A clinician typically determines the diagnosis of a muscle spasm after considering the individual’s full history of symptoms and physical examination. The clinician may want to know about the onset of the pain, how long the muscle spasms last, and how frequently they occur. Other helpful information may include which muscle or muscles are affected, whether the spasms occur consistently in the same muscles or affect various muscles, and the circumstances surrounding the spasms. Obtaining a full personal and
medical history (e.g., occupation, hobbies, history of
genetic disorders) can help the clinician rule out underlying factors predisposing the individual to muscle spasms.
If the individual’s medical history and physical examination are not sufficient to diagnose muscle spasms, the clinician may order
blood tests to check the individual’s levels of
sodium, potassium,
calcium, and
magnesium. A
creatine phosphokinase (CPK) blood test can be used to detect
muscle breakdown. CPK is released as a result of muscle damage, which can occur if muscle spasms are prolonged.
If there is concern for arteriosclerosis, imaging tests, such as
ultrasound or magnetic resonance imaging (MRI), can be ordered to assess the blood vessels for narrowing. A computed tomography (CT) angiography, which involves injecting dye into an artery near the
groin or wrist, can also be used to assess
blood flow in the arteries.
Lastly, an
electromyography (EMG), which tests the muscle’s response to
electric stimulation, may be ordered to rule out any disorders of the
nervous system, including MS and ALS, that could potentially cause muscle spasms.