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被诊断为卵巢癌的女性:患者及护理人员的经历与观点。

Women Diagnosed with Ovarian Cancer: Patient and Carer Experiences and Perspectives.

作者信息

Boban Sharolin, Downs Jenny, Codde Jim, Cohen Paul A, Bulsara Caroline

机构信息

School of Health Sciences, University of Notre Dame Australia, Fremantle, Western Australia, Australia.

Telethon Kids Institute, Centre for Child Health Research, The University of Western Australia, Nedlands, Western Australia, Australia.

出版信息

Patient Relat Outcome Meas. 2021 Feb 16;12:33-43. doi: 10.2147/PROM.S272688. eCollection 2021.

Abstract

PURPOSE

By directly engaging with women diagnosed with ovarian cancer, this study aimed to explore and identify their view of the health symptoms and outcomes that matter most to them as they traverse their disease pathway.

BACKGROUND

Patient-reported outcome measures in ovarian cancer have tended to focus on physical symptoms rather than the more complex psychosocial aspects of living with the disease. Using a "ground-up approach", this study sought to comprehensively understand the health concerns that matter most to women with ovarian cancer as a first step in generating items for development into an ovarian cancer-specific patient-reported outcome measure.

PATIENTS AND METHODS

Following an extensive literature review, we sought to capture the "patient voice" through a qualitative descriptive approach including a community conversation with ovarian cancer patients, their carers and clinicians, and interviews and focus groups with women with ovarian cancer. Thirteen women were interviewed individually, and two focus groups were conducted. A template thematic analysis was used to analyze the data.

RESULTS

Key themes included challenges related to clinical diagnosis, treatment phase, altered relationships with family/friends, financial issues, relationships with health professionals and coping strategies. Within each key theme, several sub-themes emerged that were identified as various challenges experienced by participants. Diagnostic delay, chemotherapy and surgery-related challenges, negative impact of sexual well-being on partner relationship, communicational challenges with health professionals were among the few issues identified. In addition, self-empowerment was identified as a coping mechanism among participants.

CONCLUSION

By identifying priorities for women diagnosed with ovarian cancer we have highlighted the need for strategies to reduce diagnostic delays and improve quality of life for these women. Data will inform the development of an ovarian cancer-specific patient-reported outcome measure.

摘要

目的

通过直接与被诊断为卵巢癌的女性接触,本研究旨在探索并确定她们在经历疾病过程中认为最重要的健康症状和结果。

背景

卵巢癌患者报告的结局指标往往侧重于身体症状,而非与该疾病共存的更为复杂的心理社会方面。本研究采用“自下而上的方法”,试图全面了解对卵巢癌女性最重要的健康问题,作为生成项目以开发特定于卵巢癌的患者报告结局指标的第一步。

患者与方法

在进行广泛的文献综述后,我们试图通过定性描述性方法捕捉“患者声音”,包括与卵巢癌患者、其护理人员和临床医生进行社区对话,以及对卵巢癌女性进行访谈和焦点小组讨论。对13名女性进行了单独访谈,并开展了两个焦点小组讨论。采用模板主题分析法对数据进行分析。

结果

关键主题包括与临床诊断、治疗阶段、与家人/朋友关系改变、财务问题、与医疗专业人员的关系以及应对策略相关的挑战。在每个关键主题中,出现了几个子主题,被确定为参与者经历的各种挑战。诊断延迟、化疗和手术相关挑战、性健康对伴侣关系的负面影响、与医疗专业人员的沟通挑战等是其中少数被确定的问题。此外,自我赋权被确定为参与者的一种应对机制。

结论

通过确定被诊断为卵巢癌女性的优先事项,我们强调了需要采取策略来减少诊断延迟并改善这些女性的生活质量。数据将为开发特定于卵巢癌的患者报告结局指标提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e09/7896761/4f3176766c07/PROM-12-33-g0001.jpg

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