Literature DB >> 29187744

It is a marathon rather than a sprint: an initial exploration of unmet needs and support preferences of caregivers of children with SCI.

Susan L Ryerson Espino1,2, Erin H Kelly3,4,5, Anne Rivelli5, Kathy Zebracki3,6, Lawrence C Vogel3,7.   

Abstract

STUDY
DESIGN: Focus group study.
OBJECTIVES: Explore unmet needs and support preferences of caregivers of youth with spinal cord injury (SCI).
SETTING: One pediatric specialty rehabilitation hospital system in the United States.
METHODS: Four focus groups were conducted with a convenience sample of 26 caregivers who were primarily mothers (96%) and married (65%), and had at least some college education (85%). Children living with SCI were on average 12.8 years old (SD = 3.3, 8-18). The average age of injury was 4.7 years (SD = 4.4, 0-16.2); mean injury duration was 8.2 years (SD = 3.9, 2-16); 77% had paraplegia; and 58% were male. Focus groups were digitally recorded, transcribed verbatim, and coded using thematic analysis and NVivo.
RESULTS: Qualitative data highlighted caregiver perspectives on unmet needs relating to two phases of care: acute and rehabilitation vs. current life with SCI, and two kinds of stressors: those associated with SCI and care vs. those related to other areas of the caregivers' lives, especially their families. Caregivers described stressful interactions with care systems and community services, articulated several concerns regarding well-being of family members, and noted that both they and their children with SCI experienced isolation. Caregivers articulated preferences for additional support from professionals and peers.
CONCLUSIONS: Data suggest the need for ongoing caregiver interventions and strengthened family-centered care systems, including professional assistance navigating health systems and peer support. Intervention development would benefit from further qualitative data collection with additional caregivers of youth with SCI, including multiple family members, and families from more diverse care settings.

Entities:  

Mesh:

Year:  2017        PMID: 29187744     DOI: 10.1038/s41393-017-0022-6

Source DB:  PubMed          Journal:  Spinal Cord        ISSN: 1362-4393            Impact factor:   2.772


  43 in total

1.  Using cognitive mapping to develop a community-based family intervention.

Authors:  Richard M Shewchuk; Frank A Franklin; Kathy F Harrington; Susan L Davies; Michael Windle
Journal:  Am J Health Behav       Date:  2004 Jan-Feb

2.  Caregiving and the stress process: an overview of concepts and their measures.

Authors:  L I Pearlin; J T Mullan; S J Semple; M M Skaff
Journal:  Gerontologist       Date:  1990-10

3.  Spouses of spinal cord injury survivors: the added impact of caregiving.

Authors:  D A Weitzenkamp; K A Gerhart; S W Charlifue; G G Whiteneck; G Savic
Journal:  Arch Phys Med Rehabil       Date:  1997-08       Impact factor: 3.966

4.  Quality of life of primary caregivers of spinal cord injury survivors living in the community: controlled study with short form-36 questionnaire.

Authors:  H Unalan; B Gençosmanoğlu; K Akgün; S Karamehmetoğlu; H Tuna; K Ones; A Rahimpenah; E Uzun; F Tüzün
Journal:  Spinal Cord       Date:  2001-06       Impact factor: 2.772

Review 5.  Parenting stress among caregivers of children with chronic illness: a systematic review.

Authors:  Melissa K Cousino; Rebecca A Hazen
Journal:  J Pediatr Psychol       Date:  2013-07-10

6.  Health-related quality of life after pediatric spinal cord injury.

Authors:  Sylvia I Garma; Erin H Kelly; Erica Z Daharsh; Lawrence C Vogel
Journal:  J Pediatr Psychol       Date:  2010-04-30

Review 7.  Caregiving services in spinal cord injury: a systematic review of the literature.

Authors:  E M Smith; N Boucher; W C Miller
Journal:  Spinal Cord       Date:  2016-02-23       Impact factor: 2.772

Review 8.  Developing a spinal cord injury research strategy using a structured process of evidence review and stakeholder dialogue. Part II: Background to a research strategy.

Authors:  P Bragge; L Piccenna; J Middleton; S Williams; G Creasey; S Dunlop; D Brown; R Gruen
Journal:  Spinal Cord       Date:  2015-06-23       Impact factor: 2.772

9.  Experience of rehabilitation following spinal cord injury: a meta-synthesis of qualitative findings.

Authors:  K Whalley Hammell
Journal:  Spinal Cord       Date:  2007-02-20       Impact factor: 2.772

10.  Family burden after traumatic brain injury in children.

Authors:  Mary E Aitken; Melissa L McCarthy; Beth S Slomine; Ru Ding; Dennis R Durbin; Kenneth M Jaffe; Charles N Paidas; Andrea M Dorsch; James R Christensen; Ellen J Mackenzie
Journal:  Pediatrics       Date:  2009-01       Impact factor: 7.124

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  3 in total

1.  Coping, Social Support, and Caregiver Well-Being With Families Living With SCI: A Mixed Methods Study.

Authors:  Susan L Ryerson Espino; Kerry O'Rourke; Erin H Kelly; Alicia M January; Lawrence C Vogel
Journal:  Top Spinal Cord Inj Rehabil       Date:  2022-01-19

2.  From Lost in the System to Empowered Parent-Researcher.

Authors:  Elin Salmiranta; Kristina Areskoug Josefsson
Journal:  J Patient Exp       Date:  2021-03-03

3.  Who are the beneficiaries and what are the reasons for non-utilization of care respite and support services? A cross-sectional study on family caregivers.

Authors:  Jianan Huang; Nadja Münzel; Anke Scheel-Sailer; Armin Gemperli
Journal:  BMC Health Serv Res       Date:  2021-07-02       Impact factor: 2.655

  3 in total

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