Poyurovsky Michael, Bergman Josef, Pashinian Artashez, Weizman Abraham
aTirat Carmel Mental Health Center, Tirat Carmel bRappaport Faculty of Medicine, Technion, Israel Institute of Technology, Haifa cGeha Mental Health Center and Felsenstein Medical Research Institute, Petah Tiqva dSackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Int Clin Psychopharmacol. 2014 Sep;29(5):296-8. doi: 10.1097/YIC.0000000000000035.
Low-dose mirtazapine was found to be efficacious for neuroleptic-induced akathisia. We evaluated whether mirtazapine is also effective for akathisia induced by the partial dopamine D2 receptor agonist aripiprazole. Medical charts were retrospectively analyzed for eight patients who developed akathisia while being treated with aripiprazole. All scored at least 2 (mild akathisia) on the Barnes Akathisia Rating Scale (BARS) and were treated with mirtazapine (15 mg/day) for a mean of 8.5 days. There was a statistically significant reduction in the BARS subjective, distress, and global (P<0.01 to P<0.001), but not objective (P=0.21) subscales. Five (62.5%) patients fulfilled the criteria of response, a decrease of at least two points on the BARS global subscale. Low-dose mirtazapine was well tolerated, and mild sedation, the only side effect (three patients), was transient. A large-scale controlled investigation is warranted to substantiate clinical utility of mirtazapine for akathisia induced by aripiprazole and other second-generation antipsychotics.
低剂量米氮平被发现对抗精神病药物所致静坐不能有效。我们评估了米氮平对部分多巴胺D2受体激动剂阿立哌唑所致静坐不能是否也有效。对8例在接受阿立哌唑治疗时出现静坐不能的患者的病历进行了回顾性分析。所有患者在巴恩斯静坐不能评定量表(BARS)上的得分至少为2分(轻度静坐不能),并接受米氮平(15毫克/天)治疗,平均治疗8.5天。BARS主观、痛苦和总体量表得分有统计学显著降低(P<0.01至P<0.001),但客观量表得分无显著降低(P=0.21)。5例(62.5%)患者达到反应标准,即BARS总体量表得分至少降低2分。低剂量米氮平耐受性良好,唯一的副作用(3例患者)为轻度镇静,且为一过性。有必要进行大规模对照研究,以证实米氮平对阿立哌唑及其他第二代抗精神病药物所致静坐不能的临床效用。