Is the MyoPro Right for My Patients?
What is the MyoPro’s Intended Use?
The MyoPro, an upper limb orthosis, is a compensatory device to increase the ability to perform functional tasks with the affected limb. The user voluntarily activates movement of the orthotic device with their remaining electromyography (EMG) muscle signal.
What is the MyoPro’s Indication for Use?
The MyoPro is indicated for use by adolescents (ages 12+), adults (ages 18+), veterans, diagnosed with long-term muscle weakness OR partial paralysis.
Is the MyoPro covered by medical insurance?
MyoPro may be covered by most insurance companies, Medicare Advantage plans, and the U.S. Veterans Administration.
Is Myomo’s technology similar to electrical stimulation?
No. The MyoPro does NOT stimulate a User’s muscles with an external electrical impulse. This orthosis uses passive sensors on the surface of the skin to detect electrical signal within a muscle (electromyography).
What are the MyoPro’s Contraindications?
- Insufficient myoelectric signal output from at least one muscle group needed to activate the desired powered joint (for example, biceps or triceps signal to extend the affected elbow).
- Severe shoulder subluxation.
- Excessive pain in shoulder, arm or hand during facilitated range of motion.
- Contraindicated during recovery from acute injury such as trauma, infection, or skin condition.
- Upper extremity contracture(s) that prevent functional movement to benefit from the orthosis.
- Rigid spasticity in the affected muscle groups.
- Arm circumferences and lengths that are outside build specifications required to be fit with the orthosis.
- Cognitive or behavioral impairment that would inhibit safe use of the orthosis.
- Other medical issue which interferes with safe use of the device for functional improvement.