It has been known for some time that intravascular coagulation with thrombin and platelet activation, coupled with fibrinolysis, is present in patients presenting with symptomatic aortic dissection. The differential diagnosis of myocardial infarction and aortic dissection has received a diagnostic boost from the development of point-of-care testing, which rapidly reports plasma Troponin T and D-dimer levels from a small blood sample. Thus, it is not surprising that the authors of this paper [1Paparella D. Rotunno C. Guida P. et al.Hemostasis alterations in patients with acute aortic dissection.Ann Thorac Surg. 2011; 91: 1364-1370Abstract Full Text Full Text PDF PubMed Scopus (47) Google Scholar] have demonstrated the rather remarkable levels of D-dimer, plasmin-antiplasmin ratio, and platelet factor IV levels in their group of patients who underwent operation for acute aortic dissection. It is also not surprising that patients who present to the operating room with ongoing consumptive coagulopathy would be a bleeding risk with a large aortic resection and grafting procedure. Therefore, their data regarding this process sets the stage for potential studies to assess treatment or, at least, amelioration of this condition. It is well known now that contact of blood with tissue factor from the patient's wound causes thrombin formation and platelet activation, which causes the coagulopathy during cardiopulmonary bypass. The administration of drugs, such as Alpha-Amino Caproic acid, can diminish the fibrinolysis associated with this process, which accentuates bleeding. Unfortunately, the actual dosing schedule of this compound has not been completely worked out (especially in complicated, high risk operations), and comparing post-bypass D-dimer levels and using increasing doses of Alpha-Amino Caproic acid to treat ongoing fibrinolysis has not been systematically studied. The other commonly used anti-fibrinolytic agent, Tranexamic acid, has also had very few studies regarding effectiveness against ongoing fibrinolysis, and large doses have been shown to be associated with a high incidence of seizures. The most powerful antifibrinolytic agent, Aprotinin, is now off the market and out of the picture. There are other recombinant proteinase inhibitors being studied, but these will not be available for patients for some time. It appears to me that studies to evaluate the importance of diminishing the consumptive coagulopathy not only associated with aortic dissection, but also with other major operations involving the aortic arch, redo surgery, and left ventricular assist device implantation are urgently needed. I, personally, hope the authors of this paper will begin studies such as that and that this will be followed by similar studies across the length and breadth of cardiac surgery. Hemostasis Alterations in Patients With Acute Aortic DissectionThe Annals of Thoracic SurgeryVol. 91Issue 5PreviewSurgery for acute aortic dissection (AAD) is frequently complicated by excessive postoperative bleeding and blood product transfusion. Blood flow through the nonendothelialized false lumen is a potential trigger for the activation of the hemostatic system; however, the physiopathology of the aortic dissection induced coagulopathy has never been precisely studied. The aim of the present study is the evaluation of the coagulation and fibrinolytic systems and platelet activation in patients undergoing surgery for AAD. Full-Text PDF
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