2016, Número 4
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Rev Hematol Mex 2016; 17 (4)
Síndrome de anticuerpos antifosfolipídicos; patogénesis, diagnóstico y tratamiento
Cruz-Contreras DG
Idioma: Español
Referencias bibliográficas: 20
Paginas: 256-261
Archivo PDF: 405.50 Kb.
RESUMEN
El síndrome antifosfolipídico es una afección caracterizada por producir
un estado hipercoagulable mediado por anticuerpos, puede ser
primario o secundario a enfermedad reumatológica o neoplásica. Los
anticuerpos implicados son las anticardiolipinas (IgG e IgM), antiβ2
glicoproteína 1 y el anticoagulante lúpico. Quien lo padece tiene
eventos trombóticos venoarteriales de repetición, que en algunos
casos pueden ser de difícil control e incluso mortales. Existen los
criterios de Sapporo revisados en 2006 para establecer el diagnóstico;
estos criterios incluyen datos clínicos y de laboratorio. Debido a que
los eventos trombóticos de estos pacientes tienden a la repetición, el
tratamiento es por largo tiempo y en ocasiones de manera indefinida.
El tratamiento está encaminado a revertir el estado hipercoagulable,
se prescribe de primera línea y en pacientes no embarazadas se prescriben
antagonistas de la vitamina K, con INR objetivo en 2.5. En los
casos de embarazo o sospecha del mismo el tratamiento se basa en
heparina de bajo peso molecular en ocasiones aunado a ácido acetilsalicílico.
En la actualidad se publican resultados de los estudios que
utilizan como tratamiento los nuevos anticoagulantes orales. Aún se
desconoce la necesidad de profilaxis antitrombótica en los pacientes
con anticuerpos positivos, pero que aún no han trombosado.
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