Current Advances in Palliative and Hospice Care

A special issue of Medical Sciences (ISSN 2076-3271).

Deadline for manuscript submissions: closed (31 December 2018) | Viewed by 35812

Special Issue Editors


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Guest Editor
Department of Palliative Medicine, University Hospital Cologne, Koeln, Germany
Interests: MS; brain tumor; desire to die; caring community
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Guest Editor
1. Professeur Ordinaire, Faculté de Biologie et de Médecine, Centre Hospitalier Universitaire Vaudois, Université de Lausanne, CH-1010 Lausanne, Switzerland
2. Directeur Académique, Institut Universitaire de Formation et de Recherche en Soins, CH-1010 Lausanne, Switzerland
Interests: palliative medicine

Special Issue Information

Dear Colleagues,

This Special Issue will summarize recent advances in the field of palliative and hospice care. This will include a review of relevant publications within the last two years, and will cover the broad range of topics relevant for clinicians in the field. Topics will include symptom control, psycho-social care, bereavement, early integration and spirituality as examples for the clinical part. The policy section will contain information on the WHO opioid policy, caring community and integrating palliative and hospice care. Education will cover, capacity building, competence and leadership. Ethics will include, the wish for hastening death, as well as other relevant issues.

Prof. Dr. Raymond D. Voltz
Dr. Philip Larkin
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Medical Sciences is an international peer-reviewed open access quarterly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 1400 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • Policy
  • Practice
  • Clinical
  • Education
  • Ethics

Published Papers (3 papers)

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Research

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9 pages, 729 KiB  
Article
Advances and Challenges in European Paediatric Palliative Care
by Lorna K Fraser, Myra Bluebond-Langner and Julie Ling
Med. Sci. 2020, 8(2), 20; https://doi.org/10.3390/medsci8020020 - 17 Apr 2020
Cited by 22 | Viewed by 4800
Abstract
Advances in both public health and medical interventions have resulted in a reduction in childhood mortality worldwide over the last few decades; however, children still have life-threatening conditions that require palliative care. Children’s palliative care is a specialty that differs from palliative care [...] Read more.
Advances in both public health and medical interventions have resulted in a reduction in childhood mortality worldwide over the last few decades; however, children still have life-threatening conditions that require palliative care. Children’s palliative care is a specialty that differs from palliative care for adults in many ways. This paper discusses some of the challenges, and some of the recent advances in paediatric palliative care. Developing responsive services requires good epidemiological data, as well as a clarity on services currently available and a robust definition of the group of children who would benefit from palliative care. Once a child is diagnosed with a life-limiting condition or life-limiting illness, parents face a number of complex and difficult decisions; not only about care and treatment, but also about the place of care and ultimately, place of death. The best way to address the needs of children requiring palliative care and their families is complex and requires further research and the routine collection of high-quality data. Although research in children’s palliative care has dramatically increased, there is still a dearth of evidence on key components of palliative care notably decision making, communication and pain and symptom management specifically as it relates to children. This evidence is required in order to ensure that the care that these children and their families require is delivered. Full article
(This article belongs to the Special Issue Current Advances in Palliative and Hospice Care)
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Review

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16 pages, 311 KiB  
Review
Current Advances in Palliative & Hospice Care: Problems and Needs of Relatives and Family Caregivers During Palliative and Hospice Care—An Overview of Current Literature
by Karin Oechsle
Med. Sci. 2019, 7(3), 43; https://doi.org/10.3390/medsci7030043 - 12 Mar 2019
Cited by 23 | Viewed by 7748
Abstract
Palliative and hospice care aims to improve quality of life of patients’ relatives, but still little is known about their specific problems and needs. We present a comprehensive literature update. Narrative review to present an expert overview of peer-reviewed, English-written original research publications [...] Read more.
Palliative and hospice care aims to improve quality of life of patients’ relatives, but still little is known about their specific problems and needs. We present a comprehensive literature update. Narrative review to present an expert overview of peer-reviewed, English-written original research publications and reviews on psychosocial and existential problems, supportive needs as well as interventions for relatives during the patients’ disease trajectory published between January 2017 and November 2018. A total of 64 publications were included. Relatives report high rates of psychological and existential distress, burden and psychological morbidity during the total disease trajectory of the patient. In addition, relatives report an alarmingly high number of unmet needs with information being the central issue. Relatives’ problems and needs are part of complex systems influenced by various socio-demographic factors and patient–relatives-interactions and dependency between different psychological phenomena. First support interventions for relatives during disease trajectory have proven feasible and secondary data from randomized studies suggest beneficial effects of providing early palliative care also for relatives. Relatives should be addressed to a still larger extent in the daily practice of palliative and hospice care, thus further research to reveal more detailed systematic information is needed to improve relatives’ psychological burden and quality of life. Full article
(This article belongs to the Special Issue Current Advances in Palliative and Hospice Care)
21 pages, 677 KiB  
Review
Spiritual Care in Palliative Care: A Systematic Review of the Recent European Literature
by Marie-José H. E. Gijsberts, Anke I. Liefbroer, René Otten and Erik Olsman
Med. Sci. 2019, 7(2), 25; https://doi.org/10.3390/medsci7020025 - 07 Feb 2019
Cited by 124 | Viewed by 22744
Abstract
Many studies on spiritual care in palliative care are performed in the US, leaving other continents unexplored. The objective of this systematic review is to map the recent studies on spiritual care in palliative care in Europe. PubMed, CINAHL, ATLA, PsycINFO, ERIC, IBSS, [...] Read more.
Many studies on spiritual care in palliative care are performed in the US, leaving other continents unexplored. The objective of this systematic review is to map the recent studies on spiritual care in palliative care in Europe. PubMed, CINAHL, ATLA, PsycINFO, ERIC, IBSS, Web of Science, EMBASE, and other databases were searched. Included were European studies published in a peer-reviewed journal in 2015, 2016, or 2017. The characteristics of the included studies were analyzed and a narrative synthesis of the extracted data was performed. 53 articles were included. Spiritual care was seen as attention for spirituality, presence, empowerment, and bringing peace. It implied creative, narrative, and ritual work. Though several studies reported positive effects of spiritual care, like the easing of discomfort, the evidence for spiritual care is low. Requirements for implementation of spiritual care in (palliative) care were: Developing spiritual competency, including self-reflection, and visibility of spirituality and spiritual care, which are required from spiritual counselors that they participated in existing organizational structures. This study has provided insight into spiritual care in palliative care in Europe. Future studies are necessary to develop appropriate patient outcomes and to investigate the effects of spiritual care more fully. Full article
(This article belongs to the Special Issue Current Advances in Palliative and Hospice Care)
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