scholarly journals 'Palliative care is a human right'

2009 ◽  
Vol 21 (2) ◽  
pp. 76-79 ◽  
Author(s):  
Farzana Khan ◽  
Nezumuddin Ahmad ◽  
Mostak Anwar
Keyword(s):  
Palliative Care ◽  
Unmet Needs ◽  
Human Right ◽  
Care Services ◽  
The World ◽  
Care Policies ◽  
Palliative Care Services ◽  
The Right ◽  
Basic Standard

Palliative care is about achieving the highest quality of life (QOL) and promoting comfort and dignity for patients with incurable and life limiting diseases. Palliative care advocacy has been strengthened by pronouncing that ‘the provision of palliative care is a human right'. International covenants have agreed upon this. There are huge unmet needs of patients with life-limiting illnesses in Bangladesh as well as in the world. The majority of countries have neither formal palliative care policies nor integrated palliative care services to meet basic standard guidelines in the provision of palliative care. The nature of the right in the context of international and Bangladesh perspective is discussed here. Journal of BSA, 2008; 21(2): 76-79

scholarly journals Identifying Palliative Care Needs in Assisted Living

2020 ◽  
Vol 4 (Supplement_1) ◽  
pp. 788-788
Author(s):  
Daniel David ◽  
Abraham Brody ◽  
Tina Sadarangani ◽  
Bei Wu ◽  
Tara Cortez
Keyword(s):  
Palliative Care ◽  
Assisted Living ◽  
Unmet Needs ◽  
Care Needs ◽  
Code Status ◽  
Care Services ◽  
Palliative Care Services ◽  
Advance Care ◽  
Palliative Care Needs

Abstract Many residents of Assisted Living (AL) confront serious illness and therefore might benefit from greater access to Palliative Care Services to improve quality of life. We surveyed resident records and AL nursing staff to identify patients in need of Palliative Care. Preliminary findings showed that nurses predicted 23% would not be alive and 49% would no longer live in AL. A majority of residents were over the age of 90, yet 30% did not have a reported code status. These findings suggest that a substantial portion of AL residents may have unmet needs with respect to palliative care. Future interventions are needed to support advance care planning conversations and make palliative care more accessible to this population.

Barriers to the delivery of palliative care

2015 ◽  
Author(s):  
Barry J.A. Laird
Keyword(s):  
Palliative Care ◽  
Clinical Care ◽  
World Health ◽  
Human Right ◽  
Care Services ◽  
The World ◽  
Effective Delivery ◽  
Palliative Care Services ◽  
The Many ◽  
Health Organization

This chapter discusses several key barriers to the delivery of palliative care, firstly considering the definition of ‘palliative care’. It describes the World Health Organization (WHO) definition and notes that the ideology of palliative care being a concept with which to approach management of patients may still not be fully understood. Furthermore, the differences between generalist and specialist palliative care may also contribute to confusion. Although palliative care as a concept has largely been embraced throughout the world, its implementation into routine clinical care is lacking. Essential to the change from palliative care being a principle available to the few, to being available to all, and a human right, is the need to address the many barriers to the efficient and effective delivery of high-quality palliative care. The chapter argues that the WHO is the key group necessary to develop palliative care worldwide and, together with international palliative care organizations, to help countries advance palliative care services.

Global Palliative Care

2019 ◽  
pp. 868-876
Author(s):  
Virginia LeBaron ◽  
Annette Galassi
Keyword(s):  
Palliative Care ◽  
Universal Access ◽  
Emerging Infectious Diseases ◽  
World Health ◽  
Noncommunicable Diseases ◽  
Human Right ◽  
Middle Income ◽  
Care Services ◽  
The World ◽  
Palliative Care Services

Access to quality palliative care and pain relief is increasingly viewed as a fundamental human right, as evidenced by the landmark Palliative Care Resolution passed by the World Health Assembly in 2014. Despite this, millions of people around the world continue to suffer without access to palliative care services—especially if they are poor, members of minority or marginalized groups, or live in low- and middle-income countries. The aging of the world’s population, combined with the rising incidence of noncommunicable diseases and the uncertainty of new, emerging infectious diseases, make the need for universal access to quality palliative care a global imperative. All nurses, regardless of their role or where they practice, can play a critical part in palliative care at the global level through advocacy, training, research, cultural exchange, and mentorship and by advocating for vulnerable populations.

What is palliative care?

2020 ◽  
Vol 14 (1) ◽  
pp. 19-26
Author(s):  
Francis Odukwe ◽  
Francis Ezeh
Keyword(s):  
Palliative Care ◽  
End Of Life ◽  
World Health Organisation ◽  
World Health ◽  
Care Services ◽  
Care Specialist ◽  
The World ◽  
Palliative Care Services ◽  
Serious Injuries

In 1990, the World Health Organisation (WHO) recognised palliative care as a distinct specialty dedicated to relieving suffering and improving quality of life for patients with life-limiting illnesses or serious injuries. Fourteen years later, the WHO in its publication ‘ Global Atlas of Palliative Care at the End of Life’, projected that, ‘each year in the world, around 377 per 100,000 of the adult (over 15 years of age) population and 63 per 100,000 of the child population (under 15 years of age) will require “palliative care at the end of life’. This article will discuss what constitutes palliative care, the different elements of palliative care, the approaches to palliative care, specialist palliative care services, end of life care and where GPs fit into this area. We will also be sharing tips on providing palliative care as a GP and for GP trainees.

scholarly journals Pravo na palijativnu skrb za djecu u Republici Hrvatskoj

2020 ◽  
Vol 55 (2) ◽  
pp. 82-91
Author(s):  
Marina Milić Babić ◽  
Marina Hranj
Keyword(s):  
Palliative Care ◽  
Right To Health ◽  
Human Right ◽  
Her Family ◽  
Right To Health Care ◽  
Starting Point ◽  
The Family ◽  
The Republic ◽  
The Right

Palliative care for children means active, complete care on physical, psychological, social and spiritual levels, and it includes collaboration and active work with the family. Palliative care for children lasts during the period of illness and continues after the death of the child in the form of expert assistance to the family in their grief. Such care follows the principles of individual, holistic, transdisciplinary and biopsychosocial-spiritual approaches that come together in promoting the quality of life of a child and his or her family. Numerous legal sources are the starting point for defining palliative care for children as a fundamental human right to health care, as well as for defining basic actions within this fundamental right. The right to palliative care includes rights from different systems, and collaboration and linking of different disciplines are needed in order to meet the needs of the child and his family. The aim of this paper is to present crucial knowledge in the field of palliative care for children and to examine how this right is implemented and legally regulated in the Republic of Croatia.

Measuring Quality of Care in Palliative Care Services

2000 ◽  
Vol 3 (2) ◽  
pp. 229-236 ◽  
Author(s):  
Irene J. Higginson ◽  
Anna L. Romer
Keyword(s):  
Palliative Care ◽  
Quality Of Care ◽  
Care Services ◽  
Palliative Care Services
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