Literature DB >> 31253494

Measuring quality of life in palliative care for Parkinson's disease: A clinimetric comparison.

Samantha K Holden1, Claire E Koljack2, Lindsay P Prizer3, Stefan H Sillau2, Janis M Miyasaki4, Benzi M Kluger2.   

Abstract

INTRODUCTION: Quality of life (QOL) assessments allow for more complete evaluation of patients' lived experiences in relation to chronic conditions, such as Parkinson's disease (PD). In palliative care, such instruments are vital to ensure QOL issues are catalogued and addressed for patients. However, little is known regarding the psychometric properties of quality of life scales for use in palliative care for PD, specifically.
METHODS: 210 participants with parkinsonian disorders, who participated in a larger palliative intervention clinical trial, completed four quality of life scales (PDQ-39, PROMIS-29, QOL-AD, and McGill QOL) at baseline and post-intervention. Psychometric properties, including internal consistency and concurrent validity, were examined. Factor analyses were performed to evaluate relationships between scale items. Minimal clinically important differences (MCID) and responsiveness were calculated for each scale.
RESULTS: All scales demonstrated good internal consistency and concurrent validity. Factor analyses revealed few deviations from the defined subdomains of the scales. Mean absolute MCID values were estimated at 12.7, 10.9, 3.9, and 18.9 for PDQ-39, PROMIS-29, QOL-AD, and McGill QOL, respectively. The PDQ-39 and PROMIS-29 demonstrated higher responsiveness to palliative intervention, while the QOL-AD was more responsive in the control group.
CONCLUSIONS: The PDQ-39, PROMIS-29, QOL-AD, and McGill QOL are all valid for use in PD palliative care, though subdomains of the scales in this population may differ slightly from those initially defined. We recommend the use of PDQ-39 and PROMIS-29 as outcome measures in clinical trials for palliative care in PD, though the QOL-AD may be superior for tracking disease progression.
Copyright © 2019 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Outcome measures; Palliative care; Parkinson disease; Psychometrics; Quality of life

Mesh:

Year:  2019        PMID: 31253494      PMCID: PMC6774894          DOI: 10.1016/j.parkreldis.2019.06.018

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN: 1353-8020            Impact factor:   4.891


  30 in total

Review 1.  Recommended methods for determining responsiveness and minimally important differences for patient-reported outcomes.

Authors:  Dennis Revicki; Ron D Hays; David Cella; Jeff Sloan
Journal:  J Clin Epidemiol       Date:  2007-08-03       Impact factor: 6.437

2.  PDQ-39: a review of the development, validation and application of a Parkinson's disease quality of life questionnaire and its associated measures.

Authors:  V Peto; C Jenkinson; R Fitzpatrick
Journal:  J Neurol       Date:  1998-05       Impact factor: 4.849

Review 3.  Palliative care and Parkinson's disease: Meeting summary and recommendations for clinical research.

Authors:  Benzi M Kluger; Siobhán Fox; Suzanne Timmons; Maya Katz; Nicholas B Galifianakis; Indu Subramanian; Julie H Carter; Miriam J Johnson; Edward W Richfield; David Bekelman; Jean S Kutner; Janis Miyasaki
Journal:  Parkinsonism Relat Disord       Date:  2017-01-11       Impact factor: 4.891

4.  Determining minimally important differences for the PDQ-39 Parkinson's disease questionnaire.

Authors:  V Peto; C Jenkinson; R Fitzpatrick
Journal:  Age Ageing       Date:  2001-07       Impact factor: 10.668

5.  Living with cancer: "good" days and "bad" days--what produces them? Can the McGill quality of life questionnaire distinguish between them?

Authors:  S R Cohen; B M Mount
Journal:  Cancer       Date:  2000-10-15       Impact factor: 6.860

6.  Transcultural adaptation and psychometric validation of a French-language version of the QoL-AD.

Authors:  Aurore Wolak; Jean-Luc Novella; Moustapha Drame; Francis Guillemin; Laura Di Pollina; Joël Ankri; Jean-Pierre Aquino; Isabella Morrone; François Blanchard; Damien Jolly
Journal:  Aging Ment Health       Date:  2009-07       Impact factor: 3.658

Review 7.  Palliative Care in Neurology.

Authors:  Maisha T Robinson; Robert G Holloway
Journal:  Mayo Clin Proc       Date:  2017-10       Impact factor: 7.616

8.  Universal health outcome measures for older persons with multiple chronic conditions.

Authors: 
Journal:  J Am Geriatr Soc       Date:  2012-11-29       Impact factor: 5.562

9.  Symptoms and quality of life in late stage Parkinson syndromes: a longitudinal community study of predictive factors.

Authors:  Irene J Higginson; Wei Gao; Tariq Zaffer Saleem; K Ray Chaudhuri; Rachel Burman; Paul McCrone; Peter Nigel Leigh
Journal:  PLoS One       Date:  2012-11-07       Impact factor: 3.240

10.  Inter-rater agreement of the Quality of Life-Alzheimer's Disease (QoL-AD) self-rating and proxy rating scale: secondary analysis of RightTimePlaceCare data.

Authors:  Josephine Römhild; Steffen Fleischer; Gabriele Meyer; Astrid Stephan; Sandra Zwakhalen; Helena Leino-Kilpi; Adelaida Zabalegui; Kai Saks; Maria Soto-Martin; Caroline Sutcliffe; Ingalill Rahm Hallberg; Almuth Berg
Journal:  Health Qual Life Outcomes       Date:  2018-06-28       Impact factor: 3.186

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  3 in total

Review 1.  Palliative Care for Parkinson's Spectrum Disorders: an Emerging Approach.

Authors:  Maya Katz
Journal:  Neurotherapeutics       Date:  2021-01-13       Impact factor: 7.620

2.  Impact of disease stage and age at Parkinson's onset on patients' primary concerns: Insights for targeted management.

Authors:  Roongroj Bhidayasiri; Thanatat Boonmongkol; Yuwadee Thongchuam; Saisamorn Phumphid; Nitinan Kantachadvanich; Pattamon Panyakaew; Priya Jagota; Rachaneewan Plengsri; Marisa Chokpatcharavate; Onanong Phokaewvarangkul
Journal:  PLoS One       Date:  2020-12-02       Impact factor: 3.240

Review 3.  Palliative Care Intervention Trials for Adults Living With Progressive Central Nervous System Diseases and Their Caregivers: A Systematic Review.

Authors:  HeatherE Leeper; Diane Cooper; TerriS Armstrong
Journal:  J Pain Symptom Manage       Date:  2021-06-18       Impact factor: 3.612

  3 in total

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