Pangkanon Suthipong, Sawasdivorn Siraporn, Kuptanon Chulaluck, Chotigeat Uraiwan, Vandepitte Warunee
J Med Assoc Thai. 2014 Jun;97 Suppl 6:S182-8.
Deaths attributed to birth defects are a major cause of infant and under-five mortality as well as lifetime disabilities among those who survive. In Thailand, birth defects contribute to 21% of neonatal deaths. There is currently no systematic registry for congenital anomalies in Thailand. Queen Sirikit National Institute of Child Health has initiated a Thailand Birth Defects Registry to capture birth defects among newborn infants.
To establish the national birth defects registry in order to determine the burden of birth defects in Thailand.
The birth defects data come from four main sources: National Birth Registry Database; National Health Security Office's reimbursement database; Online Birth Defect Registry Database designed to capture new cases that were detected later; and birth defects data from 20 participated hospitals. All data are linked by unique 13-digit national identification number and International Classification of Diseases (ICD)-10 codes. This registry includes 19 common structural birth defects conditions and pilots in 20 hospitals. The registry is hospital-based, hybrid reporting system, including only live births whose information was collected up to 1 year of age.
3,696 infants out of 67,813 live births (8.28% of total live births in Thailand) were diagnosed with congenital anomalies. The prevalence rate of major anomalies was 26.12 per 1,000 live births. The five most common birth defects were congenital heart defects, limb anomalies, cleft lip/cleft palate, Down syndrome, and congenital hydrocephalus respectively.
The present study established the Birth Defects Registry by collecting data from four databases in Thailand. Information obtained from this registry and surveillance is essential in the planning for effective intervention programs for birth defects. The authors suggest that this program should be integrated in the existing public health system to ensure sustainability.
出生缺陷导致的死亡是婴儿和五岁以下儿童死亡的主要原因,也是幸存者终身残疾的主要原因。在泰国,出生缺陷导致21%的新生儿死亡。泰国目前没有先天性异常的系统登记处。诗丽吉王后国家儿童健康研究所已启动泰国出生缺陷登记处,以记录新生儿中的出生缺陷情况。
建立国家出生缺陷登记处以确定泰国出生缺陷的负担。
出生缺陷数据来自四个主要来源:国家出生登记数据库;国家健康保险办公室的报销数据库;旨在收集后来发现的新病例的在线出生缺陷登记数据库;以及来自20家参与医院的出生缺陷数据。所有数据通过唯一的13位数字国家识别号和国际疾病分类(ICD)-10编码进行链接。该登记处包括19种常见的结构性出生缺陷情况,并在20家医院进行试点。该登记处是基于医院的混合报告系统,仅包括信息收集至1岁的活产儿。
在67813例活产儿中,有3696例(占泰国活产儿总数的8.28%)被诊断患有先天性异常。主要异常的患病率为每1000例活产儿26.12例。最常见的五种出生缺陷分别是先天性心脏病、肢体异常、唇腭裂、唐氏综合征和先天性脑积水。
本研究通过收集泰国四个数据库的数据建立了出生缺陷登记处。从该登记处和监测中获得的信息对于规划有效的出生缺陷干预项目至关重要。作者建议该项目应纳入现有的公共卫生系统以确保可持续性。