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Optimized regimens of combined medications for the treatment of major depressive disorder: a double-blind, randomized-controlled trial

INTRODUCTION: This study investigated if optimized dose regimens of escitalopram and bupropion combination from treatment initiation can be superior to either drug alone in speed of onset, remission rate, and maintenance of therapeutic efficacy. METHODS: Patients from a single site (N=85) within a l...

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Autores principales: Zuilhof, Zoë, Norris, Sandhaya, Blondeau, Claude, Tessier, Pierre, Blier, Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257360/
https://www.ncbi.nlm.nih.gov/pubmed/30538479
http://dx.doi.org/10.2147/NDT.S175203
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author Zuilhof, Zoë
Norris, Sandhaya
Blondeau, Claude
Tessier, Pierre
Blier, Pierre
author_facet Zuilhof, Zoë
Norris, Sandhaya
Blondeau, Claude
Tessier, Pierre
Blier, Pierre
author_sort Zuilhof, Zoë
collection PubMed
description INTRODUCTION: This study investigated if optimized dose regimens of escitalopram and bupropion combination from treatment initiation can be superior to either drug alone in speed of onset, remission rate, and maintenance of therapeutic efficacy. METHODS: Patients from a single site (N=85) within a larger double-blind 12-week trial (N=245) showed a lower dropout rate (14% vs 40%) and used higher doses; therefore, this cohort was analyzed separately. Uniquely at this single site, after 12 weeks, non-remitters on a single drug received the other one in addition and combination non-remitters underwent a switch of escitalopram for duloxetine for a 6-week period. Escitalopram could be given up to 40 mg/day and bupropion up to 450 mg/day. A 6-month prolongation was then implemented in remitters, maintaining the double-blind design throughout. Remission was defined as ≤7 on the 17-item Hamilton Rating Scale for Depression, as in the initial publication. RESULTS: At week 2, combination treatment was superior in remission rate (5/28) compared with both bupropion (0/26) and escitalopram monotherapies (0/31; P=0.03 and P=0.02, respectively). The week 12 remission rate of combination treatment showed a higher rate (15/28) relative to bupropion monotherapy (7/26; P=0.04), but not statistically different from escitalopram monotherapy (11/31; P=0.13). The 6-week augmentation produced remission in 7/21 monotherapy non-remitters and 0/6 in the switch group (P=0.13). Remission was sustained in 28/31 patients enrolled in the 6-month maintenance. CONCLUSION: These results suggest that combination of escitalopram and bupropion from treatment initiation is superior to either monotherapy in speed of onset. The addition of a second drug in non-remitters can lead to additional remissions, as shown with other combinations of medications. Treatment prolongation using optimized regimens leads to low relapse rates.
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spelling pubmed-62573602018-12-11 Optimized regimens of combined medications for the treatment of major depressive disorder: a double-blind, randomized-controlled trial Zuilhof, Zoë Norris, Sandhaya Blondeau, Claude Tessier, Pierre Blier, Pierre Neuropsychiatr Dis Treat Original Research INTRODUCTION: This study investigated if optimized dose regimens of escitalopram and bupropion combination from treatment initiation can be superior to either drug alone in speed of onset, remission rate, and maintenance of therapeutic efficacy. METHODS: Patients from a single site (N=85) within a larger double-blind 12-week trial (N=245) showed a lower dropout rate (14% vs 40%) and used higher doses; therefore, this cohort was analyzed separately. Uniquely at this single site, after 12 weeks, non-remitters on a single drug received the other one in addition and combination non-remitters underwent a switch of escitalopram for duloxetine for a 6-week period. Escitalopram could be given up to 40 mg/day and bupropion up to 450 mg/day. A 6-month prolongation was then implemented in remitters, maintaining the double-blind design throughout. Remission was defined as ≤7 on the 17-item Hamilton Rating Scale for Depression, as in the initial publication. RESULTS: At week 2, combination treatment was superior in remission rate (5/28) compared with both bupropion (0/26) and escitalopram monotherapies (0/31; P=0.03 and P=0.02, respectively). The week 12 remission rate of combination treatment showed a higher rate (15/28) relative to bupropion monotherapy (7/26; P=0.04), but not statistically different from escitalopram monotherapy (11/31; P=0.13). The 6-week augmentation produced remission in 7/21 monotherapy non-remitters and 0/6 in the switch group (P=0.13). Remission was sustained in 28/31 patients enrolled in the 6-month maintenance. CONCLUSION: These results suggest that combination of escitalopram and bupropion from treatment initiation is superior to either monotherapy in speed of onset. The addition of a second drug in non-remitters can lead to additional remissions, as shown with other combinations of medications. Treatment prolongation using optimized regimens leads to low relapse rates. Dove Medical Press 2018-11-22 /pmc/articles/PMC6257360/ /pubmed/30538479 http://dx.doi.org/10.2147/NDT.S175203 Text en © 2018 Zuilhof et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Zuilhof, Zoë
Norris, Sandhaya
Blondeau, Claude
Tessier, Pierre
Blier, Pierre
Optimized regimens of combined medications for the treatment of major depressive disorder: a double-blind, randomized-controlled trial
title Optimized regimens of combined medications for the treatment of major depressive disorder: a double-blind, randomized-controlled trial
title_full Optimized regimens of combined medications for the treatment of major depressive disorder: a double-blind, randomized-controlled trial
title_fullStr Optimized regimens of combined medications for the treatment of major depressive disorder: a double-blind, randomized-controlled trial
title_full_unstemmed Optimized regimens of combined medications for the treatment of major depressive disorder: a double-blind, randomized-controlled trial
title_short Optimized regimens of combined medications for the treatment of major depressive disorder: a double-blind, randomized-controlled trial
title_sort optimized regimens of combined medications for the treatment of major depressive disorder: a double-blind, randomized-controlled trial
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257360/
https://www.ncbi.nlm.nih.gov/pubmed/30538479
http://dx.doi.org/10.2147/NDT.S175203
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