Fractures
Treatment of fractures
Clubfoot
OI
Scoliosis
Legg-Calve Perthes Disease
Hip Dysplasia
Cerebral Palsy
Spina bifida
Muscular Dystrophy
100

This is the reason that fractures heal quicker in children than adults? 

Children have a thicker periosteum and a good blood supply 

100

Expected assessment findings with fractures? 

Pain

crepitus 

deformity 

edema 

ecchymosis

decreased use of the affected area

100

What is clubfoot 

Deformity of the ankle or foot (can be unilateral or bilateral)

100

What is Osteogenesis Imperfecta?

A condition where the bones break easily or have deformity 

Inherited connective tissue disorder 

Can often be mistaken for abuse 

100

What is scoliosis? 

A lateral curve of the spine 

Can also affect the ribs due to the rotation 

100

What is legg-calve-perthes disease? 

Impaired circulation to the femoral head that results in necrosis 

100

What is hip dysplasia? 

Abnormal development of the hip structures 

100

What is Cerebral Palsy? 

A non progressive impairment of motor function, especially that of muscle control, coordination and posture 

100

What is spina bifida? 

A neural tube defect present at birth and is characterized by failure of the osseous spine to close with CNS effects.  

Can affect anywhere from brain/skill to spine

100

What is muscular dystrophy? 

A group of inherited disorders with progressive degeneration of symmetric skeletal muscle groups causing progressive muscle weakness and wasting, which can lead to disability and deformity.

200

Fractures in this area can cause altered bone growth

Epiphyseal plates (growth plates) 

Adults do not have these! 

200

Neuro checks for fractures would consist of what? 

Sensation 

Skin temperature 

Skin color 

Capillary refill 

Pulses 

Movement

200

What are the risk factors for clubfoot? 

Heredity 

More common in males 

200

What are the risk factors for OI? 

Having a parent with OI-MOST COMMON WAY

(autosomal dominant-need only 1 copy of the abnormal gene) 

Can be autosomal recessive (both parents are carriers) but less common 

New mutations are found in(de novo) but not as common 


200

What are the 2 types of scoliosis? 

Idiopathic (typically occurs at puberty) 

Neuromuscular (found with other disorders) 

200

What are the 3 stages of Legg-calve-perthes disease? 

Synovitis

Necrotic 

fragmentation

Reconstruction


200

Who is at higher risk for hip dysplasia? 


firstborn 

Females 

family history

breech

improper swaddling 

joint instability 

oligohydramnios 

LGA 

200

What are the 2 types of Cerebral palsy? 

Congenital (present at birth) 

Acquired (obtained after birth) 

Then the types are broken down into their clinical classifications: 

1. Spastic (80% of the cases) 

2. Dyskinetic (15% of the cases) 

3. Ataxic (5% of the cases) 

200

What are the risk factors for spina bifida? 

Medications

drug use

Maternal malnutrition

insufficient folic acid intake

exposure to radiation/ chemicals

genetic predisposition 

200

What are the risk factors for muscular dystrophy? 

Genetics 

300

X-rays that reveal old fractures can be a sign of what? 

Osteogenesis Imperfecta 

or 

Child abuse 

300

What types of medications do we use for fractures? 

antibiotics 

analgesics 

Opioids

Vaccinations (tetanus) 

300

What are the expected findings for a patient with clubfoot? 

Affected foot is shorter and smaller 

May have an empty heel pad 

May have a visible plantar crease at the mid foot

300

What are the signs and symptoms of OI? 

Multiple bone fractures

blue sclera

early hearing loss

small discolored teeth

300

What are the risk factors for scoliosis? 

Genetics (can run in families) 

Female gender 8-15 years of age 

300

What are the risk factors for Legg-calve-perthes disease? 

2-12 years of age 

males

trauma 

decreased circulation 

Inflammation


300

How do we diagnose hip dysplasia? 

Infants: Physical exam (Barlow and ortolani-can hear clicks and clunks as the hip goes in and out of the hip socket) 

Unequal gluteal folds can be a clue (not diagnostic) 

Ultrasound (if less than 6 months)-the hip is not ossified prior to 6 months and will not show up on X-ray 

xray-over 4-6 months of age 


300

What are some risk factors for Cerebral palsy? 

Prenatal: malnutrition, drug use, genetics, infections, placental insufficiency, bleeding, RH incompatability

Perinatal: infections, sepsis, seizures, preeclampsia, PROM, prolonged labor, premature birth, meconium aspiration, asphyxia 

Postnatal: anoxia to the brain, stroke, cerebral infections, brain injury or trauma 

300

How do we diagnose spina bifida? 

Prenatal ultrasound 

amniocentesis 


300

What are the expected findings for muscular dystrophy? 

Fatigue

muscle weakness

lordosis

delayed motor skills

learning difficulties

Progressive loss of muscle mass

400

There are several types of fractures (14 to be exact).  Name 2 

Bend, buckle, greenstick, transverse, oblique, spiral, growth plate, stress, complete, incomplete, simple/closed, compound/open, complicated, comminuted 

400

Name 4 types of traction

Skin traction 

Skeletal traction

Halo traction

Manual

400

Treatment for clubfoot 

Casting and bracing 

Usually begins pretty early on in the first month of life 

400

How do we diagnose OI? 

Bone biopsy

400

How do we screen for scoliosis? 

Typically done during yearly exams 

Have patient bend over and touch their toes (look for any curvature of the back or uneven hips) 

Can also look at shoulders while standing to see if they are even 

Xrays, CT or MRI 

400

What are the expected findings for Legg-calve-perthes? 

Intermittent PAINLESS limp initially-then progresses to the following: 

hip stiffness 

pain: hip, groin, thigh or knee 

listed ROM (especially abduction/internal rotation) 

shortening of the affected leg (muscle wasting) 

400

What would we see clinically with hip dysplasia? 

asymmetry 

limited hip abduction (affected leg will not move out as far as the other) 

clicking sound 

Widened perineum 

toe walking on 1 foot 

limping 

waddle gait 


400

Expected findings for cerebral palsy 

Motor (choking, poor feedings, tongue thrusting, asymmetric crawl, early hand preference, toe walking)

Reflex (Persistent moro or tonic neck reflex, hyperreflexia)

Posturing (Ridge posture and extremities, scissoring and extension of the legs)

Muscle Tone (arching back, stiff posture, difficult diapering child)

Associating Conditions (vision, speech, or hearing impairments, seizures, cogitative impairments, difficulty meeting developing milestones) 

400

What are the types of spina bifida? 

Spina bifida occulta (defect is below the skin within the spinal column) 

Meningocele (protruding sac containing CSF)

myelomeningocele (protruding sac containing CSF and nerves)

400

How is muscular dystrophy diagnosed? 

Muscle biopsy 

Genetics 

EMG 

500

Risk factors for fractures 

obesity 

poor nutrition 

500

What is the purpose of casting? 

Immobilization and maintaining bone alignment 

500

What is important to teach parents of children with clubfoot? 

Cast care 

Braces/application

Routine appointments for close monitoring 

500

What is the treatment of OI? 

Supportive care-NO CURE

Bisphosphonates (Zometa)-to increase bone mineral density 

Physical Therapy (strengthen muscles) 

Gentle handling 

Surgery (Rodding as needed) to help support long bones 

Bone marrow transplant is investigational 


500

Treatment for Scoliosis 

bracing (usually around 20 degrees) 

surgery (good rule of thumb is about 50 degrees)

Treatment will depend on degree of curvature and the patient's age and the amount of growth that is left. 

500

How do we diagnose this? 

MRI of hip and pelvis 

500

What is the treatment for hip dysplasia? 

Pavlik harness 

Surgery 

Spica casting 


500

How do we diagnose Cerebral Palsy? 

Complete neurological data collection

Metabolic and genetic testing

General movement data collection

MRI

EEG

Ultrasound

500

What physical signs might you expect to see with spina bifida occulta

Dimpling of skin  

Tufts of hair 

Port wine angioma nevi (flat area of pigmentation)


500

What are the complications of muscular dystrophy? 

Obesity (inability to exercise-often wheel chair bound) 

Contractures

Scoliosis

Infection

Respiratory compromise

600

What are some complications you would need to consider when taking care of a patient with a known fracture? 

Compartment syndrome

Embolism (Fat with long bone fractures like tibia, femur or pelvis or pulmonary if the patient is immobilized for a long period of time) 

Osteomyelitis (could the patient have this????))

Infection (teach patients and parents what to watch for with fractures-this is mostly for those that are open)


600

When treating patients with fractures and/or sprains, what is important to teach for at home care? 

(hint: RICE) 

Rest 

Ice

Compression

Elevation 

600

What other 2 disorders are commonly seen with clubfoot? 

Spinabifida

Cerebral palsy 

600

What interprofessional collaboration may be needed with these patients? 

  • Orthopedic provider
  • Dietician
  • Pharmacist
  • Physical therapist
  • Infectious disease specialist
  • Dentist
  • Genetic specialist
600

What is the surgical procedure called to correct scoliosis? 

Posterior spinal fusion 

600

What is the treatment for Legg Calve Perthes Disease? 

Surgical: Osteotomy of hip or femur 

600

What complications might you see in hip dysplasia? 

Osteonecrosis 

600

Complications with cerebral palsy

aspiration 

injury 

Skin integrity

600

What might you see on exam with spina bifida cystic (MYELOMENINGOCELE AND MENINGOCELE) 

Flaccid muscles flaccid paralysis, absent deep tendon reflex  

Lack of bowel control

Constant dribbling of urine or urine overflow

Foot contractures

Spinal curvature abnormalities (scoliosis, kyphosis)

Protruding sac midline of the osseous spine

600

What is the main cause of death in a muscular dystrophy patient? 

Respiratory compromise

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