Thoracic stenosis causing lateral compression of the spinal cord in two immature Dogues de Bordeaux.

This case report describes a novel developmental vertebral malformation in two young Dogues de Bordeaux, which was diagnosed by magnetic resonance imaging. Both dogs were treated surgically with reasonable success.

Radiographic and clinical features of carpal varus associated with chronic sprain of the lateral collateral ligament complex in 10 dogs.

Lameness associated with carpal varus deformity was recognised in 10 dogs, eight of which were Dobermann Pinschers. The dogs had a mean age of seven years and nine months. Carpal varus was usually bilateral with concurrent carpal hyperflexion and pronation. Carpal varus was present prior to the onset of lameness in four cases. With stress radiography the median angle of varus deviation in all carpi was 14.6 degrees , and an increase in the size of the ulnar /ulnar carpal bone joint space was seen in six of the seven dogs. Radiographic changes included: enthesophyte formation at the proximolateral aspect of metacarpal V, periarticular soft tissue swelling, especially lateral, bone proliferation at the carpometacarpal joint I and enthesophyte formation at metacarpophalangeal joint V. Four dogs were admitted for problems other than carpal varus and lameness was not treated. Five dogs were treated with nonsteroidal anti-inflammatory drugs, but lameness was not completely resolved and became exacerbated with exercise. One dog was successfully treated by pancarpal arthrodesis.

Impaction grafting with morsellised allograft and tricalcium phosphate-hydroxyapatite: incorporation within ovine metaphyseal bone defects.

An ovine model was used to investigate the in vivo properties of impacted tricalcium phosphate-hydroxyapatite (TCP-HA) aggregates, varying in chemical composition (ratio of TCP to HA) and particle size distribution (8 versus 3 particle size ranges). All pellets were impacted to a standard compactive effort. Eight sheep underwent implantation of pellets in 4 metaphyseal defects in both rear limbs. Treatment groups consisted of: (1) allograft (clinical control). (2) 50/50 allograft/80% HA/20% TCP in 8 particle size ranges, (3) 50/50 allograft/80% TCP/20% HA in 8 sizes and (4) 50/50 allograft/80% HA/20% TCP in only 3 sizes of particles. Healing of defects was evaluated at 14 weeks with computed tomography, histology and histomorphometry. The computer tomography (CT) density measured in all defects containing synthetic agents was higher than in defects filled with allograft alone (p<0.01). Defects containing 8 sizes of 80% HA/ 20% TCP granules (group 2) achieved lower histological scores and contained less bone than the clinical control (p<0.05), whereas groups 3 and 4 did not differ from the control. Although all synthetic agents were osteoconductive, our results suggest that increasing the ratio of TCP over HA and limiting the number of particle size ranges to 3 instead of 8 improve the performance of impacted aggregates as graft expanders. Evaluation under loading conditions of morsellised allograft expanded with 80% TCP/20% HA (BoneSave) in 3 particle size ranges is warranted.