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Strategic use of new generation antidepressants for depression: SUN(^_^)D study protocol.

机译:新一代抗抑郁药在抑郁症中的战略应用:SUN (^_^) D研究方案。

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摘要

[Background] After more than half a century of modern psychopharmacology, with billions of dollars spent on antidepressants annually world-wide, we lack good evidence to guide our everyday decisions in conducting antidepressant treatment of patients with major depression. First we did not know which antidepressant to use as first line treatment. Second we do not know which dosage we should be aiming at with that antidepressant. Because more than half of the patients with major depression starting treatment do not remit after adequate trial with the first agent, they will need a second line treatment. Dose escalation, augmentation and switching are the three often recommended second line strategies but we do not know which is better than the others. Moreover, we do not know when to start considering this second line treatment. The recently published multiple-treatments meta-analysis of 12 new generation antidepressants has provided some partial answers to the first question. Starting with these findings, this proposed trial aims to establish the optimum 1st line and 2nd line antidepressant treatment strategy among adult patients with a non-psychotic unipolar major depressive episode. [Methods] SUN(^_^)D, the Strategic Use of New generation antidepressants for Depression, is an assessor-blinded, parallel-group, multi-centre randomised controlled trial. Step I is a cluster-randomised trial comparing titration up to the minimum vs maximum of the recommended dose range among patients starting with sertraline. The primary outcome is the change in the Patient Health Questionnaire (PHQ)-9 scores administered by a blinded rater via telephone at week 1 through 3. Step II is an individually randomised trial comparing staying on sertraline, augmentation of sertraline with mirtazapine, and switching to mirtazapine among patients who have not remitted on the first line treatment by week 3. The primary outcome is the change in the PHQ-9 scores at week 4 through 9. Step III represents a continuation phase to Steps I and II and aims to establish longer-term effectiveness and acceptability of the above-examined treatment strategies up to week 25. The trial is supported by the Grant-in-Aid by the Ministry of Health, Labour and Welfare, Japan. [Discussion]SUN(^_^)D promises to be a pragmatic large trial to answer important clinical questions that every clinician treating patients with major depression faces in his/her daily practices concerning its first- and second-line treatments. [Trial registration]ClinicalTrials.gov: NCT01109693
机译:[背景]经过半个多世纪的现代心理药理学研究,全球每年在抗抑郁药上的花费达数十亿美元,我们缺乏良好的证据来指导我们在进行重性抑郁症患者抗抑郁治疗方面的日常决策。首先,我们不知道使用哪种抗抑郁药作为一线治疗药物。其次,我们不知道该抗抑郁药应针对的剂量。因为超过一半的患有严重抑郁症的开始治疗的患者在使用第一种药物进行充分的试验后仍未缓解,因此他们将需要第二线治疗。剂量递增,增加和切换是经常推荐的三线策略,但我们不知道哪种策略比其他方法更好。而且,我们不知道何时开始考虑进行第二线治疗。最近发表的对12种新一代抗抑郁药的多元治疗荟萃分析为第一个问题提供了部分答案。从这些发现出发,该拟议的试验旨在为患有非精神病性单相严重抑郁发作的成年患者建立最佳的一线和二线抗抑郁治疗策略。 [方法] SUN (^_^) D是治疗抑郁症的新一代抗抑郁药的战略用途,是一项评估者盲法,平行组,多中心,随机对照试验。步骤I是一项整群随机试验,比较从舍曲林开始的患者中滴定剂量到建议剂量范围的最小与最大。主要结果是在第1至3周通过盲人评估者通过电话进行的患者健康问卷(PHQ)-9评分的变化。步骤II是一项单独的随机试验,比较了维持舍曲林,米氮平增加舍曲林和转用在第3周前未接受一线治疗的患者中使用米氮平的情况。主要结果是第4周至第9周PHQ-9得分的变化。步骤III代表了步骤I和II的延续阶段,旨在建立直至25周,上述治疗策略的长期有效性和可接受性。该试验得到日本厚生劳动省的补助金支持。 [讨论] SUN (^_^) D有望成为一项务实的大型试验,以回答每位治疗重度抑郁症患者的临床医生在其一线和二线治疗的日常实践中都面临的重要临床问题。 [试验注册] ClinicalTrials.gov:NCT01109693

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