Grinspan Zachary M, Knupp Kelly G, Patel Anup D, Yozawitz Elissa G, Wusthoff Courtney J, Wirrell Elaine C, Valencia Ignacio, Singhal Nilika S, Nordli Douglas R, Mytinger John R, Mitchell Wendy G, Keator Cynthia G, Loddenkemper Tobias, Hussain Shaun A, Harini Chellamani, Gaillard William D, Fernandez Ivan S, Coryell Jason, Chu Catherine J, Berg Anne T, Shellhaas Renee A
From Weill Cornell Medicine (Z.M.G.), New York, NY; University of Colorado Anschutz Medical Campus (K.G.K.), Aurora; Nationwide Children's Hospital (A.D.P., J.R.M.), Ohio State University, Columbus; Montefiore Medicine (E.G.Y.), Bronx, NY; Stanford University (C.J.W.), Palo Alto, CA; Mayo Clinic (E.W.), Rochester, MN; Drexel University College of Medicine (I.V.), Philadelphia, PA; University of California San Francisco (N.S.S.); University of Chicago Medicine (D.R.N.), IL; Children's Hospital of Los Angeles (W.M.), CA; Cook Children's Hospital (C.G.K.), Fort Worth, TX; Boston Children's Hospital (T.L., C.H., I.S.F.), MA; University of California Los Angeles (S.A.H.); Children's National Hospital (W.D.G.), Washington, DC; Oregon Health Services University (J.C.), Portland; Massachusetts General Hospital (C.J.C.), Boston; Lurie Children's Hospital (A.T.B.), Chicago, IL; and University of Michigan (R.A.S.), Ann Arbor.
Neurology. 2021 Sep 20;97(12):e1217-e1228. doi: 10.1212/WNL.0000000000012511.
To compare the effectiveness of initial treatment for infantile spasms.
The National Infantile Spasms Consortium prospectively followed up children with new-onset infantile spasms that began at age 2 to 24 months at 23 US centers (2012-2018). Freedom from treatment failure at 60 days required no second treatment for infantile spasms and no clinical spasms after 30 days of treatment initiation. We managed treatment selection bias with propensity score weighting and within-center correlation with generalized estimating equations.
Freedom from treatment failure rates were as follows: adrenocorticotropic hormone (ACTH) 88 of 190 (46%), oral steroids 42 of 95 (44%), vigabatrin 32 of 87 (37%), and nonstandard therapy 4 of 51 (8%). Changing from oral steroids to ACTH was not estimated to affect response (observed 44% estimated to change to 44% [95% confidence interval 34%-54%]). Changing from nonstandard therapy to ACTH would improve response from 8% to 39% (17%-67%), and changing to oral steroids would improve response from 8% to 38% (15%-68%). There were large but not statistically significant estimated effects of changing from vigabatrin to ACTH (29% to 42% [15%-75%]), from vigabatrin to oral steroids (29% to 42% [28%-57%]), and from nonstandard therapy to vigabatrin (8% to 20% [6%-50%]). Among children treated with vigabatrin, those with tuberous sclerosis complex (TSC) responded more often than others (62% vs 29%; < 0.05).
Compared to nonstandard therapy, ACTH and oral steroids are superior for initial treatment of infantile spasms. The estimated effectiveness of vigabatrin is between that of ACTH/oral steroids and nonstandard therapy, although the sample was underpowered for statistical confidence. When used, vigabatrin worked best for TSC.
This study provides Class III evidence that for children with new-onset infantile spasms, ACTH or oral steroids were superior to nonstandard therapies.
比较婴儿痉挛症初始治疗的有效性。
美国国家婴儿痉挛症联盟前瞻性地随访了23个美国中心(2012 - 2018年)年龄在2至24个月开始出现新发婴儿痉挛症的儿童。60天无治疗失败定义为无需进行第二次婴儿痉挛症治疗且在开始治疗30天后无临床痉挛发作。我们采用倾向得分加权和广义估计方程处理中心内相关性来管理治疗选择偏倚。
无治疗失败率如下:促肾上腺皮质激素(ACTH)190例中有88例(46%),口服类固醇95例中有42例(44%),氨己烯酸87例中有32例(37%),非标准疗法51例中有4例(8%)。从口服类固醇改为ACTH预计不会影响反应(观察到的44%预计变为44%[95%置信区间34% - 54%])。从非标准疗法改为ACTH会使反应从8%提高到39%(17% - 67%),改为口服类固醇会使反应从8%提高到38%(15% - 68%)。从氨己烯酸改为ACTH(29%至42%[15% - 75%])、从氨己烯酸改为口服类固醇(29%至42%[28% - 57%])以及从非标准疗法改为氨己烯酸(8%至20%[6% - 50%])有较大但无统计学显著意义的估计效应。在接受氨己烯酸治疗的儿童中,患有结节性硬化症(TSC)的儿童比其他儿童反应更频繁(62%对29%;<0.05)。
与非标准疗法相比,ACTH和口服类固醇在婴儿痉挛症的初始治疗中更具优势。氨己烯酸的估计有效性介于ACTH/口服类固醇和非标准疗法之间,尽管样本量不足以获得统计学上的置信度。使用时,氨己烯酸对TSC效果最佳。
本研究提供了III类证据,即对于新发婴儿痉挛症儿童,ACTH或口服类固醇优于非标准疗法。