Ziegenbein Marc, Kropp Stefan, Kuenzel Heike E
Department of Social Psychiatry and Psychotherapy, Hanover Medical School (MHH), Hannover, Germany.
Clin Neuropharmacol. 2005 Sep-Oct;28(5):220-4. doi: 10.1097/01.wnf.0000183446.58529.30.
Therapeutic options for patients with treatment-resistant schizophrenia are limited. In such patients, combined application of atypical antipsychotic drugs is an often-used strategy. The authors tested the hypothesis that the combination of ziprasidone and clozapine would lead to an improvement in this patient group.
Nine patients with treatment-resistant schizophrenia participated in this open clinical trial and received a combination regimen of ziprasidone and clozapine. Patients had to have remained on a stable dose of clozapine for at least 6 months to ensure a reasonable opportunity to respond to clozapine monotherapy. Clinical status was evaluated at baseline, and at 3 and 6 months' follow-up using the Brief Psychiatric Rating Scale (BPRS).
All patients completed the 6-month combination treatment. The mental state of 7 patients (77.8%) was improved and there was a significant reduction in the mean BPRS score over the 6 months treatment. The coadministration of ziprasidone in clozapine-treated patients did not result in a corresponding increase in side effects. The combination allowed a 18% reduction of the daily clozapine dose.
The combined application of clozapine and ziprasidone follows a neurobiologic rationale and appears to be safe and well tolerated without increasing the risk of side effects.
难治性精神分裂症患者的治疗选择有限。对于这类患者,联合应用非典型抗精神病药物是常用策略。作者检验了齐拉西酮与氯氮平联合应用会使该患者群体病情改善的假设。
9例难治性精神分裂症患者参与了这项开放性临床试验,并接受了齐拉西酮与氯氮平的联合治疗方案。患者必须已维持氯氮平稳定剂量至少6个月,以确保有合理机会对氯氮平单药治疗产生反应。在基线时以及使用简明精神病评定量表(BPRS)在3个月和6个月随访时评估临床状态。
所有患者均完成了6个月的联合治疗。7例患者(77.8%)的精神状态得到改善,且在6个月的治疗期间BPRS平均得分显著降低。在接受氯氮平治疗的患者中联合使用齐拉西酮并未导致副作用相应增加。联合用药使氯氮平每日剂量减少了18%。
氯氮平与齐拉西酮联合应用符合神经生物学原理,似乎安全且耐受性良好,不会增加副作用风险。