2015, Número 3
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Residente 2015; 10 (3)
Sobre el tratamiento de la enfermedad pulmonar intersticial en artritis reumatoide
Ponce-Campos SD, Martín-Márquez BT, Chávez-García D, Olvera-Palafox CN, Cardona-Müller D, Ponce-Muñoz M, Díaz-Rizo V, González-López L
Idioma: Español
Referencias bibliográficas: 45
Paginas: 132-141
Archivo PDF: 236.90 Kb.
RESUMEN
La artritis reumatoide (AR) es una enfermedad inflamatoria de las articulaciones sinoviales que frecuentemente cursa con manifestaciones sistémicas. La enfermedad pulmonar intersticial (EPI) constituye una de las manifestaciones de esta afectación extraarticular con mayor impacto en la mortalidad. La EPI puede presentarse en servicios clínicos de reumatología afectando alrededor de 3-4% de los pacientes con AR, pero la supervivencia se afecta significativamente sobre todo en individuos con una enfermedad severa; se calcula que la supervivencia puede ser de dos a tres años tras su diagnóstico. Es muy relevante el diagnóstico temprano de esta complicación con el fin de iniciar un tratamiento multidisciplinario. En el establecimiento del diagnóstico, las radiografías de tórax son de baja utilidad en etapas tempranas de la enfermedad, ya que ofrecen una baja sensibilidad y revelan datos anormales sólo en enfermedad severa o etapas tardías. Por ello, deberá considerarse en aquellos sujetos con sospecha de EPI un abordaje diagnóstico integral en el que participen los especialistas de medicina interna, neumología, reumatología y cardiología; este abordaje inicial requiere pruebas de función pulmonar y la tomografía axial computarizada de alta resolución. Esta revisión describe la epidemiología y los factores etiológicos relacionados con el desarrollo de esta entidad; asimismo, se revisan las características clínicas, los métodos de evaluación diagnóstica y la evidencia de los tratamientos utilizados para la EPI, en particular, corticosteroides, inmunosupresores y agentes biológicos.
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