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父母对有关其子女医学诊断知识的需求。

Parents' needs for knowledge concerning the medical diagnosis of their children.

作者信息

Starke Mikaela, Möller Anders

机构信息

Department of Social Work, Göteborg Pediatric Growth Research Center, Sahlgrenska Academy of Göteborg University, Sweden.

出版信息

J Child Health Care. 2002 Dec;6(4):245-57. doi: 10.1177/136749350200600402.

Abstract

It is reported that parents can handle their reactions of having a child with a chronic illness by seeking information and gaining knowledge about the diagnosis. It has been suggested that this is a way for parents to restore order in a chaotic existence. A complement to this perspective is to focus on what it means to be a parent and what is included in parenthood. The purpose of the present study was to increase our understanding of parents' need for knowledge. Interviews were conducted with parents (n = 44) who have experienced receiving a diagnosis of Turner Syndrome (TS) for their daughter, in order to explore the parents' motives and strategies for seeking information about the condition. Out of the 44 parents interviewed, 26 (21 mothers and 5 fathers) had sought information. It was found that the motives for seeking information were, to some extent, related to the parents' experiences of the consultation at the time of diagnosis. Twenty-three parents (21 mothers and 2 fathers) were dissatisfied with the information provided by the physician, while 21 (12 mothers and 9 fathers) were satisfied. Among the dissatisfied parents 16 (15 mothers and 1 father) sought information, and among the satisfied 10 parents (6 mothers and 4 fathers) sought information when they received the diagnosis for their daughter. The mothers described different strategies to gain information. They attended the library to borrow medical literature, looked up the syndrome in reference books, read articles in newspapers and asked questions of other mothers who had daughters with TS. However, it was found that the dissatisfied mothers used more and different strategies to find information compared with the fathers and the mothers who were satisfied. The motives of all the parents were to learn more about the condition. However, the dissatisfied mothers reported that they sought information because they found it important to control the actions of the professionals. The mothers that were satisfied with the information argued that they sought information in order to be able to explain the condition to others.

摘要

据报道,父母可以通过寻求信息和了解诊断情况来应对孩子患有慢性病的反应。有人认为,这是父母在混乱生活中恢复秩序的一种方式。对这一观点的补充是关注作为父母意味着什么以及为人父母包含哪些内容。本研究的目的是增进我们对父母知识需求的理解。对那些女儿被诊断患有特纳综合征(TS)的父母(n = 44)进行了访谈,以探讨父母寻求该病症信息的动机和策略。在接受访谈的44位父母中,有26位(21位母亲和5位父亲)寻求了信息。结果发现,寻求信息的动机在一定程度上与父母在诊断时的咨询经历有关。23位父母(21位母亲和2位父亲)对医生提供的信息不满意,而21位(12位母亲和9位父亲)表示满意。在不满意的父母中,有16位(15位母亲和1位父亲)寻求了信息,在满意的父母中,有10位(6位母亲和4位父亲)在女儿被诊断时寻求了信息。母亲们描述了获取信息的不同策略。她们去图书馆借阅医学文献,在参考书中查找该综合征,阅读报纸上的文章,并向其他有患TS女儿的母亲提问。然而,发现与父亲和满意的母亲相比,不满意的母亲使用了更多且不同的策略来获取信息。所有父母的动机都是更多地了解病情。然而,不满意的母亲报告说,她们寻求信息是因为她们觉得控制专业人员的行为很重要。对信息满意的母亲则认为,她们寻求信息是为了能够向他人解释病情。

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