Manufacturers and suppliers, described here as sponsors, who wish to have products approved and listed for use in Australian hospitals must follow a defined process. They must obtain an Australian Registered Therapeutic Goods number (ARTG) for the product to be used. For benefits to be paid for prostheses used under private health insurance arrangements a catalogue number is obtained after being approved through the Prosthesis Listing Advisory Committee (PLAC). Under PLAC each group of like prostheses is assessed by a Clinical Advisory group. (Hip Prosthesis Clinical Advisory Group, Knee Prosthesis Clinical Advisory Group). Existing criteria are being enhanced as to the levels of evidence required for listing approval. Essentially for joint replacements which are weight-bearing and in category three a two year clinical trial will almost always be necessary for any new prosthesis. Products must bw considered as non-inferior to comparator products.
The advent of the Australian National Joint Replacement Registry has been an outstanding success in identifying prosthesis with higher than average failure rates, but it is principally a measure of revision rates for specific prostheses. In order to consider the causes of failure it is necessary to start at the point where prostheses are able to enter the Australian market through the Therapeutic Goods administration, Australian Registered Therapeutic Goods list (ARTG) and consider each of the steps of the joint replacement procedure from that point to well beyond the operation date. This ARTG listing process as it now exists is described and an explanation of how this process may need to be reformed if the occasionally very inadequate prosthesis is to be eliminated from the Australian market. Other matters that may be predictors of variable outcomes include hospital case volume, surgeon experience, patient selection and pre-operative planning. Intra-operative factors that lead to failure, including from infection, will include surgical approaches, operative technique, instrumentation, wound care and theatre discipline. Post operatively patient factors, particularly falls and osteoporosis, will influence long-term outcomes as will prosthesis performance. Further concern has been the advocacy by some by what might be considered, fashionable orthopaedics, but the literature to date has demonstrated little benefit from endeavours such as minimal invasive surgery and two-incision hip replacement. Gender specific prostheses and navigation have yet to make their mark as a universally accepted method of performing joint replacement surgery and there may be some negative issues with these matters.
The reproduction of ideal offset is an aim of hip replacement. Determining this measurement from traditional radiology techniques is inaccurate because femoral neck anteversion will foreshorten the femoral neck offset in a standard two dimensional x-ray making the measurement “apparent”. A novel method of determining offset is presented. A computer software program has been developed for pre-operative planning of joint replacements, (Orthopaedic Work Station) The program relies on using a CT scout film for magnification correction and to determine measurement parameters including leg length difference. It was recognised that by collecting extra cross-sectional references that three-dimensional measurement of offset would be possible. The CT scanner has software that allows determination of:
The location of the centre of the femoral head The centroid of the femoral shaft at a point just below the lesser trochanter The centroid of the femoral shaft at a point 150mm below the lesser trochanter For this study the line joining the two centroids is considered the longitudinal axis of the femur. The CT scanner has software that also allows for the centroids to be moved along the longitudinal axis into the plane represented by a perpendicular line from the longitudinal axis to the centre of the femoral head. It is a simple matter to measure the distance between the centroid and the centre of the femoral head to obtain a true offset. A phantom femur was measured using the radiology method described and then measured directly. Exact correlation was established. A study of inter-observer measurement has shown statistically consistent agreement using six observers in twenty cadaver femurs. The method is accurate and uses existing data collected as part of the pre-operative planning process. CT scanning prior to hip replacement, gives less radiation exposure and is more efficient with respect to radiology services than conventional radiology. An intraoperative study may require ethics approval.
In relation to the conduct of this study, one or more the authors have received, or are likely to receive direct material benefits.
Various assumptions must be made during total hip replacement when placing the acetabular component within the reamed acetabulum with regards to its orientation. Various methods have been described for different acetabular components, some relying on knowledge of the existing anatomy and some relying on the use of jigs to align the component. Many of these assumptions are based on opinion rather than science and the current study was designed to define the position of the acetabulum in relation to a fixed position of the pelvis. A neutral position of the pelvis must be defined and this is represented by having a line from the anterior superior iliac spine to the pubis fixed in the coronal plane and taking measurements of the perpendicular axis of the pelvis taken from this. A variety of measurements were made using measurement techniques and the conclusion was reached that the average angle for operative inclination is 43 degrees ± 5 degrees and the average angle for operative anteversion is 29 degrees ± 8 degrees. These figures should give a preliminary guide to the correct placement of the acetabular socket in total hip replacement although other factors may need to be taken into account.
At this time the majority of acetabular replacements in total hip replacement rely on bone ingrowth or bone ongrowth. Long term success has been well established but is this success the result of good luck or good management? Numerous systems exist with the simplest perhaps being that of the placement of a hemispherical cup in a hemispherically reamed acetabulum. Beyond this, a wide variety of added complexity exists with the presumption that these increased complexities provide improved stability and hence more secure primary and secondary fixation. The computer model that has been established demonstrates the geometry of fixation of hemispherical cups as compared to rim fit cups and looks at the requirements of acetabular distortion before secure fixation can be achieved. The model attempts to explain why on some occasions an apparently ideally reamed acetabulum is not secure without some form of augmentation of fixation. The model provides a basis for considering the various options of acetabular fixation.
Shelf arthroplasty is briefly reviewed in historical perspective and the results in 45 hips (39 patients) which had undergone this procedure at the Royal Children's Hospital are presented. The majority of these patients were adolescents who had previously been treated for congenital dislocation or subluxation of the hip. The indications for operation and the operative technique are discussed. Clinical examination was carried out upon 33 of the 39 patients at an average of 11 years after operation. The results suggested that where pain had been an indication for operation almost 80 percent of the hips remained relatively free of symptoms at the time of follow-up and in those patients where acetabular dysplasia had been an indication, the coverage remained good and pain had not appeared. It is concluded that the shelf operation is useful for dealing with both pain and dysplasia in the adolescent.