1. Origins and effects of the 2014–2016 national strategy for palliative care in Croatia
- Author
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Anna Sagan, Aleksandar Džakula, Karmen Lončarek, and Renata Marđetko
- Subjects
BIOMEDICINE AND HEALTHCARE. Clinical Medical Sciences ,Palliative care ,Croatia ,Professionalization ,Health Services Accessibility ,Reimbursement Mechanisms ,03 medical and health sciences ,0302 clinical medicine ,Nursing ,policy development ,palliative care ,health care provision ,health care organization ,health care reform ,Health care organization ,Political science ,General election ,Health care ,Humans ,Health care provision ,National level ,030212 general & internal medicine ,Strategic planning ,Health care reform ,business.industry ,BIOMEDICINA I ZDRAVSTVO. Kliničke medicinske znanosti ,Health Policy ,Policy development ,030220 oncology & carcinogenesis ,Government Regulation ,Christian ministry ,business - Abstract
Croatia is among the last countries in Europe to develop organized palliative care at the national level. Real changes in this area started after the parliamentary elections in 2011 and culminated in the 2013 adoption of the Strategic Plan for Palliative Care Development 2014–2016. The National Board for Palliative Care (NBPC), appointed by the Ministry of Health, was in charge of creating a scalable palliative care model and national guidelines. The Board drew on experiences from both neighbouring countries with similar societies and/or health care models (Bosnia and Herzegovina, Poland) and an international leader in palliative care (United Kingdom). It recognised that provision of palliative care in Croatia, thus far based on volunteering and isolated enthusiastic activities, needed to be improved through professionalization, regulation, and organized development. A variety of policy measures was used to implement these changes, including the introduction of professional guidelines and new payment models. The development of new palliative care structures and services significantly increased the number of patients who could access palliative care, from around 1–2% of patients needing such care in 2011 to 20–35% in 2014. It also ensured the provision of more appropriate services at each point of the palliative care pathway. The Strategy was extended for the 2017–2020 period.
- Published
- 2018
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