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This report is the product of a multi-stakeholder process launched by the King Baudouin Foundation in 2007 to examine the possibilities of improving patient participation in health-care policy.The project consisted of an inductive process in which a diverse group of stakeholders were questioned, using both individual interviews and group discussions. The results of these interviews were analysed and summarised to obtain an overview of the current debate on patient participation in Belgium.To help clarify the wealth of interview material, a number of dimensions of patient participation were distinguished, namely : participation activities, participation levels, relevant players and definition of the term patient . Also examined were the contextual factors liable to promote or hinder the developmentof a more participatory model in Belgium, as well as the associated risks. The analysis was structured around four basic premises, each tying patient participation to a specific goal. These were : better resource management ; higher quality care ; increased self-reliance ; and better representation of particular social players.These insights formed the basis for interaction with the wider stakeholder community in a series of multi-stakeholder dialogues. The first two sessions spawned a host of interesting thoughts on such issues as: the representation of patients who are unable to express themselves ; the need for an integrated approach (both from the policy perspective and in terms of individual patients and their various needs) ; the possibility of a self-reinforcing dynamic for making patient organisations more representative ; and the need for arbitration methods as a means of moving beyond individual interests at policy level.This part of the process culminated in the stakeholder day on 12 October 2007, which generated a raft of practical proposals for improving patient participation in health-care policy. Participants gave priority to the following issues, in order of importance : the professionalisation of patient organisations (i. e. developing stable and sustainable competencies to ensure effective participation in policy) ; the representation of patient organisations at macro-level ; fostering a more participatory culture among care providers ; involving patients in assessing the quality of care ; and improving the interaction between mutual insurance companies and patients/patient organisations.The stakeholders also proposed packages of practical measures for moving the process forward. One thing that emerged very markedly was the desire to continue and intensify the process of dialogue and discussion, both in the context of patient organisations and with other stakeholders.This report therefore marks an important but temporary consolidation stage in an expanding multistakeholder dynamic. The Foundation will use the results of the project as the basis for further initiatives to improve patient participation.
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Participatie van patiënten wordt gezien als de manier om het onderzoek in de gezondheidszorg te verbeteren, maar ook om een betere kwaliteit en nauwkeuriger afgestemd beleid te ontwikkelen. Het moet leiden tot een gezondheidszorg die patiënten en cliënten centraal stelt. De praktijk is echter weerbarstig. En ondanks de reuzenstappen die zijn gemaakt staan er nog veel vragen open over hoe participatie daadwerkelijk gerealiseerd kan worden. Meer is niet beter, zo weten we inmiddels, maar wanneer is het dan voldoende of goed? Vragen die in dit boek bediscussieerd worden zijn: * Hoe staat het met de patiëntenparticipatie in onderzoek, kwaliteit en beleid binnen de gezondheidszorg? * Is het daadwerkelijk gelukt om patiëntenparticipatie in te weven in het gezondheidszorgsysteem en het wetenschappelijk onderzoek? * Welke aspecten zijn daarbij uit het oog geraakt of onderbelicht gebleven? * Moeten we de doelen bijstellen, nieuwe vormen van samenwerking zoeken en nieuwe tools ontwikkelen of kunnen we op de ingeslagen wegen verder? Aan de hand van spraakmakende casuïstiek en dertien essays expliciteren Christine Dedding en Meralda Slager de spanningsvelden rondom patiëntenparticipatie, ten einde richting voor de toekomst te bepalen. Dr. Christine Dedding is medisch antropoloog en als universitair docent en onderzoeker werkzaam bij het Athena Instituut van de VU. Tevens is zij mede initiatiefnemer van De Participatietafel. Dr. Meralda Slager is gezondheidswetenschapper en als hoofddocent werkzaam bij de Academie voor Gezondheidszorg aan de Haagse Hogeschool. Daarvoor werkte zij bij ZonMw en was ze onder meer verantwoordelijk voor het ZonMw/VSBfonds-programma Patiëntenparticipatie in onderzoek, kwaliteit en beleid.
#SBIB:316.334.3M40 --- Patiëntenparticipatie --- Medische sociologie: zorgenverstrekkers, relatie met hulpvragers --- 616.083.5/9 --- Patient Participation --- Health Care --- Delivery of Health Care --- W 84.7 Patient care planning. Progressive health care (General) --- PXL-Healthcare 2017 --- maatschappelijke zorg --- patiëntenzorg --- patiëntenparticipatie --- empowerment --- Sociology of minorities --- Sociology of health
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"This book examines the challenges countries are facing with regard to providing and paying for long-term care. With populations ageing and the need for long-term care growing rapidly, this book looks at such issues as: future demographic trends, policies to support family carers, long-term care workers, financing arrangements, long-term care insurance, and getting better value for money in long-term care."--Publisher description.
Aged --- Long-Term Care --- Insurance --- Public Policy --- Health Policy --- W 84.7 Patient care planning. Progressive health care (General) --- #SBIB:316.334.3M50 --- #SBIB:35H436 --- Organisatie van de gezondheidszorg: algemeen, beleid --- Beleidssectoren: welzijn, volksgezondheid en cultuur --- Long-term care insurance --- Older people --- Aging people --- Elderly people --- Old people --- Older adults --- Older persons --- Senior citizens --- Seniors (Older people) --- Age groups --- Persons --- Gerontocracy --- Gerontology --- Old age --- Health insurance --- Insurance, Long-term care --- Long-term care --- Long-term care&delete& --- Finance --- Government policy
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