Literature DB >> 31046569

Challenges to Family Management for Caregivers of Adolescent and Young Adult Survivors of Childhood Brain Tumors [Formula: see text].

Nicole SanGiacomo1,2, Jennifer Toth1,2, Wendy Hobbie1, Elizabeth Broden2, Elizabeth Ver Hoeve2,3, Kathleen A Knafl4, Lamia Barakat1,2, Sue Ogle1, Janet A Deatrick2.   

Abstract

Due to the complexity of cancer late effects, the education required to provide anticipatory guidance and support to the caregivers of adolescent and young adult (AYA) survivors of childhood brain tumors can be difficult. Therefore, identifying challenges to family management (FM) could be helpful in anticipating complications with the integration of tumor and treatment late effects into family life. Building on previous research that described FM for children with chronic conditions, children who survived cancer, and the Family Management Styles Framework, the purpose of this study was to identify FM challenges for caregivers of AYA survivors of childhood brain tumors to guide clinical practice and research. Directed content analysis was used to identify FM challenges in data from semistructured interviews with 45 maternal caregivers for AYA survivors of childhood brain tumors living with them. Caregivers were largely White (89%) with an average age of 52 years, educated beyond the high school level (67%), and were partnered or married (53%). On average, caregivers had been caring for the AYA for 21 years since diagnosis, and 56% of their survivors had moderate functional restrictions. A primary and a secondary analyst were assigned to the data for each interview and completed a single summary matrix. A list of challenges was created by the research team based on Family Management Styles Framework, the literature, and clinical expertise. Seven core challenges to FM were identified: ensuring survivor well-being, supporting survivor independence, encouraging sibling well-being, planning family activities, sustaining parents as caregivers, attending to survivor late effects, and providing support and advocacy.

Entities:  

Keywords:  adolescents and young adults; challenges; family functioning; family management; oncology

Mesh:

Year:  2019        PMID: 31046569      PMCID: PMC6791045          DOI: 10.1177/1043454219844229

Source DB:  PubMed          Journal:  J Pediatr Oncol Nurs        ISSN: 1043-4542            Impact factor:   1.636


  23 in total

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Authors:  Lioness Ayres; Karen Kavanaugh; Kathleen A Knafl
Journal:  Qual Health Res       Date:  2003-07

Review 2.  Care of children and adolescents with type 1 diabetes: a statement of the American Diabetes Association.

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Journal:  Diabetes Care       Date:  2005-01       Impact factor: 19.112

3.  Three approaches to qualitative content analysis.

Authors:  Hsiu-Fang Hsieh; Sarah E Shannon
Journal:  Qual Health Res       Date:  2005-11

4.  Maternal Caregiving Demands for Adolescent and Young Adult Survivors of Pediatric Brain Tumors.

Authors:  Erica Palma; Janet A Deatrick; Wendy L Hobbie; Sue K Ogle; Kyoko Kobayashi; Linda Maldonado
Journal:  Oncol Nurs Forum       Date:  2015-05       Impact factor: 2.172

5.  Oncology Nurses' Knowledge, Confidence, and Practice in Addressing Caregiver Strain and Burden

Authors:  Margaret M Irwin; William Dudley; Laurel Northouse; Donna L Berry; Gail A Mallory
Journal:  Oncol Nurs Forum       Date:  2018-03-01       Impact factor: 2.172

6.  Patterns of family management of childhood chronic conditions and their relationship to child and family functioning.

Authors:  Kathleen A Knafl; Janet A Deatrick; George J Knafl; Agatha M Gallo; Margaret Grey; Jane Dixon
Journal:  J Pediatr Nurs       Date:  2013-04-19       Impact factor: 2.145

7.  Advancing a comprehensive cancer care agenda for children and their families: Institute of Medicine Workshop highlights and next steps.

Authors:  Rebecca Kirch; Gregory Reaman; Chris Feudtner; Lori Wiener; Lisa A Schwartz; Lillian Sung; Joanne Wolfe
Journal:  CA Cancer J Clin       Date:  2016-05-04       Impact factor: 508.702

Review 8.  Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members.

Authors:  Barbara P Yawn; George R Buchanan; Araba N Afenyi-Annan; Samir K Ballas; Kathryn L Hassell; Andra H James; Lanetta Jordan; Sophie M Lanzkron; Richard Lottenberg; William J Savage; Paula J Tanabe; Russell E Ware; M Hassan Murad; Jonathan C Goldsmith; Eduardo Ortiz; Robinson Fulwood; Ann Horton; Joylene John-Sowah
Journal:  JAMA       Date:  2014-09-10       Impact factor: 56.272

Review 9.  Psychosocial Assessment as a Standard of Care in Pediatric Cancer.

Authors:  Anne E Kazak; Annah N Abrams; Jaime Banks; Jennifer Christofferson; Stephen DiDonato; Martha A Grootenhuis; Marianne Kabour; Avi Madan-Swain; Sunita K Patel; Sima Zadeh; Mary Jo Kupst
Journal:  Pediatr Blood Cancer       Date:  2015-12       Impact factor: 3.167

10.  The cumulative burden of surviving childhood cancer: an initial report from the St Jude Lifetime Cohort Study (SJLIFE).

Authors:  Nickhill Bhakta; Qi Liu; Kirsten K Ness; Malek Baassiri; Hesham Eissa; Frederick Yeo; Wassim Chemaitilly; Matthew J Ehrhardt; Johnnie Bass; Michael W Bishop; Kyla Shelton; Lu Lu; Sujuan Huang; Zhenghong Li; Eric Caron; Jennifer Lanctot; Carrie Howell; Timothy Folse; Vijaya Joshi; Daniel M Green; Daniel A Mulrooney; Gregory T Armstrong; Kevin R Krull; Tara M Brinkman; Raja B Khan; Deo K Srivastava; Melissa M Hudson; Yutaka Yasui; Leslie L Robison
Journal:  Lancet       Date:  2017-09-08       Impact factor: 79.321

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  1 in total

1.  Psychosocial functioning of caregivers of pediatric brain tumor survivors.

Authors:  Carolyn R Bates; Diane Fairclough; Robert B Noll; Maru E Barrera; Mary Jo Kupst; Anna M Egan; Maria A Gartstein; Emily L Ach; Cynthia A Gerhardt; Kathryn Vannatta
Journal:  Pediatr Blood Cancer       Date:  2022-01-19       Impact factor: 3.167

  1 in total

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