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47 Cards in this Set
- Front
- Back
What is Cerebral Palsey
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delayed gross motor development - delays all motor skills
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What are Seizures
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atypical electrical discharge in the neurons of the cerebral cortex
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3 types of Meningitis
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1. Haempohilus influenzae B (Hib)
2. Strep pneumoniae - very common 3. Neisseria meningitidis - upper respiratory organism |
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What is Muscular Dystrophy
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a group of genetic disorders w/ microscopic changes in specific muscles, muscle wasting, loss of strength in skeletal and voluntary muscles.
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Diagnosis of Cerebral Palsey
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pattern of weakness, onset, developmental delays
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Clinical manifestations of Meningitis
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Headache, anorextia, N&V, change in LOC, seizure, rash, nuchal rigidity, joint pain, photophobia, temp >103
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Clinical manifestations of Seizures from Birth to Toddlers
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Fever, URI, metabolic disorders, malformation of CNS, perinatal brain injury.
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Clinical manifestations of Seizures from older children to adults
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trauma, tumors, CV disease
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Clinical manifestations of Seizures from Toddlers to older children
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CNS infection, neurodegenerative disorders, genetic seizure disorder
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Etiology of MD
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A flawed gene causes MD. The gene for dystrophin is normally found in the X chromosome, if defective then no dystrophin and MD results
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Describe Duchenne Muscular Dystrophy
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onset <5 years of age
rapidly progressive respiratory and cardiac failure children affected are late to walk pseudohypertrophy of calf muscles gradually become clumsy frequent falls loss of mobility b4 age 12 death b4 mid 20s |
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Describe Becker Muscular Dystrophy
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Onset in teens or early adulthood
progressive slow and unpredictable course walk becomes wide and waddling, walking on toes loss of strength in hips, pelvis, thighs, shoulders gradually becomes clumsy frequent falls loss of mobility rare b4 30 death from respiratory problems in 50s-60s |
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Diagnostic tests for MD
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biopsy of muscle for dystrophin levels
Blood creatine kinase >3000 MRI of muscle fibers EMG to measure action potentials Genetic: blood/muscle tissue |
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Treatments for MD
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PT, ROM to prevent complication r/t immobility
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Meds for MD
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Albuterol: suppress immune response
Steroids: treat everything Creatinine: increases strength Calcium blockers |
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What does Gentamycin do?
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in 10% of cases it bypasses the defective gene allowing dystrophin to be made.
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Describe Becker Muscular Dystrophy
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Onset in teens or early adulthood
progressive slow and unpredictable course walk becomes wide and waddling, walking on toes loss of strength in hips, pelvis, thighs, shoulders gradually becomes clumsy frequent falls loss of mobility rare b4 30 death from respiratory problems in 50s-60s |
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Diagnostic tests for MD
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biopsy of muscle for dystrophin levels
Blood creatine kinase >3000 MRI of muscle fibers EMG to measure action potentials Genetic: blood/muscle tissue |
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Treatments for MD
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PT, ROM to prevent complication r/t immobility
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Meds for MD
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Albuterol: suppress immune response
Steroids: treat everything Creatinine: increases strength Calcium blockers |
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What does Gentamycin do?
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in 10% of cases it bypasses the defective gene allowing dystrophin to be made.
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Manifestations of Cerebral Palsey
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*Delayed Gross motor development - Universal sign of CP
Abnormal motor performance, increased muscle tone, abnormal postures, reflex abnormalities - persistance of plantar, palmar, moro reflexes |
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Possible manifestations of CP
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Mental retardation: <30% of children have any deficit.
>70% have typical function |
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Sensory impairment of CP
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nystagmus (rapid eye movements), hearing loss, amblyopia (lazy eye)
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Other manifestations of CP
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drooling, respiratory problems, constipation, dental probs, seizures, orthopedic probs.
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What is spastic CP?
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most common type of CP
Increased tone w/ poor control attempts at movement worsten problem very limited fine motor skill |
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What is Dyskinetic CP?
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abnormal voluntary movement
athetosis: slow wormlike undulating, writhing movement worsen with stress and during adolescence involves muscles of breathing and speech |
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What is Ataxic CP?
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wide-based gait
rapid repetitive movements done poorly purposeful movement worsens condition. |
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Therapy goals for CP?
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lessen symptoms
PT, OT, Speech & Language therapy to: establish communication facilitate ambulation provide education promote typical socialization |
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Meds used in treatment of CP
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Valium, Robaxin, dantrium, Baclofen, Botox
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_____ is the most common serious neurological problem affecting nearly 1% of children
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Epilepsy
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Partial Seizure:
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originates in a single area or manifests on one side of body.
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Simple partial seizure:
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no loss of consciousness
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Complex partial seizure:
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Impaired or loss of consciousness.
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Generalized seizures:
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occur bilaterally or from several sites. manifestations on both sides of body
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Absence seizures:
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sudden loss of awaremenss
children can have up to 300-400 in 1 day |
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Myoclonic seizure
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sudden, violent muscle contraction - one or many, usually in arms
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Tonic-clonic seizure:
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sudden onset of rapid alternating muscle flexion/extention
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Seizure Meds:
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Dilantin-phenytoin - oldest, usually first drug of choice.
Not used for absence seizures, liver disease, pregnancy |
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More seizure meds:
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valproate acid: Depakene: used in all seizure types
Not used in Liver disease, pregnancy May cause liver failure or bone marrow failure Monitor labs, don't crush |
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Diet used for Tx of Seizures:
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Ketogenic Diet: high fat, low carbs, very strict.
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Vagal Nerve Stimulator
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Used in Tx of seizures. Vagus influences no. of seizures - stimulator applies current to vagus until seizures abate
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How is meningitis spread?
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Coughing, kissing, sneezing
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Who is at greatest risk for meningitis
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children <5, elderly, teens & young adults
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Labs for viral meningitis
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WBC low: <500
Protein: 50-500 mg/dL Glucose: normal Urine: clear, slightly cloudy |
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Labs for bacterial meningitis
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WBC high: >1000
Protein: >500 mg/dL Glucose: low Urine: turbid/cloudy |
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Tx for meningitis
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IV fluids
antibiotics: ampicillin, penicillin, cephalosporin Codeine for cephalgia Tylenol or ASA for fever >102 Lasix for diuresis |