特立尼达和多巴哥子宫内膜异位症妇女生活质量横断面研究。

IF 2.3 Q2 OBSTETRICS & GYNECOLOGY
Frontiers in global women's health Pub Date : 2024-08-22 eCollection Date: 2024-01-01 DOI:10.3389/fgwh.2024.1359741
Raveed Khan, Rameez Baksh, Terika J Wallace, Mikael Aimable, Vineeta Bujhawan, Justin Cumberbatch, Enrie Julian Marbella, Dana Phagoo, Sanathkumar Ramjattan, Akshita Shavili
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引用次数: 0

摘要

导言:子宫内膜异位症是一种慢性妇科疾病,目前尚无根治方法,对患者的生活质量(QoL)造成了不利影响。本研究深入探讨了特立尼达和多巴哥子宫内膜异位症患者的经历,重点关注他们的生活质量、疼痛严重程度以及对疾病的接受程度:向特立尼达和多巴哥子宫内膜异位症协会的 160 名成员发放了调查问卷。采用的调查工具是 WHOQOL-BREF,该工具可测量生活质量、疼痛严重程度和对疾病的接受程度[疾病接受度量表(AIS)]:受访者的平均年龄为 38.65 岁。生活质量得分平均为 3.41,其中 "环境 "方面得分最高(12.84),"社会关系 "方面得分最低(11.88)。Cronbach's alpha 表明,"环境"(ɑ = 0.909)和 "AIS"(ɑ = 0.882)的内部一致性极佳。独立样本 t 检验显示,失业参与者的平均 QoL 分数较低。方差分析显示,"健康状况 "和 "确诊子宫内膜异位症后的年数 "的平均 QoL 分数存在显著差异。所有 QoL 领域之间均呈正相关。身体健康和社会关系领域之间呈中度正相关(ρ = 0.558)。所有其他领域之间都有很强的相关性(0.6 ρ 讨论):研究结果强调了了解疼痛严重程度等决定因素的重要性,以改善对子宫内膜异位症患者的护理和支持。探索对疾病的接受程度对于提高这些患者的生活质量至关重要,这突出表明需要采取有针对性的干预措施,在医疗的同时提供心理和社会支持。这项研究表明,接受疾病对子宫内膜异位症患者的整体生活质量有着举足轻重的作用。要提高护理质量,需要全面了解影响生活质量的因素,尤其是疼痛的严重程度,还需要采取综合方法为子宫内膜异位症患者提供支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A cross-sectional study on the quality of life of women with endometriosis in Trinidad and Tobago.

Introduction: Endometriosis is a chronic gynecological condition that lacks a definitive cure and adversely impacts the quality of life (QoL) of those affected. This study delves into the experiences of individuals with endometriosis in Trinidad and Tobago, focusing on their quality of life, pain severity, and acceptance of illness.

Methods: Surveys were distributed among 160 members of the Trinidad and Tobago Endometriosis Association. The survey instrument utilized was the WHOQOL-BREF, which measures QoL, pain severity, and acceptance of illness [the Acceptance of Illness Scale (AIS)].

Results: The average age of respondents was 38.65 years. Quality of life scores averaged 3.41, with the "environment" aspect scoring highest (12.84) and "social relationships" scoring lowest (11.88). Cronbach's alpha indicated excellent internal consistency for "environment" (ɑ = 0.909) and the "AIS" (ɑ = 0.882). The independent samples t-test revealed lower mean QoL scores for unemployed participants. Analysis of variance revealed significant differences in mean QoL scores for "health status" and "years since endometriosis diagnosis." All the QoL domains were positively correlated with each other. There were moderate positive correlations between the physical health and social relationships domains (ρ = 0.558). All other domains were strongly correlated with each other (0.6 < ρ < 0.8). Pain intensity and acceptance of illness had mean scores of 24.15 and 6.57, respectively. Variations in quality of life were observed for health status and duration since diagnosis, impacting mostly on the domain of physical health. Acceptance of illness emerged as a significant influencer of overall quality of life, assisting individuals in navigating the challenges posed by endometriosis.

Discussion: The findings underscore the importance of understanding determinants, such as pain severity to improve care and support for those with endometriosis. Exploring acceptance of illness is critical in improving the quality of life of these individuals, highlighting the need for tailored interventions that encompass psychological and social support alongside medical treatment. This study demonstrates the pivotal role of acceptance of illness in the overall quality of life of endometriosis patients. Improving the quality of care requires a comprehensive understanding of the factors influencing quality of life, particularly pain severity and the need for a holistic approach to support individuals grappling with endometriosis.

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