Sociedad Americana de Hirudoterapia

EULAR recommendations for the management of antiphospholipid syndrome in adults.

Research article published in Annals of the rheumatic diseases (2019)

Última actualización: 18 de junio de 2026Revisado por: ASH Editorial Board
Artículo de investigación — revisión de evidenciaReferencia del artículo
Evidence: Research reportEnsayos clínicosDesarrollo de fármacosTektonidou et al. · Annals of the rheumatic diseases, 2019

Abstract

The objective was to develop evidence-based recommendations for the management of antiphospholipid syndrome (APS) in adults. Based on evidence from a systematic literature review and expert opinion, overarching principles and recommendations were formulated and voted. High-risk antiphospholipid antibody (aPL) profile is associated with greater risk for thrombotic and obstetric APS. Risk modification includes screening for and management of cardiovascular and venous thrombosis risk factors, patient education about treatment adherence, and lifestyle counselling. Low-dose aspirin (LDA) is recommended for asymptomatic aPL carriers, patients with systemic lupus erythematosus without prior thrombotic or obstetric APS, and non-pregnant women with a history of obstetric APS only, all with high-risk aPL profiles. Patients with APS and first unprovoked venous thrombosis should receive long-term treatment with vitamin K antagonists (VKA) with a target international normalised ratio (INR) of 2-3. In patients with APS with first arterial thrombosis, treatment with VKA with INR 2-3 or INR 3-4 is recommended, considering the individual's bleeding/thrombosis risk. Rivaroxaban should not be used in patients with APS with triple aPL positivity. For patients with recurrent arterial or venous thrombosis despite adequate treatment, addition of LDA, increase of INR target to 3-4 or switch to low molecular weight heparin may be considered. In women with prior obstetric APS, combination treatment with LDA and prophylactic dosage heparin during pregnancy is recommended. In patients with recurrent pregnancy complications, increase of heparin to therapeutic dose, addition of hydroxychloroquine or addition of low-dose prednisolone in the first trimester may be considered. These recommendations aim to guide treatment in adults with APS. High-quality evidence is limited, indicating a need for more research.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeJournal ArticleResearch Support, N.I.H., IntramuralResearch Support, Non-U.S. Gov't
Indexed MeSH termsAdultAntibodies, AntiphospholipidAnticoagulantsAntiphospholipid SyndromeFemaleHumansMalePractice Guidelines as TopicPregnancyPregnancy ComplicationsRheumatologyRisk Factors

Resumen

The objective was to develop evidence-based recommendations for the management of antiphospholipid syndrome (APS) in adults. Based on evidence from a systematic literature review and expert opinion, overarching principles and recommendations were formulated and voted.

Por qué esto importa para la hirudoterapia

Esta guía formuló recomendaciones basadas en evidencia para el manejo del síndrome antifosfolipídico (SAF) en adultos, detallando estrategias farmacológicas que incluyen ácido acetilsalicílico a dosis bajas, antagonistas de la vitamina K, heparina e hidroxicloroquina según los perfiles de riesgo trombótico y obstétrico. El resumen se centra por completo en la anticoagulación sistémica convencional y en terapias inmunomoduladoras. Para la American Society of Hirudotherapy, el manejo de los estados de hipercoagulabilidad severos es conceptualmente adyacente al estudio de los mecanismos anticoagulantes. Sin embargo, el resumen no contiene ninguna mención de sanguijuelas, hirudoterapia, el secretoma de la sanguijuela ni ninguna terapia anticoagulante localizada, lo que hace que su relevancia sea puramente de contexto.

Citación

EULAR recommendations for the management of antiphospholipid syndrome in adults.

Tektonidou et al. · Annals of the rheumatic diseases, 2019

Contexto clínico relacionado

Añadido a la biblioteca ASH: May 28, 2026 · Última actualización del sitio: 18 de junio de 2026

Este sitio web proporciona información educativa y no constituye consejo médico, diagnóstico ni recomendaciones de tratamiento. La terapia con sanguijuelas medicinales conlleva riesgos clínicamente significativos y debe ser realizada únicamente por profesionales calificados bajo protocolos aprobados institucionalmente. La autorización 510(k) de la FDA para sanguijuelas medicinales se limita a indicaciones específicas; las discusiones sobre uso investigativo y fuera de indicación se señalan correspondientemente. Para orientación médica específica, consulte a un profesional de salud calificado.