Interdisciplinary School of Health sciences, University of Ottawa, 25 University Private, Ottawa, ON K1N 7K4, Canada.
University of Parakou, Faculty of Medicine, Parakou, Benin.
Int Health. 2023 Jan 3;15(1):56-66. doi: 10.1093/inthealth/ihac028.
Polycystic ovary syndrome (PCOS) is a complex, chronic condition characterized by anovulation, polycystic ovarian morphology and hyperandrogenism that requires lifelong management. To reduce the risk of comorbidity and to manage symptoms, lifestyle management and pharmaceuticals such as oral contraceptives are the most common forms of treatment and should be tailored to the individual patient. The literature to date has shown PCOS patients to experience widespread dissatisfaction with the amount and quality of information they receive from providers, along with lower levels of trust in physicians. Little is known about the lived experiences of women managing PCOS in Canada, across age groups.
In-depth remote interviews explored women's lived experiences managing PCOS and the barriers and facilitators they encountered in their management journeys. Data were analyzed using thematic analysis and interpretive description methodology.
Twenty-five in-depth, telephone interviews conducted with participants (aged 18-63 y) across Canada revealed participants lacking sufficient information and guidance from physicians, especially in primary care. Areas in need of more guidance included lifestyle management and mental health. Lack of empathy and weight bias among physicians were also perceived by participants. Older participants received little guidance on treatment options postmenopause. Loss of trust and withdrawal from seeking medical care were prominent themes, along with greater self-reliance on self-management, including self-educating and self-experimenting with treatments.
Most women in this study were frustrated with the level of involvement and information provision from their doctors. Key recommendations are identified for the provision of care to younger and older patients with PCOS. Improved education for physicians may be needed to improve the quality of healthcare provision for PCOS.
多囊卵巢综合征(PCOS)是一种复杂的慢性疾病,其特征是排卵障碍、多囊卵巢形态和高雄激素血症,需要终身管理。为了降低合并症的风险并管理症状,生活方式管理和避孕药等药物是最常见的治疗方法,应根据个体患者进行调整。迄今为止的文献表明,PCOS 患者普遍对从提供者那里获得的信息量和质量不满意,对医生的信任度也较低。关于加拿大不同年龄段的女性在管理 PCOS 方面的生活体验,知之甚少。
深入的远程访谈探讨了女性在管理 PCOS 方面的生活体验,以及她们在管理过程中遇到的障碍和促进因素。使用主题分析和解释性描述方法对数据进行分析。
在加拿大各地对 25 名参与者(年龄 18-63 岁)进行了深入的电话访谈,结果显示参与者从医生那里获得的信息和指导不足,尤其是在初级保健方面。需要更多指导的领域包括生活方式管理和心理健康。参与者还认为医生缺乏同理心和体重偏见。年长的参与者在绝经后几乎没有得到关于治疗选择的指导。失去信任和退出寻求医疗保健是突出的主题,同时也更加依赖自我管理,包括自我教育和自我试验治疗。
本研究中的大多数女性对医生的参与程度和信息提供感到不满。为年轻和年长的 PCOS 患者提供护理提出了关键建议。可能需要对医生进行更多教育,以提高 PCOS 医疗服务的质量。