医院临终关怀:家属的自由文字记录。

IF 2 4区 医学 Q3 HEALTH CARE SCIENCES & SERVICES
Sandra Kurkowski, Johannes Radon, Annika R Vogt, Martin Weber, Stephanie Stiel, Christoph Ostgathe, Maria Heckel
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引用次数: 0

摘要

背景:姑息关怀致力于改善不治之症患者的生活质量。这种方法包括为患者的亲人提供充分的支持。因此,亲人在为其下一代提供临终关怀方面有着亲身经历。目的:在德语地区临终关怀评估(CODE-GER)问卷调查的定量结果基础上,进一步确定亲人认为对提高临终关怀质量非常重要的质量方面:设计:在 "临终关怀评估"(CODETM)德语地区问卷的验证研究中,要求亲人对 CODE-GER 的每个项目同时发表评论(自由文本)。Philipp Mayring 采用定性内容分析法对这些自由文本记录进行了分析:2016年4月至2017年3月期间,在两所大学医院(姑息治疗和非姑息治疗病房)中预期死亡的患者(n=237)的亲人:从1261篇自由文本笔记中提取了993个相关段落。对于亲人而言,护理质量的重要方面是信息/沟通、尊重患者和/或亲人的意愿、参与生命末期的决策(患者的意愿)以及有可能说再见:对于亲人来说,重要的是要认真对待他们的悲伤,让他们了解情况,护理人员要尊重病人的意愿,并在情感上给予支持:本研究已在德国临床试验注册中心注册(DRKS00013916)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hospital end-of-life care: families' free-text notes.

Background: Palliative care strives to improve quality of life for patients with incurable diseases. This approach includes adequate support of the patients' loved ones. Consequently, loved ones have personal experiences of providing end-of-life care for their next. This is a resource for information and may help to investigate the loved ones' perspectives on need for improvements.

Aim: To identify further quality aspects considered important by loved ones to improve the quality of care at the end of life as an addition to quantitative results from the Care of the Dying Evaluation for the German-speaking area (CODE-GER) questionnaire.

Design: Within the validation study of the questionnaire 'Care of the Dying Evaluation' (CODETM) GER, loved ones were asked to comment (free text) in parallel on each item of the CODE-GER. These free-text notes were analysed with the qualitative content analysis method by Philipp Mayring.

Setting/participants: Loved ones of patients (n=237), who had died an expected death in two university hospitals (palliative and non-palliative care units) during the period from April 2016 to March 2017.

Results: 993 relevant paragraphs were extracted out of 1261 free-text notes. For loved ones, important aspects of quality of care are information/communication, respect of the patient's and/or loved one's will, involvement in decision-making at the end of life (patient's volition) and having the possibility to say goodbye.

Conclusions: It is important for loved ones to be taken seriously in their sorrows, to be informed, that the caregivers respect the patients' will and to be emotionally supported.

Trial registration number: This study was registered at the German Clinical Trials Register (DRKS00013916).

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来源期刊
BMJ Supportive & Palliative Care
BMJ Supportive & Palliative Care Medicine-Medicine (miscellaneous)
CiteScore
4.60
自引率
7.40%
发文量
170
期刊介绍: Published quarterly in print and continuously online, BMJ Supportive & Palliative Care aims to connect many disciplines and specialties throughout the world by providing high quality, clinically relevant research, reviews, comment, information and news of international importance. We hold an inclusive view of supportive and palliative care research and we are able to call on expertise to critique the whole range of methodologies within the subject, including those working in transitional research, clinical trials, epidemiology, behavioural sciences, ethics and health service research. Articles with relevance to clinical practice and clinical service development will be considered for publication. In an international context, many different categories of clinician and healthcare workers do clinical work associated with palliative medicine, specialist or generalist palliative care, supportive care, psychosocial-oncology and end of life care. We wish to engage many specialties, not only those traditionally associated with supportive and palliative care. We hope to extend the readership to doctors, nurses, other healthcare workers and researchers in medical and surgical specialties, including but not limited to cardiology, gastroenterology, geriatrics, neurology, oncology, paediatrics, primary care, psychiatry, psychology, renal medicine, respiratory medicine.
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