Abstract
Introduction and Aims: Bone cement (Polymethylmethacrylate) is commonly used to augment internal fixation in osteoporotic bone. An inconsistency exists among surgeons regarding the appropriate mixing time for bone cement to achieve optimal screw purchase. The study addresses the effect of cement viscosity on fixation augmentation in both healthy and simulated osteoporotic canine bone.
Method: Fourteen canine femora were plated using eight-hole DC plates and 3.5mm screws, repairing transverse diaphyseal osteotomies with and without a gap. In the left femora, cement was mixed for one minute (liquid) prior to injection into drilled and tapped holes that were either properly sized (2.5mm) or over-drilled (3.2mm) to simulate osteoporotic bone. In the right femora, cement was mixed for five minutes prior to injection (thick paste). Four-point bending stiffness for each plated construct was normalised to baseline stiffness, followed by failure loading.
Results: Within the properly sized holes, there were no significant differences in bending stiffness with or without a gap at the fracture site. The liquid cement had a force to failure 77% greater than that of cement as a paste (p< 0.05).
Within the over-sized holes simulating osteoporotic bone, there was no difference between liquid and paste without a gap. With a gap, liquid cement demonstrated an increased bending stiffness of 24% (p< 0.05) and force to failure was 92% higher (p< 0.05).
Bone cement in its liquid state may provide increased structural support in the setting of an osteoporotic fracture, possibly due to increased interdigitation of the cement with the screw threads and bone.
Conclusion: In a canine diaphyseal fracture model, screw insertion into liquid cement achieves greater bending stiffness and resists a greater load to failure than insertion into cement with the consistency of a paste.
These abstracts were prepared by Editorial Secretary, George Sikorski. Correspondence should be addressed to Australian Orthopaedic Association, Ground Floor, The William Bland Centre, 229 Macquarie Street, Sydney, NSW 2000, Australia.
At least one of the authors is receiving or has received material benefits or support from a commercial source.
