Literature DB >> 28937333

Provider-Prioritized Domains of Quality in Pediatric Home-Based Hospice and Palliative Care: A Study of the Ohio Pediatric Palliative Care and End-of-Life Network.

Rachel Thienprayoon1,2, Melissa San Julian Mark2, Daniel Grossoehme3.   

Abstract

BACKGROUND: Children receiving hospice and palliative care (HPC) differ from adults in important ways. Children are more likely to have rare diagnoses, less likely to have cancer, have longer lengths of stay on hospice, and are more likely to be technology dependent than adults. The National Consensus Project (NCP) in Palliative Care established domains of quality for HPC, but these domains have not been evaluated for applicability in children.
OBJECTIVES: This study aims to establish consensus stakeholder-prioritized domains of high-quality pediatric home-based hospice and palliative care (HBHPC).
DESIGN: Mixed methods design. SETTING/
SUBJECTS: Providers from the Ohio Pediatric Palliative Care and End-of-life Network. MEASUREMENTS: Using a modified Delphi technique, providers were surveyed regarding the NCP quality domains for HPC.
RESULTS: There was strong consensus on the applicability of each domain to the participants' practices (median scores ranged from 0.97 to 1.0 with interquartile ranges = 0). Consensus on the rank importance of the eight domains was not achieved. Qualitative data included challenges with NCP domain 3 (Psychological and Psychiatric Aspects of Care). It was recommended that titles should remain consistent with adult standards, but domain definitions should be broadened for pediatric HBHPC. Continuity and coordination of care should be added as a ninth domain of quality in pediatric HBHPC.
CONCLUSIONS: All eight NCP domains were validated in pediatric HBHPC. A ninth domain, Continuity and Coordination of Care, was also added. Ranking the domains was not recommended as consensus indicated weighting them as equally integrated standards. Future studies are needed to evaluate parent- and patient-prioritized domains of quality in pediatric HBHPC and to validate and map pediatric-specific indicators to these domains.

Entities:  

Keywords:  domains; home-based hospice and palliative care; pediatric palliative care; quality

Mesh:

Year:  2017        PMID: 28937333      PMCID: PMC5972768          DOI: 10.1089/jpm.2017.0333

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


  7 in total

1.  Improved quality of life at end of life related to home-based palliative care in children with cancer.

Authors:  Stefan J Friedrichsdorf; Andrea Postier; Jill Dreyfus; Kaci Osenga; Susan Sencer; Joanne Wolfe
Journal:  J Palliat Med       Date:  2014-11-17       Impact factor: 2.947

2.  Exposure to home-based pediatric palliative and hospice care and its impact on hospital and emergency care charges at a single institution.

Authors:  Andrea Postier; Jody Chrastek; Sean Nugent; Kaci Osenga; Stefan J Friedrichsdorf
Journal:  J Palliat Med       Date:  2013-12-31       Impact factor: 2.947

3.  Cost Analysis and Policy Implications of a Pediatric Palliative Care Program.

Authors:  Daphna Gans; Max W Hadler; Xiao Chen; Shang-Hua Wu; Robert Dimand; Jill M Abramson; Betty Ferrell; Allison L Diamant; Gerald F Kominski
Journal:  J Pain Symptom Manage       Date:  2016-05-24       Impact factor: 3.612

4.  American Academy of Pediatrics. Committee on Bioethics and Committee on Hospital Care. Palliative care for children.

Authors: 
Journal:  Pediatrics       Date:  2000-08       Impact factor: 7.124

5.  Hospice Care for Children With Cancer: Where Do These Children Die?

Authors:  Rachel Thienprayoon; Simon C Lee; David Leonard; Naomi Winick
Journal:  J Pediatr Hematol Oncol       Date:  2015-07       Impact factor: 1.289

6.  Comparison of pediatric and adult hospice patients using electronic medical record data from nine hospices in the United States, 2008-2012.

Authors:  Laura Dingfield; Laura Bender; Pamela Harris; Kristina Newport; Margo Hoover-Regan; Chris Feudtner; Sheila Clifford; David Casarett
Journal:  J Palliat Med       Date:  2014-11-20       Impact factor: 2.947

Review 7.  Pediatric palliative care in the community.

Authors:  Erica C Kaye; Jared Rubenstein; Deena Levine; Justin N Baker; Devon Dabbs; Sarah E Friebert
Journal:  CA Cancer J Clin       Date:  2015-05-07       Impact factor: 508.702

  7 in total
  4 in total

1.  Defining Provider-Prioritized Domains of Quality in Pediatric Home-Based Hospice and Palliative Care: A Study of the Ohio Pediatric Palliative Care and End-of-Life Network.

Authors:  Rachel Thienprayoon; Evaline Alessandrini; Millicent Frimpong-Manso; Daniel Grossoehme
Journal:  J Palliat Med       Date:  2018-06-29       Impact factor: 2.947

Review 2.  A systematic concept analysis of 'technology dependent': challenging the terminology.

Authors:  Maria Brenner; Denise Alexander; Mary Brigid Quirke; Jessica Eustace-Cook; Piet Leroy; Jay Berry; Martina Healy; Carmel Doyle; Kate Masterson
Journal:  Eur J Pediatr       Date:  2020-07-24       Impact factor: 3.183

3.  Developing a family-reported measure of experiences with home-based pediatric palliative and hospice care: a multi-method, multi-stakeholder approach.

Authors:  Jackelyn Y Boyden; Chris Feudtner; Janet A Deatrick; Kimberley Widger; Gwenn LaRagione; Blyth Lord; Mary Ersek
Journal:  BMC Palliat Care       Date:  2021-01-14       Impact factor: 3.234

4.  Long-Term Follow-Up of Legacy Services Offered by Children's Hospitals in the United States.

Authors:  Terrah Foster Akard; Samantha Burley; Maggie C Root; Mary S Dietrich; Brittany Cowfer; Kim Mooney-Doyle
Journal:  Palliat Med Rep       Date:  2021-08-13
  4 in total

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