Literature DB >> 21245433

Parent reports of quality of life for pediatric patients with cancer with no realistic chance of cure.

Deborah Tomlinson1, Pamela S Hinds, Ute Bartels, Eleanor Hendershot, Lillian Sung.   

Abstract

PURPOSE: To compare quality of life of children with cancer with no reasonable chance of cure reported by parents 6 months or fewer versus more than 6 months before death. PATIENTS AND METHODS: This cross-sectional study included children between the ages of 2 and 18 years with cancer and no reasonable chance of cure at The Hospital for Sick Children, Toronto, Ontario, Canada. Parents reported quality of life on behalf of their children. Outcomes were the PedsQL 4.0 Generic Core Scales, Acute Cancer Module, and Multidimensional Fatigue Scale.
RESULTS: Seventy-three parents of children participated. Compared with children who survived more than 6 months (n = 43), those who died at 6 months or fewer (n = 30) had significantly worse physical health (mean difference, 15.9; 95% CI, 1.8 to 30.0; P = .028), more pain and hurt (mean difference, 15.5; 95% CI, 0.9 to 30.0; P = .037), and worse general fatigue (mean difference, 15.8; 95% CI, 2.4 to 29.1; P = .021) and sleep/rest fatigue (mean difference, 16.0; 95% CI, 3.5 to 28.5; P = .013). Among the entire cohort, those with leukemia/lymphoma had worse physical and psychosocial quality of life compared with those with solid or brain tumors. Recent stem-cell transplantation was associated with worse psychosocial health.
CONCLUSION: Parents of children with cancer reported worse physical health, pain, and fatigue proximal to death. Those with leukemia/lymphoma were at higher risk for impaired quality of life. This knowledge can help in the design of targeted interventions to improve quality of life for children dying as a result of cancer.

Entities:  

Mesh:

Year:  2011        PMID: 21245433     DOI: 10.1200/JCO.2010.31.4047

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


  18 in total

1.  The Effect of Fatigue-Related Education on Pediatric Oncology Patients' Fatigue and Quality of Life.

Authors:  Aslı Akdeniz Kudubes; Murat Bektas; Kamer Mutafoğlu
Journal:  J Cancer Educ       Date:  2019-12       Impact factor: 2.037

2.  Understanding Treatment Burden and Quality of Life Impact of Participating in an Early-Phase Pediatric Oncology Clinical Trial: A Pilot Study.

Authors:  Stacey Crane; Lori Backus; Beth Stockman; Janet S Carpenter; Li Lin; Joan Haase
Journal:  J Pediatr Oncol Nurs       Date:  2017-08-29       Impact factor: 1.636

3.  Improving the care of children with advanced cancer by using an electronic patient-reported feedback intervention: results from the PediQUEST randomized controlled trial.

Authors:  Joanne Wolfe; Liliana Orellana; E Francis Cook; Christina Ullrich; Tammy Kang; Jeffrey Russell Geyer; Chris Feudtner; Jane C Weeks; Veronica Dussel
Journal:  J Clin Oncol       Date:  2014-03-10       Impact factor: 44.544

4.  Referral practices of pediatric oncologists to specialized palliative care.

Authors:  Kirsten Wentlandt; Monika K Krzyzanowska; Nadia Swami; Gary Rodin; Lisa W Le; Lillian Sung; Camilla Zimmermann
Journal:  Support Care Cancer       Date:  2014-03-27       Impact factor: 3.603

Review 5.  Considering quality of life for children with cancer: a systematic review of patient-reported outcome measures and the development of a conceptual model.

Authors:  Samantha J Anthony; Enid Selkirk; Lillian Sung; Robert J Klaassen; David Dix; Katrin Scheinemann; Anne F Klassen
Journal:  Qual Life Res       Date:  2013-08-02       Impact factor: 4.147

6.  Fatigue and health related quality of life in children and adolescents with cancer.

Authors:  Michelle Darezzo Rodrigues Nunes; Eufemia Jacob; Emiliana Omena Bomfim; Luis Carlos Lopes-Junior; Regina Aparecida Garcia de Lima; Milena Floria-Santos; Lucila Castanheira Nascimento
Journal:  Eur J Oncol Nurs       Date:  2017-05-13       Impact factor: 2.398

7.  Symptoms and Distress in Children With Advanced Cancer: Prospective Patient-Reported Outcomes From the PediQUEST Study.

Authors:  Joanne Wolfe; Liliana Orellana; Christina Ullrich; E Francis Cook; Tammy I Kang; Abby Rosenberg; Russ Geyer; Chris Feudtner; Veronica Dussel
Journal:  J Clin Oncol       Date:  2015-04-27       Impact factor: 44.544

8.  Children with minimal chance for cure: parent proxy of the child's health-related quality of life and the effect on parental physical and mental health during treatment.

Authors:  Belinda N Mandrell; Justin Baker; Deena Levine; Jami Gattuso; Nancy West; April Sykes; Amar Gajjar; Alberto Broniscer
Journal:  J Neurooncol       Date:  2016-06-25       Impact factor: 4.130

Review 9.  Palliative care for children with cancer.

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

10.  Quality of Life in Children With Advanced Cancer: A Report From the PediQUEST Study.

Authors:  Abby R Rosenberg; Liliana Orellana; Christina Ullrich; Tammy Kang; J Russell Geyer; Chris Feudtner; Veronica Dussel; Joanne Wolfe
Journal:  J Pain Symptom Manage       Date:  2016-05-21       Impact factor: 3.612

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.