Your browser doesn't support javascript.
loading
Comparison of the Efficacy and Safety of Aripiprazole Versus Bupropion Augmentation in Patients With Major Depressive Disorder Unresponsive to Selective Serotonin Reuptake Inhibitors: A Randomized, Prospective, Open-Label Study.
Cheon, Eun-Jin; Lee, Kwang-Hun; Park, Young-Woo; Lee, Jong-Hun; Koo, Bon-Hoon; Lee, Seung-Jae; Sung, Hyung-Mo.
Affiliation
  • Cheon EJ; From the *Department of Psychiatry, Yeungnam University College of Medicine, Yeungnam University Medical Center, Daegu; †Department of Neuropsychiatry, Dongguk University Kyungju Hospital, Kyungju; ‡Department of Neuropsychiatry, Daegu Fatima Hospital; §Department of Psychiatry, Catholic University of Daegu School of Medicine; ∥Department of Psychiatry, Kyungpook National University School of Medicine, Daegu; and ¶Department of Neuropsychiatry, College of Medicine, Pochon Cha University, Cha Hos
J Clin Psychopharmacol ; 37(2): 193-199, 2017 Apr.
Article de En | MEDLINE | ID: mdl-28129308
ABSTRACT

PURPOSE:

The purpose of this study was to compare the efficacy and safety of aripiprazole versus bupropion augmentation in patients with major depressive disorder (MDD) unresponsive to selective serotonin reuptake inhibitors (SSRIs).

METHODS:

This is the first randomized, prospective, open-label, direct comparison study between aripiprazole and bupropion augmentation. Participants had at least moderately severe depressive symptoms after 4 weeks or more of SSRI treatment. A total of 103 patients were randomized to either aripiprazole (n = 56) or bupropion (n = 47) augmentation for 6 weeks. Concomitant use of psychotropic agents was prohibited. Montgomery Asberg Depression Rating Scale, 17-item Hamilton Depression Rating scale, Iowa Fatigue Scale, Drug-Induced Extrapyramidal Symptoms Scale, Psychotropic-Related Sexual Dysfunction Questionnaire scores were obtained at baseline and after 1, 2, 4, and 6 weeks of treatment.

RESULTS:

Overall, both treatments significantly improved depressive symptoms without causing serious adverse events. There were no significant differences in the Montgomery Asberg Depression Rating Scale, 17-item Hamilton Depression Rating scale, and Iowa Fatigue Scale scores, and response rates. However, significant differences in remission rates between the 2 groups were evident at week 6 (55.4% vs 34.0%, respectively; P = 0.031), favoring aripiprazole over bupropion. There were no significant differences in adverse sexual events, extrapyramidal symptoms, or akathisia between the 2 groups.

CONCLUSIONS:

The present study suggests that aripiprazole augmentation is at least comparable to bupropion augmentation in combination with SSRI in terms of efficacy and tolerability in patients with MDD. Both aripiprazole and bupropion could help reduce sexual dysfunction and fatigue in patients with MDD. Aripiprazole and bupropion may offer effective and safe augmentation strategies in patients with MDD who are unresponsive to SSRIs. Double-blinded trials are warranted to confirm the present findings.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Neuroleptiques / / Bupropion / Inbiteurs sélectifs de la recapture de la sérotonine / Inhibiteurs de la capture de la dopamine / Trouble dépressif majeur / Trouble dépressif résistant aux traitements / Aripiprazole Type d'étude: Clinical_trials / Observational_studies Limites: Adult / Female / Humans / Male / Middle aged Langue: En Journal: J Clin Psychopharmacol Année: 2017 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Neuroleptiques / / Bupropion / Inbiteurs sélectifs de la recapture de la sérotonine / Inhibiteurs de la capture de la dopamine / Trouble dépressif majeur / Trouble dépressif résistant aux traitements / Aripiprazole Type d'étude: Clinical_trials / Observational_studies Limites: Adult / Female / Humans / Male / Middle aged Langue: En Journal: J Clin Psychopharmacol Année: 2017 Type de document: Article