Literature DB >> 27749945

Ethics, Emotions, and the Skills of Talking About Progressing Disease With Terminally Ill Adolescents: A Review.

Abby R Rosenberg1, Joanne Wolfe2, Lori Wiener3, Maureen Lyon4, Chris Feudtner5.   

Abstract

Importance: For clinicians caring for adolescent patients living with progressive, life-threatening illness, discussions regarding prognosis, goals of care, and treatment options can be extremely challenging. While clinicians should respect and help to facilitate adolescents' emerging autonomy, they often must also work with parents' wishes to protect patients from the emotional distress of hearing bad news. Observations: We reviewed the ethical justifications for and against truth-telling, and we considered the published ethical and practice guidance, as well as the perspectives of patients, parents, and clinicians involved in these cases. We also explored particular challenges with respect to the cultural context, timing, and content of conversations at the end of adolescents' lives. In most cases, clinicians should gently but persistently engage adolescents directly in conversations about their disease prognosis and corresponding hopes, worries, and goals. These conversations need to occur multiple times, allowing significant time in each discussion for exploration of patient and family values. While truth-telling does not cause the types of harm that parents and clinicians may fear, discussing this kind of difficult news is almost always emotionally distressing. We suggest some "phrases that help" when clinicians strive to deepen understanding and facilitate difficult conversations with adolescents, parents, and other family members. Conclusions and Relevance: The pediatrician's opportunities to engage in difficult conversations about poor prognosis may be rare, but such conversations can be crucial. These discussions affect how patients live at the end of their lives, how they die, and how their families go on. Improved understanding of basic principles of communication, as well as augmented understanding of patient, family, and clinician perspectives may better enable us to navigate these important conversations.

Entities:  

Mesh:

Year:  2016        PMID: 27749945      PMCID: PMC5636611          DOI: 10.1001/jamapediatrics.2016.2142

Source DB:  PubMed          Journal:  JAMA Pediatr        ISSN: 2168-6203            Impact factor:   16.193


  61 in total

1.  Collusion in doctor-patient communication about imminent death: an ethnographic study.

Authors:  A M The; T Hak; G Koëter; G van Der Wal
Journal:  BMJ       Date:  2000-12-02

2.  Differences in parent-provider concordance regarding prognosis and goals of care among children with advanced cancer.

Authors:  Abby R Rosenberg; Liliana Orellana; Tammy I Kang; J Russell Geyer; Chris Feudtner; Veronica Dussel; Joanne Wolfe
Journal:  J Clin Oncol       Date:  2014-09-20       Impact factor: 44.544

3.  On a communitarian approach to bioethics.

Authors:  Amitai Etzioni
Journal:  Theor Med Bioeth       Date:  2011-10

4.  Trends in End-of-Life Care in Pediatric Hematology, Oncology, and Stem Cell Transplant Patients.

Authors:  Katharine E Brock; Angela Steineck; Clare J Twist
Journal:  Pediatr Blood Cancer       Date:  2015-10-29       Impact factor: 3.167

5.  Prognostic disclosure to patients with cancer near the end of life.

Authors:  E B Lamont; N A Christakis
Journal:  Ann Intern Med       Date:  2001-06-19       Impact factor: 25.391

6.  End-of-life care preferences of pediatric patients with cancer.

Authors:  Pamela S Hinds; Donna Drew; Linda L Oakes; Maryam Fouladi; Sheri L Spunt; Christopher Church; Wayne L Furman
Journal:  J Clin Oncol       Date:  2005-09-19       Impact factor: 44.544

7.  Care-related distress: a nationwide study of parents who lost their child to cancer.

Authors:  Ulrika Kreicbergs; Unnur Valdimarsdóttir; Erik Onelöv; Olle Björk; Gunnar Steineck; Jan-Inge Henter
Journal:  J Clin Oncol       Date:  2005-09-19       Impact factor: 44.544

8.  Patients' expectations about effects of chemotherapy for advanced cancer.

Authors:  Jane C Weeks; Paul J Catalano; Angel Cronin; Matthew D Finkelman; Jennifer W Mack; Nancy L Keating; Deborah Schrag
Journal:  N Engl J Med       Date:  2012-10-25       Impact factor: 91.245

9.  Parents' views of cancer-directed therapy for children with no realistic chance for cure.

Authors:  Jennifer W Mack; Steven Joffe; Joanne M Hilden; Jan Watterson; Caron Moore; Jane C Weeks; Joanne Wolfe
Journal:  J Clin Oncol       Date:  2008-09-08       Impact factor: 44.544

Review 10.  Collaborative communication in pediatric palliative care: a foundation for problem-solving and decision-making.

Authors:  Chris Feudtner
Journal:  Pediatr Clin North Am       Date:  2007-10       Impact factor: 3.278

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  17 in total

1.  Taboo Topics in Adolescent and Young Adult Oncology: Strategies for Managing Challenging but Important Conversations Central to Adolescent and Young Adult Cancer Survivorship.

Authors:  Giselle K Perez; John M Salsman; Kaitlyn Fladeboe; Anne C Kirchhoff; Elyse R Park; Abby R Rosenberg
Journal:  Am Soc Clin Oncol Educ Book       Date:  2020-03

2.  Family-centred advanced care planning with adolescents living with HIV is perceived as important, helpful and meaningful.

Authors:  Lori Wiener; Abby R Rosenberg
Journal:  Evid Based Nurs       Date:  2017-06-13

3.  Commentary: Treating the Pediatric Cancer Patient: Insights That Have Stood the Test of Time.

Authors:  Lori Wiener; Myra Bluebond-Langner
Journal:  J Pediatr Psychol       Date:  2019-08-01

Review 4.  Communication About Dying, Death, and Bereavement: A Systematic Review of Children's Literature.

Authors:  Marina N F Arruda-Colli; Meaghann S Weaver; Lori Wiener
Journal:  J Palliat Med       Date:  2017-03-27       Impact factor: 2.947

5.  Regret and unfinished business in parents bereaved by cancer: A mixed methods study.

Authors:  Wendy G Lichtenthal; Kailey E Roberts; Corinne Catarozoli; Elizabeth Schofield; Jason M Holland; Justin J Fogarty; Taylor C Coats; Lamia P Barakat; Justin N Baker; Tara M Brinkman; Robert A Neimeyer; Holly G Prigerson; Talia Zaider; William Breitbart; Lori Wiener
Journal:  Palliat Med       Date:  2020-02-05       Impact factor: 4.762

Review 6.  Pediatric Palliative Care in Oncology.

Authors:  Jennifer Snaman; Sarah McCarthy; Lori Wiener; Joanne Wolfe
Journal:  J Clin Oncol       Date:  2020-02-05       Impact factor: 44.544

Review 7.  Truth Telling in the Setting of Cultural Differences and Incurable Pediatric Illness: A Review.

Authors:  Abby R Rosenberg; Helene Starks; Yoram Unguru; Chris Feudtner; Douglas Diekema
Journal:  JAMA Pediatr       Date:  2017-11-01       Impact factor: 16.193

8.  End-of-Life Communication Needs for Adolescents and Young Adults with Cancer: Recommendations for Research and Practice.

Authors:  Ursula M Sansom-Daly; Claire E Wakefield; Pandora Patterson; Richard J Cohn; Abby R Rosenberg; Lori Wiener; Joanna E Fardell
Journal:  J Adolesc Young Adult Oncol       Date:  2019-10-29       Impact factor: 2.223

9.  Considerations for the cross-cultural adaptation of an advance care planning guide for youth with cancer.

Authors:  Marina Noronha Ferraz de Arruda-Colli; Ursula Sansom-Daly; Manoel Antônio Dos Santos; Lori Wiener
Journal:  Clin Pract Pediatr Psychol       Date:  2018-12

10.  To Disclose or Not to Disclose: A Case Highlighting the Challenge of Conflicts in Pediatric Disclosure.

Authors:  Isaac Martinez; Anna Hoppmann; Sam Perna; Paul Byrd; Joanne Wolfe; Jamie Aye; Emily E Johnston
Journal:  J Pain Symptom Manage       Date:  2020-09-02       Impact factor: 3.612

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