Literature DB >> 31873053

Identifying the Prevalence and Correlates of Caregiver-Reported Symptoms in Home Hospice Patients at the End of Life.

Veerawat Phongtankuel1, Jeanne A Teresi2,3, Joseph P Eimicke2, Jian X Kong2, Ronald D Adelman1, Holly G Prigerson1, Sara J Czaja1, Ariel Shalev1, Ritchell Dignam4, Rosemary Baughn4, M Cary Reid1.   

Abstract

Background: Symptoms (e.g., pain, shortness of breath, and fatigue) at the end of life (EoL) are common. Although symptoms can contribute to poor quality of life at the EoL, much remains unknown regarding their prevalence and correlates in home hospice care.
Objectives: To determine the prevalence and correlates of caregiver-reported symptoms in home hospice patients during the last week before discharge using the Edmonton Symptom Assessment Scale (ESAS). Design: This is a cross-sectional study measuring perceived patient symptoms using caregiver proxy data. Bivariate and multivariate analyses were conducted to examine patient and caregiver characteristics associated with ESAS scores. Setting/Subjects: Subjects were from an urban nonprofit home hospice organization. Measurements: Symptoms were measured using the ESAS.
Results: The mean ESAS score was 51.2 (SD ±17.4). In bivariate analyses, higher perceived symptom score was associated with younger patient age (p < 0.001), younger caregiver age (p < 0.001), having a cancer diagnosis (p = 0.006), and lower caregiver comfort level managing symptoms (p < 0.001). Regression model analyses showed that younger patient age (p = 0.0009, p = 0.0036) and lower caregiver comfort level managing symptoms (p = 0.0047, p < 0.0001) were associated uniquely with higher symptom scores. Conclusions: Multiple symptoms of high severity were perceived by caregivers in the last week on home hospice. Patient age and caregiver comfort level in managing symptoms were associated with higher symptom scores. Further work is needed to improve management and treatment of symptoms in this care setting.

Entities:  

Keywords:  end of life; hospice care; palliative care; symptoms

Year:  2019        PMID: 31873053      PMCID: PMC7232637          DOI: 10.1089/jpm.2019.0324

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  22 in total

1.  Symptom burden at the end of life: hospice providers' perceptions.

Authors:  J S Kutner; C T Kassner; D E Nowels
Journal:  J Pain Symptom Manage       Date:  2001-06       Impact factor: 3.612

2.  The memorial symptom assessment scale: modified for use in understanding family caregivers' perceptions of cancer patients' symptom experiences.

Authors:  Michelle M Lobchuk
Journal:  J Pain Symptom Manage       Date:  2003-07       Impact factor: 3.612

3.  Feasibility of a Study To Test the Effectiveness of a Dyspnea Assessment and Treatment Bundle To Improve Family Caregiving of Patients in Home Hospice.

Authors:  Margaret L Campbell; Lindsey McErlane
Journal:  J Palliat Med       Date:  2018-11       Impact factor: 2.947

Review 4.  A review of the literature on multiple symptoms, their predictors, and associated outcomes in patients with advanced cancer.

Authors:  Stephanie Gilbertson-White; Bradley E Aouizerat; Thierry Jahan; Christine Miaskowski
Journal:  Palliat Support Care       Date:  2011-03

5.  Symptom distress and quality of life in patients with cancer newly admitted to hospice home care.

Authors:  Susan C McMillan; Brent J Small
Journal:  Oncol Nurs Forum       Date:  2002 Nov-Dec       Impact factor: 2.172

6.  Prevalence and characteristics of breakthrough pain in cancer patients admitted to a hospice.

Authors:  G Zeppetella; C A O'Doherty; S Collins
Journal:  J Pain Symptom Manage       Date:  2000-08       Impact factor: 3.612

7.  Symptom prevalence in the last week of life.

Authors:  C Conill; E Verger; I Henríquez; N Saiz; M Espier; F Lugo; A Garrigos
Journal:  J Pain Symptom Manage       Date:  1997-12       Impact factor: 3.612

8.  Validation of the Edmonton Symptom Assessment Scale.

Authors:  V T Chang; S S Hwang; M Feuerman
Journal:  Cancer       Date:  2000-05-01       Impact factor: 6.860

9.  Symptom burden in the last week of life.

Authors:  Marianne Klinkenberg; Dick L Willems; Gerrit van der Wal; Dorly J H Deeg
Journal:  J Pain Symptom Manage       Date:  2004-01       Impact factor: 3.612

10.  Comfort level of caregivers of cancer patients receiving palliative care.

Authors:  Maisa Vitória Gayoso; Marla Andréia Garcia de Avila; Thays Antunes da Silva; Rúbia Aguiar Alencar
Journal:  Rev Lat Am Enfermagem       Date:  2018-08-09
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  2 in total

1.  Understanding the Experience of Cancer Pain From the Perspective of Patients and Family Caregivers to Inform Design of an In-Home Smart Health System: Multimethod Approach.

Authors:  Virginia LeBaron; Rachel Bennett; Ridwan Alam; Leslie Blackhall; Kate Gordon; James Hayes; Nutta Homdee; Randy Jones; Yudel Martinez; Emmanuel Ogunjirin; Tanya Thomas; John Lach
Journal:  JMIR Form Res       Date:  2020-08-26

2.  Impact of Palliative Care in Evaluating and Relieving Symptoms in Patients with Advanced Cancer. Results from the DEMETRA Study.

Authors:  Oscar Corli; Giacomo Pellegrini; Cristina Bosetti; Luca Riva; Matteo Crippa; Emanuele Amodio; Gianlorenzo Scaccabarozzi
Journal:  Int J Environ Res Public Health       Date:  2020-11-14       Impact factor: 3.390

  2 in total

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