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首页> 外文期刊>The New England journal of medicine >Lack of benefit of a single dose of synthetic human secretin in the treatment of autism and pervasive developmental disorder (see comments)
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Lack of benefit of a single dose of synthetic human secretin in the treatment of autism and pervasive developmental disorder (see comments)

机译:单一剂量的合成人促胰液素在自闭症和普遍性发育障碍的治疗中缺乏益处(参见评论)

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摘要

BACKGROUND: Secretin is a peptide hormone that stimulates pancreatic secretion. After recent publicity about a child with autism whose condition markedly improved after a single dose of secretin, thousands of children with autistic disorders may have received secretin injections. METHODS: We conducted a double-blind, placebo-controlled trial of a single intravenous dose of synthetic human secretin in 60 children (age, 3 to 14 years) with autism or pervasive developmental disorder. The children were randomly assigned to treatment with an intravenous infusion of synthetic human secretin (0.4 microg per kilogram of body weight) or saline placebo. We used standardized behavioral measures of the primary and secondary features of autism, including the Autism Behavior Checklist, to assess the degree of impairment at base line and over the course of a four-week period after treatment. RESULTS: Of the 60 children, 4 could not be evaluated - 2 received secretin outside the study, and 2 did not return for follow-up. Thus, 56 children (28 in each group) completed the study. As compared with placebo, secretin treatment was not associated with significant improvements in any of the outcome measures. Among the children in the secretin group, the mean total score on the Autism Behavior Checklist at base line was 59.0 (range of possible values, 0 to 158, with a larger value corresponding to greater impairment), and among those in the placebo group it was 63.2. The mean decreases in scores over the four-week period were 8.9 in the secretin group and 17.8 in the placebo group (mean difference, -8.9; 95 percent confidence interval, -19.4 to 1.6; P=0.11). None of the children had treatment-limiting adverse effects. After they were told the results, 69 percent of the parents of the children in this study said they remained interested in secretin as a treatment for their children. CONCLUSIONS: A single dose of synthetic human secretin is not an effective treatment for autism or pervasive developmental disorder.
机译:背景:促胰液素是一种刺激胰腺分泌的肽激素。在最近对自闭症儿童进行了一次宣传之后,单剂量服用促胰液素后病情明显好转,成千上万的自闭症儿童可能接受了促胰液素注射。方法:我们对60名自闭症或普遍性发育障碍儿童进行了单次静脉内剂量的合成人促胰液素的静脉注射双盲,安慰剂对照试验。这些孩子被随机分配接受合成人促胰液素(每公斤体重0.4微克)或生理盐水安慰剂的静脉输注治疗。我们使用了包括自闭症行为清单在内的自闭症主要和次要特征的标准化行为测量,以评估基线水平以及治疗后四周内的损伤程度。结果:在60名儿童中,有4名无法评估-2名在研究之外接受了促胰液素,还有2名没有返回进行随访。因此,有56名儿童(每组28名)完成了研究。与安慰剂相比,促胰液素治疗与任何结局指标均无明显改善。在促胰液素组的孩子中,自闭症行为检查表上的基线平均总分是59.0(可能值的范围是0到158,值越大表示损伤越大),而在安慰剂组中则是是63.2。在四周的时间内,促胰液素组的平均得分降低为8.9,而安慰剂组为17.8(平均值差异为-8.9; 95%的置信区间为-19.4至1.6; P = 0.11)。没有一个孩子有限制治疗的副作用。在将结果告知他们后,在这项研究中,有69%的孩子的父母表示,他们仍然对促胰液素有兴趣作为治疗孩子的方法。结论:单剂量的合成人促胰液素不能有效治疗自闭症或广泛性发育障碍。

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