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阿立哌唑合并5-羟色胺再摄取抑制剂与氯米帕明治疗5-羟色胺再摄取抑制剂无效强迫障碍的临床对照研究 被引量:2

A controlled clinical study of aripiprazole combined with SSRIs vs.chlorimi-pramine in treatment of SSRIs refractory obsessive-compulsive disorder
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摘要 目的探索5-羟色胺再摄取抑制剂(SSRIs)治疗无效的强迫障碍的治疗方案。方法将73例强迫障碍患者随机分为3组:(1)增效剂组26例,在原用SSRIs药物剂量不变的基础上加用阿立哌唑治疗,起始量为5 mg·d^(-1),最大剂量不超过20 mg·d^(-1);(2)换药组24例,停用SSRIs药,换为氯米帕明单药治疗,初始剂量50~75 mg·d^(-1),逐渐增加至150~225 mg·d^(-1);(3)对照组23例,继续使用原SSRIs药单药治疗。疗程均为12 wk。用Yale-Brown强迫量表(Y-BOCS)、大体评定量表(GAS)评定疗效,并观察不良反应。结果治疗wk 8、wk 12末增效剂组和换药组Y-BOCS、Y-BOCS强迫思维、Y-BOCS强迫行为和GAS评分均无显著差异(P>0.05)。治疗wk 12末,增效剂组4项评分均与对照组有非常显著差异(P<0.01),换药组除Y-BOCS强迫思维外其余3项评分与对照组比较均有显著差异(P<0.01)。增效剂组、换药组和对照组显效率分别为50%、38%、13%:换药组和增效剂组显效率无显著差异(x^2=0.79,P>0.05),增效剂组和对照组有非常显著差异(x^2=7.58,P<0.01),换药组和对照组相比无显著差异(x^2=3.70,P=0.055)。换药组不良反应发生率和增效剂组相比无显著差异(P>0.05);2组和对照组相比,均有显著差异(P<0.05)。结论对于SSRIs治疗效果不理想的强迫障碍,可使用阿立哌唑增效或换为氯米帕明作为候选的治疗方案,二者疗效和安全性相近。 AIM To explore the treatment (SSRIs) refractory obsessive-compulsive disorder plan in the treatment of selective serotonin reuptake inhibitors METHODS Seventy-three patients with obsessive compulsive disorder were randomly assigned to three groups: (1) augmentation treatment group (n = 26) was treated by aripiprazole based upon preceding SSRIs, with the initial dose 5 mg·d-1 and maximum dose 20 mg·d-1; (2) switch treatment group (n = 24) stopped taking SSRIs with the change of chlorimipramine, from initial dose 50 - 75 mg·d-1 increased up to 150 - 225 mg·d-1 gradually; (3) control group (n = 23) continued the SSRIs monotherapy as before. The treatment course was 12 weeks in all three groups. Yale-Brown Obsessive Compulsive Scale (Y-BOCS) and Global Assessment Scale (GAS) were used to evaluate the therapeutic efficacy, and adverse drug reactions were observed. RESULTS At the end of wk 8 and wk 12 of the treatment, there were no significant differences between the augmentation treatment group and the switch treatment group in scores of the Y-BOCS, Y-BOCS obsessions, Y-BOCS compulsions and GAS (P 〉 0.05). At the end of wk 12, there were significant differences in the four scores between the augmentation treatment group and the control group (P 〈 0.01), and except scores of Y-BOCS obsessions, there were significant differences in other three scores between the switch treatment group and the control group (P 〈 0.01) . The significant improvement rate of the augmentation treatment group, switch treatment group and control group was 50%, 38% and 13% respectively: there were no significant differences between the augmentation treatment group and the switch treatment group or the control group (χ2 = 0.79, P 〉 0.05; χ2 = 3.70, P = 0.055 ). But the differences between the augmentation treatment group and the control group were significant (χ2 = 7.58, P 〈 0.01) . Furthermore, the adverse reaction incidence between the augmentation treatment group and the switch treatment group had no differences (P 〉 0.05), and they both had significant difference compard with the control group (P 〈 0.05). CONCLUSION Aripiprazole augmentation and chlormipramine switch could be the candidate treatment plan in the treatment of SSRIs refractory obsessive-compulsive disorder. The curative effect and the safety were similar in these two plans.
出处 《中国新药与临床杂志》 CAS CSCD 北大核心 2012年第9期553-556,共4页 Chinese Journal of New Drugs and Clinical Remedies
关键词 阿立哌唑 氯米帕明 强迫性障碍 血清素摄取抑制药 临床对照试验 aripiprazole chlorimipramine obsessive-compulsive disorder selective serotonin reuptakeinhibitors controlled clinical trials
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  • 1KARNO M, GOLDING JM, SORENSON SB, et al. The epidemiology of obsessive-compulsive disorder in five US communities [J]. Arch Gen Psychiatry, 1988, 45 (12): 1094- 1099.
  • 2MURRAY CJ, LOPEZ AD. Regional patterns of disability-free life expectancy and disability-adjusted life expectancy: global Burden of Disease Study[J]. Lancet, 1997, 349 (9062) : 1347- 1352.
  • 3BLIER P, HABIB R, FLAMENT MF. Pharmacotherapies in the management of obsessive-compulsive disorder[J]. Can J Psychiatry, 2006, 51(7): 417-430.
  • 4喻东山.强迫症的药物治疗进展[J].中国全科医学,2009,12(8):663-665. 被引量:13
  • 5FINEBERG NA, PAMPALONI I, PALLANTI S, et al. Sustained response versus relapse: the pharmacotherapeutic goal for obsessive-compulsive disorder [J]. Int Clin Psyehopharmacol, 2007, 22(6): 313-322.
  • 6BLOCH MH, LANDEROS-WEISENBERGER A, KELMENDI B, etal. A systematic review: antipsychotic augmentation with treatment refractory obsessive-compulsive disorder[J]. Mol Psy- chiatry, 2006, 11(7): 622-632.
  • 7BOYER WF, FEIGHNER JP. An overview of paroxetine [J]. J Clin Psychiatry, 1992, 53 Suppl: 3-6.
  • 8GOODMAN WK, MCDOUGLE CJ, PRICE LH, et al. Beyond the serotonin hypothesis: A role for dopamine in some forms of obsessive-compulsive disorder? [J]. J Clin Psychiatry, 1990, 51 Suppl: 36-43.
  • 9KAPUR S, REMINGTON G. Serotonin-dopamine interaction and its relevance to schizophrenia [J]. Am J Psychiatry, 1996, 153 (4) : 466-476.
  • 10STEIN DJ. Neurobioloy of the obsessive-compulsive specstrum disorders[J]. Biol Psychiatry, 2000, 47(4) : 296-304.

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