Literature DB >> 17933614

Psychosocial and spiritual needs of children living with a life-limiting illness.

Mary McSherry1, Kathy Kehoe, Jean M Carroll, Tammy I Kang, Mary T Rourke.   

Abstract

Quality end-of-life care includes the management of distressing symptoms; provisions of care, including the assessment and management of psychosocial and spiritual needs; and respite from diagnosis through death and bereavement. Meeting the palliative care goal of improved quality of life depends on medical and nursing practitioners understatnding and effectively assessing psychosocial symptoms.

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Year:  2007        PMID： 17933614     DOI： 10.1016/j.pcl.2007.08.002

Source DB:  PubMed          Journal:  Pediatr Clin North Am        ISSN： 0031-3955            Impact factor:   3.278


  8 in total

Review 1.  Pediatric palliative care - The role of the patient's family.

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

Review 2.  End-of-Life and Bereavement Care in Pediatric Intensive Care Units.

Authors:  Markita L Suttle; Tammara L Jenkins; Robert F Tamburro
Journal:  Pediatr Clin North Am       Date:  2017-08-18       Impact factor: 3.278

3.  How parents of children receiving pediatric palliative care use religion, spirituality, or life philosophy in tough times.

Authors:  Kari R Hexem; Cynthia J Mollen; Karen Carroll; Dexter A Lanctot; Chris Feudtner
Journal:  J Palliat Med       Date:  2011-01       Impact factor: 2.947

4.  Measuring quality of life in pediatric palliative care: challenges and potential solutions.

Authors:  I-Chan Huang; Elizabeth A Shenkman; Vanessa L Madden; Susan Vadaparampil; Gwendolyn Quinn; Caprice A Knapp
Journal:  Palliat Med       Date:  2009-12-10       Impact factor: 4.762

5.  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

6.  "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

7.  From the Child's Word to Clinical Intervention: Novel, New, and Innovative Approaches to Symptoms in Pediatric Palliative Care.

Authors:  Katharine E Brock; Joanne Wolfe; Christina Ullrich
Journal:  Children (Basel)       Date:  2018-03-28

Review 8.  Palliative Care for Children with Central Nervous System Malignancies.

Authors:  Peter H Baenziger; Karen Moody
Journal:  Bioengineering (Basel)       Date:  2018-10-13
  8 in total

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