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The Journal of Pain & Palliative Care Pharmacotherapy is a quarterly peer-reviewed medical journal covering advances in acute, chronic, and end-of-life symptom management. It is published by Informa Healthcare and the editor in chief is Arthur G. Lipman (University of Utah Health Sciences Center).
In 1999, the Pain and Palliative Care Society established the 'Neighbourhood Network in Palliative Care', aimed at increasing community participation in palliative care. In 2003, the Institute was shifted to a separate building for training, research and patient care.
Palliative care (derived from the Latin root palliare, meaning "to cloak") is an interdisciplinary medical caregiving approach aimed at optimising quality of life and mitigating or reducing suffering among people with serious, complex, and often terminal illnesses. [1] Within the published literature, many definitions of palliative care exist.
Rajagopal is one of the founders of Pain and Palliative Care Society (PPCS) in Medical College, Calicut, Kerala in 1993. [32] In 1995, PPCS was recognized as a model demonstration project by the World Health Organization for community based palliative care activities. It set up an Institute of Palliative Medicine (IPM), with numerous link centres.
It is a continuation of the PRN Forum (Pain Research News forum), a bimonthly journal published from 1982 to 1985. [1] It is the official journal of the American Academy of Hospice and Palliative Medicine and the National Hospice and Palliative Care Organization. It was formally the official journal of the United States Cancer Pain Relief ...
Pain management practitioners come from all fields of medicine. In addition to medical practitioners, a pain management team may often benefit from the input of pharmacists, physiotherapists, clinical psychologists and occupational therapists, among others. Together the multidisciplinary team can help create a package of care suitable to the ...
Palliative care got its start as hospice care delivered largely by caregivers at religious institutions. The first formal hospice was founded in 1948 by the British physician Dame Cicely Saunders in order to care for patients with terminal illnesses. [2] She defined key physical, emotional, social, and spiritual dimensions of distress in her work.
According to the Global Atlas of Palliative Care at the End of Life, 78% of adults and 98% of children in need of palliative care at the end of life live in low and middle-income countries. Nevertheless, hospice and palliative care provision in Egypt is limited and sparsely available relative to the size of the population. [59]