Literature DB >> 17403912

Patient-reported outcomes in end-of-life research in pediatric oncology.

Pamela S Hinds1, Jennifer Brandon, Caitlin Allen, Nobuko Hijiya, Rachel Newsome, Javier R Kane.   

Abstract

OBJECTIVE: The purpose of this review of published literature was to identify the number and focus of empirically based papers that included research methods used to directly solicit patient-reported outcomes (PRO) from pediatric oncology patients at end of life.
METHODS: Key terms including "pediatric or child and oncology or cancer and end of life or palliative or hospice or dying" were used with five data bases (PubMed, Ovid, Cochrane, PsycInfo & PsycArticles, and CINAHL) for English language literature published between January, 2001 and June, 2006. All retrieved documents were independently reviewed by a panel of six (nurses, physicians, and one psychologist) with backgrounds in pediatric oncology.
RESULTS: Thirty-five publications were identified but nine (25.7%) were eliminated from the analysis as they did not meet inclusion criteria. Of the remaining 26, four (15.4%) included patient-reported outcomes, six (23.1%) included parent only-reported outcomes, and five (19.2%) included staff only-reported outcomes. Nine (34.6%) were retrospective medical record reviews. Two (7.7%) included parent and record review data or parent and physician reports.
CONCLUSIONS: Empirically-based end-of-life publications in pediatric oncology are relatively few in number and nearly 85% of completed studies do not include PRO.

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Year:  2007        PMID: 17403912     DOI: 10.1093/jpepsy/jsm004

Source DB:  PubMed          Journal:  J Pediatr Psychol        ISSN: 0146-8693


  9 in total

Review 1.  Palliative Care as a Standard of Care in Pediatric Oncology.

Authors:  Meaghann S Weaver; Katherine E Heinze; Katherine P Kelly; Lori Wiener; Robert L Casey; Cynthia J Bell; Joanne Wolfe; Amy M Garee; Anne Watson; Pamela S Hinds
Journal:  Pediatr Blood Cancer       Date:  2015-12       Impact factor: 3.167

2.  Feasibility of Conducting a Palliative Care Randomized Controlled Trial in Children With Advanced Cancer: Assessment of the PediQUEST Study.

Authors:  Veronica Dussel; Liliana Orellana; Natalie Soto; Kun Chen; Christina Ullrich; Tammy I Kang; Jeffrey R Geyer; Chris Feudtner; Joanne Wolfe
Journal:  J Pain Symptom Manage       Date:  2015-01-30       Impact factor: 3.612

Review 3.  Establishing psychosocial palliative care standards for children and adolescents with cancer and their families: An integrative review.

Authors:  Meaghann S Weaver; Katherine E Heinze; Cynthia J Bell; Lori Wiener; Amy M Garee; Katherine P Kelly; Robert L Casey; Anne Watson; Pamela S Hinds
Journal:  Palliat Med       Date:  2015-04-28       Impact factor: 4.762

4.  Symptoms in children with advanced cancer: child and nurse reports.

Authors:  Lois Van Cleve; Cynthia E Muñoz; Marilyn Savedra; Matt Riggs; Elizabeth Bossert; Marcia Grant; Kathleen Adlard
Journal:  Cancer Nurs       Date:  2012 Mar-Apr       Impact factor: 2.592

5.  Voices of children and adolescents on phase 1 or phase 2 cancer trials: A new trial endpoint?

Authors:  Pamela S Hinds; Jichuan Wang; Emily Dunn Stern; Catherine Fiona Macpherson; Claire M Wharton; Ruthanna Okorosobo; Yao Iris Cheng; Heather E Gross; Holly J Meany; Shana Jacobs
Journal:  Cancer       Date:  2017-06-05       Impact factor: 6.860

6.  Psychosocial Needs and Preferences for Care among Adolescent and Young Adult Cancer Patients (Ages 15-39): A Qualitative Study.

Authors:  Viswatej Avutu; Kathleen A Lynch; Marie E Barnett; Jacqueline A Vera; Julia L Glade Bender; William D Tap; Thomas M Atkinson
Journal:  Cancers (Basel)       Date:  2022-01-29       Impact factor: 6.575

7.  From qualitative work to intervention development in pediatric oncology palliative care research.

Authors:  Terrah Foster Akard; Mary Jo Gilmer; Debra L Friedman; Barbara Given; Verna L Hendricks-Ferguson; Pamela S Hinds
Journal:  J Pediatr Oncol Nurs       Date:  2013-04-30       Impact factor: 1.636

8.  Trending Longitudinal Agreement between Parent and Child Perceptions of Quality of Life for Pediatric Palliative Care Patients.

Authors:  Meaghann S Weaver; Cheryl Darnall; Sue Bace; Catherine Vail; Andrew MacFadyen; Christopher Wichman
Journal:  Children (Basel)       Date:  2017-08-01

9.  Comparison of child and family reports of health-related quality of life in pediatric acute lymphoblastic leukemia patients after induction therapy.

Authors:  Shohei Nakajima; Iori Sato; Takafumi Soejima; Katsuyoshi Koh; Motohiro Kato; Yasuhiro Okamoto; Toshihiko Imamura; Miho Maeda; Yasushi Ishida; Atsushi Manabe; Kiyoko Kamibeppu
Journal:  BMC Pediatr       Date:  2020-08-19       Impact factor: 2.125

  9 in total

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