Women's Menopausal Experiences in the UK: A Systemic Literature Review of Qualitative Studies

IF 3.2 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Health Expectations Pub Date : 2025-01-29 DOI:10.1111/hex.70167
Ailin Anto, Arunima Basu, Rania Selim, Andreas B. Eisingerich
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Abstract

Background

Menopause, defined as the cessation of periods for over 12 months, can have a profound impact on women in numerous ways. Understanding women's experiences of menopause can lead to improved care and support during this transformative period.

Objectives

The objective of this systematic review is to identify and summarise published qualitative studies that consider the lived experiences of women with menopause in the UK and to serve as a basis for future research in the field of menopause.

Search Strategy

EMBASE, MEDLINE and PsycINFO databases were searched initially in March, and then updated in April 2024.

Inclusion Criteria

Peer-reviewed papers with full text available in English, focused on women experiencing menopause in the UK, studies published from January 2000 to April 2024, qualitative or mixed methods study design with qualitative analysis.

Data Extraction and Synthesis

Two authors independently performed title and abstract screening for eligibility. Conflicting opinions were resolved with a third author. Reviewers familiarised themselves with the data and coded the text line by line. Thematic analysis was utilised to place the codes into broader themes. All studies were assessed using an appropriate quality assessment tool.

Main Results

Thirty-two studies were included in the review with 3462 participants involved. 173 primary codes were extracted and organised into subthemes and 3 overarching themes. These key themes were the biopsychosocial dimensions of menopause, understanding of menopause and strategies to manage menopause.

Discussion

Menopausal experiences documented in the literature are shaped by a range of individual and societal factors. While initiatives to support menopausal women are in place, this review also identifies key knowledge gaps and marginalised groups that would benefit from targeted research and interventions. It emphasises that menopause is not merely a collection of symptoms, but, for many, a pivotal life transition. A deeper understanding of these experiences allows us to more effectively support women through this significant phase of life.

Conclusions

This review concluded that the menopausal experience extends beyond physical symptoms, also affecting mental health, personal and professional life, and self-identity. Additionally, menopause is shaped by individual life experiences and various personal factors.

Patient or Public Contributions

The studies analysed in this review contain original data from women in the UK undergoing menopause. The qualitative data delves into their experiences with symptoms, accessing various sources of support from NHS and non-NHS sources as well as alternative therapies.

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英国妇女的更年期经历:定性研究的系统文献综述。
背景:绝经,定义为月经停止超过12个月,可以在许多方面对女性产生深远的影响。了解妇女的更年期经历可以在这一变革时期改善护理和支持。目的:本系统综述的目的是识别和总结已发表的定性研究,这些研究考虑了英国更年期妇女的生活经历,并作为更年期领域未来研究的基础。检索策略:EMBASE、MEDLINE和PsycINFO数据库于2024年3月开始检索,并于2024年4月更新。纳入标准:同行评议的论文,有英文全文,关注英国更年期妇女,2000年1月至2024年4月发表的研究,定性或混合方法研究设计与定性分析。数据提取和综合:两位作者独立进行了标题和摘要筛选。相互矛盾的意见由第三位作者来解决。审稿人熟悉数据并逐行编码文本。主题分析被用于将代码置于更广泛的主题中。使用适当的质量评估工具对所有研究进行评估。主要结果:本综述纳入32项研究,涉及3462名受试者。抽取了173个主要代码,并将其组织为分主题和3个总主题。这些关键主题是更年期的生物心理社会维度,更年期的理解和管理更年期的策略。讨论:文献记载的更年期经历是由一系列个人和社会因素形成的。虽然支持更年期妇女的举措已经到位,但本次审查还确定了关键的知识差距和边缘化群体,这些群体将从有针对性的研究和干预措施中受益。它强调更年期不仅仅是一系列症状的集合,而且对许多人来说,是一个关键的生命转变。对这些经历有了更深入的了解,我们就能更有效地支持女性度过这一重要的人生阶段。结论:本综述的结论是,绝经期经历不仅影响身体症状,还影响心理健康、个人和职业生活以及自我认同。此外,更年期是由个人生活经历和各种个人因素决定的。患者或公众贡献:本综述分析的研究包含来自英国绝经期妇女的原始数据。定性数据深入研究了他们的症状经历,从NHS和非NHS来源获得各种支持以及替代疗法。
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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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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