Osteoporosis is a systemic skeletal disease defined by reduced bone mineral density (BMD) and microarchitectural deterioration, increasing the risk of fractures.1,2 It is a major public health issue, affecting millions of Australians over 50 years of age. The condition is largely asymptomatic until a fracture occurs, leading to underdiagnosis and undertreatment.1
Fractures related to osteoporosis, particularly hip and vertebral fractures, are associated with increased mortality and morbidity, loss of independence and quality of life. There is insufficient evidence to recommend population-based systematic screening with BMD measurement for reduction of osteoporotic fractures in Australia, and case-finding is recommended, including with the use of a fracture risk assessment tool, particularly the Fracture Risk Assessment Tool, FRAX®.
A comprehensive list of non-modifiable and modifiable risk factors for osteoporosis can be found here.
Risk factors1,2
All postmenopausal women and men > 50 years old should undergo a risk factor assessment for osteoporosis even in the absence of fracture
Risk factors include:
non-modifiable factors, eg age ≥70 years, parent with hip fracture or other types of minimal trauma fracture
lifestyle factors, eg smoking, low muscle mass, immobility
certain comorbid conditions, eg early menopause, rheumatoid arthritis, hypogonadism, coeliac disease
medications that cause bone loss, eg glucocorticoids, aromatase inhibitors
Patients at very high risk include those with DXA T-score ≤ -3.0 and:
recent fracture within 2 years, and/or
history of 2 or more minimal trauma fractures, and/or
clinical risk factors (see above), and/or
FRAX risk of major osteoporotic fracture (MOF) ≥30% (ie involving vertebra, hip, humerus, and forearm) or hip risk ≥4.5%
Bone mineral density (BMD) assessment should be measured at a minimum of two sites, including the lumbar spine and hip1
DXA is the gold standard for diagnosis of osteoporosis and is used to guide treatment
WHO definitions for postmenopausal women and men >50 years old:
normal BMD: T-score ≥ -1.0
osteopenia: T-score between -1.0 and -2.5
osteoporosis: T-score ≤ -2.5 at the femoral neck
severe osteoporosis as defined by the International Osteoporosis Foundation: T-score ≤ -2.5 and history of at least one fragility fracture3
Patients at very high risk: refer to bone specialist for treatment.
Patients who have sustained a minimal trauma fracture:
at hip or vertebra: commence treatment with a provisional diagnosis of osteoporosis; DXA may be performed to monitor BMD but not necessary for initiating treatment
at site other than hip or vertebra: refer for DXA
if T-score ≤ -1.5, commence treatment
if T-score > -1.5, investigate other causes of fracture
Patients at risk with no history of fracture:
with non-modifiable or lifestyle factors:
perform FRAX assessment and refer for DXA if ≥10%
if DXA T-score ≤ -2.5, commence treatment
if DXA T-score between -1.5 and -2.5, recalculate FRAX to account for T-score and treat only if MOF risk ≥20% or hip fracture risk ≥3%
with comorbidities or medications known to increase osteoporosis risk:
perform DXA and treat or calculate FRAX as per algorithm for non-modifiable or lifestyle factors above
Review the flowchart for osteoporosis risk assessment, diagnosis, and management here.
Calcium and vitamin D:1
1300 mg/day for women >50 years
1000 mg/day for men 50-70 years
1300 mg/day for men >70 years
adequate calcium intake should be ensured, preferably through diet.:
consider calcium supplementation for all frail older patients, and in patients on osteoporosis treatment with inadequate dietary calcium
vitamin D supplementation (800-1000 IU/day) is recommended in frail older patients, and for individuals with serum 25 hydroxyvitamin D < 50 nmol/L
Protein intake of 1.0-1.2 g/kg body weight can improve bone and muscle health1
Exercise can reduce fracture risk:1
weight-bearing impact exercises (eg, walking, dancing) should be done most days
resistance training (at least twice per week) is crucial for maintaining muscle strength and reducing falls
Proactive falls risk assessment and fall prevention strategies based on risk, including:1
physiotherapy referral for tailored exercises targeting balance, gait, and strength
education on falls prevention
medication review
foot health and footwear
appropriate vision correction
Bisphosphonates (oral alendronate, risedronate, or IV zoledronic acid):1
for primary prevention of vertebral fractures from osteopenia in women >10 years postmenopause
to reduce fractures in postmenopausal women and men >50 years at high fracture risk
most common adverse effects are gastrointestinal; atypical fracture of the femur is rare, as is medication-related osteonecrosis of the jaw; consider dental review prior to treatment
upper GIT disorders (eg, Barrett’s oesophagus or ulcers) are contraindications
reassess need for therapy after 5–10 years if T-score ≥ -2.5 and no recent fractures
Denosumab:1
alternative to bisphosphonates in men and postmenopausal women at high fracture risk
administered as subcutaneous injection
avoids gastrointestinal adverse effects found with biphosphonates
therapy should not be abruptly stopped - transition to a bisphosphonate is necessary to prevent rebound fractures
Romosozumab:1
an osteoanabolic agent recommended for very high-risk patients as first-line therapy
administered with monthly subcutaneous injection
contraindicated in patients with history of stroke or myocardial infarction due to increased cardiovascular risk
note this is the most recent addition to pharmacological therapies for osteoporosis (PBS listed in 2021), so evidence is limited
conditional PBS approval requires a consultant physician to initiate this medication
Menopausal hormone therapy (MHT):1
consider oestrogen replacement therapy in women within 10 years of menopause for osteoporosis prevention but requires careful risk-benefit assessment
selective oestrogen receptor modulators may be considered, if at risk of vertebral fracture and other agents not tolerated, particularly in younger postmenopausal women with personal or family history of breast cancer
Recombinant human parathyroid hormone (teriparatide) is reserved for patients with very high fracture risk or those experiencing fractures despite antiresorptive therapy1
recurrent or multiple fractures despite adequate treatment (may require first-line osteoanabolic therapy)1
BMD T-score ≤ -3 and patient is taking glucocorticoids, or has multiple risk factors indicating imminent or very high fracture risk1
atypical femoral fractures in patients on long-term bisphosphonates (may require reassessment of biphosphonate therapy)1
symptoms suggestive of secondary osteoporosis, such as unintentional weight loss, gastrointestinal disorders (e.g., coeliac disease), or hormonal disorders (e.g., hyperthyroidism).
concurrent chronic kidney disease2
osteoporosis post-transplant2
Adjust monitoring frequency depending on fracture risk or other risk factors
Reassess fracture risk, medication side effects, and therapy adherence every 6–12 months for patients on pharmacological therapy
Repeat DXA to reevaluate risk and/or monitor response to treatment:
for patients with osteoporosis, prior to modifying pharmacological therapy or if a new minimal trauma fracture is sustained while on treatment
aim to use the same instrument to enhance comparability of results
regular DXA scans may help to improve patient compliance with therapy
for patients not on pharmacotherapy, consider repeating scans after minimum 2 years to reliably detect BMD change; however, in high-risk patients, consider annual scans
Bone turnover markers may be used in specialist settings to assess treatment efficacy
RACGP, Healthy Bones Australia. Osteoporosis management and fracture prevention in postmenopausal women and men over 50 years of age. 2024. (last accessed March 2025).
Therapeutic Guidelines. Osteoporosis and minimal-trauma fracture. 2024. (last accessed March 2025).
International Osteoporosis Foundation. Diagnosis. 2025. (last accessed April 2025).
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