SPECIAL ARTICLE |
Care of the Dying Adolescent: Special Considerations
From the Division of Pediatric Hematology/Oncology and Blood and Bone Marrow Transplantation, DeVos Childrens Hospital, Grand Rapids, Michigan; and Department of Pediatrics and Human Development, Michigan State University College of Human Medicine, East Lansing, Michigan
More than 3000 adolescents in the United States die annually from the effects of chronic illness. Providing appropriate end-of-life care for these patients is particularly challenging because of several developmental, ethical, and legal considerations relevant to this age group. Developmental issues relate to the ways in which life-threatening illness alters the normal physical and psychological changes associated with adolescence, including attainment of independence, social skills, peer acceptance, and a healthy self-image. Ethical and legal issues arise from the fact that many terminally ill adolescents <18 years of age lack ordinary legal authority to make binding medical decisions (including discontinuation of their treatment), yet they meet functional criteria for having the competence to do so. In such situations, a broad medical, ethical, and legal consensus supports giving decisional authority to the minor patient. Even when full decisional authority is not appropriate, strong moral arguments exist for taking serious account of the young adolescents treatment preferences. In supporting the dying adolescent, an atmosphere promoting excellent communication and sound decision-making should be fostered as early as possible during preterminal care and maintained thereafter. Once palliative-care strategies become the clinical focus, psychosocial support sensitive to the adolescents developmental stage must be provided. Using these principles, clinicians can play a crucial role in helping the adolescent, in the face of death, to experience richness of life and the dignity of self-determination.
Key Words: adolescents children death and dying decision-making end of life minors palliative care
Received for publication Apr 3, 2003; Accepted Sep 2, 2003.
![]()
CiteULike
Connotea
Del.icio.us
Digg
Facebook
Reddit
Technorati
Twitter What's this?
This article has been cited by other articles:
![]() |
J. Cassano, K. Nagel, and L. O'Mara Talking With Others Who "Just Know": Perceptions of Adolescents With Cancer Who Participate in a Teen Group Journal of Pediatric Oncology Nursing, July 1, 2008; 25(4): 193 - 199. [Abstract] [PDF] |
||||
![]() |
B. Ewing Children's Wishes: Holistic Revelations in Art J Holist Nurs, June 1, 2008; 26(2): 147 - 154. [Abstract] [PDF] |
||||
![]() |
K. Hendrickson and R. McCorkle A Dimensional Analysis of the Concept: Good Death of a Child With Cancer Journal of Pediatric Oncology Nursing, June 1, 2008; 25(3): 127 - 138. [Abstract] [PDF] |
||||
![]() |
T. M. Kremer, R. G. Zwerdling, P. H. Michelson, and B. P. O'Sullivan Intensive Care Management of the Patient With Cystic Fibrosis J Intensive Care Med, May 1, 2008; 23(3): 159 - 177. [Abstract] [PDF] |
||||
![]() |
E. E. Callaghan Achieving Balance: A Case Study Examination of an Adolescent Coping With Life-Limiting Cancer Journal of Pediatric Oncology Nursing, December 1, 2007; 24(6): 334 - 339. [Abstract] [PDF] |
||||
![]() |
P. S. Hinds, D. Drew, L. L. Oakes, M. Fouladi, S. L. Spunt, C. Church, and W. L. Furman End-of-Life Care Preferences of Pediatric Patients With Cancer J. Clin. Oncol., December 20, 2005; 23(36): 9146 - 9154. [Abstract] [Full Text] [PDF] |
||||
![]() |
American Society for Parenteral and Enteral Nutrit, and Task Force on Standards for Specialized Nutrit, Jane Balint, Catherine Crill, and Kimberly Klotz Standards for Specialized Nutrition Support: Hospitalized Pediatric Patients Nutr Clin Pract, February 1, 2005; 20(1): 103 - 116. [Full Text] [PDF] |
||||









