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Social construction of biopsychosocial and medical experiences of women with polycystic ovary syndrome

机译:多囊卵巢综合征女性生物学生理学和医学经验的社会建构

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Abstract Aim To explore the perceived biopsychosocial and medical experiences of women with polycystic ovary syndrome, as presented in stories written by women on a social support website. Design Qualitative descriptive using low inference content analysis, guided by the social construction of illness theoretical framework. Methods In July 2018, 95 of 379 website stories were randomly selected. The stories were analysed, ending in September 2018. Results Three major themes aligning with framework constructs were identified: Biopsychosocial struggles and management: “I can't even look in the mirror without wanting to cry,” Sociocultural navigation: “I feel all alone and no one understands me.” and Healthcare encounters: “I don't feel like I’m getting the help I need”. These themes revealed that Polycystic ovary syndrome (PCOS) has biological and experiential components, which exist independently of each other and hold social and cultural meanings. Conclusion Care for women with PCOS should be multidisciplinary, multidimensional, and multi‐level to ameliorate biopsychosocial issues. Provider (physicians, nurse practitioners, physician assistants) education about PCOS is necessary to enhance timely diagnosis and implement individualized treatment strategies. Non‐advanced practice nurses are in a unique position to have an impact on patient satisfaction and clinical outcomes by providing and reinforcing patient education, coordinating management processes, counselling via telephone or in‐person appointments and facilitating referrals to ancillary providers. Evidence‐based and accessible psychosocial supports and interventions will lead to improved self‐esteem and effective coping skills, and reduced stigma‐related stress. Lastly, policy changes are warranted to address access to care, health insurance inequities and inadequate funding for PCOS‐related research. Impact Increased awareness of PCOS and its biopsychosocial aspects will aid providers with timely diagnosis and meaningful treatment plans. Women with PCOS will gain acknowledgment, acceptance, and insight towards health care and self‐management.
机译:摘要目的探讨妇女在社会支持网站上妇女撰写的故事中妇女的感知生物学和医学体验。使用低推理内容分析的设计定性描述性,由疾病社会建构的理论框架为指导。方法2018年7月,379个网站故事中的95个是随机选择的。在2018年9月结束的情况下分析了故事。结果确定了与框架构建体保持一致的三个主要主题:活检性斗争和管理:“我甚至不能在不想哭泣的情况下看镜子,”社会文化导航:“我觉得独自一人没有人理解我。“和医疗保健遭遇:“我不觉得我得到了我需要的帮助”。这些主题揭示了多囊卵巢综合征(PCOS)具有生物学和体验组分,其彼此独立存在并保持社会和文化含义。结论应有PCOS的妇女应有多学科,多维和多层次,以改善生物心细胞问题。提供者(医师,护士从业者,医师助理)关于PCOS的教育是为了提高及时诊断和实施个性化治疗策略。非高级练习护士通过提供和加强患者教育,协调管理流程,通过电话或亲本预约,促进辅助提供商的推荐,对患者满意度和临床结果产生影响,对患者满意度和临床结果产生影响。基于证据和可访问的心理社会支持和干预措施将导致自尊和有效的应对技能提高,降低耻辱相关的压力。最后,有必要进行政策变革来处理护理,健康保险不公平,以及对PCOS相关研究的资金不足。影响提高了PCOS的意识及其活检性问题,将援助提供者及时诊断和有意义的治疗计划。 PCOS的妇女将获得对医疗保健和自我管理的承认,接受和洞察力。

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