• 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

相似文献

1
Epidemiology of major congenital heart defects in Sweden, 1981-1986.1981 - 1986年瑞典主要先天性心脏缺陷的流行病学
J Epidemiol Community Health. 1992 Jun;46(3):211-5. doi: 10.1136/jech.46.3.211.
2
Monitoring of congenital cardiac defects.先天性心脏缺陷的监测。
Pediatr Cardiol. 1987;8(4):247-56. doi: 10.1007/BF02427537.
3
Increased prevalence of congenital heart defects in monozygotic and dizygotic twins.先天性心脏缺陷在单卵双胎和双卵双胎中的发生率增加。
Circulation. 2013 Sep 10;128(11):1182-8. doi: 10.1161/CIRCULATIONAHA.113.002453. Epub 2013 Aug 8.
4
The epidemiology of cardiovascular defects, part I: a study based on data from three large registries of congenital malformations.心血管缺陷的流行病学,第一部分:一项基于三个大型先天性畸形登记处数据的研究。
Pediatr Cardiol. 2003 May-Jun;24(3):195-221. doi: 10.1007/s00246-002-9401-6. Epub 2003 Mar 14.
5
Maternal smoking and congenital heart defects.母亲吸烟与先天性心脏缺陷
Eur J Epidemiol. 1999 Sep;15(8):731-7. doi: 10.1023/a:1007671631188.
6
[Epidemiology and registry of congenital heart disease in Costa Rica].[哥斯达黎加先天性心脏病的流行病学与登记情况]
Rev Panam Salud Publica. 2011 Jul;30(1):31-8.
7
The epidemiology of cardiovascular defects, part 2: a study based on data from three large registries of congenital malformations.心血管缺陷的流行病学,第2部分:基于三个大型先天性畸形登记处数据的研究。
Pediatr Cardiol. 2003 May-Jun;24(3):222-35. doi: 10.1007/s00246-002-9402-5. Epub 2003 Mar 17.
8
Noncardiac malformations at major congenital heart defects.主要先天性心脏缺陷中的非心脏畸形。
Pediatr Cardiol. 1997 Jan-Feb;18(1):11-8. doi: 10.1007/s002469900101.
9
Recurrence risk for major congenital heart defects in Sweden: a registry study.瑞典主要先天性心脏缺陷的复发风险:一项登记研究。
Genet Epidemiol. 1994;11(2):131-40. doi: 10.1002/gepi.1370110204.
10
Cardiovascular malformations among preterm infants.早产儿中的心血管畸形。
Pediatrics. 2005 Dec;116(6):e833-8. doi: 10.1542/peds.2005-0397.

引用本文的文献

1
Investigation of Genetic Causes in Patients with Congenital Heart Disease in Qatar: Findings from the Sidra Cardiac Registry.卡塔尔先天性心脏病患者遗传病因研究:锡德拉心脏登记处的发现。
Genes (Basel). 2022 Jul 30;13(8):1369. doi: 10.3390/genes13081369.
2
KinCor, a national registry for paediatric patients with congenital and other types of heart disease in the Netherlands: aims, design and interim results.KinCor,荷兰先天性及其他类型心脏病儿科患者的国家登记处:目标、设计与中期结果。
Neth Heart J. 2016 Nov;24(11):628-639. doi: 10.1007/s12471-016-0892-9.
3
The pattern of congenital heart defects arising from reduced Tbx5 expression is altered in a Down syndrome mouse model.在唐氏综合征小鼠模型中,因Tbx5表达降低而产生的先天性心脏缺陷模式发生了改变。
BMC Dev Biol. 2015 Jul 25;15:30. doi: 10.1186/s12861-015-0080-y.
4
Congenital heart disease and chromossomopathies detected by the karyotype.通过核型分析检测到的先天性心脏病和染色体病
Rev Paul Pediatr. 2014 Jun;32(2):262-71. doi: 10.1590/0103-0582201432213213.
5
Chromosomal abnormalities in patients with congenital heart disease.先天性心脏病患者的染色体异常。
Arq Bras Cardiol. 2013 Dec;101(6):495-501. doi: 10.5935/abc.20130204. Epub 2013 Oct 22.
6
Population-based treated prevalence of congenital heart disease in a pediatric cohort.儿科队列中基于人群的先天性心脏病治疗患病率。
Pediatr Cardiol. 2013 Mar;34(3):606-11. doi: 10.1007/s00246-012-0505-3. Epub 2012 Sep 14.
7
Sex ratio imbalance in transposition of the great arteries and possible agricultural environmental risk factors.大动脉转位中的性别比例失衡及可能的农业环境风险因素。
Images Paediatr Cardiol. 2001 Jul;3(3):10-4.
8
The contribution of chromosomal abnormalities to congenital heart defects: a population-based study.染色体异常对先天性心脏病的影响:一项基于人群的研究。
Pediatr Cardiol. 2011 Dec;32(8):1147-57. doi: 10.1007/s00246-011-0034-5. Epub 2011 Jul 5.
9
Increased prevalence of cardiovascular defects among 56,709 California twin pairs.加利福尼亚州56,709对双胞胎中心血管缺陷患病率上升。
Am J Med Genet A. 2009 May;149A(5):877-86. doi: 10.1002/ajmg.a.32745.
10
Getting to the heart of the matter: epidemiology of cyanotic heart defects.直击问题核心:青紫型先天性心脏病的流行病学
Pediatr Cardiol. 2008 May;29(3):484-97. doi: 10.1007/s00246-007-9185-9. Epub 2008 Jan 10.

本文引用的文献

1
Cardiac malformation in mongolism: a prospective study of 184 mongoloid children.蒙古症患儿的心脏畸形:对184名蒙古症儿童的前瞻性研究。
Am J Med. 1961 Nov;31:726-35. doi: 10.1016/0002-9343(61)90157-7.
2
The incidence of congenital heart disease in children born in Gothenburg 1941-1950.1941年至1950年在哥德堡出生儿童的先天性心脏病发病率。
Br Heart J. 1959 Jan;21(1):40-50. doi: 10.1136/hrt.21.1.40.
3
Congenital malformation in twins.双胞胎的先天性畸形
Am J Hum Genet. 1980 Jan;32(1):69-78.
4
Malformations in twins and their siblings, Norway, 1967-79.1967 - 1979年挪威双胞胎及其兄弟姐妹的畸形情况。
Acta Genet Med Gemellol (Roma). 1984;33(1):87-95. doi: 10.1017/s0001566000007558.
5
A Swedish register of congenital malformations. Experience with continuous registration during 2 years with special reference to multiple malformations.瑞典先天性畸形登记处。关于连续两年登记情况的经验,特别提及多发畸形。
Pediatrics. 1968 Apr;41(4):765-76.
6
Congenital heart disease: prevalence at livebirth. The Baltimore-Washington Infant Study.先天性心脏病:活产时的患病率。巴尔的摩-华盛顿婴儿研究。
Am J Epidemiol. 1985 Jan;121(1):31-6. doi: 10.1093/oxfordjournals.aje.a113979.
7
Congenital malformations in twins: a population study.
Acta Genet Med Gemellol (Roma). 1986;35(3-4):167-78. doi: 10.1017/s0001566000005687.
8
Search for teratogenic risks with the aid of malformation registries.
Teratology. 1987 Feb;35(1):47-52. doi: 10.1002/tera.1420350108.
9
Monitoring of congenital cardiac defects.先天性心脏缺陷的监测。
Pediatr Cardiol. 1987;8(4):247-56. doi: 10.1007/BF02427537.
10
Congenital cardiovascular malformations in twins and triplets from a population-based study.
Am J Dis Child. 1989 Dec;143(12):1461-3. doi: 10.1001/archpedi.1989.02150240083023.

1981 - 1986年瑞典主要先天性心脏缺陷的流行病学

Epidemiology of major congenital heart defects in Sweden, 1981-1986.

作者信息

Pradat P

机构信息

Department of Embryology, University of Lund, Sweden.

出版信息

J Epidemiol Community Health. 1992 Jun;46(3):211-5. doi: 10.1136/jech.46.3.211.

DOI:10.1136/jech.46.3.211
PMID:1645073
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1059552/
Abstract

STUDY OBJECTIVE

The aim was to make an epidemiological study of major congenital heart defects and to make comparisons between groups of heart defects regarding different epidemiological variables.

DESIGN

The cases with congenital heart defects were identified from two Swedish registries: the Registry of Congenital Malformations and the Child Cardiology Registry. A classification with nine groups of heart defects is proposed.

SETTING

This was a national survey in Sweden during the period 1981-1986. The total number of cases reported during the six years was 1605. Cases that presented a patent ductus arteriosus only and a birthweight below 2500 g were excluded.

MEASUREMENTS AND MAIN RESULTS

The prevalence at birth was 2.8 per 1000. When cases with a chromosomal anomaly were excluded, no maternal age effect was observed except a possible under-risk for women above 40 years. The risk for a heart defect seems to increase with increasing parity independent of age. A higher risk was also observed among twin infants compared with singletons although no specificity in cardiac malformation type appeared. Sex ratio, the tendency for having an associated extracardiac malformation, and the proportion of isolated v non-isolated cardiac defects differed between the different groups of heart malformations.

CONCLUSIONS

The differences observed between groups of defects indicate different aetiologies and show that this classification may be suitable for further analyses of congenital heart defects.

摘要

研究目的

旨在对主要先天性心脏缺陷进行流行病学研究,并就不同的流行病学变量对心脏缺陷组进行比较。

设计

先天性心脏缺陷病例来自两个瑞典登记处:先天性畸形登记处和儿童心脏病登记处。提出了一种将心脏缺陷分为九组的分类方法。

背景

这是一项1981 - 1986年期间在瑞典进行的全国性调查。六年期间报告的病例总数为1605例。仅患有动脉导管未闭且出生体重低于2500克的病例被排除。

测量与主要结果

出生时的患病率为每1000例中有2.8例。排除染色体异常病例后,未观察到母亲年龄的影响,除了40岁以上女性可能存在风险不足的情况。心脏缺陷的风险似乎随着产次增加而增加,与年龄无关。与单胎婴儿相比,双胎婴儿中观察到的风险也更高,尽管心脏畸形类型没有特异性。不同心脏畸形组之间的性别比例、伴有心外畸形的倾向以及孤立性与非孤立性心脏缺陷的比例有所不同。

结论

不同缺陷组之间观察到的差异表明病因不同,并表明这种分类可能适用于先天性心脏缺陷的进一步分析。