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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
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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
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Pain Sensation
Modulation? |
Modulated in the midbrain by chemicals called endogenous opioids (endorphins, enkephalins, and ndynorphins)
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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 |
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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 |
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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.
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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
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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 |
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Motor Function
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Voluntary control of motor fx is directed by the motor cortex, which consists of the primary, premotor, and supplementary motor cortex
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Muscle Tone
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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.
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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
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Disorders of Musculoskeletal Function
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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. |
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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
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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
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Myastenia Gravis (MA)
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weak eye closure, pytosis, diplopia, fatigue, late paralysis, blank facial appearance, nasal vocal tones, frequent nasal regurgitation, eyelids drooping, head bobbing, decreased resp. muscles
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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;
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Myastenia Gravis (MA)
Treatment? |
anticolinesterse drugs- neostigmine and pyridostigmine; immunosuppressant therapy; IV IG; plasmapheresis; thymectomy
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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
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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.
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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
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Disorders of the Basal Ganglia
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Alteration in or abnormal muscle movements that result from disorders of the cerebellum and basal ganglia. The basal ganglia organize & then release basic movements
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Parkinson Disease
Degenerative disorder of the Basal Ganglia |
involves destruction of nigrostriatal pathway, & reduction of striatal concentrations of dopamine. depleting dopamine producing neurons.
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Disorders of the Basal Ganglia
Parkinson Disease- How? |
• Onset in 40-50s, more males
• #1 neurological disorder |
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Disorders of the Basal Ganglia
Parkinson Disease- Treatment? |
diet (increase calorie, decrease protein), surgery (pallidotomy), PT, meds (anticholinergics)
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Upper Motor Neuron Disorders
Amyotrophic Lateral Sclerosis "Lou Gehrig" |
A devastating neuro disorder that selectively affects motor function
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Upper Motor Neuron Disorders
Amyotrophic Lateral Sclerosis "Lou Gehrig" - Who? |
Affects people from 55-60 yrs of age; twice as many men than women
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Upper Motor Neuron Disorders
Amyotrophic Lateral Sclerosis "Lou Gehrig" - SxS, Treatment? |
rapid, progressive weakness; intellect remains intact
Treatment: no cure, supportive care only |
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Demyelinating Disorders
Multiple Sclerosis- What? |
Loss of myelin on the nerve fibers throughout the CNS
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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
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Demyelinating Disorders
Multiple Sclerosis- SxS? |
Exacerbations and remissions are usual
S & S: decrease sensation, motor impairments (spasticity), visual problems, cognitive changes, fatigue |
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Demyelinating Disorders
Multiple Sclerosis- Treatment? |
PT, meds (immunosuppressors, muscle relaxers, antidepressants, bladder control agents)
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Spinal Cord Injures
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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 |
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Spinal Cord Injures
Primary and Secondary damage |
Primary – bone fracture/dislocation, nerve tissue tearing
Secondary – bleeding, edema, necrosis |
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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 |
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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
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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
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Spinal Cord Injures (SCI
Central cord syndrome |
damage to central aspect, UEs more involved than LEs.
sensory loss is less than motor loss |
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Spinal Cord Injures (SCI
Posterior cord syndrome |
damage to post columns, proprio/touch/vibration loss only, rare
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Early Medical Management of SPI
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Immobilization to stabilize the spine and prevent cord damage-
High doses of methylprednisolone |
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Early Medical Management of SPI
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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
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Increased Intracranial Pressure
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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 |
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Increased Intracranial Pressure
How it presents? |
change in LOC is earliest sign
Late sign: widened pulse pressure, irreg. resp., bradycardia. Hydrocephalus- |
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Head and Brain Injury
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from MVAs, falls, other accidents. Patient is typically young male. There is usually primary and secondary damage.
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Traumatic Brain Injury (TBI)
Coup-contrecoup injury |
when the mechanical forces inducing head injury causes bouncing of the brain in the closed skull
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Traumatic Brain Injury (TBI)
Concussion |
momentary interruption of brain function with or without loss of consciousness
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Traumatic Brain Injury (TBI)
Contusion |
is a bruise to the cortical surface of the brain caused by blunt head trauma
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Levels of Consciousness
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Consciousness depends of the reticular activating system (RAS) and both cerebral hemispheres
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Brain Death
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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 |
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CVA - Stroke
What? |
Stroke or infarct (cerebrovascular accident) – 3rd leading cause of death in US, leading cause of disability
common in men and blacks |
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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
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CVA - Stroke
Hemorrhagic |
Hemorrhagic strokes caused by bleeding into the brain tissue, are less common but account for higher fatality rate.
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CVA - Stroke
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TIA- usually no lasting deficits, clear within 24 h-
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Risk Factors for CVA
Primary- |
Primary- HTN, Heart disease, Diabetes, Smoking, TIA’s, Age, Race
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Risk Factors for CVA
Secondary- |
Secondary- Physical inactivity, Obesity, High cholesterol, Alcohol/drug abuse, Polycyhemia, Sickle cell disease, hx of CVA
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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. |
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CVA - Stroke
Deficits. |
Motor deficits most common
then language, sensation, & cognition. |
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Common Primary Deficits of CVA
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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 |
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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 |
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Infectious Disorders
Meningitis |
infection of the pia mater, arachnoid, and subarachnoid space. can be bacterial, viral, or fungal. Most common: bacteria- Neisseria, Strep
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Infectious Disorders
Meningitis |
* Most common in college age group
* Symptoms- fever, HA, N & V, neck rigidity, fatigue |
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Infectious Disorders
Encephalitis |
generalized infection of the brain or spinal cord. caused by a virus, toxins, or vaccine.
common in US is herpes simplex |
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Infectious Disorders
Encephalitis |
Edema, necrosis, hemorrhage
*Symptoms- fever, HA, neck rigidity, confusion, seizures |
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Infectious Disorders
Treatment? |
Symptomatic, IV antibiotics, antifungal, antivirals, supportive care, prevention of complications
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Brain Tumors
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2% of all aggressive neoplasms- 2nd common type of CA in children.
(astrocytomas)- in adults |
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Brain Tumors
SxS |
headache, nausea, vomiting, mental changes, papilledema, visual disturbances, alterations in motor and sensory functions and seizures
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Brain Tumors
Treat? |
Physical exam, visual field testing, CT, MRI, skull x-ray, brain scans, EEG, cerebral angiography: surgery, irradiation, chemotherapy
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Seizures
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A sudden uncoordinated neuron discharge from a known or unknown cause
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Unprovoked Seizure
aka primary or idiopathic |
no known cause, thought to be genetic. Epilepsy-
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Provoked Seizure
aka secondary or symptomatic |
include febrile, those precipitated by systemic metabolic conditions, and after primary CNS insult occurrence
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Partial Seizures
Simple partial seizures |
One hemisphere, no loss of consciousness, generalized symptoms (lights flashing, sweating, dream states). May have an aura
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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
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Generalized Seizures
Typical Absence seizures |
generalized disturbance in consciousness, nonconvulsive. Usually, only in children and stop at adulthood
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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
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Generalized Seizures
Atonic/akinetic |
sudden loss of muscle tone that leads to falling. “Drop attacks”
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Generalized Seizure
Myoclonic |
brief involuntary muscle contractions d/t cerebral stimulus. Bilateral jerking of muscles of face, trunk, or extremities.
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Generalized Seizures
Tonic-Clonic: (Grand mal) |
most common of the generalized. Aura, LOC, incontinence, post-ictal phase
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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)
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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 |
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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 |
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Dementia
Alzheimer’s Disease |
STM loss, short attention span, decreased reasoning, behavioral changes, decrease language skills
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