Literature DB >> 21109490

Parents' views on information in childhood cancer care.

Anne Kästel1, Karin Enskär, Olle Björk.   

Abstract

PURPOSE: The aim of the study is to highlight parents' views on information in childhood cancer care.
METHOD: A qualitative design, appropriate to gain a holistic view, has been chosen. Eight families with children diagnosed with cancer, of various ages and gender and from various backgrounds, participated in five interviews each during the first year of the child's illness.
RESULTS: If the parents' needs were fulfilled, they were better equipped to handle the illness of their child, which is totally dependant on how the matter of information is dealt with. Information is a complex and demanding issue for the persons involved and the families' views were divergent in this area. Sometimes they seemed to obtain the information successfully and sometimes there were great problems in this respect. Therefore their preferences must be considered.
CONCLUSION: There has to be an improvement from the aspects of what, when and how information is provided. The major findings of this study indicate that the families need better support and more distinct instructions to be able to cope with the situation.
Copyright © 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 21109490     DOI: 10.1016/j.ejon.2010.10.007

Source DB:  PubMed          Journal:  Eur J Oncol Nurs        ISSN: 1462-3889            Impact factor:   2.398


  10 in total

1.  Decision-making in childhood cancer: parents' and adolescents' views and perceptions.

Authors:  Eden G Robertson; Claire E Wakefield; Joanne Shaw; Anne-Sophie Darlington; Brittany C McGill; Richard J Cohn; Joanna E Fardell
Journal:  Support Care Cancer       Date:  2019-03-18       Impact factor: 3.603

2.  Identifying unmet informational needs in the inpatient setting to increase patient and caregiver engagement in the context of pediatric hematopoietic stem cell transplantation.

Authors:  Elizabeth Kaziunas; David A Hanauer; Mark S Ackerman; Sung Won Choi
Journal:  J Am Med Inform Assoc       Date:  2015-10-28       Impact factor: 4.497

3.  Pediatric oncology nurses' perceptions of prognosis-related communication.

Authors:  Amy R Newman; Kristin Haglund; Cheryl C Rodgers
Journal:  Nurs Outlook       Date:  2018-11-15       Impact factor: 3.250

Review 4.  Communication in pediatric oncology: State of the field and research agenda.

Authors:  Bryan A Sisk; Jennifer W Mack; Rachel Ashworth; James DuBois
Journal:  Pediatr Blood Cancer       Date:  2017-07-27       Impact factor: 3.167

5.  Protecting family interests: an interview study with foreign-born parents struggling on in childhood cancer care.

Authors:  Pernilla Pergert; Solvig Ekblad; Olle Björk; Karin Enskär; Tom Andrews
Journal:  Int J Pediatr       Date:  2012-03-04

6.  Information needs of Malaysian parents of children with cancer: A qualitative study.

Authors:  Chai-Eng Tan; Sie Chong Doris Lau; Zarina Abdul Latiff; Chee Chan Lee; Kok Hoi Teh; Sherina Mohd Sidik
Journal:  Asia Pac J Oncol Nurs       Date:  2021-12-25

7.  Nurses' Perceptions of Prognosis-Related Communication.

Authors:  Ahmad Mahmoud Saleh
Journal:  Asian Pac J Cancer Prev       Date:  2022-03-01

8.  Person-centred information to parents in paediatric oncology (the PIFBO study): A study protocol of an ongoing RCT.

Authors:  Anders Ringnér; Maria Björk; Cecilia Olsson; Ulla Hällgren Graneheim
Journal:  BMC Nurs       Date:  2015-12-21

Review 9.  New Trends and Recent Care Approaches in Pediatric Oncology Nursing.

Authors:  Ebru Kilicarslan Toruner; Naime Altay
Journal:  Asia Pac J Oncol Nurs       Date:  2018 Apr-Jun

10.  Medical procedures in children using a conceptual framework that keeps a focus on human dimensions of care - a discussion paper.

Authors:  Katarina Karlsson; Kathleen Galvin; Laura Darcy
Journal:  Int J Qual Stud Health Well-being       Date:  2019-12
  10 in total

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