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Treatment of Mood Disorders in Multiple Sclerosis

机译:多发性硬化症的情绪障碍治疗

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摘要

Multiple sclerosis (MS) is a chronic demyelinating disease of the central nervous system with a significant comorbidity with depressive disorders. Prevalence rates for major depressive disorder (MDD) range from 36 % to 54 % and the rate is around 22 % for adjustment disorders. Selective serotonin reuptake inhibitors (SSRIs) are considered well-tolerated first-line treatment. Tricyclic antidepressants (TCAs) and monoamine oxidase inhibitors (MAOIs) are generally reserved for second-line use after SSRIs, because of sedating or anticholinergic side effects. SNRIs, with the exception of duloxetine, and combinations of newer antidepressants have failed to treat depression due to their side effects profile and frequent interaction with other drugs. Among SSRIs, sertraline is usually the first option, starting at 25 mg/day and increasing to 50 mg/day; and waiting a few weeks to assess drug effects before increasing the dose. The maximum is generally 200 mg/day in a single dose. Paroxetine is the second choice, starting at 10 mg/day for the first 5 days, and then at 20 mg/day thereafter. The maximum dose is about 50 mg/day in a single dose. Fluvoxamine is used at 100-200 mg/day, starting with 25 mg/day, and increasing 25 mg/day every 5 days until 200 mg/day is reached. We should take into account increasing blood level amounts of MS treatments (corticosteroids and cyclophosphamide) with fluvoxamine. With duloxetine, doses will be at 60-120 mg/day. The initial dose for depression is 40 mg/day in two doses; it can increase to 60 mg/day in one to two doses if necessary. The maximum dose is generally 120 mg/day. Duloxetine may increase liver problems through interaction with these MS treatments: teriflunomide, interferon beta-1a, and interferon beta-1b. Considering psychotherapy, only cognitive behavior therapy and mindfulness-based interventions have shown efficacy in improving depression disorders in MS. A comprehensive treatment for depression should include pharmacotherapy and psychotherapy.
机译:多发性硬化症(MS)是一种中枢神经系统的慢性脱髓鞘疾病,伴有抑郁症。重度抑郁症(MDD)的患病率在36%至54%之间,而调节障碍的患病率约为22%。选择性5-羟色胺再摄取抑制剂(SSRI)被认为是耐受性良好的一线治疗。三环类抗抑郁药(TCA)和单胺氧化酶抑制剂(MAOI)通常由于镇静或抗胆碱能副作用而保留给SSRI后的二线使用。由于度洛西汀的副作用以及与其他药物的频繁相互作用,除度洛西汀以外,SNRI和新型抗抑郁药的组合均无法治疗抑郁症。在SSRI中,舍曲林通常是首选,剂量从25毫克/天开始,增加到50毫克/天。然后等待几周以评估药物效果,然后再增加剂量。单次剂量最大值通常为200毫克/天。帕罗西汀是第二选择,头5天以10毫克/天开始,然后以20毫克/天开始。单次剂量的最大剂量约为50毫克/天。氟伏沙明的使用量为100-200 mg /天,从25 mg /天开始,每5天增加25 mg /天,直到达到200 mg /天。我们应考虑用氟伏沙明增加MS治疗(皮质类固醇和环磷酰胺)的血药水平。使用度洛西汀时,剂量为60-120 mg /天。抑郁的初始剂量为40毫克/天,分两次服用;如果有必要,它可以以一到两剂的剂量增加到60毫克/天。最大剂量通常为120毫克/天。度洛西汀可能通过与下列特效药物(特立氟胺,干扰素β-1a和干扰素β-1b)的相互作用而加剧肝脏问题。考虑到心理治疗,只有认知行为疗法和基于正念的干预措施才显示出改善MS抑郁症的功效。抑郁症的综合治疗应包括药物治疗和心理治疗。

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