Literature DB >> 19365164

The assessment and management of family distress during palliative care.

Talia Zaider1, David Kissane.   

Abstract

PURPOSE OF REVIEW: In the advanced stages of illness, families manage multiple caregiving demands while facing the emotional task of preparing for the loss of their loved one. Palliative care settings are well suited to identifying families at risk for elevated distress, and providing support as they navigate this process. This review summarizes current research in the assessment and management of family distress at the end of life. RECENT
FINDINGS: The recent literature on families of terminally ill cancer patients has provided a more precise description of the relational and cultural factors that contribute to family distress. Studies eliciting the perspectives of family members on what is needed at the end of life affirm the importance of supportive communication and continuity of psychosocial care into bereavement. Other developments include efforts to establish guidelines for conducting family meetings in the palliative care setting, and to train palliative care practitioners in family-centered assessment techniques. Finally, there is a limited but growing evidence base for the utility of delivering family-focused psychosocial interventions during palliative care.
SUMMARY: The knowledge gained from current research on what is most salient to family members during palliative care is critical for ensuring effective delivery of supportive services and collaborative engagement in those services.

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Mesh:

Year:  2009        PMID: 19365164      PMCID: PMC5557503          DOI: 10.1097/SPC.0b013e328325a5ab

Source DB:  PubMed          Journal:  Curr Opin Support Palliat Care        ISSN: 1751-4258            Impact factor:   2.302


  25 in total

Review 1.  Family support at end of life.

Authors:  Karin T Kirchhoff; April I Faas
Journal:  AACN Adv Crit Care       Date:  2007 Oct-Dec

Review 2.  A review of distress and its management in couples facing end-of-life cancer.

Authors:  Linda M McLean; Jennifer M Jones
Journal:  Psychooncology       Date:  2007-07       Impact factor: 3.894

3.  What questions do family caregivers want to discuss with health care providers in order to prepare for the death of a loved one? An ethnographic study of caregivers of patients at end of life.

Authors:  Randy Scott Hebert; Richard Schulz; Valire Copeland; Robert M Arnold
Journal:  J Palliat Med       Date:  2008-04       Impact factor: 2.947

4.  Evaluation of a psycho-educational group programme for family caregivers in home-based palliative care.

Authors:  P Hudson; K Quinn; L Kristjanson; T Thomas; M Braithwaite; J Fisher; M Cockayne
Journal:  Palliat Med       Date:  2008-04       Impact factor: 4.762

Review 5.  Preparing caregivers for the death of a loved one: a theoretical framework and suggestions for future research.

Authors:  Randy S Hebert; Holly G Prigerson; Richard Schulz; Robert M Arnold
Journal:  J Palliat Med       Date:  2006-10       Impact factor: 2.947

6.  Cancer and the family: an integrative model.

Authors:  John S Rolland
Journal:  Cancer       Date:  2005-12-01       Impact factor: 6.860

Review 7.  The psychological impact of cancer on patients' partners and other key relatives: a review.

Authors:  C Pitceathly; P Maguire
Journal:  Eur J Cancer       Date:  2003-07       Impact factor: 9.162

8.  Health-related quality of life in significant others of patients dying from lung cancer.

Authors:  C Persson; U Ostlund; A Wennman-Larsen; Y Wengström; P Gustavsson
Journal:  Palliat Med       Date:  2008-04       Impact factor: 4.762

9.  Associations between end-of-life discussions, patient mental health, medical care near death, and caregiver bereavement adjustment.

Authors:  Alexi A Wright; Baohui Zhang; Alaka Ray; Jennifer W Mack; Elizabeth Trice; Tracy Balboni; Susan L Mitchell; Vicki A Jackson; Susan D Block; Paul K Maciejewski; Holly G Prigerson
Journal:  JAMA       Date:  2008-10-08       Impact factor: 56.272

10.  The psychological impact of a cancer diagnosis on families: the influence of family functioning and patients' illness characteristics on depression and anxiety.

Authors:  Ben Edwards; Valerie Clarke
Journal:  Psychooncology       Date:  2004-08       Impact factor: 3.894

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  9 in total

1.  Experience of meaning in life in bereaved informal caregivers of palliative care patients.

Authors:  Monika Brandstätter; Monika Kögler; Urs Baumann; Veronika Fensterer; Helmut Küchenhoff; Gian Domenico Borasio; Martin Johannes Fegg
Journal:  Support Care Cancer       Date:  2014-01-03       Impact factor: 3.603

2.  Parenting while living with advanced cancer: A qualitative study.

Authors:  Eliza M Park; Devon K Check; Mi-Kyung Song; Katherine E Reeder-Hayes; Laura C Hanson; Justin M Yopp; Donald L Rosenstein; Deborah K Mayer
Journal:  Palliat Med       Date:  2016-08-06       Impact factor: 4.762

Review 3.  Can early palliative care with anticancer treatment improve overall survival and patient-related outcomes in advanced lung cancer patients? A review of the literature.

Authors:  Massimo Ambroggi; Claudia Biasini; Ilaria Toscani; Elena Orlandi; Raffaella Berte; Martina Mazzari; Luigi Cavanna
Journal:  Support Care Cancer       Date:  2018-04-27       Impact factor: 3.603

Review 4.  Holistic view of patients with melanoma of the skin: how can health systems create value and achieve better clinical outcomes?

Authors:  Patrícia Redondo; Matilde Ribeiro; Machado Lopes; Marina Borges; Francisco Rocha Gonçalves
Journal:  Ecancermedicalscience       Date:  2019-08-27

5.  Biopsychosocial and Spiritual Implications of Patients With COVID-19 Dying in Isolation.

Authors:  Thushara Galbadage; Brent M Peterson; David C Wang; Jeffrey S Wang; Richard S Gunasekera
Journal:  Front Psychol       Date:  2020-11-17

6.  Long-distance caregiving at the end of life: a protocol for an exploratory qualitative study in Germany.

Authors:  Franziska A Herbst; Nils Schneider; Stephanie Stiel
Journal:  BMC Palliat Care       Date:  2022-05-12       Impact factor: 3.113

Review 7.  Development of a set of process and structure indicators for palliative care: the Europall project.

Authors:  Kathrin Woitha; Karen Van Beek; Nisar Ahmed; Jeroen Hasselaar; Jean-Marc Mollard; Isabelle Colombet; Lukas Radbruch; Kris Vissers; Yvonne Engels
Journal:  BMC Health Serv Res       Date:  2012-11-02       Impact factor: 2.655

8.  Double Burden of COVID-19 Pandemic and Military Occupation: Mental Health Among a Palestinian University Community in the West Bank.

Authors:  Rula Ghandour; Rasha Ghanayem; Farah Alkhanafsa; Ayah Alsharif; Hiba Asfour; Aisha Hoshiya; Amani Masalmeh; Muna Nadi; Laila Othman; Sameera Ryahe; Yasmeen Wahdan; Shatha Wahsh; Ala'a Yamani; Rita Giacaman
Journal:  Ann Glob Health       Date:  2020-10-08       Impact factor: 2.462

Review 9.  Developing an integrated model of community-based palliative care into the primary health care (PHC) for terminally ill cancer patients in Iran.

Authors:  Suzanne Hojjat-Assari; Maryam Rassouli; Maxwell Madani; Heshmatolah Heydari
Journal:  BMC Palliat Care       Date:  2021-06-28       Impact factor: 3.234

  9 in total

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