Sachs Gary S, Grossman Fred, Ghaemi S Nassir, Okamoto Akiko, Bowden Charles L
Bipolar Research Program, Department of Psychiatry, Massachusetts General Hospital, 50 Staniford Street, Suite 580, Boston, MA 02114, USA.
Am J Psychiatry. 2002 Jul;159(7):1146-54. doi: 10.1176/appi.ajp.159.7.1146.
The study assessed the efficacy and safety of risperidone as an adjunctive agent to mood stabilizers in the treatment of acute mania.
This 3-week randomized, double-blind, placebo-controlled study included 156 bipolar disorder patients with a current manic or mixed episode who received a mood stabilizer (lithium or divalproex) and placebo, risperidone, or haloperidol. The primary efficacy measure was the Young Mania Rating Scale. Other assessments used the Brief Psychiatric Rating Scale, the Clinical Global Impression scale, and safety measures.
The trial was discontinued by 25 (49%) of the 51 placebo group patients, 18 (35%) of the 52 risperidone group patients, and 28 (53%) of the 53 haloperidol group patients. Mean modal doses were 3.8 mg/day (SD=1.8) of risperidone and 6.2 mg/day (SD=2.9) of haloperidol. Significantly greater reductions in Young Mania Rating Scale scores at endpoint and over time were seen in the risperidone group and in the haloperidol group, compared with the placebo group. Young Mania Rating Scale total scores improved with risperidone and with haloperidol both in patients with psychotic features and in those without psychotic features at baseline. Extrapyramidal Symptom Rating Scale total scores at endpoint were significantly higher in the haloperidol patients than in the placebo patients. Antiparkinsonian medications were received by 8%, 17%, and 38% of patients in the placebo, risperidone, and haloperidol groups, respectively.
Risperidone plus a mood stabilizer was more efficacious than a mood stabilizer alone, and as efficacious as haloperidol plus a mood stabilizer, for the rapid control of manic symptoms and was well tolerated.
本研究评估利培酮作为心境稳定剂辅助药物治疗急性躁狂症的疗效和安全性。
这项为期3周的随机、双盲、安慰剂对照研究纳入了156名双相情感障碍且目前处于躁狂或混合发作的患者,他们接受了一种心境稳定剂(锂盐或丙戊酸)以及安慰剂、利培酮或氟哌啶醇治疗。主要疗效指标为杨氏躁狂评定量表。其他评估采用简明精神病评定量表、临床总体印象量表以及安全性指标。
51名安慰剂组患者中有25名(49%)、52名利培酮组患者中有18名(35%)、53名氟哌啶醇组患者中有28名(53%)中断试验。利培酮的平均模态剂量为3.8毫克/天(标准差=1.8),氟哌啶醇为6.2毫克/天(标准差=2.9)。与安慰剂组相比,利培酮组和氟哌啶醇组在研究终点及整个研究期间杨氏躁狂评定量表评分的降低幅度显著更大。无论基线时有无精神病性特征的患者,利培酮和氟哌啶醇均使杨氏躁狂评定量表总分得到改善。研究终点时,氟哌啶醇组患者的锥体外系症状评定量表总分显著高于安慰剂组患者。安慰剂组、利培酮组和氟哌啶醇组分别有8%、17%和38%的患者接受了抗帕金森药物治疗。
利培酮加心境稳定剂在快速控制躁狂症状方面比单用心境稳定剂更有效,且与氟哌啶醇加心境稳定剂疗效相当,耐受性良好。