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Hemophilia is an X-linked, recessive bleeding disorder. Improvements in factor replacement therapy and overall approach to hemophilia management have increased the lifespan and quality of life for patients with hemophilia. Thus, they are presenting for cardiac surgery related to age-related atherosclerosis, vascular disorders, and degenerative valvular disease. Although challenging, cardiac surgery can be performed safely with appropriate planning, using a multidisciplinary approach. This article provides a narrative review and framework for the perioperative management of patients with hemophilia A and B undergoing cardiac surgery. [ABSTRACT FROM AUTHOR]

Hemophilia is a congenital bleeding disorder characterized by episodic hemorrhages that can be spontaneous or trauma related and can pose challenges in the emergency department both in diagnosis and management. Timely infusions of hemostatic clotting factors can control bleeding in most circumstances and significantly minimize sequelae. Hemorrhages in some anatomical areas such as the central nervous system, within the abdomen, or into restricted spaces in extremities require a high index of suspicion for early detection. Patients with hemophilia with inhibitors against specific clotting factors can be particularly challenging to treat. Patients with acquired hemophilia can present with severe spontaneous bleeding. Prompt correction of factor deficiencies by infusing an appropriately dosed replacement product is fundamental to effective emergency hemophilia management. [Copyright &y& Elsevier]

Abstract: Introduction: Thrombin and plasmin are the key enzymes involved in coagulation and fibrinolysis, respectively. Plasma coagulative and fibrinolytic potentials in normal children and adults, and in representative pathologically altered hemostatic states, were evaluated via simultaneous assessment of thrombin and plasmin generation. Materials and Methods: An assay of Simultaneous Thrombin and Plasmin generation (STP) was developed to measure thrombin and plasmin in plasma using individual fluorometric substrates. Coagulation is initiated with dilute tissue factor, phospholipid, and calcium in platelet-poor plasma; fibrinolysis is accelerated via tissue plasminogen activator (tPA). Abnormal states of hemostasis were investigated. Results: STP assay reproducibility and normal adult and pediatric values for measured and calculated parameters have been established. Onset of both thrombin and plasmin generation was significantly delayed in children relative to adults (p<0.001) and the maximum amplitudes of thrombin and plasmin generation were less in children than adults (p<0.01). No significant differences were measured among pediatric age groups. The most profound impairments in thrombin generation were observed for extrinsic and common pathway factor deficiencies, with the exception of afibrinogenemia. Plasmin generation was severely impaired in deficiencies of fibrinogen and plasminogen as well as with decreased tPA reagent concentration and addition of aminocaproic acid. Plasmin generation was greatly enhanced by alpha-2-antiplasmin deficiency and excess tPA reagent. Conclusion: Simultaneous assessment of thrombin and plasmin generation in plasma shows promise for affording an enhanced understanding of overall coagulative and fibrinolytic functions in physiological and pathologically altered states of hemostasis in children and adults. [Copyright &y& Elsevier]