Literature DB >> 30723074

Symptom burden in malignant and non-malignant disease on admission to a palliative care unit.

David See1,2, Brian Le3,4, Alexandra Gorelik2,5, Peter Eastman3,4,6.   

Abstract

BACKGROUND: There is increasing recognition that patients with non-malignant diseases have comparable physical and psychosocial symptom burden to patients with cancer. There is currently limited data directly comparing symptom burden between these patient groups.
OBJECTIVE: To investigate differences in symptom burden between patients with malignant and non-malignant conditions admitted to a palliative care unit (PCU).
METHOD: A cross-sectional study involving 186 patients admitted to a PCU was undertaken. Patients were dichotomised into malignant or non-malignant disease categories. Symptom burden at admission was assessed using the Symptom Assessment Scale and Palliative Care Problem Severity Score. Group differences in symptoms were analysed using univariate and multivariate approaches.
RESULTS: One hundred patients (53.8%) had cancer, with upper gastrointestinal the most common type (18.0%). Among the 86 patients with non-malignant disease, neurological conditions were most prevalent (40.7%). Patients admitted with non-malignant diseases were older, more functionally impaired and more likely to be deteriorating or terminal. A malignant diagnosis was associated with a higher likelihood of clinician-assessed pain, patient-assessed pain, fatigue, psychological/spiritual symptoms and other symptoms. However, when adjusted for confounders, disease category ceased to be a significant predictor of symptom burden. Younger patients experienced worse pain and patients in terminal phase experienced less symptom burden.
CONCLUSION: Symptom burden was similar between patients with malignant and non-malignant disease after adjustment for confounders. Further research is needed to understand the palliative care needs of patients with non-malignant disease. © Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  cancer; chronic conditions; clinical assessment; end of life care; symptoms and symptom management

Year:  2019        PMID: 30723074     DOI: 10.1136/bmjspcare-2018-001560

Source DB:  PubMed          Journal:  BMJ Support Palliat Care        ISSN: 2045-435X            Impact factor:   3.568


  4 in total

1.  Socioeconomic inequalities in the place of death in urban small areas of three Mediterranean cities.

Authors:  Andreu Nolasco; Manuel Fernández-Alcántara; Pamela Pereyra-Zamora; María José Cabañero-Martínez; José M Copete; Adriana Oliva-Arocas; Julio Cabrero-García
Journal:  Int J Equity Health       Date:  2020-12-03

2.  Healthcare utilisation trajectories in patients dying from chronic obstructive pulmonary disease, heart failure or cancer: a nationwide register-based cohort study.

Authors:  Anne Høy Seemann Vestergaard; Christian Fynbo Christiansen; Mette Asbjoern Neergaard; Jan Brink Valentin; Søren Paaske Johnsen
Journal:  BMJ Open       Date:  2021-11-24       Impact factor: 2.692

3.  Virtual reality reduces pain in palliative care-A feasibility trial.

Authors:  Miriam Guenther; Dennis Görlich; Florian Bernhardt; Esther Pogatzki-Zahn; Burkhard Dasch; Janina Krueger; Philipp Lenz
Journal:  BMC Palliat Care       Date:  2022-10-05       Impact factor: 3.113

4.  Systematic symptom and problem assessment at admission to the palliative care ward - perspectives and prognostic impacts.

Authors:  Anja Coym; Anneke Ullrich; Lisa Kathrin Hackspiel; Mareike Ahrenholz; Carsten Bokemeyer; Karin Oechsle
Journal:  BMC Palliat Care       Date:  2020-05-28       Impact factor: 3.234

  4 in total

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