J Midwifery Womens Health. 2012 Sep-Oct;57(5):489-94. doi: 10.1111/j.1542-2011.2012.00187.x.
Despite the high prevalence of pelvic organ prolapse, many women suffer in silence, lacking the language and opportunity to describe their condition. There are limited descriptions of women's experiences with pelvic organ prolapse in the literature. This qualitative study addressed the knowledge and experience of women with pelvic organ prolapse.
Semistructured interviews were conducted with 13 women who had been previously diagnosed with pelvic organ prolapse. Transcripts of the interviews were reviewed and coded using a process of content analysis compared against the framework of authoritative knowledge, developed by Brigitte Jordan.
By applying the concept of authoritative knowledge, we identified 3 themes of how women construct understanding about pelvic organ prolapse and how they demonstrate deference to the authoritative knowledge of medical providers. First, we found through women's narratives that authoritative knowledge was held by the health care provider and is considered consequential and legitimate by all participants. Second, women reported that the health care provider's authoritative knowledge was valued over personal, experiential knowledge. Finally, women described how they work with their health care providers to create a system of authoritative knowledge as they seek treatment for or discuss their condition. Throughout the narratives, women's experiences are not legitimized by the women or the medical community, perpetuating the "hidden" nature of these conditions.
This analysis provides qualitative evidence of Jordan's authoritative knowledge: women and health care providers contribute to dimensions of authoritative knowledge surrounding pelvic organ prolapse. Despite what women experience, the health care provider's definition and understanding of pelvic organ prolapse is seen as legitimate and consequential. Because of their construction of their condition, and the power dynamic at play, women are silenced, and their expertise about their bodies is delegitimized, limiting their active participation in seeking care for this condition.
尽管盆腔器官脱垂的患病率很高,但许多女性默默忍受,缺乏描述自身状况的语言和机会。文献中对女性盆腔器官脱垂体验的描述有限。本定性研究旨在探讨女性对盆腔器官脱垂的认知和经验。
对 13 名先前被诊断为盆腔器官脱垂的女性进行半结构式访谈。使用 Brigitte Jordan 提出的权威知识框架,对访谈记录进行审查和编码,并进行内容分析。
通过应用权威知识的概念,我们确定了女性构建对盆腔器官脱垂的理解以及如何表现出对医疗提供者权威知识的尊重的 3 个主题。首先,我们发现,通过女性的叙述,权威知识由医疗保健提供者掌握,所有参与者都认为其具有重要性和合法性。其次,女性报告说,医疗保健提供者的权威知识比个人经验知识更有价值。最后,女性描述了她们如何在寻求治疗或讨论病情时与医疗保健提供者合作,建立权威知识体系。在整个叙述中,女性的经历没有得到女性或医疗界的认可,使这些情况继续处于“隐蔽”状态。
本分析提供了 Jordan 权威知识的定性证据:女性和医疗保健提供者对围绕盆腔器官脱垂的权威知识维度做出了贡献。尽管女性有自己的体验,但医疗保健提供者对盆腔器官脱垂的定义和理解被视为合法且有重要影响。由于她们对自身状况的构建以及权力动态的作用,女性被噤声,她们对自身身体的专业知识被否定,限制了她们积极参与寻求治疗的机会。