Telepalliation creates a sense of security: A qualitative study of patients with cancer receiving palliative care.

IF 3.9 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Jarl Voss Andersen Sigaard, Elisabet Dortea Ragnvaldsdóttir Joensen, Una Rósa Birgisdóttir, Helle Spindler, Birthe Dinesen
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Abstract

Background: With the aging population and increasing prevalence of chronic illnesses, the demand for palliative care is rising. However, only a small percentage of patients in need receive palliative care. Many prefer home-based care, valuing continuous support and communication from healthcare professionals. Telepalliative care, utilizing telehealth technology, may enhance home-based palliative care by improving access to professionals, facilitating communication, and offering a cost-effective approach.

Aim: The aim of this study was to explore patients' experiences with the functionality of the Telepalliation program while receiving specialized palliative care.

Design: Qualitative sub-study within the multimethod randomized control trial (RCT) on the Telepal platform (ClinicalTrials.gov: NCT04995848) using semi-structured individual interviews inspired by Brinkmann & Kvale. Data was thematically coded using NVIVO 12.0 software.

Setting/participants: The study was conducted at the University Hospital of Southern Denmark. Eighteen were randomly selected for interviews. Eligible patients were over 18, receiving specialized palliative care, and diagnosed with cancer, terminal heart failure, chronic obstructive pulmonary disease, or motor neuron disease.

Results: Four key themes emerged: "Sense of coherence," "Telepal platform," "Roles of spouse/partner and relatives," and "Cross-sector collaboration." The program improved patients' sense of security and coherence by enhancing communication with healthcare professionals. Some challenges arose due to fatigue and questionnaire volume. The platform also successfully integrated relatives into the care process.

Conclusions: The Telepal program enhanced communication, continuity, and personalized care, improving the sense of security for patients and families, though some patients faced challenges with fatigue and questionnaire burden.

临终关怀创造了一种安全感:一项接受姑息治疗的癌症患者的定性研究。
背景:随着人口老龄化和慢性病患病率的增加,对姑息治疗的需求正在上升。然而,只有一小部分有需要的患者接受了姑息治疗。许多人更喜欢家庭护理,重视医疗保健专业人员的持续支持和沟通。利用远程医疗技术的远程姑息治疗可以通过改善获得专业人员的机会、促进沟通和提供具有成本效益的方法来加强家庭姑息治疗。目的:本研究的目的是探讨患者在接受专业姑息治疗时对远端治疗功能的体验。设计:在Telepal平台(ClinicalTrials.gov: NCT04995848)上进行多方法随机对照试验(RCT)的定性子研究,采用半结构化的个人访谈,灵感来自Brinkmann & Kvale。使用NVIVO 12.0软件对数据进行主题编码。环境/参与者:本研究在南丹麦大学医院进行。随机抽取18人进行访谈。符合条件的患者年龄在18岁以上,接受专门的姑息治疗,并被诊断患有癌症、晚期心力衰竭、慢性阻塞性肺疾病或运动神经元疾病。结果:出现了四个关键主题:“一致性”、“远程平台”、“配偶/伴侣和亲属的角色”和“跨部门协作”。该计划通过加强与医疗保健专业人员的沟通,提高了患者的安全感和一致性。由于疲劳和问卷量,出现了一些挑战。该平台还成功地将亲属融入到护理过程中。结论:尽管部分患者面临疲劳和问卷负担的挑战,但远程护理项目增强了沟通、连续性和个性化护理,提高了患者和家属的安全感。
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来源期刊
Palliative Medicine
Palliative Medicine 医学-公共卫生、环境卫生与职业卫生
CiteScore
7.60
自引率
9.10%
发文量
125
审稿时长
6-12 weeks
期刊介绍: Palliative Medicine is a highly ranked, peer reviewed scholarly journal dedicated to improving knowledge and clinical practice in the palliative care of patients with far advanced disease. This outstanding journal features editorials, original papers, review articles, case reports, correspondence and book reviews. Essential reading for all members of the palliative care team. This journal is a member of the Committee on Publication Ethics (COPE).
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