El-Hage W, Fakra E
Clinique Psychiatrique Universitaire, Centre Expert Dépression Résistante Fondation FondaMental, CHRU de Tours, 37044 Tours cedex 9, France; UMR Inserm U930, Université François Rabelais de Tours, Tours, France.
Pôle Universitaire de Psychiatrie, CHU Saint-Etienne, 5 Chemin de la Marendière 42055 Saint-Etienne cedex 2, France.
Encephale. 2016 Feb;42(1 Suppl 1):1S39-47. doi: 10.1016/S0013-7006(16)30018-5.
Only one third of patients suffering from depression will achieve a satisfactory response with first line treatments and more than half of patients will fail to obtain at least 50 % reduction in their symptoms after 3 months of treatment. This article presents a review of the scientific arguments supporting the various therapeutic strategies when confronted to a first treatment failure after an adequate drug trial. Several pharmacological approaches are possible. A first and classical approach is adjusting the drug dosage (optimization). This strategy is coherent with the pharmacological profile of some antidepressant drugs (tricyclic antidepressants, tetracyclic antidepressants, venlafaxine). There is no scientific basis to a dose-effect relationship with the selective serotonin reuptake inhibitors (SSRIs), as minimal doses of these drugs correspond to a high ratio of serotonin transporter occupation; however increasing doses of SSRIs constitutes a usual practice, endorsed by several experts. A second classic strategy is changing an inefficient antidepressant drug to another antidepressant drug (switch). Theoretically, a different pharmacological class should have more chances to be successful; however, in the case of a failure with an SSRI, an inter-class switch has not consistently proven to be superior to an intra-class switch. In some cases, association of antidepressant drugs can also be an advantageous strategy (combination), particularly in the case of partial response with the first prescribed drug. Due to its particular mechanism of action, mirtazapine is often a drug of choice in the case of such an association. Finally, another approach to recommend in case of partial response is associating an antidepressant drug to another class of drugs, such as lithium, atypical antipsychotics or thyroid hormones (potentiation). Lithium has unfailingly proven its efficacy in case of resistance, but the utilization of atypical antipsychotics, at low-doses, has become increasingly common, certainly, because they are easier to handle. Aside from the pharmacological options, we can consider a number of other strategies, first among them is psychotherapy. Most studies assessing the efficacy of psychotherapy were conducted with this therapy as a first-line treatment. More studies of psychotherapy in depression after unsatisfactory response are distinctly needed. Available data seem to indicate that psychotherapy constitutes an efficient alternative, regardless of the type of psychotherapy (results are more robust in cognitive and behavioural therapies and brief interpersonal psychotherapy, in relation with the greater number of studies using these therapies), with effect sizes comparable to the ones obtained with pharmacological options. Among other strategies, physical exercise has been getting more attention lately, even though evidence in this indication remains deceiving for the moment. Lastly, neuromodulation techniques have an unquestionable place. The rTMS has been largely tested with interesting results. Given the time and staff necessary to conduct this therapy, the question has now switched to how precisely select the patients who will most benefit from rTMs, and how long and at what pace should the sessions take place. ECT is undoubtedly the most efficient treatment, but, apart from life-threatening melancholia and other restricted exceptions, it is usually indicated in multi-resistant depression. Some authors suggest using this therapy earlier, as chronicity of the disease is itself a factor of poor response. Finally, this article reviews also the most recent French and International guidelines in managing patients having showed an unsatisfactory response to a first-line treatment.
仅三分之一的抑郁症患者对一线治疗会产生满意的反应,超过半数的患者在治疗3个月后症状减轻不到50%。本文综述了在充分的药物试验后首次治疗失败时支持各种治疗策略的科学依据。有几种药理学方法可供选择。第一种经典方法是调整药物剂量(优化)。该策略与某些抗抑郁药物(三环类抗抑郁药、四环类抗抑郁药、文拉法辛)的药理学特性相符。选择性5-羟色胺再摄取抑制剂(SSRI)不存在剂量-效应关系的科学依据,因为这些药物的最小剂量就对应着较高的5-羟色胺转运体占有率;然而,增加SSRI的剂量是一种常见做法,得到了多位专家的认可。第二种经典策略是将无效的抗抑郁药物换成另一种抗抑郁药物(换药)。理论上,不同的药理学类别成功的机会更大;然而,在SSRI治疗失败的情况下,类间换药并未始终被证明优于类内换药。在某些情况下,联合使用抗抑郁药物也可能是一种有利的策略(联合用药),特别是在对首次处方药物部分有效的情况下。由于其独特的作用机制,米氮平在这种联合用药的情况下通常是首选药物。最后,在部分有效的情况下推荐的另一种方法是将抗抑郁药物与另一类药物联合使用,如锂盐、非典型抗精神病药物或甲状腺激素(增效)。锂盐在耐药情况下已被确凿证明有效,但低剂量使用非典型抗精神病药物越来越普遍,这当然是因为它们更容易使用。除了药理学选择外,我们还可以考虑许多其他策略,其中首先是心理治疗。大多数评估心理治疗疗效的研究都是将这种治疗作为一线治疗进行的。显然需要更多关于心理治疗在反应不佳的抑郁症患者中的研究。现有数据似乎表明,心理治疗是一种有效的替代方法,无论心理治疗的类型如何(认知行为疗法和简短人际心理治疗的结果更强,因为使用这些疗法的研究更多),其效应大小与药理学选择相当。在其他策略中,体育锻炼最近受到了更多关注,尽管目前这方面的证据仍然令人困惑。最后,神经调节技术有着无可争议的地位。重复经颅磁刺激(rTMS)已经得到了大量测试,结果令人感兴趣。考虑到进行这种治疗所需的时间和人员,现在的问题已经转向如何精确选择最能从rTMS中获益的患者,以及治疗疗程应该持续多长时间和以何种速度进行。电休克疗法(ECT)无疑是最有效的治疗方法,但除了危及生命的忧郁症和其他有限的例外情况外,它通常用于多重耐药性抑郁症。一些作者建议更早使用这种疗法,因为疾病的慢性本身就是反应不佳的一个因素。最后,本文还综述了法国和国际上最新的关于管理对一线治疗反应不佳患者的指南。