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一项关于普瑞巴林作为门诊治疗抵抗性双相情感障碍患者急性和维持期辅助治疗的开放性试验。

An open trial of pregabalin as an acute and maintenance adjunctive treatment for outpatients with treatment resistant bipolar disorder.

机构信息

Sutter Community Hospitals, Sacramento, CA, USA.

出版信息

J Affect Disord. 2013 May;147(1-3):407-10. doi: 10.1016/j.jad.2012.09.005. Epub 2012 Oct 4.

Abstract

BACKGROUND

Pregabalin is a structural analog of GABA, similar to gabapentin. It does not have a FDA indication for any psychiatric disorder in the USA. There has been one case report of the successful use of pregabalin as an augmenting agent in a patient with Bipolar Disorder (BD). In the present open label study, not subsidized by the manufacturer, the investigators prospectively evaluated the acute and maintenance efficacy of pregabalin as an adjunctive medication for a group of treatment refractory outpatients with BD.

METHODS

Older adolescent and adult outpatients with any type of DSM-IV diagnosed BD, who were considered treatment nonresponders to multiple standard medications for BD, were treated with adjunctive pregabalin. The baseline mood state before initiation of pregabalin was compared to the mood state after an acute trial of pregabalin using the Clinical Global Impression-Bipolar Version Scale (CGI-BP). All acute responders were treated for a minimum of two months. Follow-up maintenance treatment data was obtained for the acute pregabalin responders for three years after the 18 month acute phase of the study.

RESULTS

Fifty-eight total patients were treated adjunctively with pregabalin. Twenty-four (41%) were rated as acute responders. For the acute responders, pregabalin produced either a mood stabilizing effect, antidepressant effect or antimanic effect. Intolerable side-effects were the most common reason (79%) for a failed acute trial of pregabalin. None of the side effects resulted in serious medical complications. No patient abused pregabalin, and there were no adverse drug-drug interactions despite an average of 3.3 concurrent other psychiatric medications. The maintenance data revealed that 10 (42%) of the original 24 acute pregabalin responders were still taking pregabalin as an add-on medicine for an average of 45.2 months (range 42-48, SD: 2.35).

LIMITATIONS

This study has an open label observation design.

CONCLUSIONS

The results of this preliminary open study suggest that pregabalin is a safe and effective acute and maintenance adjunctive treatment for a significant number of treatment-resistant outpatients with any type of BPD. It appears to have mood stabilizing and antidepressant properties in addition to antimanic effects. Similar studies using a double-blind, randomly controlled design would be useful to confirm the reliability and validity of the results of this study.

摘要

背景

普瑞巴林是 GABA 的结构类似物,类似于加巴喷丁。它在美国没有 FDA 批准用于任何精神疾病。有一例成功使用普瑞巴林作为双相情感障碍(BD)患者增效剂的病例报告。在本非资助于制造商的开放标签研究中,研究人员前瞻性评估了普瑞巴林作为一组治疗难治性 BD 门诊患者辅助药物的急性和维持疗效。

方法

任何类型的 DSM-IV 诊断为 BD 的年长青少年和成年门诊患者,被认为对多种 BD 标准药物无反应,接受辅助普瑞巴林治疗。在开始普瑞巴林治疗前的基础情绪状态与使用临床总体印象-双相版本量表(CGI-BP)进行的普瑞巴林急性试验后的情绪状态进行比较。所有急性反应者均至少治疗两个月。对急性普瑞巴林反应者进行为期三年的随访维持治疗数据,随访时间为研究急性阶段 18 个月后。

结果

共有 58 名患者接受普瑞巴林辅助治疗。24 名(41%)被评为急性反应者。对于急性反应者,普瑞巴林产生了稳定情绪、抗抑郁或抗躁狂作用。无法耐受副作用是普瑞巴林急性试验失败的最常见原因(79%)。没有副作用导致严重的医疗并发症。没有患者滥用普瑞巴林,尽管平均有 3.3 种其他精神科药物同时使用,但没有药物相互作用的不良事件。维持数据显示,24 名急性普瑞巴林反应者中有 10 名(42%)仍在服用普瑞巴林作为辅助药物,平均时间为 45.2 个月(范围 42-48,SD:2.35)。

局限性

本研究为开放标签观察设计。

结论

这项初步开放研究的结果表明,普瑞巴林是一种安全有效的急性和维持性辅助治疗方法,适用于许多治疗抵抗的门诊患者,无论哪种类型的 BPD。它似乎具有稳定情绪和抗抑郁作用,以及抗躁狂作用。使用双盲、随机对照设计的类似研究将有助于证实本研究结果的可靠性和有效性。

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