Make the most of the
MG-ADL scale

Patient portrayal

The image above is a patient portrayal and partial depiction of the MG-ADL scale, which assesses the impact of gMG on daily functions of 8 signs or symptoms that are typically affected in gMG. Each function is scored from 0-3: 0 represents normal function and 3 represents the loss of ability to perform that function. A total score can range from 0 to 24.

gMG=generalized myasthenia gravis; MG-ADL=Myasthenia Gravis Activities of Daily Living.

Explore the symptoms your patients may experience1

Talking

Normal

Intermittent slurring or nasal speech

Constant slurring or nasal speech, but can be understood

Difficult to understand speech

Chewing

Normal

Fatigue with solid food

Fatigue with soft food

Gastric tube

Swallowing

Normal

Rare episode of choking

Frequent choking necessitating changes in diet

Gastric tube

Breathing

Normal

Shortness of breath with exertion

Shortness of breath at rest

Ventilator dependence

Impairment of ability to brush teeth or comb hair

None

Extra effort, but no rest periods needed

Rest periods needed

Cannot do one of these functions

Impairment of ability to arise from a chair

None

Mild, sometimes uses arms

Moderate, always uses arms

Severe, requires assistance

Double vision

None

Occurs, but not daily

Daily, but not constant

Constant

Eyelid droop

None

Occurs, but not daily

Daily, but not constant

Constant

Tracking changes with the MG-ADL scale1,2

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:

  • Frequent choking necessitating changes in diet to normal function
  • Shortness of breath at rest to normal breathing
  • Experiencing double vision daily to not experiencing it at all

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

Choking Scale
Choking scale mobile

What could life look like with an MG-ADL score of 0 or 1?

MG-ADL=Myasthenia Gravis Activities of Daily Living; MSE=Minimal Symptom Expression.

Profiled headshot of Dr. Jeffrey Rosenfeld
Of course, the MG-ADL [score] is not just numbers on a scale.
Reductions [in MG-ADL score] translate into very real improvements for patients.

—Jeffrey Rosenfeld, MD, PhD
Medical Director, The Center for Restorative Neurology
Loma Linda, CA

MG-ADL=Myasthenia Gravis Activities of Daily Living.

Lowering patient scores could raise the bar on outcomes3

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