Literature DB >> 28944533

Parents spend an average of nine hours a day providing palliative care for children at home and need to maintain an average of five life-saving devices.

P Lazzarin1, B Schiavon1, L Brugnaro2, F Benini1.   

Abstract

AIM: This Italian study investigated home-based palliative care for young children and how long it took parents to meet their needs.
METHODS: The study population consisted of 33 families with a child under the responsibility of the Veneto Regional Center for Pediatric Palliative Care, northern Italy, who needed medical support in at least two of the following areas: respiratory, feeding, pain and seizures.
RESULTS: The children had a mean age of 6.8 ± 4.7 years. We found that 72% of the patients needed medical devices for feeding, 36% had a tracheostomy and 55% were on mechanical ventilatory support. The children needed an average of five different life-supporting medical appliances, and the time taken to provide for their care increased significantly with each additional appliance (p = 0.016). Their most time-consuming daily needs were feeding (174 minutes) and support when they woke up at night (67 minutes). The average daily time that parents spent taking care of their child amounted to eight hours and 54 minutes per day.
CONCLUSION: Parents providing palliative care for children with life-limiting diseases spent an average of nine hours a day caring for them each day and had to maintain an average of five medical appliances. ©2017 Foundation Acta Paediatrica. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  Carers; Home-based care; Life-limiting diseases; Paediatric palliative care; Parents

Mesh:

Year:  2017        PMID: 28944533     DOI: 10.1111/apa.14098

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN: 0803-5253            Impact factor:   2.299


  8 in total

1.  Children with medical complexity and paediatric palliative care: a retrospective cross-sectional survey of prevalence and needs.

Authors:  S Amarri; A Ottaviani; A Campagna; L De Panfilis
Journal:  Ital J Pediatr       Date:  2021-05-12       Impact factor: 2.638

2.  Measuring the Impact of the Home Health Nursing Shortage on Family Caregivers of Children Receiving Palliative Care.

Authors:  Meaghann S Weaver; Brittany Wichman; Sue Bace; Denice Schroeder; Catherine Vail; Chris Wichman; Andrew Macfadyen
Journal:  J Hosp Palliat Nurs       Date:  2018-05-02       Impact factor: 1.918

3.  Supporting Parent Caregivers of Children with Life-Limiting Illness.

Authors:  Kendra D Koch; Barbara L Jones
Journal:  Children (Basel)       Date:  2018-06-26

Review 4.  Palliative Care for Children in Hospital: Essential Roles.

Authors:  Ross Drake
Journal:  Children (Basel)       Date:  2018-02-19

5.  Home-Based Care for Children with Serious Illness: Ecological Framework and Research Implications.

Authors:  Jackelyn Y Boyden; Douglas L Hill; Gwenn LaRagione; Joanne Wolfe; Chris Feudtner
Journal:  Children (Basel)       Date:  2022-07-26

6.  Parents Are the Experts: A Qualitative Study of the Experiences of Parents of Children With Severe Neurological Impairment During Decision-Making.

Authors:  Jori F Bogetz; Amy Trowbridge; Hannah Lewis; Kelly J Shipman; Danielle Jonas; Julie Hauer; Abby R Rosenberg
Journal:  J Pain Symptom Manage       Date:  2021-06-17       Impact factor: 3.612

7.  Keeping Hope Possible Toolkit: The Development and Evaluation of a Psychosocial Intervention for Parents of Infants, Children and Adolescents with Life Limiting and Life Threatening Illnesses.

Authors:  Jill M G Bally; Meridith Burles; Shelley Spurr; Lorraine Holtslander; Heather Hodgson-Viden; Roona Sinha; Marcelline Zimmer
Journal:  Children (Basel)       Date:  2021-03-12

8.  The First Step to Initiate Pediatric Palliative Care: Identify Patient Needs and Cooperation of Medical Staff.

Authors:  Su Hyun Bae; Yeo Hyang Kim
Journal:  Healthcare (Basel)       Date:  2022-01-09
  8 in total

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