Literature DB >> 24026980

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

Daniela Carli Buttenschoen1, Jarad Stephan, Sharon Watanabe, Cheryl Nekolaichuk.   

Abstract

OBJECTIVES: The ESAS is a clinical symptom assessment tool developed for patients receiving palliative care for pain and symptom control. Recent studies have indicated that patients have difficulty understanding terminology and correct use of the ESAS, and that they appreciate the presence of a health care provider (HCP) to assist with ESAS completion. As appropriate assessment translates into effective treatment, it is important that HCPs have a good understanding of the tool. The purpose of this study was to assess HCPs' use, knowledge, and training needs of the ESAS.
METHODS: One hundred ninety-three HCPs in palliative care and chronic pain, who used the ESAS, were invited to participate in a survey.
RESULTS: The response rate was 43 % (n = 83), with 62 % nurses, 26 % physicians, and 12 % other specialties. Most participants were palliative care specialists (79 %). The majority (77 %) had a good understanding of the ESAS terms. Knowledge problems included distinguishing tiredness and drowsiness (25 %), interpreting shortness of breath as a combination of subjective and objective symptoms (19 %), not indicating current symptom level (14 %), and reverse scoring of well-being (13 %) and appetite (9 %). Reported challenges were misinterpretation of some ESAS terms, assessing patients with impaired communication, and lack of time and reliability of caregiver assessments. Participants offered suggestions regarding how their knowledge and use of the ESAS could be improved.
CONCLUSIONS: Suggestions for improving ESAS administration and training were to include term definitions and examples of how to ask about terms that might be challenging for patients. Furthermore, initial and ongoing training sessions might help to clarify issues with the tool.

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Year:  2013        PMID: 24026980     DOI: 10.1007/s00520-013-1955-8

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  29 in total

1.  A comparison of patient and proxy symptom assessments in advanced cancer patients.

Authors:  C L Nekolaichuk; E Bruera; K Spachynski; T MacEachern; J Hanson; T O Maguire
Journal:  Palliat Med       Date:  1999-07       Impact factor: 4.762

2.  Palliative care nurses' perceptions of the Edmonton Symptom Assessment Scale: a pilot survey.

Authors:  Sharon Watanabe; Sandra McKinnon; Karen Macmillan; John Hanson
Journal:  Int J Palliat Nurs       Date:  2006-03

3.  Monitoring symptoms in patients with advanced illness in long-term care: A pilot study.

Authors:  John R Brechtl; Shaiqua Murshed; Peter Homel; Marilyn Bookbinder
Journal:  J Pain Symptom Manage       Date:  2006-08       Impact factor: 3.612

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

Authors:  Irmelin Bergh; Ingela Lundin Kvalem; Nina Aass; Marianne Jensen Hjermstad
Journal:  Palliat Med       Date:  2011-01-19       Impact factor: 4.762

5.  Clinical competence in palliative nursing in Norway: the importance of good care routines.

Authors:  Kari Slåtten; Lisbeth Fagerström; Ove Edvard Hatlevik
Journal:  Int J Palliat Nurs       Date:  2010-02

6.  Does the medical record cover the symptoms experienced by cancer patients receiving palliative care? A comparison of the record and patient self-rating.

Authors:  A S Strömgren; M Groenvold; L Pedersen; A K Olsen; M Spile; P Sjøgren
Journal:  J Pain Symptom Manage       Date:  2001-03       Impact factor: 3.612

7.  Assessing the reliability of patient, nurse, and family caregiver symptom ratings in hospitalized advanced cancer patients.

Authors:  C L Nekolaichuk; T O Maguire; M Suarez-Almazor; W T Rogers; E Bruera
Journal:  J Clin Oncol       Date:  1999-11       Impact factor: 44.544

8.  Pain intensity assessment by bedside nurses and palliative care consultants: a retrospective study.

Authors:  Eduardo Bruera; Jie S Willey; Patricia A Ewert-Flannagan; Mary K Cline; Guddi Kaur; Loren Shen; Tao Zhang; J Lynn Palmer
Journal:  Support Care Cancer       Date:  2004-10-06       Impact factor: 3.603

9.  The Edmonton symptom assessment system--what do patients think?

Authors:  Sharon Watanabe; Cheryl Nekolaichuk; Crystal Beaumont; Asifa Mawani
Journal:  Support Care Cancer       Date:  2008-10-25       Impact factor: 3.603

10.  Benefits and challenges in use of a standardized symptom assessment instrument in hospice.

Authors:  Dena Schulman-Green; Emily J Cherlin; Ruth McCorkle; Melissa D A Carlson; Karen Beckman Pace; Janet Neigh; Meliessa Hennessy; R Johnson-Hurzeler; Elizabeth H Bradley
Journal:  J Palliat Med       Date:  2010-02       Impact factor: 2.947

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  5 in total

Review 1.  The Edmonton Symptom Assessment System 25 Years Later: Past, Present, and Future Developments.

Authors:  David Hui; Eduardo Bruera
Journal:  J Pain Symptom Manage       Date:  2016-12-29       Impact factor: 3.612

2.  Gaps in the Management of Depression Symptoms Following Cancer Diagnosis: A Population-Based Analysis of Prospective Patient-Reported Outcomes.

Authors:  Julie Hallet; Laura E Davis; Elie Isenberg-Grzeda; Alyson L Mahar; Haoyu Zhao; Victoria Zuk; Lesley Moody; Natalie G Coburn
Journal:  Oncologist       Date:  2020-02-26

3.  Population-based study of the prevalence and management of self-reported high pain scores in patients with non-resected pancreatic adenocarcinoma.

Authors:  S Tung; N G Coburn; L E Davis; A L Mahar; S Myrehaug; H Zhao; C C Earle; A Nathens; J Hallet
Journal:  Br J Surg       Date:  2019-11       Impact factor: 6.939

4.  Challenges in virtual collection of patient-reported data: a prospective cohort study conducted in COVID-19 era.

Authors:  Karineh Kazazian; Jessica Bogach; Wendy Johnston; Deanna Ng; Carol J Swallow
Journal:  Support Care Cancer       Date:  2022-06-07       Impact factor: 3.359

5.  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

  5 in total

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