Gascon Generoso G
Department of Neuroscience, MBC J-76, King Faisal Specialist Hospital and Research Center, PO Box 40047, Jeddah 21499, Saudi Arabia.
J Child Neurol. 2003 Dec;18(12):819-27. doi: 10.1177/088307380301801201.
The efficacy of oral inosiplex alone (group A) versus combined treatment of inosiplex (Isoprinosine) and intraventricular interferon-alpha2b (Intron A) (group B) in patients with subacute sclerosing panencephalitis (SSPE) was compared. One hundred and twenty-one patients who met the diagnostic criteria for subacute sclerosing panencephalitis and presented at stage 2 or less were randomized into group A or B. Data were analyzable on 67 patients who met the inclusion criteria and adhered to the protocol. The inosiplex dosage was 100 mg/kg/day to a maximum of 3 g/day, taken orally in three divided doses for 6 months. Interferon-alpha2b started with 100,000 U/m2 and escalated to 1,000,000 U/m2 over 5 inpatient days and then 1,000,000 U/m2 twice a week for 6 months. Neurologic status was rated by the Neurological Disability Index, Brief Assessment Examination, and stages. Kaplan-Meier survival rates were not statistically significant between group A and group B (log-rank test chi2 = .1374, P = .7109). In longitudinal morbidity analyses, regression results were fitted to three outcome measures: the Neurological Disability Index, the Brief Assessment Examination, and stage. Group medians of the estimated regression slopes were then compared using the Wilcoxon rank-sum test. There was no statistically significant difference between the two groups on any of these three measures. Morbidity comparisons of clinical classification of outcomes (improvement, stabilization, worsening after treatment stopped, deterioration) also showed no statistically significant difference between groups. There were no statistically significant differences between the two treatment groups on any efficacy measure. However, the observed rates of satisfactory outcome (stabilization, improvement) of 34% in group A and 35% in group B were higher than the spontaneous remission rates of 5 to 10% reported in the literature, suggesting that treatment was superior to no treatment.
比较了单独口服肌苷片(A组)与肌苷片(异丙肌苷)联合脑室内注射α-干扰素2b(重组干扰素α-2b)(B组)治疗亚急性硬化性全脑炎(SSPE)患者的疗效。121例符合亚急性硬化性全脑炎诊断标准且处于2期及以下的患者被随机分为A组或B组。对67例符合纳入标准并遵守方案的患者进行了数据分析。肌苷片剂量为100mg/kg/天,最大剂量为3g/天,分三次口服,共服用6个月。α-干扰素2b起始剂量为100,000U/m²,在5个住院日内逐渐增至1,000,000U/m²,然后每周两次,每次1,000,000U/m²,共6个月。通过神经功能障碍指数、简易评估检查和分期对神经状态进行评分。A组和B组的Kaplan-Meier生存率无统计学显著差异(对数秩检验χ² = 0.1374,P = 0.7109)。在纵向发病率分析中,将回归结果拟合到三个结局指标:神经功能障碍指数、简易评估检查和分期。然后使用Wilcoxon秩和检验比较估计回归斜率的组中位数。在这三个指标中的任何一个上,两组之间均无统计学显著差异。对治疗停止后的结局(改善、稳定、恶化、病情恶化)进行临床分类的发病率比较也显示两组之间无统计学显著差异。在任何疗效指标上,两个治疗组之间均无统计学显著差异。然而,A组观察到的满意结局(稳定、改善)率为34%,B组为35%,高于文献报道的5%至10%的自发缓解率,表明治疗优于不治疗。