Brar Jaspreet S, Parepally Haranath, Chalasani Lokaranjit, Gopalani Aziz, Appel Nicole, Chengappa K N Roy
School of Medicine, Western Psychiatric Institute & Clinic and University of Pittsburgh, Pittsburgh, Pennsylvania 15213, USA.
Ann Clin Psychiatry. 2008 Jul-Sep;20(3):139-44. doi: 10.1080/10401230802177755.
Tardive dyskinesia is a serious adverse event, which is associated mainly with the use of the first-generation antipsychotic agents. Convergent data from clinical trials suggest that second-generation antipsychotic agents are less likely to cause tardive dyskinesia. However, the data with regard to the effect of switching from first- to second-generation antipsychotic agents on pre-existing dyskinetic symptoms during routine clinical care is sparse.
Sixty-three patients with DSM-IV schizophrenia or schizoaffective disorder (n = 61) or bipolar I disorder (n = 2) consecutively admitted to a state hospital, who were treated either with olanzapine (n = 35) or conventional antipsychotic agents (n = 28) by physician choice, were enrolled in the study. The severity and frequency of tardive dyskinetic symptoms using the Abnormal Involuntary Movement Scale were assessed in the two medication groups at baseline, 8 weeks, and 6 months.
There were statistically significant reductions in the prevalence and severity of dyskinetic symptoms at 8 weeks and 6 months for the group treated with olanzapine but not for those treated with conventional agents.
These preliminary data suggest that olanzapine may be a treatment option for subjects with tardive dyskinesia. However, the question whether olanzapine treats, ameliorates, or masks preexisting tardive dyskinesia was difficult to answer, as no dosage reduction or withdrawal was undertaken.
迟发性运动障碍是一种严重的不良事件,主要与第一代抗精神病药物的使用有关。临床试验的汇总数据表明,第二代抗精神病药物引发迟发性运动障碍的可能性较小。然而,在常规临床护理中,关于从第一代抗精神病药物转换为第二代抗精神病药物对既往运动障碍症状影响的数据却很稀少。
连续入住一家国立医院的63例患有DSM-IV精神分裂症或分裂情感性障碍(n = 61)或双相I型障碍(n = 2)的患者参与了该研究,这些患者根据医生的选择分别接受奥氮平治疗(n = 35)或传统抗精神病药物治疗(n = 28)。在基线、8周和6个月时,使用异常不自主运动量表评估两个药物治疗组中迟发性运动障碍症状的严重程度和频率。
接受奥氮平治疗的组在8周和6个月时,运动障碍症状的患病率和严重程度有统计学意义的降低,而接受传统药物治疗的组则没有。
这些初步数据表明,奥氮平可能是迟发性运动障碍患者的一种治疗选择。然而,由于未进行剂量减少或停药,奥氮平是治疗、改善还是掩盖既往存在的迟发性运动障碍这一问题难以回答。