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80 Cards in this Set

  • Front
  • Back
Pain Sensation

The fast pathway?
for sharply discriminated pain, moves directly from the receptor to the spinal cord using myelinated A fibers and from the spinal cord to the thalamus using the neospinothalamic tract
Pain Sensation

The slow pathway?
for continuously conducted pain, is transmitted to the spinal cord using unmyelinated C fibers & from the spinal cord to the thalamus using the slower-conducting paleospinothalamic tract
Pain Sensation

Modulation?
Modulated in the midbrain by chemicals called endogenous opioids (endorphins, enkephalins, and ndynorphins)
Types of Pain

Cutaneous & Deep somatic
Cutaneous pain- arises from superficial structures like skin and subcu tissues (ex. Papercut)
Deep somatic pain- originates in deep body structures, such as the periosteum, muscles, tendons, joints, and blood vessels
Types of Pain

Visceral & Referred
Visceral Pain- has its origin in the organs and is one of the most common pains produced by disease
Referred Pain- pain that is perceived at a site different from its point of origin but innervated by the same spinal segment
Types of pain

Acute?
Acute Pain- short duration and remits when the underlying pathologic process has resolved; warning system; It can produce physical manifestations, such as tachycardia, reflective of increased sympathetic activity.
Types of pain

Chronic?
Chronic Pain- elicited by an injury but may be perpetuated by factors that are both pathologically and physically remote from the originating cause. It extends for long periods of time and generally represents low levels of an underlying pathologic process that does not explain the presence or extent of the pain.; It can produce loss of appetite, sleep disturbances, depression
Pain

Headache
a common disorder that is caused by a number of conditions (Can be primary or secondary)
Migraine- caused by changes in serotonin levels and inflammation of the cerebral vascular system
Cluster- ANS caused cerebral vascular dilation
Tension- sustained contraction of scalp muscles
Motor Function
Voluntary control of motor fx is directed by the motor cortex, which consists of the primary, premotor, and supplementary motor cortex
Muscle Tone
Muscle tone is maintained through the combined function of the stretch reflex and the extrapyramidal system that monitors and buffers UMN innervation of the LMNs.
Disorders of Musculoskeletal Function

Hypotonia/Hypertonia
is a condition of less-than-normal muscle tone; and Hypertonia or spacticity is a condition of excessive tone
Disorders of Musculoskeletal Function
Paresis refers to weakness in muscle fx, and paralysis refers to a loss of muscle movement.
UMN lesions produce spastic paralysis and LMN lesions flaccid paralysis.
Skeletal Muscle Disorders

Muscular Dystrophy (MD)
most common form is Duchenne MD
a term applied to a number of genetic disorders that produce progressive degen. & necrosis of skeletal muscle fibers, replaces with fat and conn. tissue which leads to (pseudohypertrphy) muscle weakness
Disorders of the Neuromuscular Junction

Myastenia Gravis (MA)
autoimmune; antibodies block, destroy, or weaken the neuroreceptor Ach, causing a failure in transmission of nerve impulses at the NMJ
Myastenia Gravis (MA)
weak eye closure, pytosis, diplopia, fatigue, late paralysis, blank facial appearance, nasal vocal tones, frequent nasal regurgitation, eyelids drooping, head bobbing, decreased resp. muscles
Myastenia Gravis (MA)

Dx?
Tensilon test confirms; after giving I.V. edrophonium or neostigmine muscle fx improves in 30 to 60 seconds and last for 30 minutes; nerve stimulation tests;
Myastenia Gravis (MA)

Treatment?
anticolinesterse drugs- neostigmine and pyridostigmine; immunosuppressant therapy; IV IG; plasmapheresis; thymectomy
Carpal Tunnel Syndrome

Peripheral Nerve Disorder
a compression mononeuropathy
inflammation or fibrosis of the tendon sheaths that pass through the carpal tunnel usually causes edema and compression of the median nerve. Causes: weakness, pain, burning, numbness, or tingling
Guillain-Barre Syndrome

Peripheral Nerve Disorder
autoimmune: polyneuropathy; involves demyelination or axonal degeneration:
causes progressive ascending muscle weakness and loss of tendon reflexes. may progress to resp. muscles.
Herniated Disks

A herniated intervertebral disk-
protrusion of the nucleus pulposus into the spinal canal. Usually, at (L4 or L5 to S1) or (C6 to C7 and C5 to C6). The SxS are localized to the area of the body innervated by the affected nerves w/ pain and motor/sensory deficits
Disorders of the Basal Ganglia
Alteration in or abnormal muscle movements that result from disorders of the cerebellum and basal ganglia. The basal ganglia organize & then release basic movements
Parkinson Disease

Degenerative disorder of the Basal Ganglia
involves destruction of nigrostriatal pathway, & reduction of striatal concentrations of dopamine. depleting dopamine producing neurons.
Disorders of the Basal Ganglia

Parkinson Disease- How?
• Onset in 40-50s, more males
• #1 neurological disorder
Disorders of the Basal Ganglia

Parkinson Disease- Treatment?
diet (increase calorie, decrease protein), surgery (pallidotomy), PT, meds (anticholinergics)
Upper Motor Neuron Disorders

Amyotrophic Lateral Sclerosis
"Lou Gehrig"
A devastating neuro disorder that selectively affects motor function
Upper Motor Neuron Disorders

Amyotrophic Lateral Sclerosis
"Lou Gehrig" - Who?
Affects people from 55-60 yrs of age; twice as many men than women
Upper Motor Neuron Disorders

Amyotrophic Lateral Sclerosis
"Lou Gehrig" - SxS, Treatment?
rapid, progressive weakness; intellect remains intact
Treatment: no cure, supportive care only
Demyelinating Disorders

Multiple Sclerosis- What?
Loss of myelin on the nerve fibers throughout the CNS
Demyelinating Disorders

Multiple Sclerosis- What?
most common nontramatic cause of neuro disability among young and middle-aged adults; women double compared to men; immune-mediated disorder that occurs in genetically susceptible individuals
Demyelinating Disorders

Multiple Sclerosis- SxS?
Exacerbations and remissions are usual
S & S: decrease sensation, motor impairments (spasticity), visual problems, cognitive changes, fatigue
Demyelinating Disorders

Multiple Sclerosis- Treatment?
PT, meds (immunosuppressors, muscle relaxers, antidepressants, bladder control agents)
Spinal Cord Injures
Described by the last intact spinal nerve and the vertebral level (C5, C6)
May be temporary or permanent
Causes- traumatic, non-traumatic
Typical patient is a young male
Spinal Cord Injures

Primary and Secondary damage
Primary – bone fracture/dislocation, nerve tissue tearing
Secondary – bleeding, edema, necrosis
Spinal Cord Injures (SCI)

Classification of permanent SCI
Paraplegic or quadriplegic
Initial period of spinal shock- all function is lost, end of shock indicated by positive bulbocav ernosus reflex (stimulation of genitals elicits contraction of anus)
Complete or Incomplete
Spinal Cord Injures (SCI)

Brown-Sequard-
damage to one side only, usually from GSW or stabbing, loss of motor & proprio/touch/vibration ipsilaterally, loss of pain/temp contralaterally
Spinal Cord Injures (SCI)

Anterior cord syndrome
damage to anteriolateral 2/3, usually from flexion forces, symmetrical loss of motor & pain/temp, other sensory remains
Spinal Cord Injures (SCI

Central cord syndrome
damage to central aspect, UEs more involved than LEs.
sensory loss is less than motor loss
Spinal Cord Injures (SCI

Posterior cord syndrome
damage to post columns, proprio/touch/vibration loss only, rare
Early Medical Management of SPI
Immobilization to stabilize the spine and prevent cord damage-
High doses of methylprednisolone
Early Medical Management of SPI
These patients require the best nursing care to prevent development of complications d/t immobility. Use psychotherapeutic approach. GOAL is to restore or maintain function and /or adaptation
Increased Intracranial Pressure
Common pathway for brain injury.
Possible causes?
^ tissue volume from tumor, edema, bleeding-
^ blood volume of cerebral vessels or obstruction-
^ production, decreased absorption, or obstructed circulation of CSF
Increased Intracranial Pressure

How it presents?
change in LOC is earliest sign
Late sign: widened pulse pressure, irreg. resp., bradycardia. Hydrocephalus-
Head and Brain Injury
from MVAs, falls, other accidents. Patient is typically young male. There is usually primary and secondary damage.
Traumatic Brain Injury (TBI)

Coup-contrecoup injury
when the mechanical forces inducing head injury causes bouncing of the brain in the closed skull
Traumatic Brain Injury (TBI)

Concussion
momentary interruption of brain function with or without loss of consciousness
Traumatic Brain Injury (TBI)

Contusion
is a bruise to the cortical surface of the brain caused by blunt head trauma
Levels of Consciousness
Consciousness depends of the reticular activating system (RAS) and both cerebral hemispheres
Brain Death
Defined as the irreversible loss of function of the brain, including brain stem-
Clinical exam must disclose at least the absence of responsiveness, brain stem reflexes, and respiratory effort
CVA - Stroke

What?
Stroke or infarct (cerebrovascular accident) – 3rd leading cause of death in US, leading cause of disability
common in men and blacks
CVA - Stroke

2 main types. Ischemic & Hemorrhagic.
Ischemic strokes caused by interruption of blood flow in cerebral vessels, most common type. Thrombi common cause, within atherosclerotic vessels, & @ bifurcations
CVA - Stroke

Hemorrhagic
Hemorrhagic strokes caused by bleeding into the brain tissue, are less common but account for higher fatality rate.
CVA - Stroke
TIA- usually no lasting deficits, clear within 24 h-
Risk Factors for CVA

Primary-
Primary- HTN, Heart disease, Diabetes, Smoking, TIA’s, Age, Race
Risk Factors for CVA

Secondary-
Secondary- Physical inactivity, Obesity, High cholesterol, Alcohol/drug abuse, Polycyhemia, Sickle cell disease, hx of CVA
CVA - Stroke

Treatments?
Tx has changed since 1990s
extra emphasis on salvaging brain tissue and preventing long-term damage during ischemic strokes. use proper position & effective ROM.
CVA - Stroke

Deficits.
Motor deficits most common
then language, sensation, & cognition.
Common Primary Deficits of CVA
Sensory loss contralaterally
Motor- contralateral hemiparesis, UE % face more involved then LE
Cognitive impairment- more often with Anterior Cerebral Artery CVAs
Perceptual problems- neglect, apraxia if on right
Speech- aphasia if on left
Hemianopsia- loss of ½ of visual field
Depression
CVA - Stroke

Treats?
Preservation of Brain Tissue- Time is tissue
IV thrombolytic therapy: with CT confirmation of no bleed- tPA, Redavase within 3 hours of onset of symptoms
Oral anticoagulants- aspirin
Prevent complications and recurrence
Manage BP
Rehabilitation
Infectious Disorders

Meningitis
infection of the pia mater, arachnoid, and subarachnoid space. can be bacterial, viral, or fungal. Most common: bacteria- Neisseria, Strep
Infectious Disorders

Meningitis
* Most common in college age group
* Symptoms- fever, HA, N & V, neck rigidity, fatigue
Infectious Disorders

Encephalitis
generalized infection of the brain or spinal cord. caused by a virus, toxins, or vaccine.
common in US is herpes simplex
Infectious Disorders

Encephalitis
Edema, necrosis, hemorrhage
*Symptoms- fever, HA, neck rigidity, confusion, seizures
Infectious Disorders

Treatment?
Symptomatic, IV antibiotics, antifungal, antivirals, supportive care, prevention of complications
Brain Tumors
2% of all aggressive neoplasms- 2nd common type of CA in children.
(astrocytomas)- in adults
Brain Tumors

SxS
headache, nausea, vomiting, mental changes, papilledema, visual disturbances, alterations in motor and sensory functions and seizures
Brain Tumors

Treat?
Physical exam, visual field testing, CT, MRI, skull x-ray, brain scans, EEG, cerebral angiography: surgery, irradiation, chemotherapy
Seizures
A sudden uncoordinated neuron discharge from a known or unknown cause
Unprovoked Seizure
aka primary or idiopathic
no known cause, thought to be genetic. Epilepsy-
Provoked Seizure
aka secondary or symptomatic
include febrile, those precipitated by systemic metabolic conditions, and after primary CNS insult occurrence
Partial Seizures
Simple partial seizures
One hemisphere, no loss of consciousness, generalized symptoms (lights flashing, sweating, dream states). May have an aura
Partial Seizures
Complex partial seizures
often temporal lobe with loss of consciousness & responsiveness. Usually starts w/ 1 hemisphere and progresses to involve both psychomotor seizures. Repetitive, non-purpose activities
Generalized Seizures
Typical Absence seizures
generalized disturbance in consciousness, nonconvulsive. Usually, only in children and stop at adulthood
Generalized Seizures
Atypical absence seizure
greater alteration in muscle tone and less abrupt onset & cessation. Need EEG to determine. Typical anti-seizure meds may increase frequency of atypical absence type
Generalized Seizures
Atonic/akinetic
sudden loss of muscle tone that leads to falling. “Drop attacks”
Generalized Seizure
Myoclonic
brief involuntary muscle contractions d/t cerebral stimulus. Bilateral jerking of muscles of face, trunk, or extremities.
Generalized Seizures
Tonic-Clonic: (Grand mal)
most common of the generalized. Aura, LOC, incontinence, post-ictal phase
Seizure-
Treatment
Protect from injury, protect airway, Pharmacological agents (more than 20- mainly suppress the repetitive firing of neurons, or inhibit electrical impulse, surgical intervention (may be an option)
Status Epilepticus
Seizures that do not stop spontaneously or occur without a recovery period
if not treated can cause resp failure and death. Higher morbidity in young and old.
Treatment: Airway- intubation, IV, admin of muscle relaxants and/or generalized paralyzing agents
Dementia
Alzheimer’s Disease- the most common
Unknown cause
*More women than men
*Microscopic “tangles” and plaques w/ slow gradual onset, usually 50-65
* Usually not with other medical problems
Dementia
Alzheimer’s Disease
STM loss, short attention span, decreased reasoning, behavioral changes, decrease language skills