The efficacy and tolerability of lamotrigine adjunctive/monotherapy in patients with partial seizures refractory to poly-AEDs

Chunjie Song , Huiling Chen , Xiaoyong Wang , Hui Wang , Qi Wan
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引用次数: 4

Abstract

Objective

This study was designed as an open-label trial to assess the effects of changing the antiepileptic drugs (AEDs) regi- men to lamotrigine (LTG) as adjunctive/monotherapy in patients with partial seizures who were dissatisfied with their drug regimen because of intractable seizures.

Methods

The patients were recruited from multicenters using the following criteria: age⩾18 years; at least 3 seizures per month during the last 16 weeks; previous use of at least 3 AEDs. The study involved a baseline phase and 2 experimental phases: LTG was first added to the regimen, and then patients could gradually change to LTG monotherapy if their seizures were reduced by at least 50 percent/month. Tolerability, the primary end point, was assessed using the Liverpool Adverse Experience Profile (LAEP). Secondary end points included quality of life, as measured with the Quality of Life in Epilepsy-31 inventory. Reductions in seizures from baseline throughout each phase were also analyzed.

Results

One hundred and fourteen patients aged between 18 and 52 years (age 27.8±13.2 years; 71 men and 43 women) were enrolled. After adding LTG, 105 patients (92.11%) completed adjunctive therapy. Upon completion of the adjunctive phase, mean improvement from baseline was 2.6 points on the LAEP (p=0.037). The overall score on the QOLIE-31 improved by 8.49 points from baseline (p=0.023). At the end of the trial, 26 (22.81%) of patients completed LTG monotherapy, and 65 patients (57.02%) experienced at least 50% reduction in seizure frequency compared to baseline, The mean improvement from baseline was 5.1 points on the LAEP (p=0.0059), and the overall score on the QOLIE-31 score improved by 12.72 points from baseline(p=0.0071). Twenty-two (19.30%) patients reported adverse effects and 9 patients discontinued participation in the trial because of adverse effects.

Conclusion

For patients with partial seizures who were dissatisfied with their AED regimen because of intractable seizures, adding LTG to the drug regimen was well tolerated and effective in improving the quality of life and controlling seizures. Furthermore, switching to LTG monotherapy was associated with further improvement.

拉莫三嗪辅助/单药治疗多抗癫痫药难治性部分发作患者的疗效和耐受性
目的:本研究是一项开放标签试验,旨在评估将抗癫痫药物(aed)方案改为拉莫三嗪(LTG)作为辅助/单药治疗因难治性癫痫发作而对其药物方案不满意的部分癫痫发作患者的效果。方法使用以下标准从多中心招募患者:年龄大于或等于18岁;在过去16周内每月至少发作3次;既往使用过至少3种aed。该研究包括基线期和2个实验期:首先将LTG添加到方案中,然后如果患者的癫痫发作减少至少50% /月,患者可以逐渐改为LTG单药治疗。耐受性,主要终点,评估使用利物浦不良经历档案(LAEP)。次要终点包括生活质量,用癫痫-31量表的生活质量来衡量。还分析了每个阶段癫痫发作从基线的减少情况。结果18 ~ 52岁患者114例(年龄27.8±13.2岁;71名男性和43名女性)被纳入研究。添加LTG后,105例患者(92.11%)完成了辅助治疗。辅助期结束后,LAEP平均较基线改善2.6分(p=0.037)。QOLIE-31总分较基线提高8.49分(p=0.023)。试验结束时,26例(22.81%)患者完成LTG单药治疗,65例(57.02%)患者癫痫发作频率较基线降低至少50%,LAEP平均较基线改善5.1分(p=0.0059), QOLIE-31评分总分较基线改善12.72分(p=0.0071)。22例(19.30%)患者报告了不良反应,9例患者因不良反应而停止参与试验。结论对于因难治性癫痫发作而对AED方案不满意的部分癫痫患者,在药物方案基础上加用LTG可改善生活质量,有效控制癫痫发作。此外,切换到LTG单药治疗与进一步改善相关。
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