NP619 Module 7 & 8 Flashcards

(55 cards)

1
Q

Treatment of club feet

A

More common in boys
The cause is unknown
Serial casting is the treatment for 6-8 weeks with cast changes weekly
surgery possible between 3-18 months
OUR ROLE is to make sure that baby is growing and that someone is doing weight checks

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2
Q

Metatarsus Adductus

A
can affect one or both feet
from position in utero
Ankle has full plantar and dorsiflexion
Do not x-ray
do not worry unless no resolution by 6 months
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3
Q

Torticollis-Contracture of the sternocleidomastoid muscle

occur from position in birth canal, etc

A

Crook in the neck
What we consider after meningitis
TX: ROM, motrin, older children can maybe use some flexeril

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4
Q

Subluxation of the elbow-Most common at ages 1-3

A

entrapment of the annular ligament
Dx by Hx: partial dislocation of the head of radius, arises from the sudden jerk or pull of a toddlers arm
Arm=motionless, slight flextion, pronation, adduction, radial head is tender

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5
Q

Tx of the nursemaids elbow

A
Cup elbow
appl pressure over the radial head
thumb in the antecubital fossa
apply slight longitudinal traction by grasping the wrist
supinate (palm up) and flex (to 90 degrees) forearm
palpable click felt with reduction
child uses arm within 15 minutes
can use sling 1-2 days
if it does not work-do x-ray
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6
Q

Scoliosis=lateral curve of 11 degrees or greater of spine

A
Long term consequences:
unpleasant deformities
back pain
social and psychological problems
limited job opportunities
Screening: inconclusive.  some states mandate! 
TX=bracing has limited effect.
maybe exercise, electrical stimulation and surgery if really severe
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7
Q

Cobb angle

A

Used for scoliosis
Angle of 10 is minimum angulation to define scoliosis
Significant = 25-30 degrees
Severe=45-50 degrees

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8
Q

Sport physicals

A

Who can participate
Used to meet legal and insurance requirements
counsel on health related issues
Do 6 weeks before pre-season
leading reasons for disqualifying from participation:rhythm and conduction abnormalities
systemic hypertension
valvular heart disease

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9
Q

Sports

A
Red flags=asthma, mono, SOB w/exercise
palpitations
seizures
family hx of early heart disease
LOC
hx of fx. Strains, sprains, spec equipment
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10
Q

Sports

A

ABSOLUTE NO=carditis
leading causes of sudden cardiac death are
hypertrophic cardiomyopathy, coronary artery anomalies, myocarditis, and aortic stenosis

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11
Q

Pectus carinatum

A

The sternum is bowed
Usually does not present with problems
Cosmetic issues-may be fixed with surgery

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12
Q

Pectus Excavatum

A

Funnel chest
1 in 500-1000
when moderate or severe it can cause abnormalities of the heart or lungs
can correct with surgery

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13
Q

Osgood-Schlatter syndrome

A

Common in adolescents
(especially in athletes during growth spurts)
inflammation of anterior proximal tibial tuberosity PULL OF THE LARGE POWERFUL MUSCLWS IN THE FRONT OF THE THIGH
resolves in 6-12 months
knee looks normal but pain over patellar grooves no instability of the knee

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14
Q

Genus varus-persistant bowing may be sign of underlying disruption of growth centers of the knee

A

Bowlegs
common in children under 2
By 2 they become knock kneed
be concerned if area between the knee is greater than 5-6 inches
Can be associated with Rickettes or Blount dx (early walking or obesity)

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15
Q

Genus valgum (knock knees)

A

lateral angulation of the tibia relative to the femur in the coronal plane, persisting into adulthood
Normal in 30 month old and will generally show spontaneous correction
Excessive (5-6 inches between ankles) persisting in the older child 6-8 years old is abnormal
Tx = bracing

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16
Q

Septic Arthritis=usually involves hip joint

A

source of infection can be anywhere
joint is hot, swollen, impaired mobility
complication=necrosis of femoral head
Dx features=younger than 3, HIGH fevers, ill appearing, refusing to walk

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17
Q

Toxic or transient synovitis

A

limp associated with Upper respiratory dx
low grade fever
child refuses to walk, appears well, decreased internal rotation, normal WBC, ESR <25, blood culture, hip aspiration =neg, x-rays nge, ultrasound of hip = neg (more reliable in detecting fluid)
Tx: resolves in 3-7 days, give ibuprofen
complications 2% will develop Legg-Calve Perthes Disease
position for less pain

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18
Q

Legg-Calve Perthes Disease

A

Develops over time
Usually 4-8 years old (white males)
DX= limp without hip pain, knee pain is referred, loss of internal rotation, loss of abduction, over all decreased ROM
x-ray shows flattening or deformity of femoral head leads to avascular necrosis
TX=decrease activity, surgery if severe
can lead to degenerative hip disease

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19
Q

Salter-Harris System Criteria

A

Type I horizontal fracture through the physis
Type II Fx through the physis, extending into the metaphysis
Type III Fx throu the epiphysis, extending into the physis
Type IV Fx through the epiphysis, physis and metaphysis
Type V crush injury of the physis

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20
Q

Salter-Harris

A

Greenstick=cortex broken on tension side but intact on compression side
Transverse=perpendicular to long axis of the bone
buckle=bone compression causes a buckle or bend rather than break
Spiral=zig-zag course around the bone
oblique=at an angle to long axis of the bone
comminuted=fx with 3 or more fragments

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21
Q

RICEM

A
Rest
ice
compression
elevation
mobility
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22
Q

Cerebral palsy

A

neurological brain disorder
life long condition
affects communication between brain and the muscles, causing permanent state of uncoordiated movement and posturing
result of an episode that cause lack of oxygen to the brain

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23
Q

CP-establish and diagnose that motor deficits are static and nonprogressing (fine and gross motor skills not devleoping)
Can do an MRI or EEG

A

prenatal factors
infections, maternal anoxia, ABO incompatibility)
perinatal factors=anoxia, prolonged labor, resp. obstruction, and others stuff
POSTER: posturing, oropharyngeal problems, strabismus, tone, evolutional responses, reflexesCan be tx with BtA for spacisidy

24
Q

Muscular Dystrophy=genetic, x-linked autosomal recessive degeneration of muscles

A
babies=diminshed reflexes
flat affect
floppy
later they are clumsy, toe-walking
Need to look at their development
25
MD-Creatinine Kinase is elevated | can do a muscle biopsy
Refer to Neuro Referr to PT/OT Refer to First Steps program
26
Hip dysplasia=more common in girls | breech and familial
not sure when it displaces so must check FOR A FULL YEAR!!!! If not caught it affects movility and abnormalities of the femoral head and the acetabelum Get a plain frog leg view or ultrasound
27
Ortolani= (click of entry) 90 degree hip abduction and feel if hip moves smoothly or do you feel a click or clunk abduct the hips 90 with index finger palpate hip joint for clicks, clunks = dislocated femoral head reduced
Barlow=(click of exit) push down and see if you can put joint out of socket one hip at a time-knee flexed and extended Thigh back and out!! Hips are adducted
28
Ortolani and Barlow are used only 6-8 weeks
Galeazzi is noted with the observed discrepancy in knee heights when infant is supine. the sacrum is flat on the table and the knees and hips are bent
29
Pavlik harness is used on infants
worn 3 mos by children 3 mos and younger and older children 4 mos or older a period of double their age. Should be worn 23 hours a day Traction or cast would be next.
30
Refer to Ortho is clunk!!
Click may just be ligament
31
Sports
Repetitive motion is the problem
32
Craniosynostosis
The premature closing of suture lines 2 most common forms: Scaphocephaly (boat head) long and narrow Sagittal suture fuses, Most common. 54-58% Brachycephaly is if the coronal sutures fuse too soon, the head is flattened. 18-29%
33
``` Microcephaly - <2 standard deviations below norm for age, gender and gestational Premature closure of suture line hypoxic encephalopathy congenital infection ```
``` Macrocephaly>2 standard deviations above normal for age, gender and gestation Hydrocephalis enlarged ventricular system megaencephaly-from metabolic conditions 97th percentile and higher ```
34
Plagiocephaly-positional molding | occipital flattening
Ask if it was round at birth teach parents to turn head treat torticollis with stretching orthotic device-helmet
35
Meningitis- late winter, early spring viral=summer and fall.
household or close contacts (individuals who slept and ate in the same household with the patient) and intimate nonhousehold contacts who have had mucosal exposure to the patient’s secretions (such as a boyfriend or girlfriend). Individuals who have had direct exposure to the patient’s secretions through shared utensils or toothbrushes, kissing, and school/daycare contacts in the prior seven days should receive chemoprophylaxis.four or more hours with the index case for 5-7 days before the illness
36
meningitis types- Treat with Rifampin Cipro or rocephin rifampin given in a 600 mg dose for adults, 10 mg/kg every dose for children older than 1 month, 5 mg/kg every dose for neonates (age less than or equal to 30 days) orally every 12 hours for a total of four doses.
``` S. pneumoniae (47%), N meningitidis (25%), ```
37
The article says
Close contact (for more than eight hours) with someone with N. meningitidis infection Contact with oral secretions of someone with N. meningitidis infection
38
Kernig and Brudzinski signs
poorly sensitive but highly specific for bacterial meningitis. K=patient supine flex knee and thigh to 90 degrees pain in the hamstring when leg is extended is a + sign B=flex neck and reflex flexion of the hips is a + sign
39
Meningitis in children-fever, petechial (nipple line & down) or purpural rash on trunk, legs, mucus membranes, flu-like symptoms, classic signs of HA, vomiting, photophobia, nuchal rigidity, full fontanel, poor feeding
A recent history of upper respiratory tract infection is common in children with bacterial meningitis; children are also more likely than adults to experience a seizure.12 The illness course varies, with progression over hours to several days.
40
Suture lines close= 2-3 years Anterior fontanel 15-18 mos Posterior fontanel= 2 mos
Abuse-call CPS and police | ASK; who, what, where, when
41
Primitive reflexes
Something wrong in the brain or CNS
42
Shaken baby syndrome
``` Lethargy / decreased muscle tone Extreme irritability Decreased appetite, poor feeding or vomiting for no apparent reason Grab-type bruises on arms or chest No smiling or vocalization Poor sucking or swallowing Rigidity or posturing Difficulty breathing Seizures Head or forehead appears larger than usual or soft-spot on head appears to be bulging Inability to lift head Inability of eyes to focus or track movement or unequal size of pupils ```
43
`Closed head injuries
No LOC, minor head injury normal mental status, no abnormal findings or focal findings on exam, including fundoscopic, no evidence of skull fx THEN YOU CAN OBSERVE WITH NO CT/SKULL FILMS
44
For LOC<1 minute and neg exam you can still observe or get a cranial CT scan. Skull films and MRI are not recommended
Helmets cut risk for head injury by 80% if worn properly | If worn wrong, then twice as likely to have a head injury
45
Headaches
Tension-like a band around the head. Migraine=pain, n/v, visual changes common vs classic (aura)
46
Brain tumors-Chronic recurrent headaches
worse on wakening may improve with vomiting ``` Variables that predict a presence of a space-occupying lesion include: HA of less than 1 month absence of family hx of migraine abnormal neurological findings on exam gait abnormalities occurrence of seizures ```
47
Neuroimaging study on a routine basis is not recommended in children with recurrent headaches and a normal neurologic examination
Should only be considered with an abnormal neurologic exam or other physical findings that suggest CNS disease
48
Treatment of migraines in children
``` >5 with features from below lasts 1-72 hours bilateral or uni (frontal or temporal) pulsating moderate to severe intensit aggravated by routine physical activities AND n/v photophobia ```
49
Acetaminophen is probably effective
Children <6 ibuprofen is effective and acetaminophen Work on triggers Give antiemetic early for nausea Child must be 12 for migraine triptans A neurologist can give a triptan earlier if he wants. You should refer for this if younger than 12
50
Seizures
chronic that recur without any external disorder REFER Order lab tests based on historic or clinical findings such as vomiting dehydration, or failure to return to baseline alertness
51
Consider toxicology if question of drug use or exposure
In the child with a NONFEBRILE first seizure, LP is of limited value. The EEG is recommended as part of the neurodiagnostic evaluation of the child with an apparent first unprovoked seizure.
52
If a neuro-imaging study is obtained, MRI is the preferred modality.
Consider MRI with a signficant cognitive or motor impairment unexplained abnormalities a seizure of partial onset with or without secondary generalization an EEG that does not represent a benign partial epilepsy of childhood or primary generalized epilepsy in children under 1 year of age
53
Seiaures
medication is typically started after 2 unprovoked seizures Involve neuro and peds monotherapy is the gold standard routine blood tests may actually lead to unnecessary changes and more problems in asymptomatic patients, BUT do if suspect toxicity therapy maintained for two years of seizure free period and then d/c?
54
Psuedo seizure vs true seizure
Psuedo=The EEG may be normal Look for in children who have witnessed a seizure in another, who have seizures that occur in the same situations, does not decrease with anticonvulsants, and whose seizures appear "suggestable" True -Seizure is like epilepsy. Brain activity depolarization of the neurons is widespread
55
NPs and seizures
Discuss safety issues with the parents. Drowning, machinery, careful of being in high places,