Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA
Boston Center for Endometriosis, Boston, Massachusetts, USA.
BMJ Open. 2022 Apr 27;12(4):e052765. doi: 10.1136/bmjopen-2021-052765.
To examine women's perceptions of endometriosis-associated disease burden and its impact on life decisions and goal attainment.
An anonymous online survey was distributed in October 2018 through the social media network MyEndometriosisTeam.com.
Women aged 19 years and older living in several English-speaking countries who self-identified as having endometriosis.
Patients' perspectives on how endometriosis has affected their work, education, relationships, overall life decisions and attainment of goals. Subanalyses were performed for women who identified as 'less positive about the future' (LPAF) or had 'not reached their full potential' (NRFP) due to endometriosis.
743 women completed the survey. Women reported high levels of pain when pain was at its worst (mean score, 8.9 on severity scale of 0 (no pain) to 10 (worst imaginable pain)) and most (56%, n=415) experienced pain daily. Women reported other negative experiences attributed to endometriosis, including emergency department visits (66%, n=485), multiple surgeries (55%, n=406) and prescription treatments for symptoms of endometriosis (72%, n=529). Women indicated that they believed endometriosis had a negative impact on their educational and professional achievements, social lives/relationships and overall physical health. Most women 'somewhat agreed'/'strongly agreed' that endometriosis caused them to lose time in life (81%, n=601), feel LPAF (80%, n=589) and feel they had NRFP (75%, n=556). Women who identified as LPAF or NRFP generally reported more negative experiences than those who were non-LPAF or non-NRFP.
Women who completed this survey reported pain and negative experiences related to endometriosis that were perceived to negatively impact major life-course decisions and attainment of goals. Greater practitioner awareness of the impact that endometriosis has on a woman's life course and the importance of meaningful dialogue with patients may be important for improving long-term management of the disease and help identify women who are most vulnerable.
探讨女性对与子宫内膜异位症相关疾病负担的认知及其对生活决策和目标实现的影响。
2018 年 10 月,通过社交媒体网络 MyEndometriosisTeam.com 发布匿名在线调查。
年龄在 19 岁及以上、居住在几个英语国家、自我诊断为子宫内膜异位症的女性。
患者对子宫内膜异位症如何影响其工作、教育、人际关系、整体生活决策和目标实现的看法。对因子宫内膜异位症而被认定为“对未来不那么乐观”(LPAF)或“未充分发挥潜力”(NRFP)的女性进行了亚分析。
743 名女性完成了调查。当疼痛最严重时,女性报告疼痛程度很高(严重程度量表评分为 0(无痛)至 10(最严重可想象的疼痛),平均得分为 8.9),大多数女性(56%,n=415)每天都有疼痛。女性报告了其他与子宫内膜异位症有关的负面经历,包括急诊就诊(66%,n=485)、多次手术(55%,n=406)和处方治疗子宫内膜异位症症状(72%,n=529)。女性表示,她们认为子宫内膜异位症对她们的教育和专业成就、社会生活/人际关系和整体身体健康产生了负面影响。大多数女性“有些同意”/“强烈同意”(81%,n=601)子宫内膜异位症使她们的生活时间减少,“对未来不那么乐观”(80%,n=589),感到自己“未充分发挥潜力”(75%,n=556)。被认定为 LPAF 或 NRFP 的女性通常比非 LPAF 或非 NRFP 的女性报告了更多的负面经历。
完成这项调查的女性报告了与子宫内膜异位症相关的疼痛和负面经历,这些经历被认为对重大生活决策和目标实现产生负面影响。提高从业者对子宫内膜异位症对女性生活轨迹的影响以及与患者进行有意义对话的重要性的认识,可能对改善疾病的长期管理和帮助识别最脆弱的患者很重要。