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Canadian consensus on osteoporosis. Preventing osteoporosis among postmenopausal women.

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VOL 49: APRIL • AVRIL 2003 Canadian Family Physician Le Médecin de famille canadien 487

Canadian consensus on osteoporosis

Preventing osteoporosis among postmenopausal women

Summarized from a statement of the Society of Obstetricians and Gynaecologists of Canada

T

he Society of Obstetricians and Gynaecologists of Canada has brought together an advisory committee made up of national experts on menopause to assist the Society in reviewing the findings of the Women’s Health Initiative (WHI) study.1 The WHI is a landmark study, the first large combined continuous hormone replacement therapy (HRT) clinical trial to confirm a reduction in inci- dence of osteoporotic fracture. Accordingly, women who choose combined continuous HRT can anticipate protec- tion from osteoporotic fractures.

How should results be applied to patients?

Further analysis of WHI results will help determine specific risk factors to help physicians individualize therapy. Although more than two thirds of women in the WHI study were older than 60 years, there were 5522 women aged 50 to 60 years, more than in any pre- vious study and more than the sum of patients in nearly all previous randomized controlled trials.

Recommendations

• Evaluation of risk of fractures in postmenopausal women should include assessment with bone mineral density measurement for those at increased risk. Central (hip and spine) measurements by dual-energy x-ray absorp- tiometry (DXA) are the most accurate and precise mea- surements of bone density available, making them useful for both risk assessment and follow up. Peripheral bone mass measurements (eg, ultrasound or DXA measure- ments in radius, phalanx, or heel) are useful for assess- ing risk of fracture, but cannot be used for follow-up assessment.

• Physicians should be aware that a prevalent vertebral or nonvertebral fragility fracture markedly increases risk of future fracture.

• Markers of bone resorption, while useful for document- ing group responses in large clinical trials, have no clear place in follow-up evaluation of individual patients.

• Women should be encouraged to take adequate amounts of calcium and vitamin D, to have good nutrition and exercise, and to avoid poor lifestyle habits (smoking, alco- hol). Normal exposure to estrogen during reproductive life, and exercise, contribute to optimal achievement and maintenance of genetically determined peak bone mass.

These recommendations apply to all women; for early postmenopausal women, adequate calcium and vitamin D intake alone is insufficient to maintain bone mass.

• Although combining antiresorptive therapies might be synergistic in increasing bone mineral density, their effect on fracture has not been proven. Combination therapy should be reserved for patients not responding to single-agent antiresorptive therapy.

Summary of key points

• The goal of osteoporosis management is to prevent frac- tures. Treatment could be associated with substantial increases in bone mineral density.

• Postmenopausal bone loss can be prevented effectively by antiresorptive therapy, such as estrogen replacement, selective estrogen receptor modulators, or bisphospho- nate therapy.

• Treatment with alendronate or risedronate has been demonstrated to decrease both vertebral and nonverte- bral fractures, including hip fractures; treatment with ral- oxifene or calcitonin has been demonstrated to reduce vertebral fractures; treatment with estrogen or etidro- nate appears to reduce vertebral fractures. Physicians should consider a range of treatments for osteoporosis.

• According to the WHI study,1 continuous combined HRT was effective at reducing risk of hip fractures (five fewer cases per 10 000 women yearly). Vertebral and other fractures were also reduced.

Reference

1. Writing Group for the Women’s Health Initiative Investigators. Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results from the Women’s Health Initiative randomized controlled trial. JAMA 2002;288:321-33.

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