Marras Connie, Herrmann Nathan, Anderson Geoffrey M, Fischer Hadas D, Wang Xuesong, Rochon Paula A
Morton and Gloria Shulman Movement Disorders Centre, Toronto Western Hospital, Toronto, Ontario, Canada.
Am J Geriatr Pharmacother. 2012 Dec;10(6):381-9. doi: 10.1016/j.amjopharm.2012.11.001.
Differences between atypical antipsychotics in their potential to cause parkinsonism and risk factors for antipsychotic-induced parkinsonism are not well established. There is a particular paucity of information on this in real-world use of these drugs, outside of clinical trial settings.
We compared the incidence of parkinsonism after new treatment with risperidone, olanzapine, or quetiapine in patients with dementia and examined the effects of dose and sex on the risk of parkinsonism.
Administrative data from Ontario, Canada between 2002 and 2010 were used to compare the incidence of a diagnostic code for parkinsonism or prescription of an anti-Parkinson medication among patients with dementia who were newly prescribed quetiapine, olanzapine, or risperidone.
From 15,939 person-years of observation, 421 patients developed parkinsonism. Using low-dose risperidone as the reference group, the adjusted hazard ratios for developing parkinsonism were 0.49 (95% CI, 0.07-3.53) for low-dose olanzapine and 1.18 (95% CI, 0.84-1.66) for low-dose quetiapine. Comparing across drugs within the most commonly prescribed dose ranges, the incidence of parkinsonism was higher in the medium-dose olanzapine group compared with the low-dose risperidone group (hazard ratio 1.66; 95% CI 23-2.23). The adjusted hazard ratio for developing parkinsonism for men (compared with women) was 2.29 (95% CI, 1.88- 2.79).
We found no evidence that the risk of drug-induced parkinsonism in older adults with dementia was different among quetiapine, olanzapine, or risperidone, challenging the notion that the drugs differed in their propensity to cause parkinsonism. Men appeared to be at higher risk of parkinsonism as a adverse event than women.
非典型抗精神病药物在引发帕金森症方面的差异以及抗精神病药物所致帕金森症的风险因素尚未完全明确。在临床试验环境之外,这些药物在实际应用中的相关信息尤为匮乏。
我们比较了使用利培酮、奥氮平或喹硫平对痴呆患者进行新治疗后帕金森症的发生率,并研究了剂量和性别对帕金森症风险的影响。
利用加拿大安大略省2002年至2010年的管理数据,比较新开具喹硫平、奥氮平或利培酮的痴呆患者中帕金森症诊断代码或抗帕金森药物处方的发生率。
在15939人年的观察期内,421例患者出现帕金森症。以低剂量利培酮作为参照组,低剂量奥氮平发生帕金森症的校正风险比为0.49(95%可信区间,0.07 - 3.53),低剂量喹硫平为1.18(95%可信区间,0.84 - 1.66)。在最常用剂量范围内比较不同药物,中剂量奥氮平组帕金森症的发生率高于低剂量利培酮组(风险比1.66;95%可信区间23 - 2.23)。男性(与女性相比)发生帕金森症的校正风险比为2.29(95%可信区间,1.88 - 2.79)。
我们没有发现证据表明喹硫平、奥氮平或利培酮在老年痴呆患者中诱发药物性帕金森症的风险存在差异,这对这些药物在引发帕金森症倾向方面存在差异的观点提出了挑战。男性作为不良事件发生帕金森症的风险似乎高于女性。