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Investigation and management of osteoporosis in aged trauma patients: a treatment algorithm adapted to the German guidelines for osteoporosis

Journal of Orthopaedic Surgery and Research volume 12, Article number: 86 (2017) Cite this article

Abstract

Background

Osteoporosis-associated fractures are of increasing importance in trauma surgery. Systematic diagnostics and treatment of osteoporosis during a hospital stay, however, remain inadequate. Therefore, a specific algorithm for diagnosing and treating osteoporosis in trauma surgery patients was developed based on the DVO (German Osteology Society) guideline for osteoporosis from 2014.

Methods

In a first step, the individuals’ age and risk profile for osteoporosis is identified considering specific fractures indicating osteoporosis and risk factors assessed by a specific questionnaire. In addition, physical activity, risk of falls, dietary habits and the individuals’ medication are considered. Basic osteoporosis laboratory tests, a bone densitometry by dual-energy X-ray absorptiometry (DXA) and, if needed, X-rays of the spine are carried out to identify prevalent vertebral body fractures.

Results

Based on the treatment algorithm adapted to the new guidelines for osteoporosis in the majority of proximal femoral fractures, treatment of osteoporosis could already be indicated without prior DXA. In case of preexisting glucocorticoid therapy, a history of previous fractures or other risk factors according to the risk questionnaire, the threshold of treatment has to be adjusted given the table of T-scores.

Conclusions

The treatment algorithm for diagnosing and treating osteoporosis in in-patient trauma surgery patients can help identify high-risk patients systematically and efficiently. As a result, osteoporosis-associated fractures or failure of osteosynthesis could be reduced, yet a prospective validation of the algorithm has to be completed.

Background

Osteoporosis is a frequent underlying disease in elderly patients with fractures following low-energy trauma which is often identified too late or not at all, and therefore, trauma surgeons play a key role in the investigation and management of the disease.

Manifest osteoporosis leads to limited life expectancy and quality of life. Osteoporotic fractures are often accompanied by the loss of independence. The prevalence of osteoporosis in female patients >75 years old is estimated at 59.2% [1]. It is assumed that in the Federal Republic of Germany 6.3–7.8 million people suffer from osteoporosis [1, 2]. Up to 27% of the patients have already suffered a fracture. Patients who have had multiple fractures run an 85% risk of suffering another fracture within a year if not treated with drugs [3]. However, only 21% of osteoporosis patients in Germany receive guideline-oriented treatment [1]. A possible explanation for inadequate diagnostics and treatment of osteoporosis is certainly the increasing complexity of a guideline-oriented procedure. The DVO guideline creates transparency in view of the increasingly complex scientific evidence. Adapted to the current osteoporosis guideline of the DVO (Dachverband Osteologie = German Osteology Society) from 2014 [4], a diagnostics and treatment algorithm for treating inpatients in trauma surgery has been developed in order to eliminate the deficit in treatment. This algorithm has been developed to make use of existing scientific evidence pragmatically in trauma surgery on a daily basis. The aims of this algorithm are to improve on the one hand the deficit in diagnosing osteoporosis as an underlying disease in trauma patients and, on the other hand, to reduce the deficit in treatment of osteoporosis as a systemic skeletal disorder to reduce following osteoporotic fractures.

Methods

Identification of patients related to osteoporosis

Patients with fracture

In general, a distinction has to be made between patients with and without fractures typical of osteoporosis (thoracic and lumbar vertebral fractures, proximal femoral fractures, proximal humerus fractures and distal radius fractures) [5]. Additional clarification is advisable in female patients >50 and male patients >60 years old who have already suffered a fracture indicating osteoporosis. In a previous examination of trauma surgical patients with such a fracture, osteoporosis was established in 56.2% of women >50 and 59% of men >60 years old [6].

Patients without fracture

It is always important to establish whether women >70 and men >80 years old are suffering from osteoporosis, whereas for younger patients, this only makes sense if there are specific risk factors (DVO guideline 2014). Specific risk questionnaires are a reliable and cost-effective method of determining the individual risk [7]. The individual risk of fractures can be determined reliably from the evidence-based risk factors. The FRAX and the Q-Fracture score, for example, are internationally accepted means for calculating osteoporosis-associated risks of fractures [8, 9]. The risk model of the DVO represents a further means for calculating the risk of fractures. We developed a risk questionnaire based on this (Fig. 1). The yes/no questions are clearly comprehensible for any patient and offer only one possible answer. Once one of the questions is answered by “yes”, the risk profile is assumed to be positive and it has to be established whether the patient is suffering from osteoporosis or not. In a later step of the algorithm, the risk profile is taken up again and will influence the therapeutic decision based on the T-score determined by dual-energy X-ray absorptiometry (DXA) (if necessary, the treatment threshold has to be raised by +0.5). In addition, individual physical activity, risk of falling, dietary habits and current medication will be included. In clinical practice, this enables the doctor in charge to decide individually how to diagnose and treat osteoporosis in a time-saving and cost-effective way.

Fig. 1
figure 1

Osteoporosis risk questionnaire

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Diagnostics of patients related to osteoporosis

Evaluation of basic laboratory tests

The first step of the entire diagnostic process leading to the diagnosis of osteoporosis is the laboratory diagnostics (Fig. 2). As the decrease in bone density in terms of secondary osteoporosis may be caused by hitherto unknown co-morbidities or changes in the metabolism, it is important to establish the most important risk factors that can be identified in a laboratory [10]. In addition to that, basic laboratory tests contribute to checking important contraindications for medical treatment. Table 1 shows a list of important co-morbidities caused by specific changes in laboratory findings.

Fig. 2
figure 2

Osteoporosis diagnostic algorithm

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Table 1 List of most important causes related to changes in laboratory findings, according to the DVO guideline 2014 [4]
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Indication of vertebral body fractures

Vertebral body fractures are a common sign of osteoporosis. Prevalent vertebral fractures are associated with high risk of impaired function and additional fractures. Due to static changes such as kyphosis and the shortening of the affected vertebral sections, they may cause numerous clinical symptoms and syndromes [11], like progressive kyphosis of the thoracic spine (“dowagers hump”), the loss of height >4–10 cm and typical skin folds appear that run down the back laterally to the flanks, referred as “fir tree phenomenon”. Often spinal compression fractures occur clinically asymptomatically and without previous trauma. They account for 11–15% of osteoporotic fractures [12]. As a result, the risk of further vertebral body fractures increases considerably [13]. Furthermore, degenerative changes in the vertebral column and vertebral fractures have a significant influence on bone densitometry by DXA, as such changes may lead to an incorrectly high bone densitometry [14, 15].

Since up to 75% of vertebral fractures do not come to clinical attention at the time of their occurrence, spine imaging with X-ray is required for their detection. For vertebral fracture assessment on standard lateral spine radiographs, the Genant semiquantitative method is used as the gold standard [16]. With this method, vertebral fractures can be graduated from 0 (normal) up to III (severe). Form and extent (loss of height) of the fracture were characterized. Multiple vertebral body fractures I° (Genant) or singular vertebral body fractures II–III° (Genant) in female patients >50 and male patients >60 years old need specific medical treatment, independent of the bone density measured by DXA according to the DVO guideline 2014. In this respect, the morphology of the vertebral column plays an important part in diagnosing and treating osteoporosis. Therefore, the synopsis of clinical signs of vertebral fractures and the severity of vertebral fractures according to Genant play a very important role in our algorithm to start immediately a specific treatment of osteoporosis.

Fractures of the femoral neck or pertrochanteric fractures

Proximal femoral fractures as femoral neck fractures and pertrochanteric fractures are diagnosed by radiography. For characterization of femoral neck fractures, the classification of Garden is frequently used. Pertrochanteric fractures are classified by the AO/OTA classification. As indicated in the osteoporosis algorithm, there is a specific link for “proximal femoral fractures”: according to the published draft of the DVO guideline 2014, the indication for specific medical treatment of osteoporosis was set for all patients with fractures of the femoral neck and a T-score <−2 as well as for those with a low-trauma pertrochanteric fracture (independent of the T-score). This indication for treatment of osteoporosis was reduced in the subsequently adopted version of the DVO guideline 2014 and replaced by the statement that treatment is generally indicated even without measuring bone density in typical radiological and/or clinical aspects of proximal femoral fractures [4]. In the authors’ opinion, however, the above mentioned femoral fractures have a significant relevance as a diagnostic criterion for the initiation of osteoporosis treatment, because of the high risk of mortality associated with these, the high risk of follow-up fractures and the influence on the quality of life connected with that [17].

This criterion was nevertheless taken up in the algorithm, because it helps to significantly facilitate the start of the treatment of osteoporosis in trauma surgical practice (Fig. 2). Osteoporosis treatment with drugs initiated after a proximal femoral fracture is accompanied by a significant reduction in new fractures and optimised survival [18]. The Working Group Geriatric Traumatology of the German Society for Trauma Surgery (AG Alterstraumatologie der Deutschen Gesellschaft für Unfallchirurgie) predicts that the number of proximal femoral fractures will rise dramatically by 351% by 2050 due to demographic development [19]. This estimate underlines the importance of ascertaining the diagnosis for osteoporosis mentioned above.

Bone densitometry

The definition of Osteoporosis by the World Health Organisation (WHO) is characterized by using a densitometric definition based on areal bone mineral density measured with DXA [20]. Due to this and solid data, low costs and a low level of exposure to radiation, bone densitometry by DXA is still used as the gold standard for analysing bone density [21]. A decrease in bone density raises the risk of an osteoporotic fracture [22]. Data for bone density in the area of the lumbar column (lumbar column body 1–4) and of the proximal femur collected during that process are compared with the data for bone density in a standard control group (i.e. T-score). Together with the age of the patient and the individual risk factors, this score forms the basis for the decision for a specific osteoporosis treatment. DXA as diagnostic part can be found in our algorithm at different points: important for a pragmatic approach is from our point of view that there are two important fractures (vertebral fractures and proximal femoral fractures) where the diagnosis osteoporosis is clear and a specific medication can be started without initial DXA as diagnostic part.

Risk factors relevant for treatment

A large number of risk factors have significant influence on the bone metabolism and the development of osteoporosis. In addition to the risk factors for the decision for a specific osteoporosis treatment already mentioned above, medical treatment with glucocorticoids should also be considered; the risk of suffering an osteoporotic vertebral body fracture during this treatment is significantly increased [23]. Therefore, specific medical treatment is already indicated when the T-score is ≤−1.5 and when treated daily with 7.5 mg prednisolone (see Fig. 2 for T-score chart).

Individual fracture anamnesis is also of considerable relevance for the risk of suffering further fractures [24]. According to the DVO risk calculation, this risk factor leads to a raising of the treatment threshold by means of the T-score by +1.0. Other risk factors may also lead to a raising of the treatment threshold by +0.5 and are therefore to be collected consistently using the risk questionnaire mentioned above (Fig. 1) in order to make an individual identification of osteoporosis according to the attached T-score chart (Fig. 2) possible.

Treatment of osteoporosis

After having detected risk patients by means of our risk questionnaire and having diagnosed osteoporosis according to our algorithm, specific treatment of the osteoporosis is initiated (Fig. 3). A negative impact on the healing of fractures caused by anti-resorptive treatment by bisphosphonates cannot be proved [25, 26]. Ingrowth of prostheses (also cemented ones) [27, 28] is supported by anti-resorptive treatment. There are clinical studies that show that the osteoanabolic treatment of fractures with teriparatide has a positive influence on the healing process [29, 30].

Fig. 3
figure 3

Osteoporosis treatment algorithm (adapted from Schray D et al. 2016 [51])

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If there are any questions concerning treatment strategies for complex osteological issues or for patients with a serious course of the disease, we have an osteological team constantly available for consultation by the colleagues on the ward in our clinic.

When choosing a drug for specific treatment of osteoporosis, the specific registration for the relevant indication and the lack of contraindications must be considered. The basis for this is the latest expert information.

Basic treatment

According to the guidelines of the DVO, the basic treatment stays the intake of 1000 mg calcium/day via nutrition, supplemented by 800–1000 IU vitamin D/day as a maintenance dose.

Vitamin D deficiency

A 25-hydroxy-vitamin D concentration in the serum <50 nmol/l or <20 ng/ml is accompanied by a moderately increased risk of proximal femoral fractures and non-vertebral fractures in elderly men and post-menopausal women [29,30,31,32]. The osteologically recommended range for adequate treatment is a serum level of 30–150 ng/ml (75–375 nmol/l) [33,34,35,36]. The synthesis of vitamin D3 in the skin under the impact of UV-light decreases with age, which is due to less exposure to sunlight and a reduction in the functioning of the skin [34, 37, 38]. Because there is a high proportion of elderly and very old people as patients in trauma surgery and geriatric traumatology and because it is by definition a question of manifest osteoporosis (with previous fracture), we generally recommend that the 25-hydroxy-vitamin D level in this group of patients be initially checked, in accordance with the DVO decision in individual cases. Studies show that only 7% of patients with a proximal femoral fracture have a sufficient 25-OH-vitamin D level.

If hypovitaminosis D (with secondary hyperparathyroidism) is proved, we recommend compensation with 20,000 IU Dekristol/week along with serum-calcium check-ups until the 25-OH-vitamin D level is in the desired area mentioned above (and the iPTH has normalised). High-dose treatment with a single administration of 50,000 IU vitamin D is accompanied by a higher risk of falling and fracture [39, 40].

It is important not to forget that vitamin D is a liposoluble vitamin that needs fat from nutrition for adequate resorption. Therefore, we recommend that it is taken with a meal or thereafter to avoid soberness.

Calcium supplementation

Calcium is found not only in milk and dairy products. A good basis for a diet with a sufficient supply of calcium for the patients is mineral water rich in calcium, containing approximately 400–500 mg of calcium. This is also possible on a trauma surgery ward. It should be possible to manage about 1000 mg of calcium in combination with a balanced diet containing vegetables, herbs and dairy products such as yoghurt, hard cheese and curds. Of course, there are situations when this is not possible (lactose or other intolerances). Then, an adequate and individual supplementation with calcium is necessary; thus, a total calcium intake of 1000 mg calcium per day is recommended following either supplementation or nutritional intake or a combination thereof. If treated with glucocorticoids, a supplementation with 1000 mg calcium/day is generally recommended.

Patients who have to ingest a proton pump inhibitor (PPI) permanently are a special case. Instead of calcium carbonate, calcium gluconate or calcium citrate is to be administered. For the elderly (>65 years), the long-term intake of a PPI in particular means a higher risk of falling and therefore a higher risk of fracture-associated in-patient treatment [41], decreased trabecular bone mineral density [42], as well as a significantly increased risk of vertebral fractures and hip fractures [43]. Therefore, the indication for PPI treatment and the risk-benefit ratio are to be regularly checked.

Specific medical treatment of osteoporosis

Strontium ranelates, SERMs (selective oestrogen receptor modulators: ralixofene, bazedoxifene) and a hormone replacement therapy (HRT) with oestrogens (possibly in combination with a gestagen) are not suitable for use (initiation of specific medical treatment) on a trauma surgical ward due to a poor risk benefit ratio, e.g. risk of thrombosis associated with oral HRT. The recommended drugs for the treatment of osteoporosis are listed in Tables 2 and 3.

Table 2 Approval status of selected drugs for specific treatment of osteoporosis
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Table 3 Overview of the treatment efficiency of specific osteoporosis treatment for post-menopausal women [4]
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Oral bisphosphonates

For the intake of oral bisphosphonate patients have to be able to sit up straight for 30 min, renal function has to be sufficiently good (GFR >30 ml/min) and the expected compliance has to be high.

Before initiating anti-resorptive treatment it is essential to look at the patient’s dental chart or at the condition of the jaws (pressure sores) if the patient has dentures. It is recommended that the dentist be informed about the treatment. Regular visits to the dentist for check-ups are also recommended [44].

If it is decided to initiate anti-resorptive treatment with an oral bisphosphonate during a hospital stay, the combination with a proton pump inhibitor (PPI) such as omeprazole is problematic. The resorption rate in the stomach is already very low to start with and is significantly reduced or made impossible by the administration of a PPI [45]. In view of currently available studies, we in this case recommend risedronate 35 mg/week [46, 47].

It is possible to administer 150 mg p.o. of the oral bisphosphonate ibandronate once a month.

The intake frequency must also be considered in terms of compliance; the lower the intake frequency, the better the compliance tends to be [48].

IV-bisphosphonate

Bisphosphonates that are injected intravenously may be used when the enteral administration of bisphosphonates is not possible (see above). This requires a GFR >30 ml/min.

Zoledronate (5 mg/year) and ibandronate (3 mg/3 months) are available for this. Zoledronate has been proved to reduce the fracture rate and mortality significantly [49]. This is only true, however, after a time interval of 2 weeks after the operation of a proximal femoral fracture. At this point, patients with an uneventful postoperative course are usually no longer on a trauma surgery ward. From an osteological point of view, it also makes sense to wait with the administration of an iv-bisphosphonate until 6 weeks after a fracture.

Teriparatide

Teriparatide (rhPTH 1–34: shortened, recombined form of the human parathormone (1–84)) is an osteoanabolic osteoporosis treatment method that leads to the (re-) augmentation of bone substance and that can reconstruct the micro-architecture of the bone. The osteoanabolic effect (stimulation of proliferation and differentiation of osteoblasts) is achieved by the single application of a small dose of 20 μg teriparatide per day (preferably in the evenings) and, always at the same time, administered subcutaneously by the patients themselves. Contraindications are hypercalcaemia or severe renal insufficiency, Paget’s disease or primary or secondary hyperparathyroidism. Teriparatide is restricted to a maximum treatment duration of 24 months.

Especially from a trauma surgical point of view, the osteoanabolic mechanism of action of teriparatide has on the whole a big advantage compared to anti-resorptive drugs. However, due to its high price and the complex use (daily subcutaneous administration by the patients themselves after a hospital stay), it is not a first choice drug. In a serious course of manifest osteoporosis, teriparatide is definitely to be considered and it has therefore been implemented in our in-patient algorithm.

Denosumab

The activity of RANKL on the surface of osteoclasts is specifically inhibited by the high affinity and specificity of denosumab, a fully human, monoclonal antibody of the immunoglobulin-isotype IgG2 that is applied subcutaneously (60 mg/6 months). Denosumab inhibits the binding of RANK-ligands to RANK (surface of osteoblasts) and therefore provides a therapeutic approach in the treatment of osteoporosis and other diseases with loss of bone mass.

It is not necessary to adjust the dose of denosumab for patients suffering from renal dysfunction. Other advantages are the easy subcutaneous administration every 6 months and the lack of febrile reactions in contrast to iv-bisphosphonates. Before the beginning of treatment, the calcium-serum level has to be standard. Patients are to undergo a consistent treatment with calcium and vitamin D. Patients suffering from severe renal dysfunction (Creatine Clearance <30 ml/min) or patients needing dialysis have a higher risk of hypocalcaemia. Severe vitamin D deficiency in particular can predispose patients to get severe symptomatic hypocalcaemia. That is why we recommend checking the level and balancing out the vitamin D deficiency before treatment with denosumab; therefore, an analysis of the calcium level at 7–10 days following treatment with denosumab should be considered; additionally, the cost of denosumab has to be mentioned (Table 4) and considered individually.

Table 4 Daily treatment costs of the specific medicinal treatment of osteoporosis
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Results and discussion

Osteoporosis-associated fractures are of increasing importance in trauma surgery. They can be accompanied by significant morbidity and mortality for the patients concerned. In Germany, only a small percentage of patients suffering from osteoporosis receive treatment according to [1, 50]. Algorithms for diagnosing and treating osteoporosis suitable for daily use in traumatology can contribute to improving the deficit in the comprehensive treatment of the disease as well as potentially reduce osteoporosis-associated fractures and avoid failures with regard to the fracture fixation. Based on the current guidelines of the DVO for diagnosing and treating osteoporosis, an algorithm for the diagnosis and treatment of trauma surgical in-patients has been developed. The specific requirements according to DVO guidelines to diagnose osteoporosis are laboratory diagnostics, clinical examinations and conducting a DXA. The differences of our algorithm are that according to the specific requirements for patients, who already gained osteoporotic fractures of the proximal femur or multiple vertebral body fractures I° (Genant) or singular vertebral body fractures II–III° (Genant), the diagnosis osteoporosis can be found with laboratory and radiographic diagnostics and clinical examination. This proceeding allows to start a specific treatment of osteoporosis meanwhile the surgical in-patient treatment. A pilot phase in our clinic showed that training nursing staff how to use the algorithm means significant relief for the doctor in charge. On the basis of the listed inclusion criteria, all the patients were handed the enclosed risk questionnaire. If osteoporosis was suspected, the nursing staff were then able to prepare further diagnostics; DXA and basic laboratory tests were also initiated.

It is therefore possible to diagnose osteoporosis and initiate treatment during the postoperative stay on a trauma surgical ward. For the specific treatment of osteoporosis with the oral bisphosphonate alendronate and risedronate, cost-effective and evidence grade A classified therapeutics are available. IV-bisphosphonates are in principle good alternatives for oral application. When patients are treated with zoledronate (5 mg/year), which is not to be begun earlier than 14 days after the operation, the next institution to provide treatment (e.g. rehab clinic, geriatric ward) has to guarantee cooperation. There are no studies on the time of treatment with denosumab following a fracture. Thus, denosumab can be administered immediately after the operation, taking the present data into account. It can also be used if the patient suffers from renal insufficiency, and it causes no febrile reactions to infusions. That is why we recommend this treatment after checking calcium and 25-OH-vitamin D in patients with contraindications against oral bisphosphonates and/or a severe course of the disease. Direct application during the stay in hospital has to be considered according to the relevant circumstances in the background. If the course of osteoporosis is really severe (e.g. vertebral body fractures during oral anti-resorptive treatment), teriparatide is available as an osteoanabolic substance. Risk, benefit, compliance, and cost all have to be considered individually in all drugs.

It is important to guarantee compliance immediately, in the first year. To this end, not only are the care and healing of fractures to be monitored, but the patients and if necessary their relatives are to be asked about their specific osteoporosis medication, at the latest during the out-patient appointments for postoperative follow-up checks of patients of trauma surgery. Only if the proper drugs are taken or applied can the risk of fracture really be reduced.

Further investigations are required; to complement the lack of a prospective validation of the algorithm, a prospective clinical study is ongoing.

Conclusion for practice

  • Osteoporosis is a frequent underlying disease in elderly patients with fractures following low-energy trauma which is of increasing importance for health economics.

  • The doctors in charge have a decisive function when initiating diagnostics and the treatment of osteoporosis to reduce further osteoporosis-associated fractures.

  • A treatment algorithm suitable for daily use helps all the surgeons on a trauma surgical ward to diagnose and treat osteoporosis individually.

  • The early diagnosis and treatment of osteoporosis can reduce the current deficit in treatment and the associated osteological deuteropathies as well as contribute to allowing trauma surgery patients to maintain their independence.

Abbreviations

AO/OTA:

Arbeitsgemeinschaft für Osteosynthesefragen (AO-Foundation)/Orthopaedic Trauma Association

AP:

Alkaline phosphatase

BP:

Bisphosphonate

CRP:

C-reactive protein

DVO:

Dachverband Osteologie = German Osteology Society

DXA:

Dual-energy X-ray absorptiometry

ESR:

Erythrocyte sedimentation rate

FRAX:

Fracture Risk Assessment Tool

GFR:

Glomerular filtration rate

HRT:

Hormone replacement therapy

IgG2:

Immunoglobulin-isotype 2

PPI:

Proton pump inhibitor

RANKL:

Receptor activator of nuclear factor kappa-B ligand

rhPTH:

Recombined form of the human parathormone

SC:

Subcutaneous

SERMs:

Selective oestrogen receptor modulators

TSH:

Thyroid-stimulating hormone

WHO:

World Health Organisation

References

  1. Haussler B, Gothe H, Gol D, Glaeske G, Pientka L, Felsenberg D. Epidemiology, treatment and costs of osteoporosis in Germany—the BoneEVA Study. Osteoporos Int. 2007;18(1):77–84.

    Article  CAS  PubMed  Google Scholar 

  2. Hadji P, Klein S, Gothe H, Häussler B, Kless T, Schmidt T, Steinle T, Verheyen F, Linder R. Epidemiologie der Osteoporose - Bone Evaluation Study: Eine Analyse von Krankenkassen-Routinedaten. Dtsch Arztebl Int. 2013;110(4):52–7.

    PubMed  PubMed Central  Google Scholar 

  3. Hadji P, Klein S, Haussler B, Kless T, Linder R, Rowinski-Jablokow M, Verheyen F, Gothe H. The bone evaluation study (BEST): patient care and persistence to treatment of osteoporosis in Germany. Int J Clin Pharmacol Ther. 2013;51(11):868–72.

    Article  PubMed  Google Scholar 

  4. Dachverband Osteologie. DVO Leitlinie Osteoporose 2014 (Kurzfassung und Langfassung). http://www.dv-osteologie.org/uploads/Leitlinie2014/DVO-LeitlinieOsteoporose2014KurzfassungundLangfassungVersion1a12012016.pdf.

  5. Cooper C. Osteoporosis: disease severity and consequent fracture management. Osteoporos Int. 2010;21 Suppl 2:S425–9.

    Article  PubMed  Google Scholar 

  6. 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(2):138–45.

    Article  CAS  PubMed  Google Scholar 

  7. Kolios L, Takur C, Moghaddam A, Hitzler M, Schmidt-Gayk H, Suda AJ, Honer B, Grutzner PA, Wolfl C. Anamnestic risk factor questionnaire as reliable diagnostic instrument for osteoporosis (reduced bone morphogenic density). BMC Musculoskelet Disord. 2011;12:187.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Hippisley-Cox J, Coupland C. Derivation and validation of updated QFracture algorithm to predict risk of osteoporotic fracture in primary care in the United Kingdom: prospective open cohort study. BMJ. 2012;344, e3427.

    Article  PubMed  Google Scholar 

  9. Strom O, Jonsson B, Kanis JA. Intervention thresholds for denosumab in the UK using a FRAX(R)-based cost-effectiveness analysis. Osteoporos Int. 2013;24(4):1491–502.

    Article  CAS  PubMed  Google Scholar 

  10. Jamal SA, Leiter RE, Bayoumi AM, Bauer DC, Cummings SR. Clinical utility of laboratory testing in women with osteoporosis. Osteoporos Int. 2005;16(5):534–40.

    Article  PubMed  Google Scholar 

  11. Willburger RE, Knorth H. Osteoporose der Wirbelsäule: Therapieoption und Präventionsstrategien. Dtsch Arztebl Int. 2003;100(17):1120.

    Google Scholar 

  12. Hernlund E, Svedbom A, Ivergard M, Compston J, Cooper C, Stenmark J, McCloskey EV, Jonsson B, Kanis JA. Osteoporosis in the European Union: medical management, epidemiology and economic burden. A report prepared in collaboration with the International Osteoporosis Foundation (IOF) and the European Federation of Pharmaceutical Industry Associations (EFPIA). Arch Osteoporos. 2013;8(1–2):136.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Kanis JA, Johnell O, De Laet C, Johansson H, Oden A, Delmas P, Eisman J, Fujiwara S, Garnero P, Kroger H, et al. A meta-analysis of previous fracture and subsequent fracture risk. Bone. 2004;35(2):375–82.

    Article  CAS  PubMed  Google Scholar 

  14. El Maghraoui A, Rezqi A, Mounach A, Achemlal L, Bezza A, Dehhaoui M, Ghozlani I. Vertebral fractures and abdominal aortic calcification in postmenopausal women. A cohort study. Bone. 2013;56(1):213–9.

    Article  PubMed  Google Scholar 

  15. Tenne M, McGuigan F, Besjakov J, Gerdhem P, Akesson K. Degenerative changes at the lumbar spine—implications for bone mineral density measurement in elderly women. Osteoporos Int. 2013;24(4):1419–28.

    Article  CAS  PubMed  Google Scholar 

  16. Genant HK, Wu CY, van Kuijk C, Nevitt MC. Vertebral fracture assessment using a semiquantitative technique. J Bone Miner Res. 1993;8(9):1137–48.

    Article  CAS  PubMed  Google Scholar 

  17. Jurisson M, Pisarev H, Kanis J, Borgstrom F, Svedbom A, Kallikorm R, Lember M, Uuskula A. Quality of life, resource use, and costs related to hip fracture in Estonia. Osteoporos Int. 2016;27(8):2555–66.

    Article  CAS  PubMed  Google Scholar 

  18. Lyles KW, Colon-Emeric CS, Magaziner JS, Adachi JD, Pieper CF, Mautalen C, Hyldstrup L, Recknor C, Nordsletten L, Moore KA, et al. Zoledronic acid and clinical fractures and mortality after hip fracture. N Engl J Med. 2007;357(18):1799–809.

    Article  CAS  PubMed  Google Scholar 

  19. Frerichmann U, Raschke MJ, Stockle U, Wohrmann S, Lohmann R. Proximal femoral fractures in the elderly. Data from health insurance providers on more than 23 million insured persons—part 2. Unfallchirurg. 2007;110(7):610–6.

    Article  CAS  PubMed  Google Scholar 

  20. Vogel T, Dobler T, Bitterling H, Biberthaler P, Kanz KG, Pfeifer KJ, Bartl R, Mutschler W. Osteoporosis in traumatology. Prevalence and management. Unfallchirurg. 2005;108(5):356–64.

    Article  CAS  PubMed  Google Scholar 

  21. Förtsch M, Schmidt T, Feldmann C, Maurer T. DVO-Leitlinie (DVO: Dachverband Osteologie) in der osteologischen Schwerpunktpraxis. Trauma Berufskrankh. 2014;16(2):110–21.

    Article  Google Scholar 

  22. Ahmed LA, Emaus N, Berntsen GK, Bjornerem A, Fonnebo V, Jorgensen L, Schirmer H, Stormer J, Joakimsen RM. Bone loss and the risk of non-vertebral fractures in women and men: the Tromso study. Osteoporos Int. 2010;21(9):1503–11.

    Article  CAS  PubMed  Google Scholar 

  23. Kanterewicz E, Puigoriol E, Garcia-Barrionuevo J, del Rio L, Casellas M, Peris P. Prevalence of vertebral fractures and minor vertebral deformities evaluated by DXA-assisted vertebral fracture assessment (VFA) in a population-based study of postmenopausal women: the FRODOS study. Osteoporos Int. 2014;25(5):1455–64.

    CAS  PubMed  Google Scholar 

  24. Gehlbach S, Saag KG, Adachi JD, Hooven FH, Flahive J, Boonen S, Chapurlat RD, Compston JE, Cooper C, Diez-Perez A, et al. Previous fractures at multiple sites increase the risk for subsequent fractures: the Global Longitudinal Study of Osteoporosis in Women. J Bone Miner Res. 2012;27(3):645–53.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Kim TY, Ha YC, Kang BJ, Lee YK, Koo KH. Does early administration of bisphosphonate affect fracture healing in patients with intertrochanteric fractures? J Bone Joint SurgBr. 2012;94(7):956–60.

    Article  Google Scholar 

  26. McDonald MM, Dulai S, Godfrey C, Amanat N, Sztynda T, Little DG. Bolus or weekly zoledronic acid administration does not delay endochondral fracture repair but weekly dosing enhances delays in hard callus remodeling. Bone. 2008;43(4):653–62.

    Article  CAS  PubMed  Google Scholar 

  27. Dhert WJ, Thomsen P, Blomgren AK, Esposito M, Ericson LE, Verbout AJ. Integration of press-fit implants in cortical bone: a study on interface kinetics. J Biomed Mater Res. 1998;41(4):574–83.

    Article  CAS  PubMed  Google Scholar 

  28. Nehme A, Maalouf G, Tricoire JL, Giordano G, Chiron P, Puget J. Effect of alendronate on periprosthetic bone loss after cemented primary total hip arthroplasty: a prospective randomized study. Rev Chir Orthop Reparatrice Appar Mot. 2003;89(7):593–8.

    CAS  PubMed  Google Scholar 

  29. Aspenberg P, Johansson T. Teriparatide improves early callus formation in distal radial fractures. Acta Orthop. 2010;81(2):234–6.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Neer RM, Arnaud CD, Zanchetta JR, Prince R, Gaich GA, Reginster JY, Hodsman AB, Eriksen EF, Ish-Shalom S, Genant HK, et al. Effect of parathyroid hormone (1–34) on fractures and bone mineral density in postmenopausal women with osteoporosis. N Engl J Med. 2001;344(19):1434–41.

    Article  CAS  PubMed  Google Scholar 

  31. Cauley JA, Parimi N, Ensrud KE, Bauer DC, Cawthon PM, Cummings SR, Hoffman AR, Shikany JM, Barrett-Connor E, Orwoll E, et al. Serum 25-hydroxyvitamin D and the risk of hip and nonspine fractures in older men. J Bone Miner Res. 2010;25(3):545–53.

    Article  CAS  PubMed  Google Scholar 

  32. Garnero P, Munoz F, Sornay-Rendu E, Delmas PD. Associations of vitamin D status with bone mineral density, bone turnover, bone loss and fracture risk in healthy postmenopausal women. The OFELY study. Bone. 2007;40(3):716–22.

    Article  CAS  PubMed  Google Scholar 

  33. Bischoff-Ferrari HA. Optimal serum 25-hydroxyvitamin D levels for multiple health outcomes. Adv Exp Med Biol. 2014;810:500–25.

    PubMed  Google Scholar 

  34. Bischoff-Ferrari HA, Willett WC, Orav EJ, Lips P, Meunier PJ, Lyons RA, Flicker L, Wark J, Jackson RD, Cauley JA, et al. A pooled analysis of vitamin D dose requirements for fracture prevention. N Engl J Med. 2012;367(1):40–9.

    Article  CAS  PubMed  Google Scholar 

  35. Drey M, Bollheimer C. Vitamin D supplementation in the elderly. Dtsch Med Wochenschr. 2011;136(48):2463–5.

    Article  CAS  PubMed  Google Scholar 

  36. Holick MF, Binkley NC, Bischoff-Ferrari HA, Gordon CM, Hanley DA, Heaney RP, Murad MH, Weaver CM, Endocrine S. Evaluation, treatment, and prevention of vitamin D deficiency: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2011;96(7):1911–30.

    Article  CAS  PubMed  Google Scholar 

  37. Holick MF, Matsuoka LY, Wortsman J. Age, vitamin D, and solar ultraviolet. Lancet. 1989;2(8671):1104–5.

    Article  CAS  PubMed  Google Scholar 

  38. Lips P. Vitamin D deficiency and secondary hyperparathyroidism in the elderly: consequences for bone loss and fractures and therapeutic implications. Endocr Rev. 2001;22(4):477–501.

    Article  CAS  PubMed  Google Scholar 

  39. Bacon CJ, Gamble GD, Horne AM, Scott MA, Reid IR. High-dose oral vitamin D3 supplementation in the elderly. Osteoporos Int. 2009;20(8):1407–15.

    Article  CAS  PubMed  Google Scholar 

  40. Sanders KM, Stuart AL, Williamson EJ, Simpson JA, Kotowicz MA, Young D, Nicholson GC. Annual high-dose oral vitamin D and falls and fractures in older women: a randomized controlled trial. Jama. 2010;303(18):1815–22.

    Article  CAS  PubMed  Google Scholar 

  41. Lewis JR, Barre D, Zhu K, Ivey KL, Lim EM, Hughes J, Prince RL. Long-term proton pump inhibitor therapy and falls and fractures in elderly women: a prospective cohort study. J Bone Miner Res. 2014;29(11):2489–97.

    Article  PubMed  Google Scholar 

  42. Maggio M, Lauretani F, Ceda GP, De Vita F, Bondi G, Corsonello A, Cattabiani C, Lattanzio F, Ruggiero C, Nouvenne A, et al. Use of proton pump inhibitors is associated with lower trabecular bone density in older individuals. Bone. 2013;57(2):437–42.

    Article  CAS  PubMed  Google Scholar 

  43. Ding J, Heller DA, Ahern FM, Brown TV. The relationship between proton pump inhibitor adherence and fracture risk in the elderly. Calcif Tissue Int. 2014;94(6):597–607.

    Article  CAS  PubMed  Google Scholar 

  44. Leitlinienreport zur S3-Leitlinie: Bisphosphonat- assoziierte Kiefernekrose (BP-ONJ) und andere Medikamenten-assoziierte Kiefernekrosen. AWMF-Register-Nr 007-091 2012.

  45. Gertz BJ, Holland SD, Kline WF, Matuszewski BK, Freeman A, Quan H, Lasseter KC, Mucklow JC, Porras AG. Studies of the oral bioavailability of alendronate. Clin Pharmacol Ther. 1995;58(3):288–98.

    Article  CAS  PubMed  Google Scholar 

  46. Abrahamsen B, Eiken P, Eastell R. Proton pump inhibitor use and the antifracture efficacy of alendronate. Arch Intern Med. 2011;171(11):998–1004.

    PubMed  Google Scholar 

  47. Roux C, Goldstein JL, Zhou X, Klemes A, Lindsay R. Vertebral fracture efficacy during risedronate therapy in patients using proton pump inhibitors. Osteoporos Int. 2012;23(1):277–84.

    Article  CAS  PubMed  Google Scholar 

  48. Ziller V, Kostev K, Kyvernitakis I, Boeckhoff J, Hadji P. Persistence and compliance of medications used in the treatment of osteoporosis—analysis using a large scale, representative, longitudinal German database. Int J Clin Pharmacol Ther. 2012;50(5):315–22.

    Article  CAS  PubMed  Google Scholar 

  49. Eriksen EF, Lyles KW, Colon-Emeric CS, Pieper CF, Magaziner JS, Adachi JD, Hyldstrup L, Recknor C, Nordsletten L, Lavecchia C, 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(7):1308–13.

    Article  CAS  PubMed  Google Scholar 

  50. Sunyecz JA. Zoledronic acid infusion for prevention and treatment of osteoporosis. Int J Womens Health. 2010;2:353–60.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  51. Schray D, Stumpf U, Kammerlander C, Böcker W, Neuerburg C. Diagnosis and therapy of osteoporosis in geriatric trauma patients: an update. Inn Sur Sci. 2016;1(2):65-71.

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Acknowledgements

The authors would like to thank Hella Thun (MultiMediaLabor, LMU Munich) for the graphic design of the risk assessment questionnaire and the algorithms. We also thank Melanie Rademacher for the language editing.

Funding

Not applicable.

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Not applicable.

Authors’ contributions

CN, RS and US contributed substantially to the conception and design of the algorithm. CN and US wrote the manuscript which was language edited by LM and MR (see acknowledgement). CK, WB and WM drafted the article and revised it for important intellectual content. All authors reviewed and edited the manuscript and approved the final version.

Competing interests

Within the interdisciplinary centre of osteology (Osteologisches Schwerpunktzentrum DVO), the authors C. Neuerburg, R. Schmidmaier, W. Böcker, W. Mutschler and U. Stumpf conducted a clinical trial for the testing of an anti-osteoporotic agent. The trial was supported by Amgen GmbH.

The authors C. Neuerburg, C. Kammerlander, W. Böcker, W. Mutschler, and U. Stumpf were payed for lectures or consultancy and gained conference supports by various pharmaceutical companies and the OSTAK. Ralf Schmidmaier was payed for lectures and consultancy and/or gained scientific support by Alexion, AMGEN, 4SC AG, Chugai, Celgene, Gilead, Lilly, Medac Schering, Munidpharma, Novartis, Ribosepharm, Roche and Sanofi-Aventis.

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Authors and Affiliations

  1. Department of General, Trauma and Reconstruction Surgery, Munich University Hospital LMU, Campus Großhadern, Marchioninistr. 15, 81377, Munich, Germany

    Carl Neuerburg, Lena Mittlmeier, Christian Kammerlander, Wolfgang Böcker, Wolf Mutschler & Ulla Stumpf

  2. Department of Endocrinology, Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, Munich, Germany

    Ralf Schmidmaier

  3. Department of Trauma Surgery, Medical University, Innsbruck, Austria

    Christian Kammerlander

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  1. Carl Neuerburg
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  7. Ulla Stumpf
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Correspondence to Carl Neuerburg.

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Neuerburg, C., Mittlmeier, L., Schmidmaier, R. et al. Investigation and management of osteoporosis in aged trauma patients: a treatment algorithm adapted to the German guidelines for osteoporosis. J Orthop Surg Res 12, 86 (2017). https://doi.org/10.1186/s13018-017-0585-0

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Keywords

Journal of Orthopaedic Surgery and Research

ISSN: 1749-799X