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Cancer nurses’ provision of survivorship care for patients with haematological malignancy

机译:癌症护士为血液系统恶性肿瘤患者提供生存护理

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IntroductionududMany haematological malignancy survivors report long-term post-treatment physiological and psychosocial effects.ududObjectivesududThis study examined cancer nurses’ perception of their role, confidence levels, practices and barriers in relation to survivorship care provision for patients with haematological malignancies.ududMethodsududApproximately 1300 cancer nurses were invited to participate in a survey. The survey was distributed to all cancer nurses at a Queensland tertiary cancer centre and via email through two Australian professional cancer nursing bodies.ududResultsududIn total, 423 cancer nurses (33%) completed the survey. The majority of participants agreed that all survivorship interventions included in the survey should be within their role. Nurses were least confident in discussing fertility (M=5.93, SD=2.66), employment and financial issues with patients (M=6.19, SD=2.66) and discussing information about identifying signs of cancer recurrence (M=6.43, SD=2.69), on a 11-point scale from 0 to 10 with higher scores indicating greater confidence. The least frequently performed interventions included discussing fertility, intimacy and sexuality issues, and communicating survivorship care with the patient’s primary care providers, with over 60% of participants reporting not performing these interventions often. The most significant barriers perceived by participants were lack of dedicated end-of-treatment consultation (M=2.62, SD=1.13), time (M=2.58, SD=0.94), and an appropriate physical location(M=2.21, SD=1.01), on a 5-point scale (0=not at all; 4=a great deal).ududConclusionsududThe strong support from nurses for their role in survivorship care highlights opportunities that have not yet been adequately developed. Barriers identified in this survey should be considered in the design of future survivorship care models.
机译:简介 ud ud许多血液恶性肿瘤幸存者报告了治疗后的长期生理和社会心理影响。 ud ud目标 ud ud这项研究检查了癌症护士对他们的角色,信心水平,实践以及与生存护理提供相关的障碍的看法对于血液系统恶性肿瘤患者。 ud udMethods ud ud大约1300名癌症护士被邀请参加一项调查。该调查已分发给昆士兰三级癌症中心的所有癌症护士,并通过电子邮件通过澳大利亚的两个专业癌症护理机构进行了分发。 ud udResults ud ud总共有423名癌症护士(33%)完成了调查。大多数参与者同意,调查中包括的所有生存干预措施应在其职责范围内。护士最不愿意讨论生育力(M = 5.93,SD = 2.66),与患者的就业和财务问题(M = 6.19,SD = 2.66)和讨论有关识别癌症复发迹象的信息(M = 6.43,SD = 2.69) ,从0到10的11分制,得分越高表示信心越强。执行得最少的干预措施包括讨论生育,亲密和性问题,并与患者的初级保健提供者进行生存护理沟通,超过60%的参与者报告不经常进行这些干预。参与者感知到的最大障碍是缺乏专门的治疗结束咨询(M = 2.62,SD = 1.13),时间(M = 2.58,SD = 0.94)和适当的身体位置(M = 2.21,SD = 1.01),以5分制评分(0 =完全没有; 4 =很大)。 ud ud结论 ud ud护士在生存护理中的作用的大力支持凸显了尚未得到充分发展的机会。在设计未来的生存护理模型时,应考虑本调查确定的障碍。

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