Literature DB >> 24742788

Trajectories of the multidimensional dying experience for terminally ill cancer patients.

Siew T Tang1, Li N Liu2, Kuan-Chia Lin3, Jui-Hung Chung3, Chia-Hsun Hsieh4, Wen-Chi Chou4, Po-Jung Su4.   

Abstract

CONTEXT: Studies exploring the trajectories of physical-psychological-social-spiritual dying experiences frequently treat changes in these experiences as consistent across different domains and over time.
OBJECTIVE: This prospective, longitudinal investigation was designed to characterize trajectories of the multidimensional dying experience for cancer patients in their last year of life.
METHODS: Trajectories of physical-psychological-social-spiritual/existential dimensions and overall quality of life (QOL) were identified among 313 cancer patients using mixed-effects models to test for linear, quadratic, or cubic changes. Changes in each variable were evaluated for clinical significance using minimal important difference.
RESULTS: When patients transitioned to their end of life, symptom distress, functional dependence, anxiety, and depressive symptoms slightly increased, followed by a stable status for approximately four to six months, and accelerated dramatically to the first clinically significant changes at three to four months before death. Perceived social support and post-traumatic growth declined gradually to clinically significant changes at one and four months before death, respectively. Perceived sense of burden to others increased steadily in the last year of life, with no clinically significant changes identified. Overall QOL deteriorated gradually in the last year but did not reach a clinically significant change until 2.5 months before death.
CONCLUSION: All dimensions deteriorated in the last year of life but with distinctive physical-psychological-social-spiritual/existential and overall QOL trajectories. Recognizing trajectory patterns and tipping points of accelerating deterioration in each dimension can help clinicians anticipate times of increased distress, initiate timely, effective interventions to relieve patient suffering, and facilitate high-quality end-of-life care tailored to patients' needs and preferences.
Copyright © 2014 American Academy of Hospice and Palliative Medicine. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Trajectory; functional dependence; post-traumatic growth; psychological distress; quality of life; sense of burden to others; symptom distress

Mesh:

Year:  2014        PMID: 24742788     DOI: 10.1016/j.jpainsymman.2014.01.011

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


  12 in total

1.  Coping Skills Training and Acceptance and Commitment Therapy for Symptom Management: Feasibility and Acceptability of a Brief Telephone-Delivered Protocol for Patients With Advanced Cancer.

Authors:  Jennifer C Plumb Vilardaga; Joseph G Winger; Irene Teo; Lynda Owen; Linda M Sutton; Francis J Keefe; Tamara J Somers
Journal:  J Pain Symptom Manage       Date:  2019-09-17       Impact factor: 3.612

Review 2.  The relationship between acceptance of cancer and distress: A meta-analytic review.

Authors:  Ekin Secinti; Danielle B Tometich; Shelley A Johns; Catherine E Mosher
Journal:  Clin Psychol Rev       Date:  2019-05-03

3.  Enhancing meaning in the face of advanced cancer and pain: Qualitative evaluation of a meaning-centered psychosocial pain management intervention.

Authors:  Joseph G Winger; Katherine Ramos; Karen E Steinhauser; Tamara J Somers; Laura S Porter; Arif H Kamal; William S Breitbart; Francis J Keefe
Journal:  Palliat Support Care       Date:  2020-06

4.  Symptom frequency, severity, and quality of life among persons with three disease trajectories: cancer, ALS, and CHF.

Authors:  Jiayun Xu; Marie T Nolan; Katherine Heinze; Gayane Yenokyan; Mark T Hughes; Julie Johnson; Joan Kub; Carrie Tudor; Daniel P Sulmasy; Lisa Soleymani Lehmann; Joseph J Gallo; Felicia Rockko; Mei Ching Lee
Journal:  Appl Nurs Res       Date:  2015-03-13       Impact factor: 2.257

5.  Longitudinal changes in spiritual well-being and associations with emotional distress, pain, and optimism-pessimism: a prospective observational study of terminal cancer patients admitted to a palliative care unit.

Authors:  Simeng Wang; Yumei Wang; Yilong Yang; Xinxin Zhao; Meng Cui
Journal:  Support Care Cancer       Date:  2021-06-19       Impact factor: 3.603

6.  Fear, Pain, Denial, and Spiritual Experiences in Dying Processes.

Authors:  M Renz; O Reichmuth; D Bueche; B Traichel; M Schuett Mao; T Cerny; F Strasser
Journal:  Am J Hosp Palliat Care       Date:  2017-08-21       Impact factor: 2.500

7.  Quality of life and symptom intensity over time in people with cancer receiving palliative care: Results from the international European Palliative Care Cancer Symptom study.

Authors:  Mariëtte N Verkissen; Marianne J Hjermstad; Simon Van Belle; Stein Kaasa; Luc Deliens; Koen Pardon
Journal:  PLoS One       Date:  2019-10-09       Impact factor: 3.240

8.  Nurses versus physicians' knowledge, attitude, and performance on care for the family members of dying patients.

Authors:  Abdolghani Abdollahimohammad; Mohammadreza Firouzkouhi; Fatemeh Amrollahimishvan; Nasrollah Alimohammadi
Journal:  Korean J Med Educ       Date:  2016-01-27

9.  The Turkish Validity and Reliability Study of Palliative Performance Scale.

Authors:  Gonca Oğuz; Gülçin Şenel; Nesteren Koçak; Şerife Karaca
Journal:  Asia Pac J Oncol Nurs       Date:  2021-05-31

10.  Understanding the Differences Between Oncology Patients and Oncology Health Professionals Concerning Spirituality/Religiosity: A Cross-Sectional Study.

Authors:  Mayara Goulart de Camargos; Carlos Eduardo Paiva; Eliane Marçon Barroso; Estela Cristina Carneseca; Bianca Sakamoto Ribeiro Paiva
Journal:  Medicine (Baltimore)       Date:  2015-11       Impact factor: 1.817

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