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BY-NC-ND 4.0 license Open Access Published by De Gruyter May 29, 2018

Resorbable implants in pediatric fracture treatment

  • Nicole Gabriele Grün , Patrick Lukas Holweg , Nicholas Donohue , Thomas Klestil and Annelie-Martina Weinberg EMAIL logo


Pediatric osteosynthesis has developed over the last 20 years, thereby reducing medical and economic burden, including long and expensive hospitalization. Currently, conventional and rigid alloying systems such as titanium are used for stabilization of bone fractures in children. In many cases, implants must be removed, as otherwise growth would be impeded. Biodegradable implant materials exhibit beneficial properties and would make a second removal surgery unnecessary. In the following article, we will give an overview of implant materials that are currently used in pediatric traumatology with a focus on Mg-based implants. Furthermore, we will discuss current scientific knowledge on resorbable implants, including results from pre-clinics and clinics.


Over the past decade, the need for implants in pediatric trauma has increased, although previously pediatric bone fractures were only rarely treated by osteosynthesis or not at all. The main reason for this is the exceptional ability of children’s bodies to heal and correct misalignments. However, over the last 20 years, surgical treatment of pediatric fractures has become more common and state of the art, in particular for long bone fractures. Analysis of efficiency and effort in terms of hospitalization costs and psychological effects on children have shown osteosynthesis to be the more attractive option. Furthermore, surgical tools and techniques have been adapted according to children’s requirements. Treatment of long bone fractures in children relies on a novel, not particularly rigid fixation procedure, termed elastic stable intramedullary nailing/flexible intramedullary nailing, which optimally supports fracture healing in children.

Conventional alloying systems such as titanium (Ti) are commonly used for bone fracture fixation in children. Given that conventional implants must always be removed, involving considerable effort for children and parents, the following question is frequently raised: could conventional, non-resorbable implants be replaced by resorbable implants?

While conservative methods require only a single anesthesia treatment, the antagonist of conservative methods needs two surgical interventions, meaning two anesthesia treatments. However, another important aspect is the percentage of re-reposition maneuvers that must also be taken into account regarding conservative procedures. Therefore, the major advantages of a resorbable implant are the single surgical procedure with definitive fixation of the fracture, a single anesthesia treatment, and minimized re-reposition maneuvers, compared to conservative treatment.

First, the article will give an overview of implant materials that are currently used in certain indications with a focus on magnesium-based implants. In a second part, the article will discuss current scientific knowledge on resorbable implants investigated in pre-clinical and clinical studies.

Resorbable and biocompatible materials

In general, biomaterials are used to support or even replace organs and tissues by taking over their functions. Non-resorbable and resorbable materials are currently used as implants and inlays in dental, cardiac, neuro-, and orthopedic surgery [1], [2], [3]. Especially in orthopedics and traumatology, resorbable biomaterials are well suited to support fracture healing. The optimal material should exhibit the required yield strength, good biocompatibility, and homogenous degradation, as well as functional properties to support or induce bone formation by releasing beneficial degradation products. The following section will focus on different types of resorbable biomaterials, including their advantages and disadvantages, in fracture treatment in children:

  1. Polymers

    The most prominent polymers are poly-l-lactic acid (PLLA) and poly-lactic-co-glycolic acid (PLGA), which are widely considered for use as osteosynthesis and bone grafts [4], [5]. Polymer-based implants are made of sugar derivatives such as PLLA and PLGA, with poor osteoconductivity and mechanical properties (low strength and stiffness, high brittleness). Depending on the polymer, the degradation rate varies between weeks to years. For example, poly-glycolic acid shows weak mechanical properties due to bulk degradation and induces tissue damage because of degradation-induced increase of glycolic acid concentration [6], [7]. To overcome the shortcomings associated with polymer-based implant degradation, the following issues would need to be addressed:

    1. Enzymes are needed to degrade slow polymer-based materials, which are limited in vivo.

    2. The monomer degradation rates must be controlled in fast copolymers.

    3. Polymer-based implants can only be used in non-load-bearing regions, due to their brittleness and low E-modulus.

    4. Because of the slow degradation rate, inflammatory cascades might be activated, inducing a fibrotic capsule and so-called “creeping” of the polymer-based system [8].

    Polyhydroxybutyrate (PHB) can serve as an alternative polymer. As PHB is produced by microorganisms, especially bacteria, this might cause toxicological problems. Recently, the toxicity of PHB has been dramatically reduced, thereby raising its medical potential [9]. However, concerns about the limited access of PHB-degrading enzymes are still present. Therefore, researchers are currently focused on attaching enzymes to guarantee adequate degradation of polymer- or PHB-based implants. Moreover, functional properties (i.e. osteoinductivity or osteoconductivity) of polymer-based materials have yet to be discovered.

  2. Ceramics

    Ceramics are characterized as synthetic bone replacement materials with good biocompatibility, osteoconductivity, osseointegration, and non-immunogenic properties. Ceramics are composed of hydroxyapatite (HA), or α- and β-tricalciumphosphates (TCPs). Either pure HA or a two-phase combination of HA and β-TCP are frequently used. Ceramics made of pure HA show chemically identical properties compared to naturally occurring HA, by releasing calcium and phosphate, as well as supporting osteogenesis. Nevertheless, pure HA and HA-based ceramics remain in the body for several years because of the slow degradation rate [10]. Moreover, ceramics do not constitute optimal implant materials for osteosynthesis due to their lack of load-bearing capacity.

    Two-phase ceramics include a slow (HA) and a fast (β-TCP) degradation source, which support bone formation and stability. A major disadvantage of TCPs, however, is that their biomechanical properties result in brittleness and low yield strength (6–10 MPa), and they tend to break apart [11]. In pediatric trauma care, ceramics are used to fill bone cysts.

  3. Biodegradable metals

    Biodegradable metals including iron (Fe), zinc (Zn), and magnesium (Mg) are more tensile, stable, and load bearing [12], [13], respectively, compared to polymers and ceramics. The low melting point of Fe constitutes an interesting property for processing Fe-based alloys. However, studies in our group revealed that limited access to oxygen was associated with slow degradation rates [14]. Therefore, Fe is currently not a suitable material for biodegradable metal implants, especially in children [15]. In contrast, Zn displays several disadvantages: low rigidity and deformability, as well as corrosion inhibition, which are the most important. Therefore, Zn is likely more suited as an alloying element in combination with other materials. Apart from good biocompatibility, Mg also shows favorable biomechanical properties, as already demonstrated by push-out tests ex vivo. Other studies have demonstrated the functional properties of Mg-based implants, especially their ability to support bone fracture healing [16], [17], [18].

Magnesium-based implants

In pediatric trauma surgery, it is of utmost importance to use resorbable implants without short-term and especially without long-term adverse effects. For instance, studies have demonstrated that intermetallic phases of alloying elements are traceable for several years. The effect on the growing skeleton was not investigated in any of those works [19], [20]. However, over the last decade, several studies have focused on Mg-based implants alloyed with rare-earth elements (REEs), such as yttrium or gadolinium [19], [21], [22], [23], which slow down the degradation rate and increase implant stability. Initial experiments with Mg-based alloying systems including REEs (WE43; Mg-Y-Nd-HRE) showed improved bone-implant interfaces and osseointegration compared to conventional Ti in a growing rat model. In our study, we suggested that bone formation was supported by the Mg-based WE43, which is fundamental for its application in osteosynthesis [24]. In another study, we demonstrated a slow degradation rate of the Mg-based implant WZ21 (Mg-1 wt% Zn-0.25 wt% Ca-0.15 wt% Mn-2 wt% Y). WZ21 did not induce any inflammatory response, neither immediately after implantation nor over a time period of 24 weeks. Additionally, micro-computed tomography (μCT) showed enhanced, new bone formation between 4 and 8 weeks after WZ21 implantation [25].

However, REEs have been described to be mildly toxic, without causing severe reactions in the body. These elements (REEs including gadolinium, yttrium, etc.) do not normally occur in the human body, and their harmful or beneficial effects on the growing skeleton have not been elucidated. As a result, the aim was set to develop a resorbable metallic implant based on elements occurring naturally within the body and avoiding the use of REEs, such as gadolinium or yttrium. Different research groups focused on producing implants from high-purity Mg (>99.99 wt%), which were further evaluated in vivo. Wang et al. demonstrated enhanced recruitment of stromal stem cells isolated from the bone marrow after using Mg-based interference screws in a rabbit tendon graft model that underwent anterior cruciate ligament reconstruction (ACLR) [26]. Another study showed that the corrosion of high-purity Mg is accelerated when co-implanted with Ti screws, depending on the distance between the two alloying systems. This group suggested that in close proximity, Mg-based and Ti screws might form a galvanic-like cell, which enhances Mg corrosion in vivo [27]. To investigate the shortcomings of pure Mg alloys, such as rapid gas formation, Lim et al. compared uncoated and HA-coated Mg plates by inserting these above the frontal bone of Sprague-Dawley rats. While uncoated Mg plates showed gas formation 2 weeks after insertion, HA-coated Mg plates only showed gas formation after 12 weeks [28].

A collaboration between the Medical University of Graz and the ETH Zurich developed appropriate REE-free Mg-based implants, which were evaluated in vitro and in vivo. Apart from the good biocompatibility, the biomechanical properties and controlled degradation rate were comparable with WZ21 and WE43. To develop the optimal Mg-based implant, different compositions of Mg, Zn, and Ca were investigated, especially in growing organisms.

In a first study, μCT analysis revealed extremely rapid degradation rates of ZX50 (Mg-5 wt% Zn-0.25 wt% Ca-0.15 wt% Mn) in growing rats. It is important to note that the regulation of degradation rates play a major role in bone formation. At the desired implant degradation rate, an adequate concentration of magnesium hydroxide [Mg(OH)2] and hydrogen gas develops because of pit corrosion. The insoluble Mg(OH)2 forms a protective layer around the implant surface and when the chloride level in the body rises, Mg is released from Mg(OH)2 to bind chloride and form MgCl2. This product is soluble and can therefore be transported or degraded [29]. However, fast degradation rates result in increased gas formation, which negatively influence bone formation by suppressing bone and, at worst, destroying the physis [30]. In contrast, slow degradation rates can result in chronic, inflammatory immune responses, as seen with slow polymer-based materials. Therefore, regulating degradation rates of Mg-based implants is a challenge that will determine how these implants are used not only in pediatrics but also in orthopedics and traumatology in adults.

In further studies, the Zn content was reduced and high-purity Mg was used for implant fabrication (ZX10 and ZX20). The degradation rate of ZX10 was significantly lower compared to ZX20 (manuscript in preparation). As a result, animals implanted with ZX10 showed improved bone in-growth and osseointegration. Furthermore, bone healing via callus formation was demonstrated, which has been proven to be the necessary support for fracture healing.

To simulate bone fracture fixation in children and adolescents, initial experiments were performed with Mg-based screws (ZX00) in a growing sheep model. ZX00 (Mg- 0.45 wt% Zn-0.45 wt% Ca) was transcortically implanted into the ovine tibia and compared to conventional Ti screws. The ZX00 alloying system revealed optimal biomechanical properties and controlled degradation rates in vivo. Moreover, good biocompatibility, osteoconductivity, and adequate support of callus formation were observed in the ovine model. Twelve weeks after ZX00 implantation, new bone formation and a stable bone-implant interface was demonstrated. In contrast, weaker bone formation beneath the implant was observed with Ti screws (because the load is carried over the screw and the bone degrades), which might also result in re-fracture after implant removal.

Current scientific knowledge on resorbable implants: results from pre-clinics and clinics

Therefore, pre-clinical in vivo studies in large animal models are needed to answer fundamental questions on resorbable implants in growing skeletons, based on the growing potential of children:

  1. Are there any short- or long-term adverse effects on growth associated with the implant? Long-term studies that continue until complete resorption of the implant (12–24 months) are needed.

  2. Does the implant support bone bridging and, in consequence, lead to growth arrest and bone deviation? This question could be answered only by surveillance over at least 2 years, as this period is used in pediatric trauma to judge how the implant affects a phenomenon such as growth arrest.

  3. Are there differences in the inflammatory reaction compared to adult bone?

The remaining part of this article focuses on the literature addressing the above questions. We examined in vivo studies using large immature animal models and clinical trials performed on children. Most in vivo studies use large mature or adult animals. However, in vivo studies in mature sheep showed sequestration of PLLA implants within new bone, 3 months after implantation. One year after PLLA implantation, a further tissue reaction associated with structural disintegration was observed. However, the reduced PLLA mass was subsequently replaced by avascular fibrous tissue including macrophages and multinucleated cells on the PLLA surface. Observations after 3 years displayed isolated polymer fragments indicating the longevity of this resorbable implant material [31]. Another study showed an increase in mechanical strength of polylactide carbonate (PLC) and PLLA, 6 and 12 weeks after ACLR in sheep. Interestingly, the PLC screw was entirely replaced by new bone after 52 weeks, whereas PLLA screws were not resorbed and surrounded by a fibrous layer, thereby suggesting satisfactory mechanical and osteoconductive properties of PLC [32]. One of the longest studies concerning resorbable implants in large animal models was published in 2002 by Jukkala-Partio et al. Two self-reinforced PLLA screws were used to fix subcapital femoral osteotomies in young adult sheep. The follow-up periods comprised 12 weeks, 1 year, and 3 years, as well as 7 years and 4 months (n=1). Three years after fixation, implant areas were replaced by new bone and connective tissue with some implant remnants. Tight bone was observed >7 years later, thereby indicating good mechanical properties and biocompatibility but very slow degradation rates [33]. Interestingly, Thormann et al. utilized interference screws made of the Mg alloy W4, which were coated with polyethylene glycol and implanted in the femur condyle of a sheep model. Compared to Ti, W4 screws showed enormous gas formation and a consequential bone defect after 6 and 12 weeks, and even 1 year after implantation. Moreover, W4 screws were not fully integrated in the surrounding bone tissue compared to PLLA and Ti [34]. To the best of our knowledge, Magarelli et al. were the only group to use growing sheep to investigate the biocompatibility of HA- and β-TCP-coated PLLA screws implanted into the femurs [35]. The studies described above used mature or adult ovine models or did not mention maturation status; other studies with large growing animal models focused on maxillofacial or calvarian surgery [36]. We did not find any research on the impact of resorbable implants on the growth plate.

Similar to in vivo studies using large animal models, clinical trials have especially focused on PLLA. A thorough search of the literature yielded only one clinical trial using Mg-based implants in children. However, in 2013, a new minimally invasive treatment for pediatric, diaphyseal forearm fracture was published. Conventional open reduction and internal fixation using plates was compared to this minimally invasive method. Therefore, ultra-high-strength, resorbable intramedullary nails of poly(lactide-co-glycolide) were used in 5–15-year-old children. Follow-up patients showed good union in the fractured bones and acceptable alignment. However, one re-fracture occurred due to high-energy trauma. To determine long-term outcomes, a randomized multicenter study was conducted [37]. Poircuitte et al. published a prospective monocentric study with 24 patients who had a fracture that was amenable to osteosynthesis by small-diameter screws. Some of the screws (d=2.8 mm) were made of poly-l-lactide-poly-d-lactide acid and trimethylene carbonate. Every month, patients were clinically and radiographically monitored until the end of the follow-up protocol (1 year). No instability, secondary displacement, growth disturbances, or osteolysis were observed. All fractures healed without complications [38]. Another study aimed to compare the efficacy of the open reduction and resorbable poly-d,l-lactic acid (PDLLA) pin fixation method with the closed reduction and lateral external fixation method in irreducible delayed displaced supracondylar humeral fractures (SHFs) in children. A total of 124 consecutive patients with irreducible delayed Gartland type III SHF were recruited. While 64 patients of group 1 underwent PDLLA pin fixation after open reduction, 60 patients of group 2 were treated by lateral external fixation after closed reduction. Within 8–12 weeks, all fractures healed without Volkmann contracture, non-union, infection, or myositis ossificans. Functional and cosmetic results were comparable between the two groups, indicating that both PDLLA pin fixation and lateral external fixation are reliable and safe alternatives for irreducible delayed SHF [39].

In 2015, Yu et al. presented a new technique to treat avascular necrosis of the femoral head and non-union using biodegradable Mg screws. In this study, 19 young adult patients with displaced femoral neck fractures were recruited and treated with this new technique: the fracture was fixed with Ti and pure Mg screws, and combined with the implantation of vascularized iliac grafting. Of the 19 cases, 18 showed hip union after an average duration of 4.1 months, whereas only 1 non-union was observed. The Harris hip score revealed 1 poor, 3 fair, and 14 excellent results, and avascular necrosis of the femoral head was not observed in any patient [40].

Although the authors may not have covered all publications, there have only been a few studies that focus on resorbable implants to treat pediatric fractures. To generate well-founded knowledge, research must answer the open questions on pediatric bone fractures and their treatment, in large growing animals or in clinical studies. The knowledge created so far is insufficient to recommend application and requires further investigation.

In summary, it can be said that the development of resorbable material implants constitutes a milestone in improving treatment of pediatric bone fractures.

Author Statement

  1. Research funding: Authors state no funding involved. Conflict of interest: Prof. Annelie-Martina Weinberg is a stakeholder and the CEO of BRI.TECH GmbH, but the 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. Annelie-Martina Weinberg: conceptualization; supervision; validation; writing – original draft; writing – review and editing. Nicole Gabriele Grün: data curation; investigation; methodology; project administration; writing – original draft. Patrick Lukas Holweg: investigation; methodology; software; writing – original draft. Nicholas Donohue: investigation; software; visualization; writing – review and editing. Thomas Klestil: conceptualization; formal analysis; supervision; writing – review and editing.

Publication Funding

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


[1] Soler-Botija C, Bagó JR, Llucià-Valldeperas A, Vallés-Lluch A, Castells-Sala C, Martínez-Ramos C, et al. Engineered 3D bioimplants using elastomeric scaffold, self-assembling peptide hydrogel, and adipose tissue-derived progenitor cells for cardiac regeneration. Am J Transl Res 2014;6:291–301.Search in Google Scholar PubMed

[2] Takmakov P, Ruda K, Phillips KS, Isayeva IS, Krauthamer V, Welle CG. Rapid evaluation of the durability of cortical neural implants using accelerated aging with reactive oxygen species. J Neural Eng 2015;12:026003.10.1088/1741-2560/12/2/026003Search in Google Scholar PubMed

[3] Linz C, Collmann H, Kübler A, Böhm H, Schweitzer T. Patient-specific biodegradable implant in pediatric craniofacial surgery. J Cranio-Maxillofac Surg 2017;45:1111.10.1016/j.jcms.2017.05.001Search in Google Scholar

[4] Bizenjima T, Takeuchi T, Seshima F, Saito A. Effect of poly (lactide-co-glycolide) (PLGA)-coated β-tricalcium phosphate on the healing of rat calvarial bone defects: a comparative study with pure-phase β-tricalcium phosphate. Clin Oral Implants Res 2016;27:1360–7.10.1111/clr.12744Search in Google Scholar PubMed

[5] Zhao B, Qiu X, Wang D, Li H, He X. Application of bioabsorbable screw fixation for anterior cervical decompression and bone grafting. Clinics 2016;71:320.10.6061/clinics/2016(06)06Search in Google Scholar PubMed

[6] Gunatillake P, Adhikari R. Biodegradable synthetic polymers for tissue engineering. Eur Cell Mater 2003;5:1–16.10.22203/eCM.v005a01Search in Google Scholar PubMed

[7] Gentile P, Chiono V, Carmagnola I, Hatton PV. An overview of poly(lactic-co-glycolic) acid (PLGA)-based biomaterials for bone tissue engineering. Int J Mol Sci 2014;15:3640–59.10.3390/ijms15033640Search in Google Scholar PubMed PubMed Central

[8] Parent M, Nouvel C, Koerber M, Sapin A, Maincent P, Boudier A. PLGA in situ implants formed by phase inversion: critical physicochemical parameters to modulate drug release. J Control Release 2013;172:292–304.10.1016/j.jconrel.2013.08.024Search in Google Scholar PubMed

[9] Luef KP, Stelzer F, Wiesbrock F. Poly(hydroxy alkanoate)s in medical applications. Chem Biochem Eng Q 2015;29: 287–97.10.15255/CABEQ.2014.2261Search in Google Scholar PubMed PubMed Central

[10] León B, Jansen J, editors. Thin Calcium Phosphate Coatings for Medical Implants [Internet]. New York, NY: Springer New York; 2009 [cited 2017 Oct 6]. Available from: Accessed 6 October, 2017.10.1007/978-0-387-77718-4Search in Google Scholar

[11] Black J. Biological Performance of Materials: Fundamentals of Biocompatibility, 4th ed. Boca Raton, FL: CRC Press; 2005. 528 p.10.1201/9781420057843Search in Google Scholar

[12] Moravej M, Mantovani D. Biodegradable metals for cardiovascular stent application: interests and new opportunities. Int J Mol Sci 2011;12:4250.10.3390/ijms12074250Search in Google Scholar PubMed PubMed Central

[13] Fagali NS, Grillo CA, Puntarulo S, Fernandez Lorenzo de Mele MA. Cytotoxicity of corrosion products of degradable Fe-based stents: relevance of pH and insoluble products. Colloids Surf B Biointerfaces 2015;128:480–8.10.1016/j.colsurfb.2015.02.047Search in Google Scholar PubMed

[14] Hofstetter J, Martinelli E, Pogatscher S, Schmutz P, Povoden-Karadeniz E, Weinberg AM, et al. Influence of trace impurities on the in vitro and in vivo degradation of biodegradable Mg-5Zn-0.3Ca alloys. Acta Biomater 2015;23:347–53.10.1016/j.actbio.2015.05.004Search in Google Scholar PubMed

[15] Purnama A, Hermawan H, Couet J, Mantovani D. Assessing the biocompatibility of degradable metallic materials: state-of-the-art and focus on the potential of genetic regulation. Acta Biomater 2010;6:1800–7.10.1016/j.actbio.2010.02.027Search in Google Scholar PubMed

[16] Wu L, Feyerabend F, Schilling AF, Willumeit-Römer R, Luthringer BJC. Effects of extracellular magnesium extract on the proliferation and differentiation of human osteoblasts and osteoclasts in coculture. Acta Biomater 2015;27:294–304.10.1016/j.actbio.2015.08.042Search in Google Scholar PubMed

[17] Jähn K, Saito H, Taipaleenmäki H, Gasser A, Hort N, Feyerabend F, et al. Intramedullary Mg2Ag nails augment callus formation during fracture healing in mice. Acta Biomater 2016;36:350–60.10.1016/j.actbio.2016.03.041Search in Google Scholar PubMed

[18] Zhang Y, Xu J, Ruan YC, Yu MK, O’Laughlin M, Wise H, et al. Implant-derived magnesium induces local neuronal production of CGRP to improve bone-fracture healing in rats. Nat Med 2016;22:1160.10.1038/nm.4162Search in Google Scholar PubMed PubMed Central

[19] Amerstorfer F, Fischerauer S, Fischer L, Eichler J, Draxler J, Zitek A, et al. Long-term in vivo degradation behavior and near-implant distribution of resorbed elements for magnesium alloys WZ21 and ZX50. Acta Biomater 2016;42:440–50.10.1016/j.actbio.2016.06.025Search in Google Scholar PubMed

[20] Angrisani N, Reifenrath J, Zimmermann F, Eifler R, Meyer-Lindenberg A, Vano-Herrera K, et al. Biocompatibility and degradation of LAE442-based magnesium alloys after implantation of up to 3.5 years in a rabbit model. Acta Biomater 2016;44:355–65.10.1016/j.actbio.2016.08.002Search in Google Scholar PubMed

[21] Pichler K, Kraus T, Martinelli E, Sadoghi P, Musumeci G, Uggowitzer PJ, et al. Cellular reactions to biodegradable magnesium alloys on human growth plate chondrocytes and osteoblasts. Int Orthop 2014;38:881.10.1007/s00264-013-2163-3Search in Google Scholar PubMed PubMed Central

[22] Myrissa A, Bräuer S, Martinelli E, Willumeit-Römer R, Gössler W, Weinberg A-M. Gadolinium accumulation in organs of Sprague-Dawley® rats after implantation of a biodegradable magnesium-gadolinium alloy. Acta Biomater 2017;48:521–9.10.1016/j.actbio.2016.11.024Search in Google Scholar PubMed

[23] Myrissa A, Nezha Ahmad A, Lu Y, Martinelli E, Eichler J, Szakacs G, et al. In vitro and in vivo comparison of binary Mg alloys and pure Mg. Mater Sci Eng C 2016;61:865–74.10.1016/j.msec.2015.12.064Search in Google Scholar PubMed

[24] Castellanie C, Lindtner RA, Hausbrandt P, Tschegg E, Stanzl-Tschegg SE, Zanoni G, et al. Bone-implant interface strength and osseointegration: biodegradable magnesium alloy versus standard titanium control. Acta Biomater 2011;7:432–40.10.1016/j.actbio.2010.08.020Search in Google Scholar PubMed

[25] Kraus T, Fischerauer SF, Hänzi A, Uggowitzer PJ, Löffler JF, Weinberg A-M. Magnesium alloys for temporary implants in osteosynthesis: in vivo studies of their degradation and interaction with bone. Acta Biomater 2012;8:1230–8.10.1016/j.actbio.2011.11.008Search in Google Scholar PubMed

[26] Wang J, Xu J, Song B, Chow DH, Yung PS, Qin L. Magnesium (Mg) based interference screws developed for promoting tendon graft incorporation in bone tunnel in rabbits. Acta Biomater 2017;63:393–410.10.1016/j.actbio.2017.09.018Search in Google Scholar PubMed

[27] Hou P, Han P, Zhao C, Wu H, Ni J, Zhang S, et al. Accelerating corrosion of pure magnesium Co-implanted with titanium in vivo. Sci Rep 2017;7:41924.10.1038/srep41924Search in Google Scholar PubMed PubMed Central

[28] Lim H-K, Byun S-H, Woo J-M, Kim S-M, Lee S-M, Kim B-J, et al. Biocompatibility and biocorrosion of hydroxyapatite-coated magnesium plate: animal experiment. Materials 2017;10:1149.10.3390/ma10101149Search in Google Scholar PubMed PubMed Central

[29] Witte F, Hort N, Vogt C, Cohen S, Kainer KU, Willumeit R, et al. Degradable biomaterials based on magnesium corrosion. Curr Opin Solid State Mater Sci 2008;12:63–72.10.1016/j.cossms.2009.04.001Search in Google Scholar

[30] Kraus T, Fischerauer S, Treichler S, Martinelli E, Eichler J, Myrissa A, et al. The influence of biodegradable magnesium implants on the growth plate. Acta Biomater 2018;66:109–17.10.1016/j.actbio.2017.11.031Search in Google Scholar PubMed

[31] Walton M, Cotton NJ. Long-term in vivo degradation of poly-l-lactide (PLLA) in Bone. J Biomater Appl [Internet] 2006 Mar 16 [cited 2018 Jan 30]; Available from: Accessed 30 January, 2018.10.1177/0885328206065125Search in Google Scholar PubMed

[32] Walsh W, Cotton N, Stephens P, Brunelle J, Langdown A, Auld J, et al. Comparison of poly-l-lactide and polylactide carbonate interference screws in an ovine anterior cruciate ligament reconstruction model. Arthrosc J Arthrosc Relat Surg 2007;23:757–65.e2.10.1016/j.arthro.2007.01.030Search in Google Scholar PubMed

[33] Jukkala-Partio K, Laitinen O, Vasenius J, Partio EK, Toivonen T, Tervahartiala P, et al. Healing of subcapital femoral osteotomies fixed with self-reinforced poly-l-lactide screws: an experimental long-term study in sheep. Arch Orthop Trauma Surg 2002;122:360–4.10.1007/s00402-001-0379-ySearch in Google Scholar PubMed

[34] Thormann U, Alt V, Heimann L, Gasquere C, Heiss C, Szalay G, et al. The biocompatibility of degradable magnesium interference screws: an experimental study with sheep. BioMed Res Int [Internet] 2015 [cited 2018 Jan 30]; 2015. Available from: Accessed 30 January, 2018.10.1155/2015/943603Search in Google Scholar PubMed PubMed Central

[35] Magarelli N, Savastano MA, Palmieri D, Zappacosta R, Lattanzio G, Salini V, et al. Poly-l-lactic acid β-tricalcium phosphate screws: a preliminary in vivo biocompatibility study [Internet] 2016 [cited 2018 Jan 29]. Available from: Accessed 29 January, 2018.Search in Google Scholar

[36] Peltoniemi HH, Tulamo R-M, Toivonen T, Hallikainen D, Törmälä P, Waris T. Biodegradable semirigid plate and miniscrew fixation compared with rigid titanium fixation in experimental calvarial osteotomy. J Neurosurg 1999;90:910–7.10.3171/jns.1999.90.5.0910Search in Google Scholar PubMed

[37] Sinikumpu J-J, Keränen J, Haltia A-M, Serlo W, Merikanto J. A new mini-invasive technique in treating pediatric diaphyseal forearm fractures by bioabsorbable elastic stable intramedullary nailing: a preliminary technical report. Scand J Surg [Internet] 2013 Sep 20 [cited 2018 Jan 29]. Available from: Accessed 29 January, 2018.10.1177/1457496913490459Search in Google Scholar PubMed

[38] Poircuitte JM, Popkov P, Huber DH, Polirsztok E, Lascombes P, Journeau P. Resorbable osteosynthetic devices in pediatric traumatology: a prospective series of 24 cases. Eur J Orthop Surg Traumatol 2015;25:997–1004.10.1007/s00590-015-1656-8Search in Google Scholar PubMed

[39] Li J, Fu D, Yu C, Wang S, Ze R, Tang X. Surgical management of delayed irreducible Gartland III supracondylar fractures in children: open reduction and internal fixation versus external fixation. J Shoulder Elbow Surg 2017;26:299–304.10.1016/j.jse.2016.10.006Search in Google Scholar PubMed

[40] Yu X, Zhao D, Huang S, Wang B, Zhang X, Wang W, et al. Biodegradable magnesium screws and vascularized iliac grafting for displaced femoral neck fracture in young adults. BMC Musculoskelet Disord 2015;16:329.10.1186/s12891-015-0790-0Search in Google Scholar PubMed PubMed Central

Supplementary Material:

The article ( offers reviewer assessments as supplementary material.

Received: 2018-02-01
Accepted: 2018-05-08
Published Online: 2018-05-29

©2018 Grün N.G. et al., published by De Gruyter, Berlin/Boston

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

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