Jaskiw George E, Thyrum Per T, Fuller Matthew A, Arvanitis Lisa A, Yeh Chiao
Psychiatry Service 116A(B), Louis Stokes Cleveland V.A. Medical Center, 10000 Brecksville Road, Brecksville, OH 44141, USA.
Clin Pharmacokinet. 2004;43(14):1025-35. doi: 10.2165/00003088-200443140-00005.
To assess the pharmacokinetics and tolerability of quetiapine in elderly patients with selected psychotic disorders.
This was a multicentre, open-label, 27-day, rising multiple-dose trial. Descriptive statistics summarised plasma quetiapine concentrations and pharmacokinetic parameters by trial day. A two-way analysis of variance was used to evaluate all pharmacokinetic parameters, and 90% confidence intervals of the mean differences were calculated.
Antipsychotic drugs taken prior to the study period were discontinued on day 1. Quetiapine treatment began on day 3. Doses were increased stepwise, starting at 25mg three times daily and reaching 250mg three times daily by day 21.
Twelve patients (age 63-85 years) with schizophrenia, schizoaffective disorder or bipolar disorder.
Key assessments included quetiapine plasma concentrations, and neurological and safety evaluations. Under steady-state conditions, the 100 and 250mg doses of quetiapine were not significantly different in terms of dose-normalised area under the plasma concentration-time curve within an 8-hour dose administration interval, or in dose-normalised minimum plasma concentration (C(min)) at the end of a dose administration interval. The morning C(min) values for the seven discrete dose amounts evaluated also increased linearly with dose. The apparent oral clearance, volume of distribution and half-life did not change as a function of dose. There were no serious adverse events. The most common adverse events were postural hypotension (n = 6), dizziness (n = 5) and somnolence (n = 4).
While quetiapine was well tolerated at doses up to 250mg three times daily, the potential for reduced clearance, as well as the adverse effects of postural hypotension and dizziness, indicated that quetiapine should be introduced at lower doses and titrated at a relatively slower rate in patients > or =65 years.
评估喹硫平在患有特定精神障碍的老年患者中的药代动力学及耐受性。
这是一项多中心、开放标签、为期27天的递增多剂量试验。描述性统计按试验日总结血浆喹硫平浓度及药代动力学参数。采用双向方差分析评估所有药代动力学参数,并计算平均差异的90%置信区间。
研究期前服用的抗精神病药物在第1天停用。喹硫平治疗于第3天开始。剂量逐步增加,从每日三次25mg开始,至第21天达到每日三次250mg。
12例年龄在63 - 85岁之间的精神分裂症、分裂情感性障碍或双相情感障碍患者。
主要评估包括喹硫平血浆浓度、神经学及安全性评估。在稳态条件下,100mg和250mg剂量的喹硫平在8小时给药间隔内的剂量标准化血浆浓度 - 时间曲线下面积,或给药间隔结束时的剂量标准化最低血浆浓度(C(min))方面无显著差异。所评估的七个离散剂量的早晨C(min)值也随剂量呈线性增加。表观口服清除率、分布容积和半衰期不随剂量变化。无严重不良事件。最常见的不良事件为体位性低血压(n = 6)、头晕(n = 5)和嗜睡(n = 4)。
虽然喹硫平在每日三次高达250mg的剂量下耐受性良好,但清除率降低的可能性以及体位性低血压和头晕的不良反应表明,对于≥65岁的患者,应采用较低剂量起始并以相对较慢的速率滴定喹硫平。