Literature DB >> 20413052

Factors that distinguish symptoms of most concern to parents from other symptoms of dying children.

Michele Pritchard1, Elizabeth A Burghen, Jami S Gattuso, Nancy K West, Poorna Gajjar, Deo Kumar Srivastava, Sheri L Spunt, Justin N Baker, Javier R Kane, Wayne L Furman, Pamela S Hinds.   

Abstract

In a previous study, we conducted telephone interviews with parents 6 to 10 months after their child's death from cancer, using open-ended questions to identify the type and frequency of cancer-related symptoms that most concerned them during the last week of their child's life. Because the parents identified many clinically striking symptoms (n=109) that were not of most concern to them, we conducted a secondary analysis of these interviews (48 mothers and four fathers of 52 patients) to identify descriptive factors associated with the parents' level of concern. Six descriptive factors were associated with symptoms of most concern and 10 factors with symptoms not of most concern. Ten of these 16 factors occurred in both categories, indicating that clinicians should directly query parents to identify the symptoms that concern parents the most. Six factors differed between the two categories, and only one (the continuous distress caused by a symptom that is unrelieved) was unique to the category of symptoms of most concern. Five factors (symptom present for at least one week, symptom not seen as remarkable by the parent or causing no distress to the child, symptom well managed, symptom improved, and symptoms for which the parent felt adequately prepared) were unique to the category of symptoms not of most concern. By inquiring about symptoms of most concern and factors that influence parental concern, clinicians may be better able to direct care efforts to reduce patients' and parents' distress and support parents during the difficult end-of-life period. Copyright (c) 2010 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20413052      PMCID: PMC2941146          DOI: 10.1016/j.jpainsymman.2009.08.012

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


  10 in total

1.  Symptoms and suffering at the end of life in children with cancer.

Authors:  J Wolfe; H E Grier; N Klar; S B Levin; J M Ellenbogen; S Salem-Schatz; E J Emanuel; J C Weeks
Journal:  N Engl J Med       Date:  2000-02-03       Impact factor: 91.245

2.  Symptoms in the palliative phase of children with cancer.

Authors:  J M J Theunissen; P M Hoogerbrugge; T van Achterberg; J B Prins; M J F J Vernooij-Dassen; C H M van den Ende
Journal:  Pediatr Blood Cancer       Date:  2007-08       Impact factor: 3.167

3.  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

4.  Cancer-related deaths in children and adolescents.

Authors:  Glenna Bradshaw; Pamela S Hinds; Shelly Lensing; Jami S Gattuso; Bassem I Razzouk
Journal:  J Palliat Med       Date:  2005-02       Impact factor: 2.947

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.  The symptoms of dying children.

Authors:  Ross Drake; Judy Frost; John J Collins
Journal:  J Pain Symptom Manage       Date:  2003-07       Impact factor: 3.612

8.  Parents' perspective on symptoms, quality of life, characteristics of death and end-of-life decisions for children dying from cancer.

Authors:  T Hechler; M Blankenburg; S J Friedrichsdorf; D Garske; B Hübner; A Menke; C Wamsler; J Wolfe; B Zernikow
Journal:  Klin Padiatr       Date:  2008 May-Jun       Impact factor: 1.349

9.  Parental grief after losing a child to cancer: impact of professional and social support on long-term outcomes.

Authors:  Ulrika C Kreicbergs; Patrizia Lannen; Erik Onelov; Joanne Wolfe
Journal:  J Clin Oncol       Date:  2007-08-01       Impact factor: 44.544

10.  Parental coping and bereavement outcome after the death of a child in the pediatric intensive care unit.

Authors:  K L Meert; C S Thurston; R Thomas
Journal:  Pediatr Crit Care Med       Date:  2001-10       Impact factor: 3.624

  10 in total
  5 in total

1.  Behavioral Observation of Infants With Life-Threatening or Life-Limiting Illness in the Neonatal Intensive Care Unit.

Authors:  Christine A Fortney; Stephanie D Sealschott; Rita H Pickler
Journal:  Nurs Res       Date:  2020 Sep/Oct       Impact factor: 2.381

2.  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

3.  Determinants of access to pediatric hospice care: A conceptual model.

Authors:  Lisa C Lindley
Journal:  J Hosp Palliat Nurs       Date:  2015-04       Impact factor: 1.918

4.  Decision making by parents of children with incurable cancer who opt for enrollment on a phase I trial compared with choosing a do not resuscitate/terminal care option.

Authors:  Scott H Maurer; Pamela S Hinds; Sheri L Spunt; Wayne L Furman; Javier R Kane; Justin N Baker
Journal:  J Clin Oncol       Date:  2010-05-24       Impact factor: 44.544

Review 5.  Palliative care for children with cancer.

Authors:  Elisha Waldman; Joanne Wolfe
Journal:  Nat Rev Clin Oncol       Date:  2013-01-22       Impact factor: 66.675

  5 in total

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