Bentall Operation in a Patient with Severe Hemophilia A and Marfan Syndrome by Use of a Biologic Composite Graft

dc.contributor.authorYildirim F.
dc.contributor.authorOzbakkaloglu A.
dc.contributor.authorOzturk T.
dc.contributor.authorTetik O.
dc.date.accessioned2025-04-10T11:09:29Z
dc.date.available2025-04-10T11:09:29Z
dc.date.issued2016
dc.description.abstractWe describe a patient with severe hemophilia A and Marfan syndrome who underwent an elective Bentall operation. Because of the severe hemophilia, anticoagulation could not be given postoperatively; thus, a biologic Valsalva conduit graft was used. During the procedure, factor VIII was given as a bolus dose just before incision, then by continous infusion intraoperatively to maintain the factor VIII activity level between 200% and 300%. Minimal postoperative bleeding occurred. The infusion was continued postoperatively at a lower dose until all chest tubes, pacing wires, and invasive catheters were removed. The patient was discharged on postoperative day 7 without adverse events. © 2016 The Society of Thoracic Surgeons.
dc.identifier.DOI-ID10.1016/j.athoracsur.2015.09.011
dc.identifier.urihttp://hdl.handle.net/20.500.14701/48780
dc.publisherElsevier USA
dc.titleBentall Operation in a Patient with Severe Hemophilia A and Marfan Syndrome by Use of a Biologic Composite Graft
dc.typeArticle

Files