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Department of Anesthesiology and Intensive Care, Sapienza University of Rome, Viale del Policlinico 155, Rome, 00161 Italy
(Email: vincenzo.desantis{at}uniroma1.it).
We appreciated the article by Bowman and colleagues [1]. The authors demonstrated that rescue therapy with recombinant human activated factor VII (rFVIIa) is effective in reducing transfusion requirements, correcting coagulopathy, and controlling of life-threatening bleeding in patients undergoing high-risk cardiovascular surgery. The majority of patients (94.4%) received a 90 µg/kg dose of rFVIIa. Thirty-one patients (86.1%) received only 1 dose of rFVIIa, with the majority (75%) of first-time doses given in the operating room during the operative procedure. The incidence of the combined endpoint of thrombosis between patients in the rFVIIa era who received rFVIIa (11.4%) versus those who did not receive rFVIIa (5.5%) was not significantly different statistically (p = 0.145). Significantly more patients experienced postoperative renal failure (23.1% vs 5.6%), and required dialysis (11.5% vs 1.2%) in the rFVIIa group compared with patients who did not receive rFVIIa in the rFVIIa era (p = 0.005 and 0.009, respectively).
The authors adequately pointed out the limitation that using historical control groups for comparison based on the complexity of the primary operation may have led to potential confounders. However, to allow an unbiased comparison between patients receiving rFVIIa and controls, the authors might have used the propensity score methodology. These analyses would have addressed imbalances due to measured confounders.
We found the investigation very interesting and believe it may confirm our previous data in patients with acute aortic dissection undergoing surgery with deep hypothermic circulatory arrest [2].
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