Live Discharges of Patients in Hospice Home Settings-Relief or Grief: A Narrative Study.

IF 1.4
Jacek T Soroka, Amanda L Paulson-Blom, Alla Blotsky, Jennifer L Derrick, Margaret T Mudroch
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Abstract

BackgroundApproximately 20% of hospice patients in the US are discharged alive, often due to Medicare regulations. Such discharges are frequently perceived by caregivers as abandonment or expulsion, especially when they occur without follow-up or planning for care transition.MethodsThis study explored caregiver experiences with live hospice discharge through 2 narrative interviews and institutional data from a Midwest medical center (January 2020 through December 2022). Caregiver stories were analyzed thematically to identify emotional and logistical challenges. Retrospective patient data were also reviewed to provide descriptive statistics on patient volume.ResultsOf 1556 hospice patients discharged, 107 (6.9%) were discharged alive, with a mean length of stay of 205 days-substantially longer than that for the general hospice population. Most patients were women who were diagnosed with cerebrovascular or neurologic conditions and discharged from skilled-care facilities. One of the caregivers described discharge as distressing and poorly coordinated; the other reported a positive experience shaped by prior knowledge and financial resources. Both emphasized the importance of clear communication, care planning (eg, to avoid loss of durable medical equipment), and interdisciplinary support. The caregiver's financial stability likely influenced discharge decisions and preparedness.ConclusionsLive hospice discharge can cause emotional and practical disruption, especially when not accompanied by a care transition plan or access to durable medical equipment. This study highlights the need for team-based communication, sensitivity in language, and continued support. Engaging all members of the interdisciplinary team and ensuring access to essential resources may improve caregiver confidence and continuity of care.

安宁疗护住家病人的出院:解脱或悲伤:一项叙事研究。
背景:在美国,大约20%的临终关怀病人活着出院,这通常是由于医疗保险的规定。这种出院通常被护理人员视为遗弃或驱逐,特别是在没有随访或护理过渡计划的情况下。方法本研究通过2次叙述性访谈和美国中西部某医疗中心(2020年1月至2022年12月)的机构数据,探讨临终关怀出院时的护理人员体验。按主题分析照顾者的故事,以确定情感和后勤方面的挑战。回顾性患者资料也进行了审查,以提供患者数量的描述性统计数据。结果在1556名安宁疗护病人中,107人(6.9%)活著出院,平均住院时间为205天,远长于一般安宁疗护病人。大多数患者是被诊断患有脑血管或神经系统疾病并从专业护理机构出院的妇女。其中一名护理人员形容出院时很痛苦,身体协调能力差;另一组报告了由先前知识和经济资源塑造的积极体验。双方都强调了明确沟通、护理规划(例如,避免损失耐用医疗设备)和跨学科支持的重要性。护理人员的经济稳定可能影响出院决定和准备。结论临终关怀出院会造成情绪和实际的混乱,特别是在没有护理过渡计划或无法获得耐用医疗设备的情况下。这项研究强调了团队沟通、语言敏感性和持续支持的必要性。让跨学科团队的所有成员参与进来,并确保获得必要的资源,可以提高护理人员的信心和护理的连续性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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