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

IF 1.8 Q3 HEALTH CARE SCIENCES & SERVICES Patient Related Outcome Measures Pub Date : 2021-02-16 eCollection Date: 2021-01-01 DOI:10.2147/PROM.S272688
Sharolin Boban, Jenny Downs, Jim Codde, Paul A Cohen, Caroline Bulsara
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引用次数: 12

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.

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被诊断患有卵巢癌的妇女:患者和护理者的经历和观点。
目的:通过直接接触被诊断患有卵巢癌的妇女,本研究旨在探索和确定她们对健康症状和结果的看法,这些症状和结果对她们在患病过程中最重要。背景:卵巢癌患者报告的结果测量往往侧重于身体症状,而不是更复杂的社会心理方面的生活与疾病。本研究采用“自下而上的方法”,试图全面了解对卵巢癌妇女最重要的健康问题,作为生成项目以发展为卵巢癌特异性患者报告结果测量的第一步。患者和方法:经过广泛的文献回顾,我们试图通过定性描述方法捕捉“患者的声音”,包括与卵巢癌患者、其护理人员和临床医生的社区对话,以及与卵巢癌妇女的访谈和焦点小组。13名妇女分别接受了采访,并进行了两个焦点小组的调查。采用模板专题分析对数据进行分析。结果:关键主题包括与临床诊断、治疗阶段、与家人/朋友关系的改变、财务问题、与卫生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,出现了若干次主题,这些主题被确定为参与者所经历的各种挑战。诊断延迟、化疗和手术相关的挑战、性健康对伴侣关系的负面影响、与卫生专业人员的沟通挑战是确定的少数问题之一。此外,自我授权被认为是参与者的一种应对机制。结论:通过确定诊断为卵巢癌的妇女的优先事项,我们强调了减少诊断延迟和改善这些妇女生活质量的战略的必要性。数据将为卵巢癌特异性患者报告结果测量的发展提供信息。
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Patient Related Outcome Measures
Patient Related Outcome Measures HEALTH CARE SCIENCES & SERVICES-
自引率
4.80%
发文量
27
审稿时长
16 weeks
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