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Survivorship care planning in gynecologic oncologyperspectives from patients, caregivers, and health care providers

机译:来自患者,护理人员和医疗保健提供者的妇科肿瘤诊所患者的生存护理计划

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PurposeThis qualitative study sought to describe the challenges following treatment and the preferences regarding survivorship care among patients treated for gynecological cancer, their caregivers, and health care providers.MethodsBetween July and August 2017, in-depth semi-structured interviews regarding survivorship were conducted at a large academic hospital in the USA among patients who recently completed treatment (12months) for a gynecological cancer (ovarian, endometrial, cervical, and vulvar) and their primary caregivers. A focus group was conducted among health care providers (oncologists, nurses, and fellows). Main themes were identified using descriptive content analysis.ResultsA total of 30 individuals participated in this study (13 patients, 9 caregivers, 8 health care providers). Almost all participants reported a desire for more information on how to address survivorship needs, specifically as they related to side effects, follow-up schedule, and psychological assistance. Despite this uniformly identified need for more information, preferences for survivorship care planning differed across cancer types and individuals, with respect to content, timing, and mode of delivery. Health care providers expressed challenges in communicating with patients about survivorship, a desire to shift post-treatment conversations to the goal of improving quality of life as opposed to focusing on disease recurrence, and an unmet need for disease specific and individualized survivorship care planning.ConclusionsPatients, caregivers, and health care providers each expressed a need for gynecologic cancer-tailored survivorship care resources.Implications for Cancer SurvivorsThe variation of disease types and patient and caregiver needs may require multi-faceted, individualized survivorship care planning.
机译:目的的定性研究寻求描述治疗后的挑战,对妇科癌症,护理人员和医疗保健提供者治疗的患者的生存护理的偏好。2017年7月和2017年8月,关于生存的深入半结构化访谈是在A中进行的最近完成妇科癌症(卵巢,子宫内膜,宫颈和外阴)及其主要护理人员的治疗(&12months)的大型学术医院。焦点小组是在医疗服务提供者(肿瘤学家,护士和研究员)之间进行的。使用描述性内容分析确定了主要主题。培训总共30个个人参加了本研究(13名患者,9名护理人员,8名医疗保健提供者)。几乎所有与会者都报告了有关如何解决生存需求的更多信息,特别是与副作用,后续时间表和心理援助相关的更多信息。尽管这种统一确定需要更多信息,但涉及癌症类型和个人的偏好,关于内容,时序和交付方式差异。医疗保健提供者对与患者沟通的攻击致力于将治疗后的谈话转移到改善生活质量的愿望,而不是专注于疾病复发,以及对疾病的特异性和个性化生存护理策划的未满足需求。结合,护理人员和医疗保健提供者各自表达了对妇科癌症定制的生存护理资源的需求。用于癌症类型和患者和护理人员需求的变异可能需要多刻,个性化的生存护理计划。

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