The Zucker Hillside Hospital, North Shore-Long Island Jewish Health System, Glen Oaks, NY, USA.
Neuropsychopharmacology. 2011 Jul;36(8):1738-46. doi: 10.1038/npp.2011.55. Epub 2011 Apr 20.
Tardive dyskinesia (TD) rates with second-generation antipsychotics (SGAs) are considered to be low relative to first-generation antipsychotics (FGAs), even in the particularly vulnerable elderly population. However, risk estimates are unavailable for patients naïve to FGAs. Therefore, we aimed to determine the TD incidence in particularly vulnerable, antipsychotic-naïve elderly patients treated with the SGA risperidone or olanzapine. The present work describes a prospective inception cohort study of antipsychotic-naïve elderly patients aged 55 years identified at New York Metropolitan area in-patient and out-patient geriatric psychiatry facilities and nursing homes at the time of risperidone or olanzapine initiation. At baseline, 4 weeks, and at quarterly periods, patients underwent assessments of medical and medication history, abnormal involuntary movements, and extra-pyramidal signs. TD was classified using Schooler-Kane criteria. Included in the analyses were 207 subjects (age: 79.8 years, 70.0% female, 86.5% White), predominantly diagnosed with dementia (58.9%) or a major mood disorder (30.9%), although the principal treatment target was psychosis (78.7%), with (59.4%) or without (19.3%) agitation. With risperidone (n=159) the cumulative TD rate was 5.3% (95% confidence interval (CI): 0.7, 9.9%) after 1 year (mean dose: 1.0±0.76 mg/day) and 7.2% (CI: 1.4, 12.9%) after 2 years. With olanzapine (n=48) the cumulative TD rate was 6.7% (CI: 0, 15.6%) after 1 year (mean dose: 4.3±1.9 mg/day) and 11.1% (CI: 0, 23.1%) after 2 years. TD risk was higher in females, African Americans, and patients without past antidepressant treatment or with FGA co-treatment. The TD rates for geriatric patients treated with risperidone and olanzapine were comparable and substantially lower than previously reported for similar patients in direct observation studies using FGAs. This information is relevant for all patients receiving antipsychotics, not just the especially sensitive elderly.
迟发性运动障碍 (TD) 在第二代抗精神病药物 (SGAs) 中的发生率被认为低于第一代抗精神病药物 (FGAs),即使在特别脆弱的老年人群中也是如此。然而,对于从未使用过 FGAs 的患者,风险估计是不可用的。因此,我们旨在确定 SGA 利培酮或奥氮平治疗的特别脆弱、抗精神病药物初治的老年患者中 TD 的发病率。本工作描述了一项前瞻性发病队列研究,纳入了在纽约都会区住院和门诊老年精神病学设施和疗养院初诊为 55 岁以上的抗精神病药物初治老年患者。在基线、4 周和每季度时,患者接受了医学和药物史、异常不自主运动和锥体外系体征的评估。TD 使用 Schooler-Kane 标准进行分类。纳入分析的有 207 例患者(年龄:79.8 岁,70.0%为女性,86.5%为白人),主要诊断为痴呆症(58.9%)或主要心境障碍(30.9%),尽管主要治疗目标是精神病(78.7%),伴有(59.4%)或不伴有(19.3%)激越。使用利培酮(n=159)的 1 年累积 TD 发生率为 5.3%(95%置信区间 (CI):0.7,9.9%)(平均剂量:1.0±0.76mg/天),2 年累积 TD 发生率为 7.2%(CI:1.4,12.9%)。使用奥氮平(n=48)的 1 年累积 TD 发生率为 6.7%(CI:0,15.6%)(平均剂量:4.3±1.9mg/天),2 年累积 TD 发生率为 11.1%(CI:0,23.1%)。女性、非裔美国人、没有既往抗抑郁治疗或使用 FGAs 联合治疗的患者 TD 风险更高。接受利培酮和奥氮平治疗的老年患者的 TD 发生率与之前使用 FGAs 的直接观察研究中类似患者的报告相比相当,且明显更低。这些信息与所有接受抗精神病药物治疗的患者相关,而不仅仅是特别敏感的老年人。