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The Effectiveness of Lamotrigine and Its Blood Levels for Pediatric Epilepsy

机译:乳草嗪及其对儿科癫痫血液水平的有效性

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This study was conducted to evaluate the effectiveness of lamotrigine (LTG) over 2 years and the usefulness of measuring its blood levels during the follow-up of patients with epilepsy. We measured peak blood LTG levels of 32 patients with epilepsy (9.16 +/- 3.34 years old; mean +/- SD). The blood levels were measured at 6 months, 1 year, and 2 years after reaching the LTG maintenance dosage. The effectiveness of LTG was evaluated to determine the seizure reduction rate. The patients were classified as effective cases (mean of own seizure reduction rates 50%) and ineffective cases (50%). The results were that the dosage and blood level showed positive correlations in the case of combination use with sodium valproate (VPA) (r = 0.690), carbamazepine and/or phenobarbital (r = 0.940), and others (r = 0.548). In several groups, the blood levels and efficacies did not show any positive correlations. In the cases of combination use with VPA, the blood levels of effective cases and ineffective cases were significantly different (P = 0.001). The optimal range was 8-11.5 g/mL based on the average and SD values in the effective cases. No patients had any side effects. In conclusion, no precise definition of the therapeutic range was possible because of the incomplete correlation between the blood level and seizure frequency. We recommend the optimal range of LTG as a therapeutic target without any side effects, and it was established that the range in the combination with VPA was 8-11.5 g/mL.
机译:进行该研究以评估2岁以下的乳藻(LTG)的有效性以及在癫痫患者随访期间测量其血液水平的有用性。我们测量了32例癫痫患者的峰值血液LTG水平(9.16 +/- 3.34岁;平均值+/- SD)。在达到LTG维持剂量后6个月,1年和2年测量血液水平。评估LTG的有效性以确定癫痫发作率。患者被归类为有效病例(自身癫痫发作率的平均值> 50%)和无效案例(50%)。结果是剂量和血液水平在与戊酸钠(VPA)(R = 0.690),卡巴马嗪和/或苯巴比妥(R = 0.940)和其他(R = 0.548)组合使用的情况下存在正相关性。在几组中,血液水平和效率没有显示出任何正相关。在与VPA组合使用的情况下,有效病例和无效病例的血液水平显着不同(P = 0.001)。基于有效案例中的平均值和SD值,最佳范围为8-11.5g / ml。没有患者有任何副作用。总之,由于血液水平和癫痫发作与癫痫发作之间不完全相关性,可能无法精确定义治疗范围。我们建议您作为治疗靶标的LTG的最佳范围,没有任何副作用,结果确定与VPA组合的范围为8-11.5g / ml。

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