- Open Access
Masquelet technique in military practice: specificities and future directions for combat-related bone defect reconstruction
Military Medical Research volume 9, Article number: 48 (2022)
Because of its simplicity, reliability, and replicability, the Masquelet induced membrane technique (IMT) has become one of the preferred methods for critical bone defect reconstruction in extremities. Although it is now used worldwide, few studies have been published about IMT in military practice. Bone reconstruction is particularly challenging in this context of care due to extensive soft-tissue injury, early wound infection, and even delayed management in austere conditions. Based on our clinical expertise, recent research, and a literature analysis, this narrative review provides an overview of the IMT application to combat-related bone defects. It presents technical specificities and future developments aiming to optimize IMT outcomes, including for the management of massive multi-tissue defects or bone reconstruction performed in the field with limited resources.
The reconstruction of segmental bone defects remains a challenge for military orthopedic surgeons, especially in cases of missile or blast injuries characterized by a high proportion of multi-tissue and infected defects [1,2,3,4,5]. Treatment modalities include techniques such as autologous bone graft (ABG), bone transport, vascularized bone transfer, and the two-stage Masquelet induced membrane (IM) technique (IMT; Table 1) [6, 7]. Because of its simplicity, reliability, and efficiency, even for large defects, the latter has spread globally in the last decade [8, 9]. The IMT presents strong advantages because it requires no sophisticated equipment or microsurgical skills to perform and has a healing time almost independent of the defect length . This simplicity makes it particularly adapted to bone reconstruction in military practice, especially in current high-intensity warfare where patients cannot be evacuated from the combat zone or present with multiple associated injuries [2, 3, 5, 10].
IMT is a two-stage procedure, using a cement spacer in the first stage and an ABG in the second stage. The spacer has a mechanical action, obviating fibrous tissue invasion of the recipient site, and a biological action that induces the surrounding membrane due to a foreign body reaction. The membrane then acts as a biological chamber that revascularizes the bone graft and prevents resorption [8, 9]. We believe that these two stages are beneficial when dealing with the large, multi-tissue, and infected defects encountered in wartime [2, 10]. Reconstruction of combat-related extremity injuries occurs in the aftermath of a primary damage control orthopedics (DCO) procedure and requires a sequential surgical approach to achieve infection control, soft-tissue coverage, and bone union (Fig. 1). In this context of care, the IMT matches perfectly with such consecutive reconstructive procedures [5, 11].
To date, only a few authors have reported on the Masquelet technique for reconstruction of combat-related bone defects [3, 12,13,14]. In 2019, we published the first clinical series about tibia reconstruction by IMT in soldiers . Since then, we have repeatedly published on IMT use in the various settings of our military practice. Like civilian authors, we have found that this technique achieves satisfying outcomes in bone union and complication rates [3, 12, 15,16,17,18,19,20,21,22]. We have also demonstrated that IMT is suited for bone defects of ballistic origin and can be applied in the austere environment of forward surgical units [12, 17, 22]. However, although simple, a successful IMT procedure is not easy to complete, especially when facing infected defects with limited resources [3, 18, 22]. Therefore, this review aims to present Masquelet technique tips and tricks for the reconstruction of combat-related bone defects in modern warfare.
Masquelet technique basics
How does it work?
Foreign body encapsulation membrane
The IM is an encapsulation membrane resulting from a foreign body reaction caused by the implantation of a polymethylmethacrylate (PMMA) cement spacer into the bone defect. This foreign body reaction, composed of macrophages and foreign body giant cells, is the end-stage response of the inflammatory and wound healing responses following implantation of any medical device or biomaterial . The IM is a vascularized collagen-based matrix entrapping immune cells (macrophages, lymphocytes), as well as bone-remodeling osteoclasts and osteoprogenitor cells (mesenchymal stem cells) [24, 25].
IM biological properties
From a biological perspective, the IM is a tissue regeneration chamber promoting bone graft integration and bone formation in three ways. First, the membrane acts as a physical barrier between the graft and the surrounding soft tissues, preventing macrophage invasion and subsequent graft resorption. Next, the membrane improves both angiogenesis and osteogenesis by secreting key growth factors including vascular endothelial growth factor (VEGF), transforming growth factor-β1 (TGF-β1), and bone morphogenic protein-2 (BMP-2) . Briefly, VEGF-A stimulates the formation of vascular buds on the inner surface of the membrane, which penetrate bone graft crevices and permit effective graft revascularization . BMP-2 and TGF-β1 stimulate bone formation by promoting the osteogenic differentiation of bone marrow stem cells .
Prerequisites for use
Masquelet  and Giannoudis et al.  have already detailed technical specificities for a successful IMT application. However, it should be stressed that three conditions are imperative to prevent IMT failure: prior infection eradication, appropriate soft-tissue coverage during stage 1, and stable bone fixation during stage 2.
Prior infection eradication
Infection is the single most frequent cause of IMT failure . Since they have no individual vascularization, bone grafts are directly affected by the presence of germs within the membrane, leading to subsequent graft resorption or late septic recurrence. In addition, infection alters IM osteogenic properties by decreasing local expression of growth factors, decreasing osteoblast and stem cell presence, and increasing bone resorption factors and proinflammatory cytokines [29, 30]. Thus, IMT must only be deployed once any infection is definitively eradicated or at least brought under control. In cases of infected bone defect, a prior IMT stage 0 is then crucial before cement spacer implantation [4, 31]. Stage 0 includes multiple consecutive procedures: removal of eventual internal fixation material, radical debridement of infected tissue, copious irrigation, and temporary stabilization by external fixation. Deep samples should be taken from the bone defect area and the medullary canal for microbiological analysis .
Appropriate soft-tissue coverage at stage 1
Cement spacer implantation requires not only the absence of infection but also stable soft-tissue coverage. Any secondary skin necrosis or wound dehiscence inevitably leads to cement spacer contamination, with subsequent infection and IMT failure. Thus, management of combat-related bone defects using the Masquelet technique often involves soft-tissue reconstruction using flap transfer during stage 1. The choice between micro-vascularized free flaps and pedicled (local or distant) flaps depends on the context of care, surgical resources, and associated injuries. Free flaps are more suited to stable patients managed in the ideal conditions of medical treatment facilities located outside the combat zone [1, 2]. Conversely, pedicled flaps are needed for early soft-tissue coverage in polytraumatized patients and in the austere conditions of forward surgical units where plastic surgeons are few or absent (Figs. 2 and 3) [4, 10, 32].
Stable bone fixation at stage 2
A lack of mechanical stability in the definitive bone fixation at stage 2 is the second cause of IMT failure [21, 22]. Insufficient stability affects graft revascularization (by rupture of the inner membrane vascular buds), leading to aseptic non-union and subsequent implant failure . If all bone fixations are possible, the implant choice depends on the defect location, associated infection, and surgeon’s preferences. In the absence of infection, intramedullary nailing is mechanically preferred for lower extremity fractures, and plating is preferred for upper extremity fractures and metaphyseal fractures . However, in military practice, most bone defects are primarily stabilized by external fixation and complicated by early infection. Definitive external fixation is naturally compatible with IMT use but exposes to specific issues such as poor patient tolerance, pin-track infection, and insufficient mechanical stability [4, 33]. Therefore, a sequential bone stabilization strategy is often required for a successful IMT application. Conversion from external to internal fixation can be performed in a single procedure during stage 2 despite the risk of pin-track infection between stages . However, a sequential internal fixation, including the use of a reinforced spacer at stage 1, seems preferable for infected bone defect reconstruction in locations where external fixation is not suitable, such as the upper extremity, femur, and tibial metaphysis (Figs. 4, 5 and 6) .
Optimal timing between stages
Basic research of animal found the highest osteo-inductive bioactivity after 2–4 weeks suggesting bone grafting after this short time interval [26, 35]. However, clinical, not evidence-based recommendations usually range from 4 to 8 weeks [7, 9, 34, 35]. In fact, successful outcomes were reported with bone grafting performed several months or years after spacer implantation [36, 37]. Gessmann et al.  recently studied the histological properties of IMs from 60 patients at different maturation ages (1–16 weeks). They demonstrated that mesenchymal stem cells and growth factors were found over all time points with minor changes. In addition, according to Masquelet , bone grafts at stage 2 can be considered as a foreign body that is likely to reactivate the IM biological properties. Thus, the timing for the second stage should be based on clinical factors rather than on a theoretical optimal stages interval. The only valid rule is to wait for the infection control and the perfect soft tissues healing, particularly in combat-related injuries requiring flap reconstruction .
The IMT global complication rate ranges from 26 to 49% in the literature, with two frequent complications: nonunion and infection [19, 38, 39]. Morelli et al.  found 9.6% of additional bone healing procedures after IMT application, and 26.7% of other revision surgeries. Mi et al.  compared the IMT results (from their meta-analysis of 41 papers) with those of 37 papers reporting on bone transport. They could not find any significant difference between techniques in terms of bone union, infection, malunion, and amputation; nevertheless, the refracture rate was 8.5 times higher with bone transport. Wen et al.  reported a monocentric retrospective study comparing the results of IMT, bone transport, and free vascularized fibular grafting for posttraumatic long-bone defect reconstruction in 317 patients. Overall bone union and complication rates were similar between the three techniques. Thus, IMT achieves similar outcomes to those of other reconstructive procedures in terms of bone union and complication rates but with greater ease of use .
In the literature, IMT is applied for tibia reconstruction in two-thirds of cases. It is also the site at which the complication rate is the highest, with a clear predominance of infection [38, 39]. Due to the superficial location of this bone, any timing error or complication related to soft-tissue coverage carries the risk of spacer contamination . In a recent meta-analysis, Hsu et al.  reported a postoperative infection rate of 24% after tibia reconstruction using IMT. Severe soft-tissue injury, early wound infection, and delayed soft-tissue coverage make secondary tibia nailing risky in military practice . Plating remains preferable for proximal or diaphyseal metaphyseal reconstruction, for which external fixation is poorly tolerated and causes joint stiffness (Fig. 6) [21, 33].
Diaphyseal tibia defects
Regarding the risk of infection, most diaphyseal tibia defects are stabilized by external fixation in military practice [1, 3, 21]. A modular frame should be preferred to a circular frame to allow soft-tissue reconstruction and delayed bone grafting. A unilateral frame is sufficient during the period of IM induction after stage 1, but a multiplanar frame is required at stage 2 to provide enough stability for bone graft integration (Fig. 2). Conversely, a subsequent progressive frame dynamization is necessary to enhance graft corticalization [3, 9, 21, 33]. Masquelet [8, 9] recommends the performance of tibia reconstructions pressed on the fibula and reinforced by inter-tibiofibular grafts at both ends of the reconstruction. When access to the fibula is easy during stage 1 (e.g., in the case of anterior compartment damage), an inter-tibiofibular spacer should be made (Fig. 2). In other situations where a tibial spacer is used, a bipolar inter-tibiofibular graft is added during stage 2 using an approach selected in accordance with potential vascular injury [21, 33].
Although it runs a higher risk of septic complications, locked intramedullary nailing is the best mechanical option, especially in very large tibia defects (Fig. 5). For Mauffrey et al. , nailing could allow early weight-bearing compared to external fixation, which seems questionable within an IMT procedure. Acting as a central core, the intramedullary nail also has the advantage of limiting the bone graft volume inside the membrane. This central part of the graft will be eliminated under the effect of the mechanical constraints during the graft corticalization process, ending with the formation of a new intramedullary canal .
Metaphyseal tibia defects
Proximal and distal tibia reconstructions are best achieved using plating. The primary management of such severe multi-tissue injuries usually requires DCO application with temporary external fixation. In the absence of infection, secondary plating can be performed readily during stage 1 (Fig. 3). Conversely, in cases of infected bone defect, the temporary external fixator should be converted to a reinforced spacer during stage 1 and the definitive internal fixation delayed at stage 2 after achieving extended antibiotic medication [4, 33]. Importantly, distal tibia reconstructions should also be pressed on the fibula to improve mechanical stability (Fig. 4).
Femur and upper extremity reconstruction
The complications rate is lower at the femur, humerus, and forearm levels, where soft-tissue issues are more uncommon . For mechanical and functional reasons, internal fixation should always be preferred to external fixation, using a reinforced spacer if necessary (Fig. 6) [4, 21, 33].
Femur mechanical conditions are less favorable for successful graft integration than those of the tibia. The divergence between mechanical and anatomical axes results in high varus loads, jeopardizing graft corticalization in cases of insufficient fixation stability [8, 19]. A stable internal fixation at stage 2 is then critical to achieve bone union (Fig. 1). Morwood et al.  reported that patients treated with intramedullary nailing experienced faster union, requiring fewer grafting procedures and fewer reoperations, than those treated by plating. When plate fixation is required at the distal femur, a fibular segment must often be intercalated inside the membrane on the medial aspect of the reconstruction to counteract the bending varus forces. This fibular segment can be a micro-vascularized or non-vascularized free transfer that will be revascularized by the IM [8, 9, 43].
Upper extremity defects
Humerus, radius, and ulna defects are best stabilized using plates [21, 33, 44]. The involvement of a thick soft-tissue envelope and appropriate stability of plate fixation explain the observation that failures of humerus and forearm reconstructions are infrequent [21, 44]. Humerus reconstruction by IMT may require an anterior transposition of the radial nerve through the fracture or non-union site in stage 1. The surgical approach at stage 2 is then much easier and safer since the transposed nerve is positioned on the medial side of the bone gap and protected by the membrane .
The complication rate is higher at the hand, similar to the tibia level. The superficial location of the reconstruction space leads to frequent septic failure secondary to spacer exposure or other soft-tissue coverage issues . Appropriate stable fixation can be achieved by either multiple pinning or plating depending on the defect location (i.e., phalangeal or metacarpal) [12, 46].
Massive bone defect reconstruction
Combat-related extremity injuries are often characterized by extensive soft-tissue and bone defects caused by high-velocity projectiles or explosive devices. These massive tissue destructions are frequently observed in polytraumatized patients whose associated injuries or early complications do not allow for long and complex reconstructive procedures such as micro-vascularized tissue transfer . Moreover, without exception, these sophisticated procedures are not feasible in the operation theatres [10, 32]. In addition, even under ideal conditions, the management of extensive bone defects remains challenging regarding bone stabilization, available bone stock for grafting, and time to bone union. Therefore, amputation can be considered in these massive multi-tissue defects for which vascularized transfers or bone transport seem inappropriate. In our experience, the Masquelet technique sometimes permits limb salvage in such extreme clinical presentations, provided infection is absent or under control (Fig. 5). These massive reconstructions frequently involve the combination of simultaneous pedicled flaps with a sequential internal fixation.
Extensive soft-tissue coverage at stage 1
Since micro-vascularized flaps can be hardly achieved on the battlefield or may be contraindicated by associated injuries or vascular complications (e.g., multiple venous thromboses), soft-tissue coverage of extensive defects is performed using simultaneous pedicled flaps [10, 32]. This problem is frequently encountered at the leg level, where local muscle flaps can be combined with local or distant fascio-cutaneous flaps (Fig. 5). In this context, muscle flaps are often preferred for the proximal two- thirds of the tibia (Figs. 2, 3, and 5), but cross-leg flaps are particularly straightforward for distal tibia coverage (Fig. 4). Of course, when feasible, a free latissimus dorsi flap transfer must also be considered.
Considering the large size of the bone defect and the need for dual or triple flap transfers, external fixation is not suitable. Bone stabilization at stage 1 is best achieved using a reinforced spacer with an intramedullary frame (Figs. 4 and 5). A reinforced spacer offers several advantages in this situation: 1) it is a quick and safe procedure that is perfectly suited to complex soft-tissue reconstruction, 2) the risk of bacterial adhesion is low, 3) the easy hardware removal facilitates possible subsequent bone debridement in case of septic recurrence, and 4) there are no risks related to pin-tract infection during the conversion to definitive fixation .
Massive bone grafting with highly stable fixation at stage 2
Reconstruction of large bone defects requires highly stable internal fixation during stage 2. Intramedullary nailing is preferred from a mechanical perspective. This also brings the advantage of limiting the graft volume. However, in cases of extensive bone defect, the mechanical stability obtained with a standard locked nail can be insufficient for bone graft integration within the IMT. In such situations, nailing can be combined with a locking plate or a free fibular strut placed within the membrane . This fibular segment also permits limiting the volume of cancellous bone graft, which can be considerable in cases of metaphyso-diaphyseal defect (Fig. 5). Mixing autograft with allograft or bone substitute is necessary for such massive bone grafting. Conventionally, the ratio of allograft/autograft should not exceed 1:3 because allograft does not contain stem cells or growth factors . However, Pesciallo et al.  recently found that a higher proportion of allograft (up to 64%) achieves similar union and failure rates than those reported for similar series that relied on lower allograft proportions. Masquelet  also stressed that the membrane cavity must be fully filled to avoid down-migration of the graft due to gravity in a standing position and subsequent proximal non-union.
The “Capasquelet” is an alternative strategy described by Combal et al.  for reconstruction of femoral bone defects exceeding 10 cm. This two-stage hybrid approach combines the Masquelet technique and the allograft technique with inlay of a vascularized fibula (i.e., Capanna technique) [48, 49]. At stage 2, a vascularized fibular autograft is embedded in a prepared fresh femoral allograft with a proximal and distal overlap of 2 cm. Stable bone stabilization is obtained by the combination of this inlay bone graft with a locking plate. The preliminary results of this innovative technique are encouraging with bone union being achieved within a short time, thereby allowing early full weight bearing . However, as it requires femoral allograft access and microsurgery skills, the “Capasquelet” might not be the easiest solution in a combat-related situation due to limited resources, with associated soft tissue and potential vascular lesions.
Bone reconstruction in the field
Contrary to micro-vascularized bone transfers or bone transport procedures, the Masquelet technique can be applied with limited resources in the austere environment of forward surgical units or improvised field hospitals [12, 15, 17, 22]. Although several barriers may impede its application, we believe that IMT is the best option for large bone defect reconstruction in such settings. Various technical tricks help to avoid these obstacles and achieve bone union.
Challenge 1: infection control
This is the main difficulty on the battlefield due to delayed surgical management with limited resources. Stage 0 must include serial debridement sessions with appropriate antibiotic medication and negative wound pressure therapy to avoid iterative environmental contamination [4, 43]. Next, a stable soft-tissue envelope must be reconstructed at stage 1, considering that the choices for soft-tissue coverage methods are always restricted in this setting . In addition to these surgical challenges, it is also crucial to have laboratory resources permitting bacteriological cultures with precise germ identification and to be capable of providing an adapted and extended antibiotic treatment. In the Sahel, we found that the latter point was a frequent issue when managing local patients with combat-related bone defects .
Challenge 2: limitation in surgical cement
PMMA cement can be lacking in forward surgical units that are not dedicated to performing bone reconstruction. Similarly, the absence of PMMA often precludes the use of the Masquelet technique in developing countries . To avoid this obstacle, Mozumder et al.  achieved IMT using a polypropylene spacer made from disposable syringes in Bangladesh. They observed results comparable with those obtained with a PMMA spacer for long-bone reconstruction . Successful metacarpal bone reconstructions were also achieved using disposable syringes as spacers in a forward surgical unit . A recent experimental study demonstrated that polypropylene spacers induce membrane encapsulation with histologic characteristics and bone regenerative capacities that seem like those of PMMA spacers. These findings support the possibility of a cementless Masquelet technique in cases of PMMA shortage caused by a lack of resources .
Challenge 3: limitation in available bone stock
Allograft, bone substitute, or sophisticated bone harvesting devices, such as the reamer/irrigator/aspirator (RIA), are usually not available in battlefield medical treatment facilities [43, 51]. As a result, management of large long-bone defects can be compromised by the lack of autograft during stage 2. However, various technical tricks permit limiting the required volume of cancellous graft.
The use of intramedullary nailing is critically important when the patient’s bone stock is limited or the defect is extensive. The nail acts like a central core limiting the bone graft volume to be applied inside the membrane. When intramedullary nailing is not suitable, a central fibular strut is an interesting option limiting the cancellous bone graft quantity and adding mechanical stability to the bone fixation method, be it for external fixation or plating (Figs. 3 and 5).
A non-vascularized fibular graft combined with IMT seems to be a valid alternative to the conventional micro-vascularized fibular bone transfer [8, 52,53,54,55]. The membrane ensures progressive graft revascularization, avoiding the pitfalls of non-vascularized fibular graft. Using this technique, Fitoussi and Ilharreborde  obtained satisfying results for the reconstruction of large bone defects in children. Masquelet  previously reported similar outcomes in adult patients but faced late stress fracture, which suggested insufficient graft revascularization. He subsequently improved the technique by performing multiple perforations in the fibular graft, using a 2-mm drill to permit penetration of the vascular buds generated by the membrane. Several African authors have recently reported similar results confirming the relevance of this technique in low-resource settings [54, 55]. Thus, the combination of a multiperforated fibular graft with cancellous autografts in an IM seems to be a reliable strategy to achieve bone union in local patients treated in the field for large bone defects (Figs. 3 and 5).
Under certain conditions, limb shortening may be considered to limit the extent of the bone defect. At the humerus, a 3–4 cm shortening can be tolerated without significant functional impairment (Table 1) . In the lower extremity, femur or tibia shortening must remain the exception and should not exceed 2 cm. However, such shortening should probably be contraindicated at the tibia level when the fibula is intact, since the fibula should be used as a support for tibia reconstruction [3, 6, 8, 9, 43].
Future directions to improve Masquelet technique outcomes
Various approaches are currently being developed worldwide to refine IMT and promote its efficiency. These approaches mainly focus on four different aspects: 1) substitution of the standard PMMA spacer with another biomaterial able to generate an IM exhibiting at least similar osteogenic properties to those conferred by PMMA, 2) enhancement of the quality and the viability of ABG implanted into the IM cavity, 3) substitution or combination of ABG with synthetic scaffolds presenting increased osteogenic properties, and 4) IMT conversion into a single-step procedure by performing an “off the shell” membrane strategy.
Alternative membrane inductors
Various biomaterials have been evaluated for their capacity to generate osteogenic IM in animal models as alternatives to PMMA: smooth or roughened titanium , silicone , calcium sulfate spacers , and polypropylene syringe bodies . Interestingly, Toth et al.  determined whether spacer material modification or topography alteration could change biochemical IM environment or bone reconstruction efficiency. By inducing IM in rat models using smooth or roughened PMMA and titanium, they showed that titanium induced membranes were around 35% thicker than PMMA (with better barrier properties), and the inflammatory factor IL-6 was around 35% higher in the roughened groups than smooth groups, potentially suggesting indirect repair enhancement. They concluded that smooth PMMA-IMs promoted better bone regeneration than the three other groups. According to Sagardoy et al. , silicone spacers inserted in rat bone defects generated IM with similar biological and histological properties (IM thickness, vessel density, BMP2 and VEGF content) to PMMA-triggered IM. Furthermore, the authors noted that silicone spacers were easier to remove than PMMA spacers at the end of IM induction time. In an 8-week study in an IMT rat model, Ma et al.  demonstrated that morphological characteristics of IM around calcium sulfate spacers were similar to those around PMMA, whatever the considered kinetic time. However, they suspected that calcium sulfate-IMs were thicker than PMMA-IMs and that even if not significant, endochondral ossification and higher expression levels of VEGF, TGF-1, and BMP-2 were detected in calcium sulfate-IM compared to PMMA-IM. Lastly, it was recently found that polypropylene-IM exhibited similar histologic characteristics and bone regenerative capacities to PMMA–IM [12, 20]. Overall, from the military surgery point of view and to answer recurrent clinical needs of orthopedic surgeons, a spacer that is easy to handle or insert into the bone defect (in stage 1) and convenient to extract from the IM cavity (in stage 2) will be preferred in the future.
Autologous bone grafting optimization
Sparse clinical investigations have compared bone union rates obtained with IMT using ABG collected from iliac crests and the RIA technique. Globally, a similar union rate was observed in both groups, but the graft volume collected from RIA was slightly higher (average 47 cm3 vs. 37 cm3, respectively), with few postoperative complications (including iatrogenic femur fracture) [7, 38, 51]. In an IMT rat model, Sun et al.  modified the graft harvest technique to reduce the cortical content of the graft and minimize the graft preparation time. They found that these modifications achieved a bone union rate much higher than that obtained using conventional graft harvesting (92% vs. 36%). Thus, scrupulous graft preparation could also ameliorate the outcome of the IMT procedure in patients.
The addition of biological additives (cells or growth factors) to ABG during stage 2 was proposed to support new bone formation . Experimental studies demonstrated improved bone union after incorporation of concentrated growth factors or BMP-7 in rabbits [61, 62]. However, in clinical practice, the effects of supplementing grafts with BMP-2 or BMP-7 are unclear and growth factors utilization is entirely dependent on surgeon preference . The addition of recombinant growth factors is in fact debated since no clinical comparative study has proven their value so far. Masquelet and Bégué  have observed that it could be deleterious to associate BMPs with the graft material inside the IM. Localized high density of the product and possible effects of competition with growth factors secreted by the membrane can lead to partial resorption of the graft .
Lastly, Luangphakdy et al.  found in a caprine model that a simple scrapping of the IM after spacer removal and prior to grafting may improve healing of segmental bone defects. This removal of the IM inner layer induced bleeding while preserving the mechanical and biological function of the rest of the membrane. Micro-CT showed that scrapping almost double the amount of total bone within the defect 12 weeks post-grafting.
One of the most exciting new areas is the convergence of the Masquelet technique with scaffold guided bone engineering. Scaffolds provide attractive alternatives to conventional bone grafting serving as three-dimensional structures to guide cell migration, proliferation, and differentiation. In load bearing tissues, they also serve as temporary mechanical support structures . The ability of 3D-printing allows the design and manufacture of osteoconductive scaffolds which are optimized for clinical translation in terms of pore size, layering, and degradation [66, 67]. Mainly to overcome graft limitation quantity, a huge diversity of synthetic scaffolds has been developed in preclinic models to be mixed with the ABG during stage 2 . Some of them have been tested clinically [68,69,70,71]. Tetsworth et al.  achieved very acceptable outcomes in 5 cases of femoral bone defects treated by patient-specific 3D printed titanium cages. Van Vugt et al.  implanted a combination of bioactive glass and bone marrow aspirate concentrate in 4 patients who all exhibited complete bone repair and functional recovery. In a larger series, Gupta et al.  treated 42 patients with postinfective segmental bone defects using ABG mixed with beta tri-calcium phosphate (B-TCP)-based composite ceramic (34 patients) or ABG alone (15 patients). They found that B-TCP is an efficacious bone-graft expander in the IMT despite the bone union rate of this group was lower (81% vs. 100% with index bone grafting). Always to reduce the required amount of bone graft, but also to main graft position and shape, Cho et al.  used a circumferential graft around an absorbable gelatin sponge (the gelatin sponge core was about 21.4% of the bone defect volume) leading to an 86% bone healing rate in 21 patients.
Toward a single-stage Masquelet technique
To allow a quicker healing time with fewer surgical procedures for the patient, a strategy could be to bypass the membrane induction time by applying a commercial off-the-shelf membrane concomitantly to the bone graft. Interestingly, maxillofacial surgery already uses such a strategy, better known as guided bone regeneration (GBR). In GBR, the implantation of membranes made of natural (collagen, chitosan, alginate) or synthetic polymers [resorbable aliphatic polyesters, including polylactic acid and polycaprolactone or non-resorbable polytetrafluorethylene (PTFE)] in combination with grafting materials is commonly applied to treat peri-implant bone deficiencies or alveolar bone reconstruction. GBR membranes act as passive membranes hindering the soft-tissue invasiveness of the defect. Emerging data also suggest that GBR membranes may bioactively contribute to bone regeneration . The application of GBR membranes to replace the Masquelet membrane for the treatment of long-bone defects has gained some attention in the last ten years. For example, in a rabbit model, Tarchala et al.  compared the healing efficiency of ulna bone defects treated by a standard IM or a synthetic non-resorbable PTFE membrane filled with allograft. The bone defect repair was similar in both experimental arms, underlying the promising potential for the treatment of synthetic PTFE membranes. However, because PTFE is a non-absorbable material, more experimental studies using absorbable membranes are needed to validate the streamlining toward a single-stage IMT procedure. In this context, a French research team examined the use of human amniotic membranes as Masquelet membrane alternatives. Human amniotic membranes and Masquelet IM share similar biological properties [74,75,76]: both are highly organized tissues containing growth factors such as VEGF and TGF-β1, expressing anti-inflammatory proteins and displaying osteogenic properties. Recently, Fenelon et al.  showed that no difference existed in the bone regeneration potential of femoral critical-size defects in rats between the two-step IM procedure and the single-step approach using human amniotic membranes.
All these future directions are promising approaches to improving IMT outcomes. However, in a military practice context, surgeons often deal with limited resources. Thus, valuable replacement solutions to the IMT standard of care could include ready-to-use implantable medical devices presenting large-scale manufacturing facilities, easy sterilization processes, and convenient storage modes. We believe disposable polypropylene syringe bodies are an example of a promising alternative spacer to standard PMMA cements in IMT in a military practice context or low-resource environment.
The Masquelet IMT offers a successful possibility to solve long-bone defects encountered in military practice. Reconstruction of combat-related bone defects often requires prior infection control and soft-tissue reconstruction during stage 1. Providing those requirements are met, IMT even allows bone reconstruction in the austere environment of field medical treatment facilities. However, specific surgical tactics, such as combined inter-tibiofibular grafting or sequential internal fixation, may be required. We believe that this simple, reliable, and replicable procedure should be considered as a technique of choice for the reconstruction of multi-tissue defects resulting from missile or blast injuries.
Availability of data and materials
Autologous bone graft
Bone morphogenic protein-2
Bone morphogenic protein-7
Beta tri-calcium phosphate
Damage control orthopedics
Guided bone regeneration
Induced membrane technique
Transforming growth factor-β1
Vascular endothelial growth factor
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The authors thank Alain Charles Masquelet for his teaching and long-term support in their clinical practice and research.
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Mathieu, L., Mourtialon, R., Durand, M. et al. Masquelet technique in military practice: specificities and future directions for combat-related bone defect reconstruction. Military Med Res 9, 48 (2022). https://doi.org/10.1186/s40779-022-00411-1
- Bone defect
- Induced membrane technique
- Gunshot wound
- Low resources
- Masquelet technique
- War surgery