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Last updated 3:46 PM on 4/15/26
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62 Terms

1
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Define a Electromyelogram (EMG) + purpose

Measure electrical charge associated with muscle contraction → Differentiate muscle vs neurological issues

2
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Define Arthroscopy

Insertion of a lens/camera directly into the joint

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Abnormal calcium, phosphate & parathyroid hormone labs meaning?

Metabolic changes, possibly secondary to renal disease or parathyroid hormone imbalance

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What is Serum CK (creatine kinase)?

Protein that leaks out of damaged muscle cells into body fluids → telling of rhabdo/muscle injury

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Healing process of fractures? (4 steps)

  1. Hematoma forms (bleeding)

  2. Inflammation (fibrin mesh + granulation tissue form)

  3. Soft callus → hard callus

  4. Bone remodeling

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General healing periods for fractures?

  • Kids: ~1 month

  • Adults: 2+ months

  • Older adults: LONG time

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Co-morbidities of impaired bone healing? (5)

  1. Anemia

  1. DM

  2. Nutritional deficits

  3. Glucocorticoids

  4. Nicotine → vasoconstricts

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Define osteomyelitis + relevance

Bone infection → common complication of fractures

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Define Compartment Syndrome + signs?

  • Pressure builds (edema turns inward) → cuts off blood flow (compresses nerves + vessels)

  • Pain + swelling + numbness

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Define Fat Emboli

Fatty marrow escapes into vein → goes to lungs → obstruction, inflammation, and
respiratory distress

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Define nonunion/malunion

Bone doesn’t heal properly

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Define Osteoporosis

  • Decrease in bone mass and density

  • Loss of bone matrix and mineralization

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2 Types of Osteoporosis?

  1. Primary: postmenopausal, senile, or idiopathic

  2. Secondary: develops as a result of another disorder, like Cushing syndrome

14
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Pathophysiology of Osteoporosis? + Precursor?

Pathophysiology: reabsorption of bone by osteoclasts exceeds bone formation by osteoblasts → thin, fragile bones
○ osteopenia → precursor to full osteoporosis

15
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Risk Factor Pattern for Osteoporosis? (10)

  • Aging

  • Female/postmenopausal

  • Low calcium/vit D

  • Sedentary

  • Smoking, caffeine

  • Steroids/Cushing’s

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Key s/s of Osteoporosis? (3)

  • Back pain

  • Kyphosis (“hunchback”)

  • Spontaneous fractures (KEY)

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Diagnostic for Osteoporosis?

  • DEXA scan

  • T-score:

    • Normal: ≥ -1

    • Osteopenia: -1 to -2.5

    • Osteoporosis: ≤ -2.5

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General Treatment for Osteoporosis? (3)

  • Calcium & Vitamin D + protein

  • Weight-bearing exercise

  • Surgery

19
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Prototype Osteoporosis Meds? (2)

Alendronate (Bisphosphonate) & Raloxifene (SERM)

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Alendronate MOA?

Inhibits osteoclast-mediated bone reabsorption

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Alendronate SE/AE? (3)

SE → dyspepsia

AE → HF, esophageal damage

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Nursing considerations for Alendronate? (3)

  1. Must be taken with 8oz water 30 min before other food/fluids

  2. Must remain upright for 30 minutes after taking (esophageal damage)

  3. Also comes with vitamin D for enhanced absorption of calcium

23
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Raloxifene MOA?

Binds to specific estrogen receptors to reduce bone resorption and increase bone mineral density

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Raloxifene SE/AE? (3)

SE → Hot flashes, leg cramps
AE → Increased risk for DVT, PE, & CVA (CLOTS!)

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Nursing considerations for Raloxifene? (2)

  1. Take with calcium and vitamin D to prevent/treat hypocalcemia while on it

  2. Avoid prolonged periods of sitting, especially first 4 months of therapy (clot risk!)

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Pathophysiology of Rickets & Osteomalacia?

Deficit of vitamin D and phosphates required for absorption of calcium → lack of
calcification of cartilage formation → weak bones, deformities, compression fractures

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Rickets vs. Osteomalacia?

Children → Rickets (“bow legs”)
Adults → Osteomalacia

<p><span style="color: rgb(0, 0, 0);">Children → Rickets (“bow legs”)<br>Adults → Osteomalacia</span></p>
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Key causes of Rickets & Osteomalacia? (3)

  1. Poor diet

  2. No sunlight (lack vitamin D)

  3. Malabsorption

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Define Osteosarcoma

Neoplasm in the metaphysis of the femur, tibia, fibula in children and young adults; primarily males

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Define Ewing sarcoma

Neoplasm in diaphysis of long bones, commonly in adolescence

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Define Muscular Dystrophy (MD)

Group of inherited disorders characterized by degeneration of skeletal muscle

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Pathophysiology of MD?

Metabolic deficit of dystrophin (muscle cell membrane protein) → degeneration and necrosis of
the cell → skeletal muscle fibers replaced with fat/fibrous connective tissue & hypertrophic muscle appearance → gradual loss of muscle function

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Key s/s of MD? (3)

  1. Weakness (starts in legs)

  2. Gower’s maneuver

  3. Waddling gait

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Key MD diagnostic?

Elevated CK levels

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Typical outcome of MD?

  • No cure → focus on PT/OT

  • Death (usually by age 20) often from respiratory/cardiac failure (possible ventilation to prolong life)

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Define Osteoarthritis (OA)

“Wear and tear” damage to weight-bearing joints → can be unilateral

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Pathophysiology of Osteoarthritis (OA)?

Weight-bearing joint articular cartilage is damaged from excessive mechanical stress

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Key s/s of OA?

  • Pain with movement

  • Crepitus

  • Heberden’s nodes (DIP joints of hands)

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Treatment for OA?

  1. Minimize stress on joint, ambulatory aids, PT, OT

  2. Pain relief; 1st line medication → Acetaminophen

  3. Celecoxib (NSAID)

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Celecoxib uses? (3)

OA, rheumatoid arthritis, & ankylosing spondylitis

41
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Celecoxib MOA?

Inhibits COX-2, which normally promotes prostaglandin synthesis and inflammatory response (does not inhibit COX-1)

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Key Celecoxib AE? (3)

Tinnitus, bronchospasm, blood dyscrasias

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Nursing consideration for Celecoxib? (1)

Less risk for peptic ulcer/GI bleed than traditional NSAIDs

44
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Define Rheumatoid Arthritis (RA)

Autoimmune disorder → chronic systemic inflammatory disease with exacerbations and remissions; with each exacerbation more damage & additional joints involved

45
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RA genetic factor?

Rheumatoid factor (RF), antibody against immunoglobulin G, is present in the blood of most persons with RA

46
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Pathophysiology of initial onset RA?

Abnormal immune response → Acute inflammation of synovial membrane → Formation of exudate → Typical red, swollen, painful joint (synovitis) → Appears to recover

47
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Pathophysiology of subsequent exacerbations of RA?

Synovitis (inflammation recurs) → Granulation tissue spreads over joint causing “pannus” formation → Pannus releases enzymes that erodes cartilage → Fibrosis of joint space, limited
movement → Ankylosis (joint fixation and deformity)

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Key s/s of RA? (4)

  1. Morning stiffness (improves with movement)

  2. Swollen, warm joints

  3. Fatigue, fever (systemic)

  4. Ulnar deviation

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Medications for RA? (4)

Focus = pain control

  1. High-doses of NSAIDs/aspirin

  2. Celecoxib

  3. Corticosteroids (if severe)

  4. Disease-modifying antirheumatic agents (DMARDs)

    1. Immunosuppressant → methotrexate

    2. Immunomodulator → etanercept

    3. Antimalarials → hydrochloroquine

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Methotrexate MOA?

For RA exact MOA unknown but decreases joint inflammation and damage

51
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Key SE/AE of Methotrexate? (4)

SE → photosensitivity
AE → hepatotoxicity, bone marrow suppression → increased infection risk, gastric ulcers

52
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Nursing considerations for Methotrexate? (5)

  1. Class 1 hazardous drug → double chemo gloves

  2. Teratogenic

  3. Avoid aspirin, NSAIDs, PPIs, and alcohol

  4. Monitor labs (bone marrow suppression, liver function, GI bleeding)

  5. Take folic acid to decrease toxicity risk

53
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Etanercept MOA?

TNFI → inactivates tumor necrosis factor (TNF) which prevents it from attaching to cells synovial fluid in joints → blocked inflammatory reaction

54
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Key SE/AE of Etanercept? (2)

SE → Increased infection risk (blocks inflammation)
AE → Reactivation of latent TB

55
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Nursing considerations for Etanercept? (3)

  1. Give with methotrexate for enhanced effect

  2. Monitor for infection symptoms & CBC

  3. Test for TB before starting and periodically

56
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Define Gout (Gouty Arthritis)

Uric acid and urate crystal deposits in joints → acute inflammatory response; most commonly effects big toe

57
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Most common underlying cause of Gout?

Inadequate renal excretion → hyperuricemia (uric acid is purine metabolism waste product the kidneys excrete)

58
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Define a tophus

Large hard nodule of urate crystals in soft tissue or bone → local inflammation

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Define Ankylosing Spondylitis

Chronic, progressive autoimmune inflammatory condition of sacroiliac (SI) joints, intervertebral spaces, & costovertebral joints

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Pathophysiology of Ankylosing Spondylitis?

Vertebral joints (SI) of lower back become inflamed → calcification/fusion of joints → ankylosis → progression up spine → “poker back” → kyphosis

61
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Key s/s of Ankylosing Spondylitis? (3)

Morning body stiffness relieved by walking, rigid spine, & systemic signs (fever/anorexia)

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Treatment for Ankylosing Spondylitis?

Pain relief with anti-inflammatory meds & maintain mobility