Diagnostic accuracy of voluntary and stimulated neuromuscular jitter studies in ocular myasthenia gravis

Author:

Cosentino Giuseppe12ORCID,Prunetti Paolo2,Tammam Giulia2,Zaffina Chiara2,Gastaldi Matteo3,Tassorelli Cristina14,Alfonsi Enrico2,Todisco Massimiliano2

Affiliation:

1. Department of Brain and Behavioral Sciences University of Pavia Pavia Italy

2. Translational Neurophysiology Research Unit IRCCS Mondino Foundation Pavia Italy

3. Neuroimmunology Laboratory and Neuroimmunology Research Unit IRCCS Mondino Foundation Pavia Italy

4. Headache Science and Neurorehabilitation Center IRCCS Mondino Foundation Pavia Italy

Abstract

AbstractIntroduction/AimsThere is a lack of studies comparing the accuracy of neuromuscular jitter analysis during voluntary activation (v‐jitter study) versus axonal stimulation (s‐jitter study). The study aimed to compare these two techniques in the same population of patients with suspected ocular myasthenia gravis (OMG).MethodsFourteen control subjects (mean age: 55.5 ± 15.2 years) and 34 patients with suspected OMG (mean age: 59 ± 13.9 years) were prospectively evaluated. Twenty spike pairs and 30 individual spikes were analyzed during v‐jitter and s‐jitter study, respectively. Two different criteria for abnormal individual jitter values were evaluated: ≥ or > than 10% values exceeding the upper normal limit.ResultsOMG was diagnosed in 19 patients based on clinical and laboratory findings, without considering jitter measurements. In most patients, v‐jitter and s‐jitter analyses provided comparable results. The maximum sensitivity (89%) was achieved with s‐jitter study using the ≥10% criterion, while the maximum specificity (93%) was found with v‐jitter study using the >10% criterion.DiscussionBoth v‐jitter and s‐jitter studies showed good to very good accuracy for the diagnosis of OMG, in the absence of any statistically significant difference. Therefore, the patient's cooperation level and examiner's experience should guide the choice of performing v‐jitter or s‐jitter analysis in patients with suspected OMG.

Publisher

Wiley

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