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婴儿痉挛症的神经发育结局:一项系统综述和荟萃分析。

Neurodevelopmental outcome of infantile spasms: A systematic review and meta-analysis.

作者信息

Widjaja Elysa, Go Cristina, McCoy Blathnaid, Snead O Carter

机构信息

Diagnostic Imaging, The Hospital for Sick Children, Toronto, Ontario, Canada; Division of Neurology, The Hospital for Sick Children, Toronto, Ontario, Canada.

Division of Neurology, The Hospital for Sick Children, Toronto, Ontario, Canada.

出版信息

Epilepsy Res. 2015 Jan;109:155-62. doi: 10.1016/j.eplepsyres.2014.11.012. Epub 2014 Nov 22.

Abstract

BACKGROUND

The aims of this systematic review and meta-analysis were to assess (i) estimates of good neurodevelopmental outcome in infantile spasms (IS), (ii) if neurodevelopmental outcome has changed since the publication of the first guideline on medical treatment of IS in 2004 and (iii) effect of lead time to treatment (LTTT).

METHODS

The Medline, Embase, Cochrane, PsycINFO, Web of Science and Scopus databases, and reference lists of retrieved articles were searched. Studies inclusion criteria were: (i) >5 patients with IS, (ii) mean/median follow-up of >6 months, (iii) neurodevelopmental outcome, and (iv) randomized and observational studies. The data extracted included proportion of good neurodevelopmental outcome, year of publication, cryptogenic or symptomatic IS and LTTT.

RESULTS

Of the 1436 citations screened, 55 articles were included in final analysis, with a total of 2967 patients. The pooled estimate for good neurodevelopmental outcome was 0.236 (95% CI: 0.193-0.286). There was no difference between the proportions of good neurodevelopmental outcome for the 21 studies published after 2004 [0.264 (95% CI: 0.197-0.344)] compared to the 34 studies published before 2004 [0.220 (95% CI: 0.168-0.283)] (Q value=0.862, p=0.353). The pooled estimate of good neurodevelopmental outcome for cryptogenic IS [0.543 (95% CI: 0.458-0.625)] was higher than symptomatic IS [0.125 (95% CI: 0.09-0.171)] (Q value=69.724, p<0.001). Risk ratio of LTTT <4weeks relative to >4weeks for good neurodevelopmental outcome of 8 studies was 1.519 (95% CI: 1.064-2.169).

CONCLUSION

Neurodevelopmental outcome was overall poor in patients with IS and has not changed since the publication of first guideline on IS. Although cryptogenic IS has better prognosis than symptomatic IS, the outcome for cryptogenic IS remained poor. There was heterogeneity in neurodevelopmental outcome ascertainment methods, highlighting the need for a more standardized and comprehensive assessment of cognitive, behavioural, emotional and functional outcomes.

摘要

背景

本系统评价和荟萃分析的目的是评估:(i)婴儿痉挛症(IS)良好神经发育结局的估计值;(ii)自2004年首次发布IS药物治疗指南以来,神经发育结局是否发生变化;(iii)治疗提前期(LTTT)的影响。

方法

检索了Medline、Embase、Cochrane、PsycINFO、Web of Science和Scopus数据库以及检索到的文章的参考文献列表。研究纳入标准为:(i)超过5例IS患者;(ii)平均/中位随访时间超过6个月;(iii)神经发育结局;(iv)随机和观察性研究。提取的数据包括良好神经发育结局的比例、发表年份、隐源性或症状性IS以及LTTT。

结果

在筛选的1436篇文献中,55篇文章纳入最终分析,共2967例患者。良好神经发育结局的合并估计值为0.236(95%CI:0.193 - 0.286)。2004年后发表的21项研究中良好神经发育结局的比例[0.264(95%CI:0.197 - 0.344)]与2004年前发表的34项研究中[0.220(95%CI:0.168 - 0.283)]相比,无差异(Q值 = 0.862,p = 0.353)。隐源性IS良好神经发育结局的合并估计值[0.543(95%CI:0.458 - 0.625)]高于症状性IS[0.125(95%CI:0.09 - 0.171)](Q值 = 69.724,p < 0.001)。8项研究中,LTTT < 4周相对于> 4周时良好神经发育结局的风险比为1.519(95%CI:1.064 - 2.169)。

结论

IS患者的神经发育结局总体较差,自首次发布IS指南以来未发生变化。虽然隐源性IS的预后比症状性IS好,但隐源性IS的结局仍然较差。神经发育结局确定方法存在异质性,突出了对认知、行为、情感和功能结局进行更标准化和全面评估的必要性。

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