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Diagnosis and therapy of osteoporosis in geriatric trauma patients: an update

  • Deborah Schray , Ulla Stumpf , Christian Kammerlander , Wolfgang Böcker and Carl Neuerburg EMAIL logo
Published/Copyright: December 22, 2016

Abstract

Demographic changes confront clinicians with an increasing number of orthogeriatric patients. These patients present with comorbidities, which force their surgeons to take into consideration their medical condition. A major risk factor for fractures in orthogeriatric patients is osteoporosis in combination with frailty. To prevent subsequent fractures in these patients, we need to pay attention to adequate osteoporosis treatment in orthogeriatric patients. There is a huge treatment gap. In Germany, 77% of patients with osteoporosis are not treated adequately. Even after fragility fractures, a low percentage of patients receive a specific osteoporosis therapy. Secondary prevention is of great importance in the treatment of these patients. Diagnostics and treatment should be already initiated with the admission to the hospital. Treatment decisions need to be made individually based on the risk profile of the patients. After discharge, it is important to involve the patients’ general practitioners and to follow up on patients regularly to improve their compliance and to ensure adequate therapy. Establishing a fracture liaison service helps coordinating osteoporosis treatment during hospitalization and after discharge. Subsequent fractures can be reduced; therefore, it is an effective service for secondary prevention. The present article provides an overview of how an efficient identification and subsequent treatment of osteoporosis can be achieved in aged trauma patients.

Background

Demographic changes confront clinicians with an increasing number of orthogeriatric patients. Aged trauma patients present with various comorbidities, and these have to be addressed to secure the results of surgical intervention. Thus, fractures associated with a low-energy trauma are frequently the first sign indicating an underlying osteoporosis [1], [2]. Given the high prevalence of osteoporosis in combination with frailty, patients are at a high risk for secondary fractures. Within 5 years after an osteoporotic index fracture, 14.7% of these patients suffer another hip fracture and 32.5% another osteoporotic fracture [3].

Thus, it is crucial to screen orthogeriatric patients for an underlying osteoporosis to initiate adequate therapy, adjust the surgical procedures, and prevent subsequent fractures in these patients.

Epidemiology

In female patients older than 75 years, the prevalence of osteoporosis is 59.2% [4]. Approximately 6.3–7.8 million of German inhabitants are affected by osteoporosis [5]. However, there is a huge treatment gap, as 77% of these patients are not treated adequately [6]. Even after fragility fractures, only 16%–21% of female patients and 3.4% of male patients receive specific osteoporosis therapy [5], [7]. Given the high risk of secondary osteoporotic fractures, prevention is of great importance in the treatment of these patients.

Identification

At a first glance, the identification of patients at risk of osteoporosis appears complicated. However, there are fractures such as thoracic and lumbar vertebral fractures, proximal femur fractures, proximal humerus fractures, and fractures of the distal radius in which the prevalence of an underlying osteoporosis remains high. Osteoporosis was diagnosed in 56.2% of women older than 50 years with fragility fractures and men ages 60 years [4]. Patients with typical osteoporosis-related fractures should be screened for osteoporosis [8].

According to the guidelines for osteoporosis by the Dachverband Osteologie e.V. (DVO) 2014, patients without any fracture should generally be assessed at the age of 70 years in women and at the age of 80 years in men; in high-risk patients, a clarification in younger age might already be useful [9].

When orthogeriatric patients with fractures are admitted to hospital, risk factors for osteoporosis should be assessed by standardized questionnaires. Thus, standardized questionnaires and algorithms based on the osteoporosis guidelines of the DVO 2014 for prevention, diagnostics, and treatment of osteoporosis [9] can help to estimate the risk of a secondary fracture (downloads available at http://www.klinikum.uni-muenchen.de/Klinik-fuer-Allgemeine-Unfall-und-Wiederherstellungschirurgie/de/fach/alterstraumatologie/downloads/index.html). Internationally acknowledged to identify the osteoporosis-associated fracture risk are the FRAX- or Q-factor score [10], [11]. A diagnostic assessment in postmenopausal women and men older than 60 years is recommended as soon as a fragility fracture or an increased risk of fractures is present [12].

Osteoporosis diagnostics

The new guidelines of the DVO 2014 recommend five diagnostic steps to confirm the diagnosis of osteoporosis.

Taking the medical history should already identify risk factors for osteoporosis as mentioned above. The following subjects are important to include in the medical history: tendency to fall, medication (especially glucocorticoids, aromatase inhibitors, and the long-term intake of proton pump inhibitors, which are a potential risk factor still under discussion), and preexisting conditions such as diabetes mellitus, ankylosing spondylitis, chronic obstructive pulmonary disease (COPD), and endocrine disorders (such as hypothyroidism).

Also, a detailed clinical examination helps finding indicators for osteoporosis. Especially, the Tannenbaum phenomenon is common. In addition, a loss of height over 2 cm may indicate further diagnostics [13].

A basic blood testing consists of calcium and phosphate in serum, alkaline phosphatase, γ-glutamyltransferase (γ-GT), creatinine, C-reactive protein (CRP), thyroid-stimulating hormone (TSH), 25-OH-vitamin D3, a serum electrophoresis, and a complete blood count.

Dual X-ray absorptiometry (DXA) is the gold standard to determine bone density. Radiation exposure and costs are relatively small [8]. The lower bone density is, the higher is the risk for osteoporotic fractures [14]. Density measurements of the lumbar spine, femur, and femoral neck are set in relation to bone density values of a normal population (T-value). Treatment is based on the t-value, age of patients, and the individual risk factors. Risk factors, such as glucocorticoid therapy or multiple fractures in the past 3 years, increase the treatment threshold.

According to the DVO 2014 [9], in some cases, bone density scans are not necessary to obtain the diagnosis of an underlying osteoporosis. Thus, in patients having suffered a fragility fracture that shows radiographic signs of an osteoporosis within the spine or proximal femur (i.e. Figures 1 or 2), an underlying osteoporosis can be diagnosed without bone density measurements. Also, multiple low-graded fractures of the vertebral spine, such as a singular grade II impression of the vertebrae according to the Genant classification, go in line with an underlying osteoporosis (Figure 1) [15].

Figure 1: Preoperative CT scan with an atraumatic lumbar vertebral fracture.In this case, the diagnosis of an underlying osteoporosis can be secured without further bone density scans.
Figure 1:

Preoperative CT scan with an atraumatic lumbar vertebral fracture.

In this case, the diagnosis of an underlying osteoporosis can be secured without further bone density scans.

Figure 2: Preoperative X-ray with a pertrochanteric fracture of the proximal femur on the left side.
Figure 2:

Preoperative X-ray with a pertrochanteric fracture of the proximal femur on the left side.

Degenerative changes (i.e. of the spine) can increase the t-value. If, in these cases, bone density scans of the hip cannot be applied, quantitative computed tomography (CT) scans are recommended [16], [17].

Osteoporosis treatment

Vitamin D deficiency is widely spread among elderly patients. It is associated with muscle weakness and therefore with a tendency to fall. Aged trauma patients are at high risk to develop vitamin D deficiency because of malnutrition, reduced sunlight exposure, impaired intestinal absorption, and impaired hydroxylation in the liver and kidneys [18]. In elderly patients with hip fractures, only approximately 10% of the patients have an adequate vitamin D level [19].

Treatment algorithms can be helpful for the decision of the individual osteoporosis therapy (Figure 3).

Figure 3: LMU algorithm for the treatment of osteoporosis.
Figure 3:

LMU algorithm for the treatment of osteoporosis.

Basic treatment aims on a compensation of vitamin D level and a sufficient calcium intake. A balanced calcium homeostasis is required for the initiation of a specific osteoporosis treatment and crucial to secure fracture healing [20].

According to the DVO guidelines, a dose of approximately 1000 IU/day vitamin D is needed to maintain a normal to high vitamin D level. Vitamin D application should be adjusted to the laboratory results (Table 1). A 25-OH-vitamin D level above 75 μg/L is not recommended, as it has been shown to be associated with an increased risk of falls [21].

Table 1:

Vitamin D3 levels and treatment recommendations adapted from Amling [20].

25-OH-vitamin D3 level, mg/LCholecalciferolComments
Severe deficiency<1020,000 IU/day for 10 days then 20,000 IE/weekAdditional tests for calcium metabolism
Distinct deficiency10–2020,000 IU/day for 5 days then 20,000 IE/weekFollow up after 2–3 months
Deficiency21–3020,000 IU/weekFollow up after 2–3 months
Optimal level31–601000–2000 IU/dayMaintain level
Oversupply>100Pause therapyAddressing causes

The intake of calcium should be up to 1000 mg/day. Raising the calcium level can be achieved through diet, for example, with calcium-rich mineral water (about 400 mg/L) or dairy products such as milk, cheese, cottage cheese, or yogurt. During a therapy with glucocorticoids, calcium supplements with a dose of 1000 mg/day calcium are recommended.

As supplement, calcium carbonate is recommended. However, a high percentage of elderly patients have proton pump inhibitors among their daily medication. In these patients, calcium citrate or calcium gluconate is recommended for an adequate resorption of calcium [22].

Depending on laboratory findings, specific therapy can be initiated during hospitalization. Considering contraindications and comorbidities, a specialized physician should initiate specific therapy.

Oral bisphosphonates are the first-line medication in postmenopausal osteoporosis. In patients older than 75 years, alendronate and risedronate show a reduced risk for vertebral fractures [23]. Also, intravenously applied bisphosphonates such as ibandronate or zolendranate show a reduction of vertebral fractures and zolendronate also decreases the total fracture risk.

An intravenous therapy with bisphosphonates should not be started before 14 days after surgery to prevent accumulation around the internal fixation [24]. To avoid hypocalcemia, vitamin D levels should be normal before starting with a specific osteoporosis therapy. In some cases, an intravenous bisphosphonate therapy is recommended 6 weeks after fracture.

Studies show that intravenous therapy with bisphosphonates is not inferior to the therapy with oral bisphosphonates concerning fracture risk. The compliance of the patients might be even higher in monthly intravenous applications than in taking it orally [25], [26].

The osteoanabolic therapy with recombinant parathyroid hormone (teriparatide) is effective but costly. It can be an option when, despite adequate pretreatment, osteoporosis progresses or causes further vertebral fractures. Teriparatide received the recommendation level B of the DVO due to the superior effect compared to alendronate in treating glucocorticoid-induced osteoporosis and reducing peripheral postmenopausal osteoporotic fractures [27].

Depending on the risk profile of the patient, monoclonal antibodies, such as denosumab, are also considered as an option. Studies with denosumab show a reduction of vertebral fractures and peripheral fractures such as proximal femur fractures. Especially, in orthogeriatric patients with limited compliance associated with cognitive disorders such as dementia or patients who refuse taking more oral medication, denosumab offers advantages. Thus, a specific osteoporosis therapy with denosumab, which has to be applied only twice a year, can be secured easily, as it is injected subcutaneously, which could be handled, for example, by the nursing staff and monitored by their general practitioners [28], [29], [30].

Due to the increased risk of thrombosis, strontium ranelate, selective estrogen receptor modulators (SERMs; raloxifene and bazedoxifene), and estrogens (optionally in combination with a progestin) are not suitable for orthogeriatric patients [10], [31].

Calcitonin plays no role in first-line therapy. Only in cases with severe renal insufficiency, it might be applied because other agents are contraindicated.

Prevention

An effective prevention of subsequent fractures includes also fall prevention with muscle training, physiotherapy, and critical adjustment of the preexisting medication.

Training should concentrate on an integration of general movement, improvement of coordination, balance, posture, and flexibility [32].

Medication, which causes vertigo or dizziness, should be reduced [33]. Also, medication that reduces bone quality (e.g. glucocorticoids) or bone healing [e.g. nonsteroidal antirheumatics (NSAR)] should be avoided.

A big problem is also the compliance of these elderly patients. The literature shows that the percentage of compliant patients decreases to 50% over a period of 1 year after initiation of treatment and even to only 30% over time [34]. Women and patients with DXA were more likely to follow their doctors’ instructions, whereas older or multimorbid patients and those with a preexisting high amount of medications are more likely to not continue with their medication.

Secondary prevention via fracture liaison service (FLS) is another additional organization to comanagement to reduce subsequent fractures and postoperative complications. First mentioned in 1999, the “UK National Health Service” in Glasgow, Scotland, established one of the first FLS. Today, clinics can apply to certify through the International Osteoporosis Foundation (IOF) for FLS.

A specially trained fragility fracture nurse is taking care of the coordination of the patients’ treatment after admission to the hospital. Besides identifying patients of high risk and initiation of adequate diagnostics and osteoporosis therapy, the fragility fracture nurse is also monitoring the patients’ compliance after discharge.

This network also increases compliance by close supervision in rehabilitation and outpatient clinics [35], [36].

The rate of subsequent fractures in patients with untreated osteoporosis increases significantly within the first 2 years after the first fracture [37]. Patients with fragility fractures have an increased risk of 86% for subsequent fractures [38]. In patients with vertebral fractures, the risk of another fracture is doubled and after proximal femur fractures even trebled [39]. Recent studies show that establishing an FLS can reduce subsequent fractures by approximately 30%. Axelsson et al. stated that even a minimal resource FLS was effective in increasing investigation and treatment (Figure 4). Patients treated in an FLS setting had a re-fracture risk reduction of 51%. This indicates that an FLS can improve secondary prevention of fractures [40], [41].

Figure 4: Re-fracture rate with and without treatment of osteoporosis in an FLS setting from 2011 to 2014 [40].
Figure 4:

Re-fracture rate with and without treatment of osteoporosis in an FLS setting from 2011 to 2014 [40].

To prevent one re-fracture in 3 years, the number needed to treat (NNT) with FLS is 20 [42]. For the widely spread angiotensin-converting enzyme (ACE) inhibitors and angiotensin receptor blockers (ARBs), the NNT is 80 and 338 over a period of 4.3 years to prevent one myocardial infarction.

Allowing an early initiation of appropriate treatment, the rate of subsequent fracture can be significantly reduced [41], [43]. Another positive effect lays in the reduction of health economic cost [44], [45]. The literature shows that introducing an orthogeriatrician-led or a nurse-led FLS is cost-effective compared to usual care.

Conclusion

The management of orthogeriatric patients should not only focus on the surgical aspects of treatment but also include diagnosis and treatment of an underlying osteoporosis. Decisions should be based on the risk profile of the patients. Treatment is more complicated because of comorbidities limiting the therapy options. It is also difficult to convince these patients to follow through with their therapy even if they have already reached a high age. Therefore, it is important to involve their general practitioners and the patients themselves as an attempt to increase compliance. Thus, precise patient information about their therapy and risk of subsequent fractures is of importance. Especially, aged trauma patients tend to concentrate on their return to daily activities following fracture and neglect the necessity of osteoporosis therapy. Therefore, it is important to follow up on these patients and secure secondary fracture prevention.

FLS is a new approach that can significantly increase the efficiency of osteoporosis treatment by coordinating osteoporosis treatment during hospitalization and after discharge. It helps avoiding subsequent fractures and therefore is an effective service to secure secondary fracture prevention.

Author Statement

  1. Research funding: Authors state no funding involved. Conflict of interest: Authors state no conflict of interest. Informed consent: Informed consent is not applicable. Ethical approval: The conducted research is not related to either human or animal use.

Author Contributions

  1. Deborah Schray: writing of the manuscript. Ulla Stumpf: approval of the manuscript. Christian Kammerlander: approval of the manuscript. Wolfgang Böcker: approval of the manuscript. Carl Neuerburg: revision of the manuscript.

Publication Funding

  1. The German Society of Surgery funded the article processing charges of this article.

References

[1] Johnell O, Kanis J. Epidemiology of osteoporotic fractures. Osteoporosis Int 2005;16(Suppl 2):S3–S7.10.1007/s00198-004-1702-6Search in Google Scholar PubMed

[2] Johnell O, Kanis JA. An estimate of the worldwide prevalence and disability associated with osteoporotic fractures. Osteoporosis Int 2006;17:1726–1733.10.1007/s00198-006-0172-4Search in Google Scholar PubMed

[3] Gibson-Smith D, Klop C, Elders PJ, et al. The risk of major and any (non-hip) fragility fracture after hip fracture in the United Kingdom: 2000–2010. Osteoporosis Int 2014;25:2555–2563.10.1007/s00198-014-2799-xSearch in Google Scholar PubMed

[4] Haasters F, Prall WC, Himmler M, Polzer H, Schieker M, Mutschler W. Prevalence and management of osteoporosis in trauma surgery. Implementation of national guidelines during inpatient fracture treatment. Unfallchirurg 2015;118:138–145.10.1007/s00113-013-2500-4Search in Google Scholar PubMed

[5] Haussler B, Gothe H, Gol D, Glaeske G, Pientka L, Felsenberg D. Epidemiology, treatment and costs of osteoporosis in Germany – the BoneEVA study. Osteoporosis Int 2007;18:77–84.10.1007/s00198-006-0206-ySearch in Google Scholar PubMed

[6] Kanis JA, McCloskey E, Branco J, et al. Goal-directed treatment of osteoporosis in Europe. Osteoporosis Int 2014;25:2533–2543.10.1007/s00198-014-2787-1Search in Google Scholar PubMed

[7] Johnell K, Fastbom J. Undertreatment of osteoporosis in the oldest old? A nationwide study of over 700,000 older people. Arch Osteoporosis 2009;4:17–23.10.1007/s11657-009-0022-zSearch in Google Scholar PubMed PubMed Central

[8] Neuerburg C, Schmidmaier R, Schilling S, et al. Identifikation, Diagnostik und leitliniengerechte Osteoporosetherapie (DVO) unfallchirurgischer Patienten. Unfallchirurg 2015;118:913–924.10.1007/s00113-015-0071-2Search in Google Scholar PubMed

[9] (DVO) DOeV. Osteoporose-Leitlinien 2014. http://www.dv-osteologie.org/DVO_leitlinien/osteoporose-leitlinie-2014.Search in Google Scholar

[10] Kanis JA, McCloskey EV, Johansson H, et al. European guidance for the diagnosis and management of osteoporosis in postmenopausal women. Osteoporosis Int 2013;24:23–57.10.1007/s00198-012-2074-ySearch in Google Scholar PubMed PubMed Central

[11] McGowan B, Kanis JA, Johansson H, Silke C, Whelan B. Development and application of FRAX in the management of osteoporosis in Ireland. Arch Osteoporosis 2013;8:146.10.1007/s11657-013-0146-zSearch in Google Scholar PubMed

[12] Kolios L, Takur C, Moghaddam A, et al. Anamnestic risk factor questionnaire as reliable diagnostic instrument for osteoporosis (reduced bone morphogenic density). BMC Musculoskel Disord 2011;12:187.10.1186/1471-2474-12-187Search in Google Scholar

[13] Baum E, Peters KM. The diagnosis and treatment of primary osteoporosis according to current guidelines. Deutsches Ärzteblatt Int 2008;105:573–582.10.3238/arztebl.2008.0573Search in Google Scholar

[14] Ahmed LA, Emaus N, Berntsen GK, et al. Bone loss and the risk of non-vertebral fractures in women and men: the Tromso study. Osteoporosis Int 2010;21:1503–1511.10.1007/s00198-009-1102-zSearch in Google Scholar

[15] Genant HK, Wu CY, van Kuijk C, Nevitt MC. Vertebral fracture assessment using a semiquantitative technique. J Bone Miner Res 1993;8:1137–1148.10.1002/jbmr.5650080915Search in Google Scholar

[16] Moyad MA. Osteoporosis: a rapid review of risk factors and screening methods. Urol Oncol Semin Orig Invest 2003;21:375–379.10.1016/S1078-1439(03)00140-6Search in Google Scholar

[17] Guglielmi G, Ferrari F, Bazzocchi A. Bone mineral density and quantitative imaging. In: Peh WCG, editor. Pitfalls in diagnostic radiology. Berlin/Heidelberg: Springer, 2015:109–132.Search in Google Scholar

[18] Janssen HC, Samson MM, Verhaar HJ. Vitamin D deficiency, muscle function, and falls in elderly people. Am J Clin Nutr 2002;75:611–615.10.1093/ajcn/75.4.611Search in Google Scholar PubMed

[19] de Jong A, Woods K, Van Gestel L, Suresh M, Porteous M. Vitamin D insufficiency in osteoporotic hip fracture patients: rapid substitution therapy with high dose oral cholecalciferol (vitamin D3). Acta Orthopaed Belg 2013;79:578–586.Search in Google Scholar

[20] Amling M. Calcium and vitamin D in bone metabolism: clinical importance for fracture treatment. Unfallchirurg 2015;118:995–999.10.1007/s00113-015-0104-xSearch in Google Scholar PubMed

[21] Scharla. Therapie mit Vitamin D: gibt es Grenzen? J Miner Stoffwechsel 2014;21:51–55.Search in Google Scholar

[22] Bo-Linn GW, Davis GR, Buddrus DJ, Morawski SG, Santa Ana C, Fordtran JS. An evaluation of the importance of gastric acid secretion in the absorption of dietary calcium. J Clin Invest 1984;73:640–647.10.1172/JCI111254Search in Google Scholar PubMed PubMed Central

[23] Wells GA, Cranney A, Peterson J, et al. Alendronate for the primary and secondary prevention of osteoporotic fractures in postmenopausal women. Cochrane Database Syst Rev 2008:Cd001155.10.1002/14651858.CD001155.pub2Search in Google Scholar PubMed

[24] Eriksen EF, Lyles KW, Colon-Emeric CS, et al. Antifracture efficacy and reduction of mortality in relation to timing of the first dose of zoledronic acid after hip fracture. J Bone Miner Res 2009;24:1308–1313.10.1359/jbmr.090209Search in Google Scholar PubMed PubMed Central

[25] Horikawa A, Miyakoshi N, Shimada Y, Sugimura Y, Kodama H. A comparative study between intravenous and oral alendronate administration for the treatment of osteoporosis. SpringerPlus 2015;4:675.10.1186/s40064-015-1474-9Search in Google Scholar PubMed PubMed Central

[26] Epstein S. Ibandronate treatment for osteoporosis: rationale, preclinical, and clinical development of extended dosing regimens. Curr Osteoporosis Rep 2006;4:14–20.10.1007/s11914-006-0010-9Search in Google Scholar PubMed

[27] Nickolaus B. Osteoporose: Teriparatid bei hohem Frakturrisiko. Dtsch Arztebl Int 2010;107:A-1224.Search in Google Scholar

[28] Hanley DA, Adachi JD, Bell A, Brown V. Denosumab: mechanism of action and clinical outcomes. Int J Clin Pract 2012;66:1139–1146.10.1111/ijcp.12022Search in Google Scholar PubMed PubMed Central

[29] Lewiecki EM, Miller PD, McClung MR, et al. Two-year treatment with denosumab (AMG 162) in a randomized phase 2 study of postmenopausal women with low BMD. J Bone Miner Res 2007;22:1832–1841.10.1359/jbmr.070809Search in Google Scholar PubMed

[30] Cummings SR, San Martin J, McClung MR, et al. Denosumab for prevention of fractures in postmenopausal women with osteoporosis. N Engl J Med 2009;361:756–765.10.1056/NEJMoa0809493Search in Google Scholar PubMed

[31] Ishtiaq S, Fogelman I, Hampson G. Treatment of post-menopausal osteoporosis: beyond bisphosphonates. J Endocrinol Invest 2015;38:13–29.10.1007/s40618-014-0152-zSearch in Google Scholar PubMed

[32] Woolf AD, Akesson K. Preventing fractures in elderly people. BMJ (Clin Res Ed) 2003;327:89–95.10.1136/bmj.327.7406.89Search in Google Scholar PubMed PubMed Central

[33] Kannus P. Preventing osteoporosis, falls, and fractures among elderly people: promotion of lifelong physical activity is essential. Br Med J 1999;318:205–206.10.1136/bmj.318.7178.205Search in Google Scholar PubMed PubMed Central

[34] Gosch M, Kammerlander C, Nicholas JA. Treatment of osteoporosis in older adults. Panminerva Med 2014;56:133–143.Search in Google Scholar

[35] Eisman JA, Bogoch ER, Dell R, et al. Making the first fracture the last fracture: ASBMR task force report on secondary fracture prevention. J Bone Miner Res 2012;27:2039–2046.10.1002/jbmr.1698Search in Google Scholar PubMed

[36] Ganda K, Puech M, Chen JS, et al. Models of care for the secondary prevention of osteoporotic fractures: a systematic review and meta-analysis. Osteoporosis Int 2013;24:393–406.10.1007/s00198-012-2090-ySearch in Google Scholar PubMed

[37] Center JR, Bliuc D, Nguyen TV, Eisman JA. Risk of subsequent fracture after low-trauma fracture in men and women. J Am Med Assoc 2007;297:387–394.10.1001/jama.297.4.387Search in Google Scholar PubMed

[38] Kanis JA, Johnell O, De Laet C, et al. A meta-analysis of previous fracture and subsequent fracture risk. Bone 2004;35:375–382.10.1016/j.bone.2004.03.024Search in Google Scholar PubMed

[39] Black DM, Arden NK, Palermo L, Pearson J, Cummings SR. Prevalent vertebral deformities predict hip fractures and new vertebral deformities but not wrist fractures. Study of Osteoporotic Fractures Research Group. J Bone Miner Res 1999;14:821–828.10.1359/jbmr.1999.14.5.821Search in Google Scholar PubMed

[40] Axelsson KF, Jacobsson R, Lund D, Lorentzon M. Effectiveness of a minimal resource fracture liaison service. Osteoporosis Int 2016;27:3165–3175.10.1007/s00198-016-3643-2Search in Google Scholar PubMed PubMed Central

[41] Nakayama A, Major G, Holliday E, Attia J, Bogduk N. Evidence of effectiveness of a fracture liaison service to reduce the re-fracture rate. Osteoporosis Int 2016;27:873–879.10.1007/s00198-015-3443-0Search in Google Scholar PubMed PubMed Central

[42] Brugts JJ, van Vark L, Akkerhuis M, et al. Impact of renin-angiotensin system inhibitors on mortality and major cardiovascular endpoints in hypertension: a number-needed-to-treat analysis. Int J Cardiol 2015;181:425–429.10.1016/j.ijcard.2014.11.179Search in Google Scholar PubMed

[43] Huntjens KM, van Geel TA, van den Bergh JP, et al. Fracture liaison service: impact on subsequent nonvertebral fracture incidence and mortality. J Bone Joint Surg Am Vol 2014;96:e29.10.2106/JBJS.L.00223Search in Google Scholar PubMed

[44] Yates CJ, Chauchard MA, Liew D, Bucknill A, Wark JD. Bridging the osteoporosis treatment gap: performance and cost-effectiveness of a fracture liaison service. J Clin Densitomet 2015;18:150–156.10.1016/j.jocd.2015.01.003Search in Google Scholar PubMed

[45] Solomon DH, Patrick AR, Schousboe J, Losina E. The potential economic benefits of improved postfracture care: a cost-effectiveness analysis of a fracture liaison service in the US health-care system. J Bone Miner Res 2014;29:1667–1674.10.1002/jbmr.2180Search in Google Scholar PubMed PubMed Central


Supplemental Material:

The article (DOI: 10.1515/iss-2016-0028) offers reviewer assessments as supplementary material.


Received: 2016-10-15
Accepted: 2016-12-08
Published Online: 2016-12-22
Published in Print: 2016-12-01

©2016 Neuerburg C. et al., published by De Gruyter.

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

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