2023
DOI: 10.1007/s40120-023-00549-7
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No Evidence of Disease Activity (NEDA) as a Clinical Assessment Tool for Multiple Sclerosis: Clinician and Patient Perspectives [Narrative Review]

Scott D. Newsome,
Cherie Binns,
Ulrike W. Kaunzner
et al.
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Cited by 6 publications
(2 citation statements)
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“…Quality of life in MS patients is influenced by various factors including physical disability, cognitive function, and emotional well-being [ 13 , 14 ]. Previous studies have indicated that improvements in clinical and radiological measures of disease activity do not always correlate strongly with QoL improvements [ 15 , 16 ]. Moreover, the application of advanced MRI techniques in clinical practice has enhanced the understanding of MS pathophysiology and the monitoring of disease progression.…”
Section: Introductionmentioning
confidence: 99%
“…Quality of life in MS patients is influenced by various factors including physical disability, cognitive function, and emotional well-being [ 13 , 14 ]. Previous studies have indicated that improvements in clinical and radiological measures of disease activity do not always correlate strongly with QoL improvements [ 15 , 16 ]. Moreover, the application of advanced MRI techniques in clinical practice has enhanced the understanding of MS pathophysiology and the monitoring of disease progression.…”
Section: Introductionmentioning
confidence: 99%
“…The treatment for MS is primarily concerned with the use of immunomodulating and immunosuppressive medications, which help reduce inflammation and limit disease progression; however, these agents often come with a risk of adverse reactions, including possible infections (Ghasemi et al., 2017 ). More recent disease modifying treatments have shown great promise in the treatment of the disease, with some even striving toward the outcome known as no evidence of disease activity, which is based on a demonstration of low clinical measures or lack of disease symptoms, relapses, progression, and MRI activity (Newsome et al., 2023 ). Yet, despite the present advancements, the symptoms of fatigue and lethargy that are experienced by those with MS stand as a crucial obstacle in the way of substantial improvement in the quality of life (QoL) for sufferers (Braley & Chervin, 2010 ).…”
Section: Introductionmentioning
confidence: 99%