ArticleBMC medical ethics2020
Barriers in implementing the dying patient law: the Israeli experience - a qualitative study.
Article in BMC medical ethics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
What it found
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Who cites it
5 citing papers in PubMed.
- Cultural, religious, and demographic factors shaping Arab healthcare providers' decisions on referring Arab patients to palliative care in Israel: a qualitative study.BMC medical ethics · 2026Article
- Frames of dying: a qualitative study of end-of-life experiences of terminal Arab patients.BMC palliative care · 2025Article
- The Professional Guest: conceptualizing home visits in palliative care settings.Palliative care and social practice · 2024Article
- Ethical challenges in end-stage dementia: Perspectives of professionals and family care-givers.Nursing ethicsArticle
- Article
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Authors and funding
2 authors.
Funding
Abstract
backgroundCoping with end-of-life issues is a major challenge for governments and health systems. Despite progress in legislation, many barriers exist to its full implementation. This study is aimed at identifying these end-of-life barriers in relation to Israel.
methodsQualitative in-depth interviews using professionals and decision makers in the health-care and related systems (n = 37) were carried out, along with two focus groups based on brainstorming techniques consisting of nurses (n = 10) and social workers (n = 10). Data was managed and analyzed using Naralyzer software.
resultsQualitative analysis showed identification of six primary barriers: 1) law, procedures, and forms; 2) clinical aspects; 3) human aspects; 4) knowledge and skills of medical teams; 5) communication; and 6) resource allocation. These were further divided into 44 sub area barriers.
conclusionsThis study highlights the role of the family doctor in end-of-life by training physicians in decision-making workshops and increasing their knowledge in the field of palliative medicine. Effectively channeling resources, knowledge, and support for medical teams, by accounting for the structure and response of the units for home treatment will improve patient's access to information on and support for end-of-life laws, as well as reduce legislative barriers in other countries that face the same issues.
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