Management of antiphospholipid syndrome.
Review published in Annals of the rheumatic diseases (2018)
Abstract
Antiphospholipid syndrome, also known as 'Hughes Syndrome', is an autoimmune disease characterised by a set of clinical manifestations, almost all of which are direct or indirect sequelae of a hypercoagulable state involving the venous, and to a lesser extent the arterial vasculature. The incidence and prevalence of antiphospholipid syndrome are estimated at approximately 5 de novo cases per 100 000 per year and 40-50 cases per 100 000 individuals, respectively. The clinical spectrum of antiphospholipid syndrome involves haematological (thrombocytopaenia, venous thrombosis), obstetrical (recurrent pregnancy loss), neurological (stroke, transient ischaemic attack, migraine, seizures, cognitive dysfunction, chorea, transverse myelitis, multiple sclerosis), cardiovascular (cardiac valve disease), dermatological (livedo reticularis and racemosa, skin ulceration and necrosis), renal (glomerulonephritis, renal thrombotic microangiopathy) and orthopaedic (avascular necrosis of bones, non-traumatic fractures) manifestations, among others. In addition to the classical antiphospholipid antibodies, namely anticardiolipin antibodies and lupus anticoagulant, new autoantibodies and antibody complexes of different immunoglobulin subtypes (IgA, IgG, IgM) are now recognised as significant contributors to the pathogenesis of antiphospholipid syndrome. Anticoagulation remains the cornerstone in the management of antiphospholipid syndrome; nevertheless, new drugs and therapeutic strategies are being tested, and some have been found effective for the primary and secondary thromboprophylaxis in antiphospholipid syndrome.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Resumen
Antiphospholipid syndrome, also known as 'Hughes Syndrome', is an autoimmune disease characterised by a set of clinical manifestations, almost all of which are direct or indirect sequelae of a hypercoagulable state involving the venous, and to a lesser extent the arterial vasculature. The incidence...
Por qué esto importa para la hirudoterapia
Esta revisión abarca el espectro clínico, la fisiopatología y el manejo del síndrome antifosfolipídico, un estado hipercoagulable autoinmune tratado principalmente con anticoagulación. Describe manifestaciones en múltiples sistemas orgánicos y señala fármacos y estrategias emergentes para la tromboprofilaxis. Para ASH, el artículo aporta contexto clínico relevante acerca de estados de enfermedad trombótica en los que el tratamiento anticoagulante —el descendiente farmacológico de la hirudina derivada de sanguijuelas— desempeña un papel terapéutico central. ADVERTENCIA: el resumen no menciona sanguijuelas, hirudina, bivalirudina, hirudoterapia ni ninguna sustancia derivada de sanguijuelas; su relevancia es indirecta, limitada al dominio general de la anticoagulación en la enfermedad trombótica.
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Añadido a la biblioteca ASH: May 28, 2026 · Última actualización del sitio: June 18, 2026