In total knee arthroplasty (TKA) the knee may be found to be too stiff in extension, causing a flexion contracture. One proposed surgical technique to correct this extension deficit is to recut the distal femur, but that may lead to excessively raising the joint line. Alternatively, full extension may be gained by stripping the posterior capsule from its femoral attachment, however if this release has an adverse impact on anterior-posterior (AP) stability of the implanted knee then it may be advisable to avoid this technique. The aim of the study was therefore to investigate the effect of posterior capsular release on AP stability in TKA, and compare this to the restraint from the cruciate ligaments and different TKA inserts. Eight cadaveric knees were mounted in a six degree of freedom testing rig (Fig.1) and tested at 0°, 30°, 60° and 90° flexion with ±150 N AP force, with and without a 710 N axial compressive load. The rig allowed an AP drawer to be applied to the tibia at a fixed angle of flexion, whilst the other degrees-of-freedom were unconstrained and free to translate/ rotate. After the native knee was tested with and without the anterior cruciate ligament (ACL), a cruciate-retaining TKA (Legion; Smith & Nephew) was implanted and the tests repeated. The following stages were then performed: replacing with a deep dished insert, cutting the posterior cruciate ligament (PCL), releasing the posterior capsule using an osteotome (Fig. 2), replacing with a posterior-stabilised implant and finally using a more-constrained insert.Introduction
Methods
The primary aim of this study was to evaluate the performance
and safety of magnetically controlled growth rods in the treatment
of early onset scoliosis. Secondary aims were to evaluate the clinical
outcome, the rate of further surgery, the rate of complications,
and the durability of correction. We undertook an observational prospective cohort study of children
with early onset scoliosis, who were recruited over a one-year period
and followed up for a minimum of two years. Magnetically controlled
rods were introduced in a standardized manner with distractions
performed three-monthly thereafter. Adverse events which were both related
and unrelated to the device were recorded. Ten children, for whom
relevant key data points (such as demographic information, growth
parameters, Cobb angles, and functional outcomes) were available,
were recruited and followed up over the period of the study. There
were five boys and five girls. Their mean age was 6.2 years (2.5
to 10).Aims
Patients and Methods
