The variation of coverage and access to palliative care for cancer patients in eight European countries: an exploratory vignette approach.

IF 2.5 2区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Nathan Shuftan, Mark Dayan, Sarah Scobie, Bee Wee, Antoniya Dimova, Elka Atanasova, Liubove Murauskiene, Coralie Gandré, Zeynep Or, Gonçalo Figueiredo Augusto, Triin Habicht, Kristina Köhler, Kristiina Kahur, Bertil Axelsson, Madelon Kroneman, Judith de Jong, Anke de Veer, Wanda Bemelmans, Chantal Pereira, Ajay Aggarwal, Joanna Davies, Ewout van Ginneken, Dimitra Panteli
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Abstract

Background: Palliative care aims to maintain quality of life and offer treatment and person-centred care options for people with serious end-stage illnesses and their families. The purpose of this exploratory study was to compare the statutory coverage and access to palliative care for adult services for people with cancer in 8 European countries using a vignette approach.

Methods: We used a patient vignette to examine coverage and access to palliative care services across Europe. The palliative care vignette describes a pathway based on guidance for best practices of palliative care patients with incurable cancer. The surveys accompanying the vignette were completed by health services researchers knowledgeable on palliative care, practitioners, government officials, or teams consisting of a health systems expert working together with practitioners.

Results: Completed vignettes were received from 8 countries: Bulgaria, Estonia, France, Lithuania, the Netherlands, Portugal, Sweden and England. Services provided for palliative care envisioned in the vignette's pathway are, generally, covered by the statutory health systems. However, in some countries cost sharing exists for hospital stays, certain medicines and medical aids. Furthermore, coverage of social and financial assessments, home equipment and financial advice varied in nearly every country. Travel times to and availability of palliative care specialists were identified as challenges across nearly all countries. Organizational barriers, societal stigmas and knowledge gaps about what palliative care entails were also found to be areas in need of improvement.

Conclusions: The comparative research presented provides further insight how countries organise palliative care, how services are offered and what levels of access exist around Europe. Our study showed differences in the scope of coverage of and access to the care options in the vignette. While responses showed countries have basic levels of coverage and access to services provided, there were variations, such as availability of specialists or the extent travel and waiting times influence care delivery. Settings where patients receive services also varied. As the need for palliative care grows in the future, health ministries and insurers should be increasingly concerned with how to guarantee coverage of and access to this care, as well as aware of best practices among countries facing similar challenges.

Abstract Image

覆盖范围的变化和获得姑息治疗的癌症患者在八个欧洲国家:一个探索性的小插曲方法。
背景:姑息治疗旨在维持生活质量,为患有严重终末期疾病的患者及其家属提供治疗和以人为本的护理选择。本探索性研究的目的是比较法定覆盖率和获得姑息治疗成人服务的癌症患者在8个欧洲国家使用小插曲的方法。方法:我们使用患者小短文来检查整个欧洲姑息治疗服务的覆盖率和可及性。姑息治疗小插图描述了基于指导的途径姑息治疗患者的最佳实践无法治愈的癌症。随附小插图的调查由了解姑息治疗的卫生服务研究人员、从业人员、政府官员或由卫生系统专家与从业人员共同组成的团队完成。结果:共收到来自保加利亚、爱沙尼亚、法国、立陶宛、荷兰、葡萄牙、瑞典和英国8个国家的完整问卷。在小插图的途径所设想的姑息治疗提供的服务,通常是由法定卫生系统覆盖。但是,在一些国家,住院费用、某些药品和医疗辅助设备的费用是分担的。此外,几乎每个国家的社会和财务评估、家庭设备和财务咨询的覆盖范围各不相同。几乎所有国家都将前往姑息治疗专家的旅行时间和可获得性确定为挑战。还发现需要改进的领域包括组织障碍、社会耻辱感和关于姑息治疗需要什么的知识差距。结论:提出的比较研究提供了进一步的见解,国家如何组织姑息治疗,如何提供服务,并在欧洲存在什么水平的访问。我们的研究表明,在覆盖范围的差异和获得护理方案在小插曲。虽然答复表明各国具有基本的覆盖面和获得所提供服务的机会,但存在差异,例如是否有专家或旅行和等待时间对提供护理的影响程度。患者接受服务的环境也各不相同。随着未来对姑息治疗需求的增长,各国卫生部和保险公司应日益关注如何保证这种治疗的覆盖和获得,并了解面临类似挑战的国家之间的最佳做法。
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来源期刊
BMC Palliative Care
BMC Palliative Care HEALTH CARE SCIENCES & SERVICES-
CiteScore
4.60
自引率
9.70%
发文量
201
审稿时长
21 weeks
期刊介绍: BMC Palliative Care is an open access journal publishing original peer-reviewed research articles in the clinical, scientific, ethical and policy issues, local and international, regarding all aspects of hospice and palliative care for the dying and for those with profound suffering related to chronic illness.
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