Thursday, February 9, 2017
Wednesday, February 8, 2017
Anesthesia
General IV
Lipophilic
GABA receptor
Local Anesthesia 
Bind to Na+ channels during refractory period
High firing nerves more susceptible 
Weak bases
Ionized once inside cell so it can bind to receptor
Pain-->temperature-->touch-->pressure
Adverse effects: cardiotoxicity and seizures 
Epinephrine can be used as "adjunctive" to prolong the effects of other local anesthesia 
Myelin Diseases
Multiple Sclerosis
-chronic, autoimmune demyelinating disease
-immune response activates macrophages and their proteins
-neuro deficits separated in time
-white matter lesions
-MRI
-Uhthoff's sign
-Lhermitte's sign
-acute: mononuclear inflammatory cells, myelin breakdown, little astrogliosis, decrease in oligodendroglia, larger paler astrocytic nuclei
-chronic: decrease in inflammatory cells, complete demyelination and axonal loss, severe astrogliosis
-CSF: increased IgG, increased mononuclear cells, oligoclonal bands
Guillain-Barre Syndrome
-autoimmune demyelinating neuropathy
-ascending paralysis
-preceded by acute infection
-inflammation and demyelination
-loss of DTR
-decreased conduction velocity
-increased CSF protein
Leukodystrophies
-abnormal formation of stability of myelin
-progressive loss of cerebral function
-lysosomal or peroxisomal enzyme defects
1. Metachromatic Leukodystrophy
-defect in arylsulfatase-A --> accumulation of sulfatides
-lossof myelin and gliosis
-metachromasia
2. Krabbe's Disease (Globoid Cell Leukodystrophy)
-deficiency of galactocerebroside b-galactosidase --> galactosphingosine
-loss of myelin and oligodendrocytes
-globoid cells around blood vessels
3. Adrenoleukodystrophy
-mutation in ALD gene
-lack of catabolism of very long chain fatty acids
-elevated VLCFA in serum
-loss of myelin
-gliosis
-lymphocytic inflammation
4. Progressive Multifocal Leukoencephalopathy
-JC polyomavirus infects oligodendrocytes --> demyelination
-viral inclusions in nuclei
-foamy macrophages
-astrogliosis
-chronic, autoimmune demyelinating disease
-immune response activates macrophages and their proteins
-neuro deficits separated in time
-white matter lesions
-MRI
-Uhthoff's sign
-Lhermitte's sign
-acute: mononuclear inflammatory cells, myelin breakdown, little astrogliosis, decrease in oligodendroglia, larger paler astrocytic nuclei
-chronic: decrease in inflammatory cells, complete demyelination and axonal loss, severe astrogliosis
-CSF: increased IgG, increased mononuclear cells, oligoclonal bands
Guillain-Barre Syndrome
-autoimmune demyelinating neuropathy
-ascending paralysis
-preceded by acute infection
-inflammation and demyelination
-loss of DTR
-decreased conduction velocity
-increased CSF protein
Leukodystrophies
-abnormal formation of stability of myelin
-progressive loss of cerebral function
-lysosomal or peroxisomal enzyme defects
1. Metachromatic Leukodystrophy
-defect in arylsulfatase-A --> accumulation of sulfatides
-lossof myelin and gliosis
-metachromasia
2. Krabbe's Disease (Globoid Cell Leukodystrophy)
-deficiency of galactocerebroside b-galactosidase --> galactosphingosine
-loss of myelin and oligodendrocytes
-globoid cells around blood vessels
3. Adrenoleukodystrophy
-mutation in ALD gene
-lack of catabolism of very long chain fatty acids
-elevated VLCFA in serum
-loss of myelin
-gliosis
-lymphocytic inflammation
4. Progressive Multifocal Leukoencephalopathy
-JC polyomavirus infects oligodendrocytes --> demyelination
-viral inclusions in nuclei
-foamy macrophages
-astrogliosis
Neuromuscular Nicotinic Receptor Blockers
Succinylcholine
Aminosteriods
- Metabolized by plasma cholinesterase
 - Apnea
 - Hyperthermia
 - Bradycardia
 - Histamine
 
- Non-hepatic metabolism
 
- Laudanosine accumulates and causes seizures
 
- Cis isomer
 - Does not accumulate
 
Aminosteriods
- Hepatic and renal metabolism
 
- Difficult to achieve reversal
 
- Less potent so anesthesia for intubation
 - Hypersensitivity
 
Monday, February 6, 2017
OMM Techniques
Muscle Energy
- active direct
 - golgi tendon organ
 - position patient into the barriers
 - patient moves to freedom for 3 seconds (isometric)
 - 3 sets
 - reposition and move further into barrier
 - passive stretch at end
 
- passive
 - spindle fibers
 - decrease pain at tenderpoints
 - hold for 90 seconds
 
- decrease myofascial restriction
 
- passive indirect
 - muscle spindle
 - decrease muscle spasm
 - neutralize, compress, move to freedom for 3 to 5 seconds
 - 1 set
 
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