Vieta Eduard, Goikolea José M, Olivares José M, González-Pinto Ana, Rodriguez Alfonso, Colom Francesc, Comes Mercè, Torrent Carla, Sánchez-Moreno José
Bipolar Disorders Program, Hospital Clinic, University of Barcelona, Institut d'Investigacions Biomediques Agusti Pi Sunyer, Barcelona, Spain.
J Clin Psychiatry. 2003 Jul;64(7):834-9. doi: 10.4088/jcp.v64n0715.
The safety and efficacy of the combination of risperidone and topiramate in the long-term treatment of mania were assessed in a 12-month, multicenter open study.
Subjects (N = 58) who met DSM-IV criteria for bipolar disorder and for a manic episode received both risperidone and topiramate for the treatment of their manic symptoms. Patients with mixed episodes were excluded. Risperidone could be discontinued at any point, but patients had to be on topiramate therapy for at least 12 months to be considered completers. Efficacy was assessed with the Young Mania Rating Scale (YMRS) and a modified version of the Clinical Global Impressions for Bipolar Disorder (CGI-BP-M). Safety was assessed with systematic collection of side effect data, weight, and the Hamilton Rating Scale for Depression (HAM-D) scores, to address the risk of switch into depression.
41 patients (70.7%) completed the study. There was a significant improvement on the YMRS (p <.001) and the CGI-BP-M subscales for manic symptoms (p <.005) and long-term outcome (p <.005) from week 2 onward. Relapse rates were significantly lower during the 12-month study period compared to the precedent year (p <.0001). There was no increase in depressive symptoms as measured by the HAM-D. 37 patients (63.8 %) experienced at least 1 adverse event, the most frequent of which was somnolence (N = 7, 12.1%). At endpoint, the patients' mean weight had decreased an average of 1.1 +/- 0.4 kg.
Despite the limitations inherent to the open design, this naturalistic study suggests that the combination of risperidone and topiramate may be a valuable option for the short- and long-term treatment of mania.
在一项为期12个月的多中心开放性研究中,评估了利培酮与托吡酯联合用于躁狂症长期治疗的安全性和有效性。
符合双相情感障碍和躁狂发作DSM-IV标准的受试者(N = 58)接受利培酮和托吡酯治疗其躁狂症状。排除混合发作的患者。利培酮可在任何时间停用,但患者必须接受托吡酯治疗至少12个月才能被视为完成治疗。使用杨氏躁狂评定量表(YMRS)和双相情感障碍临床总体印象修改版(CGI-BP-M)评估疗效。通过系统收集副作用数据、体重和汉密尔顿抑郁评定量表(HAM-D)评分来评估安全性,以解决转为抑郁的风险。
41名患者(70.7%)完成了研究。从第2周起,YMRS(p <.001)以及CGI-BP-M中躁狂症状(p <.005)和长期结局(p <.005)的分量表均有显著改善。与前一年相比,12个月研究期间的复发率显著降低(p <.0001)。HAM-D测量的抑郁症状没有增加。37名患者(63.8%)经历了至少1次不良事件,最常见的是嗜睡(N = 7,12.1%)。在研究终点,患者的平均体重平均下降了1.1 +/- 0.4千克。
尽管开放性设计存在固有局限性,但这项观察性研究表明,利培酮与托吡酯联合使用可能是躁狂症短期和长期治疗的一个有价值的选择。