Toenniessen L M, Casey D E, McFarland B H
Arch Gen Psychiatry. 1985 Mar;42(3):278-84. doi: 10.1001/archpsyc.1985.01790260072009.
Although tardive dyskinesia (TD) is recognized to result from neuroleptic drug exposure, data conflict about the importance of the quantity of that exposure in producing TD. The relationship between duration of neuroleptic treatment (one to 301 months) and TD was studied in 57 elderly psychiatric inpatients. Examinations for TD and parkinsonism were quantified on the Abnormal Involuntary Movement Scale (AIMS) and on a parkinsonism severity scale. Prevalence of presumed TD was 49% and of parkinsonism 51%. Prevalence of TD increased with longer treatment, but parkinsonism was independent of treatment duration. Linear multiple regression analysis showed that the AIMS score was correlated positively with treatment duration and negatively with parkinsonism. Logistic multiple regression analysis verified these relationships and was more successful at predicting TD. The length of neuroleptic treatment necessary to produce TD was calculated from the logistic model at 10.8 months (95% confidence interval, zero to 25.6 months). These analyses showed the greatest rise in risk of TD occurred within the first two years of drug therapy.
虽然迟发性运动障碍(TD)被认为是由抗精神病药物暴露所致,但关于该暴露量在引发TD中的重要性,数据存在冲突。对57名老年精神科住院患者研究了抗精神病药物治疗时长(1至301个月)与TD之间的关系。依据异常不自主运动量表(AIMS)和帕金森症严重程度量表对TD和帕金森症进行量化检查。疑似TD的患病率为49%,帕金森症的患病率为51%。TD的患病率随治疗时间延长而增加,但帕金森症与治疗时长无关。线性多元回归分析表明,AIMS评分与治疗时长呈正相关,与帕金森症呈负相关。逻辑多元回归分析证实了这些关系,且在预测TD方面更为成功。根据逻辑模型计算得出,引发TD所需的抗精神病药物治疗时长为10.8个月(95%置信区间,0至25.6个月)。这些分析表明,药物治疗的头两年内,TD风险上升幅度最大。