Literature DB >> 23721923

Prescription patterns following first-line new generation antidepressants for depression in Japan: a naturalistic cohort study based on a large claims database.

Toshi A Furukawa1, Yoshie Onishi, Shiro Hinotsu, Aran Tajika, Nozomi Takeshima, Kiyomi Shinohara, Yusuke Ogawa, Yu Hayasaka, Koji Kawakami.   

Abstract

BACKGROUND: Several studies have described real-world prescription patterns of first-line antidepressants for depression but little is known about their fate in terms of duration, intensity and changes.
METHODS: An inception cohort of new onset non-psychotic depression initiating antidepressant treatment with a new generation antidpressive agent was identified in a large health insurance claims database in Japan between 2009 and 2010. The duration and intensity of first-line antidepressants, the timing and kind of second-line antidepressants and the total duration of antidepressant treatment were examined.
RESULTS: We identified 1592 patients. The starting dose and the maximum dose attained with the first-line agent appeared to be largely in line with the guideline recommendations although the latter tended toward the minimum of the recommended range. The continuity of the first-line antidepressant was far below the guideline recommendations, with 28% never returning after the initial prescription and 55% dropping out within 3 months. Of all the first-line antidepressants, 14% were subsequently augmented by another psychotropic agent while 17% were switched to another antidepressant after a median of 3 or 2 months, respectively. The choice of the second-line agents varied extremely widely. The total duration of antidepressant therapy was as short as a median of 4 months, with 68% stopping treatment by 6 months. LIMITATIONS: The diagnosis of non-psychotic unipolar depression in the claims database analyses remains approximate.
CONCLUSIONS: The current guidelines are grossly out of touch with the clinical realities. On the one hand, guidelines need to reflect the real-world practices; on the other hand clinicians should limit their treatment options and allow evidence-based comparative effectiveness research among them so that patients shall no longer be given less effective and more effective treatments without being able to distinguish among them.
© 2013 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Antidepressive agents; Depressive disorder; Drug administration schedule; Patient compliance

Mesh:

Substances:

Year:  2013        PMID: 23721923     DOI: 10.1016/j.jad.2013.05.015

Source DB:  PubMed          Journal:  J Affect Disord        ISSN: 0165-0327            Impact factor:   4.839


  7 in total

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4.  An observational study of duloxetine versus SSRI monotherapy for the treatment of painful physical symptoms in Japanese patients with major depressive disorder: primary analysis.

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Authors:  Ahmad Ali Eslami; Leili Rabiei; Seyed Mohammad Afzali; Saeed Hamidizadeh; Reza Masoudi
Journal:  Iran Red Crescent Med J       Date:  2016-01-02       Impact factor: 0.611

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Authors:  Tadashi Kato; Toshi A Furukawa; Akio Mantani; Ken'ichi Kurata; Hajime Kubouchi; Susumu Hirota; Hirotoshi Sato; Kazuyuki Sugishita; Bun Chino; Kahori Itoh; Yoshio Ikeda; Yoshihiro Shinagawa; Masaki Kondo; Yasumasa Okamoto; Hirokazu Fujita; Motomu Suga; Shingo Yasumoto; Naohisa Tsujino; Takeshi Inoue; Noboru Fujise; Tatsuo Akechi; Mitsuhiko Yamada; Shinji Shimodera; Norio Watanabe; Masatoshi Inagaki; Kazuhira Miki; Yusuke Ogawa; Nozomi Takeshima; Yu Hayasaka; Aran Tajika; Kiyomi Shinohara; Naohiro Yonemoto; Shiro Tanaka; Qi Zhou; Gordon H Guyatt
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  7 in total

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