摘要
背景:5-羟色胺再摄取抑制剂(SRIs)和认知行为心理治疗(CBT)是强迫症(OCD)的一线治疗方法。然而,相当一部分患者对首选治疗的反应不令人满意。已经针对耐药患者的管理研究了几种选择。 目的:本文的目的是系统地回顾有关治疗耐药成人强迫症患者的策略的现有文献。 方法:我们首先回顾了关于治疗抗性OCD定义的研究;然后,我们分析了评估耐药患者的几种不同策略的研究结果。我们将我们的评价限制在成人OCD患者中进行的双盲,安慰剂对照研究,这些患者对SRI试验的第一次充分性(就持续时间和剂量而言)的耐药性进行了记录,结果明确定义为耶鲁的减少 - 布朗强迫症量表(YBOCS)评分和/或反应/缓解率(根据YBOCS)。 结果:我们确定了安慰剂对照随机研究中阳性结果支持的五种策略:1)SRIs的抗精神病药物添加(16项RCT,其中10项阳性; 4项头对头RCT);在抗精神病药物中,现有的随机对照试验检测了氟哌啶醇(丁酰苯),匹莫齐特(二苯基丁基哌啶),利培酮(SDA:5-羟色胺 - 多巴胺拮抗剂),帕潘立酮(SDA),奥氮平(MARTA:多效受体靶向抗精神病药),喹硫平(喹硫平)的加入MARTA)和阿立哌唑(部分多巴胺激动剂); 2)CBT加药(2项阳性RCT); 3)改用静脉注射氯米帕明(SRI)给药(2例阳性RCT); 4)当第一次试验为阴性时(1个阳性RCT),改用帕罗西汀(SSRI:选择性5-羟色胺再摄取抑制剂)或文拉法辛(SNRI:血清素 - 去甲肾上腺素再摄取抑制剂); 5)向SRIs添加除抗精神病药物以外的药物(18项RCT用几种不同的化合物进行,仅有4项阳性研究)。 结论:治疗抵抗性强迫症仍然是精神科医生面临的重大挑战。迄今为止,最有效的策略是向SRIs中加入抗精神病药(阿立哌唑和利培酮);另一个有效的策略是CBT加入药物治疗。其他策略,例如转用另一种一线治疗或改用静脉内给药是有希望的,但需要在双盲研究中进一步确认。添加除抗精神病药物以外的药物仍有待研究,因为有几项阴性研究存在,而积极的研究需要确认(仅有1项阳性研究)。
关键词: 强迫症,治疗抵抗,认知行为疗法增强,抗精神病药物增强,联合治疗。
Current Medicinal Chemistry
Title:A Systematic Review of Evidence-based Treatment Strategies for Obsessive- compulsive Disorder Resistant to first-line Pharmacotherapy
Volume: 25 Issue: 41
关键词: 强迫症,治疗抵抗,认知行为疗法增强,抗精神病药物增强,联合治疗。
摘要: Background: Serotonin reuptake inhibitors (SRIs) and cognitive-behavioral psychotherapy (CBT) are first-line treatments for obsessive-compulsive disorder (OCD). However, a significant proportion of patients do not respond satisfactorily to first-choice treatments. Several options have been investigated for the management of resistant patients.
Objective: The aim of the present paper is to systematically review the available literature concerning the strategies for the treatment of resistant adult patients with OCD.
Method: We first reviewed studies concerning the definition of treatment-resistant OCD; we then analyzed results of studies evaluating several different strategies in resistant patients. We limited our review to double-blind, placebo-controlled studies performed in adult patients with OCD whose resistance to a first adequate (in terms of duration and dosage) SRI trial was documented and where outcome was clearly defined in terms of decrease in Yale-Brown Obsessive-Compulsive Scale (YBOCS) scores and/or response/ remission rates (according to the YBOCS).
Results: We identified five strategies supported by positive results in placebo-controlled randomized studies: 1) antipsychotic addition to SRIs (16 RCTs, of them 10 positive; 4 head-to-head RCTs); among antipsychotics, available RCTs examined the addition of haloperidol (butyrophenone), pimozide (diphenyl-butylpiperidine), risperidone (SDA: serotonin- dopamine antagonist), paliperidone (SDA), olanzapine (MARTA: multi-acting receptor targeted antipsychotic), quetiapine (MARTA) and aripiprazole (partial dopamine agonist); 2) CBT addition to medication (2 positive RCTs); 3) switch to intravenous clomipramine (SRI) administration (2 positive RCTs); 4) switch to paroxetine (SSRI: selective serotonin reuptake inhibitor) or venlafaxine (SNRI: serotonin-norepinephrine reuptake inhibitor) when the first trial was negative (1 positive RCT); and 5) the addition of medications other than an antipsychotic to SRIs (18 RCTs performed with several different compounds, with only 4 positive studies).
Conclusion: Treatment-resistant OCD remains a significant challenge to psychiatrists. To date, the most effective strategy is the addition of antipsychotics (aripiprazole and risperidone) to SRIs; another effective strategy is CBT addition to medications. Other strategies, such as the switch to another first-line treatment or the switch to intravenous administration are promising but need further confirmation in double-blind studies. The addition of medications other than antipsychotics remains to be studied, as several negative studies exist and positive ones need confirmation (only 1 positive study).
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Cite this article as:
A Systematic Review of Evidence-based Treatment Strategies for Obsessive- compulsive Disorder Resistant to first-line Pharmacotherapy, Current Medicinal Chemistry 2018; 25 (41) . https://dx.doi.org/10.2174/0929867325666171222163645
DOI https://dx.doi.org/10.2174/0929867325666171222163645 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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