The Seattle Pediatric Palliative Care Project: Effects on Family Satisfaction and Health-Related Quality of Life
- 1 June 2006
- journal article
- Published by Mary Ann Liebert Inc in Journal of Palliative Medicine
- Vol. 9 (3) , 716-728
- https://doi.org/10.1089/jpm.2006.9.716
Abstract
This paper presents the components of a pediatric palliative care demonstration program implemented in Seattle during the period 1999-2001. It reports findings from the evaluation of quality of life and family satisfaction among enrolled participants. The program was designed to enhance patient-provider communication using the Decision-making Tool (DMT) and experimented with co-management by clinicians and insurers to support decision making in advanced serious pediatric illness. The project design consisted of ethical decision-making, provider education, and flexible administration of health benefits through co-case management between insurers and care providers. The evaluation study design is a non-experimental pretest, posttest design comparison of pediatric quality of life and family satisfaction at program entry with repeated measures at 3 months post-program entry. Quality of life was measured with parent proxy reports of health-related quality of life using the PedsQL() Version 4.0, and family satisfaction was measured with a 31-item self-administered questionnaire designed by project staff. Forty-one patients ranging in age from infancy to 22 years old were enrolled in the program over a 2-year period. Parents consented to participate in the evaluation study. Thirty one specific diagnoses were represented in the patient population; 34% were some form of cancer. Improvements in health-related quality of life over baseline were observed for 21 matched pairs available for analysis in each domain of health-related quality of life; positive changes in reports of emotional well-being were statistically significant. Improvements over baseline in 14 of 31 family satisfaction items were statistically significant. Pediatric palliative care services that focus on effective communication, decision support, and co-case management with insurers can improve aspects of quality of life and family satisfaction.Keywords
This publication has 17 references indexed in Scilit:
- Hospital Staff and Family Perspectives Regarding Quality of Pediatric Palliative CarePediatrics, 2004
- Palliative CareNew England Journal of Medicine, 2004
- Pediatric Palliative CareNew England Journal of Medicine, 2004
- Family Perspectives on End-of-Life Care at the Last Place of CareJAMA, 2004
- The PedsQL™ in pediatric rheumatology: Reliability, validity, and responsiveness of the Pediatric Quality of Life Inventory™ generic core scales and rheumatology moduleArthritis & Rheumatism, 2002
- Pediatric palliative care: the time has come.Archives of Pediatrics & Adolescent Medicine, 2002
- The PedsQLTM 4.0 Generic Core Scales: Sensitivity, Responsiveness, and Impact on Clinical Decision-MakingJournal of Behavioral Medicine, 2002
- PedsQL™ 4.0: Reliability and Validity of the Pediatric Quality of Life Inventory™ Version 4.0 Generic Core Scales in Healthy and Patient PopulationsMedical Care, 2001
- Palliative Care for ChildrenPediatrics, 2000
- Quality of Care — What is It?New England Journal of Medicine, 1996