Venlafaxine, Paroxetine and Milnacipran for Major Depressive Disorder: A Pragmatic 24-Week Study

被引:3
|
作者
Chuang, Hui-Yu [1 ]
Chang, Yun-Hsuan [2 ,3 ]
Cheng, Ling-Yi [1 ]
Wang, Yu-Shan [1 ]
Chen, Shiou-Lan [2 ]
Chen, Shih-Heng [2 ]
Chu, Chun-Hsien [2 ]
Lee, I. Hui [2 ,4 ]
Chen, Po See [2 ,4 ]
Yeh, Tzung Lieh [2 ,4 ]
Yang, Yen Kuang [2 ,4 ]
Lu, Ru-Band [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Natl Cheng Kung Univ, Coll Med & Hosp, Inst Behav Med, Tainan 70428, Taiwan
[2] Natl Cheng Kung Univ, Coll Med & Hosp, Dept Psychiat, Tainan 70428, Taiwan
[3] Natl Cheng Kung Univ, Coll Med & Hosp, Inst Allied Hlth Sci, Tainan 70428, Taiwan
[4] Natl Cheng Kung Univ Hosp, Dept Psychiat, Tainan 70428, Taiwan
[5] Natl Cheng Kung Univ Hosp, Addict Ctr, Tainan 70428, Taiwan
[6] Natl Hlth Res Inst, Ctr Neuropsychiat Res, Zhunan 35053, Miaoli County, Taiwan
来源
CHINESE JOURNAL OF PHYSIOLOGY | 2014年 / 57卷 / 05期
关键词
milnacipran; paroxetine; remission; response; venlafaxine; RATING-SCALE; PRIMARY-CARE; REUPTAKE INHIBITOR; REMISSION; SEROTONIN; EFFICACY; RELAPSE; NORADRENALINE; RECOVERY;
D O I
10.4077/CJP.2014.BAC209
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Major depressive disorder (MDD), one of the most common psychiatric disorders in the world, is a serious, recurrent and chronic mental disorder, which is associated with significant psychosocial disability and economic burden. Until recently, short-term effectiveness of antidepressants has been measured in terms of patients' response to the medications in significantly reduced depressive symptoms. Remission, a long-term elimination of symptoms and the restoration of normal functioning, has become the primary outcome of therapy. In the current study, the efficacy of three frequently prescribed antidepressants, venlafaxine (75-225 mg/day), paroxetine (20 mg/day) and milnacipran (100 mg/day), used in treating 249 MDD patients with Hamilton Rating Scale of Depression (HRSD17) scores higher than 16 was compared. Each patient was evaluated at week 0, 1, 2, 4, 8, 12, 16, 20 and 24 in a 24-week open-label study. Eighty-two patients took venlafaxine, 97 took paroxetine and 70 patients took milnacipran. No significant differences were found between the three groups in the response condition (HRSD17 scores decreased more than 50%) after 24 weeks of follow-up. For remission, the paroxetine was the least efficacious medication than either the milnacipran (HRSD17 <= 7) or the venlafaxine (HRSD17 <= 5) by the last observation carried forward (LOCF) analysis. Our results suggest that the absence of depressive symptoms alone may not be an indicator for MDD remission, but the duration of absent depressive symptoms may be a better indicator.
引用
收藏
页码:265 / 270
页数:6
相关论文
共 50 条
  • [1] The efficacy and safety of milnacipran in patients with major depressive disorder following initial treatment failure with a selective serotonin reuptake inhibitor: a pragmatic 24-week, multicentre, open-label study
    Tasuku, Hashimoto
    Oda, Yasunori
    Hasegawa, Tadashi
    Kanahara, Nobuhisa
    Sasaki, Tsuyoshi
    Komatsu, Hideki
    Takahashi, Junpei
    Oiwa, Takahiro
    Sakashita, Kiyoshi
    Ishima, Tamaki
    Takase, Naoko
    Kikuchi, Shuichi
    Sekine, Yoshimoto
    Hashimoto, Kenji
    Lyo, Masaomi
    INTERNATIONAL JOURNAL OF PSYCHIATRY IN CLINICAL PRACTICE, 2013, 17 : 35 - 36
  • [2] Milnacipran and venlafaxine at flexible doses (up to 200 mg/d) in the outpatient treatment of adults with moderate-to-severe major depressive disorder: A 24-week randomised, double blind exploratory study
    Olie, J. -P.
    Gourion, D.
    Montagne, A.
    Rostin, M.
    Poirier, M. -F.
    ENCEPHALE-REVUE DE PSYCHIATRIE CLINIQUE BIOLOGIQUE ET THERAPEUTIQUE, 2009, 35 (06): : 595 - 604
  • [3] Efficacy of paroxetine for relapse prevention in social anxiety disorder - A 24-week study
    Stein, DJ
    Versiani, M
    Hair, T
    Kumar, R
    ARCHIVES OF GENERAL PSYCHIATRY, 2002, 59 (12) : 1111 - 1118
  • [4] Milnacipran and venlafaxine at flexible doses (up to 200 mg/day) in the outpatient treatment of adults with moderate-to-severe major depressive disorder: a 24-week randomized, double-blind exploratory study
    Olie, Jean-Pierre
    Gourion, David
    Montagne, Agnes
    Rostin, Michel
    Poirier, Marie-France
    NEUROPSYCHIATRIC DISEASE AND TREATMENT, 2010, 6 : 71 - 79
  • [5] Daily treatment of patients with major depressive disorder: an exploratory study evaluating milnacipran and venlafaxine
    Gourion, D.
    Poirier, M. F.
    Olie, J. P.
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2009, 19 : S419 - S419
  • [6] Residual symptoms in major depressive disorder after treatment with paroxetine and milnacipran
    Kesebir, S.
    Simsek, Y.
    INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2006, 9 : S235 - S235
  • [7] A randomised, placebo-controlled 24-week study evaluating adjunctive brexpiprazole in patients with major depressive disorder
    Bauer, Michael
    Hefting, Nanco
    Lindsten, Annika
    Josiassen, Mette Krog
    Hobart, Mary
    ACTA NEUROPSYCHIATRICA, 2019, 31 (01): : 27 - 35
  • [8] Paroxetine versus Venlafaxine and Escitalopram in Korean Patients with Major Depressive Disorder: A Randomized, Rater-blinded, Six-week Study
    Woo, Young Sup
    McIntyre, Roger S.
    Kim, Jung-Bum
    Lee, Min-Soo
    Kim, Jae-Min
    Yim, Hyeon Woo
    Jun, Tae-Youn
    CLINICAL PSYCHOPHARMACOLOGY AND NEUROSCIENCE, 2017, 15 (04) : 391 - 401
  • [9] Differences in immunomodulatory properties between venlafaxine and paroxetine in patients with major depressive disorder
    Chen, Chun-Yen
    Yeh, Yi-Wei
    Kuo, Shin-Chang
    Liang, Chih-Sung
    Ho, Pei-Shen
    Huang, Chang-Chih
    Yen, Che-Hung
    Shyu, Jia-Fwu
    Lu, Ru-Band
    Huang, San-Yuan
    PSYCHONEUROENDOCRINOLOGY, 2018, 87 : 108 - 118
  • [10] Dosing of aripiprazole adjunctive therapy for Asian patients with major depressive disorder: a 24-week open label trial
    Bai, Y. M.
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2011, 21 : S356 - S357