Pradat P
Department of Embryology, University of Lund, Sweden.
J Epidemiol Community Health. 1992 Jun;46(3):211-5. doi: 10.1136/jech.46.3.211.
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.
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.
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.
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.
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.
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。
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。
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。
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。
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。