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Effect of high-dose milnacipran in patients with depression

To investigate the antidepressant effect of high-dose milnacipran, we retrospectively compared three groups of inpatients with major depression; those who were given milnacipran >100–150 mg/day (high-dose milnacipran group), those treated with milnacipran at maximum doses of 50–100 mg/day (standa...

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Autores principales: Hayashi, Masatoshi, Mimura, Masaru, Otsubo, Tempei, Kamijima, Kunitoshi
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656309/
https://www.ncbi.nlm.nih.gov/pubmed/19300602
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author Hayashi, Masatoshi
Mimura, Masaru
Otsubo, Tempei
Kamijima, Kunitoshi
author_facet Hayashi, Masatoshi
Mimura, Masaru
Otsubo, Tempei
Kamijima, Kunitoshi
author_sort Hayashi, Masatoshi
collection PubMed
description To investigate the antidepressant effect of high-dose milnacipran, we retrospectively compared three groups of inpatients with major depression; those who were given milnacipran >100–150 mg/day (high-dose milnacipran group), those treated with milnacipran at maximum doses of 50–100 mg/day (standard-dose milnacipran group), and those treated with paroxetine at maximum doses of 40 mg/day (paroxetine group). The Hamilton Depression Rating Scale (HAM-D) scores of the three groups showed significant decrease at discharge compared to the scores at admission, indicating improvement of depressive symptoms for each group. However, the mean HAM-D score on admission was significantly lower for the standard-dose milnacipran group than the high-dose milnacipran and paroxetine groups. Additional intermediate assessment of the high-dose milnacipran group showed that the effect of milnacipran was dose-dependent with an additional improvement when patients were increase from 100 to 150 mg/day. These results suggest that patients suffering from moderate to severe depression with relative high HAM-D scores may benefit from treatment with high-dose milnacipran.
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spelling pubmed-26563092009-03-19 Effect of high-dose milnacipran in patients with depression Hayashi, Masatoshi Mimura, Masaru Otsubo, Tempei Kamijima, Kunitoshi Neuropsychiatr Dis Treat Letter To investigate the antidepressant effect of high-dose milnacipran, we retrospectively compared three groups of inpatients with major depression; those who were given milnacipran >100–150 mg/day (high-dose milnacipran group), those treated with milnacipran at maximum doses of 50–100 mg/day (standard-dose milnacipran group), and those treated with paroxetine at maximum doses of 40 mg/day (paroxetine group). The Hamilton Depression Rating Scale (HAM-D) scores of the three groups showed significant decrease at discharge compared to the scores at admission, indicating improvement of depressive symptoms for each group. However, the mean HAM-D score on admission was significantly lower for the standard-dose milnacipran group than the high-dose milnacipran and paroxetine groups. Additional intermediate assessment of the high-dose milnacipran group showed that the effect of milnacipran was dose-dependent with an additional improvement when patients were increase from 100 to 150 mg/day. These results suggest that patients suffering from moderate to severe depression with relative high HAM-D scores may benefit from treatment with high-dose milnacipran. Dove Medical Press 2007-10 /pmc/articles/PMC2656309/ /pubmed/19300602 Text en © 2007 Dove Medical Press Limited. All rights reserved
spellingShingle Letter
Hayashi, Masatoshi
Mimura, Masaru
Otsubo, Tempei
Kamijima, Kunitoshi
Effect of high-dose milnacipran in patients with depression
title Effect of high-dose milnacipran in patients with depression
title_full Effect of high-dose milnacipran in patients with depression
title_fullStr Effect of high-dose milnacipran in patients with depression
title_full_unstemmed Effect of high-dose milnacipran in patients with depression
title_short Effect of high-dose milnacipran in patients with depression
title_sort effect of high-dose milnacipran in patients with depression
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656309/
https://www.ncbi.nlm.nih.gov/pubmed/19300602
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