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印度一家三级保健中心唐氏综合征队列的生存分析。

Survival analysis of Down syndrome cohort in a tertiary health care center in India.

机构信息

Center of Medical Genetics, Sir Ganga Ram Hospital, Rajinder Nagar, 110060, New Delhi, India.

出版信息

Indian J Pediatr. 2013 Feb;80(2):118-23. doi: 10.1007/s12098-012-0836-3. Epub 2012 Jul 26.

Abstract

OBJECTIVE

To identify the major causes of death in Down Syndrome (DS), the ages at which mortality rates are the highest and recognize factors associated with it.

METHODS

The prospective cohort-based study was carried out in a tertiary health care center. Children with DS (n = 543) counseled at the Center of Medical Genetics, Sir Ganga Ram Hospital from 2005 through 2009 were followed up in year 2010. Survival curves and Cox's proportional hazards regression analysis were used to determine the effect of different variables on survival.

RESULTS

Total mortality was 13 %, of which 80.3 % was in children less than 2 y of age. Presence of congenital heart disease (CHD) increased the risk of mortality by 5.7 folds (p = 0.001). A definitive survival benefit after cardiac intervention was noted, although it differed with the type of CHD. Sex, maternal age at time of birth and karyotypes did not show a significant correlation with survival.

CONCLUSIONS

The higher DS infant mortality observed in the present study could be attributed to financial constraints of the families and misconceptions amongst health professionals. It is recommended that a nation-wide DS registry be created to study the morbidity and mortality in Down syndrome from birth. The findings of this study will help clinicians in making management decisions and enable better counseling.

摘要

目的

确定唐氏综合征(DS)患者的主要死亡原因、死亡率最高的年龄,并识别与之相关的因素。

方法

本研究为前瞻性队列研究,在一家三级保健中心开展。2005 年至 2009 年在 Sir Ganga Ram 医院医学遗传学中心接受咨询的唐氏综合征患儿(n=543)于 2010 年进行随访。采用生存曲线和 Cox 比例风险回归分析来确定不同变量对生存的影响。

结果

总死亡率为 13%,其中 80.3%发生在 2 岁以下儿童。先天性心脏病(CHD)的存在使死亡率增加了 5.7 倍(p=0.001)。尽管不同类型的 CHD 有所不同,但心脏干预后确实有明确的生存获益。性别、患儿母亲出生时的年龄和核型与生存无显著相关性。

结论

本研究中观察到的唐氏综合征婴儿死亡率较高可能归因于家庭的经济限制和卫生专业人员的误解。建议建立全国性的唐氏综合征登记处,以研究唐氏综合征从出生到死亡的发病率和死亡率。本研究的结果将有助于临床医生做出管理决策,并提供更好的咨询服务。

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