Literature DB >> 21518721

Parents' experiences of their children's presence in discussions with physicians about Leukemia.

Bridget Young1, Joanne Ward, Peter Salmon, Katja Gravenhorst, Jonathan Hill, Tim Eden.   

Abstract

OBJECTIVE: We aimed to examine parents' views regarding their preadolescent child's presence during discussions about serious illnesses.
METHODS: In-depth qualitative interviews with parents of children receiving treatment for acute lymphoblastic leukemia were conducted. Parents were sampled from 6 UK treatment centers. Analysis was informed by the constant comparative method and content analysis.
RESULTS: We report on interviews with 53 parents (33 mothers, 20 fathers). Parents acknowledged the benefits of communicating openly with children, but few thought that their child's presence in discussions was straightforwardly desirable. They described how their child's presence restricted their own communication with physicians, made concentrating difficult, and interfered with their efforts to care for their child emotionally. Children's presence was particularly difficult when significant issues were being discussed, including prognoses, adverse results, and certain medical procedures. Parents felt that such discussions posed a potential threat to their child, particularly when they had not first had an opportunity to discuss information with the physician separately from the child. In contrast, separate meetings enabled parents to absorb information and to convey it to their child at an appropriate time and in a reassuring way. Some parents experienced difficulties in accessing separate meetings with physicians.
CONCLUSIONS: The difficulties parents described could potentially be addressed by extending, beyond the diagnosis period, the practice of sequencing significant information so that it is communicated to parents in separate meetings before being communicated to the child and by periodically exploring with parents what information would be in each child's interests.

Entities:  

Mesh:

Year:  2011        PMID: 21518721     DOI: 10.1542/peds.2010-2402

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  9 in total

1.  Inclusion of children in the initial conversation about their cancer diagnosis: impact on parent experiences of the communication process.

Authors:  Sarah R Brand McCarthy; Tammy I Kang; Jennifer W Mack
Journal:  Support Care Cancer       Date:  2019-01-23       Impact factor: 3.603

Review 2.  Communication in pediatric oncology: State of the field and research agenda.

Authors:  Bryan A Sisk; Jennifer W Mack; Rachel Ashworth; James DuBois
Journal:  Pediatr Blood Cancer       Date:  2017-07-27       Impact factor: 3.167

3.  Multilevel barriers and facilitators of communication in pediatric oncology: A systematic review.

Authors:  Bryan A Sisk; Kieandra Harvey; Annie B Friedrich; Alison L Antes; Lauren H Yaeger; Jennifer W Mack; James M DuBois
Journal:  Pediatr Blood Cancer       Date:  2021-10-18       Impact factor: 3.167

Review 4.  Prognostic Disclosures to Children: A Historical Perspective.

Authors:  Bryan A Sisk; Myra Bluebond-Langner; Lori Wiener; Jennifer Mack; Joanne Wolfe
Journal:  Pediatrics       Date:  2016-08-25       Impact factor: 7.124

Review 5.  Understanding Effective Delivery of Patient and Family Education in Pediatric OncologyA Systematic Review From the Children's Oncology Group [Formula: see text].

Authors:  Cheryl C Rodgers; Catherine M Laing; Ruth Anne Herring; Nancy Tena; Adrianne Leonardelli; Marilyn Hockenberry; Verna Hendricks-Ferguson
Journal:  J Pediatr Oncol Nurs       Date:  2016-07-27       Impact factor: 1.636

Review 6.  Palliative care for children with cancer.

Authors:  Elisha Waldman; Joanne Wolfe
Journal:  Nat Rev Clin Oncol       Date:  2013-01-22       Impact factor: 66.675

7.  Supporting Family Decision-making for a Child Who Is Seriously Ill: Creating Synchrony and Connection.

Authors:  Vanessa N Madrigal; Katherine Patterson Kelly
Journal:  Pediatrics       Date:  2018-11       Impact factor: 7.124

8.  End of life communication among caregivers of children with cancer: A qualitative approach to understanding support desired by families.

Authors:  Ansley E Kenney; Sima Zadeh Bedoya; Cynthia A Gerhardt; Tammi Young-Saleme; Lori Wiener
Journal:  Palliat Support Care       Date:  2021-03-01

9.  Improving communication and recall of information in paediatric diabetes consultations: a qualitative study of parents' experiences and views.

Authors:  Julia Lawton; Norman Waugh; Kathryn Noyes; Kathryn Barnard; Jeni Harden; Louise Bath; John Stephen; David Rankin
Journal:  BMC Pediatr       Date:  2015-06-10       Impact factor: 2.125

  9 in total

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