Publications by authors named "E Favaloro"

Hemostasis describes the process of blood clotting homeostasis. Hemostasis reflects a balance of procoagulant and anticoagulant mechanisms that aim to prevent both bleeding and thrombosis. If hemostasis is disrupted, and bleeding or thrombosis occur, then laboratory testing may ensue to either diagnose the reason for bleeding or thrombosis, or to manage patients under therapy or treatment for bleeding or thrombosis.

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Article Synopsis
  • Von Willebrand disease (VWD) is the most common inherited bleeding disorder caused by issues with von Willebrand factor (VWF), often leading to misdiagnosis and improper management.
  • Treatment mainly involves replacing the deficient or defective VWF, with additional therapies tailored to specific patient needs, including new treatment options like FVIII replacement and antibody-based strategies.
  • The future of VWD treatment is expected to evolve significantly with personalized approaches, offering tailored therapies based on individual patient circumstances and treatment goals.
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Antiphospholipid syndrome (APS) diagnosis is dependent on the accurate detection and interpretation of antiphospholipid antibodies (aPL). Lupus anticoagulant (LA), anticardiolipin antibodies (aCL), and anti-beta2 glycoprotein I antibodies (aβ2GPI) remain the cornerstone of the laboratory part of APS diagnosis. In the 2023 American College of Rheumatology (ACR)/European Alliance of Associations for Rheumatology (EULAR) APS classification criteria, the type of laboratory parameters remain essentially unchanged compared with the updated Sapporo classification criteria, and aCL and aβ2GPI measurement are still restricted to enzyme-linked immunosorbent assays (ELISAs) with moderate and high titer aPL thresholds defined as 40 and 80 Units, respectively, and a cutoff calculated by the 99th percentile has been abandoned.

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