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Alterations in Musculoskeletal Function: Trauma, Infection, and Disease

Alterations in Musculoskeletal Function

  • Disorders of the Musculoskeletal System:
    • Bone Diseases
    • Diseases of Skeletal Muscle
    • Soft Tissue Injuries

Infections of the Bone: Osteomyelitis

  • Definition: Severe pyogenic infection of bone and local tissue.
  • Pathways of Infection:
    • Bloodstream (hematogenous)
    • Infectious agents reach bone through blood from elsewhere in the body.
    • Adjacent soft tissue
    • Common origins: burns, sinus disease, trauma, malignant tumor necrosis, periodontal infection, infected pressure ulcer.
    • Direct introduction
    • Occurs due to open fractures, penetrating wounds, surgical contamination, or prosthesis insertion.

Risk Factors

  • Common Among:
    • Children under 16 years old (mean age 6)
    • Elderly patients
    • IV drug users
    • indwelling intravascular catheter users
    • Diseases: sickle cell anemia and chronic granulomatous disease.
  • Most common pathogen: Staphylococcus aureus, followed by Streptococcus pneumoniae.

Clinical Manifestations

  • In Children:
    • High fever
    • Localized pain at the bone site
  • In Adults:
    • Fever, malaise, anorexia, night sweats, weight loss.

Healing Complications

  • If untreated:
    • Necrotic bone separates from healthy bone leading to dead segments.
    • Possible outcomes: abscess or chronic infection (Involucrum).

Treatment

  • Duration: 4 to 6 weeks of IV antibiotic therapy.
  • Possible interventions for abscess:
    • Debridement or amputation.
    • Management of chronic osteomyelitis.

Alterations in Bone Mass and Structure: Scoliosis

  • Definition: Lateral curvature of the spine, often S- or C-shaped.

Etiology and Pathogenesis

  • Possible Causes:
    • Idiopathic
    • Congenital disorders
    • Connective tissue disorders
    • Neuromuscular disorders.

Clinical Manifestations and Classifications

  • Symptoms:
    • Asymmetrical shoulders, hips, chest wall.
    • Possible respiratory problems and gastrointestinal dysfunction.

Types of Scoliosis

  • Nonstructural Scoliosis:

    • Resolves when the patient bends to the affected side.
    • No vertebral rotation present.
    • Causes include postural problems and inflammation.
  • Structural Scoliosis:

    • Fails to correct on forced bending.
    • Involves vertebral rotation and deformity.
Key Indicators of Scoliosis
  • Symptoms:
    • Uneven shoulders
    • Rib hump
    • Scapular prominence
    • Uneven hips
    • Lateral deviation of the spine.

Treatment

  • Options:
    • Bracing
    • Exercises
    • Surgical interventions for spinal alignment.

Alterations in Bone Mass and Structure: Osteoporosis

  • Definition: Most common metabolic bone disease; greater bone resorption than formation.

Key Characteristics

  • Disruption in osteoblastic/osteoclastic balance.
  • Decreased mineral and protein matrix results in fragile bones.
  • Factors influencing rate of bone loss:
    • Age
    • Genetics
    • Estrogen.

Risk Factors

  • Common Factors:
    • Family history.
    • Estrogen deficiency.
    • Small body frame.
    • Caucasian or Asian race.
    • Menopause and various diseases.

Clinical Manifestations

  • Symptoms include shortened stature, muscle wasting, back spasms, and kyphosis.

Diagnosis

  • Based on Bone Mineral Density (BMD) by dual energy x-ray absorptiometry (DXA):
    • T score < -2.5 indicates osteoporosis.
    • T score between -1.0 and -2.5 indicates osteopenia.

Treatment Options

  • Calcium and vitamin D supplements.
  • Exercise.
  • Medications:
    • Bisphosphonates
    • Recombinant human parathyroid hormone.

Alterations in Bone Mass and Structure: Rickets and Osteomalacia

  • Definition: Vitamin D deficiency affecting bone matrix mineralization leading to soft osteopenic bone.

Clinical Manifestations

  • Symptoms:

    • Kyphosis
    • Genu valgum (knock knees)
    • Genu varum (bow legs)
    • Bone pain in adults.
  • Rickets: Affects growing skeleton in children.

  • Osteomalacia: Affects mature skeleton in adults.

Etiology

  • Causes include:
    • Inadequate vitamin D, calcium, or phosphorus.
    • Poor vitamin D metabolism.
    • Renal disease.

Treatment

  • Supplementation with vitamin D, calcium, and phosphorus.

Bone Tumors: Multiple Myeloma

  • Most common primary bone tumor, a slowly growing malignancy of bone marrow.

Pathogenesis

  • Neoplastic proliferation of a single clone of plasma cells.
  • Commonly affects kidneys and the immune system.

Clinical Manifestations

  • Symptoms:
    • Predominantly bone pain.
    • Pathologic fractures.
    • Kidney dysfunction and neurologic symptoms.

Diagnosis

  • Presence of homogeneous immunoglobulin in urine and serum.
  • Confirmed by:
    • Bone marrow aspiration and biopsy.
    • Imaging tests.

Treatment

  • Aggressive combination chemotherapy and local radiation.

Diseases of Skeletal Muscle: Muscular Dystrophy

  • Group of genetically determined myopathies characterized by:
    • Progressive muscle weakness.
    • Replacement of muscle tissue with fat and fibrous tissue.
  • Classified by the pattern of inheritance, age of onset, and muscular weakness distribution.

Duchenne Muscular Dystrophy

  • Most common and severe type, inherited as X-linked trait.

Pathogenesis

  • Muscle cells lack dystrophin, leading to muscle necrosis and degeneration.

Clinical Manifestations

  • Symptoms often appear by age 3:
    • Enlarged calf muscles due to fat infiltration.
    • Proximal muscle weakness leading to frequent falls by 5-6 years old.
    • Most patients are wheelchair-bound by age 12-14 and may die by 20.

Treatment

  • Education for patients and families, corticosteroid therapy, and preservation of function.

Myasthenia Gravis

  • Chronic autoimmune disease affecting voluntary muscles.
  • Mechanism: Antibodies block or destroy acetylcholine receptors at the neuromuscular junction, causing muscle weakness.

Risk Factors

  • More common in women than men, peak onset at ages 20-30.

Clinical Manifestations

  • Initial symptoms include painless muscle weakness affecting ocular and cranial muscles and proximal limb muscles; usually improves with rest but worsens with repeated use.

Treatment Options

  • Anticholinesterase inhibitors, corticosteroids, IV immune globulin, plasmapheresis, immunosuppressive agents, and thymectomy if unresponsive to treatment.

Myasthenic Crisis vs. Cholinergic Crisis

  • Myasthenic Crisis: Insufficient medication causing sudden increases in BP and pulse.
  • Cholinergic Crisis: Excessive medication leads to muscle fasciculations, especially around the mouth.

"If you fell down yesterday, stand up today."
H. G. Wells