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Clinical Cases in Mineral and Bone Metabolism logoLink to Clinical Cases in Mineral and Bone Metabolism
. 2016 May 11;13(1):42–45. doi: 10.11138/ccmbm/2016.13.1.042

Surgical prevention of femoral neck fractures in elderly osteoporotic patients. A literature review

Eugenio Chiarello 1,, Giuseppe Tedesco 2, Matteo Cadossi 2, Paola Capra 2, Silvio Terrando 2, Andrea Miti 1, Sandro Giannini 2
PMCID: PMC4869953  PMID: 27252744

Summary

Fragility fractures of the femur are one of the major causes of morbidity and mortality worldwide.

The incidence of new contralateral hip fractures in elderly osteoporotic patients ranges from 7 to 12% within 2 years after the first fracture.

Secondary prevention can be divided in: pharmacological therapy based on the prescription of anti-osteoporotic drugs with different mechanism of action and non-pharmacological therapy which is based on modification of environmental risk factors, on a healthy diet with daily supplements of calcium and vitamin D and calcium and on the use of hip protectors.

Recently a new form of prevention is becoming achievable: surgical prevention; the rationale of surgical reinforcement is the need to increase the resistance of the femoral neck to the compression and distraction forces acting on it.

In this paper we analyse all the experimental and “on the market” device available for the surgical prevention of femoral neck fracture.

Keywords: osteoporosis, surgical prevention, femoral neck fractures

Introduction

Osteoporosis is a skeletal disorder characterized by an increased risk of fractures due to a compromised bone strength (1, 2). The strength reflects both density and quality of bone, therefore the decrease of bone mass and the microarchitectural deterioration that occur in this disease cause bone frailty leading to low energy fractures (35).

Fragility fractures are one of the major causes of morbidity and mortality worldwide. In Italy there are 80,000 new femoral neck fractures due to osteoporosis every year, with a high prevalence in women (72%) (6). Moreover it is estimated that in 2012 the cost of femoral fractures was 1.1 billion euro (7).

Osteoporosis prevalence is likely to rise due to an aging population: people older than 60 will increase by 50% over the next 40 years. Although numbers are uncertain, the latest pessimistic estimates lead us to expect a doubling of fragility fractures by 2050 (8, 9).

Moreover hip fractures are associated with an increased mortality up to 25–30% within the first year (10) and an increase of 2.5 times risk of a new fracture (11). One year after a hip fracture 40% of patients is still unable to walk independently, 60% has difficulty in at least one of the normal daily living activities and 80% experiences limitations in other activities such as driving and shopping. In addition, 27% of patients is hospitalized in a long-term care facility following a hip fracture (12).

This scenario shows how osteoporosis and femoral neck fractures represent a tremendous concern in economic and social terms, therefore new strategies must be sought for the prevention and treatment of this pathology.

Prevention of the second contralateral femoral neck fracture

In literature, the incidence of a contralateral hip fracture in elderly osteoporotic patients ranges from 7 to 12% within two years after the first femoral neck fracture, with a high percentage of symmetry between the two fractures which varies from 70 to 83% (13, 14).

Therefore it is mandatory to adopt appropriate strategies to prevent the second fracture in these patients. Currently secondary prevention focuses on pharmacological and non-pharmacological therapy.

The pharmacological secondary prevention is based on the prescription of antiosteoporotic drugs. In the market there are several classes of drugs with different mechanism of action: anti-absorbable, anabolic, hormone replacement, selective estrogen receptor modulators and monoclonal antibodies.

Bisphosphonates are anti-absorbable drugs with high tropism for the mineralized tissues. They are able to concentrate electively on remodeling bone surfaces, blocking osteoclast activity (1518).

Teriparatide (rh-PTH) is the first anabolic drug that stimulates bone formation and increases bone mineral density (19, 20).

Strontium ranelate is a drug with both anti-absorbable and anabolic actions and is able to un-couple the remodeling process stimulating osteoblast differentiation and bone formation and on the other hand decreasing resorption by a reduction in osteoclastic activity (21, 22).

Hormone replacement therapy, as the name suggests, is based on the substitution of estrogens whose production decreases in menopausal women; however this class of drugs is associated with a high risk of uterine and breast cancer and increased cardiovascular risks (2325). In order to overcome these complications, selective estrogen receptor modulators (SERMs) such as raloxifene and bazedoxifene were introduced. These drugs explicate their action on the estrogen receptors on the bone cells without having the negative effects on breast and uterus (2628).

The last class of drug to be introduced in the marked are the monoclonal antibodies. Currently only denosumab is available; this is an IgG2 human monoclonal antibody directed against RANK-L which binds with high affinity and specificity. These bindings prevent the activation of its receptor RANK present on osteoclasts’ surface thereby inhibiting their activation thus reducing both cortical and trabecular bone resorption (29, 30).

Although there are so many drugs for the treatment and prevention of osteoporosis, it has been showed that none of these attain significant efficacy for the prevention of hip fractures below three years of continuous treatment (31, 32). This combined with poor patient compliance results in a lack of efficacy of drugs for the secondary prevention of femoral neck fractures (33). Recently some Authors argue that evidence for drug therapy to prevent hip fracture is insufficient to warrant the current approach. They believe that pharmacotherapy can achieve at best a marginal reduction in hip fractures at the cost of unnecessary psychological harms, serious medical adverse events, and forgone opportunities to have greater impacts on the health of older people. Therefore they propose to regret the current approach to hip fracture prevention because it is neither viable as a public health strategy nor cost effective (34).

The non-pharmacological prevention is based on modification of environmental risk factors, on a healthy diet with daily supplements of calcium and vitamin D and on the use of hip protectors. A Cochrane review on the use of hip protectors has demonstrated that their effectiveness in reducing fractures in nursing home patients but equally it has shown that they are less effective in patients living in community. These results are probably related to the adherence of patients in wearing hip protectors due to their discomfort (35).

Currently, in addition to pharmacological and non-pharmacological prevention we need to add a new type of prevention: the surgical one.

Surgical prevention of femoral neck fracture

Cortical thinning and trabecular bone loss are both important in the frail osteoporotic bone. The cortical thinning of long bones is due to endosteal resorption and normally is compensated by periosteal bone apposition, leading to an increase in the diameter of the bone. The femoral neck is not covered by periosteum because it is an intracapsular, and therefore there isn’t bone apposition (3). This may partially explain why in osteoporotic femur the neck is the “locus minoris resistentiae”.

Moreover Holzer et al., in an in vitro study, show that in the femoral neck the cortical bone and its geometry are primarily responsible for the bone strength, whereas the trabecular bone gives a marginal contribution (less than 10%) due to morphological changes (36).

The rationale of surgical reinforcement is the need to increase the resistance of the neck to the compression and distraction forces acting on it (36, 37).

During gait the major stresses occur in the subcapital and middle-cervical regions: high compressive stress occurs inferiorly and mild distraction stress occurs superiorly (38). During a fall to the side with impact on the greater trochanter the stresses are reversed: on the superior side of the femoral neck a huge compressive stress occurs while on the inferior side there is a distraction stress (38, 39).

The concept of surgical reinforcement of the femoral neck was proposed for the first time in 1960 by Crockett (40) who described a reinforcement technique of the femoral neck characterized by percutaneous insertion of stainless-steel nails under local anesthesia. In the conclusion of his paper the Author affirmed that in case of a fracture in the reinforced neck, the patient would have a non-displaced fracture and therefore the treatment required was only rest and walking with 2 crutches.

More recently Heini et al. (41) in 2004 described another experimental technique called “femoroplasty” consisting of injection of poly-methyl-methacrylate (PMMA) inside osteoporotic femoral neck. The Author used 20 pairs of osteoporotic femurs, each pair as a case-control, to assess the surgical reinforcement. The Author inserted a low viscosity cement in a 4.5 mm hole on the lateral cortex at the base of the greater trochanter. Subsequently the femurs were tested by simulating a fall. Fracture type observed in control group matched those commonly seen in vivo; in the study group different fracture patterns were observed: trochanteric and medial fractures of the femoral neck and in three cases sub-trochanteric fractures. Moreover all the fractures occurred at the bone-cement interface. In this study group femurs had an increased breaking load greater than 82% compared to controls, and an increase in absorbed energy of 188%. However the Author concluded that there is concerns in the application of this technique in vivo due to the high volume of PM-MA necessary which generates enormous heat during polymerization (up to 60° in vivo) leading to necrosis of the femoral head. Moreover revision surgery in the event of fracture would be technically very difficult.

Other Authors (42) tested 10 pairs of osteoporotic human femurs, each pair as a case-control, augmented with about 40 ml of another low viscosity cement. They simulated a fall on the greater trochanter and confirmed the increase of breaking load and absorbed energy in the augmented femurs; however it was unknown if this increase would be enough to prevent fracture in vivo. Moreover they found that the stiffness was not significantly different between the 2 groups. They hypothesized that these results were due to the composite nature of the augmented femur: the bone governs the pre-yield behavior and once fracture occurs, it is likely that the composite formed by trabecular bone and cement determines the mechanical response.

To overcome the high temperature of polymerization, Beckmann et al. (43) tested a non-resorbable composite consisting of crosslinking resins and reinforcing glass ceramic particles already used for vertebral augmentation instead of PM-MA. The Author used 9 pairs of femur as case-control, they recorded the temperature of polymerization and simulated a fall on the great trochanter. Subsequently the fractured femurs were stabilized using either cannulated screws, a dynamic hip screw or a proximal femoral nail and they were then biomechanically tested again. As expected, breaking load and absorbed energy were significantly increased. The maximum temperature elevation (about 11°) was lower if compared with PMMA but still high if compared to the near-isotermic polymerization cement based on calcium phosphate. However, the Authors expressed concern regarding the revision surgery of the reinforced femur especially in the drilling: the composite was even harder to drill than the PM-MA. Moreover femoroplasty may directly influence the subsequent fracture of the augmented region: a distal shift of the fracture location could be assumed for in vivo condition.

Moreover De Bakker et al. (44), in a finite elements study, have shown how, reinforcing the femur with a Gamma nail, there was a 100% increase in the resistance to fracture.

Currently, to our knowledge, there is only a device on the market, for the prevention of the femoral neck fractures. Recently it has been published a finite element analysis showing that this device has led to a decrease in the risk of femoral neck fracture (−28%) and trochanteric fracture (−52%) (45).

Conclusions

Surgical prevention could become a viable solution in the prevention of femoral neck fracture in patients at risk. The right selection of patients is mandatory but also randomized controlled trials should by designed in order to prove the efficacy of the treatment.

References

  • 1.Seeman E. Pathogenesis of bone fragility in women and men. Lancet. 2002;359:1841–1850. doi: 10.1016/S0140-6736(02)08706-8. [DOI] [PubMed] [Google Scholar]
  • 2.Turner CH. The biomechanics of hip fracture. Lancet. 2005;366:98–99. doi: 10.1016/S0140-6736(05)66842-0. [DOI] [PubMed] [Google Scholar]
  • 3.Cullinane DM, Einhorn TA. Biomechanics of bone. In: Bilezikian JP, Raisz LG, Rodan GA, editors. Principles of Bone Biology. 2nd ed. Academic Press; San Diego, CA, USA: 2002. pp. 17–32. [Google Scholar]
  • 4.Keaveny TM, Yeh OC. Architecture and trabecular bone-toward an improved understanding of the biomechanical effects of age, sex and osteoporosis. J Musculoskelet Neuronal Interact. 2002;2:205–208. [PubMed] [Google Scholar]
  • 5.Seeman E, Delmas PD. Bone quality–the material and structural basis of bone strength and fragility. N Engl J Med. 2006;354:2250–2261. doi: 10.1056/NEJMra053077. [DOI] [PubMed] [Google Scholar]
  • 6.Piscitelli P, Brandi ML, Tarantino U, Baggiani A, Distante A, Muratore M, Grattagliano V, Migliore, Granata M, Guglielmi G, Gimigliano R, Iolascon G. Incidenza e costi delle fratture di femore in Italia: Studio di estensione 2003–2005. Reumatismo. 2010;62(2):113–118. doi: 10.4081/reumatismo.2010.113. [DOI] [PubMed] [Google Scholar]
  • 7.Italian Health Policy Brief, June 2012.
  • 8.http://www.nof.org/professionals/clinical-guidelines.
  • 9.Harvey N, Dennison E, Cooper C. Osteoporosis: impact on health and economics. Nat Rev Rheumatol. 2010;6:99–105. doi: 10.1038/nrrheum.2009.260. [DOI] [PubMed] [Google Scholar]
  • 10.Roberts SE, Goldacre MJ. Time trends and demography of mortality after fractured neck of femur in an English population, 1968–98: database study. BMJ. 2003 Oct 4;327(7418):771–5. doi: 10.1136/bmj.327.7418.771. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Colón-Emeric C, Kuchibhatla M, Pieper C, et al. The contribution of hip fracture to risk of subsequent fracture: Data from two longitudinal studies. Osteoporos Int. 2003;(14):879–883. doi: 10.1007/s00198-003-1460-x. [DOI] [PubMed] [Google Scholar]
  • 12.Cooper C. The crippling consequences of fractures and their impact on quality of life. Am J Med. 1997 Aug 18;103(2A):12S–17S. doi: 10.1016/s0002-9343(97)90022-x. discussion 17S–19S. [DOI] [PubMed] [Google Scholar]
  • 13.Boston DA. Bilateral fractures of the femoral neck. Injury. 1982 Nov;14(3):207–10. doi: 10.1016/0020-1383(82)90132-2. [DOI] [PubMed] [Google Scholar]
  • 14.Lönnroos E, Kautiainen H, Karppi P, Hartikainen S, Kiviranta I, Sulkava R. Incidence of second hip fractures. A population-based study. Osteoporos Int. 2007 Sep;18(9):1279–85. doi: 10.1007/s00198-007-0375-3. [DOI] [PubMed] [Google Scholar]
  • 15.Wells GA, Cranney A, Peterson J, Boucher M, Shea B, Robinson V, Coyle D, Tugwell P. Alendronate for the primary and secondary prevention of osteoporotic fractures in postmenopausal women. Cochrane Database Syst Rev. 2008;(1):CD001155. doi: 10.1002/14651858.CD001155.pub2. [DOI] [PubMed] [Google Scholar]
  • 16.Wells G, Cranney A, Peterson J, Boucher M, Shea B, Robinson V, Coyle D, Tugwell P. Risedronate for the primary and secondary prevention of osteoporotic fractures in postmenopausal women. Cochrane Database Syst Rev. 2008;(1):CD004523. doi: 10.1002/14651858.CD004523.pub3. [DOI] [PubMed] [Google Scholar]
  • 17.Black DM, Delmas PD, Eastell R, Reid IR, Boonen S, Cauley JA, Cosman F, Lakatos P, Leung PC, Man Z, Mautalen C, Mesenbrink P, Hu H, Caminis J, Tong K, Rosario-Jansen T, Krasnow J, Hue TF, Sellmeyer D, Eriksen EF, Cummings SR. Once-yearly zoledronic acid for treatment of postmenopausal osteoporosis. N Engl J Med. 2007;356:1809–1822. doi: 10.1056/NEJMoa067312. [DOI] [PubMed] [Google Scholar]
  • 18.MacLean C, Newberry S, Maglione M, McMahon M, Ranganath V, Suttorp M, Mojica W, Timmer M, Alexander A, McNamara M, Desai SB, Zhou A, Chen S, Carter J, Tringale C, Valentine D, Johnsen B, Grossman J. Systematic review: comparative effectiveness of treatments to prevent fractures in men and women with low bone density or osteoporosis. Ann Intern Med. 2008;148:197–213. doi: 10.7326/0003-4819-148-3-200802050-00198. [DOI] [PubMed] [Google Scholar]
  • 19.European Medicines Agency. EPAR summary for the public. 2009. European Public Assessment Report (EPAR) FORSTEO. [Google Scholar]
  • 20.Stroup J, Kane MP, Abu-Baker AM. Teriparatide in the treatment of osteoporosis. Am J Health Syst Pharm. 2008;65:532–539. doi: 10.2146/ajhp070171. [DOI] [PubMed] [Google Scholar]
  • 21.Meunier PJ, Roux C, Ortolani S, az-Curiel M, Compston J, Marquis P, Cormier C, Isaia G, Badurski J, Wark JD, Collette J, Reginster JY. Effects of long-term strontium ranelate treatment on vertebral fracture risk in postmenopausal women with osteoporosis. Osteoporos Int. 2009;20:1663–1673. doi: 10.1007/s00198-008-0825-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.O’Donnell S, Cranney A, Wells GA, Adachi JD, Reginster JY. Strontium ranelate for preventing and treating postmenopausal osteoporosis. Cochrane Database Syst Rev. 2006;(4):CD005326. doi: 10.1002/14651858.CD005326.pub3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Cauley JA, Robbins J, Chen Z, Cummings SR, Jackson RD, LaCroix AZ, LeBoff M, Lewis CE, McGowan J, Neuner J, Pettinger M, Stefanick ML, Wactawski-Wende J, Watts NB. Effects of estrogen plus progestin on risk of fracture and bone mineral density: the Women’s Health Initiative randomized trial. JAMA. 2003;290:1729–1738. doi: 10.1001/jama.290.13.1729. [DOI] [PubMed] [Google Scholar]
  • 24.Torgerson DJ, Bell-Syer SE. Hormone replacement therapy and prevention of nonvertebral fractures: a meta-analysis of randomized trials. JAMA. 2001;285:2891–2897. doi: 10.1001/jama.285.22.2891. [DOI] [PubMed] [Google Scholar]
  • 25.Rossouw JE, Anderson GL, Prentice RL, LaCroix AZ, Kooperberg C, Stefanick ML, Jackson RD, Beresford SA, Howard BV, Johnson KC, Kotchen JM, Ockene J. Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results from the Women’s Health Initiative randomized controlled trial. JAMA. 2002;288:321–333. doi: 10.1001/jama.288.3.321. [DOI] [PubMed] [Google Scholar]
  • 26.Silverman SL, Chines AA, Kendler DL, Kung AWC, Teglbjaerg CS, Felsenberg D, Mairon N, Constantine GD, Adachi JD for the Bazedoxifene Study Group. Sustained efficacy and safety of bazedoxifene in preventing fractures in postmenopausal women with osteoporosis: results of a 5-year, randomized, placebo-controlled study. Osteoporos Int. 2012 Jan;23(1):351–63. doi: 10.1007/s00198-011-1691-1. [DOI] [PubMed] [Google Scholar]
  • 27.Cummings SR, Ensrud K, Delmas PD, LaCroix AZ, Vukicevic S, Reid DM, Goldstein S, Sriram U, Lee A, Thompson J, Armstrong RA, Thompson DD, Powles T, Zanchetta J, Kendler, Neven P, Eastell R. Lasofoxifene in postmenopausal women with osteoporosis. N Engl J Med. 2010;362:686–696. doi: 10.1056/NEJMoa0808692. [DOI] [PubMed] [Google Scholar]
  • 28.Barrett-Connor E, Mosca L, Collins P, Geiger MJ, Grady D, Kornitzer M, McNabb MA, Wenger NK. Effects of raloxifene on cardiovascular events and breast cancer in postmenopausal women. N Engl J Med. 2006;355:125–137. doi: 10.1056/NEJMoa062462. [DOI] [PubMed] [Google Scholar]
  • 29.Cummings SR, San Martin J, McClung MR, Siris ES, Eastell R, Reid IR, Delmas P, Zoog HB, Austin M, Wang A, Kutilek S, Adami S, Zanchetta J, Libanati C, Siddhanti S, Christiansen C. Denosumab for prevention of fractures in postmenopausal women with osteoporosis. N Engl J Med. 2009;361:756–765. doi: 10.1056/NEJMoa0809493. [DOI] [PubMed] [Google Scholar]
  • 30.Papapoulos S, Bone HGI, Brandi ML, Brown JP, Chapurlat RD, Czerwinski E, Daizadeh N, Grauer A, Haller C, Krieg MA, Libanati C, Man Z, Mellstrom D, Radominski SC, Reginster JYL, Resch H, Roman Ivorra JA, Roux C, Cummings SR. Four years of denosumab exposure in women with postmenopausal osteoporosis: results from the first year extension of the FREEDOM trial. J Bone Miner Res. 2012 Mar;27(3):694–701. doi: 10.1002/jbmr.1479. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.McClung MR, Geusens P, Miller PD, Zippel H, Bensen WG, Roux C, Adami S, Fogelman I, Diamond T, Eastell R, Meunier PJ, Reginster JY. Hip Intervention Program Study Group. Effect of risedronate on the risk of hip fracture in elderly women. Hip Intervention Program Study Group. N Eng J Med. 2001;344:333–340. doi: 10.1056/NEJM200102013440503. [DOI] [PubMed] [Google Scholar]
  • 32.Black DM, Delmas PD, Eastell R, Reid IR, Boonen S, Cauley JA, Cosman F, Lakatos P, Leung PC, Man Z, Mautalen C, Mesenbrink P, Hu H, Caminis J, Tong K, Rosario-Jansen T, Krasnow J, Hue TF, Sellmeyer D, Eriksen EF, Cummings SR. Once-yearly zoledronic acid for treatment of postmenopausal osteoporosis. HORIZON Pivotal Fracture Trial. N Eng J Med. 2007;356(18):1809–1822. doi: 10.1056/NEJMoa067312. [DOI] [PubMed] [Google Scholar]
  • 33.Sheehan J, Mohamed F, Reilly M, Perry IJ. Secondary prevention following fractured neck of femur: a survey of orthopaedic surgeons practice. Ir Med J. 2000 Jun;93(4):105–7. [PubMed] [Google Scholar]
  • 34.Järvinen TL, Michaëlsson K, Jokihaara J, Collins GS, Perry TL, Mintzes B, Musini V, Erviti J, Gorricho J, Wright JM, Sievänen H. Overdiagnosis of bone fragility in the quest to prevent hip fracture. BMJ. 2015 May 26;350:h2088. doi: 10.1136/bmj.h2088. [DOI] [PubMed] [Google Scholar]
  • 35.Parker MJ, Gillespie WJ, Gillespie LD. Hip protectors for preventing hip fractures in older people. Cochrane Database Syst Rev. 2005;20:CD001255. doi: 10.1002/14651858.CD001255.pub3. [DOI] [PubMed] [Google Scholar]
  • 36.Holzer G, Von Skrbensky G, Holzer LA, Pichl W. Hip fractures and the contribution of cortical versus trabecular bone to femoral neck strength. J Bone Miner Res. 2009 Mar;24(3):468–74. doi: 10.1359/jbmr.081108. [DOI] [PubMed] [Google Scholar]
  • 37.de Bakker PM, Manske SL, Ebacher V, Oxland TR, Cripton PA, Guy P. During sideways falls proximal femur fractures initiate in the superolateral cortex: evidence from high-speed video of simulated fractures. J Biomech. 2009 Aug 25;42(12):1917–25. doi: 10.1016/j.jbiomech.2009.05.001. [DOI] [PubMed] [Google Scholar]
  • 38.Lotz JC, Cheal EJ, Hayes WC. Stress distributions within the proximal femur during gait and falls: implications for osteoporotic fracture. Osteoporos Int. 1995;5(4):252–61. doi: 10.1007/BF01774015. [DOI] [PubMed] [Google Scholar]
  • 39.Verhulp E, van Rietbergen B, Huiskes R. Load distribution in the healthy and osteoporotic human proximal femur during a fall to the side. Bone. 2008 Jan;42(1):30–5. doi: 10.1016/j.bone.2007.08.039. [DOI] [PubMed] [Google Scholar]
  • 40.Crockett GS. Osteoporosis in the elderly. Br J Clin Pract. 1960 May;14:385–90. [PubMed] [Google Scholar]
  • 41.Heini PF, Franz T, Fankhauser C, Gasser B, Ganz R. Femoroplasty-augmentation of mechanical properties in the osteoporotic proximal femur: a biomechanical investigation of PMMA reinforcement in cadaver bones. Clin Biomech (Bristol, Avon) 2004 Jun;19(5):506–12. doi: 10.1016/j.clinbiomech.2004.01.014. [DOI] [PubMed] [Google Scholar]
  • 42.Sutter EG, Mears SC, Belkoff SM. A biomechanical evaluation of femoroplasty under simulated fall conditions. J Orthop Trauma. 2010 Feb;24( 2):95–9. doi: 10.1097/BOT.0b013e3181b5c0c6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Beckmann J, Ferguson SJ, Gebauer M, Luering C, Gasser B, Heini P. Femoroplasty-augmentation of the proximal femur with a composite bone cement-feasibility, biomechanical properties and osteosynthesis potential. Med Eng Phys. 2007 Sep;29(7):755–64. doi: 10.1016/j.medengphy.2006.08.006. [DOI] [PubMed] [Google Scholar]
  • 44.De Bakker PM, Guy P, Fernlund G, Oxland TR. P452SU. Prophylactic augmentation of the contralateral femur: A finite element study. Osteoporos Int. 2006;17(Suppl 2) [Google Scholar]
  • 45.Szpalski M, Gunzburg R, Aebi M, Delimoge C, Graf N, Eberle S, Vienney C. A new approach to prevent contralateral hip fracture: Evaluation of the effectiveness of a fracture preventing implant. Clin Biomech (Bristol, Avon) 2015 Aug;30(7):713–9. doi: 10.1016/j.clinbiomech.2015.05.001. [DOI] [PubMed] [Google Scholar]

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