Myasthenia Gravis
Introduction
• Myasthenia gravis (MG) is a neuromuscular
disease that leads to fluctuating muscle
weakness and fatigue
• Caused by a breakdown in the normal
communication between nerves and muscles
• There is no cure for myasthenia gravis, but
treatment can help relieve signs and
symptoms
Signs and symptoms
• Initial complaint is a specific muscle weakness
• Extraocular muscle weakness or ptosis
• Bulbar muscle weakness is also common,
along with weakness of head extension and
flexion
• Limb weakness may be more severe
proximally than distally
• Weakness is typically least severe in the
morning and worsens as the day progresses
• Weakness is increased by exertion and
alleviated by rest
• Weakness progresses from mild to more
severe over weeks or months, with
exacerbations and remissions
• About 87% of patients have generalized
disease within 13 months after onset
• Difficulty breathing, chewing, swallowing
• Factors that worsen MG symptoms :
– Fatigue
– Illness
– Stress
– Extreme heat
– Some medications (chloroquine, procaine, lithium,
phenytoin, beta-blockers, procainamide, statins)
Diagnosis
• Neurological examination
• Edrophonium test
• Ice pack test
• Blood analysis
• Repetitive nerve stimulation
• Single-fiber electromyography (EMG)
• Pulmonary function tests
Treatment
• Cholinesterase inhibitors
• Corticosteroids
• Immunosuppressant
• Plasmapheresis
• Intravenous immunoglobulin (IVIG)
• Surgery
Physical
Rehabilitation
Introduction
• MG symptoms tend to progress over time,
usually reaching their worst within a few years
after the onset of the disease
• Muscle weakness caused by MG worsens as
the affected muscles are used repeatedly,
therefore symptoms usually improve with rest
Factors limiting daily physical
function in stable MG
• Neuromuscular fatigue
• Low CV fitness levels (20% below normal)
• Diminished physiological fitness reserve (high
energy cost of walking at peak fitness level)
• Percent body fat 2-X normal (45%) and poor
fitness contribute to mobility disability
Potential benefits of physical
therapy in MG
• Weight reduction
• Decrease in risk of hypertension, diabetes,
cholesterol
• Decrease in risk of cardiac diseases
• Decrease in risk of osteoporosis
• Mood elevation ; improve cognitive function
• Enhance baseline functional capacity,
improved mechanical efficiency
Management Strategy
• There is a lot of variance between patients with
MG
• No one exercise program is same and treatment
strategies may vary
• Evaluation-
– Strength
– Flexibility
– Mobility
– Balance
– Gait
Exercise Goals
• Enhance ability to function daily
• Decrease risk of falling
• Completion of functional tasks and
maintenance of independence
• Smoothness and coordination of activities
• Once MG is stable, consistent exercise will
elevate baseline functional capacity which will
diminish the effect of MG exarcebation
Exercise Considerations
• The dollar per day rule
• Exercise at the best time of day
• Exercise at peak dose of medication
(pyridostigmine)
• Exercise large, proximal muscle groups for
short periods of time building up only to
moderate intensity
• Do not exceed moderate intensity exercise
level
Moderate Exercise Intensity
• HR should not elevate greater than 30 bpm from
resting baseline
• Patient should not become short of breath at
peak of exercising
• MG symptoms should not become worse during
exercise (drooping of eyes)
• Patient should not be tires after 2 hours of
exercise
• Patient should not have severe residual muscle
soreness the day post exercise
Types of Exercise used in MG
• Aerobic Exercises
• Strength exercises
• Swimming
• Postural exercise
• Breathing exercise
• Strength Exercise –
– Should be done progressively
– Range of motion (flexibility) to light resistance to
full resistance
– Start with lower prescription : 3 sets of 5 reps
– If significant weakness is present, active assist
exercises may be necessary (therapist help)
• The primary goal of therapy is to build the
individual's strength to facilitate return to
work and activities of daily living
• Do not overdo resistive training to the point of
fatigue
• Swimming
– Patients should swim in water where they can
touch the bottom
– Deep water is dangerous and may cause patient to
over exert
• Postural Exercises-
– Important in assisting with breathing, speaking
and swallowing
– Keeps bones and joints in the correct alignment so
that muscles are being used properly
– Prevents fatigue because muscles are being used
more efficiently, allowing the body to use less
energy
• Breathing exercises -
– Help improve lung function
– Include inspiratory muscle training
• Pursed lip breathing
• Diaphragmatic breathing
– These exercises can improve respiratory
endurance as many people with MG have affected
respiratory muscles
Reference
• http://www.myastheniagravis.org/
• Myasthenia Gravis foundation of America
http://www.myasthenia.org/
• http://www.mdguidelines.com/
• http://www.pivotalphysio.com/
• http://www.livestrong.com/
Myasthenia gravis rehabilitation

Myasthenia gravis rehabilitation

  • 1.
  • 2.
    Introduction • Myasthenia gravis(MG) is a neuromuscular disease that leads to fluctuating muscle weakness and fatigue • Caused by a breakdown in the normal communication between nerves and muscles • There is no cure for myasthenia gravis, but treatment can help relieve signs and symptoms
  • 3.
    Signs and symptoms •Initial complaint is a specific muscle weakness • Extraocular muscle weakness or ptosis • Bulbar muscle weakness is also common, along with weakness of head extension and flexion • Limb weakness may be more severe proximally than distally • Weakness is typically least severe in the morning and worsens as the day progresses
  • 4.
    • Weakness isincreased by exertion and alleviated by rest • Weakness progresses from mild to more severe over weeks or months, with exacerbations and remissions • About 87% of patients have generalized disease within 13 months after onset • Difficulty breathing, chewing, swallowing
  • 6.
    • Factors thatworsen MG symptoms : – Fatigue – Illness – Stress – Extreme heat – Some medications (chloroquine, procaine, lithium, phenytoin, beta-blockers, procainamide, statins)
  • 7.
    Diagnosis • Neurological examination •Edrophonium test • Ice pack test • Blood analysis • Repetitive nerve stimulation • Single-fiber electromyography (EMG) • Pulmonary function tests
  • 8.
    Treatment • Cholinesterase inhibitors •Corticosteroids • Immunosuppressant • Plasmapheresis • Intravenous immunoglobulin (IVIG) • Surgery
  • 9.
  • 10.
    Introduction • MG symptomstend to progress over time, usually reaching their worst within a few years after the onset of the disease • Muscle weakness caused by MG worsens as the affected muscles are used repeatedly, therefore symptoms usually improve with rest
  • 11.
    Factors limiting dailyphysical function in stable MG • Neuromuscular fatigue • Low CV fitness levels (20% below normal) • Diminished physiological fitness reserve (high energy cost of walking at peak fitness level) • Percent body fat 2-X normal (45%) and poor fitness contribute to mobility disability
  • 14.
    Potential benefits ofphysical therapy in MG • Weight reduction • Decrease in risk of hypertension, diabetes, cholesterol • Decrease in risk of cardiac diseases • Decrease in risk of osteoporosis • Mood elevation ; improve cognitive function • Enhance baseline functional capacity, improved mechanical efficiency
  • 15.
    Management Strategy • Thereis a lot of variance between patients with MG • No one exercise program is same and treatment strategies may vary • Evaluation- – Strength – Flexibility – Mobility – Balance – Gait
  • 17.
    Exercise Goals • Enhanceability to function daily • Decrease risk of falling • Completion of functional tasks and maintenance of independence • Smoothness and coordination of activities • Once MG is stable, consistent exercise will elevate baseline functional capacity which will diminish the effect of MG exarcebation
  • 18.
    Exercise Considerations • Thedollar per day rule • Exercise at the best time of day • Exercise at peak dose of medication (pyridostigmine) • Exercise large, proximal muscle groups for short periods of time building up only to moderate intensity • Do not exceed moderate intensity exercise level
  • 19.
    Moderate Exercise Intensity •HR should not elevate greater than 30 bpm from resting baseline • Patient should not become short of breath at peak of exercising • MG symptoms should not become worse during exercise (drooping of eyes) • Patient should not be tires after 2 hours of exercise • Patient should not have severe residual muscle soreness the day post exercise
  • 20.
    Types of Exerciseused in MG • Aerobic Exercises • Strength exercises • Swimming • Postural exercise • Breathing exercise
  • 22.
    • Strength Exercise– – Should be done progressively – Range of motion (flexibility) to light resistance to full resistance – Start with lower prescription : 3 sets of 5 reps – If significant weakness is present, active assist exercises may be necessary (therapist help) • The primary goal of therapy is to build the individual's strength to facilitate return to work and activities of daily living • Do not overdo resistive training to the point of fatigue
  • 25.
    • Swimming – Patientsshould swim in water where they can touch the bottom – Deep water is dangerous and may cause patient to over exert
  • 26.
    • Postural Exercises- –Important in assisting with breathing, speaking and swallowing – Keeps bones and joints in the correct alignment so that muscles are being used properly – Prevents fatigue because muscles are being used more efficiently, allowing the body to use less energy
  • 28.
    • Breathing exercises- – Help improve lung function – Include inspiratory muscle training • Pursed lip breathing • Diaphragmatic breathing – These exercises can improve respiratory endurance as many people with MG have affected respiratory muscles
  • 31.
    Reference • http://www.myastheniagravis.org/ • MyastheniaGravis foundation of America http://www.myasthenia.org/ • http://www.mdguidelines.com/ • http://www.pivotalphysio.com/ • http://www.livestrong.com/