Lux Andrew L, Edwards Stuart W, Hancock Eleanor, Johnson Anthony L, Kennedy Colin R, Newton Richard W, O'Callaghan Finbar J K, Verity Christopher M, Osborne John P
Royal United Hospital Bath NHS Trust and the School for Health, University of Bath, Bath, UK.
Lancet Neurol. 2005 Nov;4(11):712-7. doi: 10.1016/S1474-4422(05)70199-X.
Infantile spasms is a severe infantile seizure disorder that is difficult to treat and has a high morbidity. Absence of spasms on days 13 and 14 after randomisation is more common in infants allocated hormone treatments than in those allocated vigabatrin. We sought to assess whether early control of spasms is associated with improved developmental or epilepsy outcomes.
Infants enrolled in the United Kingdom Infantile Spasms Study (UKISS) were randomly assigned hormone treatment (n=55) or vigabatrin (n=52) and were followed up until clinical assessment at 12-14 months of age. We assessed neurodevelopment with the Vineland adaptive behaviour scales (VABS) at 14 months of age on an intention to treat basis.
Of 107 infants enrolled, five died and 101 survivors reached both follow-up assessments. Absence of spasms at final clinical assessment (hormone 41/55 [75%] vs vigabatrin 39/51 [76%]) was similar in each treatment group (difference 1.9%, 95% CI -18.3% to 14.4%; chi(2)=0.05; p=0.82). Mean VABS score did not differ significantly (hormone 78.6 [SD 16.8] vs vigabatrin 77.5 [SD 12.7]; difference 1.0, 95% CI -4.9 to 7.0; t(99)=0.35, p=0.73). In infants with no identified underlying aetiology, the mean VABS score was higher in those allocated hormone treatment than in those allocated vigabatrin (88.2 [17.3] vs 78.9 [14.3]; difference 9.3, 95% CI 1.2 to 17.3; t(95)=2.28, p=0.025).
Hormone treatment controls spasms better than does vigabatrin initially, but not at 12-14 months of age. Better initial control of spasms by hormone treatment in those with no identified underlying aetiology may lead to improved developmental outcome.
婴儿痉挛症是一种严重的婴儿癫痫性疾病,难以治疗且发病率很高。随机分组后第13天和第14天无痉挛发作在接受激素治疗的婴儿中比接受vigabatrin治疗的婴儿更常见。我们试图评估痉挛的早期控制是否与改善发育或癫痫结局相关。
纳入英国婴儿痉挛症研究(UKISS)的婴儿被随机分配接受激素治疗(n = 55)或vigabatrin治疗(n = 52),并随访至12 - 14个月龄时进行临床评估。我们在14个月龄时采用文兰适应性行为量表(VABS)对意向性治疗的婴儿进行神经发育评估。
在纳入的107名婴儿中,5名死亡,101名幸存者完成了两次随访评估。各治疗组在最终临床评估时无痉挛发作的情况相似(激素治疗组41/55 [75%] 对比vigabatrin治疗组39/51 [76%])(差异1.9%,95%可信区间 - 18.3%至14.4%;χ² = 0.05;p = 0.82)。平均VABS评分无显著差异(激素治疗组78.6 [标准差16.8] 对比vigabatrin治疗组77.5 [标准差12.7];差异1.0,95%可信区间 - 4.9至7.0;t(99) = 0.35,p = 0.73)。在未发现潜在病因的婴儿中,接受激素治疗的婴儿平均VABS评分高于接受vigabatrin治疗的婴儿(88.2 [17.3] 对比78.9 [14.3];差异9.3,95%可信区间1.2至17.3;t(95) = 2.28,p = 0.025)。
激素治疗最初控制痉挛比vigabatrin更好,但在12 - 14个月龄时并非如此。在未发现潜在病因的婴儿中,激素治疗对痉挛的更好初始控制可能会导致更好的发育结局。