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Paget's Disease of Bone
Chronic condition of disorganized bone remodeling -> thick, weak bones
Pathophysiology
Excessive osteoclast activity → compensatory osteoblast response → large, disorganized bone with poor strength
Signs and Symptoms
Bone pain (especially pelvis, skull, spine, legs)\
Enlarged or deformed bones
Hearing loss (skull involvement)
Fractures
increased hat size
Risk factors
Male over 50 years old
Genetic predisposition
European Descent
viral Triggers (e.g., paramyxovirus)
Diagnostics
increased ALP (bone isoenzyme)
Normal calcium and phosphate
X-ray: Enlarged bones with thickened cortex
Bone scan: increased uptake in active lesions]
Nursing management
Monitor for fractures, pain, hearing loss
Promote safe mobility
Use assistive devices
Evaluate need for surgery if deformity is severe
Pharmacologic Treatment
Bisphosphonates (e.g., zoledronate): Suppress osteoclast activity
Calcitonin: Inhibits bone resorption
Pain management (NSAIDs, Acetaminophen
Surgical Interventions
🔩 Joint Replacement (Hip/Knee Arthroplasty)
Indication: Severe joint degeneration or deformity due to Paget’s disease
Purpose: Relieve pain and restore mobility with artificial joint
Post-op: Standard arthroplasty care — early mobilization, DVT prevention, physical therapy
🛠 Fracture Repair / Deformity Correction
Indication: Pathologic fractures or limb deformity
Purpose: Stabilizes and corrects abnormal bone architecture
Post-op: Higher bleeding risk due to hypervascular bone → monitor hemodynamics