Department of Psychiatry, Yeouido St. Mary's Hospital, The Catholic University of Korea College of Medicine, Seoul, Korea.
Psychiatry Investig. 2011 Sep;8(3):207-13. doi: 10.4306/pi.2011.8.3.207. Epub 2011 Aug 2.
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.
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.
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.
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.
本研究旨在探讨齐拉西酮联合丙戊酸钠治疗对韩国急性双相躁狂或混合发作患者的疗效和耐受性,分析齐拉西酮起始剂量与治疗效果的关系。
本研究为为期 6 周的开放性、前瞻性研究,纳入韩国急性躁狂或混合发作的双相障碍患者 65 例。根据齐拉西酮的起始剂量分为低剂量组(20-79mg/d)和标准剂量组(80mg/d)。根据临床反应和耐受性,齐拉西酮与丙戊酸钠联合使用,剂量灵活。
标准剂量组的应答率和缓解率均显著高于低剂量组。齐拉西酮联合丙戊酸钠的耐受性良好,不良反应大多为轻度,体重无统计学意义的增加。
本研究结果表明,齐拉西酮联合丙戊酸钠治疗双相障碍时,起始剂量为标准剂量优于低剂量。