Needle electromyography does not meaningfully impact findings in MR‐neurography/−myography

Author:

Sondermann Stefan1ORCID,Boppel Tobias1ORCID,Fieseler Katharina1,Schramm Peter1,Bäumer Tobias2,Trillenberg Peter3

Affiliation:

1. Department of Neuroradiology University Medical Center Schleswig‐Holstein Lübeck Germany

2. Institute of System Motor Science University of Lübeck Lübeck Germany

3. Department of Neurology University Medical Center Schleswig‐Holstein Lübeck Germany

Abstract

AbstractIntroductionMagnetic resonance neurography (MRN) and myography (MRM) are emerging imaging methods for detecting diseases of the peripheral nerve system (PNS). Most patients with PNS diseases also undergo needle electromyography (EMG). This study examined whether EMG led to lesions that were detectable using MRN/MRM and whether these lesions could impair image interpretation.MethodsTen patients who underwent clinically indicated EMG were recruited. MRN/MRM was performed before and 2–6 h after EMG, and if achievable, 2–3 days later. T2 signal intensity (SI) of the tibialis anterior muscle (TA) was quantified, and sizes and SI of the new lesions were measured. Visual rating was performed independently by three neuroradiologists.ResultsT2 lesions at the site of needle insertion, defined as focal edema, were detectable in 9/10 patients. The mean edema size was 31.72 mm2 (SD = 14.42 mm2) at the first follow‐up. Susceptibility‐weighted imaging lesions, defined as (micro) hematomas were detected in 5/10 patients (mean size, 23.85 mm2 [SD = 12.59 mm2]). General muscle SI of the TA did not differ between pre‐ and post‐EMG examinations. Lesions size was relatively small, and the readers described image interpretation as not impaired by these lesions.DiscussionThis study showed that focal edema and hematomas frequently occurred after needle EMG and could be observed using MRN/MRM. As general muscle SI was not affected and image interpretation was not impaired, we concluded that needle EMG did not interfere with MRN/MRM.

Publisher

Wiley

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