Literature DB >> 16384746

Parental decision making in pediatric cancer end-of-life care: using focus group methodology as a prephase to seek participant design input.

Deborah Tomlinson1, Michael Capra, Janet Gammon, Jocelyne Volpe, Maru Barrera, Pamela S Hinds, Eric Bouffet, Mark L Geenberg, Sylvain Baruchel, Hilary A Llewellyn-Thomas, Lillian Sung.   

Abstract

The ultimate aim of our research program is to provide strategies that facilitate parental decision-making for parents of children with cancer receiving end-of-life care. As a first step to develop this program, we needed insight into parents' reactions and opinions about the research methods planned for a larger study. In particular, we needed their opinions about the general experience of making the decision between palliative cytotoxic chemotherapy and supportive care alone and the factors that parents regard as important when making this decision. In addition, we wished to know whether the methodology proposed for the future study was easy to understand and whether it might cause unnecessary emotional trauma. Finally, we asked their opinions regarding the appropriate target sample of parents to include in the future study. Qualitative data about these issues were collected using focus group methodology involving seven participants. The comments made during the focus group discussions were content-analyzed for common themes. The results from the focus group discussion led to particular modifications in the proposed design and interview strategies planned for the future larger study. We found it was extremely beneficial to include a focus group pre-phase in a study that will interview parents in a high sensitivity area.

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Year:  2005        PMID: 16384746     DOI: 10.1016/j.ejon.2005.11.003

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


  13 in total

1.  Chemotherapy versus supportive care alone in pediatric palliative care for cancer: comparing the preferences of parents and health care professionals.

Authors:  Deborah Tomlinson; Ute Bartels; Janet Gammon; Pamela S Hinds; Jocelyne Volpe; Eric Bouffet; Dean A Regier; Sylvain Baruchel; Mark Greenberg; Maru Barrera; Hilary Llewellyn-Thomas; Lillian Sung
Journal:  CMAJ       Date:  2011-10-17       Impact factor: 8.262

2.  Complementary and alternative medicine use in pediatric cancer reported during palliative phase of disease.

Authors:  Deborah Tomlinson; Tanya Hesser; Marie-Chantal Ethier; Lillian Sung
Journal:  Support Care Cancer       Date:  2010-10-24       Impact factor: 3.603

Review 3.  Cultural and religious considerations in pediatric palliative care.

Authors:  Lori Wiener; Denice Grady McConnell; Lauren Latella; Erica Ludi
Journal:  Palliat Support Care       Date:  2012-05-22

4.  The Benefits and Burdens of Pediatric Palliative Care and End-of-Life Research: A Systematic Review.

Authors:  Meaghann S Weaver; Kim Mooney-Doyle; Katherine Patterson Kelly; Kathleen Montgomery; Amy R Newman; Christine A Fortney; Cynthia J Bell; Jessica L Spruit; Melissa Kurtz Uveges; Lori Wiener; Cynthia M Schmidt; Vanessa N Madrigal; Pamela S Hinds
Journal:  J Palliat Med       Date:  2019-03-05       Impact factor: 2.947

5.  Assessing information and service needs of young adults with cancer at a single institution: the importance of information on cancer diagnosis, fertility preservation, diet, and exercise.

Authors:  Abha A Gupta; Kim Edelstein; Alisha Albert-Green; Norma D'Agostino
Journal:  Support Care Cancer       Date:  2013-04-21       Impact factor: 3.603

6.  An evaluation of two decision-making scales for children with life-limiting illnesses.

Authors:  C Knapp; I C Huang; V Madden; S Vadaparampil; G Quinn; E Shenkman
Journal:  Palliat Med       Date:  2009-04-03       Impact factor: 4.762

7.  "Trying to be a good parent" as defined by interviews with parents who made phase I, terminal care, and resuscitation decisions for their children.

Authors:  Pamela S Hinds; Linda L Oakes; Judy Hicks; Brent Powell; Deo Kumar Srivastava; Sheri L Spunt; Joann Harper; Justin N Baker; Nancy K West; Wayne L Furman
Journal:  J Clin Oncol       Date:  2009-10-05       Impact factor: 44.544

Review 8.  Integration of palliative care practices into the ongoing care of children with cancer: individualized care planning and coordination.

Authors:  Justin N Baker; Pamela S Hinds; Sheri L Spunt; Raymond C Barfield; Caitlin Allen; Brent C Powell; Lisa H Anderson; Javier R Kane
Journal:  Pediatr Clin North Am       Date:  2008-02       Impact factor: 3.278

Review 9.  Parental decision making for children with cancer at the end of life: a meta-ethnography.

Authors:  Katherine E Heinze; Marie T Nolan
Journal:  J Pediatr Oncol Nurs       Date:  2012-09-19       Impact factor: 1.636

10.  Parental involvement in paediatric cancer treatment decisions.

Authors:  K McKenna; J Collier; M Hewitt; H Blake
Journal:  Eur J Cancer Care (Engl)       Date:  2009-10-05       Impact factor: 2.520

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