion-associated circulatory overload (TACO) is the leading cause of transfusion related morbidity and mortality. The only treatment is empirical use of furosemide. Our aim was to investigate if furosemide can prevent TACO. A randomized controlled trial was performed using a previously validat...

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Vydáno v:Scientific reports Ročník 12; číslo 1; s. 12127 - 9
Hlavní autoři: Klanderman, Robert B., Bosboom, Joachim J., Veelo, Denise P., Roelofs, Joris J. T. H., de Korte, Dirk, van Bruggen, Robin, Vogt, Liffert, van Buul, Jaap D., Hollmann, Markus W., Vroom, Margreeth B., Juffermans, Nicole P., Geerts, Bart F., Vlaar, Alexander P. J.
Médium: Journal Article
Jazyk:angličtina
Vydáno: London Nature Publishing Group UK 15.07.2022
Nature Publishing Group
Nature Portfolio
Témata:
692/1807/1809
692/308/2778
Anemia
Anesthesiology
Animals
Blood
Blood pressure
Catheters
Contractility
Ejection fraction
Furosemide
Heart
Heart failure
Heart rate
Humanities and Social Sciences
Intensive care
Laboratories
Morbidity
multidisciplinary
Ostomy
Placebos
Science
Science (multidisciplinary)
Stroke
Transfusion
Urine
Ventricle
ISSN:2045-2322, 2045-2322
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Shrnutí:Transfusion-associated circulatory overload (TACO) is the leading cause of transfusion related morbidity and mortality. The only treatment is empirical use of furosemide. Our aim was to investigate if furosemide can prevent TACO. A randomized controlled trial was performed using a previously validated two-hit rat model for TACO. Volume incompliance was induced (first hit) in anemic, anesthetized Lewis rats. Rats were randomized to placebo, low-dose (5 mg kg −1 ) or high-dose (15 mg kg −1 ) furosemide-administered prior to transfusion (second-hit) and divided over two doses. Primary outcome was change in left-ventricular end-diastolic pressure (∆LVEDP) pre- compared to post-transfusion. Secondary outcomes included changes in preload, afterload, contractility and systemic vascular resistance, as well as pulmonary outcomes. Furosemide treated animals had a significantly lower ∆LVEDP compared to placebo (p = 0.041), a dose–response effect was observed. ∆LVEDP in placebo was median + 8.7 mmHg (IQR 5.9–11), + 3.9 (2.8–5.6) in the low-dose and 1.9 (− 0.6 to 5.6) in the high-dose group. The effect of furosemide became apparent after 15 min. While urine output was significantly higher in furosemide treated animals (p = 0.03), there were no significant changes in preload, afterload, contractility or systemic vascular resistance. Furosemide rapidly and dose-dependently decreases the rise in hydrostatic pulmonary pressure following transfusion, essential for preventing TACO.
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ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-022-16465-z