Literature DB >> 16499471

Key factors affecting dying children and their families.

Pamela S Hinds1, Lisa Schum, Justin N Baker, Joanne Wolfe.   

Abstract

The death of a child alters the life and health of others immediately and for the rest of their lives. How a child dies influences parents' abilities to continue their role functions as well as siblings' abilities to make and maintain friendships, and may be the basis for health care providers' decisions to exit direct care roles. Thus, facilitating a "good death"-an obvious care priority for all involved with the dying child-ought also to be a priority for the health of bereaved families and affected health care providers. Making this a care priority is complicated by a serious lack of data, as details of the last hours or weeks of a dying child or adolescent's life are largely unknown. The purpose of this paper is to identify key factors that affect the course of dying children and adolescents and that of their bereaved survivors, and to link those key factors to needed research that could produce clinically relevant findings to improve the care of these patients. Key factors described here include suffering (physical, psychological, and spiritual), communication, decision making, prognostic ambiguities, ability of the seriously ill child to give assent to research participation, and educational preparation of health care providers to give competent end-of-life care.

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Year:  2005        PMID: 16499471     DOI: 10.1089/jpm.2005.8.s-70

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  22 in total

1.  End-of-life management in pediatric cancer.

Authors:  Claudia L Epelman
Journal:  Curr Oncol Rep       Date:  2012-04       Impact factor: 5.075

2.  An exploratory survey of end-of-life attitudes, beliefs, and experiences of adolescents with HIV/AIDS and their families.

Authors:  Patricia A Garvie; Jianping He; Jichuan Wang; Lawrence J D'Angelo; Maureen E Lyon
Journal:  J Pain Symptom Manage       Date:  2012-07-07       Impact factor: 3.612

3.  Changes in medical care at a pediatric oncology referral center after placement of a do-not-resuscitate order.

Authors:  Justin N Baker; Javier R Kane; Shesh Rai; Scott C Howard; Pamela S Hinds
Journal:  J Palliat Med       Date:  2010-10-30       Impact factor: 2.947

4.  Palliative care in the pediatric ICU: challenges and opportunities for family-centered practice.

Authors:  Ardith Doorenbos; Taryn Lindhorst; Helene Starks; Eugene Aisenberg; J Randall Curtis; Ross Hays
Journal:  J Soc Work End Life Palliat Care       Date:  2012

5.  Conducting research with end-of-life populations: overcoming recruitment challenges when working with clinical agencies.

Authors:  Dena J Fischer; Sandy C Burgener; Karen Kavanaugh; Catherine Ryan; Gail Keenan
Journal:  Appl Nurs Res       Date:  2011-06-22       Impact factor: 2.257

Review 6.  The central role of meaning in adjustment to the loss of a child to cancer: implications for the development of meaning-centered grief therapy.

Authors:  Wendy G Lichtenthal; William Breitbart
Journal:  Curr Opin Support Palliat Care       Date:  2015-03       Impact factor: 2.302

7.  Paediatric advance care planning survey: a cross-sectional examination of congruence and discordance between adolescents with HIV/AIDS and their families.

Authors:  Maureen E Lyon; Ronald H Dallas; Patricia A Garvie; Megan L Wilkins; Ana Garcia; Yao Iris Cheng; Jichuan Wang
Journal:  BMJ Support Palliat Care       Date:  2017-09-21       Impact factor: 3.568

Review 8.  Integrating palliative care into the PICU: a report from the Improving Palliative Care in the ICU Advisory Board.

Authors:  Renee Boss; Judith Nelson; David Weissman; Margaret Campbell; Randall Curtis; Jennifer Frontera; Michelle Gabriel; Dana Lustbader; Anne Mosenthal; Colleen Mulkerin; Kathleen Puntillo; Daniel Ray; Rick Bassett; Karen Brasel; Ross Hays
Journal:  Pediatr Crit Care Med       Date:  2014-10       Impact factor: 3.624

9.  Do-not-resuscitate orders and/or hospice care, psychological health, and quality of life among children/adolescents with acquired immune deficiency syndrome.

Authors:  Maureen E Lyon; Paige L Williams; Elizabeth R Woods; Nancy Hutton; Anne M Butler; Erica Sibinga; Michael T Brady; James M Oleske
Journal:  J Palliat Med       Date:  2008-04       Impact factor: 2.947

10.  Development, feasibility, and acceptability of the Family/Adolescent-Centered (FACE) Advance Care Planning intervention for adolescents with HIV.

Authors:  Maureen E Lyon; Patricia A Garvie; Linda Briggs; Jianping He; Robert McCarter; Lawrence J D'Angelo
Journal:  J Palliat Med       Date:  2009-04       Impact factor: 2.947

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