Literature DB >> 20405517

Factors influencing parental readiness to let their child with cancer die.

Marijke C Kars1, Mieke H F Grypdonck, Auke Beishuizen, Esther M M Meijer-van den Bergh, Johannes J M van Delden.   

Abstract

BACKGROUND: One in four cases of childhood cancer is incurable. In these cases death can usually be anticipated and therefore preceded by a phase of palliative care. For parents, preparing to let their child die is an extraordinarily painful process. Most struggle to preserve their child. This study identified, from a parental perspective, the main factors that influence the transition from preserving life to letting go. PROCEDURE: A multi-centre, qualitative research, study was undertaken during the end-of-life (EoL) phase, comprising single or repeated interviews with 44 parents of 23 children with incurable cancer.
RESULTS: We discovered that uncertainty, fragmentation and anxiety underpin the preserving life perspective. A perspective of letting go could be supported by a variety of factors. These included: Certainty that the child cannot be cured, postponed grief, the perception of suffering, the ability to disentangle needs and the ability to parent meaningfully. Hope, creating a peaceful parent-child relationship, and the attitude of professionals, could support movements in either direction. Of these, certainty, and in most cases postponed grief, were pre-conditions for the transition towards letting go. Strategies such as not challenging the parents' suppression of grief, creating certainty about the child's condition and supporting parents in efforts to redefine their parental role, supported progress towards accepting a letting go perspective.
CONCLUSIONS: Parents' internal struggle between a preserving frame of mind and one of letting go is influenced by a combination of factors. However, professionals can influence some of these factors in order to facilitate this transition. Copyright 2010 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2010        PMID: 20405517     DOI: 10.1002/pbc.22532

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  10 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 - The role of the patient's family.

Authors:  Carl Friedrich Classen
Journal:  World J Clin Pediatr       Date:  2012-10-08

3.  Changes Over Time in Good-Parent Beliefs Among Parents of Children With Serious Illness: A Two-Year Cohort Study.

Authors:  Douglas L Hill; Jennifer A Faerber; Yimei Li; Victoria A Miller; Karen W Carroll; Wynne Morrison; Pamela S Hinds; Chris Feudtner
Journal:  J Pain Symptom Manage       Date:  2019-04-23       Impact factor: 3.612

4.  Changes in Parental Hopes for Seriously Ill Children.

Authors:  Douglas L Hill; Pamela G Nathanson; Karen W Carroll; Theodore E Schall; Victoria A Miller; Chris Feudtner
Journal:  Pediatrics       Date:  2018-04       Impact factor: 7.124

5.  Parent Grief 1-13 Months After Death in Neonatal and Pediatric Intensive Care Units.

Authors:  JoAnne M Youngblut; Dorothy Brooten; Joy Glaze; Teresita Promise; Changwon Yoo
Journal:  J Loss Trauma       Date:  2016-05-09

6.  Prognostic accuracy of antenatal neonatology consultation.

Authors:  S Kukora; N Gollehon; G Weiner; N Laventhal
Journal:  J Perinatol       Date:  2016-09-29       Impact factor: 2.521

Review 7.  The under reporting of recruitment strategies in research with children with life-threatening illnesses: A systematic review.

Authors:  Briony F Hudson; Linda Jm Oostendorp; Bridget Candy; Victoria Vickerstaff; Louise Jones; Monica Lakhanpaul; Myra Bluebond-Langner; Paddy Stone
Journal:  Palliat Med       Date:  2016-09-08       Impact factor: 4.762

8.  Aims and tasks in parental caregiving for children receiving palliative care at home: a qualitative study.

Authors:  Lisa M Verberne; Marijke C Kars; Antoinette Y N Schouten-van Meeteren; Diederik K Bosman; Derk A Colenbrander; Martha A Grootenhuis; Johannes J M van Delden
Journal:  Eur J Pediatr       Date:  2017-01-11       Impact factor: 3.183

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.  A conceptual model of barriers and facilitators to primary clinical teams requesting pediatric palliative care consultation based upon a narrative review.

Authors:  Jennifer K Walter; Douglas L Hill; Concetta DiDomenico; Shefali Parikh; Chris Feudtner
Journal:  BMC Palliat Care       Date:  2019-12-21       Impact factor: 3.234

  10 in total

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