Literature DB >> 24680624

Care evaluation scale-patient version: measuring the quality of the structure and process of palliative care from the patient's perspective.

Mitsunori Miyashita1, Makoto Wada2, Tatsuya Morita3, Mayumi Ishida4, Hideki Onishi4, Satoru Tsuneto5, Yasuo Shima6.   

Abstract

CONTEXT: Recently, greater emphasis has been placed on patient-reported outcomes. However, there are only a few measures to evaluate the quality of care from the patient's perspective.
OBJECTIVES: To report the development of a scale to measure the quality of the structure and process in palliative care from the patient's perspective and examine the reliability and validity of the scale.
METHODS: A cross-sectional anonymous questionnaire was administered to cancer patients who were being treated on an oncology inpatient ward, who visited an oncology outpatient clinic at Saitama Medical University International Medical Center, or who were in an inpatient palliative unit in Japan between August 2007 and March 2008.
RESULTS: A total of 405 cancer patients participated in the study. Factor analysis revealed that the Care Evaluation Scale-Patient version (CES-P) consisted of 23 items with eight subscales: physical care by physicians, physical care by nurses, psychoexistential care, help with decision making for patients, environment, cost, availability, and coordination/consistency. The total CES-P score was correlated with satisfaction (r = 0.63) but not with quality of life (r = 0.18). The Cronbach α coefficient of the total score was 0.97, and the intraclass correlation coefficient of the total score was 0.67. The CES-P total score was not significantly correlated with the self-reported Eastern Cooperative Oncology Group performance status (ρ = -0.05).
CONCLUSION: The CES-P has sufficient validity and reliability. In addition, this scale is independent of the general physical condition of the patient.
Copyright © 2014 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Palliative care; hospice; neoplasms; quality of care; questionnaires

Mesh:

Year:  2014        PMID: 24680624     DOI: 10.1016/j.jpainsymman.2013.08.019

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


  6 in total

1.  Development of a national health policy logic model to accelerate the integration of oncology and palliative care: a nationwide Delphi survey in Japan.

Authors:  Yu Uneno; Maki Iwai; Naoto Morikawa; Keita Tagami; Yoko Matsumoto; Junko Nozato; Takaomi Kessoku; Tatsunori Shimoi; Miyuki Yoshida; Aya Miyoshi; Ikuko Sugiyama; Kazuhiro Mantani; Mai Itagaki; Akemi Yamagishi; Tatsuya Morita; Akira Inoue; Manabu Muto
Journal:  Int J Clin Oncol       Date:  2022-06-17       Impact factor: 3.850

2.  Development the Care Evaluation Scale Version 2.0: a modified version of a measure for bereaved family members to evaluate the structure and process of palliative care for cancer patient.

Authors:  Mitsunori Miyashita; Maho Aoyama; Misato Nakahata; Yuji Yamada; Mutsumi Abe; Kazuhiro Yanagihara; Akemi Shirado; Mariko Shutoh; Yoshiaki Okamoto; Jun Hamano; Aoi Miyamoto; Saki Yoshida; Kazuki Sato; Kei Hirai; Tatsuya Morita
Journal:  BMC Palliat Care       Date:  2017-01-23       Impact factor: 3.234

3.  Validation of the Chinese version of the Care Evaluation Scale for measuring the quality of structure and process of end-of-life care from the perspective of bereaved family.

Authors:  Juanjuan Zhao; Liming You; Hongmei Tao; Frances Kam Yuet Wong
Journal:  BMC Palliat Care       Date:  2021-06-22       Impact factor: 3.234

Review 4.  User-Centered Design of the consideRATE Questions, a Measure of People's Experiences When They Are Seriously Ill.

Authors:  Catherine H Saunders; Marie-Anne Durand; Peter Scalia; Kathryn B Kirkland; Meredith A MacMartin; Amber E Barnato; David W Milne; Joan Collison; Ashleigh Jaggars; Tanya Butt; Garrett Wasp; Eugene Nelson; Glyn Elwyn
Journal:  J Pain Symptom Manage       Date:  2020-08-16       Impact factor: 5.576

5.  Patients' perceptions of palliative care: adaptation of the Quality from the Patient's Perspective instrument for use in palliative care, and description of patients' perceptions of care received.

Authors:  Tuva Sandsdalen; Ingrid Rystedt; Vigdis Abrahamsen Grøndahl; Reidun Hov; Sevald Høye; Bodil Wilde-Larsson
Journal:  BMC Palliat Care       Date:  2015-11-02       Impact factor: 3.234

6.  The relationships between the combination of person- and organization-related conditions and patients' perceptions of palliative care quality.

Authors:  Tuva Sandsdalen; Sevald Høye; Ingrid Rystedt; Vigdis Abrahamsen Grøndahl; Reidun Hov; Bodil Wilde-Larsson
Journal:  BMC Palliat Care       Date:  2017-12-06       Impact factor: 3.234

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.