Neuro Diseases Flashcards
What are the main categories of neurological diseases?
Neurological Diseases, Genetic Disorders, Degenerative Disorders, Cerebral Vascular Disorders, Congenital Brain Diseases, Traumatic Brain Injury, Seizure Disorders.
What is cerebral blood flow (CBF) modulated by?
cerebral metabolic rate, cerebral perfusion pressure (CPP), arterial blood carbon dioxide (PaC02), arterial blood oxygen (Pa02), various drugs, and intracranial pathologies.
What is the normal CBF rate?
Approximately 50 mL/100g brain tissue per minute, totaling 750 mL/min which is 15% of cardiac output.
What does the Monro-Kellie hypothesis state?
Any increase in one component of intracranial volume must be offset by a decrease in another component to prevent elevated ICP.
Whats does the intracranial and spinal vault contain?
neural tissue (brain &spinal cord)
blood
CSF
What is normal ICP?
5-15mmHg
Normal volume of intracranial and spinal vault
1200-1500mL
What are the common causes of increased intracranial pressure (ICP)?
- Tumors
- Intracranial hematomas
- Infections (meningitis or encephalitis)
- Blood in the CSF
- Edema in surrounding brain tissue.
What are the methods to decrease ICP?
- Elevation of the head
- Hyperventilation
- CSF drainage
- Hyperosmotic drugs
- Diuretics
- Corticosteroids
- Surgical decompression.
What is Multiple Sclerosis (MS)?
A progressive, autoimmune demyelination of central nerve fibers, typically onset age 20-40.
What are common symptoms of Multiple Sclerosis?
- Motor weakness
- Sensory disorders
- Visual impairment
- Autonomic instability.
What triggers exacerbations in Multiple Sclerosis?
- Stress
- Elevated temperatures
- Postpartum period.
What is Myasthenia Gravis?
An autoimmune disorder characterized by antibodies against nicotinic acetylcholine receptors at the skeletal motor endplate.
What are common symptoms of Myasthenia Gravis?
- Muscle weakness, exacerbated with exercise
- Ocular symptoms (diplopia, ptosis)
- Bulbar involvement.
What is Lambert Eaton Syndrome?
An autoimmune disorder characterized by antibodies against voltage-gated calcium channels, reducing Ca++ influx and therefore ACh release at the neuromuscular junction.
What are the symptoms of Lambert Eaton Syndrome?
- Progressive limb-girdle weakness
- Dysautonomia
- Oculobulbar palsy.
What is LES commonly associated with?
Small cell lung carcinoma
What is the main treatment medication for LES?
3-4 diaminopyridine (K+channel blocker)
Special anesthetic considerations for LES?
VERY sensitive to ND-NMB and D-NMB, prefer RA over GA
What is Muscular Dystrophy?
A hereditary disorder of muscle fiber degeneration caused by breakdown of the dystrophin-glycoprotein complex.
What is the most common and severe form of Muscular Dystrophy?
Duchenne Muscular Dystrophy.
Who does Duchenne MD affect?
Only boys, onset 2-5 y, wheelchair-bound by 8-10 y
S/S of Duchenne MD
muscle wasting, kyphoscoliosis, long bone fragility, respiratory weakness, EKG changes, elevated CK
Special Anesthetic Considerations for Duchenne MD
EKG/ECHO
Hypermetabolic syndrome-have MH cart ready
Consider low dose Rocc and TIVA
RA >GA