Mikaeloff Yann, de Saint-Martin Anne, Mancini Josette, Peudenier Sylviane, Pedespan Jean-Michel, Vallée Louis, Motte Jacques, Bourgeois Marie, Arzimanoglou Alexis, Dulac Olivier, Chiron Catherine
Neuropediatric Department, Cochin-Saint-Vincent de Paul University Hospital, 82 Bd Denfert-Rochereau, 75014 Paris, France.
Epilepsy Res. 2003 Mar;53(3):225-32. doi: 10.1016/s0920-1211(03)00028-7.
To evaluate the efficacy and tolerability of topiramate (TPM) as add-on therapy in children less than 12 years of age with refractory epilepsy, according to epilepsy syndromes, we conducted an open, prospective, pragmatic and multicenter study in France. Efficacy was assessed, especially according to epilepsy syndromes, as well as tolerability. We included 207 children (41 of whom were less than 4 years of age). TPM was effective (responders with >50% decrease in seizure frequency) in 50% of 128 patients with partial epilepsy, and in 44% of 79 patients with generalized epilepsy. In case of generalized epilepsy, responders more frequently had generalized symptomatic epilepsy, severe myoclonic epilepsy and myoclono-astatic epilepsy, whereas response rate was mild in both infantile spasms and Lennox-Gastaut syndrome (LGS). Improvement was well maintained in all patients during the treatment period (median 5.6 months). Seizure frequency/severity increased (worsening) in 13% of patients with partial epilepsy and 17% with generalized epilepsy (particularly in those with infantile spasms), and resulted in withdrawal of TPM for 8%. The most frequently reported adverse events were moderate neurobehavioral and gastrointestinal disorders. Adverse events led to withdrawal of TPM from 13.5% of patients. Children less than 4 years of age had particularly good tolerability. Results confirm that TPM is effective and well tolerated in children under 12 years of age in a broad range of epilepsy syndromes, including refractory partial epilepsy, and symptomatic and myoclonic generalized epilepsy. Use of TPM should be considered in children under 4 years of age, and slow and progressive titration is important.
为了评估托吡酯(TPM)作为附加疗法治疗12岁以下难治性癫痫儿童的疗效和耐受性,我们在法国开展了一项开放、前瞻性、实用性多中心研究,该研究根据癫痫综合征进行。我们评估了疗效(尤其根据癫痫综合征)以及耐受性。我们纳入了207名儿童(其中41名年龄小于4岁)。在128例部分性癫痫患者中,50%的患者使用TPM有效(发作频率降低>50%);在79例全身性癫痫患者中,44%的患者使用TPM有效。对于全身性癫痫,有反应者更常见的是症状性全身性癫痫、严重肌阵挛性癫痫和肌阵挛-失张力性癫痫,而婴儿痉挛症和Lennox-Gastaut综合征(LGS)的反应率较低。在治疗期间(中位时间5.6个月),所有患者的病情改善情况均得到良好维持。部分性癫痫患者中有13%、全身性癫痫患者中有17%(尤其是婴儿痉挛症患者)的发作频率/严重程度增加(病情恶化),8%的患者因此停用TPM。最常报告的不良事件是中度神经行为和胃肠道疾病。不良事件导致13.5%的患者停用TPM。年龄小于4岁的儿童耐受性特别好。结果证实,TPM在12岁以下儿童的广泛癫痫综合征中有效且耐受性良好,包括难治性部分性癫痫、症状性和肌阵挛性全身性癫痫。对于4岁以下儿童应考虑使用TPM,缓慢逐步滴定很重要。