Recognition at the Heart of the Complex Situations Experienced by People With Chronic Musculoskeletal Pain.

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Mellier Jessica, Balis Aurélie, Defraine Fabian, Vanderhofstadt Quentin, Di Biagi Léa, Schetgen Marco, D'Ans Pierre, Foucart Jennifer, Mahieu Céline, Bengoetxea Ana
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Abstract

Objective: Chronic musculoskeletal pain (CMSP) is frequent in chronic diseases, decreasing the quality of life of these patients. In a survey conducted in Belgium in 2019, chronic pain was named by patients as the main factor of complexity in their lives. The objective of our research was to provide elements to understand why and how CMSP contributes to the complexity of these people's lives.

Design: Qualitative study through semi-structured interviews.

Setting: The study was conducted in Belgium with French-speaking individuals. The interviews took place at the university, in a teaching hospital, in private clinics or in individuals' homes.

Participants: We included 24 individuals with CMSP and living complex situations. The recruitment was made in two phases in agreement with the grounded theory methodology and to reach the saturation of ideas.

Results: The complexity experienced by people with CMSP turns around the notion of recognition, which can be broken down into 3 spheres: intimate, social and legal. The poor quality of listening and the fragmented vision of aid and care professionals generate a feeling of loneliness and incomprehension in the face of illness. The unsuitability of the world of work, the opacity of protocols and the attitude of medical experts reveal inequalities in access to recognition for immigrants and people of low socio-professional status.

Conclusion: The complexity of the situations experienced could be reduced by implementing health policies that facilitate: legal recognition of this illness; adaptability in the workplace; raising awareness about pain mechanisms; the risks of stigmatization and the need of interprofessional collaboration.

Patient or public contribution: Patients and the public participated in the dissemination of our research and were able to help us with recruitment through social networks (call for participation published on Facebook by the association 'Aidants proches') or word of mouth. The presentation of preliminary results at conferences as well as the publication of a public article in Belgian journals (http://www.lejournaldumedecin.com/magazine/douleurs-chroniques-un-veritable-parcours-du-combattant/article-normal-63055.html?cookie_check=1671467500%22) facilitated the contact with the public.

慢性肌肉骨骼疼痛患者所经历的复杂情况的核心认识。
目的:慢性肌肉骨骼疼痛(CMSP)是慢性疾病中的常见病,会降低患者的生活质量。2019 年在比利时进行的一项调查显示,慢性疼痛被患者称为导致生活复杂化的主要因素。我们的研究目的是提供一些要素,以了解慢性疼痛为何以及如何导致这些人的生活复杂化:设计:通过半结构式访谈进行定性研究:研究在比利时进行,对象为讲法语的个人。访谈在大学、教学医院、私人诊所或个人家中进行:我们共招募了 24 名患有 CMSP 并生活在复杂环境中的患者。根据基础理论方法,为了达到思想饱和,我们分两个阶段进行了招募:CMSP 患者所经历的复杂性围绕着 "认可 "这一概念,而 "认可 "又可细分为三个领域:亲密关系、社会关系和法律关系。倾听的质量不高,援助和护理专业人员的视野支离破碎,这些都会让患者在面对疾病时产生孤独感和不理解感。工作环境的不适应、协议的不透明以及医学专家的态度,都揭示了移民和社会职业地位低下者在获得认可方面的不平等:患者或公众的贡献:患者和公众参与了我们研究的传播,并通过社交网络("Aidants proches "协会在 Facebook 上发布的参与呼吁)或口碑帮助我们进行招募。在会议上介绍初步结果以及在比利时期刊(http://www.lejournaldumedecin.com/magazine/douleurs-chroniques-un-veritable-parcours-du-combattant/article-normal-63055.html?cookie_check=1671467500%22)上发表公开文章促进了与公众的接触。
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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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