A review of key terminology and definitions used for birth defects globally.

IF 1.5 Q4 GENETICS & HEREDITY Journal of Community Genetics Pub Date : 2023-06-01 Epub Date: 2023-04-24 DOI:10.1007/s12687-023-00642-2
H L Malherbe, B Modell, H Blencowe, K L Strong, C Aldous
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Abstract

Birth defects, also known as congenital disorders, are a significant health issue impacting at least five million births annually worldwide. For policymakers to mount a relevant healthcare response to care for those affected, the burden of disease of these conditions must be quantified. Estimates of the contribution of birth defects to under-5 child mortality and morbidity are generated by several groups globally. These estimates often differ, causing confusion for policymakers. While some differences may be attributed to the data sources and methods used, much is due to a lack of clarity in the terminology used for the group of disorders classed as "congenital". This study aimed to gain insight into the diversity of terms and definitions for birth defects, including those used routinely by relevant international/national organisations and in the peer-reviewed literature. This two-part study included (1) scoping review of peer-reviewed literature to identify terms and definitions in use for birth defects and (2) review of key websites and grey literature to identify terms and definitions used. The results of this study indicate a wide variety of terms being used, often interchangeably and undefined, in peer-reviewed publications, on institutional websites and related literature. This suggests a lack of clarity related to terminology and sets the scene for further discussion, recommending that the community of practice working on birth defects comes to a consensus on standard terminology and definitions for global uptake and implementation. Such standardisation will facilitate a common understanding of the burden of these disorders globally, regionally and within countries so that action can be taken to support affected children and their families.

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全球出生缺陷关键术语和定义回顾。
出生缺陷(又称先天性疾病)是一个重大的健康问题,每年影响全球至少 500 万新生儿。为了让政策制定者采取相应的医疗对策来照顾受影响的人群,必须对这些疾病造成的疾病负担进行量化。全球有多个团体对出生缺陷造成的 5 岁以下儿童死亡率和发病率进行了估计。这些估计值往往各不相同,给政策制定者造成困惑。虽然有些差异可能是由于数据来源和使用的方法不同造成的,但很大程度上是由于被归类为 "先天性 "疾病的术语不够清晰。本研究旨在深入了解出生缺陷术语和定义的多样性,包括相关国际/国家组织和同行评审文献中常规使用的术语和定义。这项研究由两部分组成,包括:(1)对同行评议文献进行范围界定,以确定出生缺陷的常用术语和定义;(2)对主要网站和灰色文献进行评议,以确定所用术语和定义。研究结果表明,在同行评议出版物、机构网站和相关文献中使用的术语种类繁多,而且往往相互替换,没有定义。这表明术语缺乏明确性,为进一步讨论创造了条件,建议从事出生缺陷工作的业界就标准术语和定义达成共识,以便在全球范围内推广和实施。这种标准化将有助于在全球、地区和国家内部对这些疾病造成的负担达成共识,从而采取行动为受影响的儿童及其家庭提供支持。
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来源期刊
Journal of Community Genetics
Journal of Community Genetics GENETICS & HEREDITY-
CiteScore
3.30
自引率
5.30%
发文量
54
期刊介绍: The Journal of Community Genetics is an international forum for research in the ever-expanding field of community genetics, the art and science of applying medical genetics to human communities for the benefit of their individuals. Community genetics comprises all activities which identify persons at increased genetic risk and has an interest in assessing this risk, in order to enable those at risk to make informed decisions. Community genetics services thus encompass such activities as genetic screening, registration of genetic conditions in the population, routine preconceptional and prenatal genetic consultations, public education on genetic issues, and public debate on related ethical issues. The Journal of Community Genetics has a multidisciplinary scope. It covers medical genetics, epidemiology, genetics in primary care, public health aspects of genetics, and ethical, legal, social and economic issues. Its intention is to serve as a forum for community genetics worldwide, with a focus on low- and middle-income countries. The journal features original research papers, reviews, short communications, program reports, news, and correspondence. Program reports describe illustrative projects in the field of community genetics, e.g., design and progress of an educational program or the protocol and achievement of a gene bank. Case reports describing individual patients are not accepted.
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