When to Order Electromyography (EMG)
EMG should be ordered when there is clinical suspicion of neuromuscular disease, particularly when diagnosis is uncertain, with specific indications including suspected myopathies, neuropathies, neuromuscular junction disorders, and radiculopathies that cannot be confirmed by clinical examination alone.
Primary Indications for EMG
Suspected Neuromuscular Disorders
- Myopathies and Neuropathies
Specific Clinical Scenarios
Peripheral Neuropathy Evaluation
Neuromuscular Junction Disorders
Laryngeal Disorders
Timing Considerations
Acute Setting:
- For rapidly progressive weakness to distinguish between urgent neurological conditions
- When considering surgical intervention for radiculopathies or entrapment neuropathies
Subacute/Chronic Setting:
- At least 3 weeks after onset of symptoms to allow development of denervation changes in neurogenic conditions 4
- For monitoring disease progression in chronic neuromuscular disorders
EMG as Part of a Diagnostic Algorithm
First-line Diagnostic Steps:
- Clinical assessment of muscle strength using validated tools (e.g., Medical Research Council scale)
- Basic laboratory testing (CK, electrolytes, thyroid function, inflammatory markers)
When to Order EMG:
- After initial assessment suggests neuromuscular pathology
- Before invasive procedures like muscle biopsy to guide site selection 5
- When distinguishing between neurogenic and myopathic causes is necessary
EMG in Conjunction with Other Tests:
- With nerve conduction studies (NCS) for comprehensive electrodiagnostic assessment
- Before MRI in non-acute cases to help direct imaging focus
- To complement serological testing for myositis-specific antibodies
Special Considerations
Pediatric Patients
- For juvenile dermatomyositis, EMG may be used when diagnosis is uncertain, but MRI is often preferred 4
- Consider age-appropriate normative values when interpreting results
Respiratory Muscle Assessment
- When respiratory muscle weakness is suspected but not confirmed by pulmonary function tests 4
- For patients with neuromuscular disorders showing signs of respiratory compromise
Follow-up EMG
- Not recommended for routine monitoring of disease activity in patients with stable symptoms 4
- Should be considered only when there is uncertainty about new or worsening symptoms 4
Diagnostic Yield and Limitations
- EMG has approximately 87% sensitivity and 65% specificity for detecting abnormalities confirmed by muscle biopsy 5
- False negatives can occur in:
- Early stages of disease
- Certain myopathies (e.g., mitochondrial myopathies, central core myopathy) 5
- Patchy or focal muscle involvement
Common Pitfalls to Avoid
- Ordering EMG too early after acute nerve injury (before denervation changes develop)
- Relying solely on EMG without clinical correlation
- Failure to recognize that normal EMG does not exclude all neuromuscular disorders
- Repeating EMG unnecessarily in patients with stable symptoms 4
EMG remains a valuable diagnostic tool when used appropriately as part of a comprehensive evaluation of neuromuscular symptoms, but should be ordered judiciously based on specific clinical indications rather than as a routine screening test.