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Exploring the Reasons for the Tiny Percentage of Patients on Home Hemodialysis

机译:探索接受家庭血液透析的患者比例偏低的原因

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The number of patients requiring renal replacement therapy continues to grow. When patients are told they need a life-sustaining treatment, it is a profound experience that impacts all aspects of their lives and the lives of their families. In the United States, the stark reality is the majority of patients are treated with in-center hemodialysis, and only a very small percentage with a home dialysis therapy, such as peritoneal dialysis or home hemodialysis. Why is this? Do patients not factor in preference, independence, or quality and maintenance of a normal life? Or is it that as a renal community, nephrology nurses do not expose patients to the knowledge they need and promote involvement in this decision-making? Is patient autonomy being fostered? This article explores the reasons for the tiny percentage of patients on home dialysis and suggests strategies to address the education needed, the dynamics of why patients decide on a therapy, patient selection characteristics, and myths of who is and is not a candidate.
机译:需要肾脏替代治疗的患者数量继续增长。当告知患者他们需要维持生命的治疗时,这是一次深刻的经历,会影响到他们生活的各个方面以及家庭生活。在美国,严峻的现实是大多数患者接受中心血液透析治疗,只有很少一部分患者接受家庭透析疗法,例如腹膜透析或家庭血液透析。为什么是这样?患者是否不考虑偏爱,独立性或正常生活的质量和维持?还是作为肾脏社区,肾病学护士不会让患者了解他们所需的知识并促进其参与决策?是否培养患者自主权?本文探讨了接受家庭透析的患者比例偏低的原因,并提出了解决所需教育的策略,患者决定治疗方案的动态,患者选择特征以及谁是或不是候选人的神话。

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