Literature DB >> 9743822

Measuring quality of life for patients with terminal illness: the Missoula-VITAS quality of life index.

I R Byock1, M P Merriman.   

Abstract

Quality of life (QOL) is an important outcome measure in caring for terminally ill patients. The Missoula-VITAS Quality of Life index (MVQOLI) has been developed to provide a measure of quality of life that is meaningful to both clinicians and patients. Unique features of the instrument include its focus on the terminal phase of life, the item structure and a scoring system that allows the weighting of each dimension of QOL by the respondent, and the subjective wording of the items that allows respondents to interpret the measured elements according to their own experience. The validity and reliability of the patient-reported survey instrument were tested by administering the 25-item questionnaire to 257 patients in 10 community-based hospices. Participants were incurably ill with predicted survival of six months or less. Exclusion criteria included inability to communicate, dementia, or psychological symptoms that might be intensified by completing the index. Reliability and validity of the new index were examined using standard statistical and psychometrical analyses. The MVQOLI demonstrated internal consistency (Cronbach's alpha = 0.77). MVQOLI total scores were correlated with scores on the Multidimensional Quality of Life Scale--Cancer 2 and with patient-reported global QOL ratings. MVQOLI scores did not correlate with observer-rated functional status scores indicating divergent validity. The MVQOLI could be completed by patients of varied educational level, age, functional status, and length of time with a terminal illness. The instrument is designed to contribute to the task of planning care by evaluating patient-identified sources of distress, strength and satisfaction, including issues of life closure. This information contributes to crafting highly specific interventions. Further studies are necessary to determine the usefulness of the instrument in measuring outcomes of end-of-life care in nonhospice settings, and for racial and diagnostic groups under-represented in this sample.

Entities:  

Mesh:

Year:  1998        PMID: 9743822     DOI: 10.1191/026921698670234618

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  33 in total

1.  Quality of life as conveyed by pediatric patients with cancer.

Authors:  P S Hinds; J S Gattuso; A Fletcher; E Baker; B Coleman; T Jackson; A Jacobs-Levine; D June; S N Rai; S Lensing; C H Pui
Journal:  Qual Life Res       Date:  2004-05       Impact factor: 4.147

2.  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

3.  The feasibility, reliability and validity of the McGill Quality of Life Questionnaire-Cardiff Short Form (MQOL-CSF) in palliative care population.

Authors:  Pei Lin Lua; Sam Salek; Ilora Finlay; Chris Lloyd-Richards
Journal:  Qual Life Res       Date:  2005-09       Impact factor: 4.147

4.  Measuring health-related quality of life in high-grade glioma patients at the end of life using a proxy-reported retrospective questionnaire.

Authors:  Eefje M Sizoo; Linda Dirven; Jaap C Reijneveld; Tjeerd J Postma; Jan J Heimans; Luc Deliens; H Roeline W Pasman; Martin J B Taphoorn
Journal:  J Neurooncol       Date:  2013-10-29       Impact factor: 4.130

5.  The Quality of Dying and Death Questionnaire (QODD): empirical domains and theoretical perspectives.

Authors:  Lois Downey; J Randall Curtis; William E Lafferty; Jerald R Herting; Ruth A Engelberg
Journal:  J Pain Symptom Manage       Date:  2009-09-25       Impact factor: 3.612

6.  Palliative care symptom assessment for patients with cancer in the emergency department: validation of the Screen for Palliative and End-of-life care needs in the Emergency Department instrument.

Authors:  Christopher T Richards; Michael A Gisondi; Chih-Hung Chang; D Mark Courtney; Kirsten G Engel; Linda Emanuel; Tammie Quest
Journal:  J Palliat Med       Date:  2011-05-06       Impact factor: 2.947

7.  Measuring health-related quality of life in patients with advanced cancer: a systematic review of self-administered measurement instruments.

Authors:  Janneke van Roij; Heidi Fransen; Lonneke van de Poll-Franse; Myrte Zijlstra; Natasja Raijmakers
Journal:  Qual Life Res       Date:  2018-02-10       Impact factor: 4.147

8.  What matters most in end-of-life care: perceptions of seriously ill patients and their family members.

Authors:  Daren K Heyland; Peter Dodek; Graeme Rocker; Dianne Groll; Amiram Gafni; Deb Pichora; Sam Shortt; Joan Tranmer; Neil Lazar; Jim Kutsogiannis; Miu Lam
Journal:  CMAJ       Date:  2006-02-28       Impact factor: 8.262

9.  Preliminary report of a palliative care and case management project in an emergency department for chronically ill elderly patients.

Authors:  Sean O' Mahony; Arthur Blank; Janice Simpson; Judy Persaud; Bernadette Huvane; Susan McAllen; Michelle Davitt; Marlene McHugh; Allen Hutcheson; Serife Karakas; Philip Higgins; Peter Selwyn
Journal:  J Urban Health       Date:  2008-05       Impact factor: 3.671

10.  Validation of a core outcome measure for palliative care in Africa: the APCA African Palliative Outcome Scale.

Authors:  Richard Harding; Lucy Selman; Godfrey Agupio; Natalya Dinat; Julia Downing; Liz Gwyther; Thandi Mashao; Keletso Mmoledi; Tony Moll; Lydia Mpanga Sebuyira; Barbara Panjatovic; Irene J Higginson
Journal:  Health Qual Life Outcomes       Date:  2010-01-25       Impact factor: 3.186

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.