Literature DB >> 19822277

Bereaved parents' perceptions about when their child's cancer-related death would occur.

Michele Pritchard1, Deo Kumar Srivastava, James O Okuma, Brent Powell, Elizabeth Burghen, Nancy K West, Jami S Gattuso, Sheri L Spunt, Justin N Baker, Javier Kane, Wayne L Furman, Pamela S Hinds.   

Abstract

Parents of terminally ill children with cancer frequently ask clinicians when their child will die. Such information helps parents prepare for the child's death. To identify how parents perceived when their child's cancer-related death would occur, we conducted a secondary analysis of telephone interviews with 49 bereaved parents 6-10 months after their child's death to extract their descriptions of this occurrence. The parents knew in advance that their child was going to die, but they described when their child's death would occur in three different ways: anticipated (parents observed changes that alerted them that death was imminent; n=22, 52.4%), surprising (parents were surprised that their child died on that particular day; n=13, 31.0%), and overdue (parents had been waiting for the end of their child's apparent suffering; n=7, 16.7%). These categories did not differ by patients' diagnosis, sex, or location of death but differed slightly by symptom patterns. Parents who reported the occurrence of their child's death as surprising reported fewer symptom changes on the last day of their child's life, compared with the last week of life, than did the parents in the other two categories. These findings indicate that parents of children with terminal cancer can perceive when their child's death would occur very differently: Some are surprised, whereas others feel they have waited too long for their child's release from suffering. Clinicians can use these descriptions and the associated symptom patterns to help families prepare for their child's last week and last day.

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Year:  2009        PMID: 19822277      PMCID: PMC2941143          DOI: 10.1016/j.jpainsymman.2009.01.005

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  11 in total

1.  The turning point: Clinical identification of dying and reorientation of care.

Authors:  Eva Jakobsson; Ingrid Bergh; Fannie Gaston-Johansson; Carl-Magnus Stolt; Joakim Ohlén
Journal:  J Palliat Med       Date:  2006-12       Impact factor: 2.947

2.  Experience of dying: concerns of dying patients and of carers.

Authors:  W Terry; L G Olson; L Wilss; G Boulton-Lewis
Journal:  Intern Med J       Date:  2006-06       Impact factor: 2.048

3.  Preparing for the end of life: preferences of patients, families, physicians, and other care providers.

Authors:  K E Steinhauser; N A Christakis; E C Clipp; M McNeilly; S Grambow; J Parker; J A Tulsky
Journal:  J Pain Symptom Manage       Date:  2001-09       Impact factor: 3.612

4.  Understanding of prognosis among parents of children who died of cancer: impact on treatment goals and integration of palliative care.

Authors:  J Wolfe; N Klar; H E Grier; J Duncan; S Salem-Schatz; E J Emanuel; J C Weeks
Journal:  JAMA       Date:  2000-11-15       Impact factor: 56.272

5.  Family perspectives on the quality of pediatric palliative care.

Authors:  Nancy Contro; Judith Larson; Sarah Scofield; Barbara Sourkes; Harvey Cohen
Journal:  Arch Pediatr Adolesc Med       Date:  2002-01

6.  Cancer-related symptoms most concerning to parents during the last week and last day of their child's life.

Authors:  Michele Pritchard; Elizabeth Burghen; Deo Kumar Srivastava; James Okuma; Lisa Anderson; Brent Powell; Wayne L Furman; Pamela S Hinds
Journal:  Pediatrics       Date:  2008-05       Impact factor: 7.124

7.  Cancer patient preferences for communication of prognosis in the metastatic setting.

Authors:  Rebecca G Hagerty; Phyllis N Butow; Peter A Ellis; Elizabeth A Lobb; Susan Pendlebury; Natasha Leighl; David Goldstein; Sing Kai Lo; Martin H N Tattersall
Journal:  J Clin Oncol       Date:  2004-05-01       Impact factor: 44.544

8.  Childhood brain tumors: parental concerns and stressors by phase of illness.

Authors:  Katherine Freeman; Christine O'Dell; Carol Meola
Journal:  J Pediatr Oncol Nurs       Date:  2004 Mar-Apr       Impact factor: 1.636

Review 9.  A systematic review of prognostic/end-of-life communication with adults in the advanced stages of a life-limiting illness: patient/caregiver preferences for the content, style, and timing of information.

Authors:  Sharon M Parker; Josephine M Clayton; Karen Hancock; Sharon Walder; Phyllis N Butow; Sue Carrick; David Currow; Davina Ghersi; Paul Glare; Rebecca Hagerty; Martin H N Tattersall
Journal:  J Pain Symptom Manage       Date:  2007-05-25       Impact factor: 3.612

10.  Understanding of prognosis and goals of care among couples whose child died of cancer.

Authors:  Kelly E Edwards; Bridget A Neville; Earl F Cook; Sarah H Aldridge; Veronica Dussel; Joanne Wolfe
Journal:  J Clin Oncol       Date:  2008-03-10       Impact factor: 44.544

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  3 in total

1.  Multiple Complex Chronic Conditions and Pediatric Hospice Utilization among California Medicaid Beneficiaries, 2007-2010.

Authors:  Lisa C Lindley
Journal:  J Palliat Med       Date:  2016-10-31       Impact factor: 2.947

Review 2.  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

Review 3.  Palliative Care in Paediatric Oncology: an Update.

Authors:  Naveen Salins; Sean Hughes; Nancy Preston
Journal:  Curr Oncol Rep       Date:  2022-01-21       Impact factor: 5.075

  3 in total

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