Comparison of legislation, regulations and national health strategies for palliative care in seven European countries (Results from the Europall Research Group): a descriptive study
Open Access
- 17 July 2013
- journal article
- research article
- Published by Springer Nature in BMC Health Services Research
- Vol. 13 (1) , 275
Abstract
Background: According to EU policy, anyone in need of palliative care should be able to have access to it. It is therefore important to investigate which palliative care topics are subject to legislation and regulations in Europe and how these are implemented in (national) health care plans. This paper aims to deliver a structured overview of the legislation, existing regulations and the different health care policies regarding palliative care in seven European countries. Methods: In 2008 an inventory of the organisation of palliative care was developed by the researchers of the Europall project. Included were two open questions about legislation, regulations, and health policy in palliative care. This questionnaire was completed using palliative care experts selected from Belgium, England, France, Germany, the Netherlands, Poland and Spain. Additionally, (grey) literature on palliative care health policy and regulations from the participating countries was collected to complete the inventory. Comparative analysis of country specific information was performed afterwards. Results: In all countries palliative care regulations and policies existed (either in laws, royal decrees, or national policies). An explicit right to palliative care was mentioned in the Belgium, French and German law. In addition, access to palliative care was mentioned by all countries, varying from explicit regulations to policy intentions in national plans. Also, all countries had a national policy on palliative care, although sometimes mainly related to national cancer plans. Differences existed in policy regarding palliative care leave, advance directives, national funding, palliative care training, research, opioids and the role of volunteers. Conclusions: Although all included European countries have policies on palliative care, countries largely differ in the presence of legislation and regulations on palliative care as well as the included topics. European healthcare policy recommendations should support palliative care access across Europe.Keywords
This publication has 15 references indexed in Scilit:
- Corrective role ofEugenia jambolanaon testicular impairment in streptozotocin-induced diabetic male albino rat: An approach through genomic and proteomic studyAndrologia, 2013
- Genome drafts of four phytoplasma strains of the ribosomal group 16SrIIIMicrobiology, 2012
- The burden of non-acute dying on society: dying of cancer and chronic disease in the European UnionBMJ Supportive & Palliative Care, 2012
- Quality indicators for palliative care: Debates and dilemmasPalliative Medicine, 2012
- Health system characteristics of quality care delivery: A comparative case study examination of palliative care for cancer patients in four regions in Ontario, CanadaPalliative Medicine, 2011
- A New Set of Quality Indicators for Palliative Care: Process and Results of the Development TrajectoryJournal of Pain and Symptom Management, 2011
- Formulary availability and regulatory barriers to accessibility of opioids for cancer pain in Europe: a report from the ESMO/EAPC Opioid Policy InitiativeAnnals of Oncology, 2010
- The Budapest Commitments: setting the goals A joint initiative by the European Association for Palliative Care, the International Association for Hospice and Palliative Care and Help the HospicesPalliative Medicine, 2007
- Realist review - a new method of systematic review designed for complex policy interventionsJournal of Health Services Research & Policy, 2005
- In briefBMJ, 2001