Literature DB >> 29288879

Development and Assessment of a Measure of Parent and Child Needs in Pediatric Palliative Care.

James P Donnelly1, Kim Downing2, Jason Cloen3, Patricia Fragen4, Alyssa W Gupton3, Jen Misasi2, Kelly Michelson5.   

Abstract

CONTEXT: Pediatric palliative care has no evidence-based needs assessment measure. The Parent and Child Needs Survey (PCNeeds) is a new instrument designed to assess the needs of children in palliative care, including children receiving end-of-life care, and their families.
OBJECTIVES: This study examines the psychometrics of and respondents' perceptions about the PCNeeds.
METHODS: Parents of children in four outpatient pediatric palliative care programs completed the PCNeeds and the World Health Organization Quality of Life-Brief tool (WHOQOL-BREF). Parents answered questions about demographics and the experience of completing the PCNeeds. Internal scale reliability was measured with Cronbach's alpha. Validity was assessed by correlating the PCNeeds total and subscale scores with the WHOQOL-BREF subscales. Additional respondent perceptions were obtained via written comments and analyzed using content analysis.
RESULTS: The 93 respondents were predominantly female (n = 69, 74%); white (n = 79, 85%); college graduates (n = 71, 76%); and married or partnered (n = 75, 81%). Internal reliability was acceptable (Cronbach's α = 0.83), and validity correlations with the WHOQOL-BREF subscales were consistent with theoretical expectations (moderate negative correlations ranging from -0.36 to -0.51). The most frequently cited need not addressed by our survey was sibling impact (n = 17, 18%). Twelve parents (13%) indicated that no content was missing. The least met needs were financial impact, family impact, and the child's physical problems besides pain. Sixty-eight percent of parents (n = 63) rated completion of the survey as "easy" or "very easy."
CONCLUSION: Initial psychometric analysis of the PCNeeds is encouraging, but further study of reliability and validity with more diverse respondents is needed.
Copyright © 2017 American Academy of Hospice and Palliative Medicine. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Pediatric palliative care; hospice; needs assessment

Mesh:

Year:  2017        PMID: 29288879      PMCID: PMC6282185          DOI: 10.1016/j.jpainsymman.2017.12.484

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  4 in total

Review 1.  Pediatric palliative care in the intensive care unit and questions of quality: a review of the determinants and mechanisms of high-quality palliative care in the pediatric intensive care unit (PICU).

Authors:  Sara Rhodes Short; Rachel Thienprayoon
Journal:  Transl Pediatr       Date:  2018-10

2.  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

3.  Paediatric palliative screening scale as a useful tool for clinicians' assessment of palliative care needs of pediatric patients: a retrospective cohort study.

Authors:  In Gyu Song; Seung Yeon Kwon; Yoon Jung Chang; Min Sun Kim; Sung Hoon Jeong; Seung Min Hahn; Kyu Tae Han; So-Jung Park; Jin Young Choi
Journal:  BMC Palliat Care       Date:  2021-05-24       Impact factor: 3.234

4.  Evaluation of Primary Caregiver Parents' Quality of Life in Pediatric Palliative Care with the WHOQOL-Bref (TR).

Authors:  Nilgün Harputluoğlu; Senem Alkan Özdemir; Ünsal Yılmaz; Tanju Çelik
Journal:  Turk Arch Pediatr       Date:  2021-09
  4 in total

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