Literature DB >> 16499457

Introduction: papers from the National Institutes of Health State-of-the-Science Conference on Improving End-of-Life Care.

P A Grady1.   

Abstract

A 1997 Institute of Medicine report cited growing public concern about the quality of care in the U.S. health care system for persons at the end of life. The National Institute of Nursing Research (NINR), the lead Institute at the National Institutes of Health for end-of-life research, has conducted a number of public forums to gather information and to assist in identifying research priorities. The complexity of biomedical research requires new methods of discovery, and scientists must use a broad approach and explore new models of team science. In December 2004, NINR and the NIH Office of Medical Applications of Research, along with many co-sponsors, held an interdisciplinary State-of-the-Science Conference on Improving End-of-Life Care. The conference panel identified many gaps in our current state of knowledge and provided suggestions for future research directions. This supplement presents papers from a distinguished group of scientists with a wide range of backgrounds who participated in this state-of-the-science conference.

Entities:  

Mesh:

Year:  2005        PMID: 16499457     DOI: 10.1089/jpm.2005.8.s-1

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  13 in total

1.  Identifying Key Priorities for Future Palliative Care Research Using an Innovative Analytic Approach.

Authors:  Catherine Riffin; Karl Pillemer; Emily K Chen; Marcus Warmington; Ronald D Adelman; M C Reid
Journal:  Am J Public Health       Date:  2015-01       Impact factor: 9.308

2.  Practice-Based Research Priorities for Palliative Care: Results From a Research-to-Practice Consensus Workshop.

Authors:  Karl Pillemer; Emily K Chen; Catherine Riffin; Holly Prigerson; M C Reid
Journal:  Am J Public Health       Date:  2015-09-17       Impact factor: 9.308

3.  FAmily CEntered (FACE) advance care planning: Study design and methods for a patient-centered communication and decision-making intervention for patients with HIV/AIDS and their surrogate decision-makers.

Authors:  Allison L Kimmel; Jichuan Wang; Rachel K Scott; Linda Briggs; Maureen E Lyon
Journal:  Contemp Clin Trials       Date:  2015-06-02       Impact factor: 2.226

4.  Why is high-quality research on palliative care so hard to do? Barriers to improved research from a survey of palliative care researchers.

Authors:  Emily K Chen; Catherine Riffin; M Cary Reid; Ronald Adelman; Marcus Warmington; Sonal S Mehta; Karl Pillemer
Journal:  J Palliat Med       Date:  2014-06-02       Impact factor: 2.947

5.  A Qualitative Inquiry on Palliative and End-of-Life Care Policy Reform.

Authors:  Hannah C Schreibeis-Baum; Lea E Xenakis; Emily K Chen; Mark Hanson; Sangeeta Ahluwalia; Gery Ryan; Karl A Lorenz
Journal:  J Palliat Med       Date:  2016-04       Impact factor: 2.947

6.  Acceptability of Family-Centered Advanced Care Planning for Adolescents With HIV.

Authors:  Ronald H Dallas; Allison Kimmel; Megan L Wilkins; Sohail Rana; Ana Garcia; Yao I Cheng; Jichuan Wang; Maureen E Lyon
Journal:  Pediatrics       Date:  2016-11-01       Impact factor: 7.124

7.  A randomized clinical trial of adolescents with HIV/AIDS: pediatric advance care planning.

Authors:  Maureen E Lyon; Lawrence J D'Angelo; Ronald H Dallas; Pamela S Hinds; Patricia A Garvie; Megan L Wilkins; Ana Garcia; Linda Briggs; Patricia M Flynn; Sohail R Rana; Yao Iris Cheng; Jichuan Wang
Journal:  AIDS Care       Date:  2017-03-30

8.  Research participation by older adults at end of life: barriers and solutions.

Authors:  Melissa Lehan Mackin; Keela Herr; Kimberly Bergen-Jackson; Perry Fine; Chris Forcucci; Sara Sanders
Journal:  Res Gerontol Nurs       Date:  2009-04-30       Impact factor: 1.571

Review 9.  Pain and symptom management in palliative care and at end of life.

Authors:  Diana J Wilkie; Miriam O Ezenwa
Journal:  Nurs Outlook       Date:  2012-09-14       Impact factor: 3.250

10.  Is it safe? Talking to teens with HIV/AIDS about death and dying: a 3-month evaluation of Family Centered Advance Care (FACE) planning - anxiety, depression, quality of life.

Authors:  Maureen E Lyon; Patricia A Garvie; Linda Briggs; Jianping He; Robert Malow; Lawrence J D'Angelo; Robert McCarter
Journal:  HIV AIDS (Auckl)       Date:  2010-02-18
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