Literature DB >> 19956979

Parental experience at the end-of-life in children with cancer: 'preservation' and 'letting go' in relation to loss.

Marijke C Kars1, Mieke H F Grypdonck, Maria C de Korte-Verhoef, Willem A Kamps, Esther M M Meijer-van den Bergh, Marian A Verkerk, Johannes J M van Delden.   

Abstract

PURPOSE: For children with incurable cancer death usually is anticipated and preceded by a phase of palliative care. Despite recognition that parents have difficulty adapting to a palliative perspective there is little insight into this process. This study explored, from a parental perspective, the process parents go through when cure is no longer a possibility. PARTICIPANTS AND METHODS: A multicenter study using qualitative research was undertaken during the EoL phase. One-time and repeated open interviews were conducted with 44 parents of 23 children with incurable cancer.
RESULTS: Feelings of loss play a prominent role during the EoL phase. Dealing with loss is a process of stepwise relinquishing that becomes manifest in an internal struggle between preservation and letting go. Preservation means that parents try to maintain the child's status quo. Letting go means parents give up their resistance to loss in service of their child's well-being. Although the relative measure of each changes over time, parents have great difficulty making the transition because it implies a change in source of control. A timely completion of this transition positively influences the child's well-being as well as the evaluation of enacted parenthood.
CONCLUSION: For parents the essence of the palliative process is not to accept death but to deal with the loss of their child. Although the need to avoid loss and gain control by means of preservation is fully understandable, the study indicated that parents who made the transition to letting go had an increased receptiveness of their child's real situation and needs.

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Year:  2009        PMID: 19956979     DOI: 10.1007/s00520-009-0785-1

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  28 in total

1.  Reembodying qualitative inquiry.

Authors:  Margarete Sandelowski
Journal:  Qual Health Res       Date:  2002-01

Review 2.  Making words count: the value of qualitative research.

Authors:  Ros Johnson; Jackie Waterfield
Journal:  Physiother Res Int       Date:  2004

Review 3.  Paediatric palliative care: challenges and emerging ideas.

Authors:  Stephen Liben; Danai Papadatou; Joanne Wolfe
Journal:  Lancet       Date:  2008-03-08       Impact factor: 79.321

4.  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

5.  Parent and physician perspectives on quality of care at the end of life in children with cancer.

Authors:  Jennifer W Mack; Joanne M Hilden; Jan Watterson; Caron Moore; Brian Turner; Holcombe E Grier; Jane C Weeks; Joanne Wolfe
Journal:  J Clin Oncol       Date:  2005-09-19       Impact factor: 44.544

6.  Choices and control: parental experiences in pediatric terminal home care.

Authors:  J L Vickers; C Carlisle
Journal:  J Pediatr Oncol Nurs       Date:  2000-01       Impact factor: 1.636

7.  Caring for the child with cancer at the close of life: "there are people who make it, and I'm hoping I'm one of them".

Authors:  Craig A Hurwitz; Janet Duncan; Joanne Wolfe
Journal:  JAMA       Date:  2004-11-03       Impact factor: 56.272

8.  Parents' intellectual and emotional awareness of their child's impending death to cancer: a population-based long-term follow-up study.

Authors:  Unnur Valdimarsdóttir; Ulrika Kreicbergs; Arna Hauksdóttir; Hayley Hunt; Erik Onelöv; Jan-Inge Henter; Gunnar Steineck
Journal:  Lancet Oncol       Date:  2007-08       Impact factor: 41.316

Review 9.  Hospice and palliative care.

Authors:  P Rousseau
Journal:  Dis Mon       Date:  1995-12       Impact factor: 3.800

Review 10.  End-of-life research as a priority for pediatric oncology.

Authors:  Pamela S Hinds; Michele Pritchard; Joann Harper
Journal:  J Pediatr Oncol Nurs       Date:  2004 May-Jun       Impact factor: 1.636

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  16 in total

1.  The family's experience of the child and/or teenager in palliative care: fluctuating between hope and hopelessness in a world changed by losses.

Authors:  Maira Deguer Misko; Maiara Rodrigues dos Santos; Carolliny Rossi de Faria Ichikawa; Regina Aparecida Garcia de Lima; Regina Szylit Bousso
Journal:  Rev Lat Am Enfermagem       Date:  2015 May-Jun

Review 2.  Pediatric palliative care-when quality of life becomes the main focus of treatment.

Authors:  Eva Bergstraesser
Journal:  Eur J Pediatr       Date:  2012-04-03       Impact factor: 3.183

3.  Challenging patient deaths in pediatric oncology.

Authors:  Leeat Granek; Ute Bartels; Katrin Scheinemann; Maru Barrera
Journal:  Support Care Cancer       Date:  2015-01-14       Impact factor: 3.603

4.  Family interactions in childhood leukemia: an exploratory descriptive study.

Authors:  Jaefar Moghaddasi; Fariba Taleghani; Alireza Moafi; Azadeh Malekian; Mahrokh Keshvari; Mahnaz Ilkhani
Journal:  Support Care Cancer       Date:  2018-06-11       Impact factor: 3.603

5.  Referral practices of pediatric oncologists to specialized palliative care.

Authors:  Kirsten Wentlandt; Monika K Krzyzanowska; Nadia Swami; Gary Rodin; Lisa W Le; Lillian Sung; Camilla Zimmermann
Journal:  Support Care Cancer       Date:  2014-03-27       Impact factor: 3.603

6.  Parenting in Childhood Life-Threatening Illness: A Mixed-Methods Study.

Authors:  Kim Mooney-Doyle; Janet A Deatrick; Connie M Ulrich; Salimah H Meghani; Chris Feudtner
Journal:  J Palliat Med       Date:  2017-10-03       Impact factor: 2.947

7.  'From activating towards caring': shifts in care approaches at the end of life of people with intellectual disabilities; a qualitative study of the perspectives of relatives, care-staff and physicians.

Authors:  Nienke Bekkema; Anke J E de Veer; Cees M P M Hertogh; Anneke L Francke
Journal:  BMC Palliat Care       Date:  2015-07-25       Impact factor: 3.234

Review 8.  Current understanding of decision-making in adolescents with cancer: A narrative systematic review.

Authors:  Emma Day; Louise Jones; Richard Langner; Myra Bluebond-Langner
Journal:  Palliat Med       Date:  2016-05-09       Impact factor: 4.762

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

Review 10.  Palliative care and quality of life in neuro-oncology.

Authors:  Naveen Mummudi; Rakesh Jalali
Journal:  F1000Prime Rep       Date:  2014-08-01
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