Literature DB >> 27272911

Children with cancer share their views: tell the truth but leave room for hope.

Li Jalmsell1,2, Malin Lövgren3,4, Ulrika Kreicbergs3,4, Jan-Inge Henter3, Britt-Marie Frost5.   

Abstract

AIM: One in five children diagnosed with cancer will die from the disease. The aim of the study was to explore how children with cancer want to receive bad news about their disease, such as when no more treatment options are available.
METHODS: We conducted individual interviews with ten children with cancer, aged seven to 17 years, at a single paediatric oncology unit in central Sweden. Interviews were audio-taped and analysed with systematic text condensation. Bad news was defined as information about a potentially fatal outcome, such as a disease relapse, or information that the treatment administered was no longer working and that there was no more treatment possible.
RESULTS: All children expressed that they wanted truthful information and they did not want to be excluded from bad news regarding their illness. They wanted to be informed as positively as possible, allowing them to maintain hope, and in words that they could understand. They also wanted to receive any bad news at the same time as their parents.
CONCLUSION: Children with cancer want to be fully informed about their disease, but they also wanted it to be relayed as positively as possible so that they could stay hopeful. ©2016 Foundation Acta Paediatrica. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  Communication; End-of-life care; Ethics; Paediatric oncology; Palliative care

Mesh:

Year:  2016        PMID: 27272911     DOI: 10.1111/apa.13496

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN: 0803-5253            Impact factor:   2.299


  12 in total

1.  Communication preferences of pediatric cancer patients: talking about prognosis and their future life.

Authors:  Sarah R Brand; Karen Fasciano; Jennifer W Mack
Journal:  Support Care Cancer       Date:  2016-10-17       Impact factor: 3.603

2.  Living with the cerebellar mutism syndrome: long-term challenges of the diagnosis.

Authors:  Morten Wibroe; Marianne Vie Ingersgaard; Hanne Bækgaard Larsen; Marianne Juhler; Karin Piil
Journal:  Acta Neurochir (Wien)       Date:  2020-07-03       Impact factor: 2.216

3.  Information needs of children with leukemia and their parents' perspectives of their information needs: a qualitative study.

Authors:  Noyuri Yamaji; Yasuko Nagamatsu; Kyoko Kobayashi; Daisuke Hasegawa; Yuki Yuza; Erika Ota
Journal:  BMC Pediatr       Date:  2022-07-13       Impact factor: 2.567

4.  Specialist paediatric palliative care for children and young people with cancer: A mixed-methods systematic review.

Authors:  Johanna Taylor; Alison Booth; Bryony Beresford; Bob Phillips; Kath Wright; Lorna Fraser
Journal:  Palliat Med       Date:  2020-05-02       Impact factor: 4.762

Review 5.  Discussing Prognosis with Empathy to Cancer Patients.

Authors:  Sophie Lelorain
Journal:  Curr Oncol Rep       Date:  2021-03-14       Impact factor: 5.075

Review 6.  Palliative Care in Pediatric Oncology and Hematopoietic Stem Cell Transplantation.

Authors:  Allison Uber; Jonathan S Ebelhar; Ashley Foster Lanzel; Anna Roche; Viviana Vidal-Anaya; Katharine E Brock
Journal:  Curr Oncol Rep       Date:  2022-01-21       Impact factor: 5.075

7.  "Some things are even worse than telling a child he is going to die": Pediatric oncology healthcare professionals perspectives on communicating with children about cancer and end of life.

Authors:  Anat Laronne; Leeat Granek; Lori Wiener; Paula Feder-Bubis; Hana Golan
Journal:  Pediatr Blood Cancer       Date:  2021-12-26       Impact factor: 3.838

8.  Achieving beneficial outcomes for children with life-limiting and life-threatening conditions receiving palliative care and their families: A realist review.

Authors:  Sarah Mitchell; Karina Bennett; Andrew Morris; Anne-Marie Slowther; Jane Coad; Jeremy Dale
Journal:  Palliat Med       Date:  2019-08-21       Impact factor: 4.762

9.  Important situations that capture moral distress in paediatric oncology.

Authors:  Margareta Af Sandeberg; Cecilia Bartholdson; Pernilla Pergert
Journal:  BMC Med Ethics       Date:  2020-01-13       Impact factor: 2.652

10.  Physicians working in oncology identified challenges and factors that facilitated communication with families when children could not be cured.

Authors:  Camilla Udo; Ulrika Kreicbergs; Bertil Axelsson; Olle Björk; Malin Lövgren
Journal:  Acta Paediatr       Date:  2019-07-12       Impact factor: 2.299

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