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Palliative care for patients with heart failure: facilitators and barriers - a cross sectional survey of German health care professionals

机译:心力衰竭患者的姑息治疗:促进者和障碍-德国医疗专业人员的横断面调查

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Background Compared to patients with cancer, heart failure patients are seldom candidates for palliative care. Numerous studies have investigated reasons why heart failure patients do not receive palliative care; however, none of these studies have ever evaluated the situation in the German health care setting. This study aims to identify German healthcare providers’ (HCP) perception of barriers and facilitators to palliative care of patients with chronic heart failure. Methods We conducted an online-survey with 315 nurses and physicians of different medical disciplines. Results Even though heart failure patients’ need of palliative care and its advantages has been recognized, HCP see potential for development and improvement. A lack of knowledge about the content and measures of palliative care, poor communication and unclear responsibilities between medical disciplines, difficulties to determine the right time to initiate palliative care, and the feeling not to be prepared to discuss end-of-life issues with the patient has been identified as barriers. Further, HCP believe that patients and relatives do not possess adequate knowledge about the disease and its progression and are therefore unprepared in asking questions regarding palliative care. They rather tend to demand everything possible to be done in order prolong life, and are reluctant to accept that life is limited. Overall, HCP perceive that dying is a taboo subject within our society placing palliative care on the same level as assisted dying. In addition, results indicate that HCP have an inappropriate notion of ideal medicine fearing to lose patient and are worried about the appropriateness of PC remuneration. Conclusions In order to overcome the described barriers, HCP, patients, and relatives need to be educated in palliative care. Information and education encompassing the aim, content and measures of palliative care needs to be provided for all parties in order to optimize patient care, to foster communication between healthcare professionals, patients, and relatives, and to overcome perceived barriers. Trial registration DRKS00007119
机译:背景技术与癌症患者相比,心力衰竭患者很少是姑息治疗的候选人。许多研究调查了心力衰竭患者不接受姑息治疗的原因。但是,这些研究都没有评估德国医疗机构的情况。这项研究旨在确定德国医疗保健提供者(HCP)对慢性心力衰竭患者姑息治疗的障碍和促进者的看法。方法我们对315名不同医学学科的护士和医生进行了在线调查。结果即使心力衰竭患者对姑息治疗的需求及其优势得到了认可,但HCP仍看到了发展和改善的潜力。缺乏关于姑息治疗的内容和措施的知识,医学学科之间的沟通不畅以及职责不明确,难以确定在何时开始姑息治疗的感觉,以及不愿意与死者讨论临终问题的感觉。患者已被确定为障碍。此外,HCP认为患者和亲属对这种疾病及其进展没有足够的了解,因此没有准备好询问有关姑息治疗的问题。他们宁愿要求一切可能的事情以延长寿命,却不愿接受生命有限。总体而言,HCP认为死亡是我们社会中的禁忌话题,因此姑息治疗与辅助死亡处于同等水平。此外,结果表明,HCP的理想药物概念不合适,担心失去患者,并担心PC薪酬的适当性。结论为了克服上述障碍,需要对HCP,患者和亲属进行姑息治疗教育。需要向各方提供包括姑息治疗的目的,内容和措施的信息和教育,以优化患者的护理,促进医疗保健专业人员,患者和亲属之间的沟通,并克服已知的障碍。试用注册DRKS00007119

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