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25 Cards in this Set

  • Front
  • Back
1) Fracture (Fx)
o Complete fx’s (though the bone): transverse (right angel to bones long axis), spiral (bone has been twisted), comminuted (broken in several pieces),
o Incomplete fx


Incompletefx (doesn’t go through skin
greenstick
greenstick (bone fragments still partially joined)
o Named fx: collie’s,Potts, Boxer’s

potts fracture- ankle fractures


collies fracture- lower end of the radius in the wrist


boxer- fracture in the hand

• Vessel/nerve damage leading to ischemia
secondary to trauma or casting (aggressive or early casting) Always do neurovascular assessment Can be severe
• Infection of bone
- especially with open fractures = osteomyelitis; can occur secondary to trauma or form soft tissue spread Ulcers/bed sores can cause bone infection
• Compartment syndrome
increase inflammation/pain, ischemia which leads to necrosis Each bone has compartments
• Fat emboli
secondary to escaping marrow going to veins then lungs  Yellow marrow or fat tissu
• Non-union

diagnosis,


treatment

 Bones are no knitting or stabilized – bones have movement at site

o Diagnosis- x-ray, MRI, CTo


Treatment- immobilization 6-8 weeks

• Subluxation
- is an incomplete or partial dislocation of joint or organ• Treatment- reduction
Sprain vs. Strains
tendon and ligament slowly heals – muscle heals very well because its vascular• Sprain- torn ligament or other soft tissue• Strains- overuse/stretching of soft tissue (muscle, tendon, ligament)• Treatment- symptoms, immobilize (to prevent pain), surgery
• Osteoporosis
- decrease bone mass/density, decrease matrix/mineralization (calcium)

- o Bone reabsorption (osteoclast) are greater than bone formation (osteoblast)


-

factors and treatment of osteoporosis

o Factors Age (after menopause): much more common in females than males due to decreased estrogen – produced by follicular cells – can take hormone replacement treatment (HPT) to reduce osteoporosis – happens in men but in less effect/degree• Ovarian cycle – changes occur in ovary within 28 day period Decrease mobility: happen when get older or paralyzed Hormonal- decrease estrogen, increase PTH and glucocort• Parathyroid hormone stimulates osteoclasts due to hyperparathyroidism  Dietary- decrease Calcium, Vitamin D, and protein Smokingo Treatment- diet, hormones, fluoride, and exercise
• Rickets/osteomalacia
secondary to decrease Vit D/PO42o Body cannot absorb calcium or vitamin Do Rickets = child; osteomalacia = adulto Secondary to diet, malabsorption, decrease sun exposureo Signs- decrease calcification leading to weak/soft bones causing bow legs, and decrease height – sometimes facial deformityo Treatment- diet
• Paget’s Disease- osteitis deformans
o Excessive bone destruction, replacement w abnormal bone/fibrous tissue, increase thickening of long bones (vertebrae, pelvis, skull)

- o Pathological fractures (occurs when a bone breaks in an area that is weakened by another disease process eg infection, tumors etc.), kyphosis (abnormal rearward curvature of spin; “hunchback”), head ach, cardio vascular diseaseo Progressive; > 40yrs; genetic/viral?

• Bone tumors
- most malignant; primary, or secondary from breast/prostate

-

o Primary tumor

- secondary

o Primary tumor – originates in bone

- secondary – originates somewhere else

o Osteosarcoma
in metaphysis of femur, tibia, fibula – generally involves long bones
o Ewing’s sarcoma
in diaphysis (main or midsection shaft of long bone) (teens); with bone mets leads to lungs, bone pain (higher at night), pathological fractures
• Muscular Dystrophy (MD)
- several types, inherited, progressive; Duchenne’s/most common

- o Duchenne’s = x-linked recessive – heterozygous males mainly – homozygous females are fairly uncommono


Signs- skeletal muscle degeneration, secondary to decrease dystrophin = (large structural protein found in small amounts in plasma membranes of muscle fiber) leading to weakness and eventually respiratory failure.o Skeletal muscle replaced w/ fat, D.F.C.T. (scar tissue) which leads to pseudohypertrophy (excessive growth; abnormal enlargement due to increase in the size of the cells – area where muscle is attacked most)



• Fibromyalgia
- painstiffness of muscle/tendon ligament

- o No inflammation, no degeneration, no physical evidence/changeso Signs – fatigue, depression, patient may have history of trauma, stress Treatment – heat, NSAID’s, SSRI’s (selective serotonin reuptake inhibitors), physical therapy modalities SED rate – non-inflammatory blood test

• Osteoarthritis (OA

and S&S

- aka Degenerative Joint Disease (DJD)

- o Secondary to erosions of articular (hyaline) cartilage from wear and tear (age), or injury; non-inflammatory,


- o Signs – pain with use or in a.m., decrease ROM (range of motion), crepitus (crackling or popping sound – can also feel ), osteophytes (small, abnormal bone growth), narrowing of joint space (one of the hallmark signs)

• Rheumatoid arthritis (RA)
- autoimmune which leads to synovitis (antibodies vs synovial)

- ncrease inflammatory with pain and joint destruction which leads to ankylosis (bones forming single unit/stiffening and immobility of joint; 2 bones fusing together)


-  Still’s disease – juvenile R.A., increase systemic effects

• Gouty arthritis
- secondary to hyperurcemia (high concentration of uric acid in the blood) which leads to uric acid crystals (like needles) deposit in joints leading to increase pain/inflammation

- o Single join involvement

• Ankylosing spondylitis
= chronic progressive inflammatory condition of (attacks/involves): sacroiliac, intervertebral, costoverterbal joints leading to fibrosis then calcification (fusion) of joints

- igns- rigidity/kyphosis of spine, decease lung expansion