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将主要出生缺陷家族史报告作为一种公共卫生策略的效用。

Utility of family history reports of major birth defects as a public health strategy.

作者信息

Romitti Paul A

机构信息

Department of Epidemiology, C21-E GH, 200 Hawkins Dr, University of Iowa, Iowa City, IA 52242, USA.

出版信息

Pediatrics. 2007 Sep;120 Suppl 2:S71-7. doi: 10.1542/peds.2007-1010F.

Abstract

A major birth defect is an abnormality that can affect the structure or function of an organ. In the United States, major birth defects are the leading cause of infant mortality and contribute substantially to childhood disability and morbidity. Globally, these conditions lead to the death of millions of infants and children annually. Patients with 1 or more affected family members may be at increased risk for having a child with a major birth defect; thus, accurate knowledge of these conditions among family members of their patients gives the clinician the ability to provide improved risk assessment and reproductive planning. Such knowledge can also serve as motivation for patients to adhere to healthy behaviors such as folic acid use or smoking cessation. To evaluate the utility of collecting family history reports of major birth defects as a public health strategy, 6 key criteria were examined by reviewing the relevant published literature. Overall, the review showed that major birth defects satisfied several of the criteria. Additional research is needed, however, regarding the awareness of parent reports of the occurrence of these conditions among relatives and how knowledge of birth defect diagnoses and related risk factors are transmitted among relatives. Such research needs to encompass not only immediate family members but also other first-degree and second-degree relatives. In summary, routine collection of family history reports of birth defects in pediatric practice holds promise as a public health strategy to reduce the burden of morbidity, mortality, and disability associated with major birth defects.

摘要

严重出生缺陷是一种可影响器官结构或功能的异常情况。在美国,严重出生缺陷是婴儿死亡的主要原因,并且在很大程度上导致儿童残疾和发病。在全球范围内,这些情况每年导致数百万婴儿和儿童死亡。有一名或多名受影响家庭成员的患者生育患有严重出生缺陷孩子的风险可能会增加;因此,临床医生了解患者家庭成员对这些情况的准确信息,有助于提供更好的风险评估和生育规划。这些信息还可以激励患者坚持健康行为,如使用叶酸或戒烟。为了评估收集严重出生缺陷家族史报告作为一项公共卫生策略的效用,通过查阅相关已发表文献对6项关键标准进行了审查。总体而言,审查表明严重出生缺陷符合其中几项标准。然而,关于亲属对这些情况发生的父母报告的知晓情况,以及出生缺陷诊断和相关风险因素的知识在亲属之间如何传播,还需要进一步研究。此类研究不仅需要涵盖直系家庭成员,还需要包括其他一级和二级亲属。总之,在儿科实践中常规收集出生缺陷家族史报告有望成为一项公共卫生策略,以减轻与严重出生缺陷相关的发病、死亡和残疾负担。

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