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. 2020 Sep 11;34(5):557–566. doi: 10.1007/s40259-020-00443-w

Table 2.

Major clinical outcome measures for myasthenia gravis trials

Outcome Description Score
MG-ADL 8-item patient-completed assessment of common symptoms with severity rated 0–3

0–24

2-point improvement considered meaningful

QMG 13-item scoring system performed by trained rater of ocular, bulbar, extremity, axial, and respiratory muscles involved in MG with severity rated 0–3 based on objective criteria

0–39

3-point change considered meaningful

MG Composite 10-item MGC contains mix of examiner- and patient-based assessments of ocular, bulbar/facial/neck, respiratory, limb domains with more critical domains weighed more heavily

0–51

3-point change considered meaningful

MGFA Clinical Classification* Ordinal scale of 5 categories of clinical severity ranging from ocular (1) to myasthenic crisis (5) and subdivisions of bulbar predominance

Class 1: ocular

Class 2: mild

Class 3: moderate

MG-QOL15r 15-item patient-reported assessment with rating of ‘not at all’, ‘somewhat’, and ‘very much’

0–45

not at all: 0

somewhat: 1

very much: 2

MG myasthenia gravis, MG-ADL Myasthenia Gravis Activities of Daily Living, MGFA MG Foundation of America, MG-QOL15r MG-Quality of Life–revised, QMG Quantitative Myasthenia Gravis

*MGFA Classification is no longer considered an outcome measure, but was used in some studies in this manner prior to 2000