Literature DB >> 21248179

What does the answer mean? A qualitative study of how palliative cancer patients interpret and respond to the Edmonton Symptom Assessment System.

Irmelin Bergh1, Ingela Lundin Kvalem, Nina Aass, Marianne Jensen Hjermstad.   

Abstract

The Edmonton Symptom Assessment System (ESAS) is a well-known self-reporting tool for symptom assessment in palliative care. Research has shown that patients experience difficulties in the scoring and interpretation, which may lead to suboptimal treatment. The aims were to examine how palliative care cancer patients interpreted and responded to the ESAS. Eleven patients (3 F/8 M), median age 65 (34-95) with mixed diagnoses were interviewed by means of cognitive interviewing, immediately after having completed the ESAS. The highest mean scores were found with tiredness (6.3) and oral dryness (5.7). The results showed that sources of error were related to interpretation of symptoms and differences in the understanding and use of the response format. The depression and anxiety symptoms were perceived as difficult to interpret, while the appetite item was particularly prone to misunderstandings. Contextual factors, such as mood and time of the day, influenced the answers. Lack of information and feedback from staff influenced the scores. Some patients stated that they scored at random because they did not understand why and how the ESAS was used. The patients' interpretation must be considered in order to minimize errors. The ESAS should always be reviewed with the patients after completion to improve symptom management, thereby strengthening the usability of the ESAS.

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Year:  2011        PMID: 21248179     DOI: 10.1177/0269216310395985

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  13 in total

1.  Health care providers' use and knowledge of the Edmonton Symptom Assessment System (ESAS): is there a need to improve information and training?

Authors:  Daniela Carli Buttenschoen; Jarad Stephan; Sharon Watanabe; Cheryl Nekolaichuk
Journal:  Support Care Cancer       Date:  2013-09-13       Impact factor: 3.603

2.  Assessing spiritual well-being in residents of nursing homes for older people using the FACIT-Sp-12: a cognitive interviewing study.

Authors:  Sue Hall; Sharon Beatty
Journal:  Qual Life Res       Date:  2014-01-28       Impact factor: 4.147

3.  Oral health is an important issue in end-of-life cancer care.

Authors:  Petter Wilberg; Marianne J Hjermstad; Stig Ottesen; Bente B Herlofson
Journal:  Support Care Cancer       Date:  2012-03-21       Impact factor: 3.603

4.  The impact of automated screening with Edmonton Symptom Assessment System (ESAS) on health-related quality of life, supportive care needs, and patient satisfaction with care in 268 ambulatory cancer patients.

Authors:  Benjamin D Diplock; Kaitlin M C McGarragle; Willem A Mueller; Sana Haddad; Rachel Ehrlich; Dong-Hyun A Yoon; Xingshan Cao; Yaseen Al-Allaq; Paul Karanicolas; Margaret I Fitch; Jeff Myers; Alex J Mitchell; Janet W M Ellis
Journal:  Support Care Cancer       Date:  2018-06-21       Impact factor: 3.603

5.  The Edmonton Symptom Assessment System (ESAS) as a screening tool for depression and anxiety in non-advanced patients with solid or haematological malignancies on cure or follow-up.

Authors:  Carla I Ripamonti; Elena Bandieri; Maria Adelaide Pessi; Alice Maruelli; Loredana Buonaccorso; Guido Miccinesi
Journal:  Support Care Cancer       Date:  2013-11-26       Impact factor: 3.603

6.  Validation of a new instrument for self-assessment of nurses' core competencies in palliative care.

Authors:  Kari Slåtten; Ove Hatlevik; Lisbeth Fagerström
Journal:  Nurs Res Pract       Date:  2014-07-16

7.  Longitudinal validity and reliability of the Myeloma Patient Outcome Scale (MyPOS) was established using traditional, generalizability and Rasch psychometric methods.

Authors:  Christina Ramsenthaler; Wei Gao; Richard J Siegert; Steve A Schey; Poly M Edmonds; Irene J Higginson
Journal:  Qual Life Res       Date:  2017-07-27       Impact factor: 4.147

8.  A brief, patient- and proxy-reported outcome measure in advanced illness: Validity, reliability and responsiveness of the Integrated Palliative care Outcome Scale (IPOS).

Authors:  Fliss Em Murtagh; Christina Ramsenthaler; Alice Firth; Esther I Groeneveld; Natasha Lovell; Steffen T Simon; Johannes Denzel; Ping Guo; Florian Bernhardt; Eva Schildmann; Birgitt van Oorschot; Farina Hodiamont; Sabine Streitwieser; Irene J Higginson; Claudia Bausewein
Journal:  Palliat Med       Date:  2019-06-12       Impact factor: 4.762

9.  Mixed methods research in the development and evaluation of complex interventions in palliative and end-of-life care: report on the MORECare consensus exercise.

Authors:  Morag Farquhar; Nancy Preston; Catherine J Evans; Gunn Grande; Vicky Short; Hamid Benalia; Irene J Higginson; Chris Todd
Journal:  J Palliat Med       Date:  2013-11-06       Impact factor: 2.947

10.  Discovering the hidden benefits of cognitive interviewing in two languages: The first phase of a validation study of the Integrated Palliative care Outcome Scale.

Authors:  Eva K Schildmann; E Iris Groeneveld; Johannes Denzel; Alice Brown; Florian Bernhardt; Katharine Bailey; Ping Guo; Christina Ramsenthaler; Natasha Lovell; Irene J Higginson; Claudia Bausewein; Fliss Em Murtagh
Journal:  Palliat Med       Date:  2015-09-28       Impact factor: 4.762

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