Neurology
Neurological System - Week 7 Lecture Notes
Lecturer Information
Farzana Sarder, MS, PA-CArizona State University (ASU)
Assigned Reading
McCance, K.L. & Huether, S.E. (2019). Pathophysiology: The biologic basis for disease in adults and children (8th ed). Elsevier.Chapters to read:
Chapter 17: Alterations in Cognitive Systems, Cerebral Hemodynamics, and Motor Function
Chapter 18: Disorders of the Central and Peripheral Nervous System
Key Concepts
Neurological Alterations in Movement
Key terms and movement alterations:
Alterations in Muscle Tone:
Hypotonia: Decreased muscle tone
Hypertonia: Increased muscle tone
Spasticity: Hyperexcitability of stretch reflexes leading to uncontrolled movements
Dystonia: Increased voluntary muscle contraction causing repetitive movements
Rigidity: Firm, tense muscles resisting movement
Upper and Lower Motor Neurons
Upper Motor Neurons (UMN):
Origin: Brain, travel to brainstem and spinal cord.
Injury leads to hypertonia (e.g., spasticity, rigidity).
Lower Motor Neurons (LMN):
Origin: Spinal nerves, travel to muscles.
Injury leads to hypotonia (e.g., weakness, atrophy, fasciculations).
Parkinson's Disease
Pathophysiology: Loss of dopamine neurotransmitter affecting basal ganglia, leading to excess movement control loss.
Symptoms:
Hallmarks: Resting tremors, cogwheel rigidity, bradykinesia (slow movements).
Increased tone causes difficulty walking; common symptoms include unblinking stare and drooling.
Treatment:
Medications (e.g., Carbidopa, Levodopa, Amantadine).
Rehabilitation therapies to address symptoms.
Spinal Cord Injuries
Causes: Trauma (e.g., falls, vehicle accidents).
Clinical Manifestations:
Loss of function below the injury level, initial hypotonia followed by hypertonia.
Complications:
Spinal Shock: Loss of motor/sensory function/ reflexes at injury level.
Neurogenic Shock: Occurs in higher spinal injuries, causing hypotension and bradycardia.
Autonomic Dysreflexia: Hypertension and possible bradycardia in response to stimuli, common after T6 injury.
Demyelinating Disorders
Multiple Sclerosis (MS):
Autoimmune disorder causing demyelination in CNS, producing sclerotic plaques.
Symptoms: Weakness, sensory deficits, gait issues, visual disturbances.
Guillain-Barre Syndrome:
Post-infection demyelinating disorder leading to ascending paralysis and potential respiratory failure.
Neuromuscular Junction Disorders
Myasthenia Gravis:
Autoimmune destruction of acetylcholine receptors, causing muscle weakness that improves with rest.
Symptoms: Diplopia, ptosis, impaired swallowing.
Traumatic Brain Injury (TBI)
Glasgow Coma Scale (GCS):
Assessment tool for traumatic brain injury severity based on eye opening, verbal response, and motor response.
GCS score range: 3 (severe) to 15 (healthy).
Posturing:
Decorticate: Flexion indicative of cortical injury.
Decerebrate: Extension indicative of brainstem injury.
Hematomas
Epidural Hematoma:
Bleeding between the skull and dura mater, often following skull fractures. Symptoms can evolve.
Subdural Hematoma:
Bleeding beneath the dura but above brain tissue, generally related to venous bleeding.
Subarachnoid Hematoma:
Bleeding in subarachnoid space compressing brain tissue, producing various symptoms.
Cerebrovascular Accident (CVA)
Types
Ischemic Stroke:
Thrombotic and Embolic categories; require rapid intervention to restore blood flow.
Hemorrhagic Stroke:
Spontaneous bleeding, requiring careful management.
Warning Signs
Use F.A.S.T. to identify potential stroke symptoms:
Face drooping
Arm weakness
Speech difficulty
Time to call 911
Meningitis
Definition: Inflammation of the meninges, commonly due to infections.
Symptoms: Fever, headache, neck stiffness, photophobia. Lumbar puncture for diagnosis.
Key Signs: Brudzinski and Kernig signs indicate irritation.
Encephalitis
Inflammation of brain tissue, often viral, leading to more severe deficits.
Similar diagnostic procedures as for meningitis.
Final Notes
For further in-depth details, refer to Chapters 17 and 18 of the assigned textbook.
Important assignments are available in the Canvas platform.