Literature DB >> 17114660

Communication about prognosis between parents and physicians of children with cancer: parent preferences and the impact of prognostic information.

Jennifer W Mack1, Joanne Wolfe, Holcombe E Grier, Paul D Cleary, Jane C Weeks.   

Abstract

PURPOSE: Concerns about the harms of prognostic information, including distress and loss of hope, cause some physicians to avoid frank disclosure. We aimed to determine parent preferences for prognostic information about their children with cancer and the results of receiving such information. PATIENTS AND METHODS: We surveyed 194 parents of children with cancer (overall response rate, 70%), treated at the Dana-Farber Cancer Institute and Children's Hospital (Boston, MA) and the children's physicians. Our main outcome measure was parent rating of prognostic information as extremely or very upsetting.
RESULTS: The majority of parents desired as much information about prognosis as possible (87%) and wanted it expressed numerically (85%). Although 36% of parents found information about prognosis to be extremely or very upsetting, those parents were more likely to want additional information about prognosis than those who were less upset (P = .01). Parents who found information upsetting were no less likely to say that knowing prognosis was important (P = .39), that knowing prognosis helped in decision making (P = .40), or that hope for a cure kept them going (P = .72).
CONCLUSION: Although many parents find prognostic information about their children with cancer upsetting, parents who are upset by prognostic information are no less likely to want it. The upsetting nature of prognostic information does not diminish parents' desire for such information, its importance to decision making, or parents' sense of hope.

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Mesh:

Year:  2006        PMID: 17114660     DOI: 10.1200/JCO.2006.06.5326

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  85 in total

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3.  Editor's Spotlight/Take 5: Conditional survival greater than overall survival at diagnosis for Ewing's and osteosarcoma.

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4.  Seven Types of Uncertainty When Clinicians Care for Pediatric Patients With Advanced Cancer.

Authors:  Douglas L Hill; Jennifer K Walter; Julia E Szymczak; Concetta DiDomenico; Shefali Parikh; Chris Feudtner
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5.  Communication about geriatric assessment domains in advanced cancer settings: "Missed opportunities".

Authors:  Lisa M Lowenstein; Robert J Volk; Richard Street; Marie Flannery; Allison Magnuson; Ronald Epstein; Supriya G Mohile
Journal:  J Geriatr Oncol       Date:  2018-06-06       Impact factor: 3.599

6.  Adherence to medication: A nation-wide study from the Children's Cancer Hospital, Egypt.

Authors:  Hanan El Malla; Nathalie Ylitalo Helm; Ulrica Wilderäng; Yasser El Sayed Elborai; Gunnar Steineck; Ulrika Kreicbergs
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7.  Illness and end-of-life experiences of children with cancer who receive palliative care.

Authors:  Erica C Kaye; Courtney A Gushue; Samantha DeMarsh; Jonathan Jerkins; April Sykes; Zhaohua Lu; Jennifer M Snaman; Lindsay Blazin; Liza-Marie Johnson; Deena R Levine; R Ray Morrison; Justin N Baker
Journal:  Pediatr Blood Cancer       Date:  2017-12-08       Impact factor: 3.167

8.  Are we meeting the informational needs of cancer patients and families? Perception of physician communication in pediatric oncology.

Authors:  Deena R Levine; Erik Liederbach; Liza-Marie Johnson; Erica C Kaye; Holly Spraker-Perlman; Belinda Mandrell; Michele Pritchard; April Sykes; Zhaohua Lu; Dave Wendler; Justin N Baker
Journal:  Cancer       Date:  2019-01-02       Impact factor: 6.860

9.  Parental distress and desire for information regarding long-term implications of pediatric cancer treatment.

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Review 10.  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

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