Bowden Charles L, Calabrese Joseph R, Sachs Gary, Yatham Lakshmi N, Asghar Shaheen Akthar, Hompland Magne, Montgomery Paul, Earl Nancy, Smoot Tonya M, DeVeaugh-Geiss Joseph
Department of Psychiatry, University of Texas Health Science Center at San Antonio, 78229, USA.
Arch Gen Psychiatry. 2003 Apr;60(4):392-400. doi: 10.1001/archpsyc.60.4.392.
Lamotrigine has been shown to be an effective treatment for bipolar depression and rapid cycling in placebo-controlled clinical trials. This double-blind, placebo-controlled study was conducted to assess the efficacy and tolerability of lamotrigine and lithium compared with placebo for the prevention of relapse or recurrence of mood episodes in recently manic or hypomanic patients with bipolar I disorder.
After an 8- to 16-week open-label phase during which treatment with lamotrigine was initiated and other psychotropic drug regimens were discontinued, patients were randomized to lamotrigine (100-400 mg daily), lithium (0.8-1.1 mEq/L), or placebo as double-blind maintenance treatment for as long as 18 months.
Of 349 patients who met screening criteria and entered the open-label phase, 175 met stabilization criteria and were randomized to double-blind maintenance treatment (lamotrigine, 59 patients; lithium, 46 patients; and placebo, 70 patients). Both lamotrigine and lithium were superior to placebo at prolonging the time to intervention for any mood episode (lamotrigine vs placebo, P =.02; lithium vs placebo, P =.006). Lamotrigine was superior to placebo at prolonging the time to a depressive episode (P =.02). Lithium was superior to placebo at prolonging the time to a manic, hypomanic, or mixed episode (P =.006). The most common adverse event reported for lamotrigine was headache.
Both lamotrigine and lithium were superior to placebo for the prevention of relapse or recurrence of mood episodes in patients with bipolar I disorder who had recently experienced a manic or hypomanic episode. The results indicate that lamotrigine is an effective, well-tolerated maintenance treatment for bipolar disorder, particularly for prophylaxis of depression.
在安慰剂对照的临床试验中,拉莫三嗪已被证明是治疗双相抑郁症和快速循环的有效药物。本双盲、安慰剂对照研究旨在评估拉莫三嗪和锂盐与安慰剂相比,在预防近期有躁狂或轻躁狂发作的I型双相情感障碍患者情绪发作复发方面的疗效和耐受性。
在为期8至16周的开放标签阶段,启动拉莫三嗪治疗并停用其他精神药物治疗方案,之后患者被随机分配接受拉莫三嗪(每日100 - 400毫克)、锂盐(0.8 - 1.1毫当量/升)或安慰剂作为双盲维持治疗,为期长达18个月。
在349名符合筛查标准并进入开放标签阶段的患者中,175名符合稳定标准并被随机分配接受双盲维持治疗(拉莫三嗪组59例;锂盐组46例;安慰剂组70例)。拉莫三嗪和锂盐在延长任何情绪发作的干预时间方面均优于安慰剂(拉莫三嗪与安慰剂相比,P = 0.02;锂盐与安慰剂相比,P = 0.006)。拉莫三嗪在延长抑郁发作时间方面优于安慰剂(P = 0.02)。锂盐在延长躁狂、轻躁狂或混合发作时间方面优于安慰剂(P = 0.006)。报告的拉莫三嗪最常见不良事件为头痛。
拉莫三嗪和锂盐在预防近期有躁狂或轻躁狂发作的I型双相情感障碍患者情绪发作复发方面均优于安慰剂。结果表明,拉莫三嗪是双相情感障碍一种有效且耐受性良好的维持治疗药物,尤其用于预防抑郁症。