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Effect of Initial Ziprasidone Dose on Treatment Outcome of Korean Patients with Acute Manic or Mixed Episodes

机译:初始齐普拉西酮剂量对韩国急性躁狂或混合发作患者的治疗效果的影响

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Objective We investigated the efficacy and tolerability of ziprasidone combined with divalproex to determine the relationship between the initial dose of ziprasidone and the treatment effect among Korean patients with acute bipolar manic or mixed disorders. Methods This study was a 6-week, open-label, prospective investigation of Korean patients with an acute manic or mixed episode of bipolar disorder. Sixty-five patients were recruited. The patients were categorized based on the initial dose of ziprasidone as follows: low (20-79 mg/day) and standard (80 mg/day). Ziprasidone was given in combination with divalproex in flexible doses, according to the clinical response and tolerability. Results The response and remission rates were significantly higher in the standard-dose group than the low-dose group. The combination of ziprasidone and divalproex was well-tolerated and adverse events were mostly mild with no statistically significant increase in body weight. Conclusion The results of this study showed that a standard starting dose of ziprasidone in combination with divalproex for bipolar disorder is more effective than a low starting dose.
机译:目的研究齐拉西酮联合divalproex的疗效和耐受性,以确定齐拉西酮的初始剂量与韩国急性双相躁狂躁狂或混合性躁狂症患者的治疗效果之间的关系。方法该研究是对韩国急性躁狂或躁郁症混合发作的韩国患者进行的为期6周,开放标签的前瞻性研究。招募了65名患者。根据齐拉西酮的初始剂量将患者分类如下:低剂量(20-79 mg /天)和标准剂量(80 mg /天)。根据临床反应和耐受性,将齐普拉西酮与双丙戊酸钠联合以灵活剂量服用。结果标准剂量组的反应和缓解率明显高于低剂量组。 ziprasidone和divalproex的组合耐受性良好,不良事件多数为轻度,体重没有统计学上的显着增加。结论这项研究的结果表明,标准的齐拉西酮联合双丙戊酸钠治疗双相情感障碍的起始剂量比低起始剂量更有效。

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