Mothers’ Internet Journeys Through Social, Health Care, and Virtual Systems When Congenital Anomalies Are Diagnosed In Utero

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Abstract

Objective

To examine mothers’ internet usage, in conjunction with social, health care, and virtual peer support navigations, when congenital anomalies were diagnosed in utero.

Design

Qualitative descriptive, consisting of semistructured interviews.

Setting

Interview data were collected over Zoom; mothers participated from locations of their choosing.

Participants

Mothers of neonates discharged postoperatively from NICUs for uterine-diagnosed congenital anomalies. The sample was purposefully recruited from private Facebook groups for parents of children with congenital anomalies.

Intervention/Measurements

Analysis was done with deductive coding using concepts from the third iteration of the systems engineering initiative for patient safety theory. The a priori codes were health care, social, journey–benefit, journey–risk, task, and technology.

Results

Twenty-two mothers signed up for an interview; 12 completed an interview, and 10 did not. The majority (n = 8, 66%) were White, had a bachelor’s or graduate degree (n = 7, 58%) and were between 24 and 33 years of age (n = 8, 66%). Nine themes emerged: (a) Providers cautioned searching for diagnosis information but encouraged private Facebook groups for peer support, (b) Mothers’ inquiries for their own care are lacking, (c) Search for information while recognizing parent-partner’s coping differences, (d) Pace information from friends and family with patience and appreciation, (e) Manage inquiries from friends and family with group sharing, (f) Private Facebook groups provide a means of receiving and giving peer support, (g) Exposure to difficult stories on Facebook is a risk of stress, (h) Select a NICU, learn about their children’s diagnoses, participate in virtual peer support, and (i) Device features frame search strategies.

Conclusion

Mothers reflected on the internet as a burden and a source of support in their health care journeys. The ubiquity of internet access calls for mothers to include in their health care journeys the complexities of managing time spent on the internet.

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当先天性畸形在子宫内确诊时,母亲通过社会、医疗保健和虚拟系统进行的互联网之旅。
目的研究母亲在子宫内诊断出先天性畸形时,结合社交、医疗保健和虚拟同伴支持导航使用互联网的情况:设计:定性描述,包括半结构式访谈:访谈数据通过 Zoom 收集;母亲们在自己选择的地点参与访谈:因子宫诊断出先天性畸形而从新生儿重症监护室术后出院的新生儿的母亲。样本特意从先天性畸形患儿家长的私人 Facebook 群组中招募:分析采用演绎编码法,使用患者安全系统工程倡议理论中的概念。先验编码为医疗保健、社会、旅程-收益、旅程-风险、任务和技术:22 位母亲报名参加了访谈;12 位完成了访谈,10 位未完成。大多数(n = 8,66%)为白人,拥有学士或研究生学位(n = 7,58%),年龄在 24 至 33 岁之间(n = 8,66%)。共出现了九个主题(a) 医疗服务提供者提醒人们搜索诊断信息,但鼓励在 Facebook 私人群组中寻求同伴支持;(b) 缺乏母亲对自身护理的咨询;(c) 在搜索信息的同时,认识到父母与伴侣在应对方面的差异;(d) 耐心和欣赏地对待来自朋友和家人的信息、(e) 通过群组共享来管理亲友的询问;(f) Facebook 私人群组提供了接受和给予同伴支持的途径;(g) 在 Facebook 上接触困难的故事有可能造成压力;(h) 选择新生儿重症监护室,了解子女的诊断,参与虚拟同伴支持;(i) 设备功能限制了搜索策略。结论母亲们认为,在她们的医疗保健旅程中,互联网既是一种负担,也是一种支持。互联网无处不在,这就要求母亲们在其健康护理旅程中考虑到管理上网时间的复杂性。
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来源期刊
Nursing for Women''s Health
Nursing for Women''s Health Nursing-Nursing (all)
CiteScore
2.10
自引率
0.00%
发文量
90
期刊介绍: Nursing for Women"s Health publishes the most recent and compelling health care information on women"s health, newborn care and professional nursing issues. As a refereed, clinical practice journal, it provides professionals involved in providing optimum nursing care for women and their newborns with health care trends and everyday issues in a concise, practical, and easy-to-read format.
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