1. Currently available total replacement hip and knee prostheses were tested in a machine enabling flexion-extension movements to be applied whilst the prostheses were surrounded with Ringer's solution or other liquid and loaded within the physiological range. 2. Prostheses of which both components were made in cobalt-chromium-molybdenum alloy produced visible quantities of alloy particles, whose sizes ranged down to about 0·1 microns, and cobalt and molybdenum ions in solution. 3. No metallic or plastic particles were detected during tests on a hip prosthesis made of stainless steel and high density polyethylene. 4. The frictional moments in cobalt-chromium-molybdenum hip prostheses were higher than in stainless steel-polyethylene hip prostheses, by a factor of at least 2 to 1. 5. It is accepted that the conditions of these tests were probably more severe than in life, but the difference is held to be one of degree and not one of kind. 6. The particulate alloy debris, when injected in massive doses into the muscles of rats, gave an incidence of malignant tumours which was comparable to that already established for pure cobalt powder, whereas particles of several other metals, tested in the same way, gave no tumours. 7. It is argued that the particles which are known to be produced in at least some patients using cobalt-chromium-molybdenum total replacement joint prostheses constitute a risk of tumour formation which is certainly small, possibly negligible, but not accurately calculable at present. 8. The results of these tests, particularly the differences in frictional moment and in the production of particulate debris, suggest a preference for high density polyethylene as one component of a total joint replacement prosthesis

Aims

Arthroplasty surgery of the knee and hip is performed in two to three million patients annually. Periprosthetic joint infections occur in 4% of these patients. Debridement, antibiotics, and implant retention (DAIR) surgery aimed at cleaning the infected prosthesis often fails, subsequently requiring invasive revision of the complete prosthetic reconstruction. Infection-specific imaging may help to guide DAIR. In this study, we evaluated a bacteria-specific hybrid tracer (^99mTc-UBI_29-41-Cy5) and its ability to visualize the bacterial load on femoral implants using clinical-grade image guidance methods.

We aimed to obtain anthropometric data on Korean knees and to compare these with data on commonly available total knee arthroplasties (TKAs). The dimensions of the femora and tibiae of 1168 knees were measured intra-operatively. The femoral components were found to show a tendency toward mediolateral (ML) under-coverage in small femurs and ML overhang in the large femurs. The ML under-coverage was most prominent for the small prostheses. The ML/anteroposterior (ML/AP) ratio of Korean tibiae was greater than that of tibial components.

This study shows that, for different reasons, current TKAs do not provide a reasonable fit for small or large Korean knees, and that the ‘gender-specific’ and ‘stature-specific’ components help for large Korean femurs but offer less satisfactory fits for small femurs. Specific modifications of prostheses are needed for Asian knees.

1. Fourteen patients whose Kienböck's disease was treated by prosthetic replacement, and who have had an acrylic lunate prosthesis in place for periods of eight to twenty years, have been reviewed.

2. In most patients pain, weakness and limitation of movement are less than they were before operation. Four wrists are completely painless and the other ten have only occasional slight pain. The average range of antero-posterior movement is 100 degrees.

3. Radiological signs of osteoarthritis are either absent or slight in ten wrists: this is considered to be due to the success of the prosthesis in maintaining the carpal architecture, even after prolonged heavy use.

The use of silicone inner sockets, with or without the incorporation of shuttle locks, has greatly improved the function of artificial limbs. They cushion and protect the stump and provide a means for prosthetic suspension, allowing more comfortable use, especially in patients with ischaemic stumps. They also allow greater movement at the proximal joint.

1. A prosthesis under myo-electric control is described.

2. An advanced technique of proportional control of such a prosthesis is outlined.

1. The working of an electrically powered prosthesis is described.

2. The advantages of this method are discussed.

1. The use of acrylic cement in bonding femoral head prostheses to bone is described.

2. No sign of deterioration of the bond between the cement and bone has been seen in histological preparations up to three and a quarter years after operation, and no harmful effects have been recognised, or suspected, in 455 patients in whom it has been used.

3. The technique is considered justifiable in elderly patients where the medullary canal is large and the cortex of the femur is thin and brittle.

1. Experience with a refined type of implantable electrode for the myo-electric control of externally powered prostheses is reported.

2. The electrodes are externally energised by electromagnetic induction and therefore do not contain any battery cells. The myo-potentials are transmitted in frequency-modulated form and detected by a receiver placed on the skin. The implantable electrode, measuring 5x11x4 millimetres, is encapsulated in epoxy resin.

3. Six electrodes have been implanted in the forearms of two normal subjects and two below-elbow amputees. The time of implantation ranged from three to fifteen months. Macroscopically, a fibrous capsule developed around the electrodes. Histological examination showed a capsule of granulation tissue of varying thickness with slight inflammatory reaction and foreign-body giant cells.

4. In all cases except one the signals received have been of high quality as ascertained by conventional electromyography and frequency analysis. There has been no significant deterioration in signal quality during the follow-up periods.

5. The major source of failure was fatigue fracture of the gold wires making contact with the body tissues. In one case, however, the electrode was still functioning normally at the time of removal fifteen months after insertion.

6. The patients have not been inconvenienced either by the operative procedures or by the presence of the electrodes in the tissues.

Obviously these and other problems need much research, but the preliminary work already done is promising enough to indicate that a useful and dependable prosthesis could be developed to operate by the use of changes of muscle potential, and that such apparatus could be made light enough for practical use at the work-bench and in the home.

In addition to its orthopaedic interest, this case illustrates the special behaviour of fine particles of a synthetic material when implanted in the human body. These results may interest those engaged in the control of dusts in the plastics industry, for the inhalation of such dusts may well result in "implantation" of the material in the lung, with consequent histological changes.

We studied the detection of joint replacements at airport security checks in relation to their weight, using two types of detector arch. A single-source, unilateral detector showed different sensitivities for implants on different sides of a test subject.

All implants weighing more than 145 g were detected by one of the arches. The degree of detection was directly related to the logarithm of the weight of the prosthesis in patients, with a linear correlation (r² = 0.61). A bilateral arch detected all prostheses weighing over 195 g.

With their usual sensitivity settings many joint replacements were detectable; an identification pass containing the site and weight of such prostheses would help to avoid the need for body-search procedures.