SciELO - Scientific Electronic Library Online

 
vol.22 número1PREVALENCIA DE SÍNDROME METABÓLICO Y FACTORES ASOCIADOS EN PERSONAL DE SALUD DEPENDIENTE DEL GOBIERNO MUNICIPAL DE LA CIUDAD DE EL ALTO (4050 M.S.N.M.), 2013SÍNDROME DEL LÓBULO MEDIO: REPORTE DE UN CASO índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

Links relacionados

  • No hay articulos similaresSimilares en SciELO

Compartir


Revista Médica La Paz

versión On-line ISSN 1726-8958

Resumen

MURILLO NAVARRO, Luis Alejandro  y  MAMANI TARQUI, Jeannett. FIBROSIS PULMONAR IDIOPÁTICA, TRATAMIENTO CON PIRFENIDONA. Rev. Méd. La Paz [online]. 2016, vol.22, n.1, pp.36-41. ISSN 1726-8958.

Idiopathic pulmonary fibrosis is the most frequent type of interstitial pneumonia. It is characterized by an abnormal healing process, with excess fibrous tissue. It is a chronic, progressive illness, limited to the lungs with unknown etiology; it affects adults over 50 years old, with a progressive deterioration of lung function and gas exchange and a fatal outcome in a relatively short period. It has been published a new consensus document of the ATS/ERS/JRS/ALAT, about the diagnostic and treatment of these disease, and it is been suggested as a treatment a new drug that has generated great expectations, pirfenidone. It has anti-inflammatory and anti-fibrotic properties with promising results. we report the case of a patient of 60 years of age admitted to university hospital social security with an insidious respiratory symptoms, during her hospitalization she was diagnosed with idiopathic pulmonary fibrosis with clinical imaging and histopathological criteria. Treatment with Pirfenidone was initiated as recommended by consensus; monitoring the evolution and the fifth month of treatment was favorable.

Palabras clave : pulmonary fibrosis; pirfenidona.

        · resumen en Español     · texto en Español     · Español ( pdf )

 

Creative Commons License Todo el contenido de esta revista, excepto dónde está identificado, está bajo una Licencia Creative Commons