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Biomedical subjects

D Checkley

Publications and source records attributed to D Checkley.

6 recordsLinked to original sources

High-resolution NMR imaging of an antigen-induced arthritis in the rabbit knee.

High-resolution, serial, spin-echo images were obtained for an antigen-induced knee arthritis in six rabbits. The animals were imaged prior to intra-articular challenge and at various time points up to 14 weeks after challenge. Extensive high-signal inflammatory changes were seen at Day 1 in the lymph node, capsule, and surrounding muscle. The muscle and lymph node response decreased rapidly after the first week. The capsule high-signal area reached a maximum at Day 10, but was still extensive at Day 39. The infrapatellar fat pad was replaced more slowly by high signal and the appearance of high signal in both the tibia and femur was a late change. Terminal histological examination showed that the capsule and fat pad high-signal areas corresponded to fibrous and synovial proliferation. The bone changes were a result of edema and cyst formation. The separation of the various time courses of the inflammatory changes may be of value in understanding the model and evaluating potential anti-arthritic drugs.

Animals

Detection of myocardial infarction in the mini-pig using NMR imaging.

Spin-echo images of 10 myocardial infarcts in nine mini-pigs were obtained at 30 h, 3 days, and approximately 10 days postinfarction. Infarcts were not detected at all at 30 h in five out of five cases examined. At 3 days postembolization (six cases) one infarct was certainly detected, whilst at 10 days (nine cases) all infarcts were seen as high-signal areas in long TE spin-echo sequences. After 2 weeks no further infarct signal change was detected (three cases), but myocardial thinning became more evident. Using techniques similar to those reported here, early postinfarct changes in the dog have been detected by other authors. Possible reasons for this difference between pig and dog are discussed.

Animals

A method for the clinical measurement of relaxation times in magnetic resonance imaging.

A method for the determination of relaxation times in clinical magnetic resonance images is described. Three components are measured: the spin-lattice (T1) and spin-spin (T2) relaxation times and the proton density (M infinity). These components are separated in the algorithm to give increased tissue discrimination. Multiple data points are used to minimise error and increase reproducibility. Errors that arise in imaging data because of the short sequence repetition periods are considered and a technique for their reduction described. Clinical results obtained using the method are reviewed. These results demonstrate the clinical utility of the technique.

Computers