• 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

浙江省常见新生儿先天性畸形的 12 年患病率。

Twelve-year prevalence of common neonatal congenital malformations in Zhejiang Province, China.

机构信息

The Neonatal Intensive Care Unit, Women's Hospital, Zhejiang University School of Medicine, Hangzhou 310006, China.

出版信息

World J Pediatr. 2011 Nov;7(4):331-6. doi: 10.1007/s12519-011-0328-y. Epub 2011 Oct 20.

DOI:10.1007/s12519-011-0328-y
PMID:22015725
Abstract

BACKGROUND

One of the challenges that pediatricians face when examining birth defects is to understand the trends in its occurrence and provide clues to etiology. This study was undertaken to retrospectively assess the prevalence of 10 common neonatal congenital malformations by reviewing a database of all deliveries from 28 weeks up until 7 days of birth from January 1998 to December 2009 in Zhejiang Province, China.

METHODS

Ten common neonatal congenital malformations were selected for analysis. The incidence and the Cochran-Armitage Trend were assessed via SAS9.2. A P value ≤0.05 was considered statistically significant.

RESULTS

Of 83 888 perinatals, 374 (4.46‰) suffered from congenital heart diseases (CHD), 77 (0.92‰) from congenital hydrocephalus, 32 (0.38‰) from intestinal atresia/stenosis, 36 (0.43‰) from anorectal malformations, 149 (1.78‰) from kidney malformations, 139 (3.31‰) from hypospadias (male), 178 (2.12‰) from orofacial clefts (OFC), 188 (2.24‰) from polydactyly, 62 (0.74‰) from syndactyly, and 269 (3.21‰) from accessory auricle anomaly. Their trend of prevalence varied as follows: CHD, P=0.0026; hydrocephalus, P=0.0042; intestinal atresia/stenosis, P=0.0103; anorectal malformations, P=0.4332; kidney malformations, P<0.0001; hypospadias, P=0.0021; OFC, P=0.005; polydactyly, P=0.0867; syndactyly, P=0.1941; and accessory auricle anomaly, P=0.0011. The upward trend was as follows: CHD (P=0.0026), intestinal atresia/stenosis (P=0.0103), kidney malformations (P<0.0001), hypospadias (P=0.0021), OFC (P=0.005), and accessory auricle anomaly (P=0.0011). The incidence of hydrocephalus (P=0.0042) showed a downward trend. No statistical significant trend was found in anorectal malformations (P=0.4332), polydactyly (P=0.0867) and syndactyly (P=0.1941).

CONCLUSIONS

The incidences of CHD, intestinal atresia/stenosis, kidney malformations, hypospadias, OFC, and accessory auricle anomaly have increased in the last 12 years, but the incidences of anorectal malformations, polydactyly and syndactyly remain stable. The incidence of hydrocephalus shows a downward trend.

摘要

背景

儿科医生在检查出生缺陷时面临的挑战之一是了解其发生趋势,并为病因提供线索。本研究回顾性评估了从 1998 年 1 月至 2009 年 12 月浙江省所有 28 周至 7 天出生的分娩数据,分析了 10 种常见新生儿先天性畸形的患病率。

方法

选择 10 种常见新生儿先天性畸形进行分析。采用 SAS9.2 评估发病率和 Cochran-Armitage 趋势。P 值≤0.05 认为有统计学意义。

结果

83888 例围产儿中,374 例(4.46‰)患先天性心脏病(CHD),77 例(0.92‰)患先天性脑积水,32 例(0.38‰)患肠闭锁/狭窄,36 例(0.43‰)患肛门直肠畸形,149 例(1.78‰)患肾畸形,139 例(3.31‰)患尿道下裂(男性),178 例(2.12‰)患唇腭裂(OFC),188 例(2.24‰)患多指(趾)畸形,62 例(0.74‰)并指(趾)畸形,269 例(3.21‰)副耳畸形。其患病率趋势如下:CHD,P=0.0026;脑积水,P=0.0042;肠闭锁/狭窄,P=0.0103;肛门直肠畸形,P=0.4332;肾畸形,P<0.0001;尿道下裂,P=0.0021;唇腭裂,P=0.005;多指(趾)畸形,P=0.0867;并指(趾)畸形,P=0.1941;副耳畸形,P=0.0011。呈上升趋势的有:CHD(P=0.0026)、肠闭锁/狭窄(P=0.0103)、肾畸形(P<0.0001)、尿道下裂(P=0.0021)、唇腭裂(P=0.005)、副耳畸形(P=0.0011)。脑积水(P=0.0042)的发病率呈下降趋势。肛门直肠畸形(P=0.4332)、多指(趾)畸形(P=0.0867)和并指(趾)畸形(P=0.1941)无统计学意义。

结论

过去 12 年,CHD、肠闭锁/狭窄、肾畸形、尿道下裂、唇腭裂和副耳畸形的发病率有所增加,但肛门直肠畸形、多指(趾)畸形和并指(趾)畸形的发病率保持稳定。脑积水的发病率呈下降趋势。

相似文献

1
Twelve-year prevalence of common neonatal congenital malformations in Zhejiang Province, China.浙江省常见新生儿先天性畸形的 12 年患病率。
World J Pediatr. 2011 Nov;7(4):331-6. doi: 10.1007/s12519-011-0328-y. Epub 2011 Oct 20.
2
Epidemiology of congenital polydactyly and syndactyly in Hunan Province, China.中国湖南省先天性多指(趾)和并指(趾)的流行病学研究。
BMC Pregnancy Childbirth. 2024 Mar 23;24(1):216. doi: 10.1186/s12884-024-06417-y.
3
Comparison of total prevalence, perinatal prevalence, and livebirth prevalence of birth defects in Hunan Province, China, 2016-2020.2016-2020 年中国湖南省出生缺陷总患病率、围产儿患病率和活产儿患病率的比较。
Front Public Health. 2024 Sep 11;12:1297426. doi: 10.3389/fpubh.2024.1297426. eCollection 2024.
4
Epidemiology of birth defects based on a birth defect surveillance system in Southern Jiangsu, China, 2014-2018.基于 2014-2018 年中国江苏南部出生缺陷监测系统的出生缺陷流行病学研究。
J Matern Fetal Neonatal Med. 2022 Feb;35(4):745-751. doi: 10.1080/14767058.2020.1731459. Epub 2020 Feb 25.
5
The prevalence at birth of cogenital malformations at a maternity hospital in Osaka City, 1948-1990.1948 - 1990年大阪市一家妇产医院先天性畸形的出生患病率。
Jinrui Idengaku Zasshi. 1991 Sep;36(3):275-87. doi: 10.1007/BF01910546.
6
[Birth defects incidence in children from single and twin pregnancies in the Czech Republic--current data].[捷克共和国单胎和双胎妊娠儿童的出生缺陷发生率——当前数据]
Ceska Gynekol. 2009 Oct;74(5):369-82.
7
[Incidence of congenital heart defects in the Czech Republic--current data].[捷克共和国先天性心脏缺陷的发病率——当前数据]
Ceska Gynekol. 2010 May;75(3):221-42.
8
Associated congenital anomalies among cases with Down syndrome.唐氏综合征病例中的相关先天性异常。
Eur J Med Genet. 2015 Dec;58(12):674-80. doi: 10.1016/j.ejmg.2015.11.003. Epub 2015 Nov 11.
9
[Prevalence of selected congenital anomalies in the Czech Republic: congenital anomalies of the central nervous system and gastrointestinal tract].[捷克共和国特定先天性异常的患病率:中枢神经系统和胃肠道的先天性异常]
Epidemiol Mikrobiol Imunol. 2015 Mar;64(1):47-53.
10
Independent effects of maternal age and birth order on the incidence of selected congenital malformations.母亲年龄和出生顺序对特定先天性畸形发生率的独立影响。
Teratology. 1972 Dec;6(3):271-9. doi: 10.1002/tera.1420060304.

引用本文的文献

1
The Global Burden of Major Gastrointestinal Anomalies: A Global, Systematic Review of Gastrointestinal Anomaly Birth Prevalence.主要胃肠道畸形的全球负担:一项关于胃肠道畸形出生患病率的全球系统性综述。
Sage Open Pediatr. 2025 Feb 25;12:30502225251304582. doi: 10.1177/30502225251304582. eCollection 2025 Jan-Dec.
2
Practical Classification and Management of Accessory Auricle.实用的副耳分类与管理
Aesthetic Plast Surg. 2024 May;48(9):1653-1662. doi: 10.1007/s00266-023-03742-z. Epub 2023 Nov 15.
3
Cerebrospinal fluid shunt malfunctions: A reflective review.

本文引用的文献

1
High prevalence of orofacial clefts in Shanxi Province in northern China, 2003-2004.2003 - 2004年中国北方山西省口面部裂隙的高患病率
Am J Med Genet A. 2008 Oct 15;146A(20):2637-43. doi: 10.1002/ajmg.a.32492.
2
Prevalence of congenital heart defects in metropolitan Atlanta, 1998-2005.1998 - 2005年亚特兰大大都市先天性心脏缺陷的患病率
J Pediatr. 2008 Dec;153(6):807-13. doi: 10.1016/j.jpeds.2008.05.059. Epub 2008 Jul 26.
3
Oral clefts: a retrospective study of prevalence and predisposal factors in the State of Mexico.
脑积水分流故障:反思性回顾。
Childs Nerv Syst. 2023 Oct;39(10):2719-2728. doi: 10.1007/s00381-023-06070-4. Epub 2023 Jul 18.
4
The changing epidemiology of syndactyly in Chinese newborns: a nationwide surveillance-based study.中国新生儿并指症的流行病学变化:一项基于全国性监测的研究。
BMC Pregnancy Childbirth. 2023 May 10;23(1):334. doi: 10.1186/s12884-023-05660-z.
5
Congenital Hydrocephalus and Associated Risk Factors: An Institution-Based Case-Control Study, Dessie Town, North East Ethiopia.先天性脑积水及相关危险因素:埃塞俄比亚东北部德西镇一项基于机构的病例对照研究
Pediatric Health Med Ther. 2022 May 11;13:175-182. doi: 10.2147/PHMT.S364447. eCollection 2022.
6
["Tragus flap" combined with "Z" modification method in the surgical correction of congenital tragal deformity in children and literature review].["“耳屏瓣”联合“Z”改形法矫治儿童先天性耳屏畸形及文献复习"]
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2022 Apr;36(4):253-257. doi: 10.13201/j.issn.2096-7993.2022.04.003.
7
Sub-Exome Target Sequencing in a Family With Syndactyly Type IV Due to a Novel Partial Duplication of the Gene: First Case Report in Fujian Province of China.因基因新型部分重复导致的IV型并指一家系的外显子组靶向测序:中国福建省首例病例报告
Front Genet. 2020 Feb 28;11:130. doi: 10.3389/fgene.2020.00130. eCollection 2020.
8
Congenital anomalies prevalence in Addis Ababa and the Amhara region, Ethiopia: a descriptive cross-sectional study.埃塞俄比亚亚的斯亚贝巴和阿姆哈拉地区先天性异常的患病率:一项描述性横断面研究。
BMC Pediatr. 2019 Jul 11;19(1):234. doi: 10.1186/s12887-019-1596-2.
9
Epidemiological characteristics of holoprosencephaly in China, 2007-2014: A retrospective study based on the national birth defects surveillance system.中国 2007-2014 年 holoprosencephaly 的流行病学特征:基于全国出生缺陷监测系统的回顾性研究。
PLoS One. 2019 Jun 6;14(6):e0217835. doi: 10.1371/journal.pone.0217835. eCollection 2019.
10
Age-specific global epidemiology of hydrocephalus: Systematic review, metanalysis and global birth surveillance.年龄特异性全球脑积水流行病学:系统评价、荟萃分析和全球出生监测。
PLoS One. 2018 Oct 1;13(10):e0204926. doi: 10.1371/journal.pone.0204926. eCollection 2018.
唇腭裂:墨西哥州患病率及易感因素的回顾性研究
J Oral Sci. 2008 Jun;50(2):123-9. doi: 10.2334/josnusd.50.123.
4
Birth prevalence of cleft lip and palate in Northern Ireland (1981 to 2000).北爱尔兰唇腭裂的出生患病率(1981年至2000年)。
Cleft Palate Craniofac J. 2008 Mar;45(2):141-7. doi: 10.1597/06-045.1.
5
Utility of family history reports of major birth defects as a public health strategy.将主要出生缺陷家族史报告作为一种公共卫生策略的效用。
Pediatrics. 2007 Sep;120 Suppl 2:S71-7. doi: 10.1542/peds.2007-1010F.
6
Stability of prevalence rates of anorectal malformations in the Alberta Congenital Anomalies Surveillance System 1990-2004.1990 - 2004年艾伯塔省先天性异常监测系统中肛门直肠畸形患病率的稳定性
J Pediatr Surg. 2007 Aug;42(8):1417-21. doi: 10.1016/j.jpedsurg.2007.03.045.
7
A possible association between maternal glomerulonephritis and congenital intestinal atresia/stenosis--a population-based case-control study.母亲肾小球肾炎与先天性肠道闭锁/狭窄之间的可能关联——一项基于人群的病例对照研究。
Eur J Epidemiol. 2007;22(8):557-64. doi: 10.1007/s10654-007-9143-0. Epub 2007 Jun 14.
8
Birth prevalence of cryptorchidism and hypospadias in northern England, 1993-2000.1993 - 2000年英格兰北部隐睾症和尿道下裂的出生患病率。
Arch Dis Child. 2007 Jul;92(7):576-9. doi: 10.1136/adc.2006.102913. Epub 2006 Dec 1.
9
Factors associated with hypospadias in Asian newborn babies.亚洲新生儿尿道下裂的相关因素。
J Perinat Med. 2006;34(6):497-500. doi: 10.1515/JPM.2006.096.
10
Risk factors for hypospadias.尿道下裂的危险因素。
Eur J Pediatr. 2007 Jul;166(7):671-8. doi: 10.1007/s00431-006-0304-z. Epub 2006 Nov 14.