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Improving the Assessment of Quality of Life in the Clinical Care of Myeloma Patients: The Development and Validation of the Myeloma Patient Outcome Scale (MyPOS)

aut.relation.articlenumberARTN 280
aut.relation.issue1
aut.relation.journalBMC Cancer
aut.relation.startpage280
aut.relation.volume15
dc.contributor.authorOsborne, TR
dc.contributor.authorRamsenthaler, C
dc.contributor.authorSchey, SA
dc.contributor.authorSiegert, RJ
dc.contributor.authorEdmonds, PM
dc.contributor.authorHigginson, IJ
dc.date.accessioned2025-11-24T03:34:12Z
dc.date.available2025-11-24T03:34:12Z
dc.date.issued2015-04-14
dc.description.abstractBackground: Multiple myeloma is an incurable cancer with a rising incidence globally. Less toxic treatments are increasingly available, so patients are living longer and treatment decisions are increasingly guided by QOL concerns. There is no QOL assessment tool designed specifically for use in the clinical care of people with myeloma. This study aimed to develop and test the psychometric properties of a new myeloma-specific QOL questionnaire designed specifically for use in the clinical setting - the MyPOS. Methods: The MyPOS was developed using findings from a previously reported literature review and qualitative study. The prototype MyPOS was pretested using cognitive interviews in a purposive sample of myeloma patients and refined prior to field testing. The psychometric properties of the MyPOS were evaluated in a multi-centre, cross sectional survey of myeloma patients recruited from 14 hospital trusts across England. Results: The prototype MyPOS contained 33 structured and open questions. These were refined using cognitive interviews with 12 patients, and the final MyPOS contained 30 items taken forward for field-testing. The cross-sectional survey recruited 380 patients for the MyPOS validation. Mean time to complete was 7 minutes 19 seconds with 0.58% missing MyPOS items overall. Internal consistency was high (α =0.89). Factor analysis confirmed three subscales: Symptoms & Function; Emotional Response and Healthcare Support. MyPOS total scores were higher (worse QOL) in those with active disease compared to those in the stable or plateau phase (F = 11.89, p < 0.001) and were worse in those currently receiving chemotherapy (t = 3.42, p = 0.001). Scores in the Symptoms & Function subscale were higher (worse QOL) in those with worse ECOG performance status (F = 31.33, p < 0.001). Good convergent and discriminant validity were demonstrated. Conclusions: The MyPOS is the first myeloma-specific QOL questionnaire designed specifically for use in the clinical setting. The MyPOS is based on qualitative enquiry and the issues most important to patients. It is a brief, comprehensive and acceptable tool that is reliable and valid on psychometric testing. The MyPOS can now be used to support clinical decision making in the routine care of myeloma patients.
dc.identifier.citationBMC Cancer, ISSN: 1471-2407 (Print); 1471-2407 (Online), BioMed Central Ltd., 15(1), 280-. doi: 10.1186/s12885-015-1261-6
dc.identifier.doi10.1186/s12885-015-1261-6
dc.identifier.issn1471-2407
dc.identifier.issn1471-2407
dc.identifier.urihttp://hdl.handle.net/10292/20202
dc.languageeng
dc.publisherBioMed Central Ltd.
dc.relation.urihttps://bmccancer.biomedcentral.com/articles/10.1186/s12885-015-1261-6
dc.rightsThis article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
dc.rights.accessrightsOpenAccess
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectOncology
dc.subjectCancer
dc.subjectHaematology
dc.subjectMultiple myeloma
dc.subjectQuality of life
dc.subjectOutcome assessment
dc.subjectPsychometrics
dc.subjectMultiple-Myeloma
dc.subjectPsychosocial Adjustment
dc.subjectCoefficient Alpha
dc.subjectExperiences
dc.subjectNumber
dc.subjectModule
dc.subject4203 Health Services and Systems
dc.subject32 Biomedical and Clinical Sciences
dc.subject4205 Nursing
dc.subject42 Health Sciences
dc.subjectBehavioral and Social Science
dc.subjectClinical Research
dc.subjectHematology
dc.subjectRare Diseases
dc.subjectHealth Services
dc.subjectHealth Disparities
dc.subject7.1 Individual care needs
dc.subject3 Good Health and Well Being
dc.subject1112 Oncology and Carcinogenesis
dc.subject1117 Public Health and Health Services
dc.subjectOncology & Carcinogenesis
dc.subject3211 Oncology and carcinogenesis
dc.subject4202 Epidemiology
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshAged, 80 and over
dc.subject.meshEngland
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshMultiple Myeloma
dc.subject.meshPsychometrics
dc.subject.meshQuality of Life
dc.subject.meshSurveys and Questionnaires
dc.titleImproving the Assessment of Quality of Life in the Clinical Care of Myeloma Patients: The Development and Validation of the Myeloma Patient Outcome Scale (MyPOS)
dc.typeJournal Article
pubs.elements-id182894

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