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1994-2009 年,挪威唐氏综合征患儿的五年生存率因伴发的先天性心脏缺陷和心脏外畸形而有所不同。

The five-year survival of children with Down syndrome in Norway 1994-2009 differed by associated congenital heart defects and extracardiac malformations.

机构信息

Department of Global Public Health and Primary Care, Faculty of Medicine, University of Bergen, Bergen, Norway.

Department of Paediatrics, Haukeland University Hospital, Bergen, Norway.

出版信息

Acta Paediatr. 2018 May;107(5):845-853. doi: 10.1111/apa.14223. Epub 2018 Feb 7.

Abstract

AIM

We investigated the prevalence of Down syndrome in a nationwide birth cohort, focusing on congenital heart defects (CHDs), their associations with extracardiac malformations (ECM) and survival.

METHODS

National registers were used to identify Norwegian births (1994-2009) and deaths (1994-2014) and updated with hospital diagnoses. We estimated birth defect frequencies in Down syndrome and the general population, the association between CHDs and ECM and hazard ratios for death from different combinations of CHDs and ECM.

RESULTS

Down syndrome was found in 1672 of 953 450 births (17.6 per 10 000). Of the 1251 live births (13.3 per 10 000), 58% had CHD and 9% ECM. CHDs were associated with oesophageal atresia (p = 0.02) and Hirschsprung's disease (p = 0.03) but with no other malformations. The five-year survival for Down syndrome increased from 91.8% (1994-1999) to 95.8% (2000-2009) (p = 0.006), and overall survival was 92.0% with CHD and 97.4% without. Compared with Down syndrome children without CHD or ECM, the five-year mortality was similar for those with nonsevere CHDs, without or with ECM, but 4-7 times higher in those with severe CHDs without ECM and 13-28 times higher in those with severe CHDs and ECM.

CONCLUSION

Down syndrome childhood survival improved, but mortality remained high with severe CHDs and extracardiac defects.

摘要

目的

我们调查了全国性出生队列中唐氏综合征的患病率,重点关注先天性心脏病(CHD)及其与心脏外畸形(ECM)的关联和生存率。

方法

国家登记处用于识别挪威出生(1994-2009 年)和死亡(1994-2014 年)情况,并通过医院诊断进行更新。我们估计唐氏综合征和普通人群中的出生缺陷频率、CHD 和 ECM 之间的关联,以及不同 CHD 和 ECM 组合的死亡风险比。

结果

在 953450 例出生中发现了 1672 例唐氏综合征(每 10000 例 17.6 例)。在 1251 例活产中(每 10000 例 13.3 例),58%患有 CHD,9%患有 ECM。CHD 与食管闭锁(p = 0.02)和先天性巨结肠(p = 0.03)相关,但与其他畸形无关。唐氏综合征的五年生存率从 1994-1999 年的 91.8%增加到 2000-2009 年的 95.8%(p = 0.006),总生存率为 CHD 为 92.0%,无 CHD 或 ECM 为 97.4%。与无 CHD 或 ECM 的唐氏综合征患儿相比,非严重 CHD 且无或伴有 ECM 的患儿五年死亡率相似,但无 ECM 的严重 CHD 患儿死亡率高 4-7 倍,伴有 ECM 的严重 CHD 患儿死亡率高 13-28 倍。

结论

唐氏综合征儿童的生存率有所提高,但严重 CHD 和心脏外缺陷的死亡率仍然很高。

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