Article

Fatigue is among the most common and debilitating symptoms of multiple sclerosis
(MS), affecting approximately 80% of persons who have the disease. Recently, as
part of the National Institutes of Health Patient Reported Outcome Measurement
Information System (PROMIS), a bank of items was developed for measuring
self-reported fatigue. This article has two purposes. (1) To assess, from the
perspective of individuals living with MS, the relevance of a subset of items
from the PROMIS fatigue item bank. (2) To identify additional aspects of fatigue
that individuals with MS believe are important for clinicians when asking about
their fatigue experience.
CI - Copyright (c) 2013 Elsevier Inc. All rights reserved.

Langue : ANGLAIS