Details

Autor(en) / Beteiligte

• 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.

Titel

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

Ist Teil von

• Scientific reports, 2022-07, Vol.12 (1), p.12127-12127, Article 12127

Ort / Verlag

London: Nature Publishing Group

Erscheinungsjahr

2022

Link zum Volltext

Quelle

Free E-Journal (出版社公開部分のみ）

Beschreibungen/Notizen

• Abstract 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.