Talking
The MG-ADL scale is an easy-to-use tool that assesses the impact of gMG on your patients' daily functions by measuring 8 signs or symptoms that are commonly affected in gMG. Each sign or symptom is assessed on a 4-point scale, where 0 represents normal function and 3 represents the most severe impairment of that function. A total MG-ADL score ranges from 0 to 24, with higher scores indicating more impairment.1-4
Every point on the scale matters, with a 2-point reduction indicating clinically meaningful improvement in daily functions. For example, a 2-point difference can look like1,2:
When used consistently, the MG-ADL scale acts as a tool to track measurable trends over the course of a patient's disease progression.2
See the impact of each point on the MG-ADL scale with this interactive tool.
gMG=generalized myasthenia gravis; MG-ADL=Myasthenia Gravis Activities of Daily Living.
Depicting 1 out of 8 signs and symptoms measured on the MG-ADL scale for swallowing
MG-ADL=Myasthenia Gravis Activities of Daily Living; MSE=Minimal Symptom Expression.
—Jeffrey Rosenfeld, MD, PhD
Medical Director, The Center for Restorative Neurology
Loma Linda, CA
MG-ADL=Myasthenia Gravis Activities of Daily Living.
One study of 45 patients found that scores on the Myasthenia Gravis-Quality of Life 15 (MG-QOL15), a self-reported scale designed to assess patients’ quality of life and experience with MG, correlated significantly with the scores on the MG-ADL scale and other clinical evaluation scales at all visits.* A patient with a low total MG-ADL score may still be struggling. In fact, a score of 5 may appear low but can comprise subscores of 2 and 3, indicating a less than normal or complete loss of ability to perform a daily function. Therefore, aiming to decrease even a low total score through treatment strategies may lead to improvement with daily living activities.1,3,4
Using the MG-ADL scale in clinical evaluation may not only empower your patients to get involved in their treatment journey, but may also inform your treatment decisions.3
*Data was collected from 45 patients who were starting first-time immunomodulatory treatment for MG and did not have other medical conditions that would interfere with treatment with prednisone or IVIG or that the investigator considered important. Pregnant or breastfeeding individuals were excluded.3
IVIG=intravenous immunoglobulin; MG=myasthenia gravis; MG-ADL=Myasthenia Gravis Activities of Daily Living.
References: 1. Wolfe GI et al. Neurology. 1999;52(7):1487-1489. doi:10.1212/wnl.52.7.1487 2. Muppidi S et al. Muscle Nerve. 2022;65(6):630-639. doi:10.1002/mus.27476 3. Diez Porras L et al. J Clin Med. 2022;11(8):2189. doi:10.3390/jcm11082189 4. Saccà F et al. Eur J Neurol. 2023;30(12):3854-3867. doi:10.1111/ene.15872
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gMG=generalized myasthenia gravis.