index cards for chapter 53 osteo
TRANSCRIPT
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What findings can be identified with
the use of a x-ray of the spine?
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X-ray of the spine may demonstrate
a fracture, dislocation, infection,
osteoarthritis or scoliosis.
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Bone scan and blood studies
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disclose infections, tumors, and
bone marrow abnormalities.
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Computed tomography
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useful in identifying soft tissue
lesions adjacent to the vertebral
column
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Electromyogram
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used to evaluate spinal nerve root
disorder
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Osteoporosis
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Chronic metabolic disease, in whichbone loss causes decreased density andpossible fracture
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Osteopenia (low bone mass),
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When osteoclastic (bone resorption) activity is
greaterthan osteoblastic (bone building) activity.Result is decrease bone mineral density
Osteopenia is present when the T scoreis at -1 and above -2.5
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Diagnosis of osteoporosis
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based on Bone Mineral Density testingthat gives a T score.
The T score is a number of standarddeviations above or below the average
BMD. (bone marrow density)Osteoporosis T score is at or lower than
-2.5
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OsteoporosisManifistations
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Normal homeostatic bone turnover is altered and therate of bone resorptionis greater than the rate of bone
formation,
resulting in loss of total bone mass Bone becomes porous, brittle, and fragile, and break
easily under stress
Frequently result in compression fractures of the spine,fractures of the neck or intertrochanteric region of the
femur, and Colles fractures of the wrist
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OsteoporosisRisk factors
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Occurrence of osteopenia and osteoporosis Family history Previous fractures Dietary consumption of calcium Exercise patterns Onset of menopause Use of corticosteroids as well as alcohol, smoking,
and caffeine intake
Small frame/white females
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Classification ofOsteoporosis
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Generalized osteoporosisoccurs most commonly inpostmenopausal women and men in their 60s and 70s
Secondary osteoporosisresults from an associatedmedical condition such as hyperparathyroidism, long-
term drug therapy, long-term immobility(Table 53-1 p
1120)
Regional osteoporosisoccurs when a limb isimmobilized
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Causes of
Secondary osteoporosisDiseases/Conditions
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a. Diabetes mellitusb. Hyperthyroidismc. Hyperparathyroidismd.
Cushing syndrome
e. Growth hormone deficiencyf. Metabolic acidosisg. Female hypogonadismh. Pagets diseasei. Osteogenesis imperfecta
j. Rheumatoid arthritisk. Prolonged immobilizationl. Bone cancerm. Cirrhosisn. HIV/AIDSo. Chronic airway limitation
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Causes of
Secondary osteoporosisCHRONIC USE OF DRUGS
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a. Corticosteroidsb. Heparinc. Anticonvulsants
1. Phenobarbital2. Phenytoin
d. Ethanol (alcohol)e. Drugs that induce hypogonadism (decreased levels of sex hormonef. High levels of thyroid hormoneg. Cytotoxic agenth. Immunosuppressantsi. Loop diuretics
j. Aluminum-based antacids
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Assessmentosteoporosis
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Physical assessment-assess for fall risk, assess for kyphosis Psychosocial assessment-asses for pain, depression, body image Laboratory assessment-assess biochemical markers Imaging assessment
DXA-means of measuring bone mineral density (BMD),assessment for spine and hip
QCT-(measure volumetric bone mineral density)-assesschange in vertebral column. More expensive than DXA
scan
QUS(bone density test using sound waves-test heel, tibia,and patella for osteoporosis
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Osteomalacia
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Loss of bone related to vitamin D deficiency Bone softens because of inadequate deposits of
calciumand phosphorusin the bone matrix Rickets or Vitamin D deficiency in children
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Osteomalacia
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A metabolic bone disease characterized by inadequate bonemineralization
Softening and weakening of the long bonescauses pain,tenderness, and deformities caused by the bowing of bonesand
pathologic fractures
Deficiencyof activated vitamin Dcauses lack of bonemineralization and low extracellular calcium and phosphate
Causes include gastrointestinal disorders, severe renalinsufficiency, hyperparathyroidism, and dietary deficiency (Table
53-3 p 1128)
Assessment-assess GI problems (IBD, etc) The major treatment for osteomalacia is vitamin D
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OsteomalaciaCauses
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a. Vitamin D disturbance1. Inadequate production2. Lack of sunlight exposure3. Dietary deficiency4.
Abnormal metabolism5. Durg therapy1. PHENYTOIN (DILANTIN)2. FLUORIDE3. BARBITURATES
b. Live diseasec. Renal diseased. Inadequate absorption
1. Postgastrectomy2. Malabsorption syndrome
e. Inflammatory bowel diseasef. Chronic kidney diseaseg. Acute tubular disorders
1. Acidosis2. Hypophosphatemia
e. familial metabolic error1. hypophosphatemia
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Comparison of
Osteoporosis to Osteomalacia
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Osteoporosis
a. decreased bone massb. lack of calciumc. osteopenia, fractured. calcium level (low/normal)e. phosphate level (normal)f. parathyroid hormone (normal)g. alkaline Phosphatase (normal)
Osteomalacia
a. demineralized boneb. lack of vitamin Dc. pseudo fractures, Loosers zones, fracturesd. calcium level (low or normal)e. phosphate level (low or normal)f. parathyroid hormone (high or normal)g. alkaline phosphatase (high)
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Pagets Disease of the
Bone
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Chronic metabolic disorder in which bone is excessively broken down andreformed
AKA osteitis deformans Disorder of localized bone turnover Incidence:2-3% of population older than age 50 More common in men and risk increases with aging; familial predisposition has
been noted
Pathophysiology: excessive bone resorption by osteoclasts is followed byincreased osteoblastic activity. Bone structure disorganized, weak and highly
vascular
Patients are at risk for fractures, arthritis, and hearing loss
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Pagets disease
Manifestations
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Clinical Manifestations include skeletal deformities, mild to moderateaching pain, and tenderness and warmth over bones
Symptoms may be insidious and may be attributed to old age or arthritis Most patients do not have symptoms Some do c/o pain. Sites involved are usually hip and pelvis. Described as
aching, poorly defined, deep and worse with pressure. Mostly at night.
Pathologic fracture may be first symptom of disease. One complicationis osteogenic sarcoma
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Osteomyelitis
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Infection of the bone Occurs due to:
Extension of soft tissue infection Direct bone contamination Blood-board spread from another site of infection-this typically
occur in an area of bone that has been traumatized or has
lowered resistance
Causative organisms Staphylococcus aureus (70-80%) Other: Proteus and Pseudomonas species, E. coli
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Benign Bone Tumors
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Often asymptomatic and may be discovered on routine x-ray or asa curse of pathologic fracture.
Classification of tissues: Chrondrogenictumors-from cartilage Osteogenictumors-from bone Fibrogenic tumors-from fibrous tissue; most commonly
found in children
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Bone Tumors
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Primary tumors Benign tumorsare more common and generally are slow
growing and present few symptoms
Malignant-prognosis depends upon type and whether thetumor has metastasized.
Osteogenic sarcoma is the most common, and most often fatal,primary malignant bone tumor
Metastatic bone tumors more common than primary tumors
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Dupuytrens Contracture
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Slowly progressive contracture of
the palmar fascia resulting in flexionof the fourth or fifth digit of the
hand.
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Ganglion
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Round, benign cyst often foundon a wristor foot jointortendon.
Painless when touched but causejoint discomfort.
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Foot disorders
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Mortons neuroma-small tumor grows in a digital nerveof the foot. Pain involves 3
rd-4
thtoesand web between
toes.
Plantar Fascitis-inflammation of tissue involving area ofarch of foot. Severe pain especially when getting out of
bed.
Tarsal tunnel syndrome-pain and numbness in the sole
of the foot. Can be caused by ankle fracture that
compresses the posterior tibial nerve
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Pagets Disease of the
Bone
Key features
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a. Bone and joint pain (may be in single bone)1. Bone is aching2. Poorly described3.
Aggravated by walkingb. Low back and Sciatic nerve pain
c. Bowing of long bonesd. Loss of normal spinal curvaturee. Enlarged thick skullf. Pathologic fracturesg.
Osteogenic sarcoma (bone cancer)h. Flushed/Warm Skin
i. Apathy, lethargy, fatiguej. Hyperparathyroidismk. Goutl. Urinary or Renal Stonesm.
Heart failure from fluid overload