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PatientPlus articles are written by UK doctors and are based on research evidence, UK and European Guidelines. They are designed for health professionals to use, so you may find the language more technical than the condition leaflets.

See also: Osteoporosis written for patients

Osteoporosis is a progressive systemic skeletal disease characterised by reduced bone mass and micro-architectural deterioration of bone tissue. As a result, bone is increasingly fragile and more susceptible to fracture.[1] 

Osteoporotic (fragility) fractures are fractures that result from mechanical forces that would not ordinarily result in fracture. Osteoporotic fractures are defined as fractures associated with low bone mineral density (BMD) and include spine, forearm, hip and shoulder fractures.

For clinicians, managing osteoporosis is a challenge due to conflicting guidelines and as yet incomplete evidence (and therefore guidance) in important areas.

Bone density values in individuals can be expressed in relation to a reference population in standard deviation (SD); when SDs are used in relation to the young healthy population, this measurement is referred to as the T score. A Z score compares bone density to the normal at that age, and a score of -2 indicates bone density below normal for a person of that age.

BMD categories established by the World Health Organization (WHO):

  • Normal: hip BMD greater than the lower limit of normal which is taken as 1 SD below the young adult reference mean (T score ≥-1).
  • Low bone mass (osteopenia): hip BMD between 1 and 2.5 SD below the young adult reference mean (T score less than -1 but above -2.5).
  • Osteoporosis: hip BMD 2.5 SD or more below the young adult reference mean (T score ≤-2.5).
  • Severe osteoporosis: hip BMD 2.5 SD or more below the young adult reference mean in the presence of one or more fragility fractures (T score ≤-2.5 PLUS fracture).

Bone density can be measured by a number of investigative tests but the one most commonly used is dual-energy X-ray absorptiometry (abbreviated to DEXA or DXA). See the 'Investigations' section below for further details.

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  • In England and Wales more than 2 million women have osteoporosis.
  • In England and Wales there are around 180,000 fractures per year due to osteoporosis.
  • 1 in 3 women and 1 in 5 men will have an osteoporotic fracture in their lifetime.
  • Osteoporosis is in general an age-related disease. Bone formation initially exceeds bone resorption but by the third decade this has reversed resulting in a net loss of bone mass. Therefore, bone mass declines with age and this is accelerated for a time in women after menopause. Prevalence of osteoporosis increases markedly with age, from 2% at 50 years to more than 25% at 80 years in women.[1] 

Risk factors for fragility fractures[5] 

Reduced BMD is a major risk factor for fragility fracture.

As well as reduced BMD, a number of other risk factors increase fracture risk. Some do this by increasing the risk of osteoporosis, some are independent risk factors and some work in more than one way. Identification of these risk factors is important as it guides case-finding and treatment.

  • Increasing age (risk increased partly independent of reducing BMD).
  • Female sex.
  • Low body mass (<19 kg/m2) and anorexia nervosa.
  • Parental history of hip fracture.
  • Past history of fragility fracture (especially hip, wrist and spine fracture).
  • Corticosteroid therapy (current treatment at any dose orally for three months or more).
  • Cushing's syndrome.
  • Alcohol intake of three or more units per day.
  • Smoking.
  • Falls and conditions increasing the risk of falls, such as:
    • Visual impairment.
    • Lack of neuromuscular co-ordination or strength.
    • Cognitive impairment.
    • Sedative medication and alcohol.
  • Secondary causes of osteoporosis, such as:
    • Rheumatoid arthritis and other inflammatory arthropathies.
    • Prolonged immobilisation or a very sedentary lifestyle.
    • Primary hypogonadism (men and women).
    • Primary hyperparathyroidism.
    • Hyperthyroidism.
    • Post-transplantation.
    • Chronic kidney disease.
    • Gastrointestinal disease such as Crohn's disease, ulcerative colitis and coeliac disease.
    • Untreated premature menopause (<45 years) or prolonged secondary amenorrhoea.
    • Type 1 diabetes mellitus.
    • Chronic liver disease
    • Chronic obstructive pulmonary disease

Unfortunately, the process that leads to established osteoporosis is asymptomatic and the condition usually presents only after bone fracture. It is important that clinicians be alert to recognise low-trauma 'fragility fractures' (fracture caused by a force equivalent to the force of a fall from the height of an ordinary chair or less).[6] 

Fragility fractures occur most commonly in the spine (vertebrae), hip (proximal femur) and wrist (distal radius). They may also occur in the arm (humerus), pelvis, ribs and other bones.[1] Signs differ according to the fracture site.

See also separate Osteoporosis Risk Assessment and Primary Prevention article.

Diagnosis of osteoporosis

Diagnosis of osteoporosis centres on the assessment of BMD. DEXA is regarded as the gold standard technique for diagnosis. The accuracy at the hip exceeds 90%. Residual errors arise for various reasons. Incorrect diagnosis of osteoporosis can be caused by osteomalacia, osteoarthritis or soft-tissue calcification.

The WHO, the International Osteoporosis Foundation (IOF) and the National Osteoporosis Guideline Group (NOGG) recommend the use of DEXA at the hip for the diagnosis of osteoporosis. Other radiological investigations sometimes used for screening purposes are:

  • Single-energy X-ray absorptiometry (SXA).
  • Digital X-ray radiogrammetry (DXR). DXR is simpler and less time-consuming than DEXA. It can be carried out anywhere where there is the facility to perform a standard radiograph of the hand. It may be used as a screening tool for osteoporosis (for example, following Colles'/other forearm fractures), without the need for additional radiographs.
  • Ultrasonic measurement of bone, usually measured at the heel. This can be used for the assessment of fracture risk or for selection of those in need of DEXA. It is unreliable for diagnosis of osteoporosis and is associated with underdiagnosis.

Consider the following screening blood tests, in patients suffering from osteoporosis, to identify treatable underlying causes and to rule out differential diagnoses (osteomalacia, myeloma):

  • FBC and ESR or CRP.
  • U&E, LFTs, TFTs, serum calcium.
  • Testosterone/gonadotrophins in men.
  • Serum immunoglobulins and paraproteins, urinary Bence-Jones' proteins.

Assessment of fracture risk

Although osteoporosis indicates a high likelihood of fracture, many fragility fractures occur in people with bone density values above the defined level. Measurements of BMD by DEXA at the lumbar spine, femoral neck, total hip and wrist have been shown to predict future fracture occurrence. Peripheral DEXA has some predictive value but less so than measurements at the hip and spine.[7] The use of BMD alone to assess risk, however, has a high specificity but low sensitivity and most osteoporotic fractures will occur in people who do not have osteoporosis as defined by a T score of ≤2.5. Fractures can be better predicted by adding clinical risk factors that contribute to fracture risk independently of BMD. BMD should not therefore normally be routinely measured without the prior use of a risk assessment tool as follows.

The WHO risk calculator available (FRAX®) calculates the ten-year probability of a major osteoporotic fracture in people aged 40-90 (with or without BMD result). The result then leads to a position on a chart of low, intermediate and high risk and subsequent NOGG advice as to the need for treatment.

For UK populations, the QFracture® score may be more appropriate for fracture risk assessment as it was based on UK data.[7][8]It may be used for ages 30-99 and does not include BMD.

NOGG guidelines advocate the use of FRAX®, whilst National Institute for Health and Care Excellence (NICE) guidelines allow for use of either FRAX® or QFracture® but advise FRAX® where BMD is available. Scottish Intercollegiate Guidelines Network (SIGN) guidelines encourage the use of QFracture prior to BMD measurement as a risk calculation tool.

Case finding

There is no national screening protocol for osteoporosis. Guidelines from NOGG, NICE, SIGN and IOF differ, making it difficult for the clinician to choose whom to carry out risk assessments or BMD measurement upon. Broadly, consider a risk assessment in:

  • Those with a history of fragility fracture. Some guidelines suggest this should trigger BMD measurement; others suggest these should be considered for treatment without the need for further assessment.
  • Postmenopausal women with risk factors.
  • Women or men with significant risk factors.
  • Women or men on oral corticosteroid treatment. (Any dose taken continuously over three months or frequent courses. 7.5 mg prednisolone or equivalent per day over three months continuously is considered high dose by NICE and confers higher risk.)
  • All women over 65 and all men over 75 (NICE only).


As osteoporosis is an asymptomatic condition, management is centred on preventing fragility fractures, which are associated with enormous morbidity and mortality.

Treatment for osteoporosis should include not only drug treatment but also advice on lifestyle, nutrition, exercise and measures to reduce falls. Advise on smoking cessation where indicated, and moderation of alcohol intake. Advise regular weight-bearing exercise. Evidence suggests this has a modest but significant effect in improving bone density.[9] 

Ensure adequate calcium intake and vitamin D status, prescribing supplements if required.[10] Dietary calcium may be assessed by one of a number of online tools.[11][12] Elderly people who are housebound or living in a nursing home may be assumed to require vitamin D supplementation. If there is adequate dietary calcium intake of more than 1000 mg/day but a lack of vitamin D, consider prescribing 10 micrograms (400 units) of vitamin D without a full replacement dose of calcium. For people who have a dietary calcium intake of less than 1000 mg/day, prescribe 10 micrograms (400 units) of vitamin D with at least 1000 mg of calcium daily (eg, as two Calcichew D3® tablets - calcium 500 mg, colecalciferol 5 micrograms). There is ongoing research into the safety of calcium supplementation but no risk has been found where calcium is combined with vitamin D and, thus far, evidence suggests combined calcium and vitamin D are more effective than vitamin D alone in preventing fractures.[13] 

Assess for risk of falls and consider referral to a falls prevention service. Consider hip protectors. Reduce polypharmacy, especially sedatives.

The detail in the following two sections reflects NICE guidance. NOGG thresholds do not differentiate between primary and secondary prevention, other than where previous fragility fractures affect the FRAX® score upon which management advice is based. To follow NOGG guidelines on whether to treat or not, simply follow the algorithm following risk calculation in the FRAX® link above. Once the FRAX® risk has been calculated, your patient will be placed in a category on an intervention chart which will advise on subsequent management (low risk: lifestyle advice; intermediate risk: measure BMD and recalculate risk; high risk: consider treatment).

Further management in postmenopausal women who have never had an osteoporotic fragility fracture (primary prevention)[2] 


  • The first-line bisphosphonate is usually alendronate on the basis of cost.
  • Bisphosphonate treatment is only recommended in postmenopausal women aged under 65 with confirmed osteoporosis but without fragility fractures, if they have an independent clinical risk factor for fracture and at least one additional indicator of low BMD.
  • Start bisphosphonates in osteoporotic women without fragility fracture once they reach age 65 if they have any independent clinical risk factor for fracture, or over the age of 70 if they just have an indicator of low BMD.
  • The responsible physician may decide a DEXA scan is not required in women aged 75 years or older who have two or more independent clinical risk factors for fracture or indicators of low BMD.

Second-line treatments (risedronate and etidronate) may be considered if the patient is aged over 65 and unable to take alendronate:

Primary prevention - T-score treatment threshold for second-line treatment in patients without previous fragility fracture
AgeIf T score not available When alendronate not an option, treat with risedronate or etidronate at these values or worse
Risk factors = family history, alcohol >3 units/day or rheumatoid arthritis
  No fracture risk factors1 fracture risk factor2 fracture risk factors
65-69Refer for DEXANot recommended-3.5-3.0
70-74Refer for DEXA-3.5-3.0-2.5
75 or olderRefer for DEXA unless over 75 and 2 risk factors-3.0-3.0-2.5

Denosumab is a monoclonal antibody that reduces osteoclast activity (and hence bone breakdown) which is given by six-monthly subcutaneous injections. It may be a suitable option in women who are unable to comply with instructions for alendronate and either risedronate or etidronate.

Primary prevention - T-score treatment threshold for denosumab treatment in patients without previous fragility fracture[14]
AgeNumber of independent clinical risk factors for fracture
Parental history of hip fracture, alcohol intake of 4 or more units per day and rheumatoid arthritis
 No fracture risk factors1 fracture risk factor2 fracture risk factors
65-69not recommended-4.5-4.0
75 or older-4.0-4.0-3.0

Strontium ranelate is also licensed for the prevention of osteoporotic fractures in postmenopausal women with osteoporosis. The European Medicines Agency (EMA) has advised that it only be used where other medications are not tolerated and there are few cardiovascular risk factors.[15] In other situations the risks of treatment may outweigh the benefits. It should only be prescribed by specialists and for people with severe osteoporosis and high fracture risk.

Raloxifene is not recommended as a treatment option for the primary prevention of osteoporotic fragility fractures.

Further management in postmenopausal women who have had an osteoporotic fragility fracture (secondary prevention)[6] 

Bisphosphonates. Start first-line bisphosphonate (usually alendronate on the basis of cost) and consider calcium and vitamin D supplementation. If the initial alendronate is not tolerated or is inappropriate, or there is an inadequate response, the next step depends on BMD, age and risk factors:

Secondary prevention - T-score treatment threshold for second-line treatment in patients with previous fragility fracture
AgeIf T score not availableWhen alendronate not an option, treat with risedronate or etidronate at these values or worse[2]
Risk factors = family history, alcohol >3 units/day or rheumatoid arthritis
  No fracture risk factors1 fracture risk factor2 fracture risk factors
50-54Refer for DEXANot recommended-3.0-2.5
55-59Refer for DEXA-3.0-3.0-2.5
60-64Refer for DEXA-3.0-3.0-2.5
65-69Refer for DEXA-3.0-2.5-2.5
70-74Refer for DEXA-2.5-2.5-2.5
75 and overDEXA may not be required (see any local guidelines)-2.5-2.5-2.5

Raloxifene. If second bisphosphonate is not an option, treat with raloxifene at these thresholds:

Secondary prevention - T-score treatment threshold for third-line treatment in patients with previous fragility fracture
Threshold for treatment with raloxifene
Risk factors = family history, alcohol >3 units/day or rheumatoid arthritis
Age0 risk factors1 risk factor2 risk factors
50-54Not recommended-3.5-3.5
75 and over-3.0-2.5-2.5

If raloxifene is not an option, consider referral to secondary care for assessment for teriparatide, strontium or denosumab:

Strontium consideration comes with the same warnings as per the section above on primary prevention.

Denosumab may also be a treatment option for the secondary prevention with increased risk of fractures in patients who cannot comply with the special instructions for administering alendronate, risedronate or etidronate, or have an intolerance or a contra-indication to those treatments.[14]

Teriparatide is a recombinant fragment of parathyroid hormone prescribed in secondary care. It may be considered if the woman is:

  • Unable to take or has a contra-indication to or intolerance of alendronate and an alternative bisphosphonate.
  • Proven to have an unsatisfactory response to a bisphosphonate.
  • 65 or older with:
    • A T score of -4 SD or below; or 
    • A T score of -3.5 SD or below plus a history of more than two fractures.
  • 55-65 with a T score of -4 SD or below plus a history of more than two fractures.

Osteoporosis in men and premenopausal women[7][16] 

Treatment for men is less well evaluated and researched and not as extensively covered by guidelines. Management would normally be undertaken in secondary care. Alendronate, risedronate, zoledronic acid, teriparatide and strontium are approved for the treatment of osteoporosis in men. Osteoporosis is more likely to be related to a secondary cause in men, so investigation for an underlying cause is important.

Hormone replacement therapy (HRT) has an unfavourable risk-benefit ratio for older postmenopausal women but may be used for the prevention and treatment of osteoporosis in women with premature menopause or in younger postmenopausal women who have symptoms of menopause.

Further notes on pharmacological treatments[10] 

There have been no head-to-head trials of the treatment options for osteoporosis, so it is not known which is most effective.

Bisphosphonates are the mainstay of treatment. Bisphosphonates act by inhibiting the action of osteoclasts. They are, however, poorly absorbed and need to be taken separately from food. They may cause oesophageal irritation and should be taken by the patient sitting up with plenty of water. Etidronate was the first but has been superseded by the more powerful alendronate and risedronate, both of which can be taken daily or weekly, and the newer ibandronate that can be taken monthly. Less frequent dosing may improve adherence to therapy. All bisphosphonate trials have been controlled for calcium/vitamin D and so bisphosphonates have usually historically had calcium/vitamin D co-prescribed. This practice, however, is less clear in light of more recent concerns about calcium supplementation, and if there is evidence of adequate dietary calcium and adequate vitamin D status, it is probably best avoided.

Zoledronic acid (Aclasta®) is the most potent bisphosphonate, given by a single intravenous infusion once a year, and licensed for the treatment of postmenopausal osteoporosis and osteoporosis in men. It is very expensive compared with oral formulations.[17] 

The main adverse effects/concerns relating to bisphosphonates are:

  • Gastrointestinal adverse effects.
  • Poor adherence to treatment (partly due to complex instructions about taking them - the tablet is taken first thing in the morning on an empty stomach with a large glass of water. The person should be sitting upright or standing when the tablet is taken and must not lie down, eat or take other oral medication for at least 30 minutes afterwards (60 minutes for ibandronate). Most are taken on a weekly basis).
  • Osteonecrosis of the jaw.
  • Atypical femoral fractures.
  • Possible increased risk of atrial fibrillation and oesophageal cancer (evidence currently inconclusive and suggests an association rather than cause).[7] 

Raloxifene, a selective oestrogen receptor modulator (SERM), reduces postmenopausal bone loss and reduces vertebral fractures but, like HRT, may increase the risk of venous thromboembolism. Unlike HRT, however, it decreases the risk of breast cancer (oestrogen-positive tumours) but may exacerbate hot flushes. The Commission on Human Medicines (CSM) has advised that HRT should not be considered as first-line therapy for long-term prevention of osteoporosis, due to the increased risk of breast cancer and cardiovascular disease.

Parathyroid hormone peptides are given by subcutaneous injection daily for a maximum of two years (course not to be repeated).[18] Evidence of efficacy exists for vertebral but not hip fractures. Expense restricts their use. They may be considered as an alternative for men or women in whom alendronate and either risedronate or etidronate are contra-indicated or not tolerated, or where treatment with one of these options has been unsatisfactory (another fragility fracture and a decline in BMD despite treatment for one year)

  • Teriparatide (recombinant 1-34 parathyroid hormone) (Forsteo®).
  • Parathyroid hormone (the full 1-84 parathyroid hormone peptide) (Preotact®).

Where fractures have occurred, these are managed in accordance with relevant guidance. Treatment of fractures is discussed in the related separate articles Femoral Fractures, Wrist Fractures, etc.

Recently, surgical procedures for the treatment of vertebral compression fractures have been approved by NICE. Compression fractures cause:

  • Pain and morbidity associated with high doses of analgesia.
  • Loss of height.
  • Difficulty breathing.
  • Loss of mobility.
  • Gastrointestinal symptoms.
  • Difficulty sleeping.
  • Symptoms of depression.

Management aims to reduce these problems and options include:

  • Analgesia.
  • Back braces.
  • Physiotherapy.
  • Percutaneous vertebroplasty - Injection of bone cement into the vertebral body.
  • Balloon kyphoplasty - inflation of a balloon-like device into the vertebral body to restore its height, followed by injection of bone cement.

NICE advises the latter surgical options only in those with severe pain despite conservative measures, and where it has been confirmed that the pain is due to the fracture. A 2015 Cochrane review cast doubts on the benefits of these procedures.[21] 

One of the currently difficult areas for primary care clinicians managing people with osteoporosis is to know how to monitor treatment and when to stop it. There is no consensus on how often BMD should be measured for individuals on treatment; guidelines generally suggest between 2 and 5 years.

Bisphosphonates bind to bone mineral and inhibit osteoclastic bone resorption. Continual bone remodelling is important in maintaining a healthy skeleton by repairing microdamage, and there has been a theoretical concern that prolonged treatment could potentially have a weakening effect on bone. Furthermore, the bisphosphonates are retained in bone for some time after treatment is stopped, and the effects can continue for months or years after treatment has been stopped. Add to this the fact that the risk of serious adverse effects increases with length of treatment, and it is clear why the concept of a "drug holiday" has been introduced.

Unfortunately, however, there is not yet any evidence that a drug holiday reduces adverse effects, and it is not yet known at what point or for how long this break should occur.

It is clear, however, that there should be a review of the need for treatment vs the risks at some point, and this is mostly agreed to be after around five years. Where risk factors have changed (steroid treatment discontinued, for example, or T score above -2.5), this becomes a simple decision; however, in the majority of cases it is not so straightforward.

At this time, NOGG has the most clear algorithm to help determine whether to continue treatment at this point. They advise:

Review after five years of bisphosphonate treatment (three years for zoledronic acid).

  • If there have been recurrent fractures:
    • Check adherence.
    • Exclude secondary causes.
    • Reconsider treatment choice.
    • Continue treatment.
  • If no fractures, remeasure BMD and FRAX®:
    • If T score at femoral neck ≤-2.5 or above NOGG intervention threshold:
      • Check adherence.
      • Exclude secondary causes.
      • Reconsider treatment choice.
      • Continue treatment.
    • If T score at femoral neck >-2.5 or results are below NOGG intervention threshold, consider a drug holiday. Repeat BMD and FRAX® in two years.

Generally the following are likely to need to continue treatment at five years:

  • Those aged 75 years or more.
  • Those who have previously sustained a hip or vertebral fracture.
  • Those on continuous oral glucocorticoids in a dose of 7.5 mg/day prednisolone or equivalent.
  • Those who have had one or more low-trauma fractures during treatment, after exclusion of poor adherence to treatment (for example, less than 80% of treatment has been taken) and after causes of secondary osteoporosis have been excluded. In such cases the treatment option should be re-evaluated.
  • Those in whom the total hip or femoral neck BMD T score is ≤-2.5 SD.

When treatment is discontinued, reassess fracture risk after two years, or earlier if a fragility fracture is sustained.

Osteoporotic fragility fractures can cause substantial pain and severe disability, often leading to a reduced quality of life, and hip and vertebral fractures are associated with decreased life expectancy.

Hip fracture nearly always requires hospitalisation, is fatal in 20% of cases and permanently disables 50% of those affected; only 30% of patients fully recover. Surgery carries risks of complications. Fixation failure is more likely to be a problem in osteoporotic bone.

Vertebral fractures are often undiagnosed. They are associated with long-term pain and disability. One study found a year after the event, four out of five people with vertebral fracture still had significant pain and loss of quality of life.[23] One vertebral fracture increases a patient's risk of sustaining another vertebral fracture five-fold - 20% of these within a year.

Osteoporotic fractures in general cause severe pain and disability to individuals who sustain them, at an annual cost to the NHS of over £1.73 billion.

Further reading & references

  1. Osteoporosis: assessing the risk of fragility fracture; NICE Clinical Guideline (August 2012)
  2. Alendronate, etidronate, risedronate, raloxifene and strontium ranelate for the primary prevention of osteoporotic fragility fractures in postmenopausal women (amended); NICE Technology Appraisal Guidance, January 2011
  3. International Osteoporosis Foundation
  4. Osteoporosis - Prevention of fragility fractures; NICE CKS, June 2015 (UK access only)
  5. Guideline for the diagnosis and management of osteoporosis in postmenopausal women and men from the age of 50 years in the UK; National Osteoporosis Guideline Group (updated 2014)
  6. Alendronate, etidronate, risedronate, raloxifene, strontium ranelate and teriparatide for the secondary prevention of osteoporotic fragility fractures in postmenopausal women; NICE Technology Appraisal Guidance, January 2011
  7. Management of osteoporosis and the prevention of fragility fractures - A national clinical guideline; Scottish Intercollegiate Guidelines Network - SIGN, (March 2015)
  8. QFracture®-2013 risk calculator
  9. Howe TE, Shea B, Dawson LJ, et al; Exercise for preventing and treating osteoporosis in postmenopausal women. Cochrane Database Syst Rev. 2011 Jul 6;(7):CD000333. doi: 10.1002/14651858.CD000333.pub2.
  10. Poole KE, Compston JE; Bisphosphonates in the treatment of osteoporosis. BMJ. 2012 May 22;344:e3211. doi: 10.1136/bmj.e3211.
  11. Dietary Calcium Calculator; International Osteoporosis Foundation
  12. Rheumatological diseases unit: Calcium Calculator; Institute of Genetics and Molecular Medicine (IGMM), University of Edinburgh
  13. Avenell A, Mak JC, O'Connell D; Vitamin D and vitamin D analogues for preventing fractures in post-menopausal women and older men. Cochrane Database Syst Rev. 2014 Apr 14;4:CD000227. doi: 10.1002/14651858.CD000227.pub4.
  14. Denosumab for the prevention of osteoporotic fractures in postmenopausal women; NICE Technology Appraisal Guidance, October 2010
  15. Strontium ranelate: cardiovascular risk. Drug Safety update; GOV.UK. March 2014
  16. Osteoporosis Clinical Guidelines for prevention and treatment - Executive Summary; National Osteoporosis Guideline Group (NOGG) 2014
  17. Summary of Product Characteristics (SPC) - Aclasta® 5 mg solution for infusion; Novartis Pharmaceuticals UK Ltd, electronic Medicines Compendium, May 2015
  18. British National Formulary; NICE Evidence Services (UK access only)
  19. Vertebral fractures - vertebroplasty and kyphoplasty, NICE Technology Appraisal Guidance, April 2013
  20. Dionyssiotis Y; Management of osteoporotic vertebral fractures. Int J Gen Med. 2010 Jul 21;3:167-71.
  21. Buchbinder R, Golmohammadi K, Johnston RV, et al; Percutaneous vertebroplasty for osteoporotic vertebral compression fracture. Cochrane Database Syst Rev. 2015 Apr 30;4:CD006349. doi: 10.1002/14651858.CD006349.pub2.
  22. Maraka S, Kennel KA; Bisphosphonates for the prevention and treatment of osteoporosis. BMJ. 2015 Sep 2;351:h3783. doi: 10.1136/bmj.h3783.
  23. Suzuki N, Ogikubo O, Hansson T; The prognosis for pain, disability, activities of daily living and quality of life after an acute osteoporotic vertebral body fracture: its relation to fracture level, type of fracture and grade of fracture deformation. Eur Spine J. 2009 Jan;18(1):77-88. doi: 10.1007/s00586-008-0847-y. Epub 2008 Dec 12.

Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. EMIS has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.

Original Author:
Dr Hayley Willacy
Current Version:
Peer Reviewer:
Dr John Cox
Document ID:
1613 (v31)
Last Checked:
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