2015, Número 2
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Arch Neurocien 2015; 20 (2)
Revisión sistemática de la combinación olanzapina-fluoxetina como tratamiento de la depresión bipolar en adolescentes y adultos
Vargas-Huicochea I, Tamayo JM, Ruiz I
Idioma: Ingles.
Referencias bibliográficas: 47
Paginas: 122-136
Archivo PDF: 149.14 Kb.
RESUMEN
Objetivo: se evaluó la seguridad y eficacia de la combinación olanzapina- fluoxetina (COF) para tratamiento de la
depresión bipolar, en especial en estudios clínicos con duración de 8 a 12 semanas, en adultos y adolescentes.
Material y métodos: los estudios se identificaron en las bases de datos
MEDLINE, EMBASE, Cochrane Library, Web of
Knowledge, LILACS, WHOLIS, NEURO, Latindex y DIALNET (del 2000 a julio 2014). Se utilizaron términos de búsqueda
en inglés, español y vocabulario MeSH (
Medical subjet headings). Se complementaron con ensayos clínicos identificados
(
Clinical Trials.gov) y resúmenes de congresos. Se consideró la evidencia de estudios controlados aleatorizados
(ECA), estudios no aleatorizados y metanálisis.
Resultados: se recuperaron 9 publicaciones/estudios, incluyendo: 5
ECA (6 publicaciones), un estudio no aleatorizado y 2 metanálisis. Un ECA se llevó a cabo en adolescentes y otro en
una población Latinoameéricana. Los estudios enrolaron desde 34 hasta 833 pacientes, con una duración de 7 a 8
semanas y hasta 6 meses, difirieron en cuanto a la calidad metodológica y del reporte. La eficacia de COF (medida
con reducción del puntaje de escalas y porcentajes de respuesta y remisión) fue mayor en comparación con la
monoterapia con olanzapina, lamotrigina y/o placebo. El tratamiento con COF fue bien tolerado en adultos y
adolescentes. Sin embargo, hubo una mayor frecuencia de ganancia de peso, somnolencia, náusea, diarrea y elevados
parámetros metabólicos en los pacientes que recibieron COF
vs los comparadores activos o el placebo.
Conclusiones:
esta revisión muestra que el tratamiento agudo con COF es efectivo y por lo general bien tolerado en adultos y
adolescentes con depresión bipolar. La evidencia existente sugiere la ausencia de diferencias en el perfil de eficacia
y seguridad de COF entre los pacientes de América Latina y poblaciones caucásicas.
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