The Myeloma Patient Outcome Scale is the first quality of life tool developed for clinical use and validated in patients with follicular lymphoma

被引:7
|
作者
Davies, Joanna M. [1 ]
Osborne, Thomas R. [2 ]
Edmonds, Polly M. [3 ]
Schey, Steve A. [4 ]
Devereux, Steve [4 ]
Higginson, Irene J. [1 ]
Ramsenthaler, Christina [1 ,5 ]
机构
[1] Kings Coll London, Dept Palliat Care Policy & Rehabil, Fac Life Sci & Med, Cicely Saunders Inst, London, England
[2] St Josephs Hosp, London, England
[3] Kings Coll Hosp NHS Fdn Trust, Dept Palliat Care, London, England
[4] Kings Coll Hosp NHS Fdn Trust, Dept Haematol Med, London, England
[5] Munich Univ Hosp, Dept Palliat Med, Munich, Germany
关键词
factor analysis; Follicular lymphoma; non-Hodgkin lymphoma; psychometrics; quality of life; questionnaire validation; DISEASE-RELATED SYMPTOMS; MULTIPLE-MYELOMA; HEALTH-STATUS; FUNCTIONAL ASSESSMENT; CANCER-THERAPY; IMPACT; SURVIVORS; CARE; CRITERIA; PEOPLE;
D O I
10.1111/ejh.12864
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ObjectivesThe development of novel agents and an ageing population has led to an increasing number of patients with follicular lymphoma (FL) living longer with their disease. Health-related quality of life (HRQOL) is a priority for patients and should guide clinical decisions. The Myeloma Patient Outcome Scale (MyPOS), originally developed for myeloma, was validated in a cross-sectional survey recruiting 124 FL patients. MethodsContent and construct validity, structural validity using confirmatory factor analyses, reliability and acceptability were evaluated. ResultsThree subscales were indicated: symptoms and function, emotional response, and healthcare support. MyPOS symptom and function scores were higher (worse) in participants with poorer ECOG performance status (F=26.2, P<.000) and discriminated between patients on and off treatment. Good convergent and discriminant validity in comparison to the EORTC-QLQ-C30 and FACT-Lym were demonstrated. Internal consistency was good; coefficient 0.70-0.95 for the total MyPOS score and subscales. ConclusionThe MyPOS is valid, reliable and acceptable, and can be used to support clinical care of FL patients. This is the first measurement tool developed specially for use in clinical practice that has been validated for use in people with FL. Further longitudinal validation is now required to support its use in outcome measurement.
引用
收藏
页码:508 / 516
页数:9
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