Daniel David G
Bioniche Development, Inc., McLean, Va 22106-6207, USA.
J Clin Psychiatry. 2003;64 Suppl 19:40-9.
Although atypical antipsychotic agents have improved the management of patients with schizophrenia, their utility has been hindered by some limitations, including significant weight gain, glucose metabolism disturbances, and increases in total and low-density lipoprotein cholesterol and triglyceride levels. In addition to its low liability for movement disorders and its favorable tolerability record in short- and long-term clinical trials, ziprasidone is associated with a favorable metabolic safety profile (in terms of its effect on plasma lipid and glucose levels) and a negligible effect on weight. The limited effect of ziprasidone on the corrected QT interval (QTc) has also been well characterized, and experience to date has not demonstrated any increased risk of clinical events attributable to QTc prolongation. This review of pharmacokinetic and clinical trials of ziprasidone versus placebo and active comparators focuses on the safety and tolerability of both the intramuscular and oral formulations.
尽管非典型抗精神病药物改善了精神分裂症患者的治疗,但它们的效用受到一些限制,包括显著的体重增加、糖代谢紊乱以及总胆固醇、低密度脂蛋白胆固醇和甘油三酯水平升高。齐拉西酮除了导致运动障碍的可能性较低,以及在短期和长期临床试验中具有良好的耐受性记录外,还具有良好的代谢安全性(就其对血浆脂质和葡萄糖水平的影响而言),且对体重的影响可忽略不计。齐拉西酮对校正QT间期(QTc)的影响有限也已得到充分证实,迄今为止的经验并未表明因QTc延长导致临床事件的风险增加。本对齐拉西酮与安慰剂及活性对照药的药代动力学和临床试验的综述聚焦于肌肉注射和口服制剂的安全性和耐受性。