• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Chiari II型畸形的神经学预后及其与形态学表现和胎儿心率模式的相关性:一项回顾性研究。

Neurological outcomes in Chiari type II malformations and their correlation to morphological findings and fetal heart rate patterns: a retrospective study.

作者信息

Otera Yuka, Morokuma Seiichi, Fukushima Kotaro, Anami Ai, Yumoto Yasuo, Ito Yushi, Ochiai Masayuki, Hashiguchi Kimiaki, Wake Norio, Sago Haruhiko, Kato Kiyoko

机构信息

Center for Maternal-Fetal and Neonatal Medicine, National Center for Child Health and Development, Tokyo, Japan.

Department of Obstetrics and Gynecology, Kyushu University Hospital, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

出版信息

BMC Res Notes. 2015 Feb 27;8:57. doi: 10.1186/s13104-015-1014-2.

DOI:10.1186/s13104-015-1014-2
PMID:25890237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4349618/
Abstract

BACKGROUND

Correlations among Chiari type II malformation (CMII) morphological findings, the proportion of fetal heart rate patterns corresponding to the quiet phase (QP), and neurological outcomes have yet to be investigated.

FINDINGS

The correlations among the morphological findings (i.e., the degree of ventriculomegaly, myelomeningocele levels, and degree of cerebellar herniation), proportion of time spent in QP, and developmental quotients (DQs) were analyzed in 22 children. The proportion of time spent in QP was compared between children with poor neurological outcomes (n = 9) and those with good outcomes (n = 13). Pearson's correlations and the Mann-Whitney U-test were used to assess for statistical significance; P < 0.05 was considered statistically significant. No significant differences were observed between the DQs and morphological findings, but the DQs and the proportion of time spent in QP were significantly correlated (r = 0.287, P = 0.01). The proportion of time spent in QP was significantly different between children with poor outcomes and those with good outcomes (median, 11% [range, 0-32%] vs. 28% [range, 2-55%]; P = 0.006).

CONCLUSIONS

The proportion of fetal heart rate patterns corresponding to the QP might be a useful predictor of neurological outcomes in 2-year-old children with CMII.

摘要

背景

Chiari II型畸形(CMII)形态学表现、与安静期(QP)相对应的胎儿心率模式比例和神经学预后之间的相关性尚未得到研究。

研究结果

分析了22名儿童的形态学表现(即脑室扩大程度、脊髓脊膜膨出水平和小脑疝程度)、QP期所占时间比例和发育商(DQ)之间的相关性。比较了神经学预后不良儿童(n = 9)和预后良好儿童(n = 13)的QP期所占时间比例。采用Pearson相关性分析和Mann-Whitney U检验评估统计学意义;P < 0.05被认为具有统计学意义。DQ与形态学表现之间未观察到显著差异,但DQ与QP期所占时间比例显著相关(r = 0.287,P = 0.01)。预后不良儿童和预后良好儿童的QP期所占时间比例存在显著差异(中位数,11% [范围,0 - 32%] 对28% [范围,2 - 55%];P = 0.006)。

结论

与QP相对应的胎儿心率模式比例可能是CMII型2岁儿童神经学预后的有用预测指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/216e/4349618/5aefd72f3938/13104_2015_1014_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/216e/4349618/5798ec658674/13104_2015_1014_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/216e/4349618/5cbab39ff45b/13104_2015_1014_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/216e/4349618/1d45408443dd/13104_2015_1014_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/216e/4349618/a1ad48c93be1/13104_2015_1014_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/216e/4349618/5aefd72f3938/13104_2015_1014_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/216e/4349618/5798ec658674/13104_2015_1014_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/216e/4349618/5cbab39ff45b/13104_2015_1014_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/216e/4349618/1d45408443dd/13104_2015_1014_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/216e/4349618/a1ad48c93be1/13104_2015_1014_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/216e/4349618/5aefd72f3938/13104_2015_1014_Fig5_HTML.jpg

相似文献

1
Neurological outcomes in Chiari type II malformations and their correlation to morphological findings and fetal heart rate patterns: a retrospective study.Chiari II型畸形的神经学预后及其与形态学表现和胎儿心率模式的相关性:一项回顾性研究。
BMC Res Notes. 2015 Feb 27;8:57. doi: 10.1186/s13104-015-1014-2.
2
Chiari-II malformation: a biometric analysis.Chiari-II型畸形:一项生物测量分析。
Eur J Pediatr Surg. 2002 Dec;12 Suppl 1:S12-8. doi: 10.1055/s-2002-36865.
3
The clinical significance of hindbrain herniation and deformity as shown on MR images of patients with Chiari II malformation.Chiari II 畸形患者磁共振成像(MR)显示的后脑疝和畸形的临床意义。
AJNR Am J Neuroradiol. 1988 Nov-Dec;9(6):1075-8.
4
Effects of birth advancement in Chiari malformation in a surgical myelomeningocele model in rabbits.在兔脊髓脊膜膨出手术模型中 Chiari 畸形的产前进阶效应。
J Pediatr Surg. 2010 Mar;45(3):594-9. doi: 10.1016/j.jpedsurg.2009.08.003.
5
Arnold-Chiari in a fetal rat model of dysraphism.脊柱裂胎儿大鼠模型中的阿诺德-奇阿利畸形
Fetal Diagn Ther. 2005 Sep-Oct;20(5):437-41. doi: 10.1159/000086827.
6
Chiari III malformation with proatlas abnormality.伴有原寰椎异常的Chiari III型畸形
Pediatr Neurosurg. 2011;47(4):295-8. doi: 10.1159/000336753. Epub 2012 Mar 23.
7
Limbic tract anomalies in pediatric myelomeningocele and Chiari II malformation: anatomic correlations with memory and learning--initial investigation.小儿脊髓脊膜膨出和Chiari II畸形中的边缘系统通路异常:与记忆和学习的解剖学关联——初步研究
Radiology. 2006 Jul;240(1):194-202. doi: 10.1148/radiol.2401050674.
8
Tectocerebellar dysraphia with posterior encephalocele (Friede): report of the youngest case. Reappraisal of the condition uniting Cleland-Chiari (Arnold-Chiari) and Dandy-Walker syndromes.伴后颅脑膨出的顶盖小脑发育不全(弗里德):最年轻病例报告。对合并克莱兰 - 基亚里(阿诺德 - 基亚里)和丹迪 - 沃克综合征的病症的重新评估。
Clin Neuropathol. 1994 Jul-Aug;13(4):216-20.
9
Retinoic acid induced myelomeningocele in fetal rats: characterization by histopathological analysis and magnetic resonance imaging.维甲酸诱导胎鼠脊髓脊膜膨出:通过组织病理学分析和磁共振成像进行特征描述
Exp Neurol. 2005 Aug;194(2):467-75. doi: 10.1016/j.expneurol.2005.03.011.
10
Reversal of hindbrain herniation after maternal-fetal surgery for myelomeningocele subsequently impacts on brain stem function.脊髓脊膜膨出母胎手术后脑疝的逆转随后会影响脑干功能。
Neuropediatrics. 2008 Dec;39(6):359-62. doi: 10.1055/s-0029-1202835. Epub 2009 Jun 30.

本文引用的文献

1
Central nervous system findings on fetal magnetic resonance imaging and outcomes in children with spina bifida.胎儿磁共振成像的中枢神经系统表现与脊膜膨出患儿的结局。
Obstet Gynecol. 2010 Aug;116(2 Pt 1):323-329. doi: 10.1097/AOG.0b013e3181e666e8.
2
Role of prenatal ultrasound in predicting survival and mental and motor functioning in children with spina bifida.产前超声在预测脊柱裂患儿生存及精神和运动功能中的作用。
Ultrasound Obstet Gynecol. 2009 Sep;34(3):253-8. doi: 10.1002/uog.6423.
3
Chiari Type II malformation: past, present, and future.
Chiari II型畸形:过去、现在与未来。
Neurosurg Focus. 2004 Feb 15;16(2):E5. doi: 10.3171/foc.2004.16.2.6.
4
Cognitive status of young adults with spina bifida.患有脊柱裂的年轻人的认知状况。
Dev Med Child Neurol. 2003 Dec;45(12):813-20. doi: 10.1017/s0012162203001518.
5
Development of fetal and neonatal sleep and circadian rhythms.胎儿及新生儿睡眠与昼夜节律的发育
Sleep Med Rev. 2003 Aug;7(4):321-34. doi: 10.1053/smrv.2002.0243.
6
Memory functions in children with early hydrocephalus.
Neuropsychology. 1998 Oct;12(4):578-89. doi: 10.1037//0894-4105.12.4.578.
7
Developmental outcomes of children with myelomeningocele: prenatal predictors.脊髓脊膜膨出患儿的发育结局:产前预测因素
Am J Obstet Gynecol. 1997 Aug;177(2):319-24; discussion 324-6. doi: 10.1016/s0002-9378(97)70193-5.
8
Heart rate variation during fetal behavioural states 1 and 2.
Early Hum Dev. 1993 Sep;34(1-2):21-8. doi: 10.1016/0378-3782(93)90037-u.
9
Are there behavioural states in the human fetus?人类胎儿存在行为状态吗?
Early Hum Dev. 1982 Apr;6(2):177-95. doi: 10.1016/0378-3782(82)90106-2.
10
Neurological control of fetal heart rate in 20 cases of anencephalic fetuses.20例无脑儿胎儿心率的神经控制
Am J Obstet Gynecol. 1984 May 15;149(2):201-8. doi: 10.1016/0002-9378(84)90199-6.