Myasthenia gravis: Difference between revisions
Ostermayer (talk | contribs) |
Ostermayer (talk | contribs) |
||
| Line 1: | Line 1: | ||
==Background== | ==Background== | ||
*Autoantibody degradation, dysfunction, and blockade of acetylcholine receptor at the NMJ | *Autoantibody degradation, dysfunction, and blockade of acetylcholine receptor at the NMJ<ref>Medications and Myasthenia Gravis (A Reference for Health Care Professionals) [http://www.myasthenia.org/LinkClick.aspx?fileticket=JuFvZPPq2vg%3d PDF]<?ref> | ||
*Thymus is abnormal in 75% of pts | *Thymus is abnormal in 75% of pts | ||
**Thymectomy resolves or improves symptoms in most pts, especially those with a thymoma | **Thymectomy resolves or improves symptoms in most pts, especially those with a thymoma | ||
Revision as of 03:27, 31 January 2015
Background
- Autoantibody degradation, dysfunction, and blockade of acetylcholine receptor at the NMJCite error: Closing
</ref>missing for<ref>tag - Steroids
- Anticonvulsants (phenytoin, barbiturates, lithium)
- Psychotropics (haloperidol)
- Beta-blockers / calcium-channel blockers
- Local anesthetics
- Narcotics
- Anticholinergics (diphenhydramine)
- NMJ blocking agents (roc, sux)
Weakness
- Neuromuscular weakness
- Upper motor neuron:
- CVA
- Hemorrhagic stroke
- Multiple sclerosis
- Amyotrophic Lateral Sclerosis (ALS) (upper and lower motor neuron)
- Lower motor neuron:
- Spinal and bulbar muscular atrophy (Kennedy's syndrome)
- Spinal cord disease:
- Infection (Epidural abscess)
- Infarction/ischemia
- Trauma (Spinal Cord Syndromes)
- Inflammation (Transverse Myelitis)
- Degenerative (Spinal muscular atrophy)
- Tumor
- Peripheral nerve disease:
- Neuromuscular junction disease:
- Muscle disease:
- Rhabdomyolysis
- Dermatomyositis
- Polymyositis
- Alcoholic myopathy
- Upper motor neuron:
- Non-neuromuscular weakness
- Can't miss diagnoses:
- ACS
- Arrhythmia/Syncope
- Severe infection/Sepsis
- Hypoglycemia
- Periodic paralysis (electrolyte disturbance, K, Mg, Ca)
- Respiratory failure
- Emergent Diagnoses:
- Symptomatic Anemia
- Severe dehydration
- Hypothyroidism
- Polypharmacy
- Malignancy
- Aortic disease - occlusion, stenosis, dissection
- Other causes of weakness and paralysis
- Acute intermittent porphyria (ascending weakness)
- Can't miss diagnoses:
Treatment
- Always evaluate tidal volume, FEV, negative inspiratory force, ability to handle secretions
- Meds
- Pyridostigmine
- If pt's usual dose has been missed the next dose is usually doubled
- PO route: 60-90mg q4hr
- IV route: 1/30th of the PO dose (2-3mg) by slow IV infusion
- Neostigmine
- 0.5mg IV
- Pyridostigmine
- Intubation
- If possible avoid depolarizing AND non-depolarizing agents
- If pt requires paralysis use non-depolarizing agent at smaller dose
- If must use depolarizing agents, will need higher doses
- If possible avoid depolarizing AND non-depolarizing agents
- Plasmapherisis
- IVIG
See Also
Source
- Tintinalli's Emergency Medicine: A Comprehensive Study Guide, 7e (2010), Chapter 167. Chronic Neurologic Disorders
