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DOI 10.1111/trf.17819

Медицинская библиотека · Transfusion · 2024

Lack of efficacy of aprotinin over tranexamic acid in type A aortic dissection repair.

Reidy Bryan, Aston Daniel, Sitaranjan Daniel, Fazmin Ibrahim Talal, Muir Martin, Ali Jason, De Silva Ravi, Falter Florian

СтатьяНаблюдательное исследованиеПеревод в очереди

Аннотация

BACKGROUND

The role of aprotinin in modern cardiac surgery is not well defined. While licensed for use in isolated coronary artery bypass grafting it is more commonly used for cases deemed to be at an increased risk of bleeding. The relative efficacy, and safety profile, of aprotinin as compared to other antifibrinolytics in these high-risk cases is uncertain.

STUDY DESIGN AND

METHODS

A retrospective observational study with propensity matching to determine whether aprotinin versus tranexamic acid reduced bleeding or transfusion requirements in patients presenting for surgical repair of type A aortic dissection (TAD).

RESULTS

Between 2016 and 2022, 250 patients presented for repair of TAD. A total of 231 patients were included in the final analysis. Bleeding and transfusion were similar between both groups in both propensity matched and unmatched cohorts. Compared to tranexamic acid, aprotinin use did not reduce transfusion requirements for any product. Rates of bleeding in the first 12 h, return to theater and return to intensive care unit with an open packed chest were similar between groups. There was no difference in rates of renal failure, stroke, or death.

CONCLUSION

Aprotinin did not reduce the risk of bleeding or transfusion requirements in patients undergoing repair of type A aortic dissections. Efficacy of aprotinin may vary depending on the type of surgery performed and the underlying pathology.

Для цитирования: Reidy Bryan, Aston Daniel, Sitaranjan Daniel, Fazmin Ibrahim Talal, Muir Martin, Ali Jason, De Silva Ravi, Falter Florian. Lack of efficacy of aprotinin over tranexamic acid in type A aortic dissection repair.. Transfusion. 2024. DOI: 10.1111/trf.17819.

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