Keating Anne M, Aoun Suzanne L, Dean Charles E
University of Minnesota School of Medicine, Minneapolis, USA.
Clin Neuropharmacol. 2005 Mar-Apr;28(2):83-6. doi: 10.1097/01.wnf.0000159952.64640.28.
Although mania was not reported as an adverse event in the pivotal trials of ziprasidone, there have been 7 reports of ziprasidone-induced mania in 12 patients. We now report 2 additional cases wherein the introduction of ziprasidone resulted in new-onset manic episodes. In 1 case, the patient required hospitalization and lost his job. In the other, time to mania was 5 months, considerably longer than previously reported. Of the 14 cases, 9 were in a depressive episode when ziprasidone was prescribed, and 8 had a history of current or past exposure to antidepressants. Ziprasidone, like many antidepressants, can block reuptake of norepinephrine and serotonin, although mania has developed in patients treated with atypical antipsychotics that are less potent in this regard. However, ziprasidone and other atypical antipsychotics have in common a high ratio of 5-HT2a to D2 receptor blockade, which may also play a role in this phenomenon. Clinicians and patients need to be aware of the potential for the induction of mania with ziprasidone, even after lengthy exposure.
尽管在齐拉西酮的关键试验中未将躁狂报告为不良事件,但已有12例患者出现7例齐拉西酮诱发躁狂的报告。我们现在报告另外2例病例,其中齐拉西酮的使用导致新发躁狂发作。在1例病例中,患者需要住院治疗并失去了工作。在另一例中,出现躁狂的时间为5个月,比之前报告的时间长得多。在这14例病例中,9例在开具齐拉西酮处方时处于抑郁发作期,8例有当前或过去使用抗抑郁药的病史。与许多抗抑郁药一样,齐拉西酮可阻断去甲肾上腺素和5-羟色胺的再摄取,尽管在这方面作用较弱的非典型抗精神病药治疗的患者也出现了躁狂。然而,齐拉西酮和其他非典型抗精神病药的共同之处在于5-HT2a与D2受体阻断的比例较高,这也可能在这一现象中起作用。临床医生和患者需要意识到,即使长期使用齐拉西酮也有诱发躁狂的可能性。