Literature DB >> 34618616

Bereaved Parent Perspectives on the Benefits and Burdens of Technology Assistance among Children with Complex Chronic Conditions.

Jori F Bogetz1,2, Anna Revette3, Danielle DeCourcey4.   

Abstract

Background: Many children with complex chronic conditions (CCCs) are supported by medical technologies. Objective: The aim of this study was to understand bereaved parent perspectives on technology assistance among this unique population. Design: Mixed methods design was used to analyze data from the cross-sectional Survey of Caring for Children with CCCs. Setting/Subjects: Bereaved parents of children with CCCs who received care at a large academic institution in the United States and died between 2006 and 2015. Measurements: Survey items were analyzed descriptively and integrated with thematic analysis of open-response items to identify key themes pertaining to parents' perspectives on technology.
Results: 110/211 (52%) parents completed the survey and at least 1 open-response item. More than 60% of parents had children with congenital/chromosomal or central nervous system progressive CCCs, used technology at baseline, and died in the hospital. A subset of parents recalled making decisions either not to initiate (n = 26/101, 26%) or to discontinue (n = 46/104, 44%) technology at end of life. Parents described both the benefits and burdens of technology. Two themes emerged regarding technology's association with the (1) intersection with goals of care and (2) complications and regret. Within goals of care, two subthemes arose: (a) technology was necessary to give time for life extension and/or to say goodbye, and (b) technology greatly impacted the child's quality of life and symptoms. Conclusions: Parents have nuanced perspectives about the benefits and burdens of technology. It is essential to understand parent's most important goals when supporting decisions about technology assistance for children with CCCs.

Entities:  

Keywords:  children with complex chronic conditions; pediatrics; technology

Mesh:

Year:  2021        PMID: 34618616      PMCID: PMC8861906          DOI: 10.1089/jpm.2021.0221

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


  30 in total

1.  Daily living with distress and enrichment: the moral experience of families with ventilator-assisted children at home.

Authors:  Franco A Carnevale; Eren Alexander; Michael Davis; Janet Rennick; Rita Troini
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2.  Consolidated criteria for reporting qualitative research (COREQ): a 32-item checklist for interviews and focus groups.

Authors:  Allison Tong; Peter Sainsbury; Jonathan Craig
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Review 3.  Pain in Children With Severe Neurologic Impairment: Undoing Assumptions.

Authors:  Julie M Hauer
Journal:  JAMA Pediatr       Date:  2018-10-01       Impact factor: 16.193

4.  Patterns of Care at the End of Life for Children and Young Adults with Life-Threatening Complex Chronic Conditions.

Authors:  Danielle D DeCourcey; Melanie Silverman; Adeolu Oladunjoye; Emily M Balkin; Joanne Wolfe
Journal:  J Pediatr       Date:  2017-11-22       Impact factor: 4.406

5.  Regret and unfinished business in parents bereaved by cancer: A mixed methods study.

Authors:  Wendy G Lichtenthal; Kailey E Roberts; Corinne Catarozoli; Elizabeth Schofield; Jason M Holland; Justin J Fogarty; Taylor C Coats; Lamia P Barakat; Justin N Baker; Tara M Brinkman; Robert A Neimeyer; Holly G Prigerson; Talia Zaider; William Breitbart; Lori Wiener
Journal:  Palliat Med       Date:  2020-02-05       Impact factor: 4.762

6.  Adults with chronic health conditions originating in childhood: inpatient experience in children's hospitals.

Authors:  Denise M Goodman; Matthew Hall; Amanda Levin; R Scott Watson; Roberta G Williams; Samir S Shah; Anthony D Slonim
Journal:  Pediatrics       Date:  2011-06-27       Impact factor: 7.124

7.  Pediatric deaths attributable to complex chronic conditions: a population-based study of Washington State, 1980-1997.

Authors:  C Feudtner; D A Christakis; F A Connell
Journal:  Pediatrics       Date:  2000-07       Impact factor: 7.124

8.  End-of-life decision-making and satisfaction with care: parental perspectives.

Authors:  K L Meert; C S Thurston; A P Sarnaik
Journal:  Pediatr Crit Care Med       Date:  2000-10       Impact factor: 3.624

9.  Inpatient growth and resource use in 28 children's hospitals: a longitudinal, multi-institutional study.

Authors:  Jay G Berry; Matt Hall; David E Hall; Dennis Z Kuo; Eyal Cohen; Rishi Agrawal; Kenneth D Mandl; Holly Clifton; John Neff
Journal:  JAMA Pediatr       Date:  2013-02       Impact factor: 16.193

10.  Regoaling: a conceptual model of how parents of children with serious illness change medical care goals.

Authors:  Douglas L Hill; Victoria Miller; Jennifer K Walter; Karen W Carroll; Wynne E Morrison; David A Munson; Tammy I Kang; Pamela S Hinds; Chris Feudtner
Journal:  BMC Palliat Care       Date:  2014-03-13       Impact factor: 3.234

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