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Measuring the Quality of Life in Patients with Multiple Sclerosis in Clinical Practice: A Necessary Challenge
Author(s) -
Karine Baumstarck,
Laurent Boyer,
Mohamed Boucékine,
Pierre Michel,
Jean Pelletier,
Pascal Auquier
Publication year - 2013
Publication title -
multiple sclerosis international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.125
H-Index - 6
eISSN - 2090-2662
pISSN - 2090-2654
DOI - 10.1155/2013/524894
Subject(s) - clinical practice , medicine , quality of life (healthcare) , multiple sclerosis , relevance (law) , clinical significance , physical therapy , alternative medicine , quality (philosophy) , intensive care medicine , pathology , nursing , psychiatry , law , philosophy , epistemology , political science
While the physical disability aspect of multiple sclerosis (MS) is of great importance, quality of life (QoL) measurements are being considered increasingly important with regard to evaluating disease progression, treatment, and the management of care provided to MS patients. Despite the acknowledged need to consider QoL issues, QoL assessment remains underutilized in clinical practice. These issues should be explored and understood to promote the use of measuring QoL in MS clinical practice. We explore the difficulties for clinicians: choosing and determining the most appropriate QoL measure and how to best integrate QoL measurements into clinical practice. This paper discusses several avenues to provide to clinicians arguments of the clinical relevance and accuracy of QoL instruments and ultimately to enhance the use of QoL measures in clinical practice for MS patients.

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