Literature DB >> 24654223

Measuring patients' experiences with palliative care: the Consumer Quality Index Palliative Care.

Susanne J J Claessen1, Anneke L Francke, Herman J Sixma, Anke J E de Veer, Luc Deliens.   

Abstract

BACKGROUND: The Consumer Quality Index Palliative Care (CQ-index PC) is a structured questionnaire for measuring the quality of palliative care from the perspective of care users. CQ-indices assess which care aspects need quality improvement by relating answers about actual care experiences to answers about the importance of certain aspects of care.
METHODS: To improve the chance that the new instrument has good content validity, a literature study and individual and group discussions were performed, and a steering committee was consulted to establish the instrument's face and content validity. The questionnaire was administered to patients with a life expectancy of 6 months or less and/or who were receiving palliative treatment. Descriptive analyses were carried out on the items about actual care experiences and the importance of care aspects, and on 'need for improvement' scores.
RESULTS: 15 care organisations participated. 133 patients met the inclusion criteria (net response n=85). Patients considered the following aspects the most important: 'offering help in good time in acute situations', 'caregivers having the necessary expertise' and 'caregivers taking the patient seriously'. The three care aspects with the highest 'need for improvement' scores were: 'support when the patient feels depressed', 'support when the patient is anxious' and 'support when the patient has shortness of breath'.
CONCLUSIONS: The CQ-index PC provides opportunities for care organisations to assess which care aspects have the highest priority for quality improvement within their organisation. Further research is needed to assess whether the instrument has enough discriminative power to assess differences between organisations.

Entities:  

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Year:  2012        PMID: 24654223     DOI: 10.1136/bmjspcare-2011-000055

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


  8 in total

1.  A systematic review of the validity and reliability of patient-reported experience measures.

Authors:  Claudia Bull; Joshua Byrnes; Ruvini Hettiarachchi; Martin Downes
Journal:  Health Serv Res       Date:  2019-06-19       Impact factor: 3.402

2.  Palliative care for patients with cancer: do patients receive the care they consider important? A survey study.

Authors:  Marianne Heins; Jolien Hofstede; Mieke Rijken; Joke Korevaar; Gé Donker; Anneke Francke
Journal:  BMC Palliat Care       Date:  2018-04-17       Impact factor: 3.234

3.  Development and Pretesting of a Questionnaire to Assess Patient Experiences and Satisfaction with Medications (PESaM Questionnaire).

Authors:  Merel L Kimman; Adrienne H Rotteveel; Marlies Wijsenbeek; Rémy Mostard; Nelleke C Tak; Xana van Jaarsveld; Marjolein Storm; Kioa L Wijnsma; Marielle Gelens; Nicole C A J van de Kar; Jack Wetzels; Carmen D Dirksen
Journal:  Patient       Date:  2017-10       Impact factor: 3.883

4.  What are essential elements of high-quality palliative care at home? An interview study among patients and relatives faced with advanced cancer.

Authors:  M G Oosterveld-Vlug; B Custers; J Hofstede; G A Donker; P M Rijken; J C Korevaar; A L Francke
Journal:  BMC Palliat Care       Date:  2019-11-06       Impact factor: 3.234

5.  Development of a Short Form of the Questionnaire Quality from the Patient's Perspective for Palliative Care (QPP-PC).

Authors:  Tuva Sandsdalen; Vigdis Abrahamsen Grøndahl; Bodil Wilde-Larsson
Journal:  J Multidiscip Healthc       Date:  2020-06-12

6.  The effect and process evaluations of the national quality improvement programme for palliative care: the study protocol.

Authors:  Natasja Jh Raijmakers; Jolien M Hofstede; Ellen Jm de Nijs; Luc Deliens; Anneke L Francke
Journal:  BMC Palliat Care       Date:  2014-02-21       Impact factor: 3.234

7.  Study protocol: evaluation of specialized outpatient palliative care in the German state of Hesse (ELSAH study) - work package I: assessing the quality of care.

Authors:  Katrin Kuss; Hannah Seipp; Dorothée Becker; Stefan Bösner; Antje Erler; Dania Gruber; Michaela Hach; Lisa R Ulrich; Jörg Haasenritter
Journal:  BMC Palliat Care       Date:  2018-10-02       Impact factor: 3.234

8.  Quality of collaboration and information handovers in palliative care: a survey study on the perspectives of nurses in the Southwest Region of the Netherlands.

Authors:  Marijanne Engel; Andrée van der Ark; Rosanne Tamerus; Agnes van der Heide
Journal:  Eur J Public Health       Date:  2020-08-01       Impact factor: 3.367

  8 in total

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