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首页> 外文期刊>Expert opinion on pharmacotherapy >Quetiapine XR efficacy and tolerability as monotherapy and as adjunctive treatment to conventional antidepressants in the acute and maintenance treatment of major depressive disorder: a review of registration trials.
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Quetiapine XR efficacy and tolerability as monotherapy and as adjunctive treatment to conventional antidepressants in the acute and maintenance treatment of major depressive disorder: a review of registration trials.

机译:在严重抑郁症的急性和维持治疗中,喹硫平XR作为常规抗抑郁药的单一疗法和辅助疗法的疗效和耐受性:一项注册试验的综述。

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摘要

Results from pivotal registration trials in major depressive disorder cohere with outcomes from effectiveness studies indicating that the majority of individuals receiving single-agent pharmacotherapy fail to achieve and sustain symptomatic remission. Several factors provided the impetus for this review: suboptimal efficacy with existing pharmacotherapy for major depressive disorder, quetiapine XR efficacy in the acute and maintenance treatment of bipolar depression, emerging pharmacodynamic evidence that quetiapine XR (and/or its metabolites) uniquely engages monoaminergic systems salient to symptom relief in depressive syndromes, the increasing use of second-generation antipsychotics in the treatment of major depressive disorder and the recent FDA review of quetiapine XR in major depressive disorder. Studies reviewed herein are pivotal registration trials that evaluated the acute and maintenance efficacy and tolerability of quetiapine XR (as monotherapy and as adjunctive treatment) in major depressive disorder. In addition, we also review recent investigations characterizing the pharmacodynamic effect of quetiapine's principal active metabolite, norquetiapine. All studies were obtained from AstraZeneca (Wilmington, DE, USA) and have been presented at national/international scientific meetings. Taken together, extant studies demonstrated that quetiapine XR (50 - 300 mg) provides rapid and sustained symptomatic improvement in the acute and maintenance treatment of major depressive disorder. Quetiapine XR may also offer advantages relative to duloxetine in time to onset of antidepressant action. The major limitations of quetiapine XR use in major depressive disorder relate to weight gain and disrupted glucose/lipid homeostasis as well as sedation/somnolence. Quetiapine XR has tolerability advantages compared with duloxetine on measures of sexual dysfunction. The data from the studies reviewed herein also indicate that quetiapine XR poses a low risk for extrapyramidal side effects in middle-aged and elderly individuals with major depressive disorder.
机译:重大抑郁症的关键性注册试验的结果与有效性研究的结果相吻合,表明大多数接受单药药物治疗的个体无法达到并维持症状缓解。有几个因素为此次综述提供了动力:现有药物疗法对重度抑郁症的治疗效果欠佳;喹硫平XR在双相抑郁症的急性和维持治疗中的疗效;新兴的药效学证据表明喹硫平XR(和/或其代谢物)独特地参与了单胺类药物系统的显着应用。抑郁症的症状缓解,第二代抗精神病药在重度抑郁症的治疗中使用的增加以及最近FDA对喹硫平XR在重度抑郁症中的评价。本文回顾的研究是关键的注册试验,评估了喹硫平XR(作为单一疗法和辅助治疗)在重度抑郁症中的急性和维持功效以及耐受性。此外,我们还回顾了表征喹硫平的主要活性代谢产物降氮平的药效学作用的最新研究。所有研究均来自阿斯利康(美国特拉华州威尔明顿),并已提交给国家/国际科学会议。总而言之,现有研究表明,喹硫平XR(50-300 mg)在严重抑郁症的急性和维持治疗中可提供快速而持续的症状改善。喹硫平XR在抗抑郁作用发作时也可能相对于度洛西汀具有优势。在严重抑郁症中使用喹硫平XR的主要局限性在于体重增加和葡萄糖/脂质体内稳态破坏以及镇静/嗜睡。与度洛西汀相比,喹硫平XR在性功能障碍方面具有耐受性优势。本文审查的研究数据还表明,喹硫平XR在患有重度抑郁症的中年和老年人中,金字塔外副作用的风险较低。

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