探索患有先天性心脏病的年轻女性在青春期的生活经历:使用焦点小组的定性女性主义研究

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Health Expectations Pub Date : 2024-09-18 DOI:10.1111/hex.14179
Anna Tylek, Charlotte Summers, Ellen Maulder, Lindsay Welch, Lynn Calman
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引用次数: 0

摘要

目标 本研究的总体目标是探索、研究和确定患有先天性心脏病的年轻女性在从青春期向成年期过渡时所面临的经历。 设计 这是一项实证定性研究,以三个焦点小组的形式进行。研究设计和分析采用了女性主义本体论的定位,以阐明女性的声音,并提供心脏病医疗保健的另一种视角。根据研究目的,采用归纳式主题方法对数据进行分析。 参与者 研究对象包括英国的七名女性参与者(平均年龄 26 岁),她们在成长过程中均患有不同程度的先天性心脏缺陷,需要进行开胸手术。 结果 出现了三个具有前因概念的关键主题:(a) 在医疗和社会文化背景下,女性身份和母亲身份对患有先天性心脏病的年轻女性自身在青春期过渡期的潜在影响;(b) 作为一名女性,在青春期接受心脏手术对年轻女性术前、术中和术后健康的挑战;(c) 现有的在线/离线医疗保健和社会结构对女性在青春期过渡期健康的影响。 结论 本研究建立在对年轻女性和患有心脏疾病的有限探索基础之上,证实了作为一名正处于青春期的年轻女性,在患有心脏疾病的过程中存在脆弱性和挑战。这是由性别(生物特征)和性别因素(社会角色)造成的。这导致了对心理健康的短期和长期影响。这项研究表明,需要加强为患有慢性阻塞性肺病的年轻女性提供护理和心理支持。这将有助于使女性在医疗进步带来的预期寿命延长之外,获得良好的生活质量。 患者或公众的贡献 积极的参与者参与对于确保研究中真实的女性声音至关重要。这项研究得到了患有先天性心脏病的年轻女性的支持。年轻女性为研究设计、参与者招募和结果分析做出了贡献。其中两名女性还是本文的共同作者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Exploring the Lived Experiences of Young Women With Congenital Heart Disease Through Adolescence: A Qualitative Feminist Study Using Focus Groups

Objectives

The overarching aim of this study is to explore, examine and identify the experience that young women with congenital heart disease face as they transition through adolescence into womanhood.

Design

This is an empirical qualitative study conducted in the form of three focus groups. The study design and analysis adopted a feminist ontological positioning to elucidate the voice of women and offer an alternative perspective of cardiology health care. Data were analysed using the inductive thematic approach informed by the study aims.

Participants

A group of seven female participants (mean age 26) based in the United Kingdom, each with varying degrees of congenital heart defects that required open heart surgery growing up, was included in the study.

Results

Three key themes with antecedent concepts emerged: (a) the impact of womanhood and the potential influence of motherhood on the young women themselves transitioning through adolescence with CHD within medical and sociocultural contexts, (b) the challenges of being a woman and undergoing heart surgery during adolescence on the young women's health before, during and after surgery and (c) the effect of existing online/offline healthcare and social structures on women's health during transitioning through adolescence These themes were encompassed under an overarching theme of psychological complexities developed throughout the cardiac journey from diagnosis through to post-surgery.

Conclusion

This study built on the limited exploration of being a young woman and having CHD and confirmed that there are vulnerabilities and challenges in having CHD as a young woman transitioning through adolescence. This was a result of sex (biological characteristics) and gender factors (socially constructed roles). This leads to short- and long-term implications on psychological well-being. This research indicates that enhancements are needed in the provision of care and psychological support for young women with CHD. This will help to enable women to achieve a good quality of life in addition to increased life expectancy offered by medical advancements.

Patient or Public Contribution

Active participant involvement was crucial to ensure the authentic female voice in the study. This study received support from young women with congenital heart disease. Young women contributed to the study design, recruitment of participants and analysis of results. Two of the women were also co-authors of this paper.

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来源期刊
Health Expectations
Health Expectations 医学-公共卫生、环境卫生与职业卫生
CiteScore
5.20
自引率
9.40%
发文量
251
审稿时长
>12 weeks
期刊介绍: Health Expectations promotes critical thinking and informed debate about all aspects of patient and public involvement and engagement (PPIE) in health and social care, health policy and health services research including: • Person-centred care and quality improvement • Patients'' participation in decisions about disease prevention and management • Public perceptions of health services • Citizen involvement in health care policy making and priority-setting • Methods for monitoring and evaluating participation • Empowerment and consumerism • Patients'' role in safety and quality • Patient and public role in health services research • Co-production (researchers working with patients and the public) of research, health care and policy Health Expectations is a quarterly, peer-reviewed journal publishing original research, review articles and critical commentaries. It includes papers which clarify concepts, develop theories, and critically analyse and evaluate specific policies and practices. The Journal provides an inter-disciplinary and international forum in which researchers (including PPIE researchers) from a range of backgrounds and expertise can present their work to other researchers, policy-makers, health care professionals, managers, patients and consumer advocates.
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