Pharmacological management of depression: Japanese expert consensus.


Journal

Journal of affective disorders
ISSN: 1573-2517
Titre abrégé: J Affect Disord
Pays: Netherlands
ID NLM: 7906073

Informations de publication

Date de publication:
01 04 2020
Historique:
received: 31 10 2019
revised: 13 12 2019
accepted: 26 01 2020
pubmed: 15 2 2020
medline: 16 2 2021
entrez: 15 2 2020
Statut: ppublish

Résumé

Clinically relevant issues in the real-world treatment of depression have not always been captured by conventional treatment guidelines. Certified psychiatrists of the Japanese Society of Clinical Neuropsychopharmacology were asked to evaluate treatment options regarding 23 clinical situations in the treatment of depression using a 9-point Likert scale (1="disagree" and 9="agree"). According to the responses of 114 experts, the options were categorized into first-, second-, and third-line treatments. First-line antidepressants varied depending on predominant symptoms: escitalopram (mean ± standard deviation score, 7.8 ± 1.7) and sertraline (7.3 ± 1.7) were likely selected for anxiety; duloxetine (7.6 ± 1.9) and venlafaxine (7.2 ± 2.1) for loss of interest; mirtazapine for insomnia (8.2 ± 1.6), loss of appetite (7.9 ± 1.9), agitation and severe irritation (7.4 ± 2.0), and suicidal ideation (7.5 ± 1.9). While first-line treatment was switched to either an SNRI (7.7 ± 1.9) or mirtazapine (7.4 ± 2.0) in the case of non-response to an SSRI, switching to mirtazapine (7.1 ± 2.2) was recommended in the case of non-response to an SNRI, and vice versa (switching to an SNRI (7.0 ± 2.0) in the case of non-response to mirtazapine). Augmentation with aripiprazole was considered the first-line treatment for partial response to an SSRI (7.1 ± 2.3) or SNRI (7.0 ± 2.5). The evidence level of expert consensus is considered low. All included experts were Japanese. Recommendations made by experts in the field are useful and can supplement guidelines and informed decision making in real-world clinical practice. We suggest that pharmacological strategies for depression be flexible and that each patient's situational needs as well as the pharmacotherapeutic profile of medications be considered.

Sections du résumé

BACKGROUND
Clinically relevant issues in the real-world treatment of depression have not always been captured by conventional treatment guidelines.
METHODS
Certified psychiatrists of the Japanese Society of Clinical Neuropsychopharmacology were asked to evaluate treatment options regarding 23 clinical situations in the treatment of depression using a 9-point Likert scale (1="disagree" and 9="agree"). According to the responses of 114 experts, the options were categorized into first-, second-, and third-line treatments.
RESULTS
First-line antidepressants varied depending on predominant symptoms: escitalopram (mean ± standard deviation score, 7.8 ± 1.7) and sertraline (7.3 ± 1.7) were likely selected for anxiety; duloxetine (7.6 ± 1.9) and venlafaxine (7.2 ± 2.1) for loss of interest; mirtazapine for insomnia (8.2 ± 1.6), loss of appetite (7.9 ± 1.9), agitation and severe irritation (7.4 ± 2.0), and suicidal ideation (7.5 ± 1.9). While first-line treatment was switched to either an SNRI (7.7 ± 1.9) or mirtazapine (7.4 ± 2.0) in the case of non-response to an SSRI, switching to mirtazapine (7.1 ± 2.2) was recommended in the case of non-response to an SNRI, and vice versa (switching to an SNRI (7.0 ± 2.0) in the case of non-response to mirtazapine). Augmentation with aripiprazole was considered the first-line treatment for partial response to an SSRI (7.1 ± 2.3) or SNRI (7.0 ± 2.5).
LIMITATIONS
The evidence level of expert consensus is considered low. All included experts were Japanese.
CONCLUSIONS
Recommendations made by experts in the field are useful and can supplement guidelines and informed decision making in real-world clinical practice. We suggest that pharmacological strategies for depression be flexible and that each patient's situational needs as well as the pharmacotherapeutic profile of medications be considered.

Identifiants

pubmed: 32056937
pii: S0165-0327(19)33031-9
doi: 10.1016/j.jad.2020.01.149
pii:
doi:

Substances chimiques

Antidepressive Agents 0
Venlafaxine Hydrochloride 7D7RX5A8MO

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

626-632

Informations de copyright

Copyright © 2020. Published by Elsevier B.V.

Auteurs

Hitoshi Sakurai (H)

Department of Psychiatry, Massachusetts General Hospital, Boston, MA, United States; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.

Hiroyuki Uchida (H)

Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.

Masaki Kato (M)

Department of Neuropsychiatry, Kansai Medical University, Osaka, Japan.

Takefumi Suzuki (T)

Department of Neuropsychiatry, University of Yamanashi Faculty of Medicine, Yamanashi, Japan.

Hajime Baba (H)

Department of Psychiatry & Behavioral Science, Juntendo University Graduate School of Medicine, Tokyo, Japan.

Koichiro Watanabe (K)

Department of Neuropsychiatry, Kyorin University School of Medicine, Tokyo, Japan.

Ken Inada (K)

Department of Psychiatry, Tokyo Women's Medical University School of Medicine, Tokyo Japan.

Toshiaki Kikuchi (T)

Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.

Asuka Katsuki (A)

Department of Psychiatry, University of Occupational and Environmental Health, Fukuoka, Japan.

Ikuko Kishida (I)

Fujisawa Hospital, Kanagawa, Japan; Department of Psychiatry, Yokohama City University School of Medicine, Kanagawa, Japan.

Yuka Sugawara Kikuchi (Y)

Department of Psychiatry, Akita University School of Medicine, Akita, Japan.

Norio Yasui-Furukori (N)

Department of Psychiatry, Dokkyo Medical University School of Medicine, Tochigi, Japan. Electronic address: furukori@dokkyomed.ac.jp.

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