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父母使用互联网对新生儿筛查阳性的婴儿进行检查。

Internet use by parents of infants with positive newborn screens.

机构信息

University of Rochester, School of Nursing, 601 Elmwood Ave, Box SON, Rochester, NY 14642, USA.

出版信息

J Inherit Metab Dis. 2012 Sep;35(5):879-84. doi: 10.1007/s10545-011-9449-7. Epub 2012 Feb 2.

DOI:10.1007/s10545-011-9449-7
PMID:22297410
Abstract

BACKGROUND

Internet searches on health topics are common, but not enough is known about online use during serious health concerns. The aim of this study was to investigate parents' internet use and responses to online information following the referral of their newborn screen-positive infants.

METHODS

Forty-four parents were interviewed about their internet use during their infants' evaluations for a potential metabolic disorder. Responses to open-ended questions were audio taped and transcribed. Content analysis was used in analyzing the interview data.

RESULTS

An overwhelming majority of parents (89%) accessed the internet and most went online before meeting with genetic providers at metabolic treatment centers. Primary and genetic providers did not routinely recommend websites to parents. Online descriptions of metabolic disorders increased parents' anxieties. Some parents allayed their distress by enlisting others to search and filter information for them and by seeking optimistic internet content about the disorders. Parents with fewer years of education were often baffled by complex disease information. Parents found limited information about treatments or what to expect during the clinical evaluations of their infants.

CONCLUSIONS

The internet is an integral part of health care and an important source of information for newborn screening parents. Parents may benefit from recommendations of credible websites and discussions of internet information with health care providers.

摘要

背景

人们经常在互联网上搜索健康相关的话题,但对于在面临严重健康问题时如何在线使用信息,我们知之甚少。本研究旨在调查父母在其新生儿筛查阳性婴儿接受评估期间的互联网使用情况和对在线信息的反应。

方法

44 名父母接受了关于其婴儿可能患有代谢紊乱的评估期间互联网使用情况的访谈。对开放式问题的回答进行了录音和转录。采用内容分析法对访谈数据进行分析。

结果

绝大多数父母(89%)上网,大多数人在代谢治疗中心与遗传医生见面之前就上网了。初级和遗传医生通常不会向父母推荐网站。在线描述代谢紊乱会增加父母的焦虑。一些父母通过寻求他人为他们搜索和筛选信息,并寻找有关疾病的乐观网络内容来减轻他们的痛苦。受教育年限较少的父母常常对复杂的疾病信息感到困惑。父母在其婴儿的临床评估期间发现有关治疗方法或预期的信息有限。

结论

互联网是医疗保健的重要组成部分,也是新生儿筛查父母获取信息的重要来源。父母可能会受益于获得可信网站的推荐以及与医疗保健提供者讨论网络信息。

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