Literature DB >> 23102756

The development and validation of a shorter version of the Canadian Health Care Evaluation Project Questionnaire (CANHELP Lite): a novel tool to measure patient and family satisfaction with end-of-life care.

Daren K Heyland1, Xuran Jiang, Andrew G Day, S Robin Cohen.   

Abstract

CONTEXT: The recently developed Canadian Health Care Evaluation Project (CANHELP) questionnaire, which can be used to assess both patient and family satisfaction with end-of-life care, takes 40-60 minutes to complete. The length of the interview may limit its uptake and clinical utility; a shorter version would make its use more feasible.
OBJECTIVES: The purpose of this study was to develop and validate a shorter version of the CANHELP questionnaire.
METHODS: Data were collected using a cross-sectional survey of patients with advanced medical diseases and their family members. Participants completed the long version of CANHELP, a global rating of satisfaction with care (GRS), the FAMCARE scale (family members only), and a quality-of-life (QOL) questionnaire. We reduced the items on the long version based on their relationship to the GRS, the frequency of missing data, the distribution of responses, the redundancy of the items, and focus groups with frontline users. With the remaining items, we assessed internal consistency using Cronbach's alpha, and evaluated construct validity by describing the correlation of the new CANHELP Lite with the full version of CANHELP, GRS, FAMCARE, and the QOL questionnaire scores.
RESULTS: A total of 363 patients and 193 family members participated in this study. The patient version was reduced from 37 items to 20 items and the caregiver version was reduced from 38 items to 21 items. Cronbach's alphas ranged from 0.68 to 0.93 for all domains of both the patient and caregiver questionnaires. We observed a high degree of correlation between CANHELP Lite domains and overall scores and the same domains and overall scores for the full version of CANHELP. In addition, we observed moderate to strong correlation between the CANHELP Lite overall satisfaction scores and the GRS questions. There was moderate correlation between the overall family member CANHELP Lite score and overall FAMCARE score (r = 0.45) and this was similar to the correlation between the full version of CANHELP and FAMCARE scores (r = 0.41). CANHELP Lite correlated more strongly with the QOL subscale on health care than the other QOL subscales.
CONCLUSION: The CANHELP Lite questionnaire is a valid and internally consistent instrument to measure satisfaction with end-of-life care.
Copyright © 2013 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  End-of-life care; outcome assessments; palliative care; quality care; quality improvement; quality of life

Mesh:

Year:  2012        PMID: 23102756     DOI: 10.1016/j.jpainsymman.2012.07.012

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


  19 in total

1.  New measures to capture end of life concerns in Huntington disease: Meaning and Purpose and Concern with Death and Dying from HDQLIFE (a patient-reported outcomes measurement system).

Authors:  N E Carlozzi; N R Downing; M K McCormack; S G Schilling; J S Perlmutter; E A Hahn; J S Lai; S Frank; K A Quaid; J S Paulsen; D Cella; S M Goodnight; J A Miner; M A Nance
Journal:  Qual Life Res       Date:  2016-07-08       Impact factor: 4.147

2.  Fatigue among post-hematopoietic stem cell transplant patients in Jordan: prevalence and associated factors.

Authors:  Osama Abdalkareem Abdalrahman; Elham H Othman; Anas H Khalifeh; Khaled Hasan Suleiman
Journal:  Support Care Cancer       Date:  2022-06-11       Impact factor: 3.359

3.  Experiences of patients, family and professional caregivers with Integrated Palliative Care in Europe: protocol for an international, multicenter, prospective, mixed method study.

Authors:  Marlieke van der Eerden; Agnes Csikos; Csilla Busa; Sean Hughes; Lukas Radbruch; Johan Menten; Jeroen Hasselaar; Marieke Groot
Journal:  BMC Palliat Care       Date:  2014-11-21       Impact factor: 3.234

4.  Bereaved family members' perceptions of the quality of end-of-life care across four types of inpatient care settings.

Authors:  Kelli Stajduhar; Richard Sawatzky; S Robin Cohen; Daren K Heyland; Diane Allan; Darcee Bidgood; Leah Norgrove; Anne M Gadermann
Journal:  BMC Palliat Care       Date:  2017-11-25       Impact factor: 3.234

5.  "Never at ease" - family carers within integrated palliative care: a multinational, mixed method study.

Authors:  Gülay Ateş; Anne Frederieke Ebenau; Csilla Busa; Ágnes Csikos; Jeroen Hasselaar; Birgit Jaspers; Johan Menten; Sheila Payne; Karen Van Beek; Sandra Varey; Marieke Groot; Lukas Radbruch
Journal:  BMC Palliat Care       Date:  2018-03-01       Impact factor: 3.234

6.  Prospective cohort study protocol to evaluate the validity and reliability of the Quality of Trauma Care Patient-Reported Experience Measure (QTAC-PREM).

Authors:  Niklas Bobrovitz; Maria Santana; Theresa Kline; John Kortbeek; Henry T Stelfox
Journal:  BMC Health Serv Res       Date:  2013-03-14       Impact factor: 2.655

Review 7.  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

8.  Measuring engagement in advance care planning: a cross-sectional multicentre feasibility study.

Authors:  Michelle Howard; Aaron J Bonham; Daren K Heyland; Rebecca Sudore; Konrad Fassbender; Carole A Robinson; Michael McKenzie; Dawn Elston; John J You
Journal:  BMJ Open       Date:  2016-06-23       Impact factor: 2.692

Review 9.  Psychometric properties of carer-reported outcome measures in palliative care: A systematic review.

Authors:  Charlotte T J Michels; Mary Boulton; Astrid Adams; Bee Wee; Michele Peters
Journal:  Palliat Med       Date:  2015-09-25       Impact factor: 4.762

10.  The development and validation of the advance care planning questionnaire in Malaysia.

Authors:  Pauline Siew Mei Lai; Salinah Mohd Mudri; Karuthan Chinna; Sajaratulnisah Othman
Journal:  BMC Med Ethics       Date:  2016-10-18       Impact factor: 2.652

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.