Publication:
Defining a set of standardised outcome measures for newly diagnosed patients with multiple myeloma using the Delphi consensus method: the IMPORTA project.

dc.contributor.authorBlade, Joan
dc.contributor.authorCalleja, Miguel Ángel
dc.contributor.authorLahuerta, Juan José
dc.contributor.authorPoveda, José Luis
dc.contributor.authorde Paz, Héctor David
dc.contributor.authorLizán, Luis
dc.date.accessioned2023-01-25T10:04:16Z
dc.date.available2023-01-25T10:04:16Z
dc.date.issued2018-02-22
dc.description.abstractTo define a standard set of outcomes and the most appropriate instruments to measure them for managing newly diagnosed patients with multiple myeloma (MM). A literature review and five discussion groups facilitated the design of two-round Delphi questionnaire. Delphi panellists (haematologists, hospital pharmacists and patients) were identified by the scientific committee, the Spanish Program of Haematology Treatments Foundation, the Spanish Society of Hospital Pharmacies and the Spanish Community of Patients with MM. Panellist's perception about outcomes' suitability and feasibility of use was assessed on a seven-point Likert scale. Consensus was reached when at least 75% of the respondents reached agreement or disagreement. A scientific committee led the project. Fifty-one and 45 panellists participated in the first and second Delphi rounds, respectively. Consensus was reached to use overall survival, progression-free survival, minimal residual disease and treatment response to assess survival and disease control. Panellists agreed to measure health-related quality of life, pain, performance status, fatigue, psychosocial status, symptoms, self-perception on body image, sexuality and preferences/satisfaction. However, panellist did not reach consensus about the feasibility of assessing in routine practice psychosocial status, symptoms, self-perception on body image and sexuality. Consensus was reached to collect patient-reported outcomes through the European Organisation for the Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire (QLQ) Core questionnaire 30 (C30), three items from EORTC-QLQ-Multiple Myeloma (MY20) and EORTC-QLQ-Breast Cancer (BR23), pain Visual Analogue Scale, Morisky-Green and ad hoc questions about patients' preferences/satisfaction. A consensual standard set of outcomes for managing newly diagnosed patients with MM has been defined. The feasibility of its implementation in routine practice will be assessed in a future pilot study.
dc.identifier.doi10.1136/bmjopen-2017-018850
dc.identifier.essn2044-6055
dc.identifier.pmcPMC5855445
dc.identifier.pmid29472263
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5855445/pdf
dc.identifier.unpaywallURLhttps://bmjopen.bmj.com/content/bmjopen/8/2/e018850.full.pdf
dc.identifier.urihttp://hdl.handle.net/10668/12170
dc.issue.number2
dc.journal.titleBMJ open
dc.journal.titleabbreviationBMJ Open
dc.language.isoen
dc.organizationHospital Universitario Virgen Macarena
dc.page.numbere018850
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectmultiple myeloma
dc.subjectoutcome
dc.subjectpatient‐centered
dc.subjectstandardisation
dc.subject.meshBody Image
dc.subject.meshConsensus
dc.subject.meshDelphi Technique
dc.subject.meshHumans
dc.subject.meshMultiple Myeloma
dc.subject.meshPatient Preference
dc.subject.meshPatient Reported Outcome Measures
dc.subject.meshQuality of Life
dc.subject.meshReproducibility of Results
dc.subject.meshReview Literature as Topic
dc.subject.meshSexuality
dc.subject.meshSocieties, Medical
dc.subject.meshSpain
dc.titleDefining a set of standardised outcome measures for newly diagnosed patients with multiple myeloma using the Delphi consensus method: the IMPORTA project.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number8
dspace.entity.typePublication

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