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[托斯卡纳地区登记处(意大利中部托斯卡纳大区)1992 - 2009年先天性心脏缺陷的患病率、死亡率和致死率]

[Prevalence, mortality and lethality of congenital heart defects from the Tuscan Registry (Tuscany Region, Central Italy), 1992-2009].

作者信息

Baldacci Silvia, Pierini Anna, Santoro Michele, Spadoni Isabella, Bianchi Fabrizio

机构信息

Unità di epidemiologia ambientale e registri di patologia, Istituto di fisiologia clinica, Consiglio nazionale delle ricerche, Pisa.

出版信息

Epidemiol Prev. 2015 Jan-Feb;39(1):36-44.

Abstract

OBJECTIVES

to estimate prevalence, mortality and lethality of congenital heart defects (CHDs), and to evaluate time trend by comparing two birth cohorts (1992- 2000 vs. 2001-2009).

DESIGN

descriptive study using a population-based registry: the Tuscan Registry of congenital defects (RTDC), which is a member of the European network of surveillance of congenital anomalies (EUROCAT) since 1979.

SETTING AND PARTICIPANTS

CHD cases were collected by the RTDC between 1992 and 2009.

MAIN OUTCOME MEASURES

prevalence and mortality rates were calculated for all and non-chromosomal CHDs. The non-chromosomal cases were classified in three severity classes (SI, SII, SIII), according to decreasing perinatal mortality. It was estimated prevalence of: live births, foetal deaths (stillbirths and spontaneous abortions from 20 weeks gestation), terminations of pregnancy for foetal anomaly (TOPFAs) at any gestational age, and of prenatally diagnosed cases. Perinatal, neonatal and infant mortality were calculated. Early-neonatal, neonatal and infant lethality were calculated for the non-chromosomal cases.

RESULTS

3,653 cases were identified out of 486,947 live births and 1,883 stillbirths, 95% of which were non-chromosomal cases. The total average prevalence was 7.47/1,000 births. The overall prevalence decreased significantly in all CHDs (Prevalence ratio - PR: 0.86; 95%CI 0.80-0.91) as well as in non-chromosomal (PR: 0.86; 95%CI 0.80-0.92), while in the more severe defects (SI/SII combined cases) the total prevalence was stable over time. In more severe cases, prevalence of live births decreased significantly (PR: 0.83; 95%CI 0.71-0.97), while the greater increase of TOPFAs and of diagnosed cases was observed in the prenatal period. All three mortality rates reduced significantly over time. In the more severe cases, the greatest rate mortality reduction was observed for neonatal mortality (Mortality ratio - MR: 0.29; 95%CI 0.16-0.49) than perinatal (MR: 0.37; 95%CI 0.19-0.70) and infant mortality (MR: 0,40; 95%CI 0.28-0.56). In this group of CHDs, early neonatal lethality decreased from 10% to 3%, neonatal lethality from 17% to 6%, and infant lethality from 24% to 10%.

CONCLUSIONS

the results suggest that the improvements in prenatal diagnosis and in foetal and neonatal treatment and care have reduced the burden of congenital heart defects on the health of the Tuscany population.

摘要

目的

估算先天性心脏病(CHD)的患病率、死亡率和致死率,并通过比较两个出生队列(1992 - 2000年与2001 - 2009年)评估时间趋势。

设计

使用基于人群的登记系统进行描述性研究:托斯卡纳先天性缺陷登记处(RTDC),自1979年起成为欧洲先天性异常监测网络(EUROCAT)的成员。

设置和参与者

RTDC在1992年至2009年间收集CHD病例。

主要观察指标

计算所有CHD和非染色体CHD的患病率和死亡率。非染色体病例根据围产期死亡率的降低分为三个严重程度等级(SI、SII、SIII)。估算以下情况的患病率:活产、胎儿死亡(死产和妊娠20周后的自然流产)、任何孕周的胎儿异常妊娠终止(TOPFA)以及产前诊断病例。计算围产期、新生儿和婴儿死亡率。计算非染色体病例的早期新生儿、新生儿和婴儿致死率。

结果

在486,947例活产和1,883例死产中识别出3,653例病例,其中95%为非染色体病例。总平均患病率为7.47/1000例出生。所有CHD以及非染色体CHD的总体患病率均显著下降(患病率比值 - PR:0.86;95%置信区间0.80 - 0.91),而在更严重的缺陷(SI/SII合并病例)中,总体患病率随时间保持稳定。在更严重的病例中,活产患病率显著下降(PR:0.83;95%置信区间0.71 - 0.97),而在产前阶段观察到TOPFA和诊断病例的增加幅度更大。所有三种死亡率均随时间显著降低。在更严重的病例中,新生儿死亡率的下降幅度最大(死亡率比值 - MR:0.29;95%置信区间0.16 - 0.49),高于围产期(MR:0.37;95%置信区间0.19 - 0.70)和婴儿死亡率(MR:0.40;95%置信区间0.28 - 0.56)。在这组CHD中,早期新生儿致死率从10%降至3%,新生儿致死率从17%降至6%,婴儿致死率从24%降至10%。

结论

结果表明,产前诊断以及胎儿和新生儿治疗与护理的改善减轻了先天性心脏病对托斯卡纳人群健康的负担。

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