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癌症姑息治疗转诊:患者及其家庭照顾者的观点——一项系统综述

Cancer palliative care referral: patients' and family caregivers' perspectives - a systematic review.

作者信息

Patra Lipika, Ghoshal Arunangshu, Damani Anuja, Salins Naveen

机构信息

Bagchi-Karunashraya Palliative Care Centre, Bangalore Hospice Trust, Bhubaneswar, India.

University of Toronto, Toronto, Ontario, Canada.

出版信息

BMJ Support Palliat Care. 2022 Nov 3. doi: 10.1136/spcare-2022-003990.

Abstract

BACKGROUND

Despite the evidence of palliative care benefits, referrals are infrequent and delayed. Patients and their caregivers are essential stakeholders in the referral process with valuable perspectives. This review systematically explored their perceived facilitators and barriers to palliative care referral.

METHODS

4 subject-specific databases (PubMed, Cumulative Index to Nursing and Allied Health Literature, PsycINFO and EMBASE), 3 multidisciplinary databases (SCOPUS, Web of Science and Cochrane database) and 11 journals from 1 January 1990 to 31 May 2022 were searched; and scored for their methodological rigour using Hawker's tool. Findings were synthesised using Popay's Narrative Synthesis method and interpreted using decision-making theory.

RESULTS

4 themes were generated from 14 studies: (1) The timing of referral should be right and communication must be comprehensive. Delays in initiating serious illness conversations, prognostication, and decision-making hindered referral. In contrast, the presence of symptoms facilitated it. (2) Referral was equated to death, and as an inferior form of treatment, a rebranding might mitigate the stigma. (3) Referral made families feel emotional and devastated; explanation and team initiatives enabled the normalisation and positive coping. (4) Long-term holistic palliative care facilitated a positive care experience and a sense of reassurance and satisfaction, enabling a smooth transition from curative to comfort care. The late referral was associated with perceived inadequate symptom management, diminished quality of life and death and complicated bereavement issues.

CONCLUSION

Patients' and caregivers' predisposition to palliative care engagement was influenced by timely referral, comprehensive communication, perception and stigma about palliative care. Longitudinal association with the palliative care team mitigated negative perceptions and improved satisfaction and coping.

PROSPERO REGISTRATION NUMBER

CRD42018091481.

摘要

背景

尽管有证据表明姑息治疗有益,但转介却很少见且延迟。患者及其护理人员是转介过程中的重要利益相关者,有着宝贵的观点。本综述系统地探讨了他们认为的姑息治疗转介的促进因素和障碍。

方法

检索了4个特定主题数据库(PubMed、护理及相关健康文献累积索引、PsycINFO和EMBASE)、3个多学科数据库(SCOPUS、科学引文索引和考科蓝数据库)以及1990年1月1日至2022年5月31日期间的11种期刊;并使用霍克工具对其方法的严谨性进行评分。研究结果采用波佩的叙事综合法进行综合,并运用决策理论进行解读。

结果

14项研究产生了4个主题:(1)转介时机要恰当,沟通必须全面。启动重病谈话、预后判断和决策的延迟阻碍了转介。相比之下,症状的出现则促进了转介。(2)转介等同于死亡,并且作为一种较低级的治疗形式,重新定位可能会减轻这种污名。(3)转介让家属感到情绪激动和崩溃;解释和团队举措使他们能够正常应对。(4)长期的整体姑息治疗促进了积极的护理体验以及安心和满足感,使从治愈性护理到舒适性护理的过渡顺利进行。延迟转介与感觉症状管理不足、生活质量和死亡质量下降以及复杂的丧亲问题有关。

结论

患者和护理人员参与姑息治疗的倾向受及时转介、全面沟通、对姑息治疗的认知和污名的影响。与姑息治疗团队的长期联系减轻了负面认知,提高了满意度和应对能力。

PROSPERO注册号:CRD42018091481。

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