Jung Hee-Yeon, Kim Jong-Hoon, Ahn Yong-Min, Kim Seong-Chan, Hwang Samuel S, Kim Yong-Sik
Department of Psychiatry, Seoul National University College of Medicine, Seoul, Korea.
Hum Psychopharmacol. 2005 Jan;20(1):41-5. doi: 10.1002/hup.655.
The Liverpool University Neuroleptic Side-Effect Rating Scale (LUNSERS) was examined for its usefulness as a subjective measure of drug-induced parkinsonism and akathisia. Eighty-three subjects were assessed using the LUNSERS, the Simpson-Angus Scale (SAS) and the Barnes Akathisia Rating Scale (BARS), before and after a 6-week treatment with olanzapine. Significant correlations were found between the changes in scores of parkinsonism items of LUNSERS and SAS. The changes in scores of akathisia item (restlessness), extrapyramidal side effects (EPS) subscale and psychic side-effects subscale of LUNSERS were significantly correlated with those of the BARS. 'Shakiness', one item of the EPS subscale of LUNSERS, correctly classified between parkinsonism and non-parkinsonism groups with 81.0% accuracy. A combination of four items included in EPS and psychic side-effect subscales of LUNSERS identified akathisia and non-akathisia groups with 76.2% accuracy. These results suggest that the EPS and psychic side-effect subscales of LUNSERS may be useful in screening for drug-induced parkinsonism and akathisia.
对利物浦大学抗精神病药物副作用评定量表(LUNSERS)作为药物性帕金森症和静坐不能主观测量方法的实用性进行了研究。在使用奥氮平进行为期6周的治疗前后,对83名受试者使用LUNSERS、辛普森-安格斯量表(SAS)和巴恩斯静坐不能评定量表(BARS)进行了评估。发现LUNSERS帕金森症项目得分变化与SAS得分变化之间存在显著相关性。LUNSERS静坐不能项目(坐立不安)、锥体外系副作用(EPS)子量表和精神副作用子量表的得分变化与BARS的得分变化显著相关。LUNSERS的EPS子量表中的一个项目“震颤”在帕金森症组和非帕金森症组之间的正确分类准确率为81.0%。LUNSERS的EPS和精神副作用子量表中包含的四个项目的组合在识别静坐不能组和非静坐不能组方面的准确率为76.2%。这些结果表明,LUNSERS的EPS和精神副作用子量表可能有助于筛查药物性帕金森症和静坐不能。