Therapy
| Intervention | Guideline |
|---|---|
| Calcium | NIH Guidelines: If less than 65 years and receiving estrogen, 1000 mg/day; If more than 65 years or not receiving estrogen, 1500 mg/day; Divide doses into 500 mg or 600 mg/dose to improve absorption. |
| Vitamin D | 400-800 IU/day. |
| Fall Prevention Strategies | Review and implement interventions when applicable and possible |
| Evaluate for Secondary | Possible causes are evident from medical history and physical examination, and medications that affect bone, hepatic or renal disease, or malabsorption. Selected laboratory tests include: serum creatinine, alkaline phosphatase, calcium, phosphorous hematologic profile, thyroid-stimulating hormone (for everyone), 24-hr urine for calcium (deficiency in calcium absorption suspected), 24-hr urine free cortisol (signs of Cushing's syndrome), one, 25-dihydroxy serum concentration (if deficiency is suspected) and serum electrophoresis (if multiple myeloma suspected). |
| Estrogen | FDA-approved; doses are the same as those for prevention. 80-85 percent response rate to these doses. Average risk reduction for vertebral fracture is 90 percent. Average risk reduction for hip fracture is 50 percent with long-term use. Give with calcium 1000-1500 mg/day and vitamin D 400 IU. |
| Evista | FDA approved; 60mg/day. 80-85 percent response rate. Vertebral fractures decreaded by 50 percent. No statistically significant decrease in hip fractures. |
| Alendronate | FDA-approved; l0mg/day. 95 percent response rate. Vertebral fractures decreased by 63 percent. Hip fractures decreased by 51 percent. |
| Risedronate | FDA approved; 5mg/day. 95 percent response rate. Vertebral fractures decreased by 65 percent. Hip fractures decreased by 39 percent. |
| Calcitonin | FDA-approved; Nasal: 200 IU daily (alternate nostrils daily); does not treat bone pain. Spinal bone mineral density increased and spinal fracture rate reduced relative to placebo. 76 percent response rate; no data to demonstrate improvement in hip BMD or fracture rates. Injection: 100 IU SQ or IM daily. Give calcium 1500 mg/day and Vitamin D 400 IU/day. May be helpful if woman is unable to take estrogen or alendronate. |
| Anabolic Steroids | Not FDA-approved; (testosterone) No data on fracture prevention. Can cause hirsutism. Avoid in women with elevated LDL-cholesterol or low HDL-cholesterol. |
| Fluoride | Slow-release formulation awaits FDA approval. New vertebral fracture rate reduced by 69 percent. |
| Combination Therapy | Combination therapy with alendronate and estrogen or Alendronate/Estrogen calcitonin and estrogen is not currently FDA approved. Alendronate/Calcitonin Estrogen and testosterone combination showed an Estrogen/Testosterone increase in biochemical markers of bone formation but no data on BMD increase above that of estrogen alone or fracture prevention. |
| Pain Due to Osteoporosis | The only osteoporosis therapeutic agent shown to decrease bone pain is calcitonin injection. Pain is usually due to one of two causes--acute pain after a fracture or chronic back pain due to vertebral fractures. The acute pain is usually treated with immobilization and analgesic agents. Chronic pain may be treated with acetaminophen or NSAIDs. |
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