Proceedings of the Texas A&M Medical Student Grand Rounds

Utilizing 3D Printing for Better Outcomes in Osteonecrosis of the Femoral Head

July 30, 2021 Aaron Kim

Aaron Kim

Introduction. Osteonecrosis of the femoral head (ONFH) is often called the “coronary artery disease of the hip” because it is cause by similar ischemic conditions1. An occlusion of the arteries surrounding the femoral head leads to progressive necrosis, further resulting in compromised subchondral circulation, accumulation of microfractures, and eventual collapse of the subchondral bone. Because most individuals affected by ONFH are in their 30s and 40s and the fact that hip injuries are correlated with increased morbidity and mortality, 3D printed bone scaffolds can improve outcomes for this potentially deadly disease.2 The main treatment for ONFH has been core decompression which involves drilling a channel in the necrotic portion of the femoral head and allowing new bone to form. However, the growth is slow and leaves the patient vulnerable to femoral head collapse. To prevent this outcome, 3D printed bone scaffolds can be used to provide structural and cellular support to the core decompression channel while also promoting osteogenesis. Methods. First generation 3D printed porous titanium alloy rods were constructed by 3D printing Ti-6Al-4V sphere powder in a configuration that mimicked human trabecular bone with an 84.21 ± 0.19% porosity.4 Second generation scaffolds were constructed with medical grade polycaprolactone (PCL) and β-TCP 3D printed in a graded porous configuration that matched the surrounding bone tissue.5 Third generation bone scaffolds were constructed from PCL and nano-hydroxyapatite in a porous 3D printed configuration with a center channel for calcium peroxide encapsulated in gelatin spheres and bone marrow mononuclear cells.6 Results. 3D printed biodegradable scaffolds loaded with bone mesenchymal stem cells and calcium oxide were shown to increase new bone tissue ingrowth and proliferation. Bone scaffolds loaded with both calcium oxide and stem cells had greater new bone formation, revascularization, and survivability of stem cells than bone scaffolds alone or bone scaffolds with calcium carbonate6. Conclusion. These studies have shown that 3D printed degradable bone scaffolds loaded with stem cells and oxygen generating compounds have a significant increase in bone regeneration when compared to core decompression alone. This indicates that a combination of core decompression and 3D printed bone scaffolding may lead to better outcomes in the treatment of ONFH. Some limitations of this review are that all experiments were conducted on animal models and that structural support is still a limiting factor of these 3D printed bone scaffolds.

  1. Baig SA, Baig MN. Osteonecrosis of the Femoral Head: Etiology, Investigations, and Management. Cureus. 2018;10(8):e3171-e3171. doi:10.7759/cureus.3171
  2. Petek D, Hannouche D, Suva D. Osteonecrosis of the femoral head: pathophysiology and current concepts of treatment. EFORT Open Rev. 2019;4(3):85-97. doi:10.1302/2058-5241.4.180036
  3. Polo-Corrales L, Latorre-Esteves M, Ramirez-Vick JE. Scaffold design for bone regeneration. J Nanosci Nanotechnol. 2014;14(1):15-56. doi:10.1166/jnn.2014.9127
  4. Wang C, Xie Q, Yang L, et al. A 3D printed porous titanium alloy rod with biogenic lamellar configuration for treatment of the early-stage femoral head osteonecrosis in sheep. Journal of the Mechanical Behavior of Biomedical Materials. 2020/06/01/ 2020;106:103738. doi:https://doi.org/10.1016/j.jmbbm.2020.103738
  5. Kawai T, Shanjani Y, Fazeli S, et al. Customized, degradable, functionally graded scaffold for potential treatment of early stage osteonecrosis of the femoral head. J Orthop Res. Mar 2018;36(3):1002-1011. doi:10.1002/jor.23673
  6. Wang C, Xu H, Liu C, et al. CaO2/gelatin oxygen slow-releasing microspheres facilitate tissue engineering efficiency for the osteonecrosis of femoral head by enhancing the angiogenesis and survival of grafted bone marrow mesenchymal stem cells. 10.1039/D0BM02071K. Biomaterials Science. 2021;doi:10.1039/D0BM02071K

 

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