Soutullo Cesar A, Díez-Suárez Azucena, Figueroa-Quintana Ana
Child and Adolescent Psychiatry Unit, Department of Psychiatry and Medical Psychology, Clínica Universitaria, University of Navarra, 31008-Pamplona, Spain.
J Child Adolesc Psychopharmacol. 2006 Jun;16(3):357-64. doi: 10.1089/cap.2006.16.357.
Our aim was to evaluate the effectiveness, safety, and tolerability of adjunctive lamotrigine in the treatment of adolescents with bipolar disorder.
We evaluated all patients under age 18 with Diagnostic and Statistical Manual of Mental Disorders, fourth edition, text revision (DSM-IV-TR) bipolar disorder in our outpatient clinic treated with lamotrigine, using the Clinical Global Impression (CGI) scale. We rated response with the CGI-Improvement (CGI-I) scale.
Five patients (mean age = 15.5 +/- 1.8 years; range = 14-17), 1 male and 4 females, were included. One patient (20%) had bipolar I disorder, 1 (20%) had bipolar II disorder, and 3 (60%) had bipolar disorder not otherwise specified (NOS). The polarity of the episode at baseline was depressive in all patients. The mean lamotrigine dose was 100 +/- 87.5 mg/day (1.67 +/- 1.39 mg/kg/day). The mean duration of treatment was 28 +/- 28 weeks. CGI significantly improved from 5 at baseline to 3 +/- 1 at endpoint (p = 0.011). Improvement was marked or moderate in 4 patients (80%) and minimal in 1 patient (20%). One patient referred to dizziness, and there were no reports of increased cycling, worsening of mania, or skin rash.
This open, retrospective chart review suggests that lamotrigine may be effective and well tolerated as an adjunctive treatment in adolescents with bipolar disorder. Controlled trials are needed.
我们的目的是评估辅助使用拉莫三嗪治疗双相情感障碍青少年的有效性、安全性和耐受性。
我们使用临床总体印象(CGI)量表,对在我们门诊接受拉莫三嗪治疗的所有18岁以下、符合《精神疾病诊断与统计手册》第四版修订版(DSM-IV-TR)双相情感障碍诊断标准的患者进行了评估。我们使用CGI改善(CGI-I)量表对疗效进行评分。
纳入了5名患者(平均年龄 = 15.5 ± 1.8岁;范围 = 14 - 17岁),1名男性和4名女性。1名患者(20%)患有双相I型障碍,1名(20%)患有双相II型障碍,3名(60%)患有未特定指明的双相情感障碍(NOS)。所有患者基线时发作的极性均为抑郁。拉莫三嗪的平均剂量为100 ± 87.5毫克/天(1.67 ± 1.39毫克/千克/天)。平均治疗持续时间为28 ± 28周。CGI评分从基线时的5分显著改善至终点时的3 ± 1分(p = 0.011)。4名患者(80%)改善显著或中等,1名患者(20%)改善轻微。1名患者出现头晕,未报告有发作频率增加、躁狂加重或皮疹的情况。
这项开放性回顾性病历审查表明,拉莫三嗪作为双相情感障碍青少年的辅助治疗可能有效且耐受性良好。需要进行对照试验。