UBC Department of Pediatrics, BC Children's Hospital, Vancouver, BC, Canada.
Sunnybrook Health Sciences Centre, Toronto, ON, Canada.
J Pediatr Rehabil Med. 2021;14(4):643-654. doi: 10.3233/PRM-200776.
Despite an increasing number of individuals with spina bifida reaching reproductive age, there has been a paucity of research into their reproductive health care needs. The objective of this study was to better understand the reproductive health experiences of self-identified women with spina bifida using qualitative methodology.
A phenomenological study design was used to address this objective. Women with spina bifida identified their interest in participating in a semi-structured interview after completing an online reproductive health survey. Interviews were recorded and transcribed verbatim. Qualitative analysis followed a phenomenological approach using Dedoose software.
Twelve self-identified women with spina bifida participated. They described experiences in four domains: sexual education, pregnancy, labor and delivery, and postpartum. In addition, an intersecting domain of social justice and advocacy emerged. Numerous themes are described, including a lack of tailored sexual health information, impact of pregnancy on function, attitudes towards delivery method, and parenting challenges.
This study explored the continuum of reproductive health experiences of women with spina bifida. They face unique reproductive health challenges that provide an opportunity for health care providers to offer more holistic care.
尽管越来越多的脊柱裂患者达到了生育年龄,但对他们的生殖健康护理需求的研究却很少。本研究的目的是使用定性方法更好地了解自我认同的脊柱裂女性的生殖健康体验。
采用现象学研究设计来实现这一目标。在完成在线生殖健康调查后,脊柱裂女性表示有兴趣参加半结构化访谈。访谈进行了录音,并逐字转录。定性分析采用 Dedoose 软件进行现象学方法。
共有 12 名自我认同的脊柱裂女性参与。她们描述了四个领域的经验:性教育、怀孕、分娩和产后。此外,还出现了一个交叉领域的社会正义和倡导。描述了许多主题,包括缺乏针对性的性健康信息、怀孕对功能的影响、对分娩方式的态度以及育儿挑战。
本研究探讨了脊柱裂女性生殖健康体验的连续体。他们面临着独特的生殖健康挑战,这为医疗保健提供者提供了提供更全面护理的机会。