scholarly journals Better Together: The Palliative Care Research Cooperative Group as a Model for Increasing Equity in the Science of Hospice and Palliative Care

2020 ◽  
Vol 23 (5) ◽  
pp. 601-602
Author(s):  
Jean S. Kutner ◽  
Christine S. Ritchie ◽  
Kathryn I. Pollak
2012 ◽  
Vol 43 (5) ◽  
pp. 902-910 ◽  
Author(s):  
David C. Currow ◽  
Jennifer J. Tieman ◽  
Aine Greene ◽  
S. Yousuf Zafar ◽  
Jane L. Wheeler ◽  
...  

2020 ◽  
Vol 60 (1) ◽  
pp. 278-279
Author(s):  
Jean Kutner ◽  
Christine Ritchie ◽  
Kathryn Pollak ◽  
Karen Kehl ◽  
Jeri Miller

2010 ◽  
Vol 13 (12) ◽  
pp. 1407-1413 ◽  
Author(s):  
Amy P. Abernethy ◽  
Noreen M. Aziz ◽  
Ethan Basch ◽  
Janet Bull ◽  
Charles S. Cleeland ◽  
...  

2021 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Susan Lysaght Hurley ◽  
Susan DeSanto-Madeya ◽  
Christine A. Fortney ◽  
Seiko Izumi ◽  
Veerawat Phongtankuel ◽  
...  

2017 ◽  
Vol 20 (6) ◽  
pp. 584-591 ◽  
Author(s):  
Christine L. Ritchie ◽  
Kathryn I. Pollak ◽  
Karen A. Kehl ◽  
Jeri L. Miller ◽  
Jean S. Kutner

2020 ◽  
Vol 2020 ◽  
pp. 1-16
Author(s):  
Rebecca Antonacci ◽  
Carol Barrie ◽  
Sharon Baxter ◽  
Sarah Chaffey ◽  
Srini Chary ◽  
...  

Background. The demand for hospice and palliative care is growing as a result of the increase of an aging population, which is most prominent in North America. Despite the importance of the topic and an increase in hospice and palliative care utilization, there still are gaps in research and evidence within the field. Aim. To determine what gaps currently exist in hospice and palliative/end-of-life care research within the context of a North American setting to ensure that future directions are grounded in appropriate evidence. Methods. Using Arksey and O’Malley’s scoping review framework, six peer-reviewed, and four grey electronic literature databases in healthcare and the social sciences were searched in mid-2019. 111 full-text articles were retrieved, with 25 articles and reports meeting the inclusion criteria. Major themes were identified through thematic context analysis: (1) clinical, (2) system access to care, (3) research methodology, and (4) caregiving-related research gaps. Results. Findings include strategies for engaging stakeholder organizations and funding agencies, implications for other stakeholder groups such as clinicians and researchers, and highlight implications for policy (e.g., national framework discussion) and practice (e.g., healthcare provider education and training and public awareness). Conclusion. Reviewing and addressing targeted research gaps is essential to inform future directions in Canada and beyond.


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